| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:96204726-96204866 | Common:1; Rare:40 | ||||
| chr14:96363271-96363552 | Common:1; Rare:93 | ||||
| chr14:96502286-96502595 | Common:1; Rare:131 | ||||
| chr14:100238556-100238848 | Common:2; Rare:86 | ||||
| chr14:100239684-100239915 | Common:2; Rare:79 | ||||
| chr14:100375426-100375758 | Common:2; Rare:51 | ||||
| chr14:100376269-100376489 | Common:3; Rare:75 | ||||
| chr14:101809686-101809945 | Rare:56 | ||||
| chr14:101823783-101823858 | Rare:15 | ||||
| chr14:101964184-101964674 | Common:5; Rare:125; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:102084398-102084777 | Common:1; Rare:141 | ||||
| chr14:102139670-102139923 | Rare:87 | ||||
| chr14:102362862-102363094 | Rare:103 | ||||
| chr14:103123283-103123472 | Rare:33 | ||||
| chr14:103333917-103334260 | Common:3; Rare:147 |