| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103415024-103415476 | Common:6; Rare:235 | ||||
| chr8:104588984-104589137 | Common:3; Rare:62 | ||||
| chr8:108248692-108248879 | Rare:74 | ||||
| chr8:108443472-108443661 | Common:2; Rare:84 | ||||
| chr8:109334078-109334465 | Common:1; Rare:101 | ||||
| chr8:119416140-119416472 | Common:1; Rare:66 | ||||
| chr8:119416575-119416823 | Common:2; Rare:72 | ||||
| chr8:119832826-119832878 | Common:1; Rare:19 | ||||
| chr8:120445087-120445390 | Common:1; Rare:72 | ||||
| chr8:123274248-123274326 | Rare:4 | ||||
| chr8:123396350-123396562 | Common:2; Rare:96 | ||||
| chr8:123416333-123416665 | Rare:87 | ||||
| chr8:124474549-124474773 | Rare:79 | ||||
| chr8:124539024-124539283 | Common:2; Rare:128; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091707-125091871 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):3 |