| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:96208214-96208467 | Rare:129 | ||||
| chr2:96208781-96208942 | Common:3; Rare:64 | ||||
| chr2:96260574-96260669 | Rare:13 | ||||
| chr2:96265959-96266348 | Common:2; Rare:118; Clinvar:1 | ||||
| chr2:96305439-96305634 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):2 | ||||
| chr2:96335713-96335807 | Common:1; Rare:31 | ||||
| chr2:96740001-96740348 | Common:5; Rare:94 | ||||
| chr2:96842565-96842875 | Common:1; Rare:51 | ||||
| chr2:96843988-96844204 | Common:1; Rare:50 | ||||
| chr2:96857988-96858293 | Common:2; Rare:96 | ||||
| chr2:97094810-97094980 | Common:1; Rare:42 | ||||
| chr2:97645808-97646186 | Common:3; Rare:112 | ||||
| chr2:97663924-97664261 | Common:1; Rare:103 | ||||
| chr2:98444760-98445061 | Common:1; Rare:115 | ||||
| chr2:98608353-98608655 | Common:1; Rare:130; Clinvar:1; Clinvar (benign):1 |