| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102086989-102087392 | Common:5; Rare:172 | ||||
| chr14:102139637-102139932 | Rare:105 | ||||
| chr14:102305061-102305234 | Rare:49 | ||||
| chr14:102362862-102363094 | Rare:103 | ||||
| chr14:103333962-103334248 | Common:1; Rare:118 | ||||
| chr14:103385120-103385439 | Common:1; Rare:99 | ||||
| chr14:103520494-103520667 | Rare:44 | ||||
| chr14:103529058-103529235 | Common:1; Rare:51 | ||||
| chr14:103562277-103562475 | Common:1; Rare:77 | ||||
| chr14:103562624-103563244 | Common:11; Rare:256; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103673158-103673383 | Common:1; Rare:52 | ||||
| chr14:103715466-103715844 | Common:1; Rare:120 | ||||
| chr14:103921468-103921676 | Common:3; Rare:69 | ||||
| chr14:104604737-104604853 | Common:6; Rare:52 | ||||
| chr14:104752887-104753208 | Common:3; Rare:115 |