Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:75673307-75673555 | Common:1; Rare:97 | ||||
chr4:75724375-75724794 | Common:2; Rare:125 | ||||
chr4:76148375-76148577 | Common:3; Rare:61 | ||||
chr4:76586110-76586320 | Common:2; Rare:34 | ||||
chr4:76898016-76898300 | Common:1; Rare:65 | ||||
chr4:76949569-76949859 | Common:1; Rare:90 | ||||
chr4:77075961-77076066 | Common:1; Rare:59 | ||||
chr4:77076271-77076340 | Common:2; Rare:33 | ||||
chr4:77862635-77862842 | Common:2; Rare:63 | ||||
chr4:78551538-78551648 | Rare:23 | ||||
chr4:78551651-78551843 | Rare:50 | ||||
chr4:81471801-81472075 | Common:1; Rare:87 | ||||
chr4:82373944-82374309 | Common:3; Rare:108 | ||||
chr4:82429372-82429585 | Rare:131; Clinvar:10; Clinvar (benign):4 | ||||
chr4:82430428-82430634 | Common:1; Rare:81 |