| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:71698320-71698731 | Common:7; Rare:158 | ||||
| chr10:71725508-71725908 | Common:3; Rare:83; Clinvar (benign):1 | ||||
| chr10:71727156-71727481 | Common:5; Rare:78 | ||||
| chr10:71727533-71727906 | Rare:64 | ||||
| chr10:71727909-71728054 | Rare:47 | ||||
| chr10:71735998-71736602 | Common:5; Rare:180 | ||||
| chr10:71747496-71747896 | Common:4; Rare:89 | ||||
| chr10:71747971-71748139 | Common:1; Rare:32 | ||||
| chr10:71748600-71749250 | Common:5; Rare:141 | ||||
| chr10:71767160-71767500 | Common:3; Rare:57 | ||||
| chr10:71768903-71769175 | Common:4; Rare:79 | ||||
| chr10:71769338-71769901 | Common:14; Rare:199 | ||||
| chr10:71772312-71772444 | Common:1; Rare:33 | ||||
| chr10:71782480-71783293 | Common:10; Rare:306 | ||||
| chr10:71801450-71801625 | Common:1; Rare:26 |