| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107563861-107564059 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):5 | ||||
| chr7:107580114-107580285 | Common:2; Rare:64 | ||||
| chr7:107743578-107743802 | Common:3; Rare:86 | ||||
| chr7:107744053-107744184 | Rare:43 | ||||
| chr7:107891032-107891251 | Rare:103; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:108003008-108003380 | Common:3; Rare:104 | ||||
| chr7:108456264-108456738 | Common:1; Rare:166 | ||||
| chr7:108526032-108526570 | Common:6; Rare:166 | ||||
| chr7:108569484-108570008 | Common:3; Rare:188 | ||||
| chr7:111090962-111091504 | Common:1; Rare:109 | ||||
| chr7:111562470-111562553 | Rare:45 | ||||
| chr7:112206271-112206805 | Common:3; Rare:182 | ||||
| chr7:112450129-112450472 | Common:7; Rare:92 | ||||
| chr7:112450782-112451060 | Common:2; Rare:79 | ||||
| chr7:112451211-112451304 | Rare:16 |