| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:243255776-243256144 | Common:2; Rare:212; Clinvar:8; Clinvar (benign):2 | ||||
| chr1:244451821-244452304 | Common:2; Rare:275 | ||||
| chr1:244652580-244653150 | Common:9; Rare:331 | ||||
| chr1:244834949-244835368 | Rare:268 | ||||
| chr1:244835561-244835749 | Common:4; Rare:158; Clinvar (benign):9 | ||||
| chr1:244863346-244864069 | Common:7; Rare:342; Clinvar:11; Clinvar (benign):14; Clinvar (pathogenic):2 | ||||
| chr1:244864411-244864724 | Common:1; Rare:222 | ||||
| chr1:244969750-244970419 | Common:9; Rare:454 | ||||
| chr1:244970580-244970880 | Common:7; Rare:88 | ||||
| chr1:246507215-246507359 | Common:1; Rare:60 | ||||
| chr1:246566122-246566606 | Common:6; Rare:322 | ||||
| chr1:246724221-246724484 | Common:4; Rare:173 | ||||
| chr1:246931320-246931770 | Common:7; Rare:229 | ||||
| chr1:246931858-246932276 | Common:1; Rare:190 | ||||
| chr1:247078724-247078879 | Common:1; Rare:48 |