Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
---|---|---|---|---|---|
chr17 | 74962515 | 74968659 | enh4612 |
|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
---|---|---|---|---|---|---|---|---|
chr17 | 74961468 | 74965700 | TCF7L2 | GTRD | no | Colon (HCT116) | 21789177 | |
chr17 | 74961647 | 74965483 | TCF7L2 | GTRD | no | Colon (HCT116) | 21789178 | |
chr17 | 74961654 | 74965625 | TCF7L2 | GTRD | no | Colon (HCT116) | 21789179 | |
chr17 | 74962786 | 74965508 | TCF7L2 | GTRD | no | Colon (HCT116) | 21789181 | |
chr17 | 74964312 | 74964806 | TCF7L2 | GTRD | no | Colon (HCT116) | 21789185 | |
chr17 | 74964563 | 74964827 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 21789186 |
Chrom. | Start | End | Strand | Gene name | Ensembl ID | TSS of gene | Distance between TSS and SNP | Tissue | q Value | id | More |
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