| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:38782658-38782940 | Common:2; Rare:49 | ||||
| chr4:38804787-38804888 | Common:2; Rare:16 | ||||
| chr4:38805634-38805947 | Common:5; Rare:46 | ||||
| chr4:38867588-38867840 | Common:2; Rare:86 | ||||
| chr4:39032319-39032409 | Rare:19 | ||||
| chr4:39032889-39032996 | Rare:15 | ||||
| chr4:39044379-39044970 | Common:8; Rare:155 | ||||
| chr4:39182114-39182538 | Common:1; Rare:91; Clinvar:1 | ||||
| chr4:39366059-39366081 | Common:1; Rare:7 | ||||
| chr4:39366270-39366492 | Common:2; Rare:71 | ||||
| chr4:39458361-39458555 | Rare:77 | ||||
| chr4:39458803-39459165 | Common:3; Rare:190; Clinvar:4; Clinvar (benign):6 | ||||
| chr4:39459459-39459582 | Rare:26 | ||||
| chr4:39527407-39527881 | Common:2; Rare:129 | ||||
| chr4:39527945-39528095 | Common:1; Rare:35 |