| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:122781599-122781760 | Common:3; Rare:22 | ||||
| chr8:123396353-123396562 | Common:2; Rare:94 | ||||
| chr8:124474938-124475099 | Rare:48 | ||||
| chr8:124539062-124539189 | Common:1; Rare:68; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091709-125091914 | Common:2; Rare:71; Clinvar (benign):3 | ||||
| chr8:127735895-127736081 | Rare:43 | ||||
| chr8:127736119-127736307 | Common:3; Rare:43 | ||||
| chr8:133571793-133572282 | Common:1; Rare:125 | ||||
| chr8:134712994-134713215 | Common:1; Rare:70 | ||||
| chr8:140511195-140511547 | Common:3; Rare:130 | ||||
| chr8:140718510-140718896 | Rare:59 | ||||
| chr8:141001142-141001458 | Common:2; Rare:112 | ||||
| chr8:141391893-141392073 | Common:1; Rare:62 | ||||
| chr8:142669949-142670297 | Common:9; Rare:125 | ||||
| chr8:142777783-142777934 | Rare:33 |