| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:143128956-143129457 | Common:3; Rare:108 | ||||
| chr2:144331868-144332318 | Common:5; Rare:151 | ||||
| chr2:144332430-144332783 | Common:1; Rare:137 | ||||
| chr2:144517316-144517394 | Rare:33; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144517398-144517717 | Common:5; Rare:89; Clinvar (benign):1 | ||||
| chr2:144520071-144520262 | Rare:32; Clinvar:1 | ||||
| chr2:147844446-147844581 | Common:1; Rare:52 | ||||
| chr2:148020664-148021140 | Common:2; Rare:115; Clinvar (benign):2 | ||||
| chr2:148021374-148021557 | Rare:58 | ||||
| chr2:148644443-148644820 | Rare:107 | ||||
| chr2:148645108-148645469 | Rare:140 | ||||
| chr2:148645819-148645864 | Rare:16 | ||||
| chr2:148875003-148875228 | Common:3; Rare:37 | ||||
| chr2:149587274-149587495 | Common:2; Rare:49 | ||||
| chr2:149587613-149587997 | Common:1; Rare:103; Clinvar:2; Clinvar (benign):2 |