| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161258570-161258795 | Common:2; Rare:48 | ||||
| chr1:161314175-161314495 | Common:11; Rare:271; Clinvar:30; Clinvar (benign):17; Clinvar (pathogenic):3 | ||||
| chr1:161523917-161524253 | Common:9; Rare:99 | ||||
| chr1:161524318-161524718 | Common:9; Rare:183 | ||||
| chr1:161725520-161726090 | Common:7; Rare:234 | ||||
| chr1:161749596-161749835 | Rare:153 | ||||
| chr1:161749756-161749874 | Rare:53 | ||||
| chr1:161750161-161750408 | Rare:142 | ||||
| chr1:161766118-161766401 | Common:6; Rare:170 | ||||
| chr1:162069511-162070421 | Common:5; Rare:403 | ||||
| chr1:162070428-162070617 | Common:2; Rare:49 | ||||
| chr1:162497707-162497905 | Common:6; Rare:157 | ||||
| chr1:162561202-162561811 | Common:13; Rare:476 | ||||
| chr1:162790494-162790850 | Common:13; Rare:274 | ||||
| chr1:163321678-163322129 | Common:3; Rare:313 |