| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107580130-107580306 | Common:2; Rare:66 | ||||
| chr7:107743604-107743801 | Common:3; Rare:72 | ||||
| chr7:107744053-107744205 | Rare:54 | ||||
| chr7:107891016-107891256 | Rare:108; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:108526039-108526475 | Common:5; Rare:130 | ||||
| chr7:108569565-108570013 | Common:3; Rare:163 | ||||
| chr7:111090935-111091279 | Rare:68 | ||||
| chr7:112206314-112206783 | Common:2; Rare:160 | ||||
| chr7:112450184-112450477 | Common:6; Rare:86 | ||||
| chr7:112790355-112790441 | Rare:23 | ||||
| chr7:113086467-113086516 | Rare:3 | ||||
| chr7:113087695-113087910 | Rare:38 | ||||
| chr7:116499512-116499779 | Common:3; Rare:91 | ||||
| chr7:117020145-117020307 | Rare:23 | ||||
| chr7:117872206-117872384 | Common:2; Rare:39 |