| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45134348-45134722 | Rare:144 | ||||
| chr14:45135715-45136029 | Common:1; Rare:76 | ||||
| chr14:45136166-45136246 | Rare:27; Clinvar:2 | ||||
| chr14:45253036-45253700 | Common:3; Rare:212 | ||||
| chr14:45254002-45254127 | Rare:30 | ||||
| chr14:49586334-49586710 | Common:1; Rare:199 | ||||
| chr14:49598439-49598540 | Rare:24 | ||||
| chr14:49598543-49598643 | Common:2; Rare:42 | ||||
| chr14:49598648-49598792 | Common:1; Rare:64 | ||||
| chr14:49598799-49599066 | Common:1; Rare:90 | ||||
| chr14:49599114-49599345 | Rare:71 | ||||
| chr14:49600180-49600292 | Rare:22 | ||||
| chr14:49620248-49620342 | Rare:27 | ||||
| chr14:49620414-49620509 | Rare:24 | ||||
| chr14:49620534-49621171 | Common:4; Rare:214; Clinvar:10; Clinvar (benign):2 |