Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:9630950-9631325 | Common:3; Rare:121 | ||||
chr2:10122540-10122771 | Common:4; Rare:97 | ||||
chr2:10689901-10690073 | Common:4; Rare:64 | ||||
chr2:11465810-11466184 | Common:3; Rare:125 | ||||
chr2:11746509-11746671 | Common:2; Rare:54; Clinvar:4 | ||||
chr2:12716631-12717056 | Common:3; Rare:131 | ||||
chr2:16665798-16665974 | Common:4; Rare:36 | ||||
chr2:17753650-17754174 | Common:5; Rare:164; Clinvar (benign):1 | ||||
chr2:19901944-19902019 | Common:1; Rare:20 | ||||
chr2:19990043-19990223 | Rare:50 | ||||
chr2:20446860-20447074 | Common:3; Rare:80 | ||||
chr2:20651021-20651223 | Rare:53 | ||||
chr2:20823040-20823140 | Rare:39 | ||||
chr2:23940363-23940514 | Common:3; Rare:53 | ||||
chr2:24049598-24049773 | Rare:56 |