| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:10043326-10043590 | Common:3; Rare:112; Clinvar:1 | ||||
| chr2:10302715-10303010 | Common:5; Rare:90 | ||||
| chr2:10448294-10448745 | Common:1; Rare:142 | ||||
| chr2:10689897-10690285 | Common:6; Rare:110 | ||||
| chr2:11344980-11345288 | Common:3; Rare:93 | ||||
| chr2:11465855-11466306 | Common:6; Rare:131 | ||||
| chr2:12716742-12717051 | Common:1; Rare:89 | ||||
| chr2:17540440-17540718 | Common:1; Rare:66 | ||||
| chr2:17753659-17754195 | Common:6; Rare:167; Clinvar (benign):1 | ||||
| chr2:18560613-18560805 | Rare:61 | ||||
| chr2:19358579-19358758 | Rare:42 | ||||
| chr2:19901646-19901743 | Common:1; Rare:47 | ||||
| chr2:19901925-19902042 | Common:1; Rare:40 | ||||
| chr2:19975434-19975557 | Common:2; Rare:27; Clinvar (benign):1 | ||||
| chr2:19990017-19990211 | Rare:56 |