| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173168757-173168838 | Common:2; Rare:38 | ||||
| chr4:173169087-173169321 | Common:2; Rare:79 | ||||
| chr4:173333603-173333873 | Common:1; Rare:71 | ||||
| chr4:173369738-173369979 | Common:1; Rare:75 | ||||
| chr4:173370646-173370994 | Common:2; Rare:88 | ||||
| chr4:173371133-173371360 | Common:3; Rare:78 | ||||
| chr4:173530073-173530482 | Common:2; Rare:87 | ||||
| chr4:174283420-174283965 | Common:2; Rare:98 | ||||
| chr4:174522272-174522659 | Common:1; Rare:117; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:176002315-176002595 | Rare:81 | ||||
| chr4:176319677-176320079 | Common:5; Rare:127 | ||||
| chr4:177442370-177442519 | Rare:90; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182917325-182917554 | Common:4; Rare:78 | ||||
| chr4:183098999-183099151 | Common:1; Rare:57 | ||||
| chr4:183504522-183504834 | Common:3; Rare:103 |