Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
---|---|---|---|---|---|
chr17 | 36895120 | 36902180 | enh32187 |
|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
---|---|---|---|---|---|---|---|---|
chr17 | 36899321 | 36899907 | TCF7L2 | GTRD | no | Colon (HCT116) | 108252852 | |
chr17 | 36899380 | 36899964 | ZNF274 | GTRD | no | Bone Marrow (K562) | 108252853 | |
chr17 | 36899461 | 36900257 | TCF7L2 | GTRD | no | Colon (HCT116) | 108252854 | |
chr17 | 36899506 | 36900562 | TCF7L2 | GTRD | no | Colon (HCT116) | 108252855 | |
chr17 | 36899516 | 36899969 | TCF7L2 | GTRD | no | Colon (HCT116) | 108252856 | |
chr17 | 36899542 | 36900582 | TCF7L2 | GTRD | no | Colon (HCT116) | 108252857 | |
chr17 | 36899809 | 36900133 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108252858 | |
chr17 | 36899826 | 36899837 | FOXC1 | JASPAR | yes | 54128085 |
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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