| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:93184851-93185008 | Rare:50 | ||||
| chr14:93206992-93207364 | Common:3; Rare:177 | ||||
| chr14:94081130-94081402 | Common:5; Rare:82 | ||||
| chr14:95157329-95157688 | Common:4; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:95534631-95534679 | Rare:13 | ||||
| chr14:96363280-96363552 | Common:1; Rare:90 | ||||
| chr14:99480745-99481013 | Common:2; Rare:104 | ||||
| chr14:100376259-100376498 | Common:3; Rare:78 | ||||
| chr14:101809637-101809890 | Rare:51 | ||||
| chr14:102086990-102087186 | Common:3; Rare:92 | ||||
| chr14:102139684-102139935 | Rare:89 | ||||
| chr14:102305118-102305373 | Common:1; Rare:75 | ||||
| chr14:102362847-102363102 | Rare:114 | ||||
| chr14:103335831-103336062 | Rare:86 | ||||
| chr14:103529029-103529236 | Common:1; Rare:63 |