Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882060-179882341 | Common:1; Rare:65 | ||||
chr1:179882488-179882837 | Rare:167; Clinvar:7; Clinvar (benign):2 | ||||
chr1:180154670-180154898 | Common:3; Rare:77 | ||||
chr1:182839164-182839399 | Common:1; Rare:103 | ||||
chr1:182839557-182839737 | Common:2; Rare:82 | ||||
chr1:183472306-183472521 | Common:2; Rare:75 | ||||
chr1:183635666-183636094 | Common:4; Rare:123 | ||||
chr1:183805022-183805232 | Rare:55 | ||||
chr1:184051601-184051789 | Common:3; Rare:74 | ||||
chr1:184754601-184754674 | Common:1; Rare:35 | ||||
chr1:185156708-185156761 | Common:1; Rare:27 | ||||
chr1:185156922-185157294 | Common:1; Rare:101 | ||||
chr1:186375111-186375548 | Rare:116 | ||||
chr1:186375557-186375920 | Common:1; Rare:104 | ||||
chr1:186680417-186680736 | Common:2; Rare:72 |