Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
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Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
---|---|---|---|---|---|---|---|---|
chr19 | 3867569 | 3869421 | TCF7L2 | GTRD | no | Colon (HCT116) | 108368702 | |
chr19 | 3867621 | 3869696 | TCF7L2 | GTRD | no | Colon (HCT116) | 108368703 | |
chr19 | 3867673 | 3869442 | TCF7L2 | GTRD | no | Colon (HCT116) | 108368704 | |
chr19 | 3867846 | 3868090 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108368705 | |
chr19 | 3867862 | 3869553 | TCF7L2 | GTRD | no | Colon (HCT116) | 108368706 |
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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