| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:119679388-119679471 | Rare:12 | ||||
| chr2:119759436-119759998 | Common:2; Rare:168 | ||||
| chr2:120012791-120013115 | Common:2; Rare:129 | ||||
| chr2:120013131-120013577 | Common:2; Rare:149 | ||||
| chr2:120222991-120223256 | Common:7; Rare:74 | ||||
| chr2:120223260-120223632 | Common:1; Rare:118 | ||||
| chr2:120223671-120223906 | Common:3; Rare:47 | ||||
| chr2:120239648-120239925 | Common:1; Rare:60 | ||||
| chr2:120252542-120253007 | Common:3; Rare:144 | ||||
| chr2:120253125-120253370 | Common:1; Rare:62 | ||||
| chr2:120346023-120346239 | Common:3; Rare:66 | ||||
| chr2:121285170-121285379 | Common:3; Rare:74 | ||||
| chr2:121530231-121530438 | Rare:57 | ||||
| chr2:121530574-121530942 | Common:7; Rare:204; Clinvar (pathogenic):11 | ||||
| chr2:121648918-121649174 | Common:1; Rare:57 |