| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215436035-215436307 | Common:2; Rare:90 | ||||
| chr2:218270221-218270532 | Common:2; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218671954-218672315 | Common:2; Rare:97 | ||||
| chr2:219177819-219177930 | Common:3; Rare:23 | ||||
| chr2:219178156-219178255 | Common:6; Rare:63 | ||||
| chr2:219229535-219229828 | Common:1; Rare:82 | ||||
| chr2:219245442-219245526 | Rare:26 | ||||
| chr2:219498699-219498955 | Common:2; Rare:58 | ||||
| chr2:219543791-219544081 | Common:3; Rare:93 | ||||
| chr2:226795032-226795111 | Rare:35 | ||||
| chr2:230712758-230712942 | Common:2; Rare:72 | ||||
| chr2:231464170-231464260 | Rare:29 | ||||
| chr2:232550591-232550722 | Rare:52 | ||||
| chr2:237085819-237085951 | Common:1; Rare:55 | ||||
| chr2:237487141-237487287 | Common:3; Rare:40 |