Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:20786636-20786833 | Rare:76 | ||||
chr1:20787197-20787424 | Rare:110 | ||||
chr1:21290421-21290551 | Common:2; Rare:34 | ||||
chr1:21345463-21345709 | Common:3; Rare:91 | ||||
chr1:21440061-21440179 | Common:1; Rare:27 | ||||
chr1:21783017-21783313 | Common:3; Rare:108 | ||||
chr1:23019256-23019517 | Rare:76 | ||||
chr1:23344229-23344521 | Common:2; Rare:96 | ||||
chr1:23368809-23369270 | Common:3; Rare:134 | ||||
chr1:23369782-23369900 | Rare:22 | ||||
chr1:23424563-23424975 | Common:1; Rare:106 | ||||
chr1:23559335-23559671 | Common:2; Rare:147 | ||||
chr1:23691602-23691898 | Common:6; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
chr1:23743289-23743518 | Rare:85 | ||||
chr1:23778239-23778510 | Common:9; Rare:140 |