| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181261065-181261274 | Rare:71 | ||||
| chr6:693069-693209 | Rare:42 | ||||
| chr6:2245430-2245743 | Common:1; Rare:106 | ||||
| chr6:2999644-2999903 | Common:10; Rare:55 | ||||
| chr6:3118589-3118755 | Common:2; Rare:57 | ||||
| chr6:3227505-3227965 | Rare:111 | ||||
| chr6:3231730-3231862 | Rare:22 | ||||
| chr6:3258825-3259060 | Rare:91 | ||||
| chr6:3456038-3456175 | Rare:44 | ||||
| chr6:3849145-3849441 | Common:3; Rare:83 | ||||
| chr6:4021201-4021437 | Rare:104 | ||||
| chr6:5260729-5261055 | Common:4; Rare:110; Clinvar (benign):2 | ||||
| chr6:5261260-5261553 | Common:9; Rare:74 | ||||
| chr6:6002932-6003004 | Common:1; Rare:16 | ||||
| chr6:7313109-7313363 | Common:4; Rare:94 |