| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42682607-42682731 | Common:1; Rare:51 | ||||
| chr1:42683230-42683465 | Common:3; Rare:105 | ||||
| chr1:42766978-42767312 | Common:4; Rare:115; Clinvar (benign):1 | ||||
| chr1:42816936-42817141 | Common:1; Rare:58 | ||||
| chr1:42817198-42817381 | Rare:76 | ||||
| chr1:42846392-42846638 | Common:1; Rare:68 | ||||
| chr1:42958754-42959078 | Common:4; Rare:85; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:43172207-43172344 | Common:1; Rare:65 | ||||
| chr1:43270443-43270743 | Rare:54 | ||||
| chr1:43285541-43285683 | Common:2; Rare:28 | ||||
| chr1:43358666-43359011 | Common:7; Rare:108 | ||||
| chr1:43366145-43366458 | Common:2; Rare:74 | ||||
| chr1:43367591-43367728 | Common:1; Rare:24 | ||||
| chr1:43367916-43368216 | Rare:78 | ||||
| chr1:43389733-43389968 | Common:4; Rare:105; Clinvar:1 |