| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87589946-87590160 | Common:2; Rare:97; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:88963585-88963830 | Common:2; Rare:83 | ||||
| chr6:89080581-89080824 | Common:1; Rare:105 | ||||
| chr6:89081048-89081376 | Common:2; Rare:125 | ||||
| chr6:89117976-89118114 | Common:2; Rare:64 | ||||
| chr6:89145983-89146094 | Rare:33 | ||||
| chr6:89352634-89353008 | Common:1; Rare:83 | ||||
| chr6:89638434-89638549 | Common:1; Rare:25 | ||||
| chr6:89638714-89638845 | Common:3; Rare:47 | ||||
| chr6:89819700-89819856 | Rare:55 | ||||
| chr6:89829609-89829969 | Common:1; Rare:91 | ||||
| chr6:93419256-93419319 | Rare:20 | ||||
| chr6:93419329-93419385 | Rare:14 | ||||
| chr6:93419393-93419831 | Common:1; Rare:109 | ||||
| chr6:95577356-95577602 | Common:6; Rare:71 |