Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145918689-145919013 | Common:2; Rare:69 | ||||
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145957704-145957812 | Rare:34 | ||||
chr1:145958000-145958212 | Rare:49 | ||||
chr1:145964573-145964742 | Rare:43 | ||||
chr1:145996404-145996882 | Common:2; Rare:176 | ||||
chr1:147172444-147172830 | Common:1; Rare:97 | ||||
chr1:147225303-147225366 | Common:1; Rare:15 | ||||
chr1:147225369-147225711 | Common:2; Rare:59 | ||||
chr1:148458680-148459006 | Common:2; Rare:90 | ||||
chr1:148844376-148844439 | Rare:7 | ||||
chr1:148951841-148952141 | Common:5; Rare:69 | ||||
chr1:148952233-148952402 | Common:1; Rare:47 | ||||
chr1:149390482-149390608 | Rare:11 | ||||
chr1:149812099-149812560 | Common:2; Rare:196 |