| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:33513182-33513496 | Common:6; Rare:131 | ||||
| chr8:37736514-37736955 | Common:3; Rare:121 | ||||
| chr8:37762460-37762736 | Common:3; Rare:103; Clinvar (benign):1 | ||||
| chr8:37849823-37850043 | Common:2; Rare:76 | ||||
| chr8:38030221-38030289 | Common:1; Rare:13 | ||||
| chr8:38030290-38030649 | Common:3; Rare:104 | ||||
| chr8:38105441-38105556 | Common:1; Rare:42 | ||||
| chr8:38105779-38105970 | Rare:55 | ||||
| chr8:38176426-38176535 | Common:1; Rare:41 | ||||
| chr8:38176650-38177013 | Common:5; Rare:109 | ||||
| chr8:38231540-38231825 | Rare:71 | ||||
| chr8:38269103-38269315 | Rare:87 | ||||
| chr8:38386467-38386508 | Rare:12 | ||||
| chr8:38404068-38404437 | Rare:107 | ||||
| chr8:38414133-38414478 | Rare:68; Clinvar:1; Clinvar (benign):2 |