| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:32394410-32394637 | Common:1; Rare:60 | ||||
| chr1:32650918-32651318 | Common:2; Rare:150 | ||||
| chr1:32753764-32754178 | Common:4; Rare:146 | ||||
| chr1:32817240-32817674 | Rare:114; Clinvar:5 | ||||
| chr1:32895582-32895915 | Common:2; Rare:102 | ||||
| chr1:33021445-33021697 | Rare:62; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:33080992-33081158 | Common:2; Rare:38 | ||||
| chr1:33182023-33182097 | Rare:13 | ||||
| chr1:34754938-34755161 | Common:1; Rare:45 | ||||
| chr1:34759725-34759815 | Common:1; Rare:16 | ||||
| chr1:34781384-34781768 | Common:1; Rare:68; Clinvar:4; Clinvar (benign):3 | ||||
| chr1:34782041-34782336 | Rare:51 | ||||
| chr1:35031917-35032211 | Common:1; Rare:63 | ||||
| chr1:35192466-35192694 | Common:2; Rare:70 | ||||
| chr1:35192907-35193165 | Common:1; Rare:102 |