| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:108218313-108218520 | Rare:80 | ||||
| chr13:110307037-110307282 | Common:1; Rare:91; Clinvar:2; Clinvar (benign):3 | ||||
| chr13:110561656-110561889 | Common:5; Rare:82 | ||||
| chr13:110615385-110615671 | Common:2; Rare:98 | ||||
| chr13:110712986-110713266 | Common:2; Rare:125 | ||||
| chr13:110715351-110715445 | Rare:29 | ||||
| chr13:110715803-110715872 | Rare:52 | ||||
| chr13:111153595-111153721 | Common:2; Rare:59 | ||||
| chr13:113208631-113208752 | Rare:69 | ||||
| chr13:113490699-113490999 | Common:1; Rare:112 | ||||
| chr13:114281299-114281648 | Common:5; Rare:135 | ||||
| chr14:20343167-20343652 | Common:13; Rare:282 | ||||
| chr14:20413420-20413593 | Common:3; Rare:50 | ||||
| chr14:20454800-20455316 | Common:7; Rare:134 | ||||
| chr14:20684429-20684650 | Common:2; Rare:36; Clinvar (benign):2 |