| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108449098-108449260 | Rare:58 | ||||
| chr2:108534186-108534483 | Common:7; Rare:120 | ||||
| chr2:108621195-108621308 | Rare:18 | ||||
| chr2:108719365-108719546 | Common:2; Rare:74 | ||||
| chr2:109613823-109614008 | Common:2; Rare:65 | ||||
| chr2:110115700-110115948 | Common:2; Rare:66 | ||||
| chr2:110678007-110678212 | Rare:65 | ||||
| chr2:111884117-111884255 | Rare:40 | ||||
| chr2:112255009-112255139 | Common:1; Rare:57 | ||||
| chr2:112275419-112275594 | Common:1; Rare:49 | ||||
| chr2:112542129-112542493 | Common:1; Rare:112 | ||||
| chr2:112584362-112584647 | Common:1; Rare:78 | ||||
| chr2:112584772-112584854 | Rare:20 | ||||
| chr2:112645759-112645959 | Rare:78 | ||||
| chr2:112764584-112764765 | Common:1; Rare:59; Clinvar (pathogenic):1 |