| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:88963545-88963830 | Common:2; Rare:95 | ||||
| chr6:89080600-89080784 | Common:1; Rare:81 | ||||
| chr6:89081022-89081365 | Common:2; Rare:136 | ||||
| chr6:89145973-89146090 | Rare:34 | ||||
| chr6:89638434-89638537 | Common:1; Rare:22 | ||||
| chr6:89638713-89638845 | Common:3; Rare:47 | ||||
| chr6:89672229-89672561 | Common:1; Rare:67 | ||||
| chr6:89819688-89819891 | Rare:67 | ||||
| chr6:89829609-89829949 | Rare:86 | ||||
| chr6:90587000-90587334 | Common:3; Rare:92 | ||||
| chr6:93419552-93419764 | Common:1; Rare:62 | ||||
| chr6:95577404-95577590 | Common:5; Rare:54 | ||||
| chr6:96521706-96521876 | Common:5; Rare:77 | ||||
| chr6:96897812-96898012 | Common:2; Rare:77; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:97283190-97283323 | Common:2; Rare:41 |