| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:693054-693172 | Rare:42 | ||||
| chr6:1626543-1626633 | Rare:16 | ||||
| chr6:2245438-2245846 | Common:1; Rare:140 | ||||
| chr6:2999613-2999981 | Common:10; Rare:80 | ||||
| chr6:3118587-3118750 | Common:2; Rare:56 | ||||
| chr6:3231730-3231817 | Rare:15 | ||||
| chr6:3258825-3259020 | Rare:72 | ||||
| chr6:4021200-4021460 | Rare:113 | ||||
| chr6:5003662-5003843 | Common:5; Rare:56 | ||||
| chr6:5004007-5004112 | Common:1; Rare:51 | ||||
| chr6:5260648-5261059 | Common:5; Rare:150; Clinvar (benign):4 | ||||
| chr6:5261268-5261585 | Common:9; Rare:86 | ||||
| chr6:7108559-7108665 | Common:1; Rare:35 | ||||
| chr6:7313049-7313380 | Common:5; Rare:125 | ||||
| chr6:7389740-7389966 | Common:1; Rare:60 |