| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:96235510-96235681 | Common:2; Rare:150; Clinvar (benign):4 | ||||
| chr8:96261532-96262000 | Common:12; Rare:294 | ||||
| chr8:96493488-96494176 | Common:5; Rare:313 | ||||
| chr8:96494208-96494528 | Common:2; Rare:145 | ||||
| chr8:96644972-96645384 | Common:5; Rare:160 | ||||
| chr8:97643830-97644378 | Common:10; Rare:143 | ||||
| chr8:97775701-97775918 | Common:7; Rare:170 | ||||
| chr8:98045331-98045684 | Common:8; Rare:204 | ||||
| chr8:98117078-98117389 | Common:8; Rare:195 | ||||
| chr8:98825618-98826030 | Common:8; Rare:130 | ||||
| chr8:99012951-99013420 | Rare:161; Clinvar:1 | ||||
| chr8:100150551-100150706 | Rare:95 | ||||
| chr8:100212640-100213150 | Common:9; Rare:180; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:100309868-100310296 | Common:2; Rare:287 | ||||
| chr8:100722269-100722524 | Common:2; Rare:152 |