| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:3068455-3068590 | Common:1; Rare:44 | ||||
| chr6:3068830-3069071 | Common:4; Rare:174 | ||||
| chr6:3118148-3118548 | Common:8; Rare:221 | ||||
| chr6:3118569-3118773 | Common:5; Rare:128 | ||||
| chr6:3157492-3157753 | Common:14; Rare:148 | ||||
| chr6:3258768-3259068 | Rare:117 | ||||
| chr6:3455860-3456250 | Rare:154 | ||||
| chr6:3751709-3752224 | Common:10; Rare:253 | ||||
| chr6:4021124-4021467 | Common:1; Rare:252 | ||||
| chr6:4134670-4135160 | Common:8; Rare:138 | ||||
| chr6:4135130-4135410 | Common:1; Rare:94 | ||||
| chr6:5003587-5003843 | Common:12; Rare:152 | ||||
| chr6:5004003-5004141 | Common:4; Rare:115 | ||||
| chr6:5216226-5216920 | Common:8; Rare:202; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr6:5260674-5261074 | Common:12; Rare:276; Clinvar (benign):8 |