| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161177422-161177769 | Common:1; Rare:97 | ||||
| chr1:161202118-161202479 | Common:3; Rare:114; Clinvar:4; Clinvar (benign):8 | ||||
| chr1:161202667-161202770 | Common:2; Rare:13 | ||||
| chr1:161225707-161226124 | Common:10; Rare:74 | ||||
| chr1:161227220-161227690 | Common:1; Rare:111 | ||||
| chr1:161306175-161306372 | Rare:67; Clinvar:2 | ||||
| chr1:161307311-161307711 | Rare:149; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr1:161314264-161314459 | Common:4; Rare:79; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr1:161524180-161524600 | Common:7; Rare:120 | ||||
| chr1:161726349-161726465 | Rare:28 | ||||
| chr1:161749659-161750079 | Rare:153 | ||||
| chr1:161750130-161750510 | Rare:80 | ||||
| chr1:161766143-161766358 | Common:3; Rare:62 | ||||
| chr1:162023636-162023985 | Common:1; Rare:101 | ||||
| chr1:162024220-162024500 | Common:3; Rare:49 |