| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:96261557-96261943 | Common:6; Rare:129 | ||||
| chr8:98045370-98045609 | Common:3; Rare:71 | ||||
| chr8:98117144-98117325 | Common:2; Rare:61 | ||||
| chr8:99013015-99013322 | Rare:60 | ||||
| chr8:100150565-100150724 | Rare:45 | ||||
| chr8:103298580-103298895 | Common:2; Rare:76 | ||||
| chr8:103415090-103415476 | Common:6; Rare:200 | ||||
| chr8:108248706-108248874 | Rare:65 | ||||
| chr8:109334051-109334396 | Common:1; Rare:90 | ||||
| chr8:119855894-119855956 | Common:1; Rare:11 | ||||
| chr8:120445120-120445455 | Common:1; Rare:79 | ||||
| chr8:124474949-124475121 | Rare:57 | ||||
| chr8:124539054-124539204 | Common:1; Rare:79; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:126558353-126558628 | Common:1; Rare:103 | ||||
| chr8:127735836-127736073 | Rare:52 |