Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:236032507-236032830 | Common:1; Rare:82; Clinvar:1 | ||||
chr1:242001523-242001755 | Common:3; Rare:34 | ||||
chr1:244451132-244451263 | Common:2; Rare:37 | ||||
chr1:244863715-244863833 | Rare:37; Clinvar:1; Clinvar (benign):2 | ||||
chr1:244970954-244971054 | Rare:24 | ||||
chr10:246578-246843 | Rare:65 | ||||
chr10:388048-388193 | Rare:41 | ||||
chr10:633555-633878 | Common:2; Rare:70 | ||||
chr10:4995767-4995949 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
chr10:5766518-5766738 | Rare:44 | ||||
chr10:17010854-17010992 | Common:1; Rare:23 | ||||
chr10:19768008-19768266 | Common:1; Rare:55 | ||||
chr10:19839318-19839397 | Common:1; Rare:23 | ||||
chr10:22251821-22252088 | Rare:59 | ||||
chr10:29409497-29409606 | Common:1; Rare:32 |