Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:185156900-185157297 | Common:2; Rare:109 | ||||
chr1:185157420-185157540 | Common:1; Rare:38 | ||||
chr1:185317201-185317468 | Common:1; Rare:79 | ||||
chr1:186375087-186375627 | Rare:147 | ||||
chr1:186375656-186375928 | Common:1; Rare:73 | ||||
chr1:186680294-186680688 | Common:3; Rare:91 | ||||
chr1:192808788-192809184 | Common:4; Rare:160; Clinvar:1 | ||||
chr1:193059298-193059436 | Rare:58 | ||||
chr1:193059484-193059774 | Common:1; Rare:143 | ||||
chr1:193105348-193105502 | Common:2; Rare:65 | ||||
chr1:193121916-193122248 | Common:1; Rare:111; Clinvar:5; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
chr1:193186576-193186677 | Rare:14 | ||||
chr1:197902560-197902675 | Common:1; Rare:39 | ||||
chr1:198156940-198157348 | Rare:135 | ||||
chr1:200620738-200620913 | Rare:46 |