| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87472832-87473006 | Common:1; Rare:60; Clinvar (benign):4 | ||||
| chr6:87589955-87590197 | Common:3; Rare:113; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:87701200-87701463 | Common:3; Rare:67 | ||||
| chr6:87701491-87701642 | Common:1; Rare:52 | ||||
| chr6:87701675-87701928 | Common:2; Rare:93 | ||||
| chr6:87702022-87702534 | Common:6; Rare:159 | ||||
| chr6:88165791-88166465 | Common:3; Rare:195 | ||||
| chr6:88963475-88963816 | Common:2; Rare:109 | ||||
| chr6:89080571-89080818 | Common:1; Rare:106 | ||||
| chr6:89081022-89081340 | Rare:129 | ||||
| chr6:89117889-89118122 | Common:3; Rare:98 | ||||
| chr6:89145983-89146132 | Rare:48 | ||||
| chr6:89352613-89353008 | Common:2; Rare:92 | ||||
| chr6:89412087-89412455 | Common:3; Rare:83 | ||||
| chr6:89562771-89562878 | Common:1; Rare:23 |