| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:180802792-180802966 | Common:7; Rare:73 | ||||
| chr5:180861186-180861435 | Common:2; Rare:103 | ||||
| chr5:181223646-181223749 | Common:3; Rare:27 | ||||
| chr5:181261081-181261272 | Rare:65 | ||||
| chr6:2245431-2245833 | Common:1; Rare:134 | ||||
| chr6:2999621-2999893 | Common:10; Rare:58 | ||||
| chr6:3118611-3118743 | Common:2; Rare:43 | ||||
| chr6:4021183-4021415 | Rare:101 | ||||
| chr6:5004007-5004118 | Common:1; Rare:52 | ||||
| chr6:5260671-5261025 | Common:3; Rare:122; Clinvar (benign):4 | ||||
| chr6:5261253-5261553 | Common:9; Rare:76 | ||||
| chr6:6588579-6588773 | Common:1; Rare:62 | ||||
| chr6:7313105-7313380 | Common:4; Rare:103 | ||||
| chr6:7389753-7389829 | Rare:19 | ||||
| chr6:7541374-7541626 | Common:1; Rare:77 |