Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:11804458-11805716 | Common:17; Rare:430 | ||||
chr1:11805692-11806338 | Common:20; Rare:865; Clinvar:10 | ||||
chr1:11806310-11806534 | Common:6; Rare:127 | ||||
chr1:11806670-11806867 | Common:3; Rare:128 | ||||
chr1:11807360-11807760 | Common:6; Rare:75 | ||||
chr1:11925766-11926720 | Common:38; Rare:605 | ||||
chr1:11934176-11935091 | Common:32; Rare:763; Clinvar:35; Clinvar (benign):8 | ||||
chr1:11979574-11980865 | Common:34; Rare:935; Clinvar:5; Clinvar (benign):26 | ||||
chr1:12019156-12019614 | Common:30; Rare:771 | ||||
chr1:12019901-12020301 | Common:2; Rare:79 | ||||
chr1:12063198-12063390 | Common:2; Rare:52 | ||||
chr1:12063428-12064325 | Common:13; Rare:400 | ||||
chr1:12125670-12125860 | Common:2; Rare:28 | ||||
chr1:12166695-12167095 | Common:6; Rare:141 | ||||
chr1:12229790-12230190 | Common:11; Rare:375 |