Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
---|---|---|---|---|---|
chr11 | 1845929 | 1854335 | enh62113 |
|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
---|---|---|---|---|---|---|---|---|
chr11 | 1845347 | 1846540 | TCF7L2 | GTRD | no | Colon (HCT116) | 107951899 | |
chr11 | 1845379 | 1846678 | ZNF274 | GTRD | no | Blood (GM12878) | 107951900 | |
chr11 | 1845578 | 1846343 | ZNF274 | GTRD | no | Bone Marrow (K562) | 107951901 | |
chr11 | 1845636 | 1846432 | TCF7L2 | GTRD | no | Colon (HCT116) | 107951902 | |
chr11 | 1845682 | 1846377 | TCF7L2 | GTRD | no | Colon (HCT116) | 107951903 | |
chr11 | 1845821 | 1846585 | TCF7L2 | GTRD | no | Colon (HCT116) | 107951904 | |
chr11 | 1846044 | 1846531 | ZNF274 | GTRD | no | Bone Marrow (K562) | 107951905 | |
chr11 | 1846068 | 1846668 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 107951906 |
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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