| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121530574-121530908 | Common:7; Rare:163; Clinvar (pathogenic):3 | ||||
| chr2:121649385-121649701 | Common:3; Rare:91 | ||||
| chr2:121649907-121650133 | Common:1; Rare:59 | ||||
| chr2:121736712-121737220 | Common:5; Rare:202 | ||||
| chr2:121755359-121755755 | Common:5; Rare:128 | ||||
| chr2:126655821-126655936 | Rare:36 | ||||
| chr2:126655945-126656306 | Common:1; Rare:95; Clinvar:2 | ||||
| chr2:127064779-127065090 | Rare:75 | ||||
| chr2:127294077-127294219 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388257 | Common:9; Rare:156 | ||||
| chr2:127526362-127526607 | Common:2; Rare:92 | ||||
| chr2:127526792-127526880 | Rare:19 | ||||
| chr2:127811080-127811259 | Rare:56 | ||||
| chr2:127858086-127858251 | Common:2; Rare:87 | ||||
| chr2:127884306-127884624 | Common:1; Rare:62 |