Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6420690-6420863 | Common:2; Rare:41 | ||||
chr1:8022539-8022699 | Common:1; Rare:31 | ||||
chr1:8361553-8361852 | Common:2; Rare:82; Clinvar (benign):1 | ||||
chr1:9182130-9182235 | Rare:27 | ||||
chr1:9182244-9182566 | Common:2; Rare:91 | ||||
chr1:9242634-9242883 | Common:1; Rare:63 | ||||
chr1:9339014-9339097 | Common:1; Rare:20 | ||||
chr1:9687503-9687633 | Common:1; Rare:33 | ||||
chr1:10815133-10815433 | Common:1; Rare:53 | ||||
chr1:11070958-11071043 | Rare:24 | ||||
chr1:11790967-11791180 | Common:3; Rare:43 | ||||
chr1:12619044-12619282 | Rare:49 | ||||
chr1:15834900-15835158 | Common:1; Rare:113 | ||||
chr1:15835793-15836095 | Common:6; Rare:141 | ||||
chr1:16155040-16155280 | Common:1; Rare:47 |