| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:107198289-107198612 | Rare:82 | ||||
| chr7:107916587-107916906 | Common:1; Rare:75 | ||||
| chr7:107917700-107918040 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr7:107924049-107924194 | Common:3; Rare:51; Clinvar (benign):4 | ||||
| chr7:107924230-107924506 | Rare:53 | ||||
| chr7:107924630-107924650 | Rare:8 | ||||
| chr7:107933403-107933604 | Common:2; Rare:42 | ||||
| chr7:107935413-107935935 | Common:3; Rare:114; Clinvar:3; Clinvar (benign):2 | ||||
| chr7:107941171-107941238 | Rare:8 | ||||
| chr7:107944303-107944378 | Common:1; Rare:11 | ||||
| chr7:107944711-107944724 | Rare:2 | ||||
| chr7:107961306-107961678 | Common:3; Rare:105; Clinvar:1; Clinvar (benign):3 | ||||
| chr7:111205767-111205862 | Rare:17 | ||||
| chr7:112205565-112205644 | Rare:17 | ||||
| chr7:114419983-114420005 | Rare:3 |