| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51991039-51991357 | Common:2; Rare:82 | ||||
| chr3:52046638-52046775 | Rare:23 | ||||
| chr3:52074510-52074668 | Rare:21 | ||||
| chr3:52240648-52240746 | Common:1; Rare:10 | ||||
| chr3:52243912-52244076 | Rare:25 | ||||
| chr3:52298866-52298907 | Rare:6 | ||||
| chr3:52311610-52311831 | Common:2; Rare:41 | ||||
| chr3:52408572-52408837 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:52473666-52473822 | Common:5; Rare:40 | ||||
| chr3:52482153-52482219 | Rare:21 | ||||
| chr3:53180965-53181070 | Rare:22 | ||||
| chr3:54033880-54034036 | Common:6; Rare:38 | ||||
| chr3:54626375-54626430 | Rare:15 | ||||
| chr3:54627030-54627350 | Common:3; Rare:56 | ||||
| chr3:55367905-55368014 | Common:1; Rare:19 |