Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:159263225-159263321 | Common:1; Rare:30 | ||||
chr5:160419053-160419219 | Common:3; Rare:59 | ||||
chr5:160421713-160421913 | Common:1; Rare:53 | ||||
chr5:163460380-163460664 | Common:5; Rare:60 | ||||
chr5:163505444-163505628 | Common:1; Rare:50 | ||||
chr5:168486355-168486493 | Common:1; Rare:45; Clinvar (benign):1 | ||||
chr5:172834163-172834394 | Common:1; Rare:54 | ||||
chr5:173328363-173328562 | Rare:37 | ||||
chr5:176388569-176388798 | Common:4; Rare:85 | ||||
chr5:177022635-177022730 | Rare:31 | ||||
chr5:177303707-177303868 | Common:3; Rare:79 | ||||
chr5:179698668-179699009 | Common:3; Rare:108 | ||||
chr6:5004007-5004126 | Common:1; Rare:53 | ||||
chr6:13615177-13615403 | Common:2; Rare:102 | ||||
chr6:17393550-17393718 | Rare:44 |