Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42816961-42817134 | Common:1; Rare:49 | ||||
chr1:42846420-42846644 | Common:1; Rare:60 | ||||
chr1:42958803-42959020 | Common:2; Rare:52; Clinvar:3; Clinvar (benign):3 | ||||
chr1:43172228-43172328 | Common:1; Rare:55 | ||||
chr1:43367994-43368181 | Rare:48 | ||||
chr1:43389747-43389910 | Common:3; Rare:69 | ||||
chr1:43707334-43707589 | Common:2; Rare:75 | ||||
chr1:45583934-45584046 | Rare:41 | ||||
chr1:45688059-45688209 | Common:1; Rare:39 | ||||
chr1:46303604-46303730 | Common:1; Rare:36 | ||||
chr1:52055217-52055273 | Rare:17 | ||||
chr1:52056148-52056336 | Rare:59 | ||||
chr1:52404420-52404602 | Common:1; Rare:55 | ||||
chr1:53946282-53946459 | Rare:66 | ||||
chr1:54053194-54053637 | Common:6; Rare:144 |