Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11099748-11099935 | Common:3; Rare:77 | ||||
chr1:11262493-11262836 | Common:2; Rare:101 | ||||
chr1:11654829-11654931 | Common:1; Rare:23 | ||||
chr1:11691455-11691781 | Common:4; Rare:74 | ||||
chr1:11691782-11691836 | Rare:8 | ||||
chr1:11805887-11806262 | Common:2; Rare:108; Clinvar:2 | ||||
chr1:11858942-11859103 | Rare:40 | ||||
chr1:12596046-12596085 | Rare:7 | ||||
chr1:12618198-12618475 | Common:1; Rare:59 | ||||
chr1:15152440-15152615 | Rare:27 | ||||
chr1:15153070-15153117 | Common:1; Rare:9 | ||||
chr1:15526551-15526885 | Common:2; Rare:103 | ||||
chr1:15756580-15756685 | Rare:34 | ||||
chr1:16352401-16352635 | Common:4; Rare:126 | ||||
chr1:17053989-17054321 | Common:3; Rare:99; Clinvar:6; Clinvar (benign):8 |