| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:9942783-9942977 | Common:1; Rare:38 | ||||
| chr1:9943073-9943489 | Common:6; Rare:104 | ||||
| chr1:10032640-10032980 | Common:3; Rare:95 | ||||
| chr1:10365180-10365469 | Common:1; Rare:79; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:10398734-10399118 | Common:2; Rare:141 | ||||
| chr1:10430356-10430486 | Common:2; Rare:42 | ||||
| chr1:10449957-10450281 | Common:1; Rare:102 | ||||
| chr1:11055057-11055112 | Common:1; Rare:21 | ||||
| chr1:11099749-11099944 | Common:3; Rare:81 | ||||
| chr1:11262484-11262843 | Common:2; Rare:109 | ||||
| chr1:11272955-11273235 | Rare:69; Clinvar:1; Clinvar (benign):1 | ||||
| chr1:11654396-11654525 | Rare:35 | ||||
| chr1:11654811-11654938 | Common:2; Rare:35 | ||||
| chr1:11691473-11691819 | Common:4; Rare:76 | ||||
| chr1:11805905-11806265 | Common:2; Rare:100; Clinvar:1 |