| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:40691527-40691865 | Common:2; Rare:153 | ||||
| chr1:40979593-40979745 | Common:2; Rare:57 | ||||
| chr1:42335134-42335356 | Common:4; Rare:114 | ||||
| chr1:42456004-42456583 | Common:1; Rare:170 | ||||
| chr1:42463018-42463316 | Common:4; Rare:89 | ||||
| chr1:42658214-42658512 | Common:2; Rare:87 | ||||
| chr1:42682132-42682442 | Common:2; Rare:81 | ||||
| chr1:42683217-42683465 | Common:3; Rare:107 | ||||
| chr1:42766996-42767321 | Common:5; Rare:112; Clinvar (benign):1 | ||||
| chr1:42817004-42817136 | Common:1; Rare:32 | ||||
| chr1:42846401-42846636 | Common:1; Rare:65 | ||||
| chr1:42958823-42959082 | Common:4; Rare:72; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:43358838-43359006 | Rare:41 | ||||
| chr1:43367934-43368190 | Rare:63 | ||||
| chr1:43389752-43389945 | Common:3; Rare:87 |