| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:113627065-113627224 | Rare:46 | ||||
| chr2:113756612-113756742 | Common:1; Rare:45 | ||||
| chr2:113889766-113890165 | Common:8; Rare:128 | ||||
| chr2:118014068-118014214 | Common:2; Rare:86 | ||||
| chr2:119366798-119367045 | Common:1; Rare:71 | ||||
| chr2:121530583-121530889 | Common:7; Rare:129; Clinvar (pathogenic):1 | ||||
| chr2:121736736-121737236 | Common:5; Rare:201 | ||||
| chr2:126655997-126656177 | Common:1; Rare:41 | ||||
| chr2:127294094-127294214 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127811139-127811258 | Rare:37 | ||||
| chr2:128091036-128091335 | Common:8; Rare:100 | ||||
| chr2:130181553-130181708 | Common:1; Rare:56 | ||||
| chr2:130342127-130342219 | Rare:37 | ||||
| chr2:130342645-130342939 | Common:5; Rare:94 | ||||
| chr2:131105177-131105367 | Common:1; Rare:82 |