| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:108218339-108218520 | Rare:71 | ||||
| chr13:110561653-110561900 | Common:5; Rare:84 | ||||
| chr13:111153569-111153721 | Common:2; Rare:70 | ||||
| chr13:113208620-113208741 | Rare:73 | ||||
| chr13:113364080-113364445 | Common:2; Rare:26 | ||||
| chr13:113490683-113490894 | Common:1; Rare:74 | ||||
| chr13:114132530-114132736 | Rare:62 | ||||
| chr13:114234835-114235104 | Common:14; Rare:100 | ||||
| chr13:114281480-114281703 | Common:2; Rare:121 | ||||
| chr13:114281802-114282096 | Common:6; Rare:149 | ||||
| chr14:20343219-20343655 | Common:12; Rare:246 | ||||
| chr14:20413404-20413562 | Common:3; Rare:51 | ||||
| chr14:20454756-20455368 | Common:7; Rare:155 | ||||
| chr14:20684438-20684595 | Common:2; Rare:25; Clinvar (benign):2 | ||||
| chr14:21025055-21025364 | Rare:93 |