| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:89829609-89829955 | Rare:89 | ||||
| chr6:90587003-90587202 | Common:3; Rare:66 | ||||
| chr6:93419525-93419824 | Common:1; Rare:79 | ||||
| chr6:95577398-95577606 | Common:5; Rare:60 | ||||
| chr6:96521723-96521906 | Common:3; Rare:91 | ||||
| chr6:96837516-96837687 | Common:2; Rare:47 | ||||
| chr6:96897778-96898040 | Common:4; Rare:98; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:97283178-97283282 | Rare:42 | ||||
| chr6:98834385-98834630 | Common:1; Rare:60 | ||||
| chr6:99425259-99425483 | Common:2; Rare:65 | ||||
| chr6:100881179-100881482 | Common:6; Rare:111 | ||||
| chr6:101398801-101399235 | Rare:83 | ||||
| chr6:105179955-105180108 | Common:4; Rare:43 | ||||
| chr6:106325599-106325892 | Common:1; Rare:102 | ||||
| chr6:106629435-106629658 | Common:3; Rare:55 |