SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs4108 | snp | G/T | 0.412416 | 0.190055 | intron-variant | CORO2B | GRCh38.p7 | 15:68659230 | tatccctcacactct[G/T]ccaggtttaaGTATG | 10391 |
rs593719 | snp | A/G | 0.41408 | 0.188621 | intron-variant | CORO2B | GRCh38.p7 | 15:68568509 | TTTGTAGCTGAGGAC[A/G]CTGGGACCCCAAAAG | 10391 |
rs596373 | snp | C/G | 0.413582 | 0.189052 | intron-variant | CORO2B | GRCh38.p7 | 15:68570983 | TTTTTGATGATGGCA[C/G]AAAGCACTTAATCAG | 10391 |
rs597284 | snp | C/T | 0.322721 | 0.23919 | intron-variant | CORO2B | GRCh38.p7 | 15:68582231 | GAGAACTTCTAGCCC[C/T]GTGGCATTTCTCCTG | 10391 |
rs615188 | snp | C/G | 0.132751 | 0.2208 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68577243 | TAGGAATGGACCCTG[C/G]AGTTCACGGATTCAA | 10391 |
rs622851 | snp | A/G | 0.397994 | 0.201489 | intron-variant | CORO2B | GRCh38.p7 | 15:68570334 | AGTTGTTTAGAGCTT[A/G]CACCATCTATCTGCA | 10391 |
rs625937 | snp | A/C | 0.385315 | 0.212113 | intron-variant | CORO2B | GRCh38.p7 | 15:68564448 | agctgggactacagg[A/C]gcgtgccactacaac | 10391 |
rs625961 | snp | A/G | 0.372794 | 0.217765 | intron-variant | CORO2B | GRCh38.p7 | 15:68571032 | GAAAGTGCGAAGGAA[A/G]CAGAGAGGAGGGAAT | 10391 |
rs626797 | snp | A/G | 0.474634 | 0.109726 | intron-variant | CORO2B | GRCh38.p7 | 15:68564659 | AGTTTGTATCTTAGC[A/G]GATTCAAAATTATCA | 10391 |
rs628703 | snp | G/T | 0.331874 | 0.236213 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68577976 | CTTGCCAGGCTGTCC[G/T]GCTTGGAGAACCCCT | 10391 |
rs644791 | snp | C/T | 0.418974 | 0.184249 | intron-variant | CORO2B | GRCh38.p7 | 15:68566933 | ACCTGAGCTTGCCAG[C/T]GAAGAGGCAGCGTGT | 10391 |
rs656209 | snp | A/G | 0.383824 | 0.211166 | intron-variant | CORO2B | GRCh38.p7 | 15:68565237 | TTAATATATTGATAT[A/G]TTTTCTCCTGTTTTG | 10391 |
rs656812 | snp | A/G | 0.307919 | 0.243198 | intron-variant | CORO2B | GRCh38.p7 | 15:68590997 | TTTGCTGAGCCCTGT[A/G]TGCCAGGCCCTAAGC | 10391 |
rs674038 | snp | A/G | 0.381891 | 0.212379 | intron-variant | CORO2B | GRCh38.p7 | 15:68566945 | CAGCGAAGAGGCAGC[A/G]TGTCCAATAAATGAC | 10391 |
rs687209 | snp | A/G | 0.413748 | 0.188909 | intron-variant | CORO2B | GRCh38.p7 | 15:68567576 | ctcccagaggaatgt[A/G]tagggcttgctgcct | 10391 |
rs688109 | snp | C/T | 0.0205511 | 0.0992634 | intron-variant | CORO2B | GRCh38.p7 | 15:68569711 | ttttgtaagaaattg[C/T]cacagggtcttccaa | 10391 |
rs694686 | snp | C/T | 0.400504 | 0.199621 | intron-variant | CORO2B | GRCh38.p7 | 15:68576286 | CCTTGCTTTTCTAGA[C/T]CTCCCTTCTGCCTGG | 10391 |
rs728400 | snp | A/G | 0.274393 | 0.248807 | intron-variant | CORO2B | GRCh38.p7 | 15:68593035 | GGTGAGGGTCATCCC[A/G]TGGCAGAGGCATCAC | 10391 |
rs728401 | snp | A/G | 0.42574 | 0.177808 | intron-variant | CORO2B | GRCh38.p7 | 15:68593475 | TAGCAGCCAGGTCTG[A/G]ATGTAGCCCTACTCC | 10391 |
rs728402 | snp | G/T | 0.274393 | 0.248807 | intron-variant | CORO2B | GRCh38.p7 | 15:68593007 | GAAGTCCAAGAGCAT[G/T]GCACCAGCATCTGGT | 10391 |
rs746118 | snp | C/T | 0.414905 | 0.187899 | intron-variant | CORO2B | GRCh38.p7 | 15:68676481 | AAGGATAACCACCGC[C/T]GCCTAAACCCGTCAA | 10391 |
rs749555 | snp | A/G | 0.254664 | 0.249956 | intron-variant | CORO2B | GRCh38.p7 | 15:68667675 | GGCTGAGAAGGGGGA[A/G]GTAGTGAATAGAGAG | 10391 |
rs755135 | snp | A/G/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68604080 | TTGTGAGCACTGAGT[A/G/T]TATTTCATACACAGA | 10391 |
rs764204 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68593177 | atgacttaatcccct[C/T]ttaaaggccccatct | 10391 |
rs893843 | snp | G/T | 0.0696718 | 0.173152 | intron-variant | CORO2B | GRCh38.p7 | 15:68667879 | GGGCTTCGGGACCTG[G/T]AGTCCTGACCCAGCC | 10391 |
rs893844 | snp | C/G | 0.449853 | 0.150196 | intron-variant | CORO2B | GRCh38.p7 | 15:68637374 | CCTCCTGTGTGTCCA[C/G]CTTTCCCGGGTGGAG | 10391 |
rs893845 | snp | C/G | 0.447421 | 0.153379 | intron-variant | CORO2B | GRCh38.p7 | 15:68637764 | CCACATTACACAGCT[C/G]TTTCCCAGGGGGCTT | 10391 |
rs920920 | snp | A/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68566680 | CAAATAAGGCTCCAT[A/G]AGCCTGACTTCCCTT | 10391 |
rs930432 | snp | C/T | 0.0629771 | 0.165899 | intron-variant | CORO2B | GRCh38.p7 | 15:68658412 | ACCCCCACTGGCCCC[C/T]CACTGGCCGAAGGCA | 10391 |
rs930433 | snp | C/T | 0.468949 | 0.12067 | intron-variant | CORO2B | GRCh38.p7 | 15:68658368 | GATGGCAGGCGGGGA[C/T]GAGGCCCCCAGCCAG | 10391 |
rs937095 | snp | A/G | 0.496416 | 0.0421803 | intron-variant | CORO2B | GRCh38.p7 | 15:68633776 | TACTACAACGGAGCC[A/G]GCAGATCGTCCTTCT | 10391 |
rs937096 | snp | C/G | 0.497804 | 0.0611406 | intron-variant | CORO2B | GRCh38.p7 | 15:68633784 | CGGAGCCGGCAGATC[C/G]TCCTTCTCTTCCATG | 10391 |
rs937097 | snp | A/G | 0.0637235 | 0.166737 | intron-variant | CORO2B | GRCh38.p7 | 15:68707409 | AAGAATATCCACACC[A/G]CTGCACAAACTTGGA | 10391 |
rs937098 | snp | A/G | 0.338069 | 0.233974 | intron-variant | CORO2B | GRCh38.p7 | 15:68602220 | GAATAAAGCCAGTCA[A/G]CAGTTCCCCCCACTC | 10391 |
rs937099 | snp | A/C | 0.174932 | 0.238463 | intron-variant | CORO2B | GRCh38.p7 | 15:68698808 | GAGATGAGCAGGCAT[A/C]GATGAAGGGACAGGC | 10391 |
rs937100 | snp | A/G | 0.258565 | 0.249853 | intron-variant | CORO2B | GRCh38.p7 | 15:68720383 | gttacacagcagtag[A/G]tagctaatacaGGTG | 10391 |
rs937101 | snp | A/G | 0.388398 | 0.208197 | intron-variant | CORO2B | GRCh38.p7 | 15:68720168 | CATGCAGCCATCTCC[A/G]TTTCAGTTGTATCAG | 10391 |
rs937102 | snp | G/T | 0.0372196 | 0.131242 | intron-variant | CORO2B | GRCh38.p7 | 15:68710556 | GTCTCAGGGTGTGGC[G/T]GGAGAGGAAGGAGAC | 10391 |
rs937103 | snp | C/T | 0.441021 | 0.161279 | intron-variant | CORO2B | GRCh38.p7 | 15:68689370 | TGTACAATGACTGTT[C/T]AGATGGTCGGCTCAC | 10391 |
rs995971 | snp | C/G | 0.330714 | 0.236612 | intron-variant | CORO2B | GRCh38.p7 | 15:68674395 | GTCTGTAACTCGGGA[C/G]TGAAGCCAGCGAATG | 10391 |
rs1106285 | snp | C/G | 0.478104 | 0.102316 | intron-variant | CORO2B | GRCh38.p7 | 15:68677780 | CCATTCTGTGTGTCT[C/G]CTGCCTCCCCTCTCC | 10391 |
rs1123931 | snp | C/T | 0.273856 | 0.248859 | intron-variant | CORO2B | GRCh38.p7 | 15:68626982 | AGGAGTCTTGCTACA[C/T]ATCCTGTGCTCAGAG | 10391 |
rs1128848 | snp | C/G | 0.497241 | 0.037038 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68727243 | CACATAGGATCTCAT[C/G]GAGCCTCACGTCTAC | 10391 |
rs1128869 | snp | C/T | | | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68727701 | CCTCCTCCCACATTT[C/T]TGGAGCTTTTTTTTT | 10391 |
rs1317998 | snp | C/G | 0.322245 | 0.239334 | intron-variant | CORO2B | GRCh38.p7 | 15:68603680 | CTGTGCAGATGCGGA[C/G]AGAGTGAGCTCTCTG | 10391 |
rs1352833 | snp | C/T | 0.332337 | 0.236052 | intron-variant | CORO2B | GRCh38.p7 | 15:68717986 | AGTCCTTTGGCAAGT[C/T]ACAACTCTCTGAGCT | 10391 |
rs1352834 | snp | C/T | 0.202959 | 0.245534 | intron-variant | CORO2B | GRCh38.p7 | 15:68717909 | AGGTGATCAGCAGAA[C/T]ATGTTCCAAGATACT | 10391 |
rs1352835 | snp | C/T | 0.331411 | 0.236373 | intron-variant | CORO2B | GRCh38.p7 | 15:68717766 | CACATAAAGGAATTC[C/T]AGGAGCTGGAGGTAA | 10391 |
rs1352836 | snp | A/G | 0.234401 | 0.249513 | intron-variant | CORO2B | GRCh38.p7 | 15:68713308 | GTTGGGGGCTACACC[A/G]CTTCAGGAGCTCTCA | 10391 |
rs1388444 | snp | C/T | 0.132409 | 0.220618 | intron-variant | CORO2B | GRCh38.p7 | 15:68682089 | AAGCTGAAGCAGGGG[C/T]TCCTCCTACCCAGGG | 10391 |
rs1388445 | snp | C/G | 0.473818 | 0.111381 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68630871 | TTACATCCTCAAATG[C/G]AAGCAAAGGCGGGAA | 10391 |
rs1388446 | snp | A/C | 0.331179 | 0.236453 | intron-variant | CORO2B | GRCh38.p7 | 15:68718165 | ACCAACAATGTGTGC[A/C]CATGTTTCCTGTGTG | 10391 |
rs1388447 | snp | A/G | 0.232651 | 0.249397 | intron-variant | CORO2B | GRCh38.p7 | 15:68688920 | GAGGAGGGCATGGAC[A/G]CCCTGCTCCAGGATG | 10391 |
rs1388448 | snp | C/T | 0.232651 | 0.249397 | intron-variant | CORO2B | GRCh38.p7 | 15:68688798 | ATTCTGCTTCAGGAA[C/T]TTACCCCAGGGAAAT | 10391 |
rs1463700 | snp | C/T | 0.347473 | 0.230215 | intron-variant | CORO2B | GRCh38.p7 | 15:68716676 | gctcaacttaaaata[C/T]catcatcacagagag | 10391 |
rs1463701 | snp | A/G | 0.276267 | 0.248616 | intron-variant | CORO2B | GRCh38.p7 | 15:68716372 | aggtgccttgcacat[A/G]tggtctctaagcctt | 10391 |
rs1463702 | snp | A/G | 0.19646 | 0.2442 | intron-variant | CORO2B | GRCh38.p7 | 15:68711243 | CCTTTTTTTGAGGAT[A/G]TGCCTGGGGCTCGGG | 10391 |
rs1463703 | snp | G/T | 0.463774 | 0.129618 | intron-variant | CORO2B | GRCh38.p7 | 15:68710216 | CCCCAGGTCTCTCCT[G/T]AGAGATGGTGGACTT | 10391 |
rs1465997 | snp | A/G | 0.482905 | 0.0908579 | intron-variant | CORO2B | GRCh38.p7 | 15:68589185 | GAGTTCCTGTAGCAT[A/G]TGATCCCTGGTATAC | 10391 |
rs1467976 | snp | G/T | 0.0755793 | 0.179102 | intron-variant | CORO2B | GRCh38.p7 | 15:68649619 | ttatatctgtcaata[G/T]ttagcatattcaaaa | 10391 |
rs1491632 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO2B | GRCh38.p7 | 15:68611550 | GCTTTCAGTTGAAGA[C/T]ATATCCAAACAGAGA | 10391 |
rs1491633 | snp | C/T | 0.36021 | 0.224397 | intron-variant | CORO2B | GRCh38.p7 | 15:68664803 | aaaaggaaatgcaaa[C/T]agattgtaagcatac | 10391 |
rs1491634 | snp | A/G | 0.172997 | 0.237846 | intron-variant | CORO2B | GRCh38.p7 | 15:68662857 | CATTTACTGGCATAA[A/G]ATATATACAAATCTA | 10391 |
rs1491635 | snp | C/T | 0.298905 | 0.24517 | intron-variant | CORO2B | GRCh38.p7 | 15:68658842 | CATCAGGCCTCCATG[C/T]TGCATTCTGATCAGC | 10391 |
rs1491636 | snp | A/G | 0.449473 | 0.150701 | intron-variant | CORO2B | GRCh38.p7 | 15:68638254 | TCAAATGTTTACTTG[A/G]GGAGGTCAGGCTTTG | 10391 |
rs1491637 | snp | C/T | 0.258843 | 0.249844 | intron-variant | CORO2B | GRCh38.p7 | 15:68722432 | TCACACTTAGATCAA[C/T]GCGTCCACCTTTGAC | 10391 |
rs1491638 | snp | C/T | 0.25912 | 0.249834 | intron-variant | CORO2B | GRCh38.p7 | 15:68722380 | GCTTCCGAACTGCTA[C/T]GATGATTAAAACTGT | 10391 |
rs1491639 | snp | A/G | 0.301429 | 0.244653 | intron-variant | CORO2B | GRCh38.p7 | 15:68719055 | TCTTACTGATCTCCA[A/G]TCACTCTACCTGCTC | 10391 |
rs1491640 | snp | G/T | 0.475753 | 0.244715 | intron-variant | CORO2B | GRCh38.p7 | 15:68719050 | CTGATCTCCAGTCAC[G/T]CTACCTGCTCTCCTG | 10391 |
rs1491641 | snp | C/T | 0.312104 | 0.242163 | intron-variant | CORO2B | GRCh38.p7 | 15:68718916 | TTTGAAGACCCCAGT[C/T]CACAGCACATCTCTC | 10391 |
rs1542746 | snp | A/C | 0.085535 | 0.188285 | intron-variant | CORO2B | GRCh38.p7 | 15:68715317 | GGCAGCCTCGGGGCC[A/C]CTTACCTAGGCCTTT | 10391 |
rs1542747 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68624752 | ggctggagtgcaatg[G/T]catgatctcggctca | 10391 |
rs1562158 | snp | C/T | 0.250168 | 0.25 | intron-variant | CORO2B | GRCh38.p7 | 15:68558093 | CAGGGAGGGTGGGTG[C/T]GGGCAGAGAGGCTTC | 10391 |
rs1562159 | snp | A/G | 0.494013 | 0.0543839 | intron-variant | CORO2B | GRCh38.p7 | 15:68561093 | CACCCCGCGTCCCCC[A/G]GGCTCCCAGCACAAC | 10391 |
rs1562160 | snp | A/G | 0.383824 | 0.211166 | intron-variant | CORO2B | GRCh38.p7 | 15:68561112 | TCCCAGCACAACTTT[A/G]CCTCTCAATACTGGT | 10391 |
rs1562162 | snp | C/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68591218 | ACGTGGCTGGGCAGG[C/G]CAAGGAAGCTCTCTG | 10391 |
rs1562163 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68591219 | CGTGGCTGGGCAGGC[C/G]AAGGAAGCTCTCTGG | 10391 |
rs1562164 | snp | A/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68591220 | GTGGCTGGGCAGGCC[A/G]AGGAAGCTCTCTGGA | 10391 |
rs1565563 | snp | A/G | 0.180064 | 0.240019 | intron-variant | CORO2B | GRCh38.p7 | 15:68593244 | GGCTACGGTTTGAAT[A/G]TCTCTGCCAAAACTC | 10391 |
rs1565564 | snp | A/G | 0.347694 | 0.230122 | intron-variant | CORO2B | GRCh38.p7 | 15:68716891 | CTAATGCATCCCATG[A/G]ATTTAGCCCCTGCCC | 10391 |
rs1602544 | snp | A/T | 0.388964 | 0.20782 | intron-variant | CORO2B | GRCh38.p7 | 15:68662979 | gcctagaaatatttt[A/T]aaaaatttaagaaaa | 10391 |
rs1602545 | snp | A/G | 0.0685596 | 0.171987 | intron-variant | CORO2B | GRCh38.p7 | 15:68662769 | catttgcagttgaga[A/G]aaatgtaaacaaatg | 10391 |
rs1866685 | snp | A/G | 0.330947 | 0.236533 | intron-variant | CORO2B | GRCh38.p7 | 15:68638321 | GAGAGGGTAGAGCTA[A/G]TGTTGAGCAAGCACC | 10391 |
rs1866686 | snp | A/G | 0.0337553 | 0.125452 | intron-variant | CORO2B | GRCh38.p7 | 15:68641865 | agtagctgagactat[A/G]ggtgtgtaccactat | 10391 |
rs1873573 | snp | A/G | 0.463343 | 0.130326 | intron-variant | CORO2B | GRCh38.p7 | 15:68707677 | TAAAAAGAAAGAAGT[A/G]TGTGTGTCTATATGT | 10391 |
rs1907565 | snp | A/G | 0.466308 | 0.125343 | intron-variant | CORO2B | GRCh38.p7 | 15:68655226 | AACCTGGATCTTTTA[A/G]TAATAGAAGAAATAT | 10391 |
rs1966275 | snp | A/G | 0.0970103 | 0.197722 | intron-variant | CORO2B | GRCh38.p7 | 15:68650079 | GAAGAAATGCAATAT[A/G]CGATTAATCACATTA | 10391 |
rs1968979 | snp | C/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68596067 | CTGCACAACTCCCAC[C/T]TCCCCGCAAGCCACC | 10391 |
rs1975513 | snp | C/T | 0.187685 | 0.242109 | intron-variant | CORO2B | GRCh38.p7 | 15:68558403 | gacagggtctcgctt[C/T]gttaaccaggctgga | 10391 |
rs1985277 | snp | C/T | 0.289424 | 0.246872 | intron-variant | CORO2B | GRCh38.p7 | 15:68558174 | AGTTGACAGGTGAGG[C/T]TGGTGTTCTGACCCG | 10391 |
rs1994714 | snp | C/T | 0.403158 | 0.197592 | intron-variant | CORO2B | GRCh38.p7 | 15:68585096 | CTGGGAGCCTCCCAT[C/T]GCTACATTAATTAAT | 10391 |
rs1994715 | snp | C/T | 0.404035 | 0.196909 | intron-variant | CORO2B | GRCh38.p7 | 15:68584977 | GTGGCTTCTCCCCCA[C/T]TCCCCACCCCCACCC | 10391 |
rs1994716 | snp | A/G | 0.439363 | 0.163222 | intron-variant | CORO2B | GRCh38.p7 | 15:68691757 | AACAGAGAGGAGCCT[A/G]TTTAGAAGAAGGAGT | 10391 |
rs2004092 | snp | A/G | 0.416871 | 0.186156 | intron-variant | CORO2B | GRCh38.p7 | 15:68675650 | TACAAAAATAGATCT[A/G]TAAACATCTTATTTG | 10391 |
rs2017617 | snp | A/G | 0.495483 | 0.0473088 | intron-variant | CORO2B | GRCh38.p7 | 15:68560723 | GGGAGCACAGCTGGA[A/G]AGCGGCCCTGACCAG | 10391 |
rs2044342 | snp | A/T | 0.406814 | 0.194704 | intron-variant | CORO2B | GRCh38.p7 | 15:68560321 | ttcttctgagacagg[A/T]tctcgctctgtcacc | 10391 |
rs2046923 | snp | C/G | 0.4711 | 0.116682 | intron-variant | CORO2B | GRCh38.p7 | 15:68654511 | AGATCAAGCAGACTG[C/G]CAGATGCTTCAGAGG | 10391 |
rs2046924 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | CORO2B | GRCh38.p7 | 15:68654258 | CCAAATCCAGAGAAC[A/G]CCCATCCCATAACCT | 10391 |
rs2046925 | snp | A/G | 0.464735 | 0.128019 | intron-variant | CORO2B | GRCh38.p7 | 15:68654124 | CAAGCTGTCAATCTC[A/G]AGCCTCAGACAAATG | 10391 |
rs2087707 | snp | C/T | 0.47852 | 0.101384 | intron-variant | CORO2B | GRCh38.p7 | 15:68678433 | GCCCAAGTCGGCCTC[C/T]CAAAGTGTTGGGATT | 10391 |
rs2087708 | snp | A/G | 0.134119 | 0.221521 | intron-variant | CORO2B | GRCh38.p7 | 15:68678148 | GTAGGAACAGCCAGC[A/G]GCCAGTGGCACGGGT | 10391 |
rs2120859 | snp | A/G | 0.377582 | 0.214995 | intron-variant | CORO2B | GRCh38.p7 | 15:68560001 | AGAGCCTCAGACGGC[A/G]ATGCAGATCTGACCA | 10391 |
rs2120860 | snp | C/T | 0.384017 | 0.211044 | intron-variant | CORO2B | GRCh38.p7 | 15:68562795 | tcctggctaacacgg[C/T]gaaaccccgtctcta | 10391 |
rs2120861 | snp | C/T | 0.495596 | 0.0467178 | intron-variant | CORO2B | GRCh38.p7 | 15:68563013 | aaaagaaaacaaaaa[C/T]gtaatatactaaaat | 10391 |
rs2120862 | snp | C/T | 0.493837 | 0.055168 | intron-variant | CORO2B | GRCh38.p7 | 15:68563085 | agctataaattctta[C/T]aaaggaagaaagatc | 10391 |
rs2131010 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68695600 | CAGTTCCTTCCTTTT[C/T]TCCCTCCCTCCTTGT | 10391 |
rs2131011 | snp | A/G | 0.196149 | 0.244131 | intron-variant | CORO2B | GRCh38.p7 | 15:68689630 | TTGGTCCTGTCTGTC[A/G]CTGAAGCCTGGCTCC | 10391 |
rs2131012 | snp | C/G | 0.199564 | 0.24486 | intron-variant | CORO2B | GRCh38.p7 | 15:68688406 | CATGTTGGTGATCAA[C/G]AAGTTTCAGATTTTG | 10391 |
rs2131013 | snp | C/G | 0.202959 | 0.245534 | intron-variant | CORO2B | GRCh38.p7 | 15:68688330 | CATATAAAAGGATCC[C/G]TATCTAAAAAAACCA | 10391 |
rs2165257 | snp | A/G | 0.254944 | 0.249951 | intron-variant | CORO2B | GRCh38.p7 | 15:68668180 | TAAGAGTTTAGCACC[A/G]TGCCTGACACACAGT | 10391 |
rs2172197 | snp | C/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68695528 | ATGCTGAATCACACG[C/G]TTAATTTTTAAATTC | 10391 |
rs2201115 | snp | C/T | 0.461592 | 0.133149 | intron-variant | CORO2B | GRCh38.p7 | 15:68632739 | GGGACTATAGGTGCG[C/T]GCTAGCACGCTTGGC | 10391 |
rs2218171 | snp | C/T | 0.284471 | 0.247612 | intron-variant | CORO2B | GRCh38.p7 | 15:68643954 | AGGTGGGAGAATCAC[C/T]TGAACCTGGGAGACG | 10391 |
rs2291534 | snp | C/T | 0.279461 | 0.248258 | intron-variant | CORO2B | GRCh38.p7 | 15:68645102 | CCCCAAGAGCCCAGC[C/T]GAGGCCCTTCATGGC | 10391 |
rs2353383 | snp | A/G | 0.0689305 | 0.172377 | intron-variant | CORO2B | GRCh38.p7 | 15:68661389 | gttctgggtggccag[A/G]gatattgtccaatat | 10391 |
rs2415021 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68689121 | GTCCAGCCCTTCTTG[G/T]TGCTGGGACAGAACT | 10391 |
rs2415022 | snp | A/G | 0.205723 | 0.246048 | intron-variant | CORO2B | GRCh38.p7 | 15:68681481 | CAGACTTCTTCTCTG[A/G]CAGAAACACAGAACT | 10391 |
rs2415023 | snp | A/C | 0.205723 | 0.246048 | intron-variant | CORO2B | GRCh38.p7 | 15:68681480 | AGACTTCTTCTCTGA[A/C]AGAAACACAGAACTT | 10391 |
rs2415024 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CORO2B | GRCh38.p7 | 15:68645953 | AACCCCATCTCTACT[A/G]AAAATACAAAAATTA | 10391 |
rs2415025 | snp | C/T | 0.330482 | 0.236691 | intron-variant | CORO2B | GRCh38.p7 | 15:68637457 | ATGAAGGAAAGACAC[C/T]GTTATCAACTGCTCC | 10391 |
rs2452120 | snp | C/T | 0 | 0 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68577992 | GCTTGGAGAACCCCT[C/T]TGCTTCCACCTCTGC | 10391 |
rs2469486 | snp | A/G | 0 | 0 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68577870 | CCCCCAGCACTTTCC[A/G]CAGAGCAGGTGCTCA | 10391 |
rs2638049 | snp | A/G | 0.397271 | 0.202018 | intron-variant | CORO2B | GRCh38.p7 | 15:68573951 | GAAAGACTGAAGAAG[A/G]GTCAGCTAGGTGCTG | 10391 |
rs2899742 | snp | C/T | 0.360842 | 0.224085 | intron-variant | CORO2B | GRCh38.p7 | 15:68665706 | TTTTAAAAGGATATA[C/T]AATACAATAAAAAAG | 10391 |
rs2899743 | snp | C/G | 0.467234 | 0.12373 | intron-variant | CORO2B | GRCh38.p7 | 15:68629185 | TCATTCAGAACTACT[C/G]CAGAATTTCCAATGT | 10391 |
rs2899744 | snp | A/C | 0.143284 | 0.226079 | intron-variant | CORO2B | GRCh38.p7 | 15:68629088 | TGATCCCATGGCTCC[A/C]CCAGCAGACCTTGCT | 10391 |
rs3084695 | in-del | -/AC/ACACAC | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68602450 | cacacacacacacac[-/AC/ACACAC]GTTTTACCTACATGT | 10391 |
rs3084723 | in-del | -/AAAGA | 0.0689305 | 0.172377 | intron-variant | CORO2B | GRCh38.p7 | 15:68665011 | agaagccataaaaga[-/AAAGA]ctggtaaacttaaat | 10391 |
rs3084725 | in-del | -/TTTT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68647690 | tcttttttttttttt[-/TTTT]gagatggagtttcga | 10391 |
rs3736272 | snp | A/C | 0.398387 | 0.2012 | intron-variant | CORO2B | GRCh38.p7 | 15:68711532 | GAGGACCTGCGAGGG[A/C]AGATGCATGGGAGGC | 10391 |
rs3751553 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68718619 | CCTCAGCCTTTCCCC[A/T]GGCCCAGAACATCAT | 10391 |
rs3751554 | snp | C/T | 0.000553065 | 0.0166201 | synonymous-codon | CORO2B | GRCh38.p7 | 15:68718714 | GGTCATGCCCAAGCA[C/T]GGGCTGGATGTGTCA | 10391 |
rs3764204 | snp | A/G | 0.0364509 | 0.129988 | intron-variant | CORO2B | GRCh38.p7 | 15:68714268 | TTTTCCAGAGTGGGG[A/G]CTGAGCTCCAGAGAG | 10391 |
rs3985627 | in-del | -/AAAA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68576169 | aaaaaaaaaaaaaaa[-/AAAA]aagaaagaaagaaag | 10391 |
rs3985628 | in-del | -/TT/TTTT/TTTTT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68696557 | ttttttttttttttt[-/TT/TTTT/TTTTT]nnnngaggcagagtc | 10391 |
rs4078458 | snp | C/T | 0.328148 | 0.237472 | intron-variant | CORO2B | GRCh38.p7 | 15:68603718 | TTCCTGGTTTGCAGA[C/T]GGCCGTCTTCTTGCT | 10391 |
rs4272984 | snp | A/T | 0.274661 | 0.248781 | intron-variant | CORO2B | GRCh38.p7 | 15:68709448 | GATTTTCGAAAAGAT[A/T]Tttttttcgtgtttt | 10391 |
rs4299098 | snp | G/T | 0.495634 | 0.0465208 | intron-variant | CORO2B | GRCh38.p7 | 15:68561211 | AGATAAGGGGGAGGG[G/T]CTGGGAGAGGGCTGG | 10391 |
rs4335728 | snp | A/G | 0.0271762 | 0.113356 | intron-variant | CORO2B | GRCh38.p7 | 15:68604971 | acacaaaaattagcc[A/G]ggcatggtggcacac | 10391 |
rs4402500 | snp | A/G | 0.18134 | 0.240387 | intron-variant | CORO2B | GRCh38.p7 | 15:68678412 | CAGgcggtggttcac[A/G]cctgtaatcccaaca | 10391 |
rs4457947 | snp | C/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68688931 | AGGGCGTCCATGCCC[C/T]CCTCCTGGGGCTGGG | 10391 |
rs4462541 | snp | C/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68641814 | ctgcaacctccacct[C/T]ccaggctcaagccat | 10391 |
rs4482222 | snp | C/T | 0.259397 | 0.249823 | intron-variant | CORO2B | GRCh38.p7 | 15:68721420 | aagtaagaatggtca[C/T]acgggctgggcgccg | 10391 |
rs4509964 | snp | A/G | 0.031825 | 0.122064 | intron-variant | CORO2B | GRCh38.p7 | 15:68623329 | GAGCAATAGAGCAGG[A/G]GCCTTGACTGAAGCT | 10391 |
rs4522367 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68688932 | GGGCGTCCATGCCCT[C/T]CTCCTGGGGCTGGGG | 10391 |
rs4528518 | snp | A/G | 0.39121 | 0.2063 | intron-variant | CORO2B | GRCh38.p7 | 15:68721341 | aatgatgtgataaat[A/G]ggatttgctttaaaa | 10391 |
rs4550403 | snp | C/T | 0.372189 | 0.218105 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68726446 | GCTGCAGTGATCCCT[C/T]TTTCGTCCCACCCCC | 10391 |
rs4598850 | snp | A/G | 0.39121 | 0.2063 | intron-variant | CORO2B | GRCh38.p7 | 15:68721368 | aaaataacccctgag[A/G]aaagtggtgcagtgt | 10391 |
rs4776411 | snp | C/G | 0.312593 | 0.242037 | intron-variant | CORO2B | GRCh38.p7 | 15:68588631 | TCCCGATGCCCCCAG[C/G]GCTCAGACCTGCTTT | 10391 |
rs4776412 | snp | C/G | 0.252421 | 0.249988 | intron-variant | CORO2B | GRCh38.p7 | 15:68627399 | AAGTGCAGGTGGGTC[C/G]CCAGGAAGAAAGAGT | 10391 |
rs4776413 | snp | C/T | 0.0456336 | 0.143994 | intron-variant | CORO2B | GRCh38.p7 | 15:68648833 | ACACTCTTCGTAAGA[C/T]GTAAATGAGGCAAGT | 10391 |
rs4776414 | snp | A/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68650522 | GAGGCTGAGGCCGGA[A/G]AATCGCTTAAACCTG | 10391 |
rs4776416 | snp | A/G | 0.237593 | 0.249692 | intron-variant | CORO2B | GRCh38.p7 | 15:68669600 | TTCGTTGAGCTCAAT[A/G]GGCAATGCTGGCTCT | 10391 |
rs4776417 | snp | A/G | 0.138546 | 0.223781 | intron-variant | CORO2B | GRCh38.p7 | 15:68670470 | caggcatgagccatc[A/G]cgcccagccAGCAAA | 10391 |
rs4776418 | snp | A/G | 0.276267 | 0.248616 | intron-variant | CORO2B | GRCh38.p7 | 15:68699723 | TCCCAACCTCTCCTG[A/G]AGGACGTGCTCTGGG | 10391 |
rs4776419 | snp | C/T | 0.170612 | 0.240411 | intron-variant | CORO2B | GRCh38.p7 | 15:68701155 | GAGGGGCCAGTGCGC[C/T]GAGTGGGTCTTCACT | 10391 |
rs4776420 | snp | A/G | 0.463451 | 0.130149 | intron-variant | CORO2B | GRCh38.p7 | 15:68701635 | ggactacaggtgcgc[A/G]ccaccatgcccggct | 10391 |
rs4776421 | snp | A/G | 0.443866 | 0.157848 | intron-variant | CORO2B | GRCh38.p7 | 15:68703903 | AAGTGCACATGAAAA[A/G]TATAACTTGGCCAGG | 10391 |
rs4777070 | snp | G/T | 0.493386 | 0.0571263 | intron-variant | CORO2B | GRCh38.p7 | 15:68574169 | AGGGCAAGTCCGAGT[G/T]GCCCAGCAAGGGAAA | 10391 |
rs4777071 | snp | C/G | 0.494733 | 0.0510469 | intron-variant | CORO2B | GRCh38.p7 | 15:68574328 | GGCAGGCAGCAAGGG[C/G]TGGAGGAGCATCTCC | 10391 |
rs4777072 | snp | G/T | 0.463881 | 0.12944 | intron-variant | CORO2B | GRCh38.p7 | 15:68604733 | TGGGATTATGGGTGC[G/T]TTTGTTTACATGGTT | 10391 |
rs4777073 | snp | A/G | 0.242775 | 0.249896 | intron-variant | CORO2B | GRCh38.p7 | 15:68607571 | gcctgtgatcccaac[A/G]cttcaggagaccgag | 10391 |
rs4777074 | snp | G/T | 0.301681 | 0.2446 | intron-variant | CORO2B | GRCh38.p7 | 15:68607941 | CCTTTATCATCTTCT[G/T]GTCAAAATCACATGC | 10391 |
rs4777075 | snp | C/G | 0.27278 | 0.24896 | intron-variant | CORO2B | GRCh38.p7 | 15:68611070 | ACCTCAGTTCATCAA[C/G]ATGAGAAAATGCGCC | 10391 |
rs4777076 | snp | A/G | 0.408871 | 0.193029 | intron-variant | CORO2B | GRCh38.p7 | 15:68628229 | TTTAATTCTCACAGT[A/G]GTCACAGAGAAACCC | 10391 |
rs4777077 | snp | A/G | 0.237593 | 0.249692 | intron-variant, utr-variant-5-prime | CORO2B | GRCh38.p7 | 15:68632101 | TCGGAGCTAGAAGGT[A/G]GTCAGATTCCCGTTA | 10391 |
rs4777078 | snp | C/T | 0.465368 | 0.126951 | intron-variant | CORO2B | GRCh38.p7 | 15:68654906 | AGTCCCTGAGTATGC[C/T]TAGCAGTGAGCTACC | 10391 |
rs4777079 | snp | A/C | 0.465683 | 0.126415 | intron-variant | CORO2B | GRCh38.p7 | 15:68655068 | GAGGGTCCAGGGCTG[A/C]CATGGAGCCTGGTGG | 10391 |
rs4777081 | snp | A/G | 0.0693013 | 0.172766 | intron-variant | CORO2B | GRCh38.p7 | 15:68674796 | TCCAGCCTTTCCACC[A/G]GTGCCCTCATGCTCT | 10391 |
rs4777082 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68697976 | TGCTGGGAGAGTGGC[A/G]GGAAGGGCTGACCCC | 10391 |
rs4777083 | snp | C/T | 0.133093 | 0.220981 | intron-variant | CORO2B | GRCh38.p7 | 15:68704567 | CTGCTCCCTCTCCCA[C/T]GTGCAGGGACAGTTG | 10391 |
rs4777084 | snp | A/G | 0.210605 | 0.246877 | intron-variant | CORO2B | GRCh38.p7 | 15:68709644 | gtttctttggtagag[A/G]cacggtctcgctgtg | 10391 |
rs5813504 | in-del | -/G | 0.282632 | 0.247861 | intron-variant | CORO2B | GRCh38.p7 | 15:68668281 | GGCTGGGGAGGGGGG[-/G]CGCTACAGGGGATCC | 10391 |
rs5813505 | in-del | -/C | 0.254664 | 0.249956 | intron-variant | CORO2B | GRCh38.p7 | 15:68668415 | CAGTCGTTAAGATTA[-/C]ATCAGACAGTGATGG | 10391 |
rs5813506 | in-del | -/C | 0.206336 | 0.246157 | intron-variant | CORO2B | GRCh38.p7 | 15:68681402 | GGGGCCAGTGAGGAG[-/C]CCCCTGATTTGGGGG | 10391 |
rs5813507 | in-del | -/GAA | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68717696 | TAAGTAGCAGAAGAA[-/GAA]CTCAGACCGAATCTG | 10391 |
rs6494755 | snp | A/T | 0.481627 | 0.0940692 | intron-variant | CORO2B | GRCh38.p7 | 15:68587694 | CCAAGCATATACAAT[A/T]TGTTTTATATGTATT | 10391 |
rs6494756 | snp | A/G | 0.314301 | 0.241589 | intron-variant | CORO2B | GRCh38.p7 | 15:68588021 | GCGTCTGTGAAAATG[A/G]AGTTAGTAGTCTATC | 10391 |
rs6494757 | snp | A/G | 0.0876345 | 0.190099 | intron-variant | CORO2B | GRCh38.p7 | 15:68635818 | AACGGGACTCTTGTA[A/G]GCCTTGAGGCAAAGA | 10391 |
rs6494760 | snp | A/G | 0.224412 | 0.248687 | intron-variant | CORO2B | GRCh38.p7 | 15:68684492 | GTATGGCACGTACAT[A/G]TGTGTGTGTGTGTTC | 10391 |
rs6494761 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | CORO2B | GRCh38.p7 | 15:68694865 | GGGGCACCTTTTCCT[C/T]ATTTGCAGAGGTGTA | 10391 |
rs6494762 | snp | C/T | 0.446641 | 0.154377 | intron-variant | CORO2B | GRCh38.p7 | 15:68721578 | aggcgtggtggtgcg[C/T]gcctgtaatcccagc | 10391 |
rs7162636 | snp | C/G | 0.49949 | 0.0159663 | intron-variant | CORO2B | GRCh38.p7 | 15:68647999 | ctcccctgcactcca[C/G]cctgggcaacggaga | 10391 |
rs7163493 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | CORO2B | GRCh38.p7 | 15:68647764 | tgtaatcccaacact[C/T]tgggaggccaaggca | 10391 |
rs7164681 | snp | C/T | 0.0383715 | 0.133092 | utr-variant-5-prime, intron-variant | CORO2B | GRCh38.p7 | 15:68616596 | CTTCCAGGCCGCGGT[C/T]GAATGATTCTGACAA | 10391 |
rs7166042 | snp | G/T | 0.104859 | 0.203554 | intron-variant | CORO2B | GRCh38.p7 | 15:68595509 | CCTTTAGGGGACTGG[G/T]ATCCCCTTCCCTCAG | 10391 |
rs7167147 | snp | C/G | 0.030665 | 0.119967 | intron-variant | CORO2B | GRCh38.p7 | 15:68653800 | CCATTCCAGATTTCT[C/G]TAACACCCCATCACT | 10391 |
rs7167348 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | CORO2B | GRCh38.p7 | 15:68653905 | ACTGCTCTGCAGTGA[A/G]GTCTCCGCCCCTCCA | 10391 |
rs7168495 | snp | C/T | 0.193966 | 0.243639 | intron-variant | CORO2B | GRCh38.p7 | 15:68663099 | caaacaattcaaacc[C/T]gtgttgttcagaggt | 10391 |
rs7168514 | snp | C/T | 0.193966 | 0.243639 | intron-variant | CORO2B | GRCh38.p7 | 15:68663129 | tcaatcttttttaca[C/T]gaagatcaccaacta | 10391 |
rs7168630 | snp | A/G | 0.384593 | 0.210677 | intron-variant | CORO2B | GRCh38.p7 | 15:68663040 | gtcgctaaactcaaa[A/G]aaatttccaatttat | 10391 |
rs7168721 | snp | G/T | 0.391024 | 0.206427 | intron-variant | CORO2B | GRCh38.p7 | 15:68720815 | aagctattagggcca[G/T]cccatgcttgaggag | 10391 |
rs7169200 | snp | C/T | 0.493523 | 0.0565391 | intron-variant | CORO2B | GRCh38.p7 | 15:68657562 | ttatcaaaatgtata[C/T]cagaattgtgctgta | 10391 |
rs7169598 | snp | A/T | 0.193966 | 0.243639 | intron-variant | CORO2B | GRCh38.p7 | 15:68663044 | ctaaactcaaagaaa[A/T]ttccaatttattgaa | 10391 |
rs7169645 | snp | A/G | 0.479258 | 0.0997024 | intron-variant | CORO2B | GRCh38.p7 | 15:68657605 | ctatcaatgcattac[A/G]ccccatgattgagtg | 10391 |
rs7169952 | snp | C/T | 0.227074 | 0.248947 | intron-variant | CORO2B | GRCh38.p7 | 15:68663206 | atcttggagatcttt[C/T]cacatcaaatataga | 10391 |
rs7171944 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CORO2B | GRCh38.p7 | 15:68629966 | GTAATGCCCCTGCCA[A/G]AGGCACCCTGCCCTG | 10391 |
rs7171992 | snp | C/T | 0.338523 | 0.233803 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68630138 | CCCTCTTCCTCGTGG[C/T]TTCTGTAGCAATGAC | 10391 |
rs7172641 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68566759 | GCCTGTATATCCAGG[C/T]ACCCTTGGGGTGAGC | 10391 |
rs7173475 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | CORO2B | GRCh38.p7 | 15:68663526 | tgacattgtagtagg[A/C]agttttcttaacagg | 10391 |
rs7173575 | snp | A/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68685218 | CATGATAATGTTCTT[A/T]Attttgtttcgggag | 10391 |
rs7173622 | snp | C/T | 0.114387 | 0.210022 | intron-variant | CORO2B | GRCh38.p7 | 15:68568428 | ATCATCACTATTGCC[C/T]TTTACCCTCTGAGAG | 10391 |
rs7175828 | snp | C/G | 0.0182019 | 0.0936463 | intron-variant | CORO2B | GRCh38.p7 | 15:68593538 | GTTCTCTAGACACTT[C/G]TGACTGAGCTGGAAC | 10391 |
rs7176791 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68621864 | caggttcaagtgatc[C/G]tcccacctcagcctc | 10391 |
rs7177160 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2B | GRCh38.p7 | 15:68572757 | AATTTAGATCCTAAA[C/T]GACTGGAAGGATCTG | 10391 |
rs7177574 | snp | A/C | 0.100588 | 0.200439 | intron-variant | CORO2B | GRCh38.p7 | 15:68699388 | GGGGGTCACAGACAG[A/C]TTTATGGAGGACATG | 10391 |
rs7177588 | snp | A/G | 0.104504 | 0.2033 | intron-variant | CORO2B | GRCh38.p7 | 15:68699412 | GGACATGGGGCCTGA[A/G]CTAGCTGGATACAGG | 10391 |
rs7177886 | snp | A/G | 0.093777 | 0.195178 | intron-variant | CORO2B | GRCh38.p7 | 15:68699321 | CCCACCGAGTGTGGT[A/G]CATGGGAGACACTAC | 10391 |
rs7178209 | snp | A/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68685321 | gttcaagccattctc[A/C]tgcctcagcctccca | 10391 |
rs7178348 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68685314 | ctcctgggttcaagc[C/G]attctcatgcctcag | 10391 |
rs7178352 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68685320 | ggttcaagccattct[C/T]atgcctcagcctccc | 10391 |
rs7178401 | snp | C/G | 0.16976 | 0.236773 | intron-variant | CORO2B | GRCh38.p7 | 15:68661236 | acccacctcggcctc[C/G]caaagtgctgggatt | 10391 |
rs7178969 | snp | C/G | 0.443866 | 0.157848 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68639704 | CAGGGATGGGAAGCT[C/G]ACTACCTATCAAGGT | 10391 |
rs7179174 | snp | A/G | 0.00557542 | 0.0525036 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68639831 | ATGTCCCAGTCTTGC[A/G]CCTTGTGCTCATTGG | 10391 |
rs7179629 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68685300 | acttcaacctcctcc[G/T]cctgggttcaagcca | 10391 |
rs7179882 | snp | A/G | 0.093417 | 0.194889 | intron-variant | CORO2B | GRCh38.p7 | 15:68694390 | tagagaggggaaacc[A/G]aggctcagagaagtt | 10391 |
rs7180458 | snp | A/G | 0.0322114 | 0.122752 | intron-variant | CORO2B | GRCh38.p7 | 15:68694730 | GTACACCCAGCATCT[A/G]AGCGTGCGTGAACAA | 10391 |
rs7183039 | snp | A/C | 0.102014 | 0.201495 | intron-variant | CORO2B | GRCh38.p7 | 15:68595255 | GTTGGGACAAAGGGG[A/C]CCCCTCCCTCTTTCC | 10391 |
rs7183063 | snp | A/G | 0.24019 | 0.249807 | intron-variant | CORO2B | GRCh38.p7 | 15:68712995 | TAGAGTTCAGAGTGT[A/G]TGACGCCAGCCTGAA | 10391 |
rs7183225 | snp | C/T | 0.464523 | 0.128375 | intron-variant | CORO2B | GRCh38.p7 | 15:68704102 | AATATTAGCTGGTCA[C/T]GGTGGTGCGCATCTG | 10391 |
rs7359194 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68579783 | CCACTCTGTGCAGAA[A/G]GCGCTGCCCAGTCCC | 10391 |
rs7359303 | snp | A/G | 0.318656 | 0.240388 | intron-variant | CORO2B | GRCh38.p7 | 15:68694613 | GACCCAGAGATTCAG[A/G]CCTCTCTGCTGACTC | 10391 |
rs7359307 | snp | A/G | 0.320575 | 0.239832 | intron-variant | CORO2B | GRCh38.p7 | 15:68694744 | TGAGCGTGCGTGAAC[A/G]AGGCAGATCGTGGGC | 10391 |
rs7359311 | snp | A/G | 0.213635 | 0.247341 | intron-variant | CORO2B | GRCh38.p7 | 15:68695002 | CCAGCAGGGCCCAAA[A/G]ACAAAAATAAAACAC | 10391 |
rs7359316 | snp | C/T | 0.21695 | 0.247806 | intron-variant | CORO2B | GRCh38.p7 | 15:68694922 | CATGGCTGTGTGGCC[C/T]CCCTGAACCATTCAG | 10391 |
rs8023344 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68700580 | ATACCCAGGCCCTTC[C/T]CCAGGGGCTTTGGGC | 10391 |
rs8023915 | snp | A/G | 0.199873 | 0.244923 | intron-variant | CORO2B | GRCh38.p7 | 15:68719917 | GCCTCCCTCGCTGGC[A/G]TTGCAGCAGTGCTGG | 10391 |
rs8023980 | snp | C/T | 0.285257 | 0.247501 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68640738 | TGCTAAGGAAATTGC[C/T]GTCCTTTGTAGGAAA | 10391 |
rs8024177 | snp | G/T | 0.47802 | 0.102502 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68631691 | GAAGTACACACCAGG[G/T]GCCAGGGGGCAGGGT | 10391 |
rs8024675 | snp | A/G | 0.430583 | 0.172886 | intron-variant | CORO2B | GRCh38.p7 | 15:68687008 | TATTGTCTTCTTCAC[A/G]GTTGTTCTGGCATTG | 10391 |
rs8024951 | snp | C/T | 0.353803 | 0.227431 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68640603 | GAACCTAGGTTTCAC[C/T]GAATCCTAGGTCAGA | 10391 |
rs8024974 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68700830 | AGGTTTCTGTCATCT[C/T]AAGGAGAGGGAGAGA | 10391 |
rs8025334 | snp | A/G | 0.111928 | 0.208413 | intron-variant | CORO2B | GRCh38.p7 | 15:68600513 | CTGTAGGACTTAGTC[A/G]GAAAGACAAAGCGGT | 10391 |
rs8025344 | snp | G/T | 0.160609 | 0.233472 | intron-variant | CORO2B | GRCh38.p7 | 15:68619747 | CATATATATGAGTGC[G/T]TGCATGCGTGTGTGT | 10391 |
rs8026124 | snp | C/G | 0.0955749 | 0.196603 | intron-variant | CORO2B | GRCh38.p7 | 15:68636031 | CTCTGAATCAGATCC[C/G]AGCTCCTCCACTTCA | 10391 |
rs8026194 | snp | C/T | 0.485528 | 0.0838238 | intron-variant | CORO2B | GRCh38.p7 | 15:68658936 | GCTTTCTCTCCTACA[C/T]GCCTTTGCCCCGGCT | 10391 |
rs8026209 | snp | C/G | 0.0528381 | 0.153711 | intron-variant | CORO2B | GRCh38.p7 | 15:68704688 | CTTGAGACTAAGAGC[C/G]GTTCCCCCGTATCTA | 10391 |
rs8026438 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68704923 | GAAGTAACCTCCCAG[A/G]GCAACCTCTGAGCAG | 10391 |
rs8026511 | snp | C/G | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68704689 | TTGAGACTAAGAGCC[C/G]TTCCCCCGTATCTAA | 10391 |
rs8026551 | snp | A/T | 0.498908 | 0.0233371 | intron-variant | CORO2B | GRCh38.p7 | 15:68657224 | caagaagccaattat[A/T]ttgaaacacaggcca | 10391 |
rs8026784 | snp | C/T | 0.0711525 | 0.174681 | intron-variant | CORO2B | GRCh38.p7 | 15:68674944 | CAGCAAGGTGGAGCA[C/T]GAAAGGAATGAATCC | 10391 |
rs8026807 | snp | A/G | 0.117188 | 0.211804 | intron-variant | CORO2B | GRCh38.p7 | 15:68713309 | GAGAGCTCCTGAAGT[A/G]GTGTAGCCCCCAACT | 10391 |
rs8027077 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68653540 | GGAGAATGCAGCACC[A/G]TACAGGGGCTGCCCA | 10391 |
rs8027249 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68705143 | AGTAATGTATTCAAT[A/G]TCAAAGCAGAAAAGT | 10391 |
rs8027795 | snp | A/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68653930 | CCTCCAAGGGAATTC[A/G]GAGAGCCTTTTCCAA | 10391 |
rs8027940 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68653915 | AGTGAGGTCTCCGCC[C/T]CTCCAAGGGAATTCA | 10391 |
rs8028289 | snp | A/G | 0.117537 | 0.212022 | intron-variant | CORO2B | GRCh38.p7 | 15:68714128 | AAGTCAGGAGCCTGG[A/G]CCCGCACACCAGCTT | 10391 |
rs8028291 | snp | A/G | 0.117537 | 0.212022 | intron-variant | CORO2B | GRCh38.p7 | 15:68714132 | CAGGAGCCTGGGCCC[A/G]CACACCAGCTTCTCA | 10391 |
rs8028464 | snp | A/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68654065 | GTGACTTTGGAAAAG[A/G]GAGGAGAATTGTGCT | 10391 |
rs8028652 | snp | G/T | 0.0150606 | 0.0854603 | intron-variant | CORO2B | GRCh38.p7 | 15:68653618 | GCATGGCCCAGCTGG[G/T]CTTAACTCTGGAGCT | 10391 |
rs8028905 | snp | G/T | 0.281841 | 0.247964 | intron-variant | CORO2B | GRCh38.p7 | 15:68613478 | TCTCTATGTGGCAAA[G/T]CTTGAAGGACCAGTC | 10391 |
rs8028973 | snp | C/T | 0.338296 | 0.233889 | intron-variant | CORO2B | GRCh38.p7 | 15:68693076 | CTATCCTCTAATTTT[C/T]CCACAACATACAACA | 10391 |
rs8029010 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68653850 | GCTCCTCAAACCTTC[A/T]CTCCCCCAGGAAAAA | 10391 |
rs8029298 | snp | C/T | 0.197082 | 0.244335 | intron-variant | CORO2B | GRCh38.p7 | 15:68693260 | CTGGAAATGAGCCGA[C/T]AGAGATGCAGGCAGG | 10391 |
rs8030333 | snp | A/G | 0.235854 | 0.249599 | intron-variant | CORO2B | GRCh38.p7 | 15:68672257 | TAAAAAttttttgag[A/G]cagaatctcactctg | 10391 |
rs8030733 | snp | C/T | 0.345925 | 0.230864 | intron-variant | CORO2B | GRCh38.p7 | 15:68633186 | ATGCAGAATGCTACA[C/T]GACCACCTAGAATGA | 10391 |
rs8030994 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | CORO2B | GRCh38.p7 | 15:68593113 | ttctttcatcaggag[C/T]ccactcccaggataa | 10391 |
rs8031238 | snp | A/G | 0.126909 | 0.217598 | intron-variant | CORO2B | GRCh38.p7 | 15:68636424 | GGGCTTGCATTGGGT[A/G]GTGGATGCATGCTGC | 10391 |
rs8031588 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | CORO2B | GRCh38.p7 | 15:68610352 | AGGCCTAGTGAAGGG[C/G]TGGGGGCTGGCTTGG | 10391 |
rs8032109 | snp | C/T | 0.356169 | 0.226336 | intron-variant | CORO2B | GRCh38.p7 | 15:68724909 | GTTAAGCTAGAGAGT[C/T]ATTGGGGTGAAGATC | 10391 |
rs8032349 | snp | A/G | 0.199564 | 0.24486 | intron-variant | CORO2B | GRCh38.p7 | 15:68689993 | tataaattacattga[A/G]taaacttgcaattaa | 10391 |
rs8032624 | snp | A/G | 0.298398 | 0.245271 | intron-variant | CORO2B | GRCh38.p7 | 15:68725082 | AGTTCTAAATTATCA[A/G]CACAAGCCGGGCATG | 10391 |
rs8032777 | snp | C/G | 0.0792508 | 0.182605 | intron-variant | CORO2B | GRCh38.p7 | 15:68596405 | CCCTGTGGAATGAAG[C/G]GGGGATAGAGCCCCA | 10391 |
rs8032929 | snp | C/T | 0.0517044 | 0.152246 | intron-variant | CORO2B | GRCh38.p7 | 15:68684489 | CTTGTATGGCACGTA[C/T]ATATGTGTGTGTGTG | 10391 |
rs8033001 | snp | A/T | 0.203267 | 0.245593 | intron-variant | CORO2B | GRCh38.p7 | 15:68705500 | ACCCAGGGAGGGAAG[A/T]GGCTGGTATCAAATG | 10391 |
rs8033246 | snp | A/G | 0.224116 | 0.248656 | intron-variant | CORO2B | GRCh38.p7 | 15:68684543 | ACATGTGTATGTTGC[A/G]GACAGTCACTGGAAA | 10391 |
rs8033543 | snp | G/T | 0.453575 | 0.145111 | intron-variant | CORO2B | GRCh38.p7 | 15:68690112 | actattacatttgca[G/T]agtggaaatattcta | 10391 |
rs8033783 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | CORO2B | GRCh38.p7 | 15:68684830 | GGCCCGGGAGCCTGG[A/G]ACACAGGGAGCCCGA | 10391 |
rs8034347 | snp | A/G | 0.143284 | 0.226079 | intron-variant | CORO2B | GRCh38.p7 | 15:68633442 | AAAGTTTCTGCTCTA[A/G]TTTCTAGACCCTCAG | 10391 |
rs8034877 | snp | A/G | 0.391397 | 0.206172 | intron-variant | CORO2B | GRCh38.p7 | 15:68721812 | cagtgctgtggcacg[A/G]tcatagctcactata | 10391 |
rs8034916 | snp | A/G | 0.25912 | 0.249834 | intron-variant | CORO2B | GRCh38.p7 | 15:68721877 | cttagacttctgagt[A/G]gctggaactagcggc | 10391 |
rs8037496 | snp | A/G | 0.430732 | 0.172731 | intron-variant | CORO2B | GRCh38.p7 | 15:68660864 | tgtaacaatgatggt[A/G]tcttcaactatgtaa | 10391 |
rs8037940 | snp | C/T | 0.119978 | 0.213528 | intron-variant | CORO2B | GRCh38.p7 | 15:68661034 | ccaggctggagtgca[C/T]tggagtgatgtcagc | 10391 |
rs8038357 | snp | A/G | 0.118933 | 0.212888 | intron-variant | CORO2B | GRCh38.p7 | 15:68661107 | ctcaacctccccagt[A/G]gctgggattacaggt | 10391 |
rs8039274 | snp | A/G | 0.0818113 | 0.184966 | intron-variant | CORO2B | GRCh38.p7 | 15:68664374 | agttattggcggggc[A/G]tggtggctcacgctt | 10391 |
rs8039445 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CORO2B | GRCh38.p7 | 15:68590921 | CTATGCAGGGCCGGC[C/T]GCCTTCCCCATCCCT | 10391 |
rs8039918 | snp | A/G | 0.0314385 | 0.121371 | intron-variant | CORO2B | GRCh38.p7 | 15:68649003 | agcctcaatttttaa[A/G]ttatattcaataaaa | 10391 |
rs8039932 | snp | A/G | 0.0726307 | 0.176182 | intron-variant | CORO2B | GRCh38.p7 | 15:68686099 | ctggagtgcaatggc[A/G]caaccttggctcatt | 10391 |
rs8040343 | snp | A/G | 0.0803491 | 0.183626 | intron-variant | CORO2B | GRCh38.p7 | 15:68679115 | TATGGGCCTGGCACC[A/G]TGCTGGGTGTTGGGA | 10391 |
rs8041119 | snp | C/G | 0.326506 | 0.238006 | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68615997 | AGAACACCTACTGTG[C/G]GCCAGACCTGCTGGG | 10391 |
rs8041352 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | CORO2B | GRCh38.p7 | 15:68703805 | CATAATCATGTACGC[A/G]TTTTAAAGATGAAGT | 10391 |
rs8042264 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | CORO2B | GRCh38.p7 | 15:68703858 | GAAACAAACTTCATA[C/T]CATATGTATTGACTA | 10391 |
rs8042290 | snp | A/G | 0.455621 | 0.142197 | intron-variant | CORO2B | GRCh38.p7 | 15:68682752 | CCACTCAGCCAGTGT[A/G]CAGCAGAGCTGAGAT | 10391 |
rs8042712 | snp | A/C | 0.116838 | 0.211584 | intron-variant | CORO2B | GRCh38.p7 | 15:68713286 | ggatgaaaAGCAATG[A/C]CCCTGGTGAGAGCTC | 10391 |
rs9630433 | snp | C/G | 0.324855 | 0.23853 | intron-variant | CORO2B | GRCh38.p7 | 15:68605806 | ctcagctcactgcaa[C/G]ctccacctcccgggt | 10391 |
rs9630434 | snp | A/G | 0.329317 | 0.237084 | intron-variant | CORO2B | GRCh38.p7 | 15:68605811 | ctcactgcaacctcc[A/G]cctcccgggttcaag | 10391 |
rs9646210 | snp | A/C | 0.331179 | 0.236453 | intron-variant | CORO2B | GRCh38.p7 | 15:68718290 | TGGAGACACAGGAGG[A/C]TTAGGGATGACTGTT | 10391 |
rs9672308 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68686914 | caaaaaaaaaaaaag[A/G]aaataaaaaaaTGAA | 10391 |
rs9672329 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68686913 | tcaaaaaaaaaaaaa[A/G]aaaataaaaaaaTGA | 10391 |
rs9672377 | snp | A/G | 0.0252325 | 0.109451 | intron-variant | CORO2B | GRCh38.p7 | 15:68723665 | caccatcttggccag[A/G]ctgatcttgaactcc | 10391 |
rs9672449 | snp | C/T | 0.362313 | 0.223351 | intron-variant | CORO2B | GRCh38.p7 | 15:68723804 | AAAACATGCGAggtg[C/T]agtggcacccctcta | 10391 |
rs9806222 | snp | A/G | 0.48378 | 0.0885831 | intron-variant | CORO2B | GRCh38.p7 | 15:68591865 | ACGTGGTTATAGCAT[A/G]GCGAGAAGAGCACTG | 10391 |
rs9806329 | snp | A/G | 0.0376037 | 0.131863 | intron-variant | CORO2B | GRCh38.p7 | 15:68623888 | TCTCTGCAGCTGAGC[A/G]TGGGTCGCACAGACT | 10391 |
rs9806752 | snp | C/T | 0.0349115 | 0.127424 | intron-variant | CORO2B | GRCh38.p7 | 15:68648581 | tgtgaacccaggagg[C/T]ggagcttgcagtgag | 10391 |
rs9972579 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | CORO2B | GRCh38.p7 | 15:68670076 | aaaaaaaaGGGGGGG[A/G]aaaataaagaaaaat | 10391 |
rs9972587 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68670069 | ctcagaaaaaaaaaa[A/G]ggggggaaaaataaa | 10391 |
rs10083637 | snp | C/T | 0.304438 | 0.244001 | intron-variant | CORO2B | GRCh38.p7 | 15:68724621 | GTTTTTTTAGCATCA[C/T]CTTTATCAAGATTTT | 10391 |
rs10152807 | snp | C/T | 0.0387552 | 0.1337 | intron-variant | CORO2B | GRCh38.p7 | 15:68621404 | GGACCAGAGAGGCTT[C/T]GCAGCGCTGGAGACA | 10391 |
rs10152829 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | CORO2B | GRCh38.p7 | 15:68621466 | TTGGCAGGAGGAGAT[A/G]AGGAGGAGGCATTCC | 10391 |
rs10450990 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2B | GRCh38.p7 | 15:68669911 | aaaatacaaaaatta[A/G]ccaggcatgatggcg | 10391 |
rs10518781 | snp | A/G | 0.454182 | 0.144256 | intron-variant | CORO2B | GRCh38.p7 | 15:68705174 | TTGGAAGATTAACTA[A/G]TACTATCTAAATGTG | 10391 |
rs10525373 | in-del | -/ACACAC/ACACACACAC/ACACACACACACAC | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68633546 | CACACACACACACAC[lengthTooLong]TCACTCCTTGGGGAC | 10391 |
rs10543660 | in-del | -/CC | 0.480382 | 0.097079 | intron-variant | CORO2B | GRCh38.p7 | 15:68656178 | GCACCGTCCCCCCCG[-/CC]CCCCGACCCAACCAA | 10391 |
rs10548187 | in-del | -/GA | 0.140581 | 0.224783 | intron-variant | CORO2B | GRCh38.p7 | 15:68700804 | GGGCCAGCAGCCGCG[-/GA]GAGAGAGAGAGGTTT | 10391 |
rs10566834 | in-del | -/ACAC | | | intron-variant | CORO2B | GRCh38.p7 | 15:68704040 | TCTCTACACACACAT[-/ACAC]ACACACACACACACA | 10391 |
rs10579845 | in-del | -/A/AA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68673857 | AAAAAAAAAAAAAAA[-/A/AA]GGACAGTGTCCCGCT | 10391 |
rs10627263 | in-del | -/GGA | 0.0142736 | 0.0832652 | intron-variant | CORO2B | GRCh38.p7 | 15:68658300 | TCCCAATTGTTCAAT[-/GGA]GGAGGAGGAGGGCGA | 10391 |
rs10675118 | in-del | -/TTAT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68721759 | TATTTATTTATTTAT[-/TTAT]GTTTTAGAGACAGAG | 10391 |
rs10715792 | in-del | -/A | 0.467946 | 0.122472 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68640512 | AAGGCAATGCTATTT[-/A]AAAAAAAAAAAAAGG | 10391 |
rs10775197 | snp | C/G | 0.132409 | 0.220618 | intron-variant | CORO2B | GRCh38.p7 | 15:68575369 | TTTCCTCTGAGACTT[C/G]GTCTGTCACTCAGGC | 10391 |
rs10775198 | snp | A/G | 0.0325976 | 0.123435 | intron-variant | CORO2B | GRCh38.p7 | 15:68642805 | AGATCAGAGTGAGTC[A/G]GGCCTTAAAGGCTGA | 10391 |
rs10851788 | snp | C/T | 0.232651 | 0.249397 | intron-variant | CORO2B | GRCh38.p7 | 15:68688638 | GCAATGCTCATGCCA[C/T]TAAATATTCTTTGAA | 10391 |
rs10851789 | snp | A/G | 0.463451 | 0.130149 | intron-variant | CORO2B | GRCh38.p7 | 15:68705299 | AAAAATTAGCTGGGC[A/G]TGGTGGTGGGCGCCT | 10391 |
rs10851790 | snp | C/T | 0.159951 | 0.233219 | intron-variant | CORO2B | GRCh38.p7 | 15:68706208 | CTACCTGCTGGCGCC[C/T]GACCCCACACACACT | 10391 |
rs10851791 | snp | C/T | 0.362313 | 0.223351 | intron-variant | CORO2B | GRCh38.p7 | 15:68724058 | AATACAAAAATTAGC[C/T]GGGCGTGATGGCACA | 10391 |
rs11072034 | snp | A/T | 0.450985 | 0.148678 | intron-variant | CORO2B | GRCh38.p7 | 15:68567448 | tggagatgtagagct[A/T]gtggaagataagggt | 10391 |
rs11072035 | snp | C/T | 0.451608 | 0.147832 | intron-variant | CORO2B | GRCh38.p7 | 15:68571744 | CCTGGGAGATAAGCC[C/T]TGTTCTTGGGAACAG | 10391 |
rs11072036 | snp | C/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68575583 | TTGTGATCTGCCCCC[C/G]CCTCGGCCTCCCAAA | 10391 |
rs11072037 | snp | C/T | 0.455263 | 0.142713 | intron-variant | CORO2B | GRCh38.p7 | 15:68672274 | AGAATCTCACTCTGT[C/T]GCCCAGGCTGGGGTG | 10391 |
rs11072038 | snp | C/G | 0.459914 | 0.13578 | intron-variant | CORO2B | GRCh38.p7 | 15:68674821 | TGCTCTTTTCCCTCA[C/G]ACCTGCCTTCAGGAA | 10391 |
rs11072040 | snp | A/G | 0.133777 | 0.221342 | intron-variant | CORO2B | GRCh38.p7 | 15:68687764 | AACGGCCTTCCTGCT[A/G]TGACATCCCATGGCA | 10391 |
rs11072041 | snp | G/T | 0.197082 | 0.244335 | intron-variant | CORO2B | GRCh38.p7 | 15:68692826 | TTTAGTAGAGACGGG[G/T]TTTCTCCATGTTGTC | 10391 |
rs11072042 | snp | C/T | 0.439224 | 0.163383 | intron-variant | CORO2B | GRCh38.p7 | 15:68692865 | TCTCAGACTCCTGAC[C/T]TCAGGTGATCCACCC | 10391 |
rs11072043 | snp | A/C | 0.13446 | 0.221699 | intron-variant | CORO2B | GRCh38.p7 | 15:68694976 | AGCAGTGTGGCCCAG[A/C]CTGACTTGGCCCAGC | 10391 |
rs11072044 | snp | C/T | 0.239614 | 0.249784 | intron-variant | CORO2B | GRCh38.p7 | 15:68712812 | CGAAGTTGGGAGACT[C/T]GAATCTCACAGTTCC | 10391 |
rs11327515 | in-del | -/T | 0.480223 | 0.0974544 | intron-variant | CORO2B | GRCh38.p7 | 15:68656169 | CTCCCCCTCGCACCG[-/T]CCCCCCCGCCCCCCG | 10391 |
rs11332715 | in-del | -/A | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68576153 | AAAAAAAAAAAAAAA[-/A]GAAAGAAAGAAAGAA | 10391 |
rs11381045 | in-del | -/T/TT | 0 | 0 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68630432 | AAATGTTTTTTTTTT[-/T/TT]GTTCCTGGCAGGGGC | 10391 |
rs11389925 | in-del | -/A/AA | 0.14665 | 0.227637 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68577725 | AAAAAAAAAAAAAAA[-/A/AA]TTGCACAATGACCCA | 10391 |
rs11404600 | in-del | -/A | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68629812 | GGAGCTTGGGCTCTT[-/A]AACCAGCATGTGTGT | 10391 |
rs11410636 | in-del | -/A | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68673360 | GGCAACCCTGTCTCT[-/A]CAAATGAAAAAAATA | 10391 |
rs11428872 | in-del | -/C | 0.276534 | 0.248588 | intron-variant | CORO2B | GRCh38.p7 | 15:68610720 | TTGCAGAGTAGGGTA[-/C]CTCTGAGGCCCAGTC | 10391 |
rs11451826 | in-del | -/G | 0.3748 | 0.216622 | intron-variant | CORO2B | GRCh38.p7 | 15:68588856 | TATTTAACTCCTGAA[-/G]AAATTGCTGGTTATG | 10391 |
rs11462221 | in-del | -/C | 0.199873 | 0.244923 | intron-variant | CORO2B | GRCh38.p7 | 15:68709887 | GGGATGTTCCCCCCA[-/C]CCTACCACCTACCTT | 10391 |
rs11630000 | snp | A/T | 0.424659 | 0.17887 | intron-variant | CORO2B | GRCh38.p7 | 15:68662026 | aataaataaataaat[A/T]aattaattaattaat | 10391 |
rs11631477 | snp | C/T | 0.353154 | 0.227726 | intron-variant | CORO2B | GRCh38.p7 | 15:68575236 | GAGGGTGGATAAACA[C/T]CCGCTAGGCTGACAG | 10391 |
rs11631765 | snp | A/C | 0.44252 | 0.159487 | intron-variant | CORO2B | GRCh38.p7 | 15:68650453 | CCCGTCTCCACTAAA[A/C]ATACAAAACTTGGCT | 10391 |
rs11633575 | snp | A/T | 0.406641 | 0.194842 | intron-variant | CORO2B | GRCh38.p7 | 15:68706657 | GCTTTAGAGCTTCCT[A/T]CTCAAGTGCAGACAA | 10391 |
rs11633874 | snp | C/T | 0.473726 | 0.111565 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68639820 | TCAAAACCAATATGT[C/T]CCAGTCTTGCGCCTT | 10391 |
rs11634166 | snp | C/T | 0.420096 | 0.183214 | intron-variant | CORO2B | GRCh38.p7 | 15:68687520 | GTGGACTCACCATGC[C/T]GCCAGCCTTTCCAAG | 10391 |
rs11634366 | snp | G/T | 0.00398564 | 0.0444627 | intron-variant | CORO2B | GRCh38.p7 | 15:68634863 | aagggtggggcctgg[G/T]attctccatttctaa | 10391 |
rs11634526 | snp | G/T | 0.00947846 | 0.0681864 | intron-variant | CORO2B | GRCh38.p7 | 15:68594426 | CTCCAGCTCTCACCA[G/T]GTTCCCCAGCCCAGG | 10391 |
rs11634534 | snp | C/T | 0.434253 | 0.168969 | intron-variant | CORO2B | GRCh38.p7 | 15:68658313 | AATGGAGGAGGAGGG[C/T]GAGATGCATGGTGCT | 10391 |
rs11634913 | snp | A/G | 0.499879 | 0.0077866 | intron-variant | CORO2B | GRCh38.p7 | 15:68595334 | ATTTCCTCCCAGGAA[A/G]GGGGACATGGATGTC | 10391 |
rs11635636 | snp | A/T | 0.424503 | 0.179021 | intron-variant | CORO2B | GRCh38.p7 | 15:68679617 | ATTTATTGGCTCATG[A/T]GGAAACTGAAGCCCT | 10391 |
rs11636025 | snp | C/T | 0.416382 | 0.186593 | intron-variant | CORO2B | GRCh38.p7 | 15:68683655 | TATCCCTACCCATCA[C/T]ATTTAAGGCCTCGAA | 10391 |
rs11636364 | snp | A/G | 0.00952359 | 0.0683454 | intron-variant | CORO2B | GRCh38.p7 | 15:68559099 | TACCTAGAAATGCGC[A/G]AAGTGTGGCTGGGCG | 10391 |
rs11636563 | snp | G/T | 0.223819 | 0.248625 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68641443 | TGGGGATTTGGGGGA[G/T]AGAGGAAAGAAGGGC | 10391 |
rs11636615 | snp | G/T | 0.13446 | 0.221699 | intron-variant | CORO2B | GRCh38.p7 | 15:68692840 | GTTTTCTCCATGTTG[G/T]CTAGACTGGTCTCAG | 10391 |
rs11636646 | snp | C/T | 0.439224 | 0.163383 | intron-variant | CORO2B | GRCh38.p7 | 15:68692842 | TTTCTCCATGTTGTC[C/T]AGACTGGTCTCAGAC | 10391 |
rs11637058 | snp | G/T | 0.466721 | 0.124627 | intron-variant | CORO2B | GRCh38.p7 | 15:68696891 | AAGCATCTACCTGGT[G/T]CTCACTGGCAGAGCC | 10391 |
rs11637064 | snp | A/G | 0.0707826 | 0.174302 | intron-variant | CORO2B | GRCh38.p7 | 15:68666834 | ATGATAAAAATACAC[A/G]GTTTTGTAGTCAGGC | 10391 |
rs11638462 | snp | A/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68602745 | CTCTACATCAGTGAA[A/G]GAGGTTCTGTGCAAT | 10391 |
rs11639023 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CORO2B | GRCh38.p7 | 15:68591012 | gtgccaggccctaag[C/T]ggcattgagggtgca | 10391 |
rs11852724 | snp | C/G | 0.274661 | 0.248781 | intron-variant | CORO2B | GRCh38.p7 | 15:68692242 | AGAGTTAAAGATAAC[C/G]TGCGTAACCCTAATA | 10391 |
rs11855372 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | CORO2B | GRCh38.p7 | 15:68599565 | ACAAGGGCCTGAGAC[A/G]GATATAGGGAGCTTA | 10391 |
rs11855716 | snp | A/C | 0.0611083 | 0.163768 | intron-variant | CORO2B | GRCh38.p7 | 15:68712826 | tcgaatctcacagtt[A/C]caggaggagctagga | 10391 |
rs11855718 | snp | C/T | 0.0611083 | 0.163768 | intron-variant | CORO2B | GRCh38.p7 | 15:68712827 | cgaatctcacagttc[C/T]aggaggagctaggat | 10391 |
rs11856323 | snp | C/T | 0.114036 | 0.209795 | intron-variant | CORO2B | GRCh38.p7 | 15:68600650 | TATGACCATGGGTGC[C/T]GACCAGTGGGCAGAC | 10391 |
rs11856409 | snp | C/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68570888 | actcaatcctccagc[C/T]tcagccgcccacagt | 10391 |
rs11856414 | snp | A/C | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68570905 | cagccgcccacagtg[A/C]tgggattacaggcat | 10391 |
rs11856582 | snp | G/T | 0.338296 | 0.233889 | intron-variant | CORO2B | GRCh38.p7 | 15:68689257 | GGCAGCAAGGTCTCT[G/T]CCCCAGCTCTGTTGA | 10391 |
rs11856689 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CORO2B | GRCh38.p7 | 15:68644617 | AGAGATTTCTGAGGG[C/T]GTACCTGTGGATTAG | 10391 |
rs11856908 | snp | A/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68671343 | AGTTTGAGACCCAGG[A/T]AAATTGGCTCAACAT | 10391 |
rs11857162 | snp | A/C | 0.466515 | 0.124985 | intron-variant | CORO2B | GRCh38.p7 | 15:68696409 | TAAAAATTAGCCAGG[A/C]GTGGTGGCGCACCCC | 10391 |
rs11857243 | snp | A/G | 0.338296 | 0.233889 | intron-variant | CORO2B | GRCh38.p7 | 15:68689519 | TGTGTTTATATTAAT[A/G]TGCTATTATATTATC | 10391 |
rs11857348 | snp | G/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68601757 | TGCAGCTGGGGCTTA[G/T]TGGTGCTGGGGCAGG | 10391 |
rs12050853 | snp | C/T | 0.421842 | 0.181577 | intron-variant | CORO2B | GRCh38.p7 | 15:68703274 | TCCTGCCTCAGCTTC[C/T]CGAGTAGCTGGGATT | 10391 |
rs12102185 | snp | A/G | 0.0287284 | 0.116357 | intron-variant | CORO2B | GRCh38.p7 | 15:68573171 | TCAGAGGTGAAAGAC[A/G]ACACCCCAGGGCAGG | 10391 |
rs12102248 | snp | A/C | 0.380724 | 0.213099 | intron-variant | CORO2B | GRCh38.p7 | 15:68656289 | CGTGTCAAGAGACAG[A/C]TCTGTGACATCAGCA | 10391 |
rs12148095 | snp | A/G | 0.388775 | 0.207946 | intron-variant | CORO2B | GRCh38.p7 | 15:68719806 | GTTATGCATCTCCTC[A/G]TGAACTCATTTCAGA | 10391 |
rs12437455 | snp | A/G | 0.405082 | 0.196086 | intron-variant | CORO2B | GRCh38.p7 | 15:68586238 | TGTGAAGCACTTACC[A/G]TATGCCTGACATGTA | 10391 |
rs12438042 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CORO2B | GRCh38.p7 | 15:68627076 | ctgcctctgtttcta[C/T]gcctgcaaaatgggc | 10391 |
rs12438764 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68583585 | AGATGGAAGAAGCAT[C/T]GCGGGAGTGGGAGGA | 10391 |
rs12439204 | snp | C/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68646169 | AAGATTTTCCCCTTT[C/G]TGCAGCTGCTTACGT | 10391 |
rs12439338 | snp | C/G | 0.453818 | 0.144769 | intron-variant | CORO2B | GRCh38.p7 | 15:68575686 | TCCTTCTCAACCGCA[C/G]TACtccccacctcca | 10391 |
rs12440345 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68686036 | TTTTttttttttttt[C/T]tcttttttttttttt | 10391 |
rs12440542 | snp | A/G | 0.466291 | 0.202928 | intron-variant | CORO2B | GRCh38.p7 | 15:68682521 | AGAGATCACATGGCC[A/G]CAGATTGACATTCTC | 10391 |
rs12442523 | snp | C/T | 0.444533 | 0.157025 | intron-variant | CORO2B | GRCh38.p7 | 15:68702465 | GGGTTTGGTGGGATT[C/T]GTTTCCCATATTGGC | 10391 |
rs12443134 | snp | A/G | 0.214541 | 0.247473 | intron-variant | CORO2B | GRCh38.p7 | 15:68715912 | GCATATGATTCAGCA[A/G]TTCTATATTTCGGGT | 10391 |
rs12592448 | snp | C/T | 0.468047 | 0.122292 | intron-variant | CORO2B | GRCh38.p7 | 15:68659543 | cacagtaagagcccc[C/T]ctctaaaaaaatttt | 10391 |
rs12592467 | snp | G/T | 0.309154 | 0.242901 | intron-variant | CORO2B | GRCh38.p7 | 15:68717461 | AGACGGGGAGAACAG[G/T]GTGAATCCAGATGTT | 10391 |
rs12594723 | snp | A/G | 0.331411 | 0.236373 | intron-variant | CORO2B | GRCh38.p7 | 15:68717374 | TGGGAGGGGCAGGAG[A/G]AAGACAGGGAAACCA | 10391 |
rs12594757 | snp | A/G | 0.33819 | 0.249966 | intron-variant | CORO2B | GRCh38.p7 | 15:68717548 | AAAGAAGCAGGAAGG[A/G]CTCAGAATGACTCAC | 10391 |
rs12595136 | snp | C/G | 0.443732 | 0.158012 | intron-variant | CORO2B | GRCh38.p7 | 15:68584813 | GCACCCTGCAGCCTG[C/G]GGAGCTTGGGGCAGC | 10391 |
rs12898306 | snp | A/C | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68704043 | CTACACACACATACA[A/C]ACACACACACACACA | 10391 |
rs12898318 | snp | G/T | 0.263809 | 0.249618 | intron-variant | CORO2B | GRCh38.p7 | 15:68722586 | CACTAAAGCGGTTTT[G/T]TTGACAAAAGTGGAC | 10391 |
rs12898784 | snp | C/T | 0.44333 | 0.158505 | intron-variant | CORO2B | GRCh38.p7 | 15:68627805 | AGACCCTCAGGCTTA[C/T]GGGTACAGCCCCCTT | 10391 |
rs12898796 | snp | C/T | 0.202035 | 0.245356 | intron-variant | CORO2B | GRCh38.p7 | 15:68722863 | GCCTGAGGTTAAGAG[C/T]TCAAGACCAGCCTGA | 10391 |
rs12899032 | snp | G/T | 0.441568 | 0.160629 | intron-variant | CORO2B | GRCh38.p7 | 15:68585908 | GGGCAGAACAAAGTA[G/T]GACAGAGGCAGAGCC | 10391 |
rs12900292 | snp | C/G | 0.272511 | 0.248984 | intron-variant | CORO2B | GRCh38.p7 | 15:68612506 | CTGAGGTCTGGGGTA[C/G]AGCAGGAAAACTGAG | 10391 |
rs12900350 | snp | C/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68612685 | TGATGATAACTTGCT[C/G]TCTAACTGACCATGA | 10391 |
rs12901345 | snp | C/T | 0.499515 | 0.0155675 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68641021 | GGGTTGTGGAGCCAT[C/T]GATCAACAGCAGCCC | 10391 |
rs12901895 | snp | C/T | 0.206336 | 0.246157 | intron-variant | CORO2B | GRCh38.p7 | 15:68679879 | CCAGGGTCATTACCT[C/T]GGAGGTGGTGCATCT | 10391 |
rs12902396 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | CORO2B | GRCh38.p7 | 15:68562077 | GGGACTGAGGAGAAA[A/G]GCCTTAATGATGTTG | 10391 |
rs12903191 | snp | C/G | 0.330249 | 0.23677 | intron-variant | CORO2B | GRCh38.p7 | 15:68586717 | GCCTCTTTCCTTCCC[C/G]CTGCCTGCTGCTTGG | 10391 |
rs12904642 | snp | C/T | 0.225597 | 0.248806 | intron-variant | CORO2B | GRCh38.p7 | 15:68623747 | CTGGGTGAGGATTAC[C/T]GCATGCTGGATCACG | 10391 |
rs12904790 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68587049 | ATAGGGAGATATGTA[C/T]ACACACACACACACA | 10391 |
rs12904875 | snp | C/T | 0.241914 | 0.249869 | intron-variant | CORO2B | GRCh38.p7 | 15:68609968 | GGGACCCTGTAATTG[C/T]GCAACCAGCCTCTCC | 10391 |
rs12904959 | snp | A/T | 0.292008 | 0.246445 | intron-variant | CORO2B | GRCh38.p7 | 15:68597637 | CCCATCAAAAAAAAA[A/T]AAATAAATAAATAAA | 10391 |
rs12906690 | snp | C/G | 0.203267 | 0.245593 | intron-variant | CORO2B | GRCh38.p7 | 15:68702050 | cagcttgagaccagc[C/G]tggccaacatgataa | 10391 |
rs12907028 | snp | C/G | 0.444267 | 0.157354 | intron-variant | CORO2B | GRCh38.p7 | 15:68702251 | CAAGTTTTCTCACCT[C/G]TGTGGGCCTCATTTC | 10391 |
rs12907941 | snp | A/T | 0.437118 | 0.165792 | intron-variant | CORO2B | GRCh38.p7 | 15:68650356 | gagcgaaactctgtc[A/T]aaaaaaaaaaaaaaa | 10391 |
rs12908134 | snp | A/G | 0.467642 | 0.123012 | intron-variant | CORO2B | GRCh38.p7 | 15:68651248 | CCTGCCGCCCAAGCC[A/G]TGGCCGTCCCTCTAC | 10391 |
rs12908848 | snp | A/G | 0.464629 | 0.128197 | intron-variant | CORO2B | GRCh38.p7 | 15:68629826 | TTAACCAGCATGTGT[A/G]TGTGTGTGTGTGTCT | 10391 |
rs12909046 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | CORO2B | GRCh38.p7 | 15:68572156 | TCTCCAAATTGAGGA[A/G]CAGCTCTTCCAGGAG | 10391 |
rs12909503 | snp | C/T | 0.206029 | 0.246103 | intron-variant | CORO2B | GRCh38.p7 | 15:68697082 | AATGCTTAGTAGGTG[C/T]TGGATGGGATCGATG | 10391 |
rs12909736 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68714929 | AGTCAGTGATGAATG[A/T]TGGAATTTGAGATAC | 10391 |
rs12909854 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68714904 | GAATAAAGATCAGAG[C/T]CTGCAGTGTAGTCAG | 10391 |
rs12910003 | snp | A/C | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68714948 | AATTTGAGATACCCG[A/C]CAGGAGATCCTTGGT | 10391 |
rs12910005 | snp | C/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68714949 | ATTTGAGATACCCGC[C/G]AGGAGATCCTTGGTG | 10391 |
rs12910529 | snp | A/G | 0.331411 | 0.236373 | intron-variant | CORO2B | GRCh38.p7 | 15:68693689 | GACTCACCCCCTCCC[A/G]GGAAGTCATGGACTG | 10391 |
rs12910749 | snp | A/C | 0.309154 | 0.242901 | intron-variant | CORO2B | GRCh38.p7 | 15:68605956 | gtctcaaactcctga[A/C]cttgtgattcgccca | 10391 |
rs12910996 | snp | C/T | 0.282632 | 0.247861 | intron-variant | CORO2B | GRCh38.p7 | 15:68693893 | CAGTCTGGAGTGCAG[C/T]GGCACAATCTTGGCT | 10391 |
rs12911005 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68605909 | tttgtatttttagta[A/G]agacgggggtttcac | 10391 |
rs12911106 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68714923 | CAGTGTAGTCAGTGA[A/T]GAATGATGGAATTTG | 10391 |
rs12911382 | snp | A/G | 0.201727 | 0.245295 | intron-variant | CORO2B | GRCh38.p7 | 15:68721577 | caggcgtggtggtgc[A/G]cgcctgtaatcccag | 10391 |
rs12911591 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68575586 | tgatctgcccccgcc[C/T]cggcctcccaaagtg | 10391 |
rs12911725 | snp | A/G | 0.204189 | 0.245767 | intron-variant | CORO2B | GRCh38.p7 | 15:68642342 | CCCCTTGTACCCCAG[A/G]GAGAGCCTGCGGTGA | 10391 |
rs12912092 | snp | C/T | 0.0482946 | 0.147699 | intron-variant | CORO2B | GRCh38.p7 | 15:68560202 | GCTAACTGTGCTCCC[C/T]ACAGCTGGTCTGCAA | 10391 |
rs12914115 | snp | A/G | 0.372592 | 0.217879 | intron-variant | CORO2B | GRCh38.p7 | 15:68725660 | AAGTAAGAGCCATGG[A/G]CTGAGCTAGAGATGG | 10391 |
rs12915435 | snp | C/G | 0.191461 | 0.24305 | intron-variant | CORO2B | GRCh38.p7 | 15:68715888 | CTTCCTTTCAACTAA[C/G]CTGGTAATGCATATG | 10391 |
rs12915441 | snp | C/G | 0.441977 | 0.16014 | intron-variant | CORO2B | GRCh38.p7 | 15:68606430 | ATCTAGGACTGCACT[C/G]ATGGTCCCTGTGTTC | 10391 |
rs12915581 | snp | C/T | 0.192088 | 0.2432 | intron-variant | CORO2B | GRCh38.p7 | 15:68715976 | ACCTCCCGTTCCCAC[C/T]TCTGCGGGTGATCCT | 10391 |
rs12915858 | snp | C/G | 0.231189 | 0.249291 | intron-variant | CORO2B | GRCh38.p7 | 15:68625852 | TCAAGCAATCTGCCC[C/G]CCTTGGCCTCCCAAA | 10391 |
rs12915890 | snp | C/T | 0.23031 | 0.249223 | intron-variant | CORO2B | GRCh38.p7 | 15:68686098 | GCTGGAGTGCAATGG[C/T]GCAACCTTGGCTCAT | 10391 |
rs12916371 | snp | C/G | 0.0704125 | 0.17392 | intron-variant | CORO2B | GRCh38.p7 | 15:68656103 | TCCTTAGGGCAGTTT[C/G]CACTTCCAGATGGCC | 10391 |
rs12917124 | snp | A/T | | | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68578618 | GCCTCCAGGGGGCGA[A/T]CCCGACCGCCTTCTT | 10391 |
rs12917315 | snp | G/T | 0.0547245 | 0.156101 | intron-variant | CORO2B | GRCh38.p7 | 15:68569531 | cagtttatttatctg[G/T]tcacctactgaagga | 10391 |
rs12917469 | snp | A/G | 0.203267 | 0.245593 | intron-variant | CORO2B | GRCh38.p7 | 15:68704010 | ACCAACCTGGGCAAT[A/G]TGGCAAAAACCCTTT | 10391 |
rs16952259 | snp | C/T | 0.104504 | 0.2033 | intron-variant | CORO2B | GRCh38.p7 | 15:68570483 | ATCGAAGGAAACTTC[C/T]GGGTGGTGACTCATA | 10391 |
rs16952287 | snp | C/T | 0.487049 | 0.0794222 | intron-variant | CORO2B | GRCh38.p7 | 15:68596437 | GGGATCTAGGGGGAT[C/T]TTTCTGGCTGAGAGA | 10391 |
rs16952288 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | CORO2B | GRCh38.p7 | 15:68599051 | ACTTGGCTGGGCATT[C/G]AAAGCCTTCACTCTC | 10391 |
rs16952292 | snp | A/G | 0.342806 | 0.232136 | intron-variant | CORO2B | GRCh38.p7 | 15:68601655 | GCCAAGAGAACAGCT[A/G]GGAAGCGTGGCTGAG | 10391 |
rs16952295 | snp | G/T | 0.127254 | 0.217792 | intron-variant | CORO2B | GRCh38.p7 | 15:68602384 | TGATTGAGATATTTG[G/T]TCCTGCCCAAATTAG | 10391 |
rs16952299 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | CORO2B | GRCh38.p7 | 15:68602584 | AAACAGGATCCAGCT[A/G]TAACCTCCACGGTTC | 10391 |
rs16952336 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | CORO2B | GRCh38.p7 | 15:68643704 | AACTTCTTCCTTCAA[C/T]AAAGAGGAGTTTGTG | 10391 |
rs16952350 | snp | C/T | 0.180064 | 0.240019 | intron-variant | CORO2B | GRCh38.p7 | 15:68663836 | GTTTCAATTAGCATT[C/T]TTATTAAGACAGAAG | 10391 |
rs16952352 | snp | A/G | 0.16846 | 0.236329 | intron-variant | CORO2B | GRCh38.p7 | 15:68667920 | TGAGTTATTACTCCC[A/G]AAAGCCTTGGATTTC | 10391 |
rs16952370 | snp | A/C | 0.0383715 | 0.133092 | intron-variant | CORO2B | GRCh38.p7 | 15:68681928 | GGCTTCATAGATTTA[A/C]AGGGCTAGAGCTGGG | 10391 |
rs16952371 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | CORO2B | GRCh38.p7 | 15:68681960 | CAGTGGAGAGCCAGA[C/T]TTGGAACCAGATCAG | 10391 |
rs16952378 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | CORO2B | GRCh38.p7 | 15:68683956 | CTCTGATGCCTGGAT[A/G]AGGAGTTTGGCTTAT | 10391 |
rs16952380 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | CORO2B | GRCh38.p7 | 15:68685958 | AATCTAAGGGGCTTC[A/G]CAACTGAGCTGCCGC | 10391 |
rs16952387 | snp | C/G | 0.274929 | 0.248754 | intron-variant | CORO2B | GRCh38.p7 | 15:68691786 | TTCTGAATAGGTTCC[C/G]GTGATGTTGCCTAAC | 10391 |
rs16952389 | snp | A/G | 0.0410537 | 0.137264 | intron-variant | CORO2B | GRCh38.p7 | 15:68694524 | GCACTGTGTACCGGT[A/G]TTCAAGATGTACACT | 10391 |
rs16952397 | snp | C/G | 0.139903 | 0.224452 | intron-variant | CORO2B | GRCh38.p7 | 15:68695730 | ACTTAGCTGAGAGAA[C/G]TGTCCTGATTTTTCC | 10391 |
rs16952398 | snp | G/T | 0.0872718 | 0.189788 | intron-variant | CORO2B | GRCh38.p7 | 15:68699028 | TGGAGAAGCAGGACA[G/T]TGACAGACAGAAAAA | 10391 |
rs16952435 | snp | A/G | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68703880 | TATTGACTACACAGC[A/G]GGCAACAAAGTGCAC | 10391 |
rs16952446 | snp | C/T | 0.0501905 | 0.150254 | intron-variant | CORO2B | GRCh38.p7 | 15:68705135 | CTTCTCCCAGTAATG[C/T]ATTCAATGTCAAAGC | 10391 |
rs16952458 | snp | C/T | 0.0532157 | 0.154195 | intron-variant | CORO2B | GRCh38.p7 | 15:68706529 | AAAGATCTTTCTTGA[C/T]GGCCAGGGGCAACTA | 10391 |
rs16952475 | snp | C/T | 0.255782 | 0.249933 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68726578 | ATTCAGAGGATTGCT[C/T]TCCAAGGCCATAATG | 10391 |
rs17271969 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2B | GRCh38.p7 | 15:68634013 | GTCAGGGCATGTCAC[A/G]GGCAGGGAGCCTCGG | 10391 |
rs17278757 | snp | C/T | 0.208779 | 0.246578 | intron-variant | CORO2B | GRCh38.p7 | 15:68667919 | ATGAGTTATTACTCC[C/T]GAAAGCCTTGGATTT | 10391 |
rs17278924 | snp | C/G | 0.471483 | 0.115954 | intron-variant | CORO2B | GRCh38.p7 | 15:68684923 | TTTAATATCAACTTC[C/G]AGTCATAGAAGAGAG | 10391 |
rs17279331 | snp | C/G | 0.204189 | 0.245767 | intron-variant | CORO2B | GRCh38.p7 | 15:68700214 | AGGCTTGGGAGGTCA[C/G]TCGGCAAAGCTGCTG | 10391 |
rs17279860 | snp | A/T | 0.428182 | 0.17536 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68726620 | TCCCCATGATTCTCT[A/T]CAAAGCTCTTGCACA | 10391 |
rs17343452 | snp | G/T | 0.482979 | 0.0906686 | intron-variant | CORO2B | GRCh38.p7 | 15:68590388 | CCTGCACTTCTGTTC[G/T]CTCAGGTACCCCCAT | 10391 |
rs17852399 | snp | C/T | 0.0333694 | 0.124785 | synonymous-codon | CORO2B | GRCh38.p7 | 15:68714570 | TCAGGAGGACCTCTC[C/T]ATGCCCCTGATCGAA | 10391 |
rs17852400 | snp | C/G | 0 | 0 | missense | CORO2B | GRCh38.p7 | 15:68713988 | AACATGAAGCGGCTC[C/G]TCACGACAGGGGTCT | 10391 |
rs28378879 | snp | A/G | 0.0700422 | 0.173537 | intron-variant | CORO2B | GRCh38.p7 | 15:68645921 | TGGGATTGCAGGCAC[A/G]TGCCACCACGCCCAG | 10391 |
rs28396259 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68635993 | TGAGGAGCAGACAAG[A/T]AAAGGAGAGACCTCG | 10391 |
rs28401364 | snp | C/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68627037 | TGCCAAGTGGGGATC[C/T]TTAGCAAGGTACTTA | 10391 |
rs28405100 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68574270 | AGCCTGATGAGCTGA[C/G]GGGGCCAGCATGTGG | 10391 |
rs28415000 | snp | C/T | 0.197703 | 0.244469 | intron-variant | CORO2B | GRCh38.p7 | 15:68565809 | GAAATAATACCTGCT[C/T]GGGCTTTGCTGGAGC | 10391 |
rs28422483 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68560276 | TTTTCGTTCTTTTTT[C/T]TCTTTTTCTTTCTTT | 10391 |
rs28433558 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68669145 | AAAGAAAGGAAAGAA[C/G]AAAGAAAAAGAAAAG | 10391 |
rs28442184 | snp | C/T | 0.0700422 | 0.173537 | intron-variant | CORO2B | GRCh38.p7 | 15:68610928 | ACCTTCCATTCCACA[C/T]CCTCGACGCAGCCAA | 10391 |
rs28447184 | snp | C/T | 0.0715223 | 0.175059 | intron-variant | CORO2B | GRCh38.p7 | 15:68608059 | ACAGCTTTGCAGAGG[C/T]GTATGTCCTTTGACA | 10391 |
rs28455864 | snp | C/T | 0.029116 | 0.117091 | intron-variant | CORO2B | GRCh38.p7 | 15:68646776 | TCCTAGTGAACCACA[C/T]AACATGTTAAGGATG | 10391 |
rs28460647 | snp | A/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68681227 | CATCTCAAAAAAAAA[A/T]TTTTTTTTGGAAAGA | 10391 |
rs28464711 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68664638 | AGGGACAGAGCGAGA[C/G]TCTGTCTCAAAAAAA | 10391 |
rs28475385 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68641944 | GTTGCTCAGGCTAGT[A/G]TCTCCAATGCCTGGG | 10391 |
rs28477950 | snp | A/G | 0.134119 | 0.221521 | intron-variant | CORO2B | GRCh38.p7 | 15:68627519 | TTGGACTCTCTTGGG[A/G]TTGGGGAGGTGGAGG | 10391 |
rs28482210 | snp | A/G | 0.0356815 | 0.128715 | intron-variant | CORO2B | GRCh38.p7 | 15:68722442 | GACGCATTGATCTAA[A/G]TGTGAGGAAACAACT | 10391 |
rs28497933 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68581445 | GCCCGCTGGTAGTAG[C/T]TCTTCCAGTACCATA | 10391 |
rs28520615 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68628088 | GGAAGGGCCAGCATA[A/T]TTTGGGTGGGGCTTT | 10391 |
rs28526517 | snp | C/G | 0.0486741 | 0.148216 | intron-variant | CORO2B | GRCh38.p7 | 15:68646292 | CGCGCTTCAGGGAAA[C/G]TGCTTGCTGTCAGTC | 10391 |
rs28528339 | snp | A/G | 0.0995161 | 0.199636 | intron-variant | CORO2B | GRCh38.p7 | 15:68605378 | GCGGGGAAAAACTCT[A/G]TGCATCAAGATGCTC | 10391 |
rs28528746 | snp | C/T | 0.322959 | 0.239117 | intron-variant | CORO2B | GRCh38.p7 | 15:68624793 | CATCTCCTGATTCTC[C/T]TGCCTCAGCCTCCTG | 10391 |
rs28529097 | snp | A/G | 0.164219 | 0.234823 | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68614549 | GAAACTATTTTAAAG[A/G]AAAGACATGGGGACT | 10391 |
rs28529235 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | CORO2B | GRCh38.p7 | 15:68646769 | GTGAAGCTCCTAGTG[A/G]ACCACACAACATGTT | 10391 |
rs28550735 | snp | C/T | 0.0707826 | 0.174302 | intron-variant | CORO2B | GRCh38.p7 | 15:68623542 | GAGGTCAGCCTCTCC[C/T]GCCCTGCATGTAAAC | 10391 |
rs28557361 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68560258 | TTTCTCTTTCTTTTT[C/T]CTTTTTCGTTCTTTT | 10391 |
rs28574803 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68635992 | TTGAGGAGCAGACAA[A/G]TAAAGGAGAGACCTC | 10391 |
rs28578838 | snp | C/T | 0.0681886 | 0.171594 | intron-variant | CORO2B | GRCh38.p7 | 15:68622145 | GAGAATTAAATGAGA[C/T]GAAGTTGGAGAAGGA | 10391 |
rs28591182 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68560305 | TTCTTTATTTTTTTT[C/T]TTCTTCTGAGACAGG | 10391 |
rs28592947 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | CORO2B | GRCh38.p7 | 15:68585923 | TGACAGAGGCAGAGC[C/T]GCCTTCTCCATTTCC | 10391 |
rs28605084 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68633547 | CACACACACACACAC[A/T]CACTCCTTGGGGACA | 10391 |
rs28609769 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | CORO2B | GRCh38.p7 | 15:68681228 | ATCTCAAAAAAAAAT[A/T]TTTTTTTGGAAAGAA | 10391 |
rs28610166 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | CORO2B | GRCh38.p7 | 15:68608655 | TCTGCTTCCCAGTTC[C/T]TCCTCTCCTAGGGAG | 10391 |
rs28610253 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68708357 | CTTTCTTTTTTTCTT[C/T]TTTTTTTTTTTTTTT | 10391 |
rs28612127 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68708354 | TGGCTTTCTTTTTTT[C/T]TTCTTTTTTTTTTTT | 10391 |
rs28629448 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68704041 | CTCTACACACACATA[C/T]ACACACACACACACA | 10391 |
rs28634070 | snp | A/G | 0.0482946 | 0.147699 | intron-variant | CORO2B | GRCh38.p7 | 15:68561507 | AGGTAGAGGGTCCCC[A/G]GTTGTCAAGGAAACC | 10391 |
rs28635113 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2B | GRCh38.p7 | 15:68598734 | CTCTTTGCTGGGCAC[C/G]AAGGAGCTGATCTGC | 10391 |
rs28636582 | snp | A/G | 0.499035 | 0.0219437 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68578703 | CAGCGGGACACCCGA[A/G]AGCCCGGGGCGCCGC | 10391 |
rs28650434 | snp | A/T | 0.183886 | 0.241099 | intron-variant | CORO2B | GRCh38.p7 | 15:68647139 | ATAAGAAAAGCTACA[A/T]GTGTATTAGAGGAAA | 10391 |
rs28657769 | snp | A/C/G | 0.0295365 | 0.118087 | intron-variant | CORO2B | GRCh38.p7 | 15:68573969 | CAGCTAGGTGCTGAC[A/C/G]GGGAGAGAAGGGCCA | 10391 |
rs28664133 | snp | A/C | 0.0603597 | 0.1629 | intron-variant | CORO2B | GRCh38.p7 | 15:68628879 | GATGCCCTCAGTTTC[A/C]CATGTGATGTGGAAG | 10391 |
rs28675071 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68565324 | TTTTATTTAAAAAAA[A/T]TTTTATTGGCATGCA | 10391 |
rs28675117 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68574063 | AACCTGAGGACACCA[C/G]GGAGCCCCTGATGGG | 10391 |
rs28708978 | snp | A/G | 0.0670745 | 0.170406 | intron-variant | CORO2B | GRCh38.p7 | 15:68622469 | AGTGTCATTCAGTTC[A/G]ACCTGAACCTGCTAT | 10391 |
rs28712461 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68668865 | GGGTAGATCACCTGA[G/T]GTCAGGAGTTCGAGA | 10391 |
rs28727290 | snp | A/G | 0.242201 | 0.249878 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68631201 | GGTGCTTGACTCCCC[A/G]TGTCCCCCAAAGGCC | 10391 |
rs28730429 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68704039 | TTCTCTACACACACA[C/T]ACACACACACACACA | 10391 |
rs28734056 | snp | A/T | 0.0486741 | 0.148216 | intron-variant | CORO2B | GRCh38.p7 | 15:68605939 | CCATGTTGGTCAGGC[A/T]GGTCTCAAACTCCTG | 10391 |
rs28820283 | snp | A/G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68647857 | CCTGTTTCTACAAAT[A/G/T]AAAAAAAAAAAAAAG | 10391 |
rs33913544 | snp | C/T | 0.294063 | 0.246086 | synonymous-codon | CORO2B | GRCh38.p7 | 15:68718780 | TCTCAAGGGCCTGAT[C/T]GAGCCCATCTCCATG | 10391 |
rs33965107 | in-del | -/T/TT/TTT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68642035 | ACCCGGCCTAGCCTC[-/T/TT/TTT]TTTTTTTTTTTTTTT | 10391 |
rs34017433 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68675971 | ATAGAACAGAAATGG[-/C]AATAGAATATAGAAT | 10391 |
rs34035264 | in-del | -/A | | | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68631349 | GAGAACTCGAGCTCC[-/A]AAAAGTTTATGAACT | 10391 |
rs34041669 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68664991 | TATTTGTTTACATTT[-/C]CAAGTATTTAAGTTT | 10391 |
rs34054994 | snp | A/G | 0.240478 | 0.249819 | intron-variant | CORO2B | GRCh38.p7 | 15:68665899 | TCCTCTTCATTTATA[A/G]CTTTTATACCTCTGG | 10391 |
rs34058839 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68598160 | AGAGAATCGGATCCC[A/G]GAGGCTGAAGCTCAG | 10391 |
rs34065281 | snp | A/G | 0.20511 | 0.245937 | intron-variant | CORO2B | GRCh38.p7 | 15:68697733 | GCTGCAGAAGGAAGG[A/G]CACAGGTGCTGGAGC | 10391 |
rs34122295 | snp | A/G | 0.0414363 | 0.137845 | intron-variant | CORO2B | GRCh38.p7 | 15:68563442 | TGGTGAGCCTTGATC[A/G]TGCCACTGCACTCTA | 10391 |
rs34161654 | snp | C/G | 0.199873 | 0.244923 | intron-variant | CORO2B | GRCh38.p7 | 15:68707824 | GCCAGCTTGTTCCCC[C/G]TGCACCCTCTCAGTC | 10391 |
rs34202070 | snp | A/C | 0.206029 | 0.246103 | intron-variant | CORO2B | GRCh38.p7 | 15:68681111 | CCAGCTACTCGCGAA[A/C]CTGAGGCAGGAGAAT | 10391 |
rs34203964 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68673858 | AAAAAAAAAAAAAAA[-/A]GGACAGTGTCCCGCT | 10391 |
rs34213505 | in-del | -/AA | 0.186737 | 0.241863 | intron-variant | CORO2B | GRCh38.p7 | 15:68657178 | ACCCCTTCACAGAAT[-/AA]AGTTTTTAAGTATAC | 10391 |
rs34229943 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68569857 | GGAAACCGAGGTGCA[A/G]AGAGTGAAAGGCTTG | 10391 |
rs34232451 | snp | C/T | 0.209084 | 0.246629 | intron-variant | CORO2B | GRCh38.p7 | 15:68693569 | CCTGAGAGATGGAAG[C/T]ATAGCTTCTGCCTAT | 10391 |
rs34263465 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68557678 | TTATATGTAACCATT[-/C]CCATTCATTATCCCT | 10391 |
rs34267403 | in-del | -/TT | 0.0872718 | 0.189788 | intron-variant | CORO2B | GRCh38.p7 | 15:68581688 | GAGATTGGGAGACTC[-/TT]TGTTCTCTGAGGGGT | 10391 |
rs34307422 | in-del | -/TTATTTAT | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68721760 | TATTTATTTATTTAT[-/TTATTTAT]GTTTAGAGACAGAGT | 10391 |
rs34320419 | snp | A/G | 0.209388 | 0.246679 | intron-variant | CORO2B | GRCh38.p7 | 15:68689106 | AACATTTGACATTGA[A/G]GTTCTGTCCCAGCAC | 10391 |
rs34341630 | snp | C/T | 0.208474 | 0.246527 | intron-variant | CORO2B | GRCh38.p7 | 15:68682963 | CCTCTTTTCCCTCCT[C/T]GTTCCTTGGGCCAAA | 10391 |
rs34353055 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68607817 | GTGAGACCCTATCTC[-/A]AAAAAAAAAAAAAAA | 10391 |
rs34373931 | snp | A/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68673861 | AAAAAAAAAAAAAGG[A/C]CAGTGTCCCGCTAAG | 10391 |
rs34448727 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68633870 | ACCAGTTACCACATT[-/C]CCCTGGGGACAGTTT | 10391 |
rs34452374 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68627948 | TTTACTCACTCTTAC[-/T]TTCTGTACCCGAAAT | 10391 |
rs34454913 | snp | G/T | 0.453575 | 0.145111 | intron-variant | CORO2B | GRCh38.p7 | 15:68695401 | AAGCCCCACGATGTG[G/T]GGGGGATGGGAGCTA | 10391 |
rs34467049 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | CORO2B | GRCh38.p7 | 15:68563651 | TTTAGCTAGACTGAT[A/T]AAGAAAAAGGAGATA | 10391 |
rs34481026 | snp | A/G | 0.243061 | 0.249904 | intron-variant | CORO2B | GRCh38.p7 | 15:68588822 | GAAGGGGACAAAGGG[A/G]TTTAATTCCTGAGGA | 10391 |
rs34520703 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68693546 | CAAAAAAGTAGCAGG[-/G]AAAAAGACCTGAGAG | 10391 |
rs34549008 | in-del | -/C | | | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68616240 | CTTCTCATAATAATA[-/C]CCCCTGCCTCTTCCC | 10391 |
rs34564985 | snp | C/T | 0.283421 | 0.247756 | intron-variant | CORO2B | GRCh38.p7 | 15:68669225 | GCCGGAGACAGGACT[C/T]GGCCTTGAGAAGCAG | 10391 |
rs34571108 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68693624 | GTAGCCGCTAAACAT[-/G]GGAACAGCTCTTCCA | 10391 |
rs34587389 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68609163 | TTAGGCAGATACGCA[-/G]GGGAGAGGGAAAAGG | 10391 |
rs34602648 | snp | G/T | 0.0142736 | 0.0832652 | intron-variant | CORO2B | GRCh38.p7 | 15:68650281 | GCTGAGGCAGGAGAA[G/T]TGGAGGCGGAGGTTG | 10391 |
rs34605864 | snp | A/G | 0.234982 | 0.249549 | intron-variant | CORO2B | GRCh38.p7 | 15:68725348 | CACTACAGCCTGGGC[A/G]ACAAAGCGAGACTTT | 10391 |
rs34606622 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68661017 | AGACTTTTGCTGTCG[-/C]CCCAGGCTGGAGTGC | 10391 |
rs34613719 | snp | C/T | 0.201727 | 0.245295 | intron-variant | CORO2B | GRCh38.p7 | 15:68723440 | AGATACATTTGGTTT[C/T]TTTGTTGTTGTTGTT | 10391 |
rs34625907 | in-del | -/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68564308 | CATAGCAGTGAAATC[-/T]TTTTTTTTTTTTTGA | 10391 |
rs34639815 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68697969 | CTGAGGTGCTGGGAG[-/C]AGTGGCGGGAAGGGC | 10391 |
rs34675566 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68684104 | AGAGCAGACATTACA[-/G]GGGAAGGAGATAAAC | 10391 |
rs34693732 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68675398 | TAGCTCACCTTCCCA[-/G]GGGAAAGTAAAGCCT | 10391 |
rs34700098 | snp | C/T | 0.201727 | 0.245295 | intron-variant | CORO2B | GRCh38.p7 | 15:68723578 | TTTGCTTCAGCCTCC[C/T]GAGTAGCTGGGATTA | 10391 |
rs34700358 | snp | C/T | 0.206029 | 0.246103 | intron-variant | CORO2B | GRCh38.p7 | 15:68699655 | GTGTCCACCCCTCCC[C/T]GCCTTGGAGCTAGGG | 10391 |
rs34728007 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68687636 | TCAAAGATGTATTTT[-/C]CCCTGGTCTTATTCT | 10391 |
rs34752510 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68639422 | TCTGTGGGACACCCT[-/A]AAAGGAGGTGGCTAT | 10391 |
rs34754638 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68635424 | GGAGCATGGATGCTT[-/C]CCCTGAGTGGGTGCT | 10391 |
rs34784999 | in-del | -/T/TT | 0 | 0 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68630423 | CCTCGAAATGAAATG[-/T/TT]TTTTTTTTTTGTTCC | 10391 |
rs34793532 | in-del | -/A | 0.439085 | 0.163545 | intron-variant | CORO2B | GRCh38.p7 | 15:68670058 | CTCAGAAAAAAAAAA[-/A]GGGGGGGAAAAATAA | 10391 |
rs34805754 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68673538 | AAATAAAATTTTCTT[-/A]AAAAAGGAAAGTGTC | 10391 |
rs34809209 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68621767 | GGCAAGTTTCACTTC[-/T]TTTTTTTTTTTTTTT | 10391 |
rs34822749 | snp | A/T | 0.243633 | 0.249919 | intron-variant | CORO2B | GRCh38.p7 | 15:68725352 | ACAGCCTGGGCGACA[A/T]AGCGAGACTTTGTCT | 10391 |
rs34828866 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68626875 | TCTCTGTGTCAGTTT[-/C]CCCTGGAGAAGTCAT | 10391 |
rs34829475 | snp | C/T | 0.27893 | 0.24832 | intron-variant | CORO2B | GRCh38.p7 | 15:68605552 | GTGTGGGAAAATATT[C/T]GTGCTAAGTGAAAAA | 10391 |
rs34829893 | snp | A/G | 0.275464 | 0.2487 | intron-variant | CORO2B | GRCh38.p7 | 15:68689899 | CTGGGGTTGGCTTGT[A/G]TTGGCTCGTGAGAGC | 10391 |
rs34830730 | snp | A/C | 0.184838 | 0.241358 | intron-variant | CORO2B | GRCh38.p7 | 15:68651219 | CTTAGGTATTGGAGC[A/C]AGCGCCGGCTTCCCC | 10391 |
rs34838752 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68572607 | CCTTGCTGCTCACCA[-/C]CCCCCCAGCTCCAGG | 10391 |
rs34978722 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68674171 | GCTGAGAGTAGCGCA[C/G]CCACCGCCCTCTGCT | 10391 |
rs34992099 | in-del | -/T | 0.291235 | 0.246576 | intron-variant | CORO2B | GRCh38.p7 | 15:68560297 | TTCTTTCTTTCTTTA[-/T]TTTTTTTTTTCTTCT | 10391 |
rs35013919 | in-del | -/A | 0.39121 | 0.2063 | intron-variant | CORO2B | GRCh38.p7 | 15:68721186 | CACACCTGGCCCACT[-/A]ATCACTATTATTAAT | 10391 |
rs35025867 | in-del | -/G | 0.206642 | 0.246211 | intron-variant | CORO2B | GRCh38.p7 | 15:68684000 | TAGGGACCCATTGAA[-/G]ATTTTGGAGCTGGGG | 10391 |
rs35039756 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68643983 | GGAGGTTCCAGTGAG[-/C]CCGAGATCGCACCAT | 10391 |
rs35040509 | in-del | -/G | 0.0970103 | 0.197722 | intron-variant | CORO2B | GRCh38.p7 | 15:68602701 | GTAGGGATGATAGAT[-/G]GTGAGGTGTGACTGC | 10391 |
rs35044293 | snp | C/T | 0.202035 | 0.245356 | intron-variant | CORO2B | GRCh38.p7 | 15:68723680 | ACTGATCTTGAACTC[C/T]TGACCTCGTGATCCA | 10391 |
rs35045606 | in-del | -/TT | 0.464416 | 0.128553 | intron-variant | CORO2B | GRCh38.p7 | 15:68653756 | TGTAATAAAATAATA[-/TT]TTGTTTGCTTACCCA | 10391 |
rs35126856 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68683859 | AGGAGCATTGGAGGT[-/G]GGAGGTGTATAACCA | 10391 |
rs35180855 | snp | A/G | 0.29175 | 0.246489 | intron-variant | CORO2B | GRCh38.p7 | 15:68605346 | CTGGGAACCTGTCCA[A/G]AGGAAATAATCCAAA | 10391 |
rs35213918 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68646059 | GATTACAGGCATGAG[-/C]CACTGCACCTGGCCC | 10391 |
rs35215656 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68693404 | TCCTCCTTATTATTC[-/T]TGATGAGGAATCTGA | 10391 |
rs35216534 | snp | C/T | 0.268724 | 0.249298 | intron-variant | CORO2B | GRCh38.p7 | 15:68672043 | GCATGATGGGGCCCA[C/T]AGGAATAGTGAACCG | 10391 |
rs35219137 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68690666 | TTTTTTTTTTTTTTT[G/T]TGAGACAGGGTCTCA | 10391 |
rs35259414 | in-del | -/A | 0.5 | 0 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68577725 | GACTACTCCGGTCTC[-/A]AAAAAAAAAAAAAAA | 10391 |
rs35262890 | snp | A/G | 0.461703 | 0.132974 | intron-variant | CORO2B | GRCh38.p7 | 15:68652213 | CCAGGTCTCTTATTC[A/G]GGCTGCCGTTGTGAA | 10391 |
rs35267665 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68602234 | CTGACTGGCTTTATT[-/G]CCGGGGAATGACACT | 10391 |
rs35275203 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68663934 | CATCATTACTCACCA[-/G]GGAAGATGAAAATTA | 10391 |
rs35315609 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68643310 | GGGGAGGGGAGAGGC[-/T]TGGTCTGAGGTCACA | 10391 |
rs35340917 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68605711 | CAGAGGGCTCTTGGG[-/T]TTTTTTTTTTTTTTT | 10391 |
rs35373266 | multinucleotide-polymorphism | GT/TC | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68681480 | AAGTTCTGTGTTTCT[GT/TC]CAGAGAAGAAGTCTG | 10391 |
rs35400910 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68564739 | GTTTGGTTGCTCCTT[-/C]CTAAAGTAAACGGTC | 10391 |
rs35402785 | in-del | -/C | 0.107341 | 0.205301 | intron-variant | CORO2B | GRCh38.p7 | 15:68676840 | ACAGTGGCACCATCA[-/C]GACTCACTGCAGTCT | 10391 |
rs35412971 | snp | A/C | 0.338296 | 0.233889 | intron-variant | CORO2B | GRCh38.p7 | 15:68690104 | TATCTGTGACTATTA[A/C]ATTTGCATAGTGGAA | 10391 |
rs35422643 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68603514 | ACATGGTGCTGTGGG[C/T]TGAATTGTATCCCCC | 10391 |
rs35425621 | snp | A/G | 0.144296 | 0.226554 | intron-variant | CORO2B | GRCh38.p7 | 15:68704250 | GTCTGAAAAAAAAAA[A/G]GAAAACTATAACCCA | 10391 |
rs35470588 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68614557 | TTTAAAGAAAAGACA[A/T]GGGGACTAAGACAAG | 10391 |
rs35500017 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68576341 | AGCAGCACAGGAGGG[-/C]ATCAGAAACATTTTC | 10391 |
rs35506646 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68588600 | CAAATGACCTTGATC[-/T]TTTGCTCCAGATACC | 10391 |
rs35512382 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68568144 | AACCTGGGAGACACA[-/G]GGGATAAAGTTGGAG | 10391 |
rs35517352 | in-del | -/T | | | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68631930 | AGATGGCCACCAGGG[-/T]AGGGCCACATGCCAT | 10391 |
rs35538898 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68695725 | AGGAGACTTAGCTGA[A/G]AGAAGTGTCCTGATT | 10391 |
rs35555397 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68678491 | CAGCCTGGCCAACAT[-/G]GGTGAAACCCCATCT | 10391 |
rs35575862 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68632916 | TGTGAGTTAGGGGAG[-/C]AGCAGGAAGGTTACA | 10391 |
rs35583427 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68598276 | CTGGTTCCTGGCCCA[-/G]GCCATGTGGGTTTTA | 10391 |
rs35630853 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68673361 | GCAACCCTGTCTCTC[-/A]AAATGAAAAAAATAA | 10391 |
rs35636803 | in-del | -/A | 0.27893 | 0.24832 | intron-variant | CORO2B | GRCh38.p7 | 15:68647857 | TAAAAAAAAAAAAAA[-/A]GAAAAAAATTAGCCG | 10391 |
rs35649681 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68652637 | CTGGGATGGTGCATT[-/C]CTCCTTCCCCACCAC | 10391 |
rs35670506 | snp | G/T | 0.206336 | 0.246157 | intron-variant | CORO2B | GRCh38.p7 | 15:68682800 | GAATCCCAGAGTGCT[G/T]CCCTGCTGCTGTAGC | 10391 |
rs35672732 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68663154 | AACTACCTACATTGT[-/G]TCTCTCTACATCTTG | 10391 |
rs35673549 | in-del | -/GGA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68658301 | CCCAATTGTTCAATG[-/GGA]GAGGAGGAGGGCGAG | 10391 |
rs35699161 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68644035 | GCCCCATCTCAAAAA[-/C]AAACAAACAAAAAGA | 10391 |
rs35737273 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68629773 | CCTGACCTCATGACT[-/G]GGGACCCAACTCGCT | 10391 |
rs35745262 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68600245 | TCTTTCTAAAATGTG[-/A]AAAATTGCACTCCTC | 10391 |
rs35754368 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68581406 | TGCAGGAAAGGCACT[-/G]GGGGACTGCTTTGCT | 10391 |
rs35758597 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68704045 | ACACACACATACACA[-/C]ACACACACACACACA | 10391 |
rs35781971 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68690644 | GTGATCACGTTAGCT[G/T]TCTTTTTTTTTTTTT | 10391 |
rs35790887 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68678323 | TGTCAGTGTGAGCCC[-/T]TTTCTCCCCTCCCTC | 10391 |
rs35831094 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68648030 | AAGATCCTGTCTCTC[-/A]AAAAAAAAAAAAAAA | 10391 |
rs35836048 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68697422 | CATCTAATCAGTTAT[-/C]CCAAAGAAAGAAAGA | 10391 |
rs35889202 | in-del | -/A | 0.485799 | 0.0830599 | intron-variant | CORO2B | GRCh38.p7 | 15:68648331 | AACAAGATTCCAGCT[-/A]AAAAAAAAAAAAAAA | 10391 |
rs35903286 | in-del | -/GA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68608948 | ACTGGGTACTAGGAA[-/GA]GAGAGAGAGAGGAGA | 10391 |
rs35903926 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68609129 | GGAACTGGGCCTCCA[-/G]GGGATGGTTGGGATT | 10391 |
rs35923288 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68627422 | AAAGAGTGTGTTGGT[-/G]GGGGGGTGGTCAGGG | 10391 |
rs35931709 | in-del | -/A | 0.175576 | 0.238665 | intron-variant | CORO2B | GRCh38.p7 | 15:68653861 | CTTCTCTCCCCCAGG[-/A]AAAAAAAAAAAATGC | 10391 |
rs35973911 | in-del | -/A | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68705454 | AAAAAAAAAAAAAAA[-/A]GAAAGTAAATGTGCA | 10391 |
rs35994899 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68646852 | GCAAAGGCTCACAGC[-/A]AGCTCTAACACATTC | 10391 |
rs36011761 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68588857 | ATTTAACTCCTGAAA[-/G]AATTGCTGGTTATGC | 10391 |
rs36038837 | snp | A/G | 0.338523 | 0.233803 | intron-variant | CORO2B | GRCh38.p7 | 15:68689640 | TTCAGTGACAGACAG[A/G]ACCAAGTTTGGTCTC | 10391 |
rs36049258 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68671212 | CTGATACTCACCACG[-/C]ACATAATAGGAATTA | 10391 |
rs36058099 | in-del | -/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68698552 | CCAAGAGACTCTGTT[-/C]CAGTTTTGCACACAC | 10391 |
rs36077420 | snp | A/G | 0.0517425 | 0.152296 | synonymous-codon | CORO2B | GRCh38.p7 | 15:68711574 | GGATGTGGGTGAGCC[A/G]GTGAAGATGATTGAC | 10391 |
rs36088681 | snp | C/T | 0.338069 | 0.233974 | intron-variant | CORO2B | GRCh38.p7 | 15:68689627 | TTAGGAGCCAGGCTT[C/T]AGTGACAGACAGGAC | 10391 |
rs36116901 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68575092 | CCTCCATAAGAACCA[-/G]GGGACTTTTTACTTT | 10391 |
rs55661876 | snp | C/T | 0.0614824 | 0.164198 | intron-variant | CORO2B | GRCh38.p7 | 15:68570770 | TGCAGCAGAAAGAGC[C/T]GAGGATGGACCCAGG | 10391 |
rs55698022 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO2B | GRCh38.p7 | 15:68576021 | AGTCAGGTGGGGTGG[C/T]GGGCACCTGTAGTCC | 10391 |
rs55725109 | snp | C/T | 0.078151 | 0.181571 | intron-variant | CORO2B | GRCh38.p7 | 15:68617176 | GTGGGCTCCAGGGAA[C/T]GGGATGAGTCATATC | 10391 |
rs55734137 | snp | A/T | 0.275464 | 0.2487 | intron-variant | CORO2B | GRCh38.p7 | 15:68689808 | CTTTAATTTTTATGT[A/T]TGTTAAAGTAATAAA | 10391 |
rs55769311 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | CORO2B | GRCh38.p7 | 15:68610723 | GCAGAGTAGGGTACT[C/T]TGAGGCCCAGTCAAA | 10391 |
rs55770579 | snp | C/T | 0.414576 | 0.188188 | intron-variant | CORO2B | GRCh38.p7 | 15:68561906 | GCCTGTGAGCATGAC[C/T]GTGAGTGTGTGTTGT | 10391 |
rs55921407 | snp | C/T | 0.294226 | 0.246057 | intron-variant | CORO2B | GRCh38.p7 | 15:68719579 | AAGTTATTACCTCCA[C/T]AGGCCCTGGAAGAGC | 10391 |
rs55962860 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | CORO2B | GRCh38.p7 | 15:68686895 | CAAGAGCGAAACTCC[A/G]TCTCAAAAAAAAAAA | 10391 |
rs55982862 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | CORO2B | GRCh38.p7 | 15:68657207 | TACAAAATAGGATTA[C/T]GCAAGAAGCCAATTA | 10391 |
rs56030116 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | CORO2B | GRCh38.p7 | 15:68677390 | ACAGGGATAGGGCTA[A/G]CTGAAGGCCACACAG | 10391 |
rs56064717 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68673670 | AGTGAAACCCCGTTT[C/T]TACTAAAAATACAAA | 10391 |
rs56094696 | snp | A/C | 0.229429 | 0.249152 | intron-variant | CORO2B | GRCh38.p7 | 15:68686007 | GCACTAGAAATGTTG[A/C]GCTCCTACTTCTGTT | 10391 |
rs56117331 | in-del | -/ATTA | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68685770 | TGTTTGATTGATTAA[-/ATTA]ACACTTTATTTTATT | 10391 |
rs56131944 | snp | C/T | 0.0310518 | 0.120672 | intron-variant | CORO2B | GRCh38.p7 | 15:68709647 | TCTTTGGTAGAGGCA[C/T]GGTCTCGCTGTGTTG | 10391 |
rs56168498 | in-del | -/TT | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68686036 | TTTTTTTTTTTTTTT[-/TT]CTTTTTTTTTTTTTT | 10391 |
rs56175213 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68572506 | TTCATATCTGTTTTG[C/G]ATGATTTATCTGACA | 10391 |
rs56215615 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CORO2B | GRCh38.p7 | 15:68641642 | TATCAGGTCAGCATG[C/T]CCTGTGCTGGGCATA | 10391 |
rs56257732 | snp | G/T | 0.0482946 | 0.147699 | intron-variant | CORO2B | GRCh38.p7 | 15:68617157 | TCCAACAACATTGGC[G/T]TTCGTGGGCTCCAGG | 10391 |
rs56260036 | snp | A/G | 0.156319 | 0.231784 | intron-variant | CORO2B | GRCh38.p7 | 15:68710312 | GGGATAAGGCCCTGC[A/G]GTCCAAACAGCCAAA | 10391 |
rs56268459 | snp | C/T | 0.229136 | 0.249128 | intron-variant | CORO2B | GRCh38.p7 | 15:68674707 | TCAAACTCAGCAGTG[C/T]TCCATGACCTCACCA | 10391 |
rs56281900 | snp | C/G | 0.0429648 | 0.14013 | intron-variant | CORO2B | GRCh38.p7 | 15:68584388 | GAGGAAGCTGGGAAG[C/G]GTTTGAGGCTCTCCA | 10391 |
rs56299461 | snp | G/T | 0.219648 | 0.248151 | intron-variant | CORO2B | GRCh38.p7 | 15:68661121 | TGGCTGGGATTACAG[G/T]TGCCCGCCACCATGC | 10391 |
rs56322535 | snp | C/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68684783 | AGTGTTGAGGGTTGT[C/G]CAAATGTGAGTTGGG | 10391 |
rs56325107 | in-del | -/A | 0.283158 | 0.247791 | intron-variant | CORO2B | GRCh38.p7 | 15:68669798 | TGGTGGCTCATGCCT[-/A]ATAATCCCAGCACTT | 10391 |
rs56327959 | snp | C/T | 0.078151 | 0.181571 | intron-variant | CORO2B | GRCh38.p7 | 15:68617181 | CTCCAGGGAATGGGA[C/T]GAGTCATATCCTGAC | 10391 |
rs56348473 | snp | C/T | 0.093417 | 0.194889 | intron-variant | CORO2B | GRCh38.p7 | 15:68720466 | GTTTCTTTGCATGCC[C/T]GTGGCTGAAGGTCTC | 10391 |
rs56352602 | in-del | -/AA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68576176 | AAAAAAAAAAAAAAA[-/AA]GAAAGAAAGAAAGAA | 10391 |
rs56359428 | snp | C/T | 0.375 | 0.216506 | intron-variant | CORO2B | GRCh38.p7 | 15:68691451 | TAAAACGGTGAAACC[C/T]CGTCTCTACTAAAAA | 10391 |
rs56393857 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CORO2B | GRCh38.p7 | 15:68557967 | CTTCGGAAGGCCACA[A/G]CACACACCTTAAGGT | 10391 |
rs56403237 | in-del | -/AGG | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68658311 | CAATGGAGGAGGAGG[-/AGG]GCGAGATGCATGGTG | 10391 |
rs56778428 | snp | A/G | 0.0777841 | 0.181223 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68631985 | CTCTCTTGGTTGCTA[A/G]CAACAGATTCTGTTG | 10391 |
rs56816924 | snp | G/T | 0.0123036 | 0.0774623 | intron-variant | CORO2B | GRCh38.p7 | 15:68558245 | TCAAACATCTCTACA[G/T]CCAAGCCCAGCTTCT | 10391 |
rs56853652 | snp | C/T | 0.101301 | 0.200969 | intron-variant | CORO2B | GRCh38.p7 | 15:68611964 | TTCATAGAGACTGGG[C/T]CTTGCTATGTTGCCC | 10391 |
rs56944234 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68583416 | CGGTCCTGACTCATG[G/T]TCAGTGCTCTTTCCA | 10391 |
rs56990063 | snp | A/C | 0.176219 | 0.238865 | intron-variant | CORO2B | GRCh38.p7 | 15:68661900 | TAATCCCAGGTACTC[A/C]GGAGGCTGAAGCAGG | 10391 |
rs56992386 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68610961 | AGAATCCCAGGGGGA[-/A]AAAATGAAAGAAGTA | 10391 |
rs57017874 | in-del | -/A | 0.200801 | 0.245111 | intron-variant | CORO2B | GRCh38.p7 | 15:68696087 | ACAAAAAATTGAATT[-/A]AAAAAAAAAAAAACT | 10391 |
rs57119614 | snp | A/G | 0.0248432 | 0.108648 | intron-variant | CORO2B | GRCh38.p7 | 15:68721477 | TTGAGAGGCCAAGGC[A/G]GGTGGATCACCTGAG | 10391 |
rs57211959 | snp | A/G | 0.0948562 | 0.196037 | intron-variant | CORO2B | GRCh38.p7 | 15:68720117 | TTTAGCTCAGCTGGG[A/G]TTCACAGGATGCCTA | 10391 |
rs57234041 | snp | A/G | 0.337841 | 0.23406 | intron-variant | CORO2B | GRCh38.p7 | 15:68691930 | AAACACTTAATGCAC[A/G]CAGCTCTGCTCAGGG | 10391 |
rs57270255 | in-del | -/T/TT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68660988 | GTCTTTTTTTTTTTT[-/T/TT]CTGTTTTTTGAGACA | 10391 |
rs57270738 | snp | A/G | 0.0517044 | 0.152246 | intron-variant | CORO2B | GRCh38.p7 | 15:68628094 | GCCAGCATAATTTGG[A/G]TGGGGCTTTGCATAT | 10391 |
rs57390996 | snp | C/G | 0.0132419 | 0.0802845 | intron-variant | CORO2B | GRCh38.p7 | 15:68711494 | GGGACAAACACCCCA[C/G]GACCCTAGCAGCCAC | 10391 |
rs57404468 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68703167 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTTGC | 10391 |
rs57420748 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68703172 | TTTTTTTTTTTTTGA[A/G]ACGGAGTCTTGCTCT | 10391 |
rs57483551 | in-del | -/GTATA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68675949 | ATAGGGTATAATATA[-/GTATA]ATAATAGAACAGAAA | 10391 |
rs57506624 | snp | A/G/T | 0.0267878 | 0.112589 | intron-variant | CORO2B | GRCh38.p7 | 15:68581042 | GCACTGCTCTGCATC[A/G/T]TTGGGCATCCTGGCT | 10391 |
rs57588113 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | CORO2B | GRCh38.p7 | 15:68609850 | CTGTGATGGCAGGCA[A/G]GGTGGGCTGGGGTAG | 10391 |
rs57604810 | in-del | -/TT | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68709479 | TTTTTTTTTTTTTTT[-/TT]AGACAGAGTCTTGCT | 10391 |
rs57610371 | snp | C/T | 0.0562307 | 0.157967 | intron-variant | CORO2B | GRCh38.p7 | 15:68562315 | ACCTTCCAGGCAAGA[C/T]TGTACTGCTCCTTCC | 10391 |
rs57796494 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | CORO2B | GRCh38.p7 | 15:68599391 | TGCTGTGCCTGGCCC[C/T]ATAGATGTTCAATTA | 10391 |
rs57802985 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68624518 | CTGGAACTGATATTA[G/T]GAACTACCGTCCCTT | 10391 |
rs57879519 | in-del | -/AAA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68691644 | AAAAAAAAAAAAAAA[-/AAA]GAAAAGAAAAGTGGT | 10391 |
rs57995280 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | CORO2B | GRCh38.p7 | 15:68683875 | GGAGGTGTATAACCA[C/T]GGGCATGGCATGGGC | 10391 |
rs58032591 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68604630 | ATTTAAAAAAAAAAA[-/A]CCTCCCTTCTGTGTA | 10391 |
rs58055503 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2B | GRCh38.p7 | 15:68703300 | GGATTACAGGCACGC[A/G]CTACCACGCCCAGTT | 10391 |
rs58281620 | snp | A/G | 0.135143 | 0.222054 | intron-variant | CORO2B | GRCh38.p7 | 15:68664589 | GAGGCAGATCTTGCA[A/G]TGAGCCAAGATTGTG | 10391 |
rs58393972 | snp | A/G | 0.0825414 | 0.185628 | intron-variant | CORO2B | GRCh38.p7 | 15:68678711 | AGAAGGCAGCTGAGC[A/G]TGTCCAGGGATCAGC | 10391 |
rs58505142 | in-del | -/CTTTT/TCTTT | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68665012 | GTTTACCAGTCTTTT[-/CTTTT/TCTTT]ATGGCTTCTGGATCT | 10391 |
rs58509645 | snp | G/T | 0.0209421 | 0.100162 | intron-variant | CORO2B | GRCh38.p7 | 15:68671958 | AAGGTGTGTTCTAAG[G/T]GGCAGTCAGGGGCTA | 10391 |
rs58515629 | snp | A/G | 0.109461 | 0.206758 | intron-variant | CORO2B | GRCh38.p7 | 15:68582696 | GAAAACCTGTGAGCT[A/G]AAGTCTAGGCCCTTG | 10391 |
rs58635545 | in-del | -/CT | 0.236144 | 0.249616 | intron-variant | CORO2B | GRCh38.p7 | 15:68559695 | CCGGTTGGTGCAGTG[-/CT]CTCTGGGGTTCTCCC | 10391 |
rs58662532 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | CORO2B | GRCh38.p7 | 15:68576399 | GTTGGGGGCAGCAGA[C/T]TGATGTTCCTAATTA | 10391 |
rs58707488 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | CORO2B | GRCh38.p7 | 15:68629117 | CATGCTGGGGAGTGC[C/T]GAATGTATCTTGCAG | 10391 |
rs58729813 | in-del | -/CA/CACT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68587096 | ACACACACACACACA[-/CA/CACT]ATTTTTTTCTAAAGT | 10391 |
rs58769702 | snp | C/G | 0.0197687 | 0.0974348 | intron-variant | CORO2B | GRCh38.p7 | 15:68609746 | CTACTGATGGAAGGC[C/G]GTTGCTCTGGCTCTC | 10391 |
rs58813791 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2B | GRCh38.p7 | 15:68627311 | GTTTGGAGTTAGACC[C/T]GAACACAGGAAAAGC | 10391 |
rs58883519 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68708690 | CTTCCTTTTTTTTTT[-/T]ATTTTCTGAGACAGA | 10391 |
rs58947334 | snp | A/G | 0.0614824 | 0.164198 | intron-variant | CORO2B | GRCh38.p7 | 15:68594558 | ATTTCTGAATAACCA[A/G]CAGCAGATCTAAAGC | 10391 |
rs58973991 | snp | A/G | 0.0894459 | 0.191631 | intron-variant | CORO2B | GRCh38.p7 | 15:68598218 | GAGAAGAGGGCGGGC[A/G]GTCTGGCTGGAATTG | 10391 |
rs59125363 | snp | A/G | 0.0429648 | 0.14013 | intron-variant | CORO2B | GRCh38.p7 | 15:68584787 | TGCAGGCTCAGGCCC[A/G]GGGTCCTGGAGCACC | 10391 |
rs59151976 | in-del | -/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68570825 | TTTTTTTTTTTTTTT[-/T]AGAGACTGGGTCTCA | 10391 |
rs59197667 | snp | A/G | 0.0263992 | 0.111815 | intron-variant | CORO2B | GRCh38.p7 | 15:68633367 | TGAGACAGTTATCAC[A/G]GATGTTTTCAAACAA | 10391 |
rs59214666 | in-del | -/GAATA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68675993 | ATATAGAATAGAATA[-/GAATA]ATGCTAGGAGGAGAA | 10391 |
rs59224067 | snp | G/T | 0.0240643 | 0.107019 | intron-variant | CORO2B | GRCh38.p7 | 15:68597332 | ATCACTAATGCTTAT[G/T]CAGCGCTTACCATGT | 10391 |
rs59240770 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68597640 | TCAAAAAAAAAAAAA[-/A]TAAATAAATAAAAAA | 10391 |
rs59252819 | in-del | -/AG | 0.254385 | 0.249962 | intron-variant | CORO2B | GRCh38.p7 | 15:68608937 | CACTGGGTACTAGGA[-/AG]AGAGAGAGAGAGGAG | 10391 |
rs59278231 | snp | C/G/T | 0.0588605 | 0.161139 | intron-variant | CORO2B | GRCh38.p7 | 15:68617135 | GTCAGCCTTCAAGCC[C/G/T]GTGCTTTCCAACAAC | 10391 |
rs59307752 | snp | C/T | 0.136847 | 0.222927 | intron-variant | CORO2B | GRCh38.p7 | 15:68604090 | TGAGTGTATTTCATA[C/T]ACAGAAAGCATTTGG | 10391 |
rs59346349 | snp | C/T | 0.119978 | 0.213528 | intron-variant | CORO2B | GRCh38.p7 | 15:68712376 | TTCTAGTACTATAGG[C/T]TGAGCATCCCAAATC | 10391 |
rs59395548 | snp | C/T | 0.103794 | 0.20279 | intron-variant | CORO2B | GRCh38.p7 | 15:68604063 | CTTACCCCATAGAAG[C/T]GTTGTGAGCACTGAG | 10391 |
rs59467072 | in-del | -/A | 0.467845 | 0.122652 | intron-variant | CORO2B | GRCh38.p7 | 15:68562980 | AAGAAAAAAAAAAAA[-/A]GAAAGAAAAGAAAAC | 10391 |
rs59490858 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68688115 | GTAGGCACCAGTCTG[C/T]ATATTATTTCTTCAA | 10391 |
rs59509599 | in-del | -/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68642054 | TTTTTTTTTTTTTTT[-/T]GAGACAGAGTCTCAT | 10391 |
rs59594144 | snp | G/T | 0.0581099 | 0.160244 | intron-variant | CORO2B | GRCh38.p7 | 15:68620639 | TATTTCCAAAGTGCC[G/T]TCTCTGTTTTATTCT | 10391 |
rs59622370 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68702017 | GGAGGCTGAGGTGGG[C/T]GGATCACCTGAGGTC | 10391 |
rs59728031 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | CORO2B | GRCh38.p7 | 15:68587177 | GATCATCCTGGGCAA[C/T]GTAGTGAGACCCCAT | 10391 |
rs59821203 | in-del | -/A/AA | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68648048 | AAAAAAAAAAAAAAA[-/A/AA]GAGTCTGGGCATGGT | 10391 |
rs59948606 | snp | C/T | 0.232651 | 0.249397 | intron-variant | CORO2B | GRCh38.p7 | 15:68667337 | CCTCTGCTTTGCCAA[C/T]AGACTCTCCGCTTCC | 10391 |
rs60007308 | in-del | -/A | | | intron-variant | CORO2B | GRCh38.p7 | 15:68662030 | ATAAATAAATAAATT[-/A]AATTAATTAATAAAA | 10391 |
rs60150413 | in-del | -/GAAAGAA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68576175 | AAAAAAAAAAAAAAA[-/GAAAGAA]AGAAAGAAAGAAAGA | 10391 |
rs60225609 | snp | C/T | 0.0926964 | 0.194308 | downstream-variant-500B | CORO2B | GRCh38.p7 | 15:68727992 | TGGGGCGAATAATTC[C/T]TTGCTGTGGGGGCTG | 10391 |
rs60280851 | snp | A/G | 0.237593 | 0.249692 | intron-variant | CORO2B | GRCh38.p7 | 15:68666663 | TGGAGAAAGCAGGGC[A/G]GCTGTGGGCACTGGG | 10391 |
rs60503351 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68650375 | AAAAAAAAAAAAAAA[A/T]AAAAAAAAAAAAAAA | 10391 |
rs60620349 | in-del | -/AAGC/AAGCAAGC | | | intron-variant | CORO2B | GRCh38.p7 | 15:68669211 | AGCAAGCAAGCAAGC[-/AAGC/AAGCAAGC]CGGAGACAGGACTCG | 10391 |
rs60732246 | snp | C/T | 0.237014 | 0.249662 | intron-variant | CORO2B | GRCh38.p7 | 15:68668671 | GAACCTTGGAGACCA[C/T]GCCAGTTTGGATTTT | 10391 |
rs60790680 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68577745 | AAAAAAAAAAAAAAA[-/AA]TTGCACAATGACCCA | 10391 |
rs60967241 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2B | GRCh38.p7 | 15:68581081 | ACTTCCATGGTAGAG[A/G]AGCACTGCTTGGAGA | 10391 |
rs60974515 | snp | G/T | 0.153665 | 0.230694 | intron-variant | CORO2B | GRCh38.p7 | 15:68712788 | ATACGTGAGAACACT[G/T]AACCTTAGCGAAGTT | 10391 |
rs60989044 | in-del | -/GTGTGT/GTGTGTGTG/GTGTGTGTGTG/GTGTGTGTGTGTGT | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68672185 | TGTGTGTGTGTGTGT[lengthTooLong]ACTTTTTTGGTGTTT | 10391 |
rs61116087 | in-del | -/AAA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68662029 | AATAAATAAATAAAT[-/AAA]TAATTAATTAATAAA | 10391 |
rs61138113 | snp | A/G | 0.16911 | 0.236552 | intron-variant | CORO2B | GRCh38.p7 | 15:68671109 | ACTGAGGAATACAAC[A/G]CAGCCGTGAAAATCA | 10391 |
rs61139980 | snp | A/G | 0.0810805 | 0.184299 | intron-variant | CORO2B | GRCh38.p7 | 15:68625730 | CCACCTCAGCACCCC[A/G]AGTAGCTAGGACTAC | 10391 |
rs61206845 | snp | A/G | 0.148661 | 0.22854 | intron-variant | CORO2B | GRCh38.p7 | 15:68715012 | CACACACACACTCAC[A/G]TCAGCCCATCCACCT | 10391 |
rs61297577 | snp | A/C/G | 0.00119737 | 0.0244387 | intron-variant | CORO2B | GRCh38.p7 | 15:68621360 | ACCTGGAGCAAGCAC[A/C/G]ATGCAGGGAGTGCTG | 10391 |
rs61482368 | in-del | -/TACACACACA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68587049 | ATAGGGAGATATGTA[-/TACACACACA]CACACACACACACAC | 10391 |
rs61493142 | snp | A/G | 0.118933 | 0.212888 | intron-variant | CORO2B | GRCh38.p7 | 15:68708422 | CTGGAGTGCAGTGAC[A/G]TGATCTCGGCTCACT | 10391 |
rs61601464 | in-del | -/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68574286 | GGGCCAGCATGTGGG[-/G]CATGCCGCCTGGGGT | 10391 |
rs61684053 | in-del | -/T | 0.176219 | 0.238865 | intron-variant | CORO2B | GRCh38.p7 | 15:68681227 | CATCTCAAAAAAAAA[-/T]TTTTTTTTGGAAAGA | 10391 |
rs61685521 | in-del | -/A | 0.494774 | 0.0508504 | intron-variant | CORO2B | GRCh38.p7 | 15:68565316 | TTTTATTTAAAAAAA[-/A]TTTTTATTGGCATGC | 10391 |
rs61747072 | snp | C/T | 0.00325471 | 0.040209 | synonymous-codon | CORO2B | GRCh38.p7 | 15:68645330 | CGAGAGCGCAGGGGG[C/T]GGCTCCTTCCTCGTC | 10391 |
rs62002112 | snp | A/C | 0.228253 | 0.249052 | intron-variant | CORO2B | GRCh38.p7 | 15:68557636 | AGCAGTGAGGCCTCA[A/C]TACAGGCCAGACACT | 10391 |
rs62002113 | snp | A/T | 0.214843 | 0.247516 | intron-variant | CORO2B | GRCh38.p7 | 15:68561343 | GGCAGTGCCTGCAGC[A/T]CACTCTCCCCGGTCC | 10391 |
rs62002115 | snp | A/G | 0.343701 | 0.231776 | intron-variant | CORO2B | GRCh38.p7 | 15:68576148 | ACAGAGTGAGACTAC[A/G]TCGCAAAAAAAAAAA | 10391 |
rs62002123 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | CORO2B | GRCh38.p7 | 15:68580263 | TCTGGCGGTGGCCTC[A/G]GGCTTGGCCGTCCAT | 10391 |
rs62002124 | snp | A/G | 0.0622301 | 0.165053 | intron-variant | CORO2B | GRCh38.p7 | 15:68589910 | GCTGCGGCTGCCCAG[A/G]CCTGGCAGTGCATGC | 10391 |
rs62002125 | snp | G/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68595974 | CAGCGACGCCGTGGG[G/T]TGCTCCCGAGCCACG | 10391 |
rs62002126 | snp | C/G | 0.00159617 | 0.0282053 | intron-variant | CORO2B | GRCh38.p7 | 15:68600546 | TTGTTAACAGCCTCT[C/G]TCTGAACTCCGTCCC | 10391 |
rs62002127 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68602029 | TTTTTTTTTTTTTAA[A/T]TAAATGCCTTAATCC | 10391 |
rs62002128 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68605116 | GAGACTCCGTCTCAA[A/G]GAAAAAAAAAAAAAA | 10391 |
rs62002132 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | CORO2B | GRCh38.p7 | 15:68627913 | GGTGTAGAAGTTCGA[C/T]GAGGCTCTGTGCTGA | 10391 |
rs62002133 | snp | A/T | 0.192401 | 0.243274 | intron-variant | CORO2B | GRCh38.p7 | 15:68629911 | GGAAAAGCACCCCAG[A/T]AGAAAGAGTCCTTTA | 10391 |
rs62002134 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68633514 | ATGGTTACTCCAACA[C/T]ACACACACACACACA | 10391 |
rs62002135 | snp | A/G | | | intron-variant | CORO2B | GRCh38.p7 | 15:68643477 | AGAACTCAGCAGAGA[A/G]AGACAGCAAGTGGGA | 10391 |
rs62002136 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68646265 | GAGTCCCCAGAGGCC[C/T]GTGGGAGGTCACGCG | 10391 |
rs62002137 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | CORO2B | GRCh38.p7 | 15:68649069 | AAACGCTTCCTCTCA[A/G]TTTCTGTAATGGTAA | 10391 |
rs62002139 | snp | A/C | | | intron-variant | CORO2B | GRCh38.p7 | 15:68655453 | CAGAGTCAGAGGGGA[A/C]CCCAGGGATCATAGA | 10391 |
rs62002150 | snp | C/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68660689 | ATTCATATTTTGAAC[C/G]CTTCACTCCTACACA | 10391 |
rs62002151 | snp | A/C | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68669893 | GAAACCCTATCTCTA[A/C]TAAAAATACAAAAAT | 10391 |
rs62002152 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | CORO2B | GRCh38.p7 | 15:68682102 | GAACCCCTGCTTCAG[C/T]TTTCATGGTAGGGCA | 10391 |
rs62002153 | snp | A/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68684890 | CTACAATACCTGTTT[A/T]ATAATGACTCTCTCT | 10391 |
rs62002154 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68684895 | ATACCTGTTTTATAA[C/T]GACTCTCTCTCTTTT | 10391 |
rs62002155 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68691212 | CGGGCGCCTGTGGTC[C/T]CAGCTACTCGGGAGG | 10391 |
rs62004271 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CORO2B | GRCh38.p7 | 15:68696309 | ATCCCAGCACTTCGG[A/G]AGGCTGAGGCAGGTG | 10391 |
rs62004273 | snp | C/T | 0.36315 | 0.222928 | intron-variant | CORO2B | GRCh38.p7 | 15:68701630 | AGCTGGGACTACAGG[C/T]GCGCGCCACCATGCC | 10391 |
rs62004274 | snp | G/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68710691 | ATCAAGGGACTTCTT[G/T]GCCGTGTCCACCCAG | 10391 |
rs62004275 | snp | A/C | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68716773 | CCAGAATGAGCCTGG[A/C]ATGTTCTAGGAGCAG | 10391 |
rs62004276 | snp | A/C | 0.379942 | 0.213577 | intron-variant | CORO2B | GRCh38.p7 | 15:68724294 | TTTTCTTCAAGGAGG[A/C]CCTCCCTGGTTGGAA | 10391 |
rs66523805 | snp | A/G | 0.239902 | 0.249796 | intron-variant | CORO2B | GRCh38.p7 | 15:68678233 | GGTCCTGTTGTCAGA[A/G]AAGGAGTCAGGCAGA | 10391 |
rs66526622 | in-del | -/AA | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68703168 | GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA | 10391 |
rs66642682 | in-del | -/AGA | 0.331411 | 0.236373 | intron-variant | CORO2B | GRCh38.p7 | 15:68717689 | TATCTGCTAAGTAGC[-/AGA]AGAAGAACTCAGACC | 10391 |
rs66691901 | snp | A/G | 0.225597 | 0.248806 | intron-variant | CORO2B | GRCh38.p7 | 15:68673625 | GGCGAATCACTTAAG[A/G]TCAGGAGTTCGAGAC | 10391 |
rs66732052 | snp | C/T | 0.234401 | 0.249513 | intron-variant | CORO2B | GRCh38.p7 | 15:68712968 | GCTACACTTTTTTGG[C/T]GGAGCTAGAACTAGA | 10391 |
rs66786238 | snp | G/T | 0.289424 | 0.246872 | intron-variant | CORO2B | GRCh38.p7 | 15:68694478 | AAACACAGGCCTGTG[G/T]GACTCCGAAGACTAT | 10391 |
rs66814227 | snp | C/G | 0.338069 | 0.233974 | intron-variant | CORO2B | GRCh38.p7 | 15:68690875 | TCCCAGGCTGGTCTC[C/G]AACTCCTGGGCTTAA | 10391 |
rs66852519 | in-del | -/TA | 0.410061 | 0.192043 | intron-variant | CORO2B | GRCh38.p7 | 15:68587047 | CTATAGGGAGATATG[-/TA]TACACACACACACAC | 10391 |
rs66906023 | snp | A/G | 0.217551 | 0.247885 | intron-variant | CORO2B | GRCh38.p7 | 15:68591775 | CTTTCCCATCTGCCT[A/G]GGCTGCCAGATGGTT | 10391 |
rs66907150 | snp | C/T | 0.0494327 | 0.149241 | intron-variant | CORO2B | GRCh38.p7 | 15:68574557 | GGCAGAGCCTCACAC[C/T]GAGAGGTCCTCATTC | 10391 |
rs67282281 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CORO2B | GRCh38.p7 | 15:68648346 | AAAAAAAAAAAAAAA[-/A]CGAAAGAAAGAAACA | 10391 |
rs67351715 | in-del | -/CAGAGCAGTGGGGCCAGATGGAGGGT | 0.375 | 0.216506 | intron-variant | CORO2B | GRCh38.p7 | 15:68580385 | GGTCAGATGGAGGGT[-/CAGAGCAGTGGGGCCAGATGGAGGGT]TGGGGTGCAAGTGAT | 10391 |
rs67420453 | in-del | -/ATACACACAC | | | intron-variant | CORO2B | GRCh38.p7 | 15:68587048 | TATAGGGAGATATGT[-/ATACACACAC]ACACACACACACACA | 10391 |
rs67447288 | in-del | -/AGG | | | intron-variant | CORO2B | GRCh38.p7 | 15:68658310 | TCAATGGAGGAGGAG[-/AGG]GRSGAGATGCATGGT | 10391 |
rs67563610 | in-del | -/AA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68576153 | TGAGACTACGTCGCA[-/AA]AAAAAAAAAAAAAAA | 10391 |
rs67601373 | in-del | -/C | 0.166506 | 0.235645 | intron-variant | CORO2B | GRCh38.p7 | 15:68625309 | TCGAGGTATAATTTA[-/C]ATGCATTAAAAAAAC | 10391 |
rs67621638 | snp | A/G | 0.433382 | 0.169915 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68726544 | GTCTCTTCCCTTCCC[A/G]CCCTCTTGTCTTCAG | 10391 |
rs67647276 | snp | C/T | 0.314787 | 0.241459 | intron-variant | CORO2B | GRCh38.p7 | 15:68691047 | TAGAAAACTGGTTTT[C/T]GGCCAGGTGCGGTGG | 10391 |
rs67753701 | in-del | -/AA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68691625 | CGAGACTCCGTCTCA[-/AA]AAAAAAAAAAAAAAA | 10391 |
rs67758992 | in-del | -/A | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68660988 | TGTCTCAAAAAACAG[-/A]AAAAAAAAAAAGACT | 10391 |
rs67778935 | snp | C/T | 0.43309 | 0.17023 | intron-variant | CORO2B | GRCh38.p7 | 15:68668806 | AAGACAGGCCGAGCA[C/T]GGTGGCTCACGCCTG | 10391 |
rs67795069 | snp | A/G | 0.398174 | 0.201356 | intron-variant | CORO2B | GRCh38.p7 | 15:68691848 | TGGCTAGAAGCTCCT[A/G]TTATCTGATGGCCAC | 10391 |
rs67807441 | snp | A/G | 0.209997 | 0.246779 | intron-variant | CORO2B | GRCh38.p7 | 15:68589608 | TGAGTGGGAACTGGG[A/G]CTCCCCCAAGTTACT | 10391 |
rs67844713 | snp | A/G | 0.202035 | 0.245356 | intron-variant | CORO2B | GRCh38.p7 | 15:68712251 | ATGGGGAGAGATGGA[A/G]TGGAAAATATGGATG | 10391 |
rs67888371 | snp | A/G | 0.256897 | 0.249905 | intron-variant | CORO2B | GRCh38.p7 | 15:68672531 | CAATTCTCTTATCTC[A/G]GCCTTCCAAAGTGCT | 10391 |
rs68024154 | snp | C/G | 0.196771 | 0.244268 | intron-variant | CORO2B | GRCh38.p7 | 15:68721984 | TCTTAAACTCCTGGG[C/G]TCAAACAGTCCTCCC | 10391 |
rs68175317 | multinucleotide-polymorphism | AATTTGCAT/CATTTGCAG | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68690104 | TATCTGTGACTATTA[AATTTGCAT/CATTTGCAG]AGTGGAAATATTCTA | 10391 |
rs71145183 | in-del | -/T | 0.496382 | 0.0423778 | intron-variant | CORO2B | GRCh38.p7 | 15:68563488 | TTTCTTTTTTTTTTT[-/T]AAAGACAGAATTTCA | 10391 |
rs71145187 | in-del | -/TGTGTGTGTGTGTA | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68587049 | GTGTGTGTGTGTGTG[-/TGTGTGTGTGTGTA]TACATATCTCCCTAT | 10391 |
rs71145188 | in-del | -/A | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68621784 | AGGAGACCCTGTCTC[-/A]AAAAAAAAAAAAAAA | 10391 |
rs71145189 | in-del | -/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68647702 | TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTTGA | 10391 |
rs71145191 | in-del | -/C | 0.230896 | 0.249269 | intron-variant | CORO2B | GRCh38.p7 | 15:68686223 | CGTGACAGAACCCCC[-/C]TCTCTACCAAAACTA | 10391 |
rs71145192 | in-del | -/TT | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68696574 | ACTTTCCCTGGATTC[-/TT]TTTTTTTTTTTTTTT | 10391 |
rs71145193 | in-del | -/AAAAAAA | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68701503 | GCGAAACTCCGTCTC[-/AAAAAAA]AAAAAAAAAAAAAAA | 10391 |
rs71145196 | in-del | -/A | 0.375 | 0.216506 | intron-variant | CORO2B | GRCh38.p7 | 15:68721763 | AGGACTCTGTCTCTA[-/A]AACATAAATAAATAA | 10391 |
rs71209395 | multinucleotide-polymorphism | CT/TC | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68688931 | AGGGTGTCCATGCCC[CT/TC]CTCCTGGGGCTGGGG | 10391 |
rs71282000 | in-del | -/CATAAAT | 0.198634 | 0.244666 | intron-variant | CORO2B | GRCh38.p7 | 15:68721761 | GACTCTGTCTCTAAA[-/CATAAAT]ATAAATAAATAAATA | 10391 |
rs71402207 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68558329 | ACCCTGAATGGCTGG[A/G]AAGGTGGGGTTGGAG | 10391 |
rs71402208 | snp | A/T | 0.0479149 | 0.147179 | intron-variant | CORO2B | GRCh38.p7 | 15:68559341 | GTTTGGGACTCTCTC[A/T]TTCCCGGAGAATTAA | 10391 |
rs71402209 | snp | C/T | 0.0414363 | 0.137845 | intron-variant | CORO2B | GRCh38.p7 | 15:68564699 | GAGTCATTGTAAAGA[C/T]AAAGAAATGGAACCT | 10391 |
rs71402210 | snp | G/T | 0.0551013 | 0.156571 | intron-variant | CORO2B | GRCh38.p7 | 15:68566292 | TATCCCCATTTGATA[G/T]GAGAGGAAACAGGCC | 10391 |
rs71402211 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68569909 | CCTCCCACTCCACCT[C/T]CTTCTCACACACATA | 10391 |
rs71402212 | snp | G/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68570797 | CAGGCCCACTACACG[G/T]AGTTTTTTTTTTTTT | 10391 |
rs71402213 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68576875 | GCCCAGGGGTACACA[A/G]TGAGAGAAGGCATGC | 10391 |
rs71402214 | snp | A/G | 0.180383 | 0.240111 | intron-variant | CORO2B | GRCh38.p7 | 15:68584107 | GGGATCCAGGACCTT[A/G]GAGGAGAAGGACATG | 10391 |
rs71402215 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68587362 | GGCTCTGGCTGCCCA[A/G]AGCGGTGGTGTGTGG | 10391 |
rs71402216 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68590232 | AACAAAGCTGCCCCT[C/T]TGCACCACCGCCCCC | 10391 |
rs71402276 | snp | A/G | 0.317692 | 0.240661 | intron-variant | CORO2B | GRCh38.p7 | 15:68591641 | GGGGAAGGGGTTTCT[A/G]AGCCCCTAGCCCAGA | 10391 |
rs71402277 | snp | A/G | 0.375 | 0.216506 | intron-variant | CORO2B | GRCh38.p7 | 15:68594472 | GGAAGGTGCTATCTT[A/G]TATCTCCCATGGCCT | 10391 |
rs71402278 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CORO2B | GRCh38.p7 | 15:68596814 | AGATCCACAAACCCA[C/T]GGGGAGAAATGGCCG | 10391 |
rs71402279 | snp | A/C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2B | GRCh38.p7 | 15:68605762 | GAGTCTCGCTGTGTC[A/C/G]CCCAGGCGGGAGTGC | 10391 |
rs71402280 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68606093 | AGTCATGGTGGCAGA[A/G]AAGCAGATTGGGGTG | 10391 |
rs71402281 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68606116 | TTGGGGTGGGGAGAA[A/G]ACCAGTAGTTTAGCT | 10391 |
rs71402282 | snp | C/T | 0.18134 | 0.240387 | intron-variant | CORO2B | GRCh38.p7 | 15:68648070 | GGGCATGGTGGCTCA[C/T]GCCTATAATCCCAGC | 10391 |
rs71402283 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68655620 | CCACACTCACATCTC[C/T]TAAGGTGTCGATGAT | 10391 |
rs71402284 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68668218 | GGTCAGCGAGAGGGC[C/T]TAGGTCATCTGCCCC | 10391 |
rs71402285 | snp | A/G | 0.226779 | 0.248919 | intron-variant | CORO2B | GRCh38.p7 | 15:68711449 | GGCCCTGCATGGGGC[A/G]CTTCTCCCAGGGCAG | 10391 |
rs71402286 | snp | A/C | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68724666 | TAAGTTTTTATAGAA[A/C]CAACAACTCTCTTTT | 10391 |
rs71455594 | in-del | -/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68561216 | GGGGGAGGGGCTGGG[-/G]AGAGGGCTGGGCTGG | 10391 |
rs71455596 | in-del | -/TA | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68565545 | ATATATATATATATA[-/TA]TTTATAAAGCTCAAC | 10391 |
rs71455598 | in-del | -/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68593672 | TTTGTTTTTTTTTTT[-/T]GCAACTCTGAAAAGA | 10391 |
rs71455600 | in-del | -/AGCA | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68669188 | AAAAGAAAGAAAGGA[-/AGCA]AGCAAGCAAGCAAGC | 10391 |
rs71667563 | in-del | -/AC | | | intron-variant | CORO2B | GRCh38.p7 | 15:68704040 | TCTCTACACACACAT[-/AC]ACACACACACACACA | 10391 |
rs71905785 | in-del | -/GTTT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68693849 | TTTGTTTGTTTGTTT[-/GTTT]TGAGACAGAGTCTTG | 10391 |
rs71911400 | in-del | -/TT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68570800 | CCCACTACACGTAGT[-/TT]TTTTTTTTTTTTTTT | 10391 |
rs72013905 | in-del | -/CCT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68575445 | AAGTTCAAGCAATTC[-/CCT]TGCCTCAGCCTCCTG | 10391 |
rs72265225 | in-del | -/TT | | | intron-variant | CORO2B | GRCh38.p7 | 15:68560306 | TCTTTATTTTTTTTT[-/TT]CTTCTGAGACAGGTT | 10391 |
rs72283325 | in-del | -/TTTG | 0.144546 | 0.22667 | intron-variant | CORO2B | GRCh38.p7 | 15:68693826 | CAGATCTGGTTGTGA[-/TTTG]TTTGTTTGTTTGTTT | 10391 |
rs72284382 | in-del | -/CTGGG | 0.234982 | 0.249549 | intron-variant | CORO2B | GRCh38.p7 | 15:68670406 | TGATCTCTTGAAATC[-/CTGGG]CTCAAGTGATCCTCC | 10391 |
rs72376399 | in-del | -/TA | | | intron-variant | CORO2B | GRCh38.p7 | 15:68565536 | TAAAAATAAATATAT[-/TA]ATATATATATTTATA | 10391 |
rs72625781 | snp | A/C | 0.0240643 | 0.107019 | intron-variant | CORO2B | GRCh38.p7 | 15:68683563 | TACAGTTTTGGTGCA[A/C]CACCCCTCCCCCCAC | 10391 |
rs72625782 | snp | C/T | 0.237303 | 0.249677 | intron-variant | CORO2B | GRCh38.p7 | 15:68696886 | GCCACAAGCATCTAC[C/T]TGGTGCTCACTGGCA | 10391 |
rs72746565 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | CORO2B | GRCh38.p7 | 15:68564277 | GCTGTTAATGTGATT[A/G]CTTGGAGAATAATTT | 10391 |
rs72746585 | snp | G/T | 0.0376037 | 0.131863 | intron-variant | CORO2B | GRCh38.p7 | 15:68601932 | TTGGCAAGAGCTGCA[G/T]CCTCCAGAGGGGGAG | 10391 |
rs72746589 | snp | A/C | 0.039522 | 0.134904 | intron-variant | CORO2B | GRCh38.p7 | 15:68606879 | AGCTGTTTCACAGGG[A/C]AGGCACTTCGTAGGT | 10391 |
rs72746591 | snp | A/C | 0.17654 | 0.238964 | intron-variant | CORO2B | GRCh38.p7 | 15:68612387 | GAGGAGGTGTGCGTG[A/C]GAAGGGGCAGAGAAA | 10391 |
rs72746595 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | CORO2B | GRCh38.p7 | 15:68618526 | TCAAAGGCTGGGAGG[C/T]GTGAGTGCGCAGCTG | 10391 |
rs72746597 | snp | A/G | 0.0741063 | 0.177655 | intron-variant | CORO2B | GRCh38.p7 | 15:68619539 | CTGTTGGAGCTGGAA[A/G]TGTTCCAAATGGCTC | 10391 |
rs72746598 | snp | C/T | 0.0752113 | 0.178743 | intron-variant | CORO2B | GRCh38.p7 | 15:68622204 | TGCTCGGTACATTCA[C/T]GACAATTGTGGCAAT | 10391 |
rs72746601 | snp | A/G | 0.0119091 | 0.0762411 | intron-variant | CORO2B | GRCh38.p7 | 15:68628391 | GGGGAAGATAATAGC[A/G]CCTGCCTCACTGGGT | 10391 |
rs72748505 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CORO2B | GRCh38.p7 | 15:68633446 | TTTCTGCTCTAGTTT[C/T]TAGACCCTCAGCTGG | 10391 |
rs72748507 | snp | A/G | 0.102014 | 0.201495 | intron-variant | CORO2B | GRCh38.p7 | 15:68636620 | GCCCTGTGAGTTGGT[A/G]GGAGAACTGTCCTGG | 10391 |
rs72748517 | snp | A/G | 0.0520825 | 0.152737 | intron-variant | CORO2B | GRCh38.p7 | 15:68641608 | AGTGTGGACTTTGCC[A/G]GGTGGGCTCAGGAGA | 10391 |
rs72748520 | snp | A/G | 0.029116 | 0.117091 | intron-variant | CORO2B | GRCh38.p7 | 15:68647372 | CTGTGAAGAATATAT[A/G]AAGAGTTCCAGAAAA | 10391 |
rs72748523 | snp | C/T | 0.0130921 | 0.0798413 | intron-variant | CORO2B | GRCh38.p7 | 15:68651687 | TCTCTAAGTTTTTTC[C/T]CTCCACTATCCAGCA | 10391 |
rs72748524 | snp | A/G | 0.0310518 | 0.120672 | intron-variant | CORO2B | GRCh38.p7 | 15:68653912 | TGCAGTGAGGTCTCC[A/G]CCCCTCCAAGGGAAT | 10391 |
rs72748534 | snp | C/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68660989 | GTCTTTTTTTTTTTT[C/T]TGTTTTTTGAGACAG | 10391 |
rs72748537 | snp | A/G | 0.214541 | 0.247473 | intron-variant | CORO2B | GRCh38.p7 | 15:68661533 | TTCCCTTCAAGACTT[A/G]GGAGTTAGCAGCTTT | 10391 |
rs72748554 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | CORO2B | GRCh38.p7 | 15:68672776 | AGGCAGCAAACCAGG[A/C]CCCTTAGGTTATGAG | 10391 |
rs72748570 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68685769 | TTTAATTGTTTGATT[A/G]ATTAAACACTTTATT | 10391 |
rs72748595 | snp | C/G | 0.00597247 | 0.0543191 | intron-variant | CORO2B | GRCh38.p7 | 15:68707258 | CAGATGGGTAAAAAT[C/G]CAGTTTTTTAAAGGT | 10391 |
rs72750311 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | CORO2B | GRCh38.p7 | 15:68719970 | TGGAAGAGACTGGGT[A/G]TTTATGAAGGTGCTC | 10391 |
rs72750316 | snp | C/G | 0.201727 | 0.245295 | intron-variant | CORO2B | GRCh38.p7 | 15:68720532 | GAATCACATCTGAAG[C/G]CTCAACTTCCAAGTT | 10391 |
rs73425104 | snp | A/T | 0.0182019 | 0.0936463 | intron-variant | CORO2B | GRCh38.p7 | 15:68635664 | CCTTGAAAGCCTTTT[A/T]GTGTCAGGACCACAT | 10391 |
rs73425106 | snp | C/T | 0.0217236 | 0.101931 | intron-variant | CORO2B | GRCh38.p7 | 15:68636697 | AGTGACTCCAGATCA[C/T]GGCCTTCCTAAGTCC | 10391 |
rs73425118 | snp | C/T | 0.0479149 | 0.147179 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68640758 | TTTGTAGGAAATGCA[C/T]GCTGAAGTAATGAGG | 10391 |
rs73425136 | snp | C/G | 0.0205511 | 0.0992634 | intron-variant | CORO2B | GRCh38.p7 | 15:68654280 | TGGATTTGGAGTCCA[C/G]GGGGCCAGAGATGCA | 10391 |
rs73425142 | snp | C/T | 0.0138799 | 0.0821421 | intron-variant | CORO2B | GRCh38.p7 | 15:68655476 | ATCATAGATTCCAAG[C/T]GCCTTGTTGTGCCCA | 10391 |
rs73425151 | snp | A/G | 0.0341408 | 0.126114 | intron-variant | CORO2B | GRCh38.p7 | 15:68660005 | TGCTGTCAGAGGTGG[A/G]AGTGGTGGTGGAGGT | 10391 |
rs73425186 | snp | A/G | 0.0437281 | 0.141251 | intron-variant | CORO2B | GRCh38.p7 | 15:68680634 | ATTCCAGACACTGGG[A/G]TTATAGCAGAGGACA | 10391 |
rs73425191 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CORO2B | GRCh38.p7 | 15:68684069 | AACAGTGTGTAAGGT[A/G]GATTGGAGAGAGAAC | 10391 |
rs73425197 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | CORO2B | GRCh38.p7 | 15:68688485 | GATCTGGGATGCTCA[A/G]CCAGTAAGTAAAATG | 10391 |
rs73427125 | snp | A/G | 0.438806 | 0.163867 | intron-variant | CORO2B | GRCh38.p7 | 15:68692548 | CAAGATCACACCACT[A/G]CACTCCAGCCTGGGC | 10391 |
rs73427180 | snp | G/T | 0.0111196 | 0.0737302 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68726214 | CCTGCCACCCCAGGA[G/T]CCAGGCTTCCCCTCA | 10391 |
rs73440271 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | CORO2B | GRCh38.p7 | 15:68557759 | TGGCAATGCCAGGAC[C/G]TAAACCCAGGCAGCC | 10391 |
rs73440273 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CORO2B | GRCh38.p7 | 15:68562455 | CCAGAGTATAGGGCT[C/T]ATGTCTTTACATTCT | 10391 |
rs73440278 | snp | A/G | 0.0905309 | 0.192535 | intron-variant | CORO2B | GRCh38.p7 | 15:68563207 | TTAGAGTAGAGACTG[A/G]CCAGGCACCATGGCT | 10391 |
rs73440281 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO2B | GRCh38.p7 | 15:68563784 | AACTAGATGAAATCC[A/G]CAAATTCCTAGAAAG | 10391 |
rs73440287 | snp | C/T | 0.0678174 | 0.1712 | intron-variant | CORO2B | GRCh38.p7 | 15:68574966 | GAACTAATACTGCAA[C/T]GTCTTATTTACCCCA | 10391 |
rs73440291 | snp | G/T | 0.0287284 | 0.116357 | intron-variant | CORO2B | GRCh38.p7 | 15:68579437 | CGCTCGAGTCACTCC[G/T]GCCCCCAAGGACTGC | 10391 |
rs73440295 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | CORO2B | GRCh38.p7 | 15:68585825 | GGGGAAGGGTGCTGG[A/G]GGAGGAGGGTGTCCT | 10391 |
rs73440301 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | CORO2B | GRCh38.p7 | 15:68588564 | CCTGGGTCCCTGGGC[A/G]GAAAGACCAGGTTCC | 10391 |
rs73442209 | snp | A/C | 0.0217236 | 0.101931 | intron-variant | CORO2B | GRCh38.p7 | 15:68598068 | CTCCACCTTTTCTTC[A/C]GATCCAGACCCCCTC | 10391 |
rs73442210 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CORO2B | GRCh38.p7 | 15:68599469 | CTATTCTGTGCATGC[A/G]TCATAGCTTCAGCCA | 10391 |
rs73442212 | snp | G/T | 0.0513262 | 0.151752 | intron-variant | CORO2B | GRCh38.p7 | 15:68599541 | ATAAAGCCACCCAAC[G/T]CTGTCCCCACAAGGG | 10391 |
rs73442220 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | CORO2B | GRCh38.p7 | 15:68603183 | CCACTGTGTCTTACA[C/T]GCCATGGAAGTCCCA | 10391 |
rs73442221 | snp | C/T | 0.152334 | 0.230133 | intron-variant | CORO2B | GRCh38.p7 | 15:68603292 | AATTGAATGAATGAA[C/T]GAGTGGATGGATGGG | 10391 |
rs73442226 | snp | A/G | 0.0752113 | 0.178743 | intron-variant | CORO2B | GRCh38.p7 | 15:68610260 | TCATAGGACGAGACA[A/G]GTTCTCTAGCGCCTC | 10391 |
rs73442227 | snp | A/G | 0.077417 | 0.180873 | intron-variant | CORO2B | GRCh38.p7 | 15:68626572 | GGCTGACACAGATGC[A/G]GGACTCCCAGCCTTT | 10391 |
rs73442228 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | CORO2B | GRCh38.p7 | 15:68627681 | GAGATGTAAGCAGGA[A/G]ATGGCTTCTGCCCTG | 10391 |
rs73442232 | snp | A/G | 0.0792508 | 0.182605 | intron-variant | CORO2B | GRCh38.p7 | 15:68629677 | TCAGGGGACCAGCAG[A/G]AGGGTCAGTGACACG | 10391 |
rs73442234 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68631334 | CCCATTTTTATAGAT[A/G]AGAACTCGAGCTCCA | 10391 |
rs74020235 | snp | A/G | 0.0138799 | 0.0821421 | intron-variant | CORO2B | GRCh38.p7 | 15:68560039 | GCCAGCCCAGCAGGG[A/G]GATCCCGGTGGAGAC | 10391 |
rs74020237 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | CORO2B | GRCh38.p7 | 15:68575061 | AAAGAGCCCAGACTT[C/G]AGCTGACAGCATCCC | 10391 |
rs74020240 | snp | A/G | 0.0763149 | 0.179815 | intron-variant | CORO2B | GRCh38.p7 | 15:68580704 | TCAGCTGGGAGGGAT[A/G]TTAAGGTTATTAATG | 10391 |
rs74020241 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | CORO2B | GRCh38.p7 | 15:68580868 | CATGCAGCCTTCCTT[C/T]CCTGGAGGCCTGCAA | 10391 |
rs74020242 | snp | C/T | 0.102014 | 0.201495 | intron-variant | CORO2B | GRCh38.p7 | 15:68582915 | GCTCAGGGGGGTCAG[C/T]GGTCCAGGAGCAAAG | 10391 |
rs74020251 | snp | A/C | 0.0905309 | 0.192535 | intron-variant | CORO2B | GRCh38.p7 | 15:68606200 | TCAAAAAAGAGGCCT[A/C]GACCAGGAGTGGGAA | 10391 |
rs74020252 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | CORO2B | GRCh38.p7 | 15:68612423 | GACAGAGAAAAGGAG[A/T]ATGAGAAATGTCCAA | 10391 |
rs74020253 | snp | C/G | 0.0596104 | 0.162024 | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68615595 | GCCCTTGGGGTGATT[C/G]GTCATTAACCAGTCA | 10391 |
rs74020254 | snp | A/G | 0.0766824 | 0.180169 | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68615890 | GGACTGAGACAAGAA[A/G]GAAGATCATAGCCTT | 10391 |
rs74020255 | snp | C/T | 0.0807149 | 0.183963 | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68615945 | TAGAGACATAAACTT[C/T]GCCCAGATGAGCAGG | 10391 |
rs74020256 | snp | G/T | 0.0763149 | 0.179815 | utr-variant-5-prime, intron-variant | CORO2B | GRCh38.p7 | 15:68616563 | CGCCTGCTGGGTGCC[G/T]TGGGCCATTGTGCAA | 10391 |
rs74020257 | snp | C/T | 0.078151 | 0.181571 | intron-variant | CORO2B | GRCh38.p7 | 15:68616706 | CGAGGGCTAGCGTTA[C/T]CAAGGGCCCCGAGAG | 10391 |
rs74020258 | snp | A/G | 0.0479149 | 0.147179 | intron-variant | CORO2B | GRCh38.p7 | 15:68626763 | TACTTATGAAAAAAC[A/G]TCTCCACAGGTGAAG | 10391 |
rs74020259 | snp | C/T | 0.184203 | 0.241186 | intron-variant | CORO2B | GRCh38.p7 | 15:68634244 | CACTTGGTGTTTGCA[C/T]GATCTTGTGCATGAC | 10391 |
rs74020260 | snp | C/T | 0.0221141 | 0.102801 | intron-variant | CORO2B | GRCh38.p7 | 15:68642759 | GGCGCCGGCTGTCTG[C/T]GGATTCTGAGAAGGT | 10391 |
rs74020261 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68645720 | TCTTGGTTTGGAGCC[A/G]GAAGGGATGAAGACC | 10391 |
rs74020263 | snp | C/G | 0.0622301 | 0.165053 | intron-variant | CORO2B | GRCh38.p7 | 15:68654771 | GTGATGCCAAGGACT[C/G]TTACCCATCTCCAGG | 10391 |
rs74020264 | snp | G/T | 0.180064 | 0.240019 | intron-variant | CORO2B | GRCh38.p7 | 15:68664052 | CTGGAACTCTCATAC[G/T]ACACTGCTGGGAGTG | 10391 |
rs74020265 | snp | G/T | 0.0741367 | 0.177809 | intron-variant | CORO2B | GRCh38.p7 | 15:68665657 | AAAAGCTTCTTCACA[G/T]AGCTCTTATTCATTT | 10391 |
rs74020268 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CORO2B | GRCh38.p7 | 15:68666324 | AGTTCCCTTTCCAAG[A/G]TGTCACGAGGTGTCA | 10391 |
rs74020269 | snp | C/T | 0.126564 | 0.217402 | intron-variant | CORO2B | GRCh38.p7 | 15:68666798 | CTACACTATTGCAAT[C/T]ACTGCACTGAGTCCC | 10391 |
rs74020270 | snp | A/G | 0.0387552 | 0.1337 | intron-variant | CORO2B | GRCh38.p7 | 15:68667514 | GACAGGGATCTTTTC[A/G]GACAGAGAAATCTTT | 10391 |
rs74020271 | snp | A/G | 0.170408 | 0.236992 | intron-variant | CORO2B | GRCh38.p7 | 15:68677157 | CTCCCTCTCCTCCAA[A/G]CCATCTGTCAGTGCT | 10391 |
rs74020273 | snp | A/G | 0.18134 | 0.240387 | intron-variant | CORO2B | GRCh38.p7 | 15:68678117 | CTTGACTTTCCCCCC[A/G]GATGACTTGTACAGC | 10391 |
rs74020274 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | CORO2B | GRCh38.p7 | 15:68679923 | CTTACATATCCCTGA[C/T]GGAGCAAGGCTGAAG | 10391 |
rs74020277 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | CORO2B | GRCh38.p7 | 15:68693130 | GCCTCTGAGGCTTTT[C/T]TCCCCCTCTCTTTCT | 10391 |
rs74020278 | snp | A/C | 0.0607341 | 0.163335 | intron-variant | CORO2B | GRCh38.p7 | 15:68697010 | TCCTGGGAGCAGAGA[A/C]CACAGCCTATTTGGT | 10391 |
rs74020279 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68700086 | CCAGGGCCCTTCCCA[C/T]GGCCTCCCTGCCTCC | 10391 |
rs74020280 | snp | G/T | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68700204 | ATCCAGACCCAGGCT[G/T]GGGAGGTCAGTCGGC | 10391 |
rs74020281 | snp | C/T | 0.0966517 | 0.197444 | intron-variant | CORO2B | GRCh38.p7 | 15:68703615 | TCTATACCATATATA[C/T]AGACAGTGGGTACTG | 10391 |
rs74020283 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | CORO2B | GRCh38.p7 | 15:68706015 | AACCCAGAGATGCCT[C/T]AGTTACTGGGTTGCT | 10391 |
rs74020284 | snp | A/G | 0.118584 | 0.212673 | intron-variant | CORO2B | GRCh38.p7 | 15:68709110 | TTACACTGCTTCTAC[A/G]TTTTCCATATAAATG | 10391 |
rs74020287 | snp | C/T | 0.119978 | 0.213528 | intron-variant | CORO2B | GRCh38.p7 | 15:68711031 | CATTCATTCGCTACA[C/T]GCAACTGAGCAACTC | 10391 |
rs74020288 | snp | G/T | 0.0310518 | 0.120672 | intron-variant | CORO2B | GRCh38.p7 | 15:68711291 | ACCTGACAAGGAACA[G/T]GTATCCTTCTTGCTC | 10391 |
rs74020290 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CORO2B | GRCh38.p7 | 15:68712131 | TGGTGAACTTAGCTC[C/T]ACTTTTGGTCTTTGA | 10391 |
rs74020293 | snp | A/G | 0.0283406 | 0.115616 | intron-variant | CORO2B | GRCh38.p7 | 15:68717981 | CTGGAAGCTCAGAGA[A/G]TTGTAACTTGCCAAA | 10391 |
rs74020298 | snp | C/T | 0.0283406 | 0.115616 | intron-variant | CORO2B | GRCh38.p7 | 15:68718311 | GATGACTGTTCATTT[C/T]AGAGGGTAATGGGCT | 10391 |
rs74020302 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | CORO2B | GRCh38.p7 | 15:68722429 | GCTGTCAAAGGTGGA[C/T]GCATTGATCTAAGTG | 10391 |
rs74022703 | snp | A/G | 0.0383715 | 0.133092 | intron-variant | CORO2B | GRCh38.p7 | 15:68724445 | TCTCATCTTTTTTTG[A/G]GACATTGAGGTATAA | 10391 |
rs74022705 | snp | C/T | 0.136847 | 0.222927 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68726340 | AACTTGGACTTTTCC[C/T]CTGTGAAGGGGGCTG | 10391 |
rs74022706 | snp | C/T | 0.0158469 | 0.0875917 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68727192 | CCACAGCCACTCGCA[C/T]CCGTATAGCACTTTA | 10391 |
rs74246053 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68685762 | ATTGATATTTAATTG[A/T]TTGATTGATTAAACA | 10391 |
rs74320050 | snp | A/C | 0.0452528 | 0.143452 | intron-variant | CORO2B | GRCh38.p7 | 15:68721834 | CTCACTATAACCTCA[A/C]TCTCCGAGGCTCAAG | 10391 |
rs74351792 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | CORO2B | GRCh38.p7 | 15:68668648 | GTAGTCAGGGGCTGG[A/G]CTACCCAGAACCTTG | 10391 |
rs74366374 | snp | A/T | 0.0463947 | 0.145069 | intron-variant | CORO2B | GRCh38.p7 | 15:68674193 | CCCTCTGCTGGTGGA[A/T]TGCTGGTAGCACAGC | 10391 |
rs74373830 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | CORO2B | GRCh38.p7 | 15:68633627 | TGAGGCCTGGTATCT[A/G]TTTCTTTATGGGCAA | 10391 |
rs74378110 | in-del | -/CC | 0.232651 | 0.249397 | intron-variant | CORO2B | GRCh38.p7 | 15:68689121 | AGTTCTGTCCCAGCA[-/CC]AAGAAGGGCTGGACT | 10391 |
rs74387184 | snp | C/T | 0.000399281 | 0.0141238 | utr-variant-3-prime | CORO2B | GRCh38.p7 | 15:68727532 | TGCTTTTCCCATGGC[C/T]GCCCTACGGAAAATC | 10391 |
rs74387979 | snp | C/T | 0.0383715 | 0.133092 | intron-variant | CORO2B | GRCh38.p7 | 15:68676663 | CTCTGTGCTAGCATG[C/T]GCACACCGCAGCCAC | 10391 |
rs74392146 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68620878 | TTTCTCTGATGAAAT[C/T]CCCCAACAAAGGGTA | 10391 |
rs74420884 | snp | A/G | 0.0372196 | 0.131242 | intron-variant | CORO2B | GRCh38.p7 | 15:68670807 | ATATTATAATATTGG[A/G]TGCTGTCAGGGTTAT | 10391 |
rs74474124 | snp | A/C | 0.0810805 | 0.184299 | intron-variant | CORO2B | GRCh38.p7 | 15:68685132 | CCTTTACATGCTCAT[A/C]ACCTAATGTGACTTC | 10391 |
rs74479346 | snp | C/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68669187 | AGAAAAGAAAGAAAG[C/G]AAGCAAGCAAGCAAG | 10391 |
rs74489259 | snp | A/C | 0.0138799 | 0.0821421 | intron-variant | CORO2B | GRCh38.p7 | 15:68576667 | GAAAGGTCTTGAGCT[A/C]CATCCTTCTGGCTAG | 10391 |
rs74494119 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68639931 | GGGCAGGGCTTTAAG[A/G]GTAAAGGCAAAGGGC | 10391 |
rs74504286 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CORO2B | GRCh38.p7 | 15:68621152 | GTAGGGACCCTCAAG[A/G]CCATAAGCAATGTAG | 10391 |
rs74507300 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | CORO2B | GRCh38.p7 | 15:68607886 | AAGAGAGGTCAGACC[A/G]GGACTCCAGGAACAG | 10391 |
rs74522910 | snp | C/T | 0.0763149 | 0.179815 | intron-variant | CORO2B | GRCh38.p7 | 15:68649099 | ACAAAATGTTTTACA[C/T]TGTCAGTAGCACTGG | 10391 |
rs74561301 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | CORO2B | GRCh38.p7 | 15:68562126 | CCATGCCTCCATGGC[A/G]TCTGTCAGGGCAGTC | 10391 |
rs74565910 | snp | C/T | 0.0193772 | 0.0965046 | intron-variant | CORO2B | GRCh38.p7 | 15:68656563 | TCCTGGCAGCAAATG[C/T]TTCAGAACCATCCCA | 10391 |
rs74577255 | snp | A/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68662042 | AATTAATTAATTAAT[A/T]AAAATCTGTTTAGGC | 10391 |
rs74578188 | snp | C/T | 0.0372196 | 0.131242 | intron-variant | CORO2B | GRCh38.p7 | 15:68670834 | TTATAGGGAAATGGC[C/T]ATTCTCTTGAGTTGC | 10391 |
rs74627635 | snp | C/G | 0.0505692 | 0.150756 | intron-variant | CORO2B | GRCh38.p7 | 15:68568110 | CAATGGGGCCACCCC[C/G]TGGGGTTCCTTGTAG | 10391 |
rs74638951 | snp | A/G | 0.0174175 | 0.0916809 | intron-variant | CORO2B | GRCh38.p7 | 15:68609733 | AAAGGCATGAAAGCT[A/G]CTGATGGAAGGCCGT | 10391 |
rs74685292 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CORO2B | GRCh38.p7 | 15:68561958 | AATGTGGATGAGTAG[A/G]GGGAGGGCTGTAAGT | 10391 |
rs74779842 | snp | C/T | 0.0524604 | 0.153226 | intron-variant | CORO2B | GRCh38.p7 | 15:68702290 | TGCAAGGACAGTCTT[C/T]AGTAGTCATAATAAT | 10391 |
rs74802685 | snp | C/G | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68691580 | CAGTGAGCCGAGATC[C/G]CGCCACTGCACTCCA | 10391 |
rs74823898 | snp | C/T | 0.095934 | 0.196885 | intron-variant | CORO2B | GRCh38.p7 | 15:68691735 | TCCCGAGTGCAGGGC[C/T]CTGGCCACTCCTTCT | 10391 |
rs74858155 | snp | C/T | 0.103082 | 0.202275 | intron-variant | CORO2B | GRCh38.p7 | 15:68647262 | TAAATTTTTAAAAGA[C/T]AGTTTCTGTATTACA | 10391 |
rs74861322 | snp | G/T | 0.00795532 | 0.062565 | intron-variant | CORO2B | GRCh38.p7 | 15:68604419 | ACCCTATTAACAAGG[G/T]CAAAGATTGCCATCA | 10391 |
rs74920623 | snp | A/G | 0.181978 | 0.240568 | intron-variant | CORO2B | GRCh38.p7 | 15:68677389 | GACAGGGATAGGGCT[A/G]GCTGAAGGCCACACA | 10391 |
rs74932067 | in-del | -/AA | | | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68640524 | TTTAAAAAAAAAAAA[-/AA]GGTGATAGGAGTATT | 10391 |
rs74938652 | snp | A/G | 0.00993419 | 0.0697739 | intron-variant | CORO2B | GRCh38.p7 | 15:68659900 | GGCCTGGGTGACAGA[A/G]CGAGACTGTGTTTCA | 10391 |
rs74958246 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | CORO2B | GRCh38.p7 | 15:68634604 | ACCAAAGTCTGGTTC[C/G]GGGACCAATAGCTTC | 10391 |
rs74959008 | snp | C/T | 0.031825 | 0.122064 | intron-variant | CORO2B | GRCh38.p7 | 15:68655358 | TGAGCCAGGCTGAAG[C/T]CACACAGTCCTCACA | 10391 |
rs74969906 | snp | A/G | 0.0569829 | 0.158885 | intron-variant | CORO2B | GRCh38.p7 | 15:68608643 | AACATACTCCCCTCT[A/G]CTTCCCAGTTCCTCC | 10391 |
rs74996862 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68569016 | AAGCACATAAAAAAA[A/G]GAAGAAAAATACACT | 10391 |
rs75030787 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68709718 | AGTGTCCTAAATTAT[A/T]GTCACATGTGCTCTT | 10391 |
rs75031317 | snp | A/C | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68597628 | TGTTTCCCCCCCATC[A/C]AAAAAAAAAAAATAA | 10391 |
rs75046358 | snp | C/T | 0.0962929 | 0.197165 | intron-variant | CORO2B | GRCh38.p7 | 15:68702868 | GTCTCACTTTGGCAC[C/T]CAGGCTGGAGTGCTG | 10391 |
rs75089413 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | CORO2B | GRCh38.p7 | 15:68598213 | CCCTGGAGAAGAGGG[C/T]GGGCAGTCTGGCTGG | 10391 |
rs75090907 | snp | C/T | 0.448066 | 0.152544 | intron-variant | CORO2B | GRCh38.p7 | 15:68580398 | GTCAGAGCAGTGGGG[C/T]CAGATGGAGGGTTGG | 10391 |
rs75124251 | snp | A/G | 0.118235 | 0.212457 | intron-variant | CORO2B | GRCh38.p7 | 15:68659981 | AGGAGGAAGAAGAGG[A/G]GTTGGCATTGCTGTC | 10391 |
rs75132545 | snp | A/T | | | intron-variant | CORO2B | GRCh38.p7 | 15:68653757 | GTAATAAAATAATAT[A/T]TTGTTTGCTTACCCA | 10391 |
rs75139775 | snp | A/G | 0.0494327 | 0.149241 | intron-variant | CORO2B | GRCh38.p7 | 15:68692102 | GTAGGGTTCAAGAAC[A/G]CTCGCTTTTGAGAAT | 10391 |
rs75147567 | snp | A/G | 0.0919752 | 0.193722 | intron-variant | CORO2B | GRCh38.p7 | 15:68634851 | CTCATTTGAGTCAAG[A/G]GTGGGGCCTGGGATT | 10391 |
rs75169384 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | CORO2B | GRCh38.p7 | 15:68676394 | TTAGCCTTTAATTTC[C/T]GGGGGCCAATCTAGC | 10391 |
rs75172368 | snp | C/T | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68585654 | CCACCAACCCCCCAC[C/T]TACAACACAGTGGGC | 10391 |
rs75174817 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68576578 | CAAGTCACAGCCATG[A/G]GTGCAGGGTGACTGG | 10391 |
rs75188236 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CORO2B | GRCh38.p7 | 15:68607384 | ACATGATGACTTGGG[A/G]CTCCAGGAGCAAGTG | 10391 |
rs75224080 | snp | C/G | 0.0209421 | 0.100162 | intron-variant | CORO2B | GRCh38.p7 | 15:68561909 | TGTGAGCATGACCGT[C/G]AGTGTGTGTTGTGAG | 10391 |
rs75224639 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | CORO2B | GRCh38.p7 | 15:68628707 | GACAAATGGGGCCCC[A/G]AAAGGTAGATCCACT | 10391 |
rs75244597 | snp | A/G | 0.0535932 | 0.154675 | intron-variant | CORO2B | GRCh38.p7 | 15:68572553 | TTATCATGTAAATCC[A/G]TGGTTCTCAAACTGG | 10391 |
rs75268529 | snp | C/T | 0 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68691351 | AAAAAAAAGGCCGGG[C/T]GCGGTGGCTCACGCC | 10391 |
rs75284722 | snp | A/C | 0.00398564 | 0.0444627 | intron-variant | CORO2B | GRCh38.p7 | 15:68599716 | GCAGTGCCCTGGTGA[A/C]CTCATGACAGTAGTG | 10391 |
rs75316114 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68571724 | AGTACAGCTGTAACC[A/G]GTAACCTGGGAGATA | 10391 |
rs75366659 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant, upstream-variant-2KB | CORO2B | GRCh38.p7 | 15:68630113 | TCCATTACCTCGTTT[C/T]CCTCTCCACCCCTCT | 10391 |
rs75390190 | snp | C/T | 0.0158469 | 0.0875917 | intron-variant | CORO2B | GRCh38.p7 | 15:68625256 | TAGAATGGAGACAAA[C/T]GTGTCTTCAGCTAAT | 10391 |
rs75419226 | snp | C/T | 0.0146672 | 0.084371 | intron-variant | CORO2B | GRCh38.p7 | 15:68599208 | AAAGTGCGACCTCCT[C/T]CACAGAGCCTTCTCT | 10391 |
rs75420806 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | CORO2B | GRCh38.p7 | 15:68624272 | CAGTCCCAGCTGCTC[A/G]GGAGGCTGAGGCAGG | 10391 |
rs75435184 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68558221 | CGGGGCTGGTGAGCC[C/T]CCAAGGCATCAAACA | 10391 |
rs75453902 | snp | C/T | 0.0379877 | 0.132479 | intron-variant | CORO2B | GRCh38.p7 | 15:68680071 | CCCGCAGAGTGTGCA[C/T]GCTCTTGGTGGATGG | 10391 |
rs75527157 | snp | C/T | 0.021333 | 0.101051 | upstream-variant-2KB, intron-variant | CORO2B | GRCh38.p7 | 15:68616203 | CTGTCGGGGATATGG[C/T]TAATCAGAATTATCA | 10391 |
rs75546133 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | CORO2B | GRCh38.p7 | 15:68623271 | CGGCTCTTTTAAGCC[C/T]GGGCCCATGCTGCCT | 10391 |
rs75547593 | snp | G/T | 0.00199481 | 0.0315187 | intron-variant | CORO2B | GRCh38.p7 | 15:68718464 | TCTAAAGGGTCCAAT[G/T]CTAAAGCACGCACTG | 10391 |
rs75559147 | snp | A/G | 0.5 | 0 | intron-variant | CORO2B | GRCh38.p7 | 15:68605119 | ACTCCGTCTCAAGGA[A/G]AAAAAAAAAAAAAGA | 10391 |
rs75581127 | snp | A/G | 0.0217236 | 0.101931 | intron-variant | CORO2B | GRCh38.p7 | 15:68595132 | AACTCTGCAGCATTC[A/G]AGGCCAGAGAACTGG | 10391 |
rs75584912 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | CORO2B | GRCh38.p7 | 15:68571999 | GAACTCCTGAGGGGG[A/G]CAGACACAGAAGAAC | 10391 |
rs75635207 | snp | C/T | 0.0729998 | 0.176553 | intron-variant | CORO2B | GRCh38.p7 | 15:68688324 | GTAGATTGGTTTTTT[C/T]AGATAGGGATCCTTT | 10391 |
rs75636422 | snp | A/T | 0.0115144 | 0.0749975 | intron-variant | CORO2B | GRCh38.p7 | 15:68677519 | CAGCTTTTCTGGGAA[A/T]GGCCAGATGGTGGCG | 10391 |
rs75657868 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | CORO2B | GRCh38.p7 | 15:68591400 | TGCTGGGCTGGAAAT[A/G]GAGGGGCTGTATGTG | 10391 |
rs75690907 | snp | A/T | 0.0279526 | 0.114869 | intron-variant | CORO2B | GRCh38.p7 | 15:68601420 | CGGTAGGCACCGAGG[A/T]TAAAACGGTAAGTGT | 10391 |
rs75695290 | snp | C/G | 0.0232847 | 0.105357 | intron-variant | CORO2B | GRCh38.p7 | 15:68602938 | GTTTTCTTGGGGCAG[C/G]GGGTGGACACACAGC | 10391 |
rs75699447 | snp | A/C | 0.214843 | 0.247516 | intron-variant | CORO2B | GRCh38.p7 | 15:68561389 | CCTCCCTCCCCGACT[A/C]TCCCCTGCCCTCACC | 10391 |