| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:10430210-10430491 | Common:15; Rare:228 | ||||
| chr1:10430444-10430994 | Common:38; Rare:492 | ||||
| chr1:10471919-10472832 | Common:2; Rare:642 | ||||
| chr1:10472733-10473725 | Common:10; Rare:282 | ||||
| chr1:10474760-10475244 | Common:4; Rare:542; Clinvar:19; Clinvar (benign):3 | ||||
| chr1:10693582-10694312 | Common:8; Rare:356 | ||||
| chr1:10694590-10694950 | Common:2; Rare:121 | ||||
| chr1:11012102-11012851 | Common:12; Rare:434; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:11012944-11013344 | Common:3; Rare:319 | ||||
| chr1:11058790-11059192 | Common:6; Rare:199 | ||||
| chr1:11059392-11059826 | Common:3; Rare:266 | ||||
| chr1:11059770-11060702 | Common:22; Rare:1009 | ||||
| chr1:11069105-11069665 | Common:15; Rare:160 | ||||
| chr1:11098990-11099497 | Common:1; Rare:219 | ||||
| chr1:11099429-11100110 | Common:17; Rare:756 |