| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108534204-108534502 | Common:7; Rare:123 | ||||
| chr2:108719383-108719571 | Common:3; Rare:77; Clinvar (benign):2 | ||||
| chr2:109613846-109614022 | Common:2; Rare:65 | ||||
| chr2:110204935-110205071 | Common:1; Rare:60; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:112275417-112275613 | Common:1; Rare:55 | ||||
| chr2:112584400-112584639 | Common:1; Rare:66 | ||||
| chr2:112645701-112645944 | Common:1; Rare:89 | ||||
| chr2:113627046-113627303 | Common:3; Rare:77 | ||||
| chr2:113756482-113756734 | Common:2; Rare:74 | ||||
| chr2:113889709-113890174 | Common:8; Rare:152 | ||||
| chr2:117814650-117814757 | Rare:41 | ||||
| chr2:118014002-118014249 | Common:2; Rare:129 | ||||
| chr2:118088337-118088510 | Common:1; Rare:53 | ||||
| chr2:119366752-119367076 | Common:1; Rare:103 | ||||
| chr2:119679090-119679236 | Common:4; Rare:47 |