| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:98117144-98117340 | Common:4; Rare:63 | ||||
| chr8:99013036-99013315 | Rare:50 | ||||
| chr8:100150555-100150701 | Rare:47 | ||||
| chr8:102655705-102655844 | Common:1; Rare:48 | ||||
| chr8:103021002-103021132 | Rare:35 | ||||
| chr8:103415020-103415516 | Common:6; Rare:248 | ||||
| chr8:106657563-106657872 | Common:3; Rare:79 | ||||
| chr8:108248688-108248856 | Rare:67 | ||||
| chr8:108443417-108443667 | Common:4; Rare:113 | ||||
| chr8:109334060-109334427 | Common:1; Rare:98 | ||||
| chr8:116766292-116766548 | Common:4; Rare:62 | ||||
| chr8:119832797-119832888 | Common:1; Rare:44 | ||||
| chr8:120445102-120445440 | Common:1; Rare:81 | ||||
| chr8:123396359-123396555 | Common:2; Rare:89 | ||||
| chr8:124538981-124539198 | Common:2; Rare:126; Clinvar (benign):5; Clinvar (pathogenic):1 |