| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:98117030-98117366 | Common:4; Rare:121 | ||||
| chr8:99012998-99013406 | Rare:83; Clinvar:1 | ||||
| chr8:100150559-100150709 | Rare:45 | ||||
| chr8:100309897-100310254 | Common:1; Rare:128 | ||||
| chr8:100950536-100950709 | Common:8; Rare:93 | ||||
| chr8:101205522-101205881 | Common:4; Rare:115 | ||||
| chr8:101790908-101791124 | Rare:33 | ||||
| chr8:102238815-102239141 | Common:5; Rare:108; Clinvar:1; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr8:102412702-102412952 | Common:3; Rare:61 | ||||
| chr8:102864114-102864428 | Common:4; Rare:131 | ||||
| chr8:103020987-103021158 | Rare:53 | ||||
| chr8:103298730-103298927 | Common:1; Rare:49 | ||||
| chr8:103414579-103414742 | Common:5; Rare:52 | ||||
| chr8:103415071-103415511 | Common:6; Rare:221 | ||||
| chr8:104466656-104467160 | Common:5; Rare:152; Clinvar:4; Clinvar (benign):5 |