Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155053254-155053487 | Rare:48 | ||||
chr1:155194715-155194827 | Common:1; Rare:36 | ||||
chr1:155965089-155965352 | Common:1; Rare:47 | ||||
chr1:155979615-155979794 | Rare:27 | ||||
chr1:155983382-155983624 | Rare:43 | ||||
chr1:156130308-156130771 | Common:3; Rare:113; Clinvar:11; Clinvar (benign):6; Clinvar (pathogenic):6 | ||||
chr1:158024968-158024988 | Rare:1 | ||||
chr1:161216955-161217284 | Rare:52 | ||||
chr1:161530888-161531108 | Common:5; Rare:83 | ||||
chr1:161612410-161612712 | Common:7; Rare:118 | ||||
chr1:170667585-170667615 | Rare:5 | ||||
chr1:172144720-172144892 | Rare:23 | ||||
chr1:172322378-172322410 | Common:1; Rare:10 | ||||
chr1:181089812-181089877 | Rare:27 | ||||
chr1:183022409-183022713 | Common:1; Rare:55 |