| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153684143-153684285 | Common:1; Rare:47 | ||||
| chr4:173509440-173509656 | Rare:53 | ||||
| chr5:8457537-8457730 | Common:1; Rare:70 | ||||
| chr5:78510335-78510466 | Common:1; Rare:33 | ||||
| chr5:80059479-80059905 | Common:2; Rare:124 | ||||
| chr5:80070472-80070733 | Rare:65 | ||||
| chr5:112160575-112160878 | Common:2; Rare:90 | ||||
| chr5:148826469-148826632 | Common:1; Rare:44 | ||||
| chr5:150946527-150946616 | Rare:21 | ||||
| chr5:159100311-159100517 | Common:3; Rare:67 | ||||
| chr5:179832941-179833054 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:180830889-180831022 | Common:1; Rare:38 | ||||
| chr5:180831610-180831669 | Common:2; Rare:21 | ||||
| chr6:21596298-21596558 | Rare:96 | ||||
| chr6:22146268-22146345 | Rare:18 |