| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:83853483-83853644 | Common:1; Rare:49 | ||||
| chr6:84763451-84763598 | Rare:36 | ||||
| chr6:84764585-84764805 | Common:1; Rare:63 | ||||
| chr6:85449912-85450118 | Common:1; Rare:60 | ||||
| chr6:85593309-85593438 | Common:2; Rare:29 | ||||
| chr6:85593706-85593990 | Common:1; Rare:99 | ||||
| chr6:85643812-85643931 | Common:2; Rare:37 | ||||
| chr6:87155229-87155631 | Rare:116 | ||||
| chr6:87472882-87473006 | Common:1; Rare:47; Clinvar (benign):4 | ||||
| chr6:87589915-87590192 | Common:3; Rare:143; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87701857-87702085 | Common:3; Rare:69 | ||||
| chr6:87702176-87702497 | Common:2; Rare:102 | ||||
| chr6:88165830-88166310 | Common:3; Rare:141 | ||||
| chr6:88963555-88963830 | Common:2; Rare:93 | ||||
| chr6:89080571-89080824 | Common:1; Rare:107 |