| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7313109-7313380 | Common:4; Rare:101 | ||||
| chr6:7389740-7389881 | Common:1; Rare:41 | ||||
| chr6:7541368-7541684 | Common:1; Rare:94; Clinvar (benign):1 | ||||
| chr6:7541840-7542085 | Common:3; Rare:100; Clinvar:15; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr6:8435354-8435659 | Common:4; Rare:105 | ||||
| chr6:10419655-10419887 | Common:4; Rare:39 | ||||
| chr6:10694636-10694988 | Common:4; Rare:89 | ||||
| chr6:10722817-10723241 | Common:6; Rare:143 | ||||
| chr6:10747592-10747860 | Common:3; Rare:105 | ||||
| chr6:11094140-11094305 | Rare:58 | ||||
| chr6:12008629-12008789 | Common:1; Rare:39 | ||||
| chr6:13328515-13328644 | Common:2; Rare:43 | ||||
| chr6:13615170-13615512 | Common:2; Rare:141 | ||||
| chr6:16761430-16761726 | Common:2; Rare:91 | ||||
| chr6:17280843-17281020 | Common:2; Rare:53 |