Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:96721192-96721592 | Common:5; Rare:117 | ||||
chr1:96721506-96721888 | Common:7; Rare:329 | ||||
chr1:97920915-97921197 | Common:2; Rare:180; Clinvar:6; Clinvar (pathogenic):1 | ||||
chr1:98661455-98661902 | Common:9; Rare:371 | ||||
chr1:98661920-98662474 | Rare:240 | ||||
chr1:99766460-99766870 | Common:2; Rare:124 | ||||
chr1:99849945-99850229 | Common:5; Rare:235 | ||||
chr1:99850210-99850830 | Rare:178; Clinvar:5; Clinvar (benign):4 | ||||
chr1:99969812-99970110 | Rare:170 | ||||
chr1:99970110-99970290 | Common:6; Rare:63 | ||||
chr1:99970270-99970554 | Rare:134 | ||||
chr1:100037903-100038324 | Common:4; Rare:334 | ||||
chr1:100132839-100133249 | Common:7; Rare:391 | ||||
chr1:100249732-100250033 | Common:6; Rare:172; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:100266041-100266367 | Common:8; Rare:268 |