| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:119416303-119416501 | Rare:47 | ||||
| chr8:119638805-119639028 | Common:1; Rare:36 | ||||
| chr8:119832825-119832897 | Common:1; Rare:26 | ||||
| chr8:119855817-119855947 | Common:2; Rare:38 | ||||
| chr8:120125468-120125650 | Rare:31 | ||||
| chr8:120445093-120445455 | Common:1; Rare:91 | ||||
| chr8:122781599-122781934 | Common:3; Rare:64 | ||||
| chr8:123274374-123274711 | Common:2; Rare:103 | ||||
| chr8:123396365-123396557 | Common:2; Rare:87 | ||||
| chr8:124474513-124474720 | Common:1; Rare:77 | ||||
| chr8:124474963-124475099 | Rare:44 | ||||
| chr8:124538996-124539189 | Common:2; Rare:112; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091626-125091924 | Common:2; Rare:98; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126558389-126558628 | Common:1; Rare:86 | ||||
| chr8:127735804-127736092 | Common:1; Rare:65 |