| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:87589915-87590171 | Common:3; Rare:132; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr6:87702195-87702443 | Common:1; Rare:80 | ||||
| chr6:88165868-88166277 | Common:2; Rare:121 | ||||
| chr6:88963540-88963830 | Common:2; Rare:96 | ||||
| chr6:89080733-89080811 | Common:1; Rare:31 | ||||
| chr6:89081621-89081869 | Common:2; Rare:88 | ||||
| chr6:89117907-89118131 | Common:4; Rare:91 | ||||
| chr6:89562101-89562332 | Rare:45 | ||||
| chr6:89562622-89562795 | Rare:27 | ||||
| chr6:89638404-89638606 | Common:1; Rare:43 | ||||
| chr6:89638721-89638845 | Common:3; Rare:42 | ||||
| chr6:89819702-89819823 | Rare:40 | ||||
| chr6:89829609-89829964 | Rare:91 | ||||
| chr6:90296550-90296945 | Common:4; Rare:128 | ||||
| chr6:90586873-90587202 | Common:3; Rare:109 |