| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:52450514-52450936 | Common:4; Rare:284 | ||||
| chr13:52454948-52455700 | Common:37; Rare:762 | ||||
| chr13:52455763-52456176 | Common:11; Rare:279 | ||||
| chr13:52651932-52652960 | Common:34; Rare:1102 | ||||
| chr13:52738890-52739150 | Common:2; Rare:74 | ||||
| chr13:60163299-60163699 | Common:4; Rare:95; Clinvar (benign):1 | ||||
| chr13:60163762-60164213 | Common:12; Rare:599 | ||||
| chr13:60396184-60396687 | Common:11; Rare:591 | ||||
| chr13:60396614-60397014 | Common:2; Rare:167 | ||||
| chr13:60396950-60397400 | Common:8; Rare:369 | ||||
| chr13:60397420-60397710 | Common:6; Rare:195 | ||||
| chr13:67230287-67230710 | Common:10; Rare:579 | ||||
| chr13:71867085-71867573 | Common:7; Rare:240 | ||||
| chr13:72727012-72727412 | Common:6; Rare:88 | ||||
| chr13:72727527-72728002 | Common:42; Rare:1079 |