| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:105876475-105876844 | Common:6; Rare:109 | ||||
| chr7:105877364-105877400 | Rare:4 | ||||
| chr7:106284862-106285276 | Common:2; Rare:164 | ||||
| chr7:106285539-106285824 | Rare:61 | ||||
| chr7:107563861-107564028 | Common:2; Rare:99; Clinvar:1; Clinvar (benign):4 | ||||
| chr7:107580174-107580294 | Common:2; Rare:44 | ||||
| chr7:107743603-107743816 | Common:3; Rare:82 | ||||
| chr7:107744053-107744171 | Rare:37 | ||||
| chr7:107929063-107929620 | Common:4; Rare:162; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:107932336-107932640 | Rare:71; Clinvar (benign):1 | ||||
| chr7:108526032-108526223 | Rare:51 | ||||
| chr7:108569562-108570006 | Common:3; Rare:164 | ||||
| chr7:111091031-111091226 | Rare:42 | ||||
| chr7:112206329-112206783 | Common:2; Rare:155 | ||||
| chr7:112450287-112450465 | Common:4; Rare:60 |