| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85643240-85643535 | Common:1; Rare:113 | ||||
| chr6:85643808-85643954 | Common:2; Rare:42 | ||||
| chr6:87155218-87155620 | Rare:112 | ||||
| chr6:87329271-87329318 | Rare:10 | ||||
| chr6:87407748-87408026 | Common:1; Rare:58 | ||||
| chr6:87472882-87473004 | Common:1; Rare:46; Clinvar (benign):4 | ||||
| chr6:87589946-87590177 | Common:3; Rare:109; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87701860-87702085 | Common:3; Rare:69 | ||||
| chr6:87702169-87702489 | Common:3; Rare:101 | ||||
| chr6:88963549-88963830 | Common:2; Rare:94 | ||||
| chr6:89145923-89146090 | Rare:46 | ||||
| chr6:89352670-89353008 | Common:1; Rare:75 | ||||
| chr6:89638419-89638851 | Common:6; Rare:132 | ||||
| chr6:89819688-89819888 | Rare:66 | ||||
| chr6:89829599-89829964 | Rare:96 |