Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:16644646-16644789 | Common:1; Rare:2 | ||||
chr1:16895618-16895990 | Common:5; Rare:73 | ||||
chr1:16913904-16914115 | Common:7; Rare:43 | ||||
chr1:20655484-20655707 | Common:1; Rare:63; Clinvar (benign):2 | ||||
chr1:21850135-21850460 | Common:3; Rare:104; Clinvar:6 | ||||
chr1:21890046-21890379 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
chr1:22025178-22025515 | Common:7; Rare:84 | ||||
chr1:27625191-27625441 | Rare:49 | ||||
chr1:28458853-28459119 | Rare:54 | ||||
chr1:28581695-28581984 | Common:2; Rare:107 | ||||
chr1:28648296-28648605 | Common:4; Rare:89 | ||||
chr1:30756668-30757060 | Common:1; Rare:61 | ||||
chr1:33347036-33347243 | Rare:35 | ||||
chr1:35192265-35192589 | Common:2; Rare:96 | ||||
chr1:36207457-36207680 | Common:1; Rare:35 |