| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:112645644-112646056 | Common:6; Rare:346 | ||||
| chr2:112646224-112646442 | Common:5; Rare:165 | ||||
| chr2:112725810-112726171 | Common:1; Rare:61 | ||||
| chr2:112763880-112764300 | Common:5; Rare:170 | ||||
| chr2:112764575-112764859 | Common:6; Rare:253; Clinvar (pathogenic):3 | ||||
| chr2:113117580-113118000 | Common:11; Rare:169; Clinvar:5; Clinvar (benign):4 | ||||
| chr2:113157135-113157664 | Common:12; Rare:323 | ||||
| chr2:113198773-113199041 | Common:3; Rare:185 | ||||
| chr2:113235375-113235793 | Common:3; Rare:234; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:113438003-113438550 | Common:4; Rare:140 | ||||
| chr2:113627077-113627304 | Common:6; Rare:127 | ||||
| chr2:113755904-113756304 | Common:1; Rare:87 | ||||
| chr2:113756486-113757020 | Common:14; Rare:363 | ||||
| chr2:113889645-113890300 | Common:25; Rare:510 | ||||
| chr2:113890928-113891176 | Rare:101 |