| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103123034-103123061 | Rare:5 | ||||
| chr14:103123064-103123108 | Common:1; Rare:9 | ||||
| chr14:103123215-103123462 | Rare:46 | ||||
| chr14:103333962-103334253 | Common:1; Rare:122 | ||||
| chr14:103334337-103334434 | Common:2; Rare:22 | ||||
| chr14:103334658-103334944 | Common:3; Rare:122 | ||||
| chr14:103335915-103336116 | Rare:78 | ||||
| chr14:103385252-103385446 | Common:1; Rare:72 | ||||
| chr14:103385494-103385904 | Common:1; Rare:95 | ||||
| chr14:103521465-103521816 | Common:2; Rare:99 | ||||
| chr14:103529022-103529255 | Common:1; Rare:72 | ||||
| chr14:103562109-103562399 | Rare:102 | ||||
| chr14:103562592-103563053 | Common:8; Rare:181; Clinvar (benign):5 | ||||
| chr14:103629107-103629489 | Common:4; Rare:148 | ||||
| chr14:103673158-103673431 | Common:1; Rare:64 |