Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:99645623-99646367 | Rare:129 | ||||
chr1:99646379-99646663 | Common:1; Rare:57 | ||||
chr1:99667637-99667898 | Common:2; Rare:70 | ||||
chr1:99850287-99850425 | Rare:35; Clinvar:2; Clinvar (benign):1 | ||||
chr1:99969913-99970158 | Common:2; Rare:63 | ||||
chr1:100037953-100038316 | Common:1; Rare:132 | ||||
chr1:100132857-100133346 | Common:5; Rare:189 | ||||
chr1:100266092-100266670 | Common:4; Rare:201 | ||||
chr1:100351612-100351836 | Common:2; Rare:75 | ||||
chr1:100352208-100352650 | Common:1; Rare:95 | ||||
chr1:100352846-100353004 | Common:1; Rare:60; Clinvar (benign):2 | ||||
chr1:100719420-100719763 | Common:1; Rare:81 | ||||
chr1:100894610-100894987 | Common:2; Rare:84 | ||||
chr1:100895065-100895326 | Common:2; Rare:44 | ||||
chr1:100895678-100896290 | Common:1; Rare:174 |