| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:117520541-117520788 | Common:5; Rare:63 | ||||
| chr8:118951820-118952259 | Common:1; Rare:117; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832792-119832919 | Common:2; Rare:54 | ||||
| chr8:119855868-119855990 | Common:1; Rare:26 | ||||
| chr8:119873568-119873775 | Common:1; Rare:46 | ||||
| chr8:120445097-120445435 | Common:1; Rare:81 | ||||
| chr8:121641387-121641727 | Common:1; Rare:70 | ||||
| chr8:122781364-122781689 | Common:1; Rare:66 | ||||
| chr8:123042228-123042360 | Common:1; Rare:37 | ||||
| chr8:123241336-123241435 | Common:1; Rare:44 | ||||
| chr8:123416425-123416821 | Rare:106 | ||||
| chr8:124474941-124475121 | Rare:58 | ||||
| chr8:124538991-124539204 | Common:2; Rare:121; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124549873-124550052 | Rare:39; Clinvar (benign):1 | ||||
| chr8:125091725-125091914 | Common:2; Rare:66; Clinvar (benign):3 |