Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:778598-778820 | Common:4; Rare:95 | ||||
chr1:827500-827823 | Common:2; Rare:106 | ||||
chr1:1164636-1164908 | Common:1; Rare:95 | ||||
chr1:1234001-1234258 | Common:3; Rare:71 | ||||
chr1:1234276-1234538 | Common:2; Rare:61 | ||||
chr1:2229229-2229387 | Rare:50; Clinvar:2; Clinvar (benign):5 | ||||
chr1:3499866-3500213 | Common:5; Rare:85 | ||||
chr1:3781329-3781392 | Rare:25 | ||||
chr1:6467507-6467827 | Common:3; Rare:81; Clinvar:1; Clinvar (benign):1 | ||||
chr1:6468852-6469174 | Common:4; Rare:91; Clinvar:7; Clinvar (benign):5 | ||||
chr1:6470236-6470627 | Common:2; Rare:138; Clinvar:14; Clinvar (benign):5 | ||||
chr1:6475967-6476115 | Rare:50; Clinvar:6; Clinvar (benign):5 | ||||
chr1:6587778-6588105 | Rare:92 | ||||
chr1:9242602-9242867 | Common:1; Rare:64 | ||||
chr1:9244668-9244916 | Common:2; Rare:55 |