| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118014006-118014254 | Common:2; Rare:130 | ||||
| chr2:118088337-118088570 | Common:1; Rare:63 | ||||
| chr2:119366789-119367114 | Common:1; Rare:107 | ||||
| chr2:119678960-119679219 | Common:5; Rare:69 | ||||
| chr2:119759741-119759809 | Common:1; Rare:13 | ||||
| chr2:121285099-121285322 | Common:2; Rare:84 | ||||
| chr2:121530579-121530895 | Common:7; Rare:142; Clinvar (pathogenic):2 | ||||
| chr2:121649424-121649715 | Common:2; Rare:85 | ||||
| chr2:121736736-121737113 | Common:4; Rare:155 | ||||
| chr2:127294094-127294219 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387949-127388255 | Common:7; Rare:131 | ||||
| chr2:127811107-127811297 | Common:1; Rare:68 | ||||
| chr2:127858112-127858202 | Rare:45 | ||||
| chr2:127885886-127886272 | Common:1; Rare:107 | ||||
| chr2:128091057-128091335 | Common:8; Rare:93 |