Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:231710278-231710553 | Common:2; Rare:137 | ||||
chr2:231961645-231961755 | Rare:31; Clinvar:1 | ||||
chr2:232525820-232526245 | Common:3; Rare:131; Clinvar (benign):1 | ||||
chr2:232550303-232550363 | Rare:11 | ||||
chr2:232550493-232550727 | Rare:96 | ||||
chr2:232632944-232633231 | Common:3; Rare:67 | ||||
chr2:233419044-233419329 | Common:2; Rare:60 | ||||
chr2:236567563-236567802 | Common:1; Rare:70 | ||||
chr2:237085748-237085998 | Common:2; Rare:98 | ||||
chr2:237414067-237414491 | Common:3; Rare:90; Clinvar (benign):2 | ||||
chr2:237487105-237487283 | Common:3; Rare:46 | ||||
chr2:238060741-238061057 | Common:4; Rare:98 | ||||
chr2:238138483-238138752 | Common:1; Rare:52 | ||||
chr2:238203574-238203815 | Common:3; Rare:99 | ||||
chr2:239309123-239309373 | Rare:54 |