Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21176852-21177065 | Rare:58 | ||||
chr1:21290203-21290514 | Common:1; Rare:69 | ||||
chr1:21345459-21345655 | Common:2; Rare:75 | ||||
chr1:21783086-21783293 | Common:2; Rare:75 | ||||
chr1:21854609-21854979 | Common:2; Rare:138; Clinvar:5; Clinvar (benign):2 | ||||
chr1:21874614-21874949 | Common:2; Rare:98; Clinvar (benign):1 | ||||
chr1:22652867-22653301 | Common:1; Rare:93 | ||||
chr1:23019328-23019508 | Rare:55 | ||||
chr1:23368177-23368496 | Common:1; Rare:95 | ||||
chr1:23368779-23369262 | Common:4; Rare:137 | ||||
chr1:23558933-23559155 | Common:4; Rare:106 | ||||
chr1:23559159-23559661 | Common:3; Rare:219 | ||||
chr1:23778281-23778400 | Common:5; Rare:57 | ||||
chr1:23791135-23791225 | Rare:30 | ||||
chr1:23800730-23800938 | Common:1; Rare:69 |