Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179142994-179143221 | Common:1; Rare:48 | ||||
chr1:179882159-179882311 | Common:1; Rare:29 | ||||
chr1:179882478-179882957 | Common:1; Rare:237; Clinvar:10; Clinvar (benign):4 | ||||
chr1:179954697-179954814 | Rare:28 | ||||
chr1:180502270-180502697 | Common:1; Rare:150 | ||||
chr1:182839231-182839405 | Common:1; Rare:73 | ||||
chr1:183134634-183135180 | Common:3; Rare:130 | ||||
chr1:183635515-183636113 | Common:5; Rare:173 | ||||
chr1:184051376-184051771 | Common:4; Rare:110 | ||||
chr1:185156900-185157303 | Common:2; Rare:113 | ||||
chr1:185317221-185317439 | Common:1; Rare:67 | ||||
chr1:186375173-186375384 | Rare:51 | ||||
chr1:186375676-186375932 | Common:1; Rare:69 | ||||
chr1:186680399-186680715 | Common:3; Rare:70 | ||||
chr1:193029216-193029390 | Rare:50 |