| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:181261107-181261239 | Rare:41 | ||||
| chr6:1311815-1312098 | Common:2; Rare:84 | ||||
| chr6:3118597-3118735 | Common:2; Rare:44 | ||||
| chr6:3227621-3227935 | Rare:77 | ||||
| chr6:4021212-4021423 | Rare:97 | ||||
| chr6:5260719-5261025 | Common:2; Rare:96; Clinvar (benign):2 | ||||
| chr6:5261238-5261553 | Common:9; Rare:78 | ||||
| chr6:7541374-7541620 | Common:1; Rare:76 | ||||
| chr6:8435494-8435659 | Common:3; Rare:62 | ||||
| chr6:10694614-10694974 | Common:4; Rare:91 | ||||
| chr6:10722848-10723149 | Common:4; Rare:98 | ||||
| chr6:10747630-10747857 | Common:2; Rare:93 | ||||
| chr6:13328515-13328621 | Common:2; Rare:36 | ||||
| chr6:13615180-13615400 | Common:2; Rare:97 | ||||
| chr6:16761444-16761724 | Common:2; Rare:86 |