| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:100114434-100114713 | Common:2; Rare:50 | ||||
| chr3:100260688-100261048 | Rare:103 | ||||
| chr3:100261336-100261353 | Rare:4 | ||||
| chr3:100334630-100334998 | Common:3; Rare:148 | ||||
| chr3:100401398-100401586 | Common:1; Rare:35 | ||||
| chr3:100492420-100492839 | Common:11; Rare:111 | ||||
| chr3:100709203-100709721 | Common:9; Rare:156; Clinvar (benign):1 | ||||
| chr3:100765899-100765993 | Rare:22 | ||||
| chr3:101513089-101513232 | Common:7; Rare:39 | ||||
| chr3:101513284-101513310 | Rare:8 | ||||
| chr3:101513311-101513343 | Rare:7 | ||||
| chr3:101561743-101561979 | Common:2; Rare:87 | ||||
| chr3:101573995-101574371 | Common:1; Rare:123 | ||||
| chr3:101677043-101677178 | Rare:56 | ||||
| chr3:101685816-101686036 | Common:3; Rare:58 |