| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915218-34915383 | Rare:48 | ||||
| chr5:34915463-34915882 | Common:2; Rare:126 | ||||
| chr5:35617708-35617981 | Common:1; Rare:63 | ||||
| chr5:36151881-36152214 | Rare:104 | ||||
| chr5:36242116-36242330 | Common:1; Rare:59 | ||||
| chr5:36876632-36876894 | Common:1; Rare:76; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371018-37371154 | Rare:56 | ||||
| chr5:38845712-38846106 | Common:2; Rare:101 | ||||
| chr5:39074340-39074657 | Common:2; Rare:129 | ||||
| chr5:39424607-39424725 | Common:1; Rare:19 | ||||
| chr5:39424787-39425322 | Common:3; Rare:127 | ||||
| chr5:40679665-40679955 | Common:2; Rare:71 | ||||
| chr5:40755823-40756176 | Common:1; Rare:94 | ||||
| chr5:40764557-40764820 | Rare:74 | ||||
| chr5:40798068-40798326 | Rare:94 |