| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:85643209-85643696 | Common:2; Rare:175 | ||||
| chr6:85643753-85643933 | Common:3; Rare:58 | ||||
| chr6:87155268-87155624 | Rare:103 | ||||
| chr6:87589924-87590190 | Common:3; Rare:135; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr6:87701361-87701498 | Rare:40 | ||||
| chr6:87702169-87702497 | Common:3; Rare:104 | ||||
| chr6:88963458-88963830 | Common:2; Rare:118 | ||||
| chr6:89080576-89080784 | Common:1; Rare:91 | ||||
| chr6:89081470-89081706 | Common:3; Rare:70 | ||||
| chr6:89117917-89118122 | Common:3; Rare:88 | ||||
| chr6:89145973-89146330 | Rare:117 | ||||
| chr6:89638451-89638611 | Common:1; Rare:34 | ||||
| chr6:89638685-89638837 | Common:5; Rare:57 | ||||
| chr6:89819670-89819942 | Rare:86 | ||||
| chr6:89829595-89830016 | Common:2; Rare:108 |