Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:5126555-5127081 | Common:4; Rare:169 | ||||
chr20:5610885-5611169 | Common:2; Rare:102 | ||||
chr20:5911314-5911525 | Common:2; Rare:55 | ||||
chr20:5950410-5950656 | Common:8; Rare:75 | ||||
chr20:6053960-6054199 | Common:1; Rare:42 | ||||
chr20:10034829-10035114 | Common:6; Rare:112 | ||||
chr20:10218716-10218928 | Rare:47 | ||||
chr20:10673970-10674127 | Common:1; Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
chr20:13638898-13639035 | Common:1; Rare:40 | ||||
chr20:13784878-13785112 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):3 | ||||
chr20:13995157-13995573 | Common:1; Rare:109 | ||||
chr20:14337598-14337975 | Common:2; Rare:73 | ||||
chr20:15985873-15986134 | Common:1; Rare:48 | ||||
chr20:16573288-16573540 | Common:1; Rare:72 | ||||
chr20:16729951-16730064 | Rare:30 |