| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100150564-100150708 | Rare:44 | ||||
| chr8:100309868-100310231 | Common:1; Rare:119 | ||||
| chr8:100706649-100707028 | Common:10; Rare:101 | ||||
| chr8:100709131-100709735 | Common:11; Rare:150 | ||||
| chr8:100950349-100950706 | Common:11; Rare:137 | ||||
| chr8:100953254-100953445 | Common:1; Rare:35 | ||||
| chr8:100953452-100953483 | Rare:10 | ||||
| chr8:101204769-101204840 | Rare:13 | ||||
| chr8:101206001-101206094 | Rare:21 | ||||
| chr8:101491811-101492181 | Common:2; Rare:68 | ||||
| chr8:101492271-101492458 | Common:2; Rare:29 | ||||
| chr8:101492460-101492841 | Common:1; Rare:87; Clinvar (benign):2 | ||||
| chr8:102412689-102412980 | Common:3; Rare:70 | ||||
| chr8:102864071-102864434 | Common:6; Rare:146 | ||||
| chr8:103298730-103298963 | Common:2; Rare:53 |