| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:97645761-97646144 | Common:3; Rare:111 | ||||
| chr2:97663442-97663682 | Common:2; Rare:68 | ||||
| chr2:97663851-97664380 | Common:1; Rare:152 | ||||
| chr2:97713183-97713308 | Rare:22 | ||||
| chr2:97713439-97713665 | Common:1; Rare:31; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:97761194-97761325 | Common:1; Rare:34 | ||||
| chr2:97995026-97995376 | Common:3; Rare:93 | ||||
| chr2:97995380-97995553 | Common:3; Rare:57 | ||||
| chr2:97995773-97996046 | Common:3; Rare:98 | ||||
| chr2:97996186-97996499 | Common:2; Rare:96 | ||||
| chr2:98444599-98444960 | Common:1; Rare:123 | ||||
| chr2:98608375-98608725 | Common:2; Rare:137; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:98731103-98731443 | Common:3; Rare:106 | ||||
| chr2:99140865-99140965 | Rare:23 | ||||
| chr2:99141093-99141407 | Common:1; Rare:112 |