Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
---|---|---|---|---|---|
chr14 | 95980405 | 95994595 | enh15901 |
|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
---|---|---|---|---|---|---|---|---|
chr14 | 95981267 | 95981878 | TCF7L2 | GTRD | no | Colon (HCT116) | 21636731 | |
chr14 | 95981267 | 95981878 | TCF7L2 | GTRD | no | Colon (HCT116) | 108121484 | |
chr14 | 95981267 | 95981878 | TCF7L2 | GTRD | no | Colon (HCT116) | 108121485 | |
chr14 | 95981366 | 95981886 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108121486 | |
chr14 | 95981366 | 95981886 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108121487 | |
chr14 | 95981501 | 95981937 | ZZZ3 | ENCODE Uniform TFBS | no | Blood (GM12878) | 108121492 | |
chr14 | 95981557 | 95981957 | ZZZ3 | ENCODE Uniform TFBS | no | Blood (GM12878) | 108121493 | |
chr14 | 95981817 | 95981836 | REST | JASPAR | yes | 117497651 |
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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