| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100951252-100951548 | Common:3; Rare:108 | ||||
| chr8:100952407-100952770 | Common:1; Rare:114 | ||||
| chr8:100953194-100953479 | Common:1; Rare:61 | ||||
| chr8:101205278-101205897 | Common:5; Rare:191 | ||||
| chr8:101790908-101791120 | Rare:33 | ||||
| chr8:102238773-102239000 | Common:4; Rare:91; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr8:102239026-102239370 | Common:5; Rare:75; Clinvar (benign):1 | ||||
| chr8:102412235-102412555 | Common:1; Rare:95 | ||||
| chr8:102864066-102864559 | Common:7; Rare:197 | ||||
| chr8:103020855-103021137 | Common:1; Rare:79 | ||||
| chr8:103414978-103415512 | Common:6; Rare:262 | ||||
| chr8:103500475-103500683 | Common:2; Rare:56 | ||||
| chr8:103500696-103500899 | Rare:48 | ||||
| chr8:106269997-106270433 | Common:1; Rare:149 | ||||
| chr8:108248679-108248884 | Rare:85 |