| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:106270024-106270351 | Common:1; Rare:121 | ||||
| chr8:108248659-108248858 | Rare:84 | ||||
| chr8:109334016-109334412 | Common:1; Rare:115 | ||||
| chr8:109539477-109539914 | Common:2; Rare:110 | ||||
| chr8:109540074-109540202 | Common:1; Rare:29 | ||||
| chr8:116874383-116874676 | Common:2; Rare:76; Clinvar (benign):1 | ||||
| chr8:118951829-118952145 | Common:1; Rare:88; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832829-119832897 | Common:1; Rare:22 | ||||
| chr8:119855868-119855956 | Common:1; Rare:18 | ||||
| chr8:120445092-120445461 | Common:1; Rare:96 | ||||
| chr8:122781626-122781666 | Rare:3 | ||||
| chr8:123241337-123241444 | Common:1; Rare:44 | ||||
| chr8:124474978-124475110 | Rare:44 | ||||
| chr8:124538981-124539198 | Common:2; Rare:126; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091687-125091938 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 |