| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119759748-119759810 | Common:1; Rare:11 | ||||
| chr2:121530596-121530880 | Common:7; Rare:113 | ||||
| chr2:121649399-121649683 | Common:2; Rare:85 | ||||
| chr2:121755415-121755786 | Common:5; Rare:123 | ||||
| chr2:126655173-126655469 | Common:1; Rare:68 | ||||
| chr2:127294100-127294204 | Common:2; Rare:41; Clinvar (benign):2 | ||||
| chr2:127387941-127388255 | Common:8; Rare:135 | ||||
| chr2:127526429-127526673 | Common:2; Rare:83 | ||||
| chr2:127811018-127811259 | Common:1; Rare:73 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885932-127885978 | Rare:6 | ||||
| chr2:128091031-128091342 | Common:8; Rare:105 | ||||
| chr2:130181538-130181797 | Common:4; Rare:114 | ||||
| chr2:130182091-130182455 | Common:2; Rare:133 | ||||
| chr2:130342111-130342279 | Rare:72; Clinvar:1 |