Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:7954232-7954293 | Rare:10 | ||||
chr1:7961457-7961762 | Common:4; Rare:105; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878578-8878835 | Rare:130 | ||||
chr1:9943292-9943489 | Common:2; Rare:46 | ||||
chr1:10032642-10032961 | Common:3; Rare:88 | ||||
chr1:10398896-10399101 | Common:2; Rare:81 | ||||
chr1:11262493-11262776 | Common:2; Rare:86 | ||||
chr1:11654843-11654914 | Common:1; Rare:15 | ||||
chr1:11934551-11934773 | Common:3; Rare:72; Clinvar:5; Clinvar (benign):1 | ||||
chr1:12618207-12618464 | Common:1; Rare:55 | ||||
chr1:13749091-13749451 | Common:2; Rare:124 | ||||
chr1:15526583-15526885 | Common:2; Rare:92 | ||||
chr1:16352420-16352587 | Common:3; Rare:88 | ||||
chr1:19210244-19210433 | Rare:73 | ||||
chr1:19251494-19251854 | Common:6; Rare:121 |