| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:113759069-113759278 | Common:1; Rare:57 | ||||
| chr13:113835527-113835747 | Rare:80 | ||||
| chr13:113863832-113864150 | Common:2; Rare:77 | ||||
| chr13:114132512-114132829 | Common:2; Rare:96 | ||||
| chr13:114281501-114281664 | Common:2; Rare:90 | ||||
| chr14:20343178-20343644 | Common:12; Rare:273 | ||||
| chr14:20413164-20413234 | Common:1; Rare:10 | ||||
| chr14:20413413-20413558 | Common:3; Rare:45 | ||||
| chr14:20454738-20455281 | Common:7; Rare:144 | ||||
| chr14:20455406-20455702 | Rare:83 | ||||
| chr14:20684462-20684739 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:20780987-20781180 | Common:1; Rare:34 | ||||
| chr14:20989691-20990051 | Common:7; Rare:91 | ||||
| chr14:21023433-21023496 | Common:1; Rare:9 | ||||
| chr14:21024997-21025385 | Rare:120 |