| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:106285652-106286030 | Common:2; Rare:75 | ||||
| chr7:106661005-106661273 | Common:2; Rare:69 | ||||
| chr7:107563828-107564028 | Common:2; Rare:112; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:107564338-107564347 | Rare:1; Clinvar:1 | ||||
| chr7:107580147-107580307 | Common:2; Rare:61 | ||||
| chr7:107743582-107743916 | Common:5; Rare:127 | ||||
| chr7:107743996-107744190 | Common:1; Rare:62 | ||||
| chr7:108002859-108003286 | Common:1; Rare:131; Clinvar (benign):1 | ||||
| chr7:108526032-108526483 | Common:5; Rare:131 | ||||
| chr7:108569566-108570006 | Common:3; Rare:161 | ||||
| chr7:111090962-111091133 | Rare:34 | ||||
| chr7:112206318-112206804 | Common:2; Rare:172 | ||||
| chr7:112450129-112450491 | Common:7; Rare:101 | ||||
| chr7:114086191-114086568 | Common:2; Rare:138 | ||||
| chr7:114087604-114087667 | Rare:21 |