| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108621166-108621325 | Rare:26 | ||||
| chr2:108719383-108719592 | Common:3; Rare:87; Clinvar (benign):2 | ||||
| chr2:111884076-111884255 | Common:1; Rare:51 | ||||
| chr2:112275392-112275594 | Common:1; Rare:66 | ||||
| chr2:112542142-112542502 | Common:2; Rare:113 | ||||
| chr2:112584378-112584645 | Common:1; Rare:74 | ||||
| chr2:112645669-112645962 | Common:2; Rare:108 | ||||
| chr2:112764594-112764823 | Common:2; Rare:73; Clinvar (pathogenic):1 | ||||
| chr2:113278919-113279098 | Common:1; Rare:39 | ||||
| chr2:113627004-113627284 | Common:1; Rare:85 | ||||
| chr2:113756590-113756763 | Common:3; Rare:63 | ||||
| chr2:113889333-113889602 | Rare:54 | ||||
| chr2:113889765-113890321 | Common:9; Rare:169 | ||||
| chr2:118014056-118014221 | Common:2; Rare:93 | ||||
| chr2:118088329-118088532 | Common:1; Rare:57 |