| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:69232426-69233225 | Common:3; Rare:218 | ||||
| chr6:69796601-69796947 | Common:3; Rare:127; Clinvar (benign):2 | ||||
| chr6:69867340-69867610 | Common:3; Rare:65 | ||||
| chr6:70413131-70413589 | Common:2; Rare:146 | ||||
| chr6:70566837-70566995 | Common:2; Rare:61 | ||||
| chr6:70667669-70667844 | Common:2; Rare:65 | ||||
| chr6:70668170-70668650 | Common:5; Rare:140 | ||||
| chr6:70957040-70957550 | Common:5; Rare:113 | ||||
| chr6:71288699-71288842 | Rare:48 | ||||
| chr6:73262625-73263025 | Common:1; Rare:104 | ||||
| chr6:73263140-73263274 | Common:3; Rare:35 | ||||
| chr6:73461664-73461988 | Common:1; Rare:115; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:73520015-73520415 | Common:2; Rare:253 | ||||
| chr6:73521017-73521385 | Common:1; Rare:90 | ||||
| chr6:73521553-73521726 | Rare:44 |