Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:33350354-33350520 | Rare:42 | ||||
chr1:33430489-33430593 | Common:1; Rare:20 | ||||
chr1:33430718-33431293 | Common:3; Rare:170 | ||||
chr1:33472342-33472747 | Common:1; Rare:83 | ||||
chr1:34754905-34755168 | Common:1; Rare:55 | ||||
chr1:34755352-34755623 | Common:2; Rare:60 | ||||
chr1:34781120-34781567 | Common:1; Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr1:34781653-34781917 | Common:1; Rare:52; Clinvar (benign):1 | ||||
chr1:34782123-34782347 | Rare:39 | ||||
chr1:34859119-34859369 | Common:1; Rare:51 | ||||
chr1:34859608-34859965 | Common:1; Rare:84 | ||||
chr1:34984721-34985018 | Common:2; Rare:67 | ||||
chr1:34985057-34985160 | Rare:27 | ||||
chr1:34985170-34985449 | Common:2; Rare:92 | ||||
chr1:35031171-35031464 | Common:1; Rare:58 |