| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74833889-74834229 | Rare:105 | ||||
| chr2:74834529-74834853 | Common:3; Rare:92 | ||||
| chr2:74834860-74835070 | Common:1; Rare:54 | ||||
| chr2:74835094-74835391 | Common:1; Rare:73 | ||||
| chr2:74835505-74835569 | Rare:21 | ||||
| chr2:74958527-74958726 | Common:4; Rare:79 | ||||
| chr2:74958839-74959073 | Rare:87 | ||||
| chr2:75560907-75561080 | Rare:43 | ||||
| chr2:75561104-75561237 | Common:3; Rare:35 | ||||
| chr2:75561270-75561463 | Common:1; Rare:23 | ||||
| chr2:75646654-75647117 | Common:3; Rare:140 | ||||
| chr2:75710412-75710508 | Common:1; Rare:20 | ||||
| chr2:75710540-75711086 | Common:3; Rare:204 | ||||
| chr2:75711174-75711310 | Rare:27 | ||||
| chr2:84459198-84459663 | Common:4; Rare:119; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 |