| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:108588130-108588472 | Common:2; Rare:59 | ||||
| chr2:108588777-108589068 | Rare:53 | ||||
| chr2:111122449-111122612 | Common:1; Rare:64 | ||||
| chr2:112542111-112542493 | Common:1; Rare:117 | ||||
| chr2:112645713-112645944 | Common:1; Rare:84 | ||||
| chr2:112836740-112837099 | Common:1; Rare:53; Clinvar:1 | ||||
| chr2:113127365-113127633 | Rare:57 | ||||
| chr2:113627078-113627289 | Common:2; Rare:61 | ||||
| chr2:113890061-113890319 | Common:2; Rare:71 | ||||
| chr2:118013965-118014277 | Common:4; Rare:153 | ||||
| chr2:118088163-118088540 | Common:2; Rare:96 | ||||
| chr2:119366755-119367018 | Common:1; Rare:72 | ||||
| chr2:119759719-119759956 | Common:1; Rare:70 | ||||
| chr2:121530583-121530949 | Common:7; Rare:207; Clinvar (pathogenic):12 | ||||
| chr2:121650026-121650151 | Rare:33 |