| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3231733-3231836 | Rare:18 | ||||
| chr6:4021201-4021417 | Rare:96 | ||||
| chr6:5003668-5003826 | Common:5; Rare:45 | ||||
| chr6:5003998-5004102 | Common:2; Rare:52 | ||||
| chr6:5260696-5261025 | Common:3; Rare:108; Clinvar (benign):4 | ||||
| chr6:7313059-7313380 | Common:5; Rare:122 | ||||
| chr6:7389718-7389866 | Common:1; Rare:50 | ||||
| chr6:7590086-7590254 | Common:5; Rare:52 | ||||
| chr6:8102505-8102711 | Common:1; Rare:70 | ||||
| chr6:8435484-8435659 | Common:3; Rare:70 | ||||
| chr6:10556169-10556298 | Rare:33; Clinvar:1 | ||||
| chr6:10585616-10585778 | Common:3; Rare:36 | ||||
| chr6:10694603-10694988 | Common:4; Rare:103 | ||||
| chr6:10747441-10747865 | Common:4; Rare:143 | ||||
| chr6:11044326-11044619 | Common:3; Rare:95 |