| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179882990-179883172 | Common:6; Rare:126; Clinvar (benign):1 | ||||
| chr1:179954429-179955074 | Common:6; Rare:260 | ||||
| chr1:180154363-180155097 | Common:13; Rare:463 | ||||
| chr1:180229830-180230069 | Common:12; Rare:255 | ||||
| chr1:180230110-180230510 | Common:4; Rare:139; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:180502061-180502736 | Common:2; Rare:403 | ||||
| chr1:180502746-180502988 | Rare:129 | ||||
| chr1:180503108-180503846 | Common:4; Rare:203 | ||||
| chr1:180631835-180632243 | Common:10; Rare:271 | ||||
| chr1:181022674-181023306 | Common:28; Rare:514 | ||||
| chr1:181033700-181034052 | Common:1; Rare:119 | ||||
| chr1:181088456-181088981 | Common:4; Rare:448 | ||||
| chr1:182388567-182389152 | Common:4; Rare:193 | ||||
| chr1:182391152-182391533 | Common:2; Rare:187 | ||||
| chr1:182391664-182392088 | Common:12; Rare:369; Clinvar:14; Clinvar (benign):12 |