| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:110615354-110615816 | Common:7; Rare:367 | ||||
| chr13:110615750-110616150 | Common:3; Rare:123 | ||||
| chr13:110705940-110706439 | Common:10; Rare:314; Clinvar:6; Clinvar (benign):18 | ||||
| chr13:110712293-110712684 | Common:1; Rare:380 | ||||
| chr13:110712834-110713318 | Common:6; Rare:625 | ||||
| chr13:110713481-110713754 | Common:6; Rare:283 | ||||
| chr13:110714405-110715089 | Common:5; Rare:339 | ||||
| chr13:110715217-110715970 | Common:8; Rare:703 | ||||
| chr13:110914393-110914694 | Common:7; Rare:173 | ||||
| chr13:110914932-110915349 | Common:6; Rare:278 | ||||
| chr13:111153427-111153855 | Common:7; Rare:375 | ||||
| chr13:111154040-111154931 | Common:5; Rare:277 | ||||
| chr13:112587975-112588341 | Rare:216 | ||||
| chr13:112689904-112690652 | Common:6; Rare:335 | ||||
| chr13:112894140-112894425 | Common:23; Rare:201 |