| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:121285137-121285309 | Common:2; Rare:66 | ||||
| chr2:121530321-121530895 | Common:10; Rare:216; Clinvar (pathogenic):2 | ||||
| chr2:121649394-121649701 | Common:2; Rare:90 | ||||
| chr2:121649846-121650133 | Common:1; Rare:74 | ||||
| chr2:121736709-121737089 | Common:4; Rare:153 | ||||
| chr2:121755387-121755803 | Common:6; Rare:136 | ||||
| chr2:127294069-127294212 | Common:2; Rare:54; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387904-127388257 | Common:9; Rare:156 | ||||
| chr2:127526404-127526596 | Common:2; Rare:71 | ||||
| chr2:127811113-127811234 | Rare:40 | ||||
| chr2:127858112-127858198 | Rare:42 | ||||
| chr2:127885886-127885999 | Rare:31 | ||||
| chr2:128091039-128091369 | Common:8; Rare:106 | ||||
| chr2:130181546-130181696 | Common:1; Rare:53 | ||||
| chr2:130182078-130182375 | Common:2; Rare:114 |