| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103498425-103498472 | Rare:6 | ||||
| chr14:103498509-103498552 | Rare:5 | ||||
| chr14:103520255-103520564 | Rare:98 | ||||
| chr14:103529070-103529264 | Common:1; Rare:59 | ||||
| chr14:103562573-103563326 | Common:11; Rare:309; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103629263-103629346 | Rare:19 | ||||
| chr14:103629383-103629490 | Common:2; Rare:37 | ||||
| chr14:103684772-103685181 | Common:2; Rare:96 | ||||
| chr14:103714493-103714546 | Common:1; Rare:6 | ||||
| chr14:103715418-103715860 | Common:1; Rare:151 | ||||
| chr14:104689545-104689664 | Rare:28 | ||||
| chr14:104708517-104708728 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:104752995-104753275 | Common:2; Rare:109 | ||||
| chr14:104865131-104865487 | Common:4; Rare:90 | ||||
| chr14:104970434-104970825 | Common:4; Rare:72 |