| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110713008-110713266 | Common:2; Rare:114 | ||||
| chr13:111153529-111153720 | Common:2; Rare:95 | ||||
| chr13:112968311-112968472 | Rare:41 | ||||
| chr13:112969076-112969211 | Common:2; Rare:44 | ||||
| chr13:113208630-113208756 | Rare:72 | ||||
| chr13:113297030-113297271 | Common:1; Rare:95 | ||||
| chr13:113490683-113491021 | Common:1; Rare:122 | ||||
| chr13:113863841-113864142 | Common:2; Rare:77 | ||||
| chr13:114281519-114281664 | Common:2; Rare:83 | ||||
| chr14:20343161-20343661 | Common:13; Rare:293 | ||||
| chr14:20413415-20413531 | Common:3; Rare:32 | ||||
| chr14:20454768-20455320 | Common:7; Rare:145 | ||||
| chr14:20684002-20684355 | Common:15; Rare:155; Clinvar:2; Clinvar (benign):4 | ||||
| chr14:20684357-20684390 | Common:1; Rare:6; Clinvar (benign):1 | ||||
| chr14:20684418-20684756 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):3 |