Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155978129-155978262 | Common:1; Rare:35 | ||||
chr1:155978463-155978641 | Rare:46 | ||||
chr1:155979136-155979219 | Rare:11 | ||||
chr1:156053708-156053925 | Rare:59 | ||||
chr1:156054615-156054891 | Common:3; Rare:80 | ||||
chr1:156114507-156114821 | Rare:68; Clinvar:4; Clinvar (benign):1 | ||||
chr1:156193828-156194126 | Common:3; Rare:77 | ||||
chr1:156282777-156282941 | Common:1; Rare:48 | ||||
chr1:156338152-156338530 | Common:2; Rare:136 | ||||
chr1:156500489-156500691 | Rare:59 | ||||
chr1:156500768-156501124 | Common:1; Rare:129 | ||||
chr1:156591660-156591855 | Common:4; Rare:99 | ||||
chr1:156601410-156601559 | Common:2; Rare:57 | ||||
chr1:156728394-156728469 | Rare:15 | ||||
chr1:156741054-156741395 | Common:1; Rare:95 |