| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74958844-74959411 | Common:4; Rare:626 | ||||
| chr2:75646358-75646843 | Common:3; Rare:221 | ||||
| chr2:75646784-75648161 | Common:17; Rare:650 | ||||
| chr2:75710038-75710438 | Common:2; Rare:96 | ||||
| chr2:75710470-75710830 | Common:15; Rare:551 | ||||
| chr2:75710811-75711330 | Common:9; Rare:519 | ||||
| chr2:80304095-80304940 | Common:7; Rare:359 | ||||
| chr2:84459132-84459651 | Common:22; Rare:727; Clinvar:28; Clinvar (benign):29; Clinvar (pathogenic):7 | ||||
| chr2:84516270-84516540 | Common:1; Rare:73 | ||||
| chr2:84881030-84881360 | Common:2; Rare:85 | ||||
| chr2:84905070-84905460 | Common:1; Rare:146 | ||||
| chr2:84905441-84906385 | Common:10; Rare:634 | ||||
| chr2:84906989-84907389 | Common:1; Rare:112 | ||||
| chr2:84970540-84971575 | Common:33; Rare:1390 | ||||
| chr2:84971526-84972641 | Common:14; Rare:685 |