| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42335875-42336056 | Rare:39 | ||||
| chr1:42456211-42456586 | Common:1; Rare:114 | ||||
| chr1:42682155-42682426 | Common:2; Rare:70 | ||||
| chr1:42766514-42766813 | Rare:86; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr1:42766968-42767316 | Common:5; Rare:120; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr1:42816961-42817139 | Common:1; Rare:52 | ||||
| chr1:42817260-42817548 | Rare:98 | ||||
| chr1:42846391-42846642 | Common:1; Rare:71 | ||||
| chr1:42958633-42959108 | Common:4; Rare:118; Clinvar:6; Clinvar (benign):8 | ||||
| chr1:42959272-42959509 | Common:1; Rare:55 | ||||
| chr1:43172090-43172374 | Common:3; Rare:114 | ||||
| chr1:43269967-43270083 | Common:3; Rare:18 | ||||
| chr1:43358699-43359004 | Common:7; Rare:94 | ||||
| chr1:43367931-43368238 | Rare:81 | ||||
| chr1:43389742-43389966 | Common:4; Rare:102; Clinvar:1 |