Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778599-778805 | Common:4; Rare:89 | ||||
chr1:827504-827692 | Common:1; Rare:76 | ||||
chr1:2229229-2229350 | Rare:37; Clinvar:1; Clinvar (benign):5 | ||||
chr1:2354831-2355105 | Common:2; Rare:73 | ||||
chr1:2428524-2428719 | Common:1; Rare:49 | ||||
chr1:7820326-7820525 | Common:3; Rare:42 | ||||
chr1:9687529-9687633 | Common:1; Rare:27 | ||||
chr1:10622646-10623059 | Common:2; Rare:68; Clinvar:3 | ||||
chr1:12619106-12619236 | Rare:27 | ||||
chr1:13829017-13829108 | Rare:15 | ||||
chr1:15603589-15603719 | Common:3; Rare:39 | ||||
chr1:15834846-15835140 | Common:2; Rare:132 | ||||
chr1:16458796-16458877 | Rare:25 | ||||
chr1:16499211-16499371 | Rare:76 | ||||
chr1:16644637-16644790 | Common:1; Rare:2 |