| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13586788-13587031 | Common:3; Rare:80 | ||||
| chr10:14838007-14838361 | Common:2; Rare:93 | ||||
| chr10:14878607-14878901 | Common:2; Rare:94 | ||||
| chr10:14954023-14954195 | Rare:61 | ||||
| chr10:15088725-15088923 | Common:1; Rare:86 | ||||
| chr10:15097301-15097412 | Common:1; Rare:53 | ||||
| chr10:15860271-15860589 | Common:2; Rare:88 | ||||
| chr10:16817315-16817724 | Common:5; Rare:142 | ||||
| chr10:17229101-17229289 | Common:2; Rare:36 | ||||
| chr10:17617282-17617485 | Common:4; Rare:73 | ||||
| chr10:17643860-17644286 | Common:2; Rare:130 | ||||
| chr10:18651570-18651809 | Common:1; Rare:94 | ||||
| chr10:24208834-24208935 | Rare:35 | ||||
| chr10:27100461-27100582 | Common:3; Rare:38; Clinvar:2; Clinvar (benign):2 | ||||
| chr10:27154323-27154456 | Rare:37 |