| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:118014056-118014214 | Common:2; Rare:91 | ||||
| chr2:118088352-118088492 | Common:1; Rare:41 | ||||
| chr2:119366795-119367080 | Common:1; Rare:86 | ||||
| chr2:119679005-119679225 | Common:3; Rare:62 | ||||
| chr2:120252597-120252945 | Common:3; Rare:114 | ||||
| chr2:121285200-121285322 | Rare:38 | ||||
| chr2:121530579-121530884 | Common:7; Rare:127 | ||||
| chr2:121649418-121649683 | Common:2; Rare:77 | ||||
| chr2:121736846-121737261 | Common:5; Rare:155 | ||||
| chr2:127294091-127294196 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127811131-127811259 | Rare:41 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:130181553-130181777 | Common:3; Rare:99 | ||||
| chr2:130182137-130182368 | Common:2; Rare:95 | ||||
| chr2:130182438-130182569 | Common:1; Rare:50 |