Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40096904-40097475 | Common:8; Rare:390; Clinvar:25; Clinvar (benign):20; Clinvar (pathogenic):22 | ||||
chr1:40160803-40161203 | Rare:55 | ||||
chr1:40161206-40161480 | Common:4; Rare:392 | ||||
chr1:40161476-40162178 | Common:5; Rare:353 | ||||
chr1:40257449-40257840 | Common:7; Rare:156; Clinvar:3 | ||||
chr1:40257772-40258307 | Common:28; Rare:769; Clinvar:54; Clinvar (benign):5 | ||||
chr1:40258513-40258913 | Common:4; Rare:80 | ||||
chr1:40315301-40315701 | Common:10; Rare:169; Clinvar (benign):2 | ||||
chr1:40373406-40373837 | Common:6; Rare:449 | ||||
chr1:40374065-40375020 | Common:75; Rare:445 | ||||
chr1:40449800-40450591 | Common:35; Rare:827 | ||||
chr1:40450530-40450900 | Common:7; Rare:150 | ||||
chr1:40450914-40451300 | Common:2; Rare:204 | ||||
chr1:40477079-40477479 | Common:10; Rare:262 | ||||
chr1:40477660-40478160 | Common:5; Rare:120 |