| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:81937450-81937700 | Rare:54 | ||||
| chr6:85678722-85678984 | Rare:89 | ||||
| chr6:89655903-89656187 | Common:1; Rare:68 | ||||
| chr6:89720897-89721156 | Common:2; Rare:41 | ||||
| chr6:106560587-106560842 | Common:1; Rare:46 | ||||
| chr6:106561129-106561499 | Common:2; Rare:81 | ||||
| chr6:109445226-109445497 | Common:2; Rare:93 | ||||
| chr6:109453735-109454081 | Rare:136 | ||||
| chr6:111309076-111309310 | Common:1; Rare:50 | ||||
| chr6:111322073-111322237 | Rare:33 | ||||
| chr6:113873308-113873409 | Common:2; Rare:21 | ||||
| chr6:127290213-127290404 | Rare:54 | ||||
| chr6:128519240-128519297 | Rare:15 | ||||
| chr6:129460138-129460288 | Rare:47; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr6:134820568-134820580 |