Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40665405-40665782 | Common:1; Rare:92 | ||||
chr1:40691504-40691810 | Common:2; Rare:149 | ||||
chr1:40692012-40692248 | Common:2; Rare:77 | ||||
chr1:40709154-40709414 | Rare:59 | ||||
chr1:40979387-40979816 | Common:5; Rare:133 | ||||
chr1:41242087-41242383 | Rare:83 | ||||
chr1:42335095-42335417 | Common:6; Rare:154 | ||||
chr1:42456010-42456387 | Common:1; Rare:98 | ||||
chr1:42456469-42456583 | Rare:54 | ||||
chr1:42463034-42463346 | Common:4; Rare:100 | ||||
chr1:42658265-42658512 | Common:2; Rare:76 | ||||
chr1:42682101-42682448 | Common:2; Rare:95 | ||||
chr1:42682608-42682731 | Common:1; Rare:50 | ||||
chr1:42766581-42766722 | Rare:35; Clinvar:1; Clinvar (benign):1 | ||||
chr1:42767016-42767309 | Common:4; Rare:92 |