ENCODE region-wide location analyses were conducted of binding to the initiation-complex form of RNA polymerase II (Pol2), TATA-associated factor (TAF1), acetylated histone H3 (H3ac), lysine-4-dimethylated H3 (H3K4me2), suppressor of zeste 12 protein homolog (SUZ12), and lysine-27-tri-methylated H3 (H3K27me3). The analyses used chromatin extracted from IMR90 (lung fibroblast), HCT116 (colon epithelial carcinoma), HeLa (cervix epithelial adenocarcinoma), and THP1 (blood monocyte leukemia) cells. The initiation-complex form of Pol2 is associated with the transcription start site, as is TAF1. Both H3ac and H3K4me2 are associated with transcriptionally-active "open" chromatin.
This annotation follows the display conventions for composite tracks. Data for each antibody/cell line pair is displayed in a separate subtrack. See the top of the track description page for a complete list of the subtracks available for this annotation. The subtracks may be configured in a variety of ways to highlight different aspects of the displayed data. The graphical configuration options are shown at the top of the track description page, followed by the list of subtracks. To display only selected subtracks, uncheck the boxes next to the tracks you wish to hide. For more information about the graphical configuration options, click the Graph configuration help link.
Chromatin from each of the four cell lines was separately cross-linked, precipitated with antibody to one of the six proteins, sheared, amplified and hybridized to a PCR DNA tiling array produced at the Ren Lab at UC San Diego. The array was composed of 24,537 non-repetitive sequences within the 44 ENCODE regions.
For each marker, there were three biological replicates. Each experiment was normalized using the median values. The P-value and R-value were calculated using the modified single array error model (Li, Z. et al., 2003). The P-value and R-value were then derived from the weighted average results of the replicates.
The displayed values were scaled to 0 - 16, corresponding to negative log base 10 of the P-value.
Each of the experiments has three biological replicates. The array platform, the raw and normalized data for each experiment, and the image files have all been deposited at the NCBI GEO Microarray Database.
The data for this track were generated at the Ren Lab, Ludwig Institute for Cancer Research at UC San Diego.
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