Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149850720-149851290 | Common:7; Rare:56 | ||||
chr1:149886507-149887225 | Common:18; Rare:1323 | ||||
chr1:149887152-149887560 | Rare:414 | ||||
chr1:149887806-149888236 | Rare:785 | ||||
chr1:149888338-149888759 | Common:12; Rare:247 | ||||
chr1:149927639-149928039 | Common:7; Rare:563; Clinvar:2; Clinvar (benign):34 | ||||
chr1:149928225-149928413 | Common:2; Rare:57 | ||||
chr1:149928317-149928717 | Common:1; Rare:81 | ||||
chr1:149936194-149936660 | Common:8; Rare:213 | ||||
chr1:149936645-149937135 | Common:4; Rare:213 | ||||
chr1:149937330-149937730 | Common:3; Rare:60 | ||||
chr1:150009801-150010401 | Common:3; Rare:165 | ||||
chr1:150010593-150010993 | Common:9; Rare:383 | ||||
chr1:150066670-150067400 | Common:14; Rare:281 | ||||
chr1:150067480-150068193 | Common:5; Rare:611 |