| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:108248659-108248867 | Rare:84 | ||||
| chr8:108443472-108443686 | Common:2; Rare:99 | ||||
| chr8:109334009-109334412 | Common:1; Rare:117 | ||||
| chr8:109539527-109539914 | Common:2; Rare:96 | ||||
| chr8:116874611-116874946 | Common:6; Rare:141; Clinvar (benign):1 | ||||
| chr8:119832818-119832903 | Common:1; Rare:34 | ||||
| chr8:119855849-119856007 | Common:1; Rare:45 | ||||
| chr8:120445097-120445467 | Common:1; Rare:96 | ||||
| chr8:123042187-123042374 | Common:2; Rare:51 | ||||
| chr8:123241335-123241467 | Common:1; Rare:53 | ||||
| chr8:124474966-124475099 | Rare:44 | ||||
| chr8:124538981-124539204 | Common:2; Rare:127; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124728409-124728728 | Common:4; Rare:98 | ||||
| chr8:124998210-124998731 | Common:5; Rare:201 | ||||
| chr8:125091707-125091919 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):3 |