| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:16440491-16440794 | Common:6; Rare:235 | ||||
| chr1:16608080-16608779 | Common:10; Rare:11 | ||||
| chr1:16612983-16613144 | Rare:2 | ||||
| chr1:16613144-16613771 | Common:15; Rare:5 | ||||
| chr1:17011818-17012093 | Common:3; Rare:195; Clinvar:6 | ||||
| chr1:17053940-17054415 | Common:9; Rare:369; Clinvar:33; Clinvar (benign):28; Clinvar (pathogenic):1 | ||||
| chr1:17248823-17249223 | Common:3; Rare:194 | ||||
| chr1:17438395-17438940 | Common:11; Rare:373 | ||||
| chr1:17439553-17440040 | Rare:352 | ||||
| chr1:17538995-17539955 | Common:2; Rare:393 | ||||
| chr1:17539903-17540130 | Common:1; Rare:77 | ||||
| chr1:17540324-17540597 | Common:3; Rare:56 | ||||
| chr1:18480700-18481110 | Common:10; Rare:191 | ||||
| chr1:18901968-18902194 | Common:2; Rare:43 | ||||
| chr1:18902466-18903083 | Common:25; Rare:473; Clinvar:27; Clinvar (benign):1; Clinvar (pathogenic):2 |