| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:5004007-5004126 | Common:1; Rare:53 | ||||
| chr6:5260651-5261017 | Common:3; Rare:128; Clinvar (benign):4 | ||||
| chr6:5261253-5261569 | Common:9; Rare:83 | ||||
| chr6:7107501-7107879 | Rare:131 | ||||
| chr6:7313127-7313380 | Common:4; Rare:93 | ||||
| chr6:7389740-7389892 | Common:1; Rare:46 | ||||
| chr6:7541385-7541738 | Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:8102472-8102737 | Common:1; Rare:91 | ||||
| chr6:8435432-8435670 | Common:5; Rare:87 | ||||
| chr6:10694636-10694984 | Common:4; Rare:87 | ||||
| chr6:10722823-10723241 | Common:6; Rare:140 | ||||
| chr6:10747575-10747877 | Common:3; Rare:116 | ||||
| chr6:10838481-10838644 | Common:4; Rare:48; Clinvar:4 | ||||
| chr6:11093644-11093829 | Rare:59 | ||||
| chr6:11232582-11232947 | Rare:79 |