| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113889709-113890165 | Common:8; Rare:152 | ||||
| chr2:113890196-113890290 | Common:1; Rare:30 | ||||
| chr2:118014041-118014214 | Common:2; Rare:98 | ||||
| chr2:118088171-118088509 | Common:2; Rare:89 | ||||
| chr2:119366798-119367080 | Common:1; Rare:85 | ||||
| chr2:119678967-119679225 | Common:5; Rare:71 | ||||
| chr2:119759777-119759808 | Rare:9 | ||||
| chr2:120012817-120013119 | Common:2; Rare:125 | ||||
| chr2:120252612-120252964 | Common:3; Rare:115 | ||||
| chr2:121530583-121530889 | Common:7; Rare:129; Clinvar (pathogenic):1 | ||||
| chr2:121649424-121649654 | Common:2; Rare:67 | ||||
| chr2:121736741-121737111 | Common:4; Rare:151 | ||||
| chr2:126655956-126656293 | Common:1; Rare:83; Clinvar:1 | ||||
| chr2:127294086-127294185 | Common:2; Rare:41; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387958-127388255 | Common:7; Rare:130 |