| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:98117083-98117340 | Common:4; Rare:89 | ||||
| chr8:99013007-99013318 | Rare:60 | ||||
| chr8:100150555-100150701 | Rare:47 | ||||
| chr8:100951265-100951463 | Common:2; Rare:71 | ||||
| chr8:101492328-101492441 | Rare:23 | ||||
| chr8:102655699-102655850 | Common:1; Rare:55 | ||||
| chr8:103020871-103021132 | Common:1; Rare:76 | ||||
| chr8:103415084-103415512 | Common:6; Rare:215 | ||||
| chr8:106657554-106657918 | Common:5; Rare:105 | ||||
| chr8:108248679-108248872 | Rare:78 | ||||
| chr8:108443463-108443653 | Common:3; Rare:80 | ||||
| chr8:109334027-109334406 | Common:1; Rare:109 | ||||
| chr8:118951875-118952133 | Common:1; Rare:67; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832824-119832875 | Common:1; Rare:18 | ||||
| chr8:119855845-119855945 | Common:1; Rare:24 |