Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155562768-155562970 | Common:1; Rare:112 | ||||
chr1:155563088-155563251 | Rare:70 | ||||
chr1:155688652-155689113 | Common:2; Rare:145 | ||||
chr1:155859351-155859595 | Common:2; Rare:56 | ||||
chr1:155934347-155934579 | Common:1; Rare:92 | ||||
chr1:155978116-155978268 | Common:1; Rare:38 | ||||
chr1:155978446-155978635 | Rare:50 | ||||
chr1:156054682-156054878 | Common:3; Rare:57 | ||||
chr1:156061096-156061211 | Rare:26 | ||||
chr1:156114481-156114786 | Rare:63; Clinvar:3 | ||||
chr1:156135032-156135312 | Common:2; Rare:63; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr1:156193817-156194121 | Common:3; Rare:76 | ||||
chr1:156212883-156213022 | Common:1; Rare:34 | ||||
chr1:156282797-156282941 | Common:1; Rare:38 | ||||
chr1:156338152-156338481 | Common:2; Rare:118 |