| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:120252608-120252973 | Common:3; Rare:119 | ||||
| chr2:121530579-121530909 | Common:7; Rare:159; Clinvar (pathogenic):3 | ||||
| chr2:121649418-121649701 | Common:2; Rare:80 | ||||
| chr2:121649868-121650157 | Common:1; Rare:74 | ||||
| chr2:121736828-121737089 | Common:4; Rare:98 | ||||
| chr2:126655754-126656298 | Common:1; Rare:149; Clinvar:1 | ||||
| chr2:127294067-127294219 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387918-127388217 | Common:6; Rare:134 | ||||
| chr2:127526421-127526619 | Common:2; Rare:66 | ||||
| chr2:127650529-127650672 | Common:5; Rare:35 | ||||
| chr2:127675463-127675615 | Rare:35 | ||||
| chr2:127681377-127681389 | Rare:2 | ||||
| chr2:127811121-127811259 | Rare:45 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885884-127886507 | Common:2; Rare:171 |