Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:60163676-60164223 | Common:4; Rare:154; Clinvar (benign):1 | ||||
chr13:60396026-60396147 | Rare:35 | ||||
chr13:60396203-60396685 | Common:3; Rare:160 | ||||
chr13:60396854-60397236 | Rare:111 | ||||
chr13:60397392-60397600 | Common:2; Rare:71 | ||||
chr13:60397735-60397979 | Common:2; Rare:88 | ||||
chr13:67230307-67230678 | Common:2; Rare:123 | ||||
chr13:72727514-72727993 | Common:8; Rare:195 | ||||
chr13:72728105-72728118 | Rare:3 | ||||
chr13:72781442-72781662 | Rare:65 | ||||
chr13:72781853-72782282 | Common:1; Rare:151 | ||||
chr13:73058820-73059112 | Common:1; Rare:112 | ||||
chr13:74133866-74134114 | Common:1; Rare:63 | ||||
chr13:74134274-74134621 | Common:4; Rare:124 | ||||
chr13:75326697-75326919 | Common:2; Rare:41 |