| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:111153490-111153720 | Common:2; Rare:108 | ||||
| chr13:113208620-113208775 | Rare:91 | ||||
| chr13:113297016-113297274 | Common:1; Rare:103 | ||||
| chr13:113490683-113491029 | Common:1; Rare:126 | ||||
| chr13:113759078-113759278 | Common:1; Rare:54 | ||||
| chr13:114281316-114281654 | Common:5; Rare:134 | ||||
| chr14:20343167-20343644 | Common:13; Rare:280 | ||||
| chr14:20413404-20413531 | Common:3; Rare:38 | ||||
| chr14:20454762-20455316 | Common:7; Rare:143 | ||||
| chr14:20684437-20684629 | Common:2; Rare:31; Clinvar (benign):2 | ||||
| chr14:20802277-20802441 | Rare:28 | ||||
| chr14:20802796-20802965 | Common:1; Rare:23 | ||||
| chr14:21022089-21022443 | Rare:89 | ||||
| chr14:21025494-21025807 | Common:1; Rare:72 | ||||
| chr14:21437212-21437396 | Common:3; Rare:79 |