Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:45304059-45304153 | Rare:16 | ||||
chr1:45606951-45607121 | Common:1; Rare:35 | ||||
chr1:45616169-45616393 | Common:2; Rare:49 | ||||
chr1:45616397-45616677 | Common:2; Rare:76 | ||||
chr1:45656797-45656841 | Rare:13 | ||||
chr1:46001282-46001510 | Common:1; Rare:36 | ||||
chr1:46037314-46037506 | Common:1; Rare:43 | ||||
chr1:46181443-46181666 | Common:2; Rare:42 | ||||
chr1:46196056-46196232 | Common:1; Rare:30; Clinvar:2; Clinvar (benign):1 | ||||
chr1:46196747-46196973 | Common:1; Rare:72; Clinvar:8; Clinvar (benign):5 | ||||
chr1:46276032-46276245 | Common:1; Rare:33 | ||||
chr1:46717884-46718233 | Common:1; Rare:101 | ||||
chr1:48366930-48367008 | Rare:26 | ||||
chr1:51280590-51280643 | Common:1; Rare:11 | ||||
chr1:51288302-51288619 | Common:2; Rare:54 |