| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:102671631-102671836 | Common:8; Rare:31 | ||||
| chr7:102748696-102749041 | Common:2; Rare:81 | ||||
| chr7:103297347-103297462 | Common:1; Rare:37 | ||||
| chr7:103344655-103344903 | Common:1; Rare:80 | ||||
| chr7:104207941-104208112 | Common:3; Rare:85 | ||||
| chr7:105014034-105014220 | Common:3; Rare:81 | ||||
| chr7:105522180-105522391 | Common:5; Rare:75 | ||||
| chr7:105532054-105532260 | Common:3; Rare:53 | ||||
| chr7:105876481-105876843 | Common:6; Rare:108 | ||||
| chr7:106112204-106112494 | Common:3; Rare:97 | ||||
| chr7:106284911-106285485 | Common:6; Rare:200 | ||||
| chr7:106285508-106285545 | Rare:5 | ||||
| chr7:106661152-106661273 | Common:1; Rare:17 | ||||
| chr7:107168728-107169015 | Rare:97 | ||||
| chr7:107563861-107564059 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):5 |