| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197749742-197750018 | Common:1; Rare:98 | ||||
| chr3:197949886-197950269 | Common:4; Rare:114; Clinvar (benign):2 | ||||
| chr3:197950880-197950978 | Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959979-197960245 | Common:1; Rare:92 | ||||
| chr4:337532-337908 | Common:5; Rare:100 | ||||
| chr4:499121-499324 | Common:3; Rare:81 | ||||
| chr4:663657-663736 | Rare:23 | ||||
| chr4:673842-673948 | Rare:45 | ||||
| chr4:674223-674590 | Common:3; Rare:173 | ||||
| chr4:705567-705948 | Common:1; Rare:128 | ||||
| chr4:932216-932492 | Common:2; Rare:108 | ||||
| chr4:993365-993560 | Common:5; Rare:35 | ||||
| chr4:993860-993955 | Common:3; Rare:32 | ||||
| chr4:1113544-1113630 | Common:1; Rare:31 | ||||
| chr4:1720555-1720634 | Rare:24 |