| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121530532-121530885 | Common:8; Rare:139 | ||||
| chr2:121649394-121649701 | Common:2; Rare:90 | ||||
| chr2:121649927-121650146 | Rare:61 | ||||
| chr2:121736736-121737105 | Common:4; Rare:149 | ||||
| chr2:121755415-121755827 | Common:5; Rare:134 | ||||
| chr2:127294067-127294212 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387866-127388272 | Common:10; Rare:174 | ||||
| chr2:127418272-127418440 | Common:2; Rare:26 | ||||
| chr2:127526198-127526247 | Rare:14 | ||||
| chr2:127526253-127526314 | Rare:17 | ||||
| chr2:127526316-127526536 | Common:2; Rare:96 | ||||
| chr2:127526803-127527004 | Common:1; Rare:35 | ||||
| chr2:127650529-127650672 | Common:5; Rare:35 | ||||
| chr2:127811014-127811258 | Common:1; Rare:74 | ||||
| chr2:127858112-127858197 | Rare:41 |