| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:73008627-73008918 | Common:1; Rare:104 | ||||
| chr8:73293583-73293694 | Rare:67 | ||||
| chr8:73293941-73294263 | Common:2; Rare:98 | ||||
| chr8:73294427-73294602 | Common:1; Rare:64 | ||||
| chr8:73295783-73295879 | Common:2; Rare:28 | ||||
| chr8:73746812-73747284 | Common:4; Rare:138 | ||||
| chr8:73747452-73747566 | Rare:21 | ||||
| chr8:73878820-73879009 | Common:3; Rare:93 | ||||
| chr8:73972022-73972573 | Common:2; Rare:153 | ||||
| chr8:73976018-73976260 | Common:6; Rare:85; Clinvar:2; Clinvar (benign):2 | ||||
| chr8:74350001-74350054 | Rare:6 | ||||
| chr8:74350260-74350559 | Common:2; Rare:124; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:74984351-74984702 | Common:3; Rare:124 | ||||
| chr8:76681110-76681279 | Common:1; Rare:35 | ||||
| chr8:77000029-77000451 | Common:7; Rare:151; Clinvar:5 |