Chrom. | Start | End | Enhancer ID | Tissues that enhancer appears | More |
---|---|---|---|---|---|
chr17 | 1098745 | 1127875 | enh4196 |
|
|
chr17 | 1100738 | 1101160 | vista23645 |
|
Chrom. | Start | End | TF name | Source | Predicted site? | Tissue | id | More |
---|---|---|---|---|---|---|---|---|
chr17 | 1100559 | 1101005 | TCF7L2 | GTRD | no | Colon (HCT116) | 108228112 | |
chr17 | 1100749 | 1101079 | ZZZ3 | ENCODE Uniform TFBS | no | Blood (GM12878) | 21739115 | |
chr17 | 1100749 | 1101079 | ZZZ3 | ENCODE Uniform TFBS | no | Blood (GM12878) | 108228114 | |
chr17 | 1100806 | 1101037 | ZZZ3 | ENCODE Uniform TFBS | no | Blood (GM12878) | 21739116 | |
chr17 | 1100806 | 1101037 | ZZZ3 | ENCODE Uniform TFBS | no | Blood (GM12878) | 108228115 | |
chr17 | 1100813 | 1101053 | ZNF143 | ENCODE Uniform TFBS | no | Embryonic Stem Cell Line (H1-hESC) | 108228116 | |
chr17 | 1100983 | 1101000 | BCL6B | JASPAR | yes | 21180632 | ||
chr17 | 1100983 | 1101000 | BCL6B | JASPAR | yes | 52668105 |
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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