| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:97775724-97775974 | Common:4; Rare:125; Clinvar (benign):1 | ||||
| chr8:97776031-97776101 | Common:2; Rare:18 | ||||
| chr8:97868982-97869160 | Common:1; Rare:35 | ||||
| chr8:98045333-98045679 | Common:4; Rare:103 | ||||
| chr8:98117083-98117368 | Common:4; Rare:95 | ||||
| chr8:99013015-99013350 | Rare:69; Clinvar:1 | ||||
| chr8:100150551-100150712 | Rare:50 | ||||
| chr8:100310036-100310435 | Common:1; Rare:151 | ||||
| chr8:100709123-100709615 | Common:9; Rare:125 | ||||
| chr8:100712363-100712791 | Common:2; Rare:119 | ||||
| chr8:100712817-100713229 | Common:10; Rare:104 | ||||
| chr8:100950417-100950712 | Common:11; Rare:124 | ||||
| chr8:100951199-100951537 | Common:3; Rare:128 | ||||
| chr8:100952356-100952641 | Common:1; Rare:89 | ||||
| chr8:100953299-100953436 | Common:1; Rare:28 |