Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42456935-42457020 | Rare:29 | ||||
chr1:42462899-42463298 | Common:3; Rare:109 | ||||
chr1:42658017-42658083 | Rare:18 | ||||
chr1:42658214-42658509 | Common:2; Rare:86 | ||||
chr1:42658588-42658718 | Rare:29 | ||||
chr1:42681992-42682501 | Common:2; Rare:159 | ||||
chr1:42682960-42683101 | Common:1; Rare:59 | ||||
chr1:42766955-42767232 | Common:4; Rare:88; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42767243-42767515 | Common:4; Rare:103 | ||||
chr1:42816881-42816945 | Rare:14 | ||||
chr1:42817104-42817404 | Rare:110 | ||||
chr1:42846282-42846685 | Common:1; Rare:113 | ||||
chr1:42958026-42958399 | Common:6; Rare:124 | ||||
chr1:42958734-42959192 | Common:5; Rare:114; Clinvar:8; Clinvar (benign):5 | ||||
chr1:43147661-43147720 | Common:3; Rare:13 |