| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:11805900-11806276 | Common:2; Rare:102; Clinvar:1 | ||||
| chr1:11934437-11934776 | Common:5; Rare:103; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:11979948-11980484 | Common:6; Rare:147; Clinvar:1; Clinvar (benign):5 | ||||
| chr1:12019243-12019539 | Common:5; Rare:103 | ||||
| chr1:13749154-13749451 | Common:2; Rare:103 | ||||
| chr1:15526600-15526905 | Common:2; Rare:97 | ||||
| chr1:15756512-15756642 | Rare:30 | ||||
| chr1:15847531-15847802 | Rare:95 | ||||
| chr1:16237143-16237272 | Rare:42 | ||||
| chr1:16352420-16352611 | Common:3; Rare:101 | ||||
| chr1:16367005-16367255 | Common:1; Rare:74 | ||||
| chr1:16440519-16440753 | Common:2; Rare:62 | ||||
| chr1:16613484-16613692 | Common:2; Rare:1 | ||||
| chr1:17053946-17054331 | Common:3; Rare:121; Clinvar:16; Clinvar (benign):12 | ||||
| chr1:17439272-17439379 | Common:1; Rare:25 |