| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:118111384-118111540 | Rare:19; Clinvar:1 | ||||
| chr8:118111664-118111989 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):5 | ||||
| chr8:118951810-118952159 | Common:2; Rare:102; Clinvar:7; Clinvar (benign):2 | ||||
| chr8:119209005-119209092 | Common:1; Rare:21 | ||||
| chr8:119832815-119832877 | Common:1; Rare:25 | ||||
| chr8:119855868-119855956 | Common:1; Rare:18 | ||||
| chr8:120445076-120445451 | Common:1; Rare:96 | ||||
| chr8:120810913-120811223 | Common:3; Rare:86 | ||||
| chr8:120812133-120812339 | Rare:44 | ||||
| chr8:122781244-122781317 | Rare:5 | ||||
| chr8:122781631-122781913 | Common:3; Rare:55 | ||||
| chr8:123042148-123042583 | Common:3; Rare:117 | ||||
| chr8:123274427-123274745 | Common:2; Rare:100 | ||||
| chr8:123396212-123396555 | Common:2; Rare:152 | ||||
| chr8:123416321-123416743 | Rare:114 |