| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:216601271-216601552 | Common:3; Rare:65 | ||||
| chr1:217029398-217029577 | Rare:36 | ||||
| chr1:217124370-217124680 | Common:1; Rare:59 | ||||
| chr1:217134724-217135792 | Common:4; Rare:428 | ||||
| chr1:217316210-217316550 | Common:1; Rare:74 | ||||
| chr1:217422220-217422470 | Common:3; Rare:97 | ||||
| chr1:217424872-217425340 | Common:6; Rare:118 | ||||
| chr1:217556787-217557350 | Common:10; Rare:192 | ||||
| chr1:217572998-217573814 | Common:9; Rare:247 | ||||
| chr1:217574170-217575010 | Common:4; Rare:228 | ||||
| chr1:217696505-217696820 | Common:4; Rare:108 | ||||
| chr1:217713240-217713620 | Common:2; Rare:67 | ||||
| chr1:217953340-217953720 | Common:1; Rare:70 | ||||
| chr1:218164401-218164801 | Rare:179 | ||||
| chr1:218345186-218345627 | Common:4; Rare:142; Clinvar:3; Clinvar (benign):2 |