Item | Value |
---|---|
geneid | 84034 |
ensemblid | ENSG00000132205.11 |
hgncid | 19881 |
symbol | EMILIN2 |
name | elastin microfibril interfacer 2 |
refseq_nuc | NM_032048.3 |
refseq_prot | NP_114437.2 |
ensembl_nuc | ENST00000254528.4 |
ensembl_prot | ENSP00000254528.3 |
mane_status | MANE Select |
chr | chr18 |
start | 2847006 |
end | 2916003 |
strand | + |
ver | v1.2 |
region | chr18:2847006-2916003 |
region5000 | chr18:2842006-2921003 |
regionname0 | EMILIN2_chr18_2847006_2916003 |
regionname5000 | EMILIN2_chr18_2842006_2921003 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1053 | 355 | 58 | 66 | 169 | 18 | 42 | 127 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0002 | 0/0 | 1053 | 48 | 9 | 14 | 22 | 0 | 3 | 21 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0003 | 0/0 | 1053 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0004 | 0/0 | 1049 | 7 | 0 | 1 | 5 | 0 | 1 | 5 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1044): Show |
chr18 | 2842006 | 2921003 |
a0005 | 0/0 | 1053 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0006 | 0/0 | 1053 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0007 | 0/0 | 1053 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0008 | 0/0 | 1053 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0009 | 0/0 | 1053 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0010 | 0/0 | 1053 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0011 | 0/0 | 1053 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0012 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0013 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0014 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWHPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0015 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0016 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0017 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0018 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0019 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0020 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0021 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0022 | 0/0 | 1048 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1043): Show |
chr18 | 2842006 | 2921003 |
a0023 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
a0024 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | MWQPR others(1048): Show |
chr18 | 2842006 | 2921003 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3159 | 179 | 34 | 32 | 75 | 13 | 23 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0002 | 0/0 | 3159 | 61 | 2 | 4 | 47 | 1 | 7 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0003 | 0/0 | 3159 | 44 | 1 | 11 | 30 | 0 | 2 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0004 | 0/0 | 3159 | 28 | 7 | 2 | 11 | 1 | 7 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0006 | 0/0 | 3159 | 13 | 0 | 10 | 0 | 1 | 2 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0008 | 0/0 | 3159 | 10 | 3 | 6 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0013 | 0/0 | 3159 | 3 | 3 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0014 | 0/0 | 3159 | 3 | 3 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0015 | 0/0 | 3159 | 3 | 0 | 0 | 3 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0016 | 0/0 | 3159 | 3 | 3 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0023 | 0/0 | 3159 | 2 | 0 | 0 | 0 | 1 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0032 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0033 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0035 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0037 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0041 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0001c0042 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0002c0005 | 0/0 | 3159 | 22 | 5 | 5 | 11 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0002c0007 | 0/0 | 3159 | 12 | 0 | 3 | 8 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0002c0009 | 0/0 | 3159 | 7 | 1 | 3 | 3 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0002c0020 | 0/0 | 3159 | 2 | 1 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0002c0024 | 0/0 | 3159 | 2 | 1 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0002c0025 | 0/0 | 3159 | 2 | 1 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0002c0047 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0003c0010 | 0/0 | 3159 | 6 | 5 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0003c0012 | 0/0 | 3159 | 4 | 3 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0003c0045 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0003c0046 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0004c0011 | 0/0 | 3147 | 5 | 0 | 0 | 4 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3142): Show |
chr18 | 2842006 | 2921003 | ||
a0004c0039 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3142): Show |
chr18 | 2842006 | 2921003 | ||
a0004c0043 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3142): Show |
chr18 | 2842006 | 2921003 | ||
a0005c0021 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0005c0036 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0005c0038 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0006c0026 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0006c0027 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0007c0022 | 0/0 | 3159 | 2 | 0 | 2 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0008c0017 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0009c0018 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0010c0019 | 0/0 | 3159 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0011c0052 | 0/0 | 3159 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0012c0051 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0013c0031 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0014c0054 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0015c0050 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0016c0028 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0017c0053 | 0/0 | 3159 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0018c0049 | 0/0 | 3159 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0019c0048 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0020c0029 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0021c0040 | 0/0 | 3159 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0022c0034 | 0/0 | 3144 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3139): Show |
chr18 | 2842006 | 2921003 | ||
a0023c0044 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 | ||
a0024c0030 | 0/0 | 3159 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | ATGTG others(3154): Show |
chr18 | 2842006 | 2921003 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5944 | 29 | 10 | 13 | 2 | 1 | 2 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0002 | 0/0 | 5942 | 32 | 1 | 5 | 20 | 3 | 3 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0003 | 0/0 | 5942 | 38 | 0 | 5 | 25 | 1 | 7 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0005 | 0/1 | 5942 | 21 | 7 | 3 | 4 | 3 | 3 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0006 | 0/0 | 5942 | 7 | 0 | 0 | 7 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0007 | 0/0 | 5942 | 4 | 0 | 0 | 3 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0009 | 0/0 | 5942 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0010 | 0/0 | 5942 | 3 | 0 | 1 | 0 | 1 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0011 | 0/0 | 5943 | 4 | 0 | 0 | 4 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0012 | 0/0 | 5942 | 2 | 0 | 0 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0014 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0015 | 0/0 | 5943 | 2 | 0 | 0 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0016 | 0/0 | 5936 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5931): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0017 | 0/0 | 5943 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0018 | 0/0 | 5943 | 3 | 1 | 2 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0021 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0022 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0023 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0025 | 0/0 | 5942 | 2 | 0 | 1 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0027 | 0/0 | 5943 | 2 | 0 | 0 | 0 | 2 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0030 | 0/0 | 5943 | 2 | 0 | 0 | 0 | 0 | 2 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0032 | 0/0 | 5944 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0033 | 0/0 | 5944 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0034 | 0/0 | 5943 | 2 | 1 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0035 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0037 | 0/0 | 5942 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0038 | 0/0 | 5942 | 2 | 0 | 0 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0039 | 0/0 | 5943 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0044 | 0/0 | 5944 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0045 | 0/0 | 5942 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0047 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0052 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0058 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0059 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0070 | 0/0 | 5942 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0001t0071 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0001 | 0/0 | 5944 | 5 | 0 | 0 | 5 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0002 | 0/0 | 5942 | 19 | 0 | 0 | 17 | 1 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0003 | 0/0 | 5942 | 14 | 0 | 3 | 9 | 0 | 2 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0004 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0005 | 0/0 | 5942 | 5 | 1 | 0 | 2 | 0 | 2 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0006 | 0/0 | 5942 | 3 | 0 | 0 | 3 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0007 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0008 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0011 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0012 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0014 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0015 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0024 | 0/0 | 5941 | 2 | 0 | 0 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5936): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0039 | 0/0 | 5943 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0042 | 0/0 | 5942 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0049 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0067 | 0/0 | 5944 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0068 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0002t0069 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0001 | 0/0 | 5944 | 11 | 0 | 4 | 6 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0002 | 0/0 | 5942 | 9 | 0 | 0 | 8 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0003 | 0/0 | 5942 | 6 | 0 | 4 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0004 | 0/0 | 5943 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0005 | 0/0 | 5942 | 5 | 0 | 0 | 5 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0006 | 0/0 | 5942 | 4 | 0 | 0 | 4 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0007 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0012 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0015 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0016 | 0/0 | 5936 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5931): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0023 | 0/0 | 5943 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0041 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0057 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0003t0066 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0001 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0002 | 0/0 | 5942 | 8 | 0 | 0 | 5 | 0 | 3 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0003 | 0/0 | 5942 | 5 | 0 | 1 | 3 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0005 | 0/0 | 5942 | 2 | 1 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0009 | 0/0 | 5942 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0010 | 0/0 | 5942 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0013 | 0/0 | 5942 | 3 | 3 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0031 | 0/0 | 5942 | 2 | 0 | 0 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0040 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0054 | 0/0 | 5942 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0060 | 0/0 | 5943 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0064 | 0/0 | 5942 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0004t0065 | 0/0 | 5942 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0001 | 0/0 | 5944 | 5 | 0 | 5 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0002 | 0/0 | 5942 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0003 | 0/0 | 5942 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0005 | 0/0 | 5942 | 2 | 0 | 0 | 0 | 0 | 2 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0010 | 0/0 | 5942 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0032 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0033 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0006t0035 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0008t0001 | 0/0 | 5944 | 3 | 0 | 3 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0008t0002 | 0/0 | 5942 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0008t0003 | 0/0 | 5942 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0008t0021 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0008t0036 | 0/0 | 5944 | 2 | 0 | 1 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0008t0040 | 0/0 | 5942 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0013t0001 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0013t0009 | 0/0 | 5942 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0014t0001 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0014t0004 | 0/0 | 5943 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0015t0002 | 0/0 | 5942 | 2 | 0 | 0 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0015t0006 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0016t0016 | 0/0 | 5936 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5931): Show |
chr18 | 2842006 | 2921003 |
a0001c0016t0017 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0016t0061 | 0/0 | 5942 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0023t0001 | 0/0 | 5944 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0023t0002 | 0/0 | 5942 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0032t0002 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0001c0033t0022 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0035t0001 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0037t0063 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0001c0041t0014 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0001c0042t0002 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0004 | 0/0 | 5943 | 12 | 2 | 3 | 6 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0008 | 0/0 | 5943 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0026 | 0/0 | 5943 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0028 | 0/0 | 5944 | 2 | 0 | 0 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0029 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0043 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0050 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0051 | 0/0 | 5945 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5940): Show |
chr18 | 2842006 | 2921003 |
a0002c0005t0072 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0007t0004 | 0/0 | 5943 | 9 | 0 | 1 | 7 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0007t0008 | 0/0 | 5943 | 2 | 0 | 2 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0007t0046 | 0/0 | 5943 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0009t0004 | 0/0 | 5943 | 5 | 1 | 2 | 2 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0009t0008 | 0/0 | 5943 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0009t0029 | 0/0 | 5944 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0002c0020t0004 | 0/0 | 5943 | 2 | 1 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0024t0004 | 0/0 | 5943 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0024t0008 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0025t0004 | 0/0 | 5943 | 2 | 1 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0002c0047t0004 | 0/0 | 5943 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0003c0010t0001 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0003c0010t0009 | 0/0 | 5942 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0003c0010t0019 | 0/0 | 5941 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5936): Show |
chr18 | 2842006 | 2921003 |
a0003c0010t0020 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0003c0012t0001 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0003c0012t0013 | 0/0 | 5942 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0003c0012t0048 | 0/0 | 5945 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5940): Show |
chr18 | 2842006 | 2921003 |
a0003c0045t0062 | 0/0 | 5941 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5936): Show |
chr18 | 2842006 | 2921003 |
a0003c0046t0001 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0004c0011t0001 | 0/0 | 5932 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5927): Show |
chr18 | 2842006 | 2921003 |
a0004c0011t0003 | 0/0 | 5930 | 4 | 0 | 0 | 4 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5925): Show |
chr18 | 2842006 | 2921003 |
a0004c0039t0056 | 0/0 | 5931 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5926): Show |
chr18 | 2842006 | 2921003 |
a0004c0043t0003 | 0/0 | 5930 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5925): Show |
chr18 | 2842006 | 2921003 |
a0005c0021t0004 | 0/0 | 5943 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0005c0036t0004 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0005c0038t0004 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0006c0026t0053 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0006c0026t0055 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0006c0027t0001 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0007c0022t0001 | 0/0 | 5944 | 2 | 0 | 2 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0008c0017t0001 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0009c0018t0001 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0010c0019t0001 | 0/0 | 5944 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0011c0052t0001 | 0/0 | 5944 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0012c0051t0019 | 0/0 | 5941 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5936): Show |
chr18 | 2842006 | 2921003 |
a0013c0031t0003 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0014c0054t0019 | 0/0 | 5941 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5936): Show |
chr18 | 2842006 | 2921003 |
a0015c0050t0001 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0016c0028t0001 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0017c0053t0001 | 0/0 | 5944 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0018c0049t0005 | 0/0 | 5942 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0019c0048t0004 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
a0020c0029t0006 | 0/0 | 5942 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5937): Show |
chr18 | 2842006 | 2921003 |
a0021c0040t0001 | 0/0 | 5944 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0022c0034t0002 | 0/0 | 5927 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5922): Show |
chr18 | 2842006 | 2921003 |
a0023c0044t0001 | 0/0 | 5944 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5939): Show |
chr18 | 2842006 | 2921003 |
a0024c0030t0004 | 0/0 | 5943 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | AGAAG others(5938): Show |
chr18 | 2842006 | 2921003 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0022 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0384 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0402 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0403 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0415 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0418 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0001g0433 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0390 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0405 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0421 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0428 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0435 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0002g0446 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0389 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0003g0424 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0350 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0394 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0395 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0413 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0423 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0439 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0445 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0005g0448 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0006g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0006g0436 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0007g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0010g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0010g0393 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0010g0420 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0011g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0011g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0012g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0012g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0014g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0015g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0015g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0016g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0017g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0017g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0018g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0018g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0018g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0021g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0022g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0023g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0025g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0025g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0027g0406 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0027g0407 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0030g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0030g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0032g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0033g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0034g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0034g0426 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0035g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0037g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0037g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0038g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0038g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0039g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0044g0442 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0045g0443 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0047g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0052g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0058g0419 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0059g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0070g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0001t0071g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0001g0400 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0001g0425 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0002g0427 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0003g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0005g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0005g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0005g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0005g0434 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0006g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0007g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0008g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0011g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0012g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0014g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0015g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0024g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0024g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0039g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0042g0444 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0049g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0067g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0068g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0002t0069g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0416 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0001g0422 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0002g0431 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0003g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0003g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0003g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0004g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0005g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0005g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0005g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0006g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0006g0429 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0012g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0015g0432 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0016g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0023g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0041g0441 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0057g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0003t0066g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0001g0383 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0005g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0013g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0031g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0031g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0040g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0054g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0060g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0064g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0004t0065g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0010g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0032g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0033g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0006t0035g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0001g0417 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0002g0447 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0021g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0036g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0036g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0008t0040g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0013t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0013t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0013t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0014t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0014t0004g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0014t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0015t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0015t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0015t0006g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0016t0016g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0016t0017g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0016t0061g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0023t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0023t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0032t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0033t0022g0409 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0035t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0037t0063g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0041t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0001c0042t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0004g0430 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0008g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0026g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0026g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0028g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0028g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0029g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0043g0440 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0050g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0051g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0005t0072g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0004g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0008g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0007t0046g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0009t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0009t0004g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0009t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0009t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0009t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0009t0008g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0009t0029g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0020t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0020t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0024t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0024t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0025t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0025t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0002c0047t0004g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0010t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0010t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0010t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0010t0019g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0010t0020g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0010t0020g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0012t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0012t0001g0437 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0012t0013g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0012t0048g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0045t0062g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0003c0046t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0004c0011t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0004c0011t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0004c0011t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0004c0011t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0004c0011t0003g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0004c0039t0056g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0004c0043t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0005c0021t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0005c0021t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0005c0036t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0005c0038t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0006c0026t0053g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0006c0026t0055g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0006c0027t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0006c0027t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0007c0022t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0007c0022t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0008c0017t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0008c0017t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0009c0018t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0009c0018t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0010c0019t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0010c0019t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0011c0052t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0012c0051t0019g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0013c0031t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0014c0054t0019g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0015c0050t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0016c0028t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0017c0053t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0018c0049t0005g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0019c0048t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0020c0029t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0021c0040t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0022c0034t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0023c0044t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
a0024c0030t0004g0438 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0008 | t0036 | g0139 | EUR | GBR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0384 | EUR | GBR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00140 | hp1 | a0001 | c0001 | t0032 | g0232 | EUR | GBR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00140 | hp2 | a0001 | c0006 | t0010 | g0322 | EUR | GBR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00280 | hp1 | a0001 | c0023 | t0001 | g0142 | EUR | FIN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0170 | EUR | FIN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0182 | EUR | FIN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00323 | hp2 | a0001 | c0002 | t0002 | g0304 | EUR | FIN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0111 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00408 | hp2 | a0001 | c0003 | t0002 | g0301 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00423 | hp1 | a0001 | c0003 | t0007 | g0052 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0219 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00544 | hp1 | a0001 | c0002 | t0069 | g0079 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00544 | hp2 | a0001 | c0015 | t0006 | g0107 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00558 | hp1 | a0002 | c0005 | t0028 | g0317 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00558 | hp2 | a0001 | c0003 | t0006 | g0124 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00597 | hp1 | a0001 | c0003 | t0012 | g0311 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00597 | hp2 | a0001 | c0003 | t0003 | g0411 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0321 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00639 | hp1 | a0002 | c0005 | t0004 | g0193 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00639 | hp2 | a0001 | c0001 | t0025 | g0365 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0360 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00673 | hp2 | a0001 | c0033 | t0022 | g0409 | EAS | CHS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0238 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00733 | hp2 | a0001 | c0006 | t0001 | g0357 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00735 | hp1 | a0001 | c0004 | t0003 | g0227 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00735 | hp2 | a0002 | c0025 | t0004 | g0140 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00738 | hp1 | a0001 | c0003 | t0003 | g0127 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0445 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0362 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01069 | hp1 | a0002 | c0007 | t0004 | g0367 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0403 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01070 | hp2 | a0001 | c0006 | t0003 | g0230 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0402 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01074 | hp2 | a0001 | c0006 | t0033 | g0279 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01081 | hp1 | a0001 | c0006 | t0001 | g0062 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01106 | hp1 | a0003 | c0010 | t0001 | g0007 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0363 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01109 | hp1 | a0002 | c0005 | t0029 | g0231 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01109 | hp2 | a0001 | c0006 | t0002 | g0240 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01167 | hp1 | a0001 | c0006 | t0001 | g0063 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01167 | hp2 | a0001 | c0001 | t0018 | g0026 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01168 | hp2 | a0007 | c0022 | t0001 | g0197 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01169 | hp1 | a0001 | c0001 | t0018 | g0027 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01169 | hp2 | a0007 | c0022 | t0001 | g0198 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01175 | hp2 | a0001 | c0003 | t0023 | g0248 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01192 | hp1 | a0003 | c0012 | t0048 | g0008 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0423 | AMR | PUR | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01255 | hp1 | a0001 | c0006 | t0032 | g0358 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01255 | hp2 | a0002 | c0047 | t0004 | g0379 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01256 | hp1 | a0001 | c0006 | t0035 | g0174 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0168 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01257 | hp1 | a0002 | c0005 | t0004 | g0094 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0283 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01258 | hp1 | a0001 | c0002 | t0003 | g0169 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0282 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0415 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01346 | hp1 | a0011 | c0052 | t0001 | g0242 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01346 | hp2 | a0001 | c0008 | t0001 | g0138 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0410 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01358 | hp2 | a0001 | c0004 | t0001 | g0383 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01361 | hp1 | a0001 | c0008 | t0001 | g0249 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0294 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01433 | hp1 | a0001 | c0001 | t0045 | g0443 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01433 | hp2 | a0001 | c0008 | t0036 | g0141 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01496 | hp1 | a0002 | c0005 | t0004 | g0093 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01496 | hp2 | a0001 | c0006 | t0001 | g0015 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01515 | hp1 | a0001 | c0001 | t0010 | g0420 | EUR | IBS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01515 | hp2 | a0001 | c0001 | t0027 | g0406 | EUR | IBS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01516 | hp1 | a0001 | c0001 | t0005 | g0394 | EUR | IBS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0234 | EUR | IBS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0395 | EUR | IBS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01517 | hp2 | a0001 | c0001 | t0027 | g0407 | EUR | IBS | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01884 | hp1 | a0001 | c0004 | t0013 | g0004 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01884 | hp2 | a0003 | c0046 | t0001 | g0028 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01891 | hp2 | a0012 | c0051 | t0019 | g0076 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01928 | hp1 | a0001 | c0006 | t0001 | g0316 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01928 | hp2 | a0001 | c0003 | t0041 | g0441 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01934 | hp1 | a0002 | c0005 | t0008 | g0251 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01943 | hp1 | a0001 | c0003 | t0004 | g0375 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01943 | hp2 | a0001 | c0008 | t0003 | g0226 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01952 | hp1 | a0001 | c0008 | t0040 | g0176 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0233 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01975 | hp1 | a0002 | c0009 | t0008 | g0225 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0224 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01978 | hp1 | a0001 | c0035 | t0001 | g0250 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01978 | hp2 | a0001 | c0003 | t0003 | g0125 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0418 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01981 | hp2 | a0001 | c0001 | t0010 | g0323 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01993 | hp1 | a0001 | c0003 | t0003 | g0106 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01993 | hp2 | a0002 | c0024 | t0004 | g0180 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02004 | hp1 | a0002 | c0009 | t0004 | g0223 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0178 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02027 | hp2 | a0001 | c0004 | t0003 | g0102 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0044 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02055 | hp2 | a0003 | c0012 | t0013 | g0343 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02071 | hp1 | a0001 | c0002 | t0003 | g0120 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02074 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02074 | hp2 | a0001 | c0002 | t0003 | g0080 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02080 | hp1 | a0001 | c0001 | t0071 | g0319 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02080 | hp2 | a0001 | c0032 | t0002 | g0366 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02083 | hp1 | a0001 | c0003 | t0002 | g0302 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0435 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02129 | hp2 | a0001 | c0002 | t0003 | g0151 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02132 | hp1 | a0001 | c0015 | t0002 | g0288 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02132 | hp2 | a0001 | c0003 | t0066 | g0353 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02145 | hp1 | a0001 | c0013 | t0001 | g0060 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02145 | hp2 | a0001 | c0008 | t0002 | g0187 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02148 | hp1 | a0002 | c0007 | t0008 | g0247 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02155 | hp1 | a0013 | c0031 | t0003 | g0085 | EAS | CDX | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | CDX | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0396 | EAS | CDX | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02165 | hp2 | a0001 | c0001 | t0038 | g0126 | EAS | CDX | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02257 | hp1 | a0008 | c0017 | t0001 | g0074 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02257 | hp2 | a0009 | c0018 | t0001 | g0156 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0274 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02258 | hp2 | a0005 | c0038 | t0004 | g0023 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0416 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02273 | hp2 | a0002 | c0009 | t0004 | g0246 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02280 | hp1 | a0001 | c0008 | t0002 | g0447 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02280 | hp2 | a0001 | c0002 | t0005 | g0021 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02293 | hp1 | a0001 | c0003 | t0003 | g0175 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02293 | hp2 | a0001 | c0008 | t0001 | g0417 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02300 | hp1 | a0002 | c0007 | t0008 | g0177 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02300 | hp2 | a0001 | c0002 | t0042 | g0444 | AMR | PEL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02451 | hp1 | a0002 | c0005 | t0026 | g0071 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02451 | hp2 | a0001 | c0001 | t0017 | g0075 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02523 | hp1 | a0001 | c0002 | t0002 | g0320 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02523 | hp2 | a0001 | c0003 | t0005 | g0381 | EAS | KHV | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02572 | hp1 | a0002 | c0005 | t0004 | g0011 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02572 | hp2 | a0005 | c0036 | t0004 | g0046 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02602 | hp1 | a0001 | c0002 | t0003 | g0050 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02602 | hp2 | a0001 | c0023 | t0002 | g0221 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02615 | hp1 | a0001 | c0016 | t0017 | g0259 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02622 | hp1 | a0001 | c0016 | t0016 | g0029 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02622 | hp2 | a0009 | c0018 | t0001 | g0012 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02630 | hp1 | a0001 | c0013 | t0009 | g0211 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02630 | hp2 | a0006 | c0027 | t0001 | g0039 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02647 | hp1 | a0001 | c0003 | t0016 | g0061 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0065 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0166 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0389 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02698 | hp1 | a0001 | c0001 | t0025 | g0051 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02698 | hp2 | a0001 | c0004 | t0002 | g0042 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02717 | hp1 | a0001 | c0014 | t0004 | g0006 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02717 | hp2 | a0003 | c0010 | t0019 | g0216 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02723 | hp1 | a0001 | c0008 | t0021 | g0209 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02723 | hp2 | a0001 | c0004 | t0009 | g0068 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02735 | hp2 | a0001 | c0001 | t0070 | g0137 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02809 | hp1 | a0001 | c0001 | t0014 | g0033 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02809 | hp2 | a0001 | c0001 | t0052 | g0210 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02886 | hp1 | a0008 | c0017 | t0001 | g0073 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0257 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02895 | hp2 | a0005 | c0021 | t0004 | g0069 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02896 | hp1 | a0010 | c0019 | t0001 | g0035 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02896 | hp2 | a0001 | c0041 | t0014 | g0263 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02897 | hp1 | a0005 | c0021 | t0004 | g0070 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02897 | hp2 | a0010 | c0019 | t0001 | g0034 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02922 | hp1 | a0003 | c0012 | t0001 | g0437 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02922 | hp2 | a0001 | c0001 | t0059 | g0276 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0185 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02965 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02970 | hp1 | a0003 | c0012 | t0001 | g0025 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02970 | hp2 | a0001 | c0014 | t0001 | g0043 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02976 | hp1 | a0003 | c0045 | t0062 | g0005 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02976 | hp2 | a0001 | c0002 | t0014 | g0243 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0424 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03017 | hp2 | a0001 | c0002 | t0003 | g0130 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03041 | hp1 | a0001 | c0004 | t0013 | g0261 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03041 | hp2 | a0002 | c0009 | t0004 | g0260 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03098 | hp1 | a0001 | c0001 | t0034 | g0426 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03130 | hp1 | a0001 | c0004 | t0013 | g0004 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03130 | hp2 | a0001 | c0004 | t0005 | g0067 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03139 | hp1 | a0006 | c0026 | t0055 | g0032 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03195 | hp2 | a0001 | c0016 | t0061 | g0058 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03209 | hp1 | a0001 | c0014 | t0004 | g0047 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03209 | hp2 | a0014 | c0054 | t0019 | g0037 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03225 | hp1 | a0001 | c0001 | t0047 | g0064 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0364 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03239 | hp2 | a0001 | c0006 | t0005 | g0191 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03453 | hp1 | a0002 | c0005 | t0072 | g0258 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03453 | hp2 | a0015 | c0050 | t0001 | g0077 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03486 | hp2 | a0001 | c0037 | t0063 | g0361 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0188 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03491 | hp1 | a0002 | c0020 | t0004 | g0131 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03491 | hp2 | a0001 | c0001 | t0030 | g0143 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03492 | hp2 | a0001 | c0001 | t0030 | g0144 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0235 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03516 | hp2 | a0001 | c0001 | t0037 | g0212 | AFR | ESN | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03540 | hp1 | a0003 | c0010 | t0009 | g0262 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03540 | hp2 | a0001 | c0001 | t0017 | g0228 | AFR | GWD | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03579 | hp2 | a0016 | c0028 | t0001 | g0024 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0218 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03654 | hp2 | a0001 | c0004 | t0005 | g0202 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03669 | hp1 | a0004 | c0011 | t0001 | g0184 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03688 | hp1 | a0001 | c0002 | t0005 | g0434 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0350 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03704 | hp1 | a0017 | c0053 | t0001 | g0072 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03704 | hp2 | a0001 | c0004 | t0065 | g0201 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0405 | SAS | PJL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03831 | hp2 | a0001 | c0004 | t0054 | g0194 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03834 | hp1 | a0018 | c0049 | t0005 | g0236 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03834 | hp2 | a0002 | c0005 | t0004 | g0018 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03927 | hp1 | a0001 | c0001 | t0007 | g0108 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03927 | hp2 | a0001 | c0001 | t0039 | g0229 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03942 | hp1 | a0001 | c0002 | t0005 | g0351 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03942 | hp2 | a0002 | c0007 | t0004 | g0016 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04115 | hp1 | a0001 | c0004 | t0002 | g0019 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04115 | hp2 | a0001 | c0002 | t0067 | g0013 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04184 | hp2 | a0001 | c0006 | t0005 | g0237 | SAS | BEB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04199 | hp1 | a0001 | c0001 | t0034 | g0186 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04199 | hp2 | a0001 | c0001 | t0010 | g0393 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0291 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04204 | hp2 | a0001 | c0004 | t0002 | g0055 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04228 | hp1 | a0001 | c0003 | t0001 | g0199 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG04228 | hp2 | a0001 | c0002 | t0039 | g0160 | SAS | STU | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18522 | hp1 | a0001 | c0001 | t0035 | g0214 | AFR | YRI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | YRI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0382 | EAS | CHB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | CHB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0428 | EAS | CHB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | CHB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18906 | hp1 | a0006 | c0027 | t0001 | g0222 | AFR | YRI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18906 | hp2 | a0001 | c0001 | t0021 | g0253 | AFR | YRI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18941 | hp2 | a0002 | c0009 | t0004 | g0318 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0270 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18943 | hp1 | a0001 | c0003 | t0002 | g0330 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18944 | hp1 | a0001 | c0002 | t0006 | g0287 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0427 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18945 | hp2 | a0004 | c0011 | t0003 | g0148 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18946 | hp1 | a0001 | c0002 | t0003 | g0398 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18946 | hp2 | a0001 | c0002 | t0003 | g0097 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18947 | hp1 | a0002 | c0009 | t0029 | g0355 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0352 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18948 | hp1 | a0001 | c0001 | t0038 | g0300 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18948 | hp2 | a0001 | c0003 | t0002 | g0339 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18949 | hp1 | a0001 | c0001 | t0011 | g0084 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18949 | hp2 | a0002 | c0007 | t0004 | g0313 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18950 | hp1 | a0001 | c0002 | t0024 | g0162 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18950 | hp2 | a0004 | c0043 | t0003 | g0164 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0104 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0335 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18952 | hp1 | a0001 | c0003 | t0006 | g0429 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0439 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18953 | hp1 | a0001 | c0004 | t0031 | g0161 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0244 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18954 | hp2 | a0001 | c0004 | t0040 | g0113 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18957 | hp1 | a0001 | c0001 | t0011 | g0123 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0171 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18959 | hp2 | a0001 | c0002 | t0024 | g0385 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0371 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18960 | hp2 | a0001 | c0004 | t0003 | g0146 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18962 | hp1 | a0001 | c0003 | t0002 | g0338 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18962 | hp2 | a0001 | c0002 | t0011 | g0087 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18964 | hp1 | a0001 | c0002 | t0005 | g0280 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18964 | hp2 | a0001 | c0003 | t0001 | g0414 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18966 | hp1 | a0004 | c0011 | t0003 | g0397 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18966 | hp2 | a0001 | c0002 | t0008 | g0399 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18968 | hp1 | a0002 | c0005 | t0004 | g0056 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18968 | hp2 | a0001 | c0001 | t0015 | g0296 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18969 | hp1 | a0001 | c0002 | t0049 | g0157 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18969 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18970 | hp1 | a0002 | c0005 | t0004 | g0136 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18970 | hp2 | a0001 | c0001 | t0007 | g0386 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18971 | hp1 | a0002 | c0007 | t0004 | g0053 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0400 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18972 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18972 | hp2 | a0001 | c0003 | t0005 | g0154 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18973 | hp1 | a0001 | c0003 | t0005 | g0380 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18974 | hp1 | a0001 | c0001 | t0005 | g0408 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18974 | hp2 | a0001 | c0003 | t0005 | g0152 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18975 | hp1 | a0002 | c0005 | t0004 | g0165 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18975 | hp2 | a0001 | c0001 | t0023 | g0099 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0370 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18977 | hp2 | a0001 | c0003 | t0002 | g0265 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0309 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18980 | hp2 | a0001 | c0002 | t0002 | g0337 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18981 | hp1 | a0002 | c0007 | t0004 | g0312 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18981 | hp2 | a0001 | c0001 | t0022 | g0122 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18982 | hp2 | a0001 | c0003 | t0002 | g0387 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18983 | hp1 | a0001 | c0002 | t0012 | g0412 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18983 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18984 | hp1 | a0020 | c0029 | t0006 | g0135 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18984 | hp2 | a0001 | c0003 | t0003 | g0325 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18985 | hp1 | a0001 | c0004 | t0002 | g0340 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18985 | hp2 | a0021 | c0040 | t0001 | g0163 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18986 | hp1 | a0001 | c0002 | t0002 | g0268 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18986 | hp2 | a0001 | c0003 | t0006 | g0153 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18989 | hp1 | a0002 | c0005 | t0004 | g0078 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18989 | hp2 | a0001 | c0002 | t0015 | g0327 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0267 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18991 | hp1 | a0002 | c0005 | t0028 | g0401 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18991 | hp2 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18992 | hp1 | a0001 | c0003 | t0005 | g0392 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0369 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18993 | hp1 | a0001 | c0001 | t0012 | g0315 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18993 | hp2 | a0001 | c0002 | t0002 | g0391 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18994 | hp1 | a0001 | c0004 | t0003 | g0115 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18994 | hp2 | a0002 | c0005 | t0004 | g0206 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18995 | hp1 | a0001 | c0002 | t0068 | g0092 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18997 | hp2 | a0001 | c0002 | t0003 | g0324 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0132 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18998 | hp2 | a0001 | c0001 | t0005 | g0404 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0192 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18999 | hp2 | a0001 | c0001 | t0012 | g0299 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0422 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19000 | hp2 | a0001 | c0004 | t0031 | g0109 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19004 | hp2 | a0001 | c0004 | t0002 | g0129 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19005 | hp1 | a0001 | c0002 | t0006 | g0204 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19006 | hp1 | a0002 | c0005 | t0051 | g0354 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19006 | hp2 | a0001 | c0001 | t0044 | g0442 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0271 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0356 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19011 | hp1 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19011 | hp2 | a0001 | c0002 | t0005 | g0378 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19012 | hp2 | a0001 | c0042 | t0002 | g0149 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19030 | hp1 | a0002 | c0005 | t0026 | g0036 | AFR | LWK | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19043 | hp1 | a0001 | c0004 | t0064 | g0196 | AFR | LWK | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19043 | hp2 | a0003 | c0010 | t0020 | g0275 | AFR | LWK | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19056 | hp1 | a0002 | c0005 | t0004 | g0430 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0333 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19060 | hp1 | a0001 | c0015 | t0002 | g0086 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19063 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0368 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19065 | hp1 | a0001 | c0004 | t0002 | g0349 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19065 | hp2 | a0004 | c0011 | t0003 | g0329 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0376 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19066 | hp2 | a0004 | c0011 | t0003 | g0286 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19067 | hp1 | a0001 | c0001 | t0006 | g0308 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19068 | hp1 | a0002 | c0005 | t0050 | g0293 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19068 | hp2 | a0022 | c0034 | t0002 | g0347 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19070 | hp1 | a0001 | c0003 | t0015 | g0432 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0433 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19074 | hp1 | a0002 | c0007 | t0004 | g0049 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19074 | hp2 | a0002 | c0009 | t0004 | g0331 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19077 | hp1 | a0001 | c0001 | t0011 | g0158 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0372 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0425 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0388 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19079 | hp2 | a0001 | c0003 | t0002 | g0431 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19080 | hp1 | a0001 | c0002 | t0007 | g0377 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19080 | hp2 | a0001 | c0001 | t0011 | g0298 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0103 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19083 | hp1 | a0001 | c0001 | t0006 | g0436 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0285 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19084 | hp1 | a0001 | c0004 | t0002 | g0264 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19085 | hp1 | a0002 | c0005 | t0043 | g0440 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19085 | hp2 | a0002 | c0007 | t0004 | g0345 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19086 | hp1 | a0001 | c0001 | t0015 | g0332 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19086 | hp2 | a0002 | c0007 | t0004 | g0336 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19087 | hp1 | a0001 | c0003 | t0057 | g0346 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19087 | hp2 | a0002 | c0007 | t0004 | g0305 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19088 | hp2 | a0001 | c0002 | t0006 | g0134 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0421 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19090 | hp2 | a0001 | c0003 | t0006 | g0326 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19240 | hp1 | a0002 | c0005 | t0004 | g0256 | AFR | YRI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA19240 | hp2 | a0023 | c0044 | t0001 | g0272 | AFR | YRI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20129 | hp1 | a0002 | c0025 | t0004 | g0145 | AFR | ASW | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20129 | hp2 | a0001 | c0001 | t0016 | g0344 | AFR | ASW | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0446 | EUR | TSI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0413 | EUR | TSI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20805 | hp1 | a0001 | c0004 | t0060 | g0306 | EUR | TSI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20805 | hp2 | a0001 | c0001 | t0033 | g0215 | EUR | TSI | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20905 | hp1 | a0001 | c0004 | t0003 | g0020 | SAS | GIH | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20905 | hp2 | a0001 | c0001 | t0005 | g0295 | SAS | GIH | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01123 | hp1 | a0004 | c0039 | t0056 | g0017 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG01123 | hp2 | a0001 | c0001 | t0058 | g0419 | AMR | CLM | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02109 | hp1 | a0001 | c0001 | t0014 | g0213 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02109 | hp2 | a0003 | c0010 | t0009 | g0155 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02486 | hp1 | a0001 | c0001 | t0037 | g0374 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02486 | hp2 | a0006 | c0026 | t0053 | g0059 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02559 | hp1 | a0001 | c0001 | t0005 | g0241 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG02559 | hp2 | a0001 | c0004 | t0010 | g0054 | AFR | ACB | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG03471 | hp2 | a0002 | c0020 | t0004 | g0010 | AFR | MSL | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG06807 | hp1 | a0019 | c0048 | t0004 | g0252 | AFR | USA | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0390 | AFR | USA | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18955 | hp1 | a0002 | c0007 | t0046 | g0373 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA18955 | hp2 | a0001 | c0004 | t0002 | g0341 | EAS | JPT | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20300 | hp1 | a0024 | c0030 | t0004 | g0438 | AFR | USA | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA20300 | hp2 | a0002 | c0024 | t0008 | g0179 | AFR | USA | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA21309 | hp1 | a0001 | c0013 | t0001 | g0009 | AFR | LWK | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
NA21309 | hp2 | a0003 | c0010 | t0020 | g0031 | AFR | LWK | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0448 | REF | REF | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0022 | REF | REF | EMILIN2_chr18_2842006_2921003 | EMILIN2 | chr18 | 2842006 | 2921003 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:2847197 | G | T | 1 | a0014 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.9G>T | p.Gln3His | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/8 | 192/5944 | 9/3162 | 3/1053 | chr18 | 2847197 | |||
chr18:2847228 | C | A | 2 | a0008 a0016 |
3 | HG02257.hp1 HG02886.hp1 HG03579.hp2 |
missense_variant | MODERATE | c.40C>A | p.Arg14Ser | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/8 | 223/5944 | 40/3162 | 14/1053 | chr18 | 2847228 | |||
chr18:2847889 | A | G | 1 | a0017 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.215A>G | p.Tyr72Cys | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/8 | 398/5944 | 215/3162 | 72/1053 | chr18 | 2847889 | |||
chr18:2847892 | A | G | 1 | a0011 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.218A>G | p.Asn73Ser | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/8 | 401/5944 | 218/3162 | 73/1053 | chr18 | 2847892 | |||
chr18:2847919 | C | G | 2 | a0012 a0015 |
2 | HG01891.hp2 HG03453.hp2 |
missense_variant | MODERATE | c.245C>G | p.Pro82Arg | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/8 | 428/5944 | 245/3162 | 82/1053 | chr18 | 2847919 | |||
chr18:2885038 | C | T | 1 | a0018 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.332C>T | p.Pro111Leu | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/8 | 515/5944 | 332/3162 | 111/1053 | chr18 | 2885038 | |||
chr18:2885112 | C | T | 2 | a0006 a0016 |
5 | HG02486.hp2 HG02630.hp2 HG03139.hp1 others(2): Show |
missense_variant | MODERATE | c.406C>T | p.Pro136Ser | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/8 | 589/5944 | 406/3162 | 136/1053 | chr18 | 2885112 | |||
chr18:2890651 | G | A | 1 | a0020 | 1 | NA18984.hp1 | missense_variant | MODERATE | c.524G>A | p.Gly175Glu | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 707/5944 | 524/3162 | 175/1053 | chr18 | 2890651 | |||
chr18:2890770 | G | A | 3 | a0009 a0015 a0024 |
4 | HG02257.hp2 HG02622.hp2 HG03453.hp2 others(1): Show |
missense_variant | MODERATE | c.643G>A | p.Ala215Thr | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 826/5944 | 643/3162 | 215/1053 | chr18 | 2890770 | |||
chr18:2890855 | C | A | 2 | a0015 a0024 |
2 | HG03453.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.728C>A | p.Thr243Lys | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 911/5944 | 728/3162 | 243/1053 | chr18 | 2890855 | |||
chr18:2890902 | A | G | 2 | a0003 a0019 |
13 | HG01106.hp1 HG01192.hp1 HG01884.hp2 others(10): Show |
missense_variant | MODERATE | c.775A>G | p.Met259Val | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 958/5944 | 775/3162 | 259/1053 | chr18 | 2890902 | |||
chr18:2890933 | T | G | 1 | a0013 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.806T>G | p.Val269Gly | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 989/5944 | 806/3162 | 269/1053 | chr18 | 2890933 | |||
chr18:2891061 | G | A | 1 | a0010 | 2 | HG02896.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.934G>A | p.Glu312Lys | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 1117/5944 | 934/3162 | 312/1053 | chr18 | 2891061 | |||
chr18:2891212 | A | C | 1 | a0007 | 2 | HG01168.hp2 HG01169.hp2 |
missense_variant | MODERATE | c.1085A>C | p.Tyr362Ser | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 1268/5944 | 1085/3162 | 362/1053 | chr18 | 2891212 | |||
chr18:2906766 | TCCCCGAC others(21): Show |
T | 1 | a0004 | 7 | HG01123.hp1 HG03669.hp1 NA18945.hp2 others(4): Show |
frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.2360-11_2376delACG others(25): Show |
p.Lys787fs | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/8 | 2360/3162 | 787/1053 | INFO_REALIGN_3_PRIME | chr18 | 2906766 | |||
chr18:2906824 | C | G | 1 | a0023 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.2401C>G | p.Pro801Ala | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/8 | 2584/5944 | 2401/3162 | 801/1053 | chr18 | 2906824 | |||
chr18:2908958 | C | T | 2 | a0005 a0019 |
5 | HG02258.hp2 HG02572.hp2 HG02895.hp2 others(2): Show |
missense_variant | MODERATE | c.2678C>T | p.Pro893Leu | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/8 | 2861/5944 | 2678/3162 | 893/1053 | chr18 | 2908958 | |||
chr18:2909700 | T | A | 1 | a0021 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.2705T>A | p.Val902Glu | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2888/5944 | 2705/3162 | 902/1053 | chr18 | 2909700 | |||
chr18:2909702 | C | T | 4 | a0002 a0005 a0019 others(1): Show |
54 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(51): Show |
missense_variant | MODERATE | c.2707C>T | p.Pro903Ser | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2890/5944 | 2707/3162 | 903/1053 | chr18 | 2909702 | |||
chr18:2909733 | C | T | 1 | a0021 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.2738C>T | p.Thr913Ile | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2921/5944 | 2738/3162 | 913/1053 | chr18 | 2909733 | |||
chr18:2909736 | A | T | 1 | a0021 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.2741A>T | p.Gln914Leu | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2924/5944 | 2741/3162 | 914/1053 | chr18 | 2909736 | |||
chr18:2909738 | A | C | 1 | a0021 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.2743A>C | p.Lys915Gln | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2926/5944 | 2743/3162 | 915/1053 | chr18 | 2909738 | |||
chr18:2909739 | A | T | 1 | a0021 | 1 | NA18985.hp2 | missense_variant | MODERATE | c.2744A>T | p.Lys915Met | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2927/5944 | 2744/3162 | 915/1053 | chr18 | 2909739 | |||
chr18:2913222 | CGCCCTCC others(8): Show |
C | 1 | a0022 | 1 | NA19068.hp2 | disruptive_inframe_deletion | MODERATE | c.2981_2995delGCCCTC others(9): Show |
p.Arg994_Ala998del | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 3164/5944 | 2981/3162 | 994/1053 | chr18 | 2913222 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:2885120 | C | T | 10 | a0001c0006 a0001c0008 a0001c0023 others(7): Show |
36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
synonymous_variant | LOW | c.414C>T | p.Asn138Asn | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/8 | 597/5944 | 414/3162 | 138/1053 | chr18 | 2885120 | |||
chr18:2891078 | T | C | 1 | a0001c0032 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.951T>C | p.Tyr317Tyr | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 1134/5944 | 951/3162 | 317/1053 | chr18 | 2891078 | |||
chr18:2891480 | T | C | 6 | a0001c0002 a0001c0033 a0001c0035 others(3): Show |
77 | HG00323.hp2 HG00544.hp1 HG00673.hp1 others(74): Show |
synonymous_variant | LOW | c.1353T>C | p.Asn451Asn | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 1536/5944 | 1353/3162 | 451/1053 | chr18 | 2891480 | |||
chr18:2891492 | A | G | 2 | a0001c0016 a0023c0044 |
4 | HG02615.hp1 HG02622.hp1 HG03195.hp2 others(1): Show |
synonymous_variant | LOW | c.1365A>G | p.Ala455Ala | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 1548/5944 | 1365/3162 | 455/1053 | chr18 | 2891492 | |||
chr18:2891849 | C | T | 13 | a0001c0003 a0001c0008 a0001c0015 others(10): Show |
76 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(73): Show |
synonymous_variant | LOW | c.1722C>T | p.Arg574Arg | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 1905/5944 | 1722/3162 | 574/1053 | chr18 | 2891849 | |||
chr18:2892098 | G | A | 3 | a0001c0013 a0005c0036 a0009c0018 |
6 | HG02145.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
synonymous_variant | LOW | c.1971G>A | p.Pro657Pro | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 2154/5944 | 1971/3162 | 657/1053 | chr18 | 2892098 | |||
chr18:2892476 | G | A | 10 | a0001c0004 a0001c0015 a0001c0023 others(7): Show |
46 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(43): Show |
synonymous_variant | LOW | c.2349G>A | p.Gln783Gln | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/8 | 2532/5944 | 2349/3162 | 783/1053 | chr18 | 2892476 | |||
chr18:2906904 | C | T | 1 | a0002c0025 | 2 | HG00735.hp2 NA20129.hp1 |
synonymous_variant | LOW | c.2481C>T | p.Pro827Pro | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/8 | 2664/5944 | 2481/3162 | 827/1053 | chr18 | 2906904 | |||
chr18:2906985 | C | G | 1 | a0001c0014 | 3 | HG02717.hp1 HG02970.hp2 HG03209.hp1 |
synonymous_variant | LOW | c.2562C>G | p.Pro854Pro | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/8 | 2745/5944 | 2562/3162 | 854/1053 | chr18 | 2906985 | |||
chr18:2906988 | A | G | 1 | a0001c0042 | 1 | NA19012.hp2 | synonymous_variant | LOW | c.2565A>G | p.Ala855Ala | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/8 | 2748/5944 | 2565/3162 | 855/1053 | chr18 | 2906988 | |||
chr18:2909728 | G | T | 1 | a0021c0040 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.2733G>T | p.Gly911Gly | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2916/5944 | 2733/3162 | 911/1053 | chr18 | 2909728 | |||
chr18:2909734 | C | A | 1 | a0021c0040 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.2739C>A | p.Thr913Thr | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2922/5944 | 2739/3162 | 913/1053 | chr18 | 2909734 | |||
chr18:2909758 | G | C | 1 | a0021c0040 | 1 | NA18985.hp2 | synonymous_variant | LOW | c.2763G>C | p.Gly921Gly | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/8 | 2946/5944 | 2763/3162 | 921/1053 | chr18 | 2909758 | |||
chr18:2913248 | C | T | 1 | a0001c0041 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.3006C>T | p.Cys1002Cys | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 3189/5944 | 3006/3162 | 1002/1053 | chr18 | 2913248 | |||
chr18:2913359 | C | T | 3 | a0001c0037 a0003c0045 a0012c0051 |
3 | HG01891.hp2 HG02976.hp1 HG03486.hp2 |
synonymous_variant | LOW | c.3117C>T | p.Ser1039Ser | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 3300/5944 | 3117/3162 | 1039/1053 | chr18 | 2913359 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:2847040 | C | A | 1 | a0001c0003t0041 | 1 | HG01928.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/8 | 149 | chr18 | 2847040 | ||||||
chr18:2847057 | T | C | 5 | a0001c0001t0044 a0001c0001t0045 a0001c0002t0042 others(2): Show |
5 | HG01433.hp1 HG01928.hp2 HG02300.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/8 | chr18 | 2847057 | |||||||
chr18:2847086 | T | A | 1 | a0002c0007t0046 | 1 | NA18955.hp1 | 5_prime_UTR_variant | MODIFIER | c.-103T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/8 | 103 | chr18 | 2847086 | ||||||
chr18:2847163 | G | T | 1 | a0002c0005t0072 | 1 | HG03453.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-26G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/8 | chr18 | 2847163 | |||||||
chr18:2913433 | T | C | 36 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(33): Show |
115 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*29T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 29 | chr18 | 2913433 | ||||||
chr18:2913450 | T | A | 1 | a0003c0010t0020 | 2 | NA19043.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*46T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 46 | chr18 | 2913450 | ||||||
chr18:2913510 | T | C | 4 | a0001c0001t0021 a0001c0001t0047 a0001c0008t0021 others(1): Show |
4 | HG01192.hp1 HG02723.hp1 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*106T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 106 | chr18 | 2913510 | ||||||
chr18:2913581 | G | A | 31 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(28): Show |
110 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*177G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 177 | chr18 | 2913581 | ||||||
chr18:2913590 | C | T | 3 | a0001c0001t0007 a0001c0002t0007 a0001c0003t0007 |
6 | HG00423.hp1 HG03927.hp1 NA18970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*186C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 186 | chr18 | 2913590 | ||||||
chr18:2913898 | C | G | 33 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(30): Show |
107 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*494C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 494 | chr18 | 2913898 | ||||||
chr18:2913920 | G | A | 59 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0015 others(56): Show |
161 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*516G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 516 | chr18 | 2913920 | ||||||
chr18:2913960 | G | A | 1 | a0001c0002t0049 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 556 | chr18 | 2913960 | ||||||
chr18:2914075 | TA | T | 43 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0007 others(40): Show |
124 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*673delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 673 | INFO_REALIGN_3_PRIME | chr18 | 2914075 | |||||
chr18:2914083 | GTTAAT | G | 3 | a0001c0001t0016 a0001c0003t0016 a0001c0016t0016 |
3 | HG02622.hp1 HG02647.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*684_*688delTTTAA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 684 | INFO_REALIGN_3_PRIME | chr18 | 2914083 | |||||
chr18:2914111 | C | A | 1 | a0001c0001t0038 | 2 | HG02165.hp2 NA18948.hp1 |
3_prime_UTR_variant | MODIFIER | c.*707C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 707 | chr18 | 2914111 | ||||||
chr18:2914215 | C | T | 1 | a0001c0004t0065 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 811 | chr18 | 2914215 | ||||||
chr18:2914219 | G | A | 1 | a0001c0003t0066 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*815G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 815 | chr18 | 2914219 | ||||||
chr18:2914381 | T | G | 2 | a0001c0004t0013 a0003c0012t0013 |
4 | HG01884.hp1 HG02055.hp2 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*977T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 977 | chr18 | 2914381 | ||||||
chr18:2914414 | C | T | 3 | a0003c0010t0019 a0012c0051t0019 a0014c0054t0019 |
3 | HG01891.hp2 HG02717.hp2 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1010C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1010 | chr18 | 2914414 | ||||||
chr18:2914456 | C | A | 1 | a0001c0001t0052 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1052 | chr18 | 2914456 | ||||||
chr18:2914465 | C | T | 1 | a0001c0004t0064 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1061C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1061 | chr18 | 2914465 | ||||||
chr18:2914536 | G | A | 1 | a0002c0005t0050 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1132G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1132 | chr18 | 2914536 | ||||||
chr18:2914712 | T | TA | 8 | a0001c0001t0022 a0001c0001t0030 a0001c0001t0039 others(5): Show |
9 | HG00673.hp2 HG03491.hp2 HG03492.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1316dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1317 | INFO_REALIGN_3_PRIME | chr18 | 2914712 | |||||
chr18:2914780 | CT | C | 121 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(118): Show |
342 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*1378delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1378 | INFO_REALIGN_3_PRIME | chr18 | 2914780 | |||||
chr18:2914806 | G | A | 2 | a0001c0001t0017 a0001c0016t0017 |
3 | HG02451.hp2 HG02615.hp1 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1402G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1402 | chr18 | 2914806 | ||||||
chr18:2914849 | A | T | 4 | a0001c0001t0021 a0001c0004t0013 a0001c0008t0021 others(1): Show |
6 | HG01884.hp1 HG02055.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1445A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1445 | chr18 | 2914849 | ||||||
chr18:2914911 | G | A | 2 | a0001c0001t0032 a0001c0006t0032 |
2 | HG00140.hp1 HG01255.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1507G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1507 | chr18 | 2914911 | ||||||
chr18:2915002 | G | A | 1 | a0001c0001t0058 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1598G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1598 | chr18 | 2915002 | ||||||
chr18:2915020 | C | T | 1 | a0001c0008t0036 | 2 | HG00099.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1616C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1616 | chr18 | 2915020 | ||||||
chr18:2915026 | C | T | 1 | a0001c0001t0071 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1622C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1622 | chr18 | 2915026 | ||||||
chr18:2915070 | C | T | 4 | a0003c0010t0019 a0003c0045t0062 a0012c0051t0019 others(1): Show |
4 | HG01891.hp2 HG02717.hp2 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1666C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1666 | chr18 | 2915070 | ||||||
chr18:2915195 | C | T | 1 | a0001c0001t0070 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1791C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1791 | chr18 | 2915195 | ||||||
chr18:2915221 | A | G | 75 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0010 others(72): Show |
193 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1817A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1817 | chr18 | 2915221 | ||||||
chr18:2915329 | T | C | 1 | a0006c0026t0053 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1925T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1925 | chr18 | 2915329 | ||||||
chr18:2915343 | G | A | 2 | a0001c0001t0033 a0001c0006t0033 |
2 | HG01074.hp2 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1939G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1939 | chr18 | 2915343 | ||||||
chr18:2915392 | A | G | 7 | a0001c0001t0009 a0001c0001t0037 a0001c0004t0009 others(4): Show |
10 | HG02109.hp2 HG02486.hp1 HG02615.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1988A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 1988 | chr18 | 2915392 | ||||||
chr18:2915523 | C | CT | 5 | a0001c0001t0023 a0001c0003t0023 a0002c0005t0028 others(2): Show |
6 | HG00558.hp1 HG01175.hp2 HG01192.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2133dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2134 | INFO_REALIGN_3_PRIME | chr18 | 2915523 | |||||
chr18:2915523 | CT | C | 48 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(45): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2133delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2133 | INFO_REALIGN_3_PRIME | chr18 | 2915523 | |||||
chr18:2915537 | T | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(15): Show |
25 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2133T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2133 | chr18 | 2915537 | ||||||
chr18:2915584 | G | A | 2 | a0001c0001t0059 a0002c0005t0026 |
3 | HG02451.hp1 HG02922.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2180G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2180 | chr18 | 2915584 | ||||||
chr18:2915679 | C | T | 27 | a0001c0001t0014 a0001c0002t0004 a0001c0002t0014 others(24): Show |
57 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2275C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2275 | chr18 | 2915679 | ||||||
chr18:2915723 | G | A | 5 | a0001c0001t0010 a0001c0001t0025 a0001c0004t0010 others(2): Show |
8 | HG00140.hp2 HG00639.hp2 HG01515.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2319G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2319 | chr18 | 2915723 | ||||||
chr18:2915740 | C | T | 1 | a0001c0001t0052 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2336C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2336 | chr18 | 2915740 | ||||||
chr18:2915742 | C | A | 1 | a0006c0026t0055 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2338C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2338 | chr18 | 2915742 | ||||||
chr18:2915814 | C | T | 27 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0007 others(24): Show |
123 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*2410C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2410 | chr18 | 2915814 | ||||||
chr18:2915846 | G | C | 1 | a0001c0016t0061 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2442G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 8/8 | 2442 | chr18 | 2915846 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:2847363 | C | G | 88 | a0001c0001t0001g0362 a0001c0001t0001g0363 a0001c0001t0001g0384 others(85): Show |
90 | HG00099.hp2 HG00597.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.134+41C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847363 | |||||||
chr18:2847370 | G | A | 3 | a0001c0014t0004g0006 a0003c0010t0001g0007 a0003c0045t0062g0005 |
3 | HG01106.hp1 HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.134+48G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847370 | |||||||
chr18:2847421 | G | A | 5 | a0001c0013t0001g0009 a0002c0005t0004g0011 a0002c0020t0004g0010 others(2): Show |
5 | HG01192.hp1 HG02572.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.134+99G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847421 | |||||||
chr18:2847425 | G | T | 1 | a0001c0037t0063g0361 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.134+103G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847425 | |||||||
chr18:2847435 | G | A | 2 | a0001c0001t0001g0362 a0001c0001t0001g0363 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.134+113G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847435 | |||||||
chr18:2847683 | G | T | 3 | a0001c0001t0002g0446 a0001c0001t0005g0445 a0001c0008t0002g0447 |
3 | HG00738.hp2 HG02280.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.135-126G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847683 | |||||||
chr18:2847708 | C | T | 2 | a0001c0001t0003g0359 a0001c0002t0002g0360 |
2 | HG00673.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.135-101C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847708 | |||||||
chr18:2847732 | C | G | 195 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0277 others(192): Show |
196 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.135-77C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847732 | |||||||
chr18:2847746 | C | T | 88 | a0001c0001t0001g0303 a0001c0001t0001g0348 a0001c0001t0002g0294 others(85): Show |
88 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.135-63C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 1/7 | chr18 | 2847746 | |||||||
chr18:2848018 | C | T | 7 | a0001c0001t0001g0002 a0001c0003t0023g0248 a0001c0008t0001g0249 others(4): Show |
8 | HG00642.hp2 HG00741.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.257+87C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848018 | |||||||
chr18:2848067 | C | G | 1 | a0001c0037t0063g0361 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.257+136C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848067 | |||||||
chr18:2848127 | G | A | 14 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0002t0067g0013 others(11): Show |
15 | HG00642.hp2 HG00741.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.257+196G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848127 | |||||||
chr18:2848203 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.257+272C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848203 | |||||||
chr18:2848465 | G | T | 439 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(436): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
intron_variant | MODIFIER | c.257+534G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848465 | |||||||
chr18:2848506 | G | T | 2 | a0003c0012t0001g0437 a0024c0030t0004g0438 |
2 | HG02922.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.257+575G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848506 | |||||||
chr18:2848580 | G | T | 412 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0057 others(409): Show |
416 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(413): Show |
intron_variant | MODIFIER | c.257+649G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848580 | |||||||
chr18:2848593 | T | TA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0057 others(113): Show |
119 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.257+677dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2848593 | ||||||
chr18:2848593 | TAA | T | 25 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(22): Show |
25 | HG01192.hp1 HG01891.hp1 HG02572.hp1 others(22): Show |
intron_variant | MODIFIER | c.257+676_257+677del others(2): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2848593 | ||||||
chr18:2848631 | C | G | 139 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(136): Show |
142 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.257+700C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848631 | |||||||
chr18:2848639 | G | A | 14 | a0001c0001t0001g0066 a0001c0001t0005g0065 a0001c0001t0047g0064 others(11): Show |
14 | HG01081.hp1 HG01167.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.257+708G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848639 | |||||||
chr18:2848681 | T | A | 1 | a0001c0002t0005g0280 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.257+750T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848681 | |||||||
chr18:2848731 | A | G | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.257+800A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848731 | |||||||
chr18:2848806 | C | T | 1 | a0005c0038t0004g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.257+875C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848806 | |||||||
chr18:2848956 | C | G | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.257+1025C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848956 | |||||||
chr18:2848959 | G | A | 1 | a0002c0005t0004g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.257+1028G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2848959 | |||||||
chr18:2849006 | G | A | 3 | a0001c0001t0005g0044 a0001c0002t0014g0243 a0001c0014t0001g0043 |
3 | HG02055.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.257+1075G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849006 | |||||||
chr18:2849075 | C | G | 1 | a0002c0005t0004g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.257+1144C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849075 | |||||||
chr18:2849130 | G | C | 1 | a0002c0007t0046g0373 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.257+1199G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849130 | |||||||
chr18:2849132 | T | G | 1 | a0001c0006t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.257+1201T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849132 | |||||||
chr18:2849141 | G | A | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.257+1210G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849141 | |||||||
chr18:2849141 | G | C | 1 | a0017c0053t0001g0072 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.257+1210G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849141 | |||||||
chr18:2849342 | G | T | 2 | a0001c0014t0004g0006 a0003c0045t0062g0005 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.257+1411G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849342 | |||||||
chr18:2849507 | A | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0009g0041 others(5): Show |
8 | HG01192.hp1 HG02258.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+1576A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849507 | |||||||
chr18:2849641 | T | C | 2 | a0008c0017t0001g0073 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.257+1710T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849641 | |||||||
chr18:2849652 | T | C | 1 | a0001c0001t0005g0439 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.257+1721T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849652 | |||||||
chr18:2849685 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0038 others(185): Show |
192 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.257+1754A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849685 | |||||||
chr18:2849709 | A | G | 1 | a0008c0017t0001g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.257+1778A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849709 | |||||||
chr18:2849835 | C | T | 2 | a0003c0010t0001g0007 a0016c0028t0001g0024 |
2 | HG01106.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.257+1904C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849835 | |||||||
chr18:2849910 | CTTTTTTG | C | 26 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0005g0257 others(23): Show |
27 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.257+1997_257+2003d others(9): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2849910 | ||||||
chr18:2849971 | A | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0021g0253 others(1): Show |
4 | HG02886.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+2040A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849971 | |||||||
chr18:2849988 | G | A | 1 | a0002c0007t0004g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.257+2057G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2849988 | |||||||
chr18:2850074 | G | A | 10 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(7): Show |
10 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+2143G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850074 | |||||||
chr18:2850093 | A | AT | 128 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0057 others(125): Show |
129 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.257+2182dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2850093 | ||||||
chr18:2850093 | A | ATT | 18 | a0001c0001t0001g0040 a0001c0001t0001g0207 a0001c0001t0001g0208 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.257+2181_257+2182d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2850093 | ||||||
chr18:2850093 | AT | A | 12 | a0001c0001t0003g0281 a0001c0001t0005g0048 a0001c0001t0009g0041 others(9): Show |
12 | HG01192.hp1 HG01943.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+2182delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2850093 | ||||||
chr18:2850480 | A | G | 2 | a0001c0001t0033g0215 a0001c0006t0002g0240 |
2 | HG01109.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.257+2549A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850480 | |||||||
chr18:2850550 | C | T | 104 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(101): Show |
106 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.257+2619C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850550 | |||||||
chr18:2850602 | G | A | 1 | a0006c0026t0053g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.257+2671G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850602 | |||||||
chr18:2850633 | C | G | 198 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0038 others(195): Show |
201 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(198): Show |
intron_variant | MODIFIER | c.257+2702C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850633 | |||||||
chr18:2850649 | A | C | 1 | a0005c0038t0004g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.257+2718A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850649 | |||||||
chr18:2850712 | G | A | 2 | a0001c0003t0001g0282 a0001c0003t0001g0283 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.257+2781G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850712 | |||||||
chr18:2850883 | C | A | 8 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0001t0003g0190 others(5): Show |
8 | HG02145.hp2 HG02735.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+2952C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850883 | |||||||
chr18:2850895 | G | A | 5 | a0001c0001t0009g0041 a0001c0013t0001g0009 a0002c0005t0004g0011 others(2): Show |
5 | HG01192.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+2964G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850895 | |||||||
chr18:2850923 | G | C | 1 | a0001c0002t0007g0377 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.257+2992G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850923 | |||||||
chr18:2850968 | G | T | 3 | a0001c0003t0005g0152 a0001c0003t0005g0154 a0001c0003t0006g0153 |
3 | NA18972.hp2 NA18974.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.257+3037G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2850968 | |||||||
chr18:2851014 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.257+3083G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851014 | |||||||
chr18:2851090 | G | GA | 7 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0021g0253 others(4): Show |
7 | HG02886.hp2 HG03225.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+3174dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2851090 | ||||||
chr18:2851090 | GA | G | 26 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0009g0045 others(23): Show |
27 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.257+3174delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2851090 | ||||||
chr18:2851120 | G | A | 1 | a0002c0005t0072g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.257+3189G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851120 | |||||||
chr18:2851149 | A | C | 1 | a0001c0002t0003g0151 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.257+3218A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851149 | |||||||
chr18:2851180 | G | A | 22 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0005g0257 others(19): Show |
23 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.257+3249G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851180 | |||||||
chr18:2851238 | A | C | 5 | a0001c0001t0044g0442 a0001c0001t0045g0443 a0001c0002t0042g0444 others(2): Show |
5 | HG01433.hp1 HG01928.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+3307A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851238 | |||||||
chr18:2851274 | TA | T | 11 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0009g0045 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.257+3355delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2851274 | ||||||
chr18:2851297 | T | C | 1 | a0001c0001t0009g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.257+3366T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851297 | |||||||
chr18:2851384 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0057 others(130): Show |
135 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.257+3453A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851384 | |||||||
chr18:2851419 | A | C | 12 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(9): Show |
12 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.257+3488A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851419 | |||||||
chr18:2851469 | G | T | 2 | a0001c0014t0004g0006 a0003c0045t0062g0005 |
2 | HG02717.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.257+3538G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851469 | |||||||
chr18:2851521 | G | A | 5 | a0001c0014t0004g0006 a0001c0037t0063g0361 a0003c0010t0001g0007 others(2): Show |
5 | HG01106.hp1 HG02717.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+3590G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851521 | |||||||
chr18:2851638 | G | T | 1 | a0001c0006t0005g0191 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.257+3707G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851638 | |||||||
chr18:2851815 | G | C | 10 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(7): Show |
10 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.257+3884G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851815 | |||||||
chr18:2851821 | A | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0038 others(155): Show |
161 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(158): Show |
intron_variant | MODIFIER | c.257+3890A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851821 | |||||||
chr18:2851876 | C | T | 27 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0207 others(24): Show |
28 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.257+3945C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851876 | |||||||
chr18:2851892 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0021g0253 others(1): Show |
4 | HG02886.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+3961G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851892 | |||||||
chr18:2851972 | G | A | 1 | a0002c0005t0004g0078 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.257+4041G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851972 | |||||||
chr18:2851976 | G | A | 2 | a0003c0010t0001g0007 a0016c0028t0001g0024 |
2 | HG01106.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.257+4045G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2851976 | |||||||
chr18:2852030 | C | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0009g0041 others(5): Show |
8 | HG01192.hp1 HG02257.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+4099C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852030 | |||||||
chr18:2852070 | C | T | 14 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0005g0257 others(11): Show |
15 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.257+4139C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852070 | |||||||
chr18:2852164 | G | A | 1 | a0001c0002t0069g0079 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.257+4233G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852164 | |||||||
chr18:2852170 | ATGCATGT others(3): Show |
A | 1 | a0016c0028t0001g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.257+4250_257+4259d others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2852170 | ||||||
chr18:2852226 | C | T | 1 | a0002c0047t0004g0379 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.257+4295C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852226 | |||||||
chr18:2852227 | G | A | 1 | a0001c0002t0069g0079 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.257+4296G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852227 | |||||||
chr18:2852409 | G | A | 2 | a0001c0016t0016g0029 a0001c0016t0061g0058 |
2 | HG02622.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.257+4478G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852409 | |||||||
chr18:2852523 | G | A | 2 | a0001c0001t0001g0014 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.257+4592G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852523 | |||||||
chr18:2852545 | G | T | 2 | a0001c0006t0001g0357 a0001c0006t0032g0358 |
2 | HG00733.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.257+4614G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852545 | |||||||
chr18:2852549 | C | T | 2 | a0001c0001t0003g0205 a0002c0005t0004g0206 |
2 | NA18994.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.257+4618C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852549 | |||||||
chr18:2852582 | C | T | 1 | a0001c0004t0002g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.257+4651C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852582 | |||||||
chr18:2852588 | G | A | 1 | a0008c0017t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.257+4657G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852588 | |||||||
chr18:2852613 | G | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0021g0253 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+4682G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852613 | |||||||
chr18:2852653 | A | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0021g0253 others(1): Show |
4 | HG02886.hp2 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+4722A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852653 | |||||||
chr18:2852799 | G | A | 1 | a0001c0002t0004g0192 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.257+4868G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852799 | |||||||
chr18:2852821 | C | A | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.257+4890C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852821 | |||||||
chr18:2852898 | C | T | 5 | a0001c0001t0009g0041 a0001c0013t0001g0009 a0002c0005t0004g0011 others(2): Show |
5 | HG01192.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+4967C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2852898 | |||||||
chr18:2853091 | C | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(113): Show |
117 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.257+5160C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853091 | |||||||
chr18:2853139 | G | A | 9 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(6): Show |
9 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+5208G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853139 | |||||||
chr18:2853265 | TA | T | 3 | a0001c0014t0004g0006 a0001c0016t0061g0058 a0003c0045t0062g0005 |
3 | HG02717.hp1 HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.257+5339delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2853265 | ||||||
chr18:2853281 | C | T | 2 | a0001c0001t0001g0255 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.257+5350C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853281 | |||||||
chr18:2853335 | G | A | 106 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(103): Show |
107 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.257+5404G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853335 | |||||||
chr18:2853358 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0021g0253 a0019c0048t0004g0252 |
3 | HG03225.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.257+5427G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853358 | |||||||
chr18:2853387 | T | C | 445 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(442): Show |
449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.257+5456T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853387 | |||||||
chr18:2853457 | A | C | 6 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+5526A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853457 | |||||||
chr18:2853478 | T | TTGTA | 9 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(6): Show |
9 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+5549_257+5550i others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2853478 | ||||||
chr18:2853500 | A | G | 5 | a0001c0001t0009g0041 a0001c0013t0001g0009 a0002c0005t0004g0011 others(2): Show |
5 | HG01192.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+5569A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853500 | |||||||
chr18:2853698 | G | A | 9 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(6): Show |
9 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+5767G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853698 | |||||||
chr18:2853718 | C | T | 2 | a0001c0001t0003g0001 a0001c0001t0003g0234 |
3 | HG01074.hp1 HG01192.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.257+5787C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853718 | |||||||
chr18:2853723 | A | G | 5 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+5792A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853723 | |||||||
chr18:2853760 | C | A | 1 | a0001c0002t0003g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.257+5829C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853760 | |||||||
chr18:2853763 | T | C | 3 | a0001c0001t0001g0254 a0001c0001t0021g0253 a0019c0048t0004g0252 |
3 | HG03225.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.257+5832T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853763 | |||||||
chr18:2853818 | T | G | 9 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(6): Show |
9 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+5887T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853818 | |||||||
chr18:2853820 | A | C | 109 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(106): Show |
110 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.257+5889A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853820 | |||||||
chr18:2853822 | G | A | 1 | a0001c0001t0002g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.257+5891G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853822 | |||||||
chr18:2853829 | T | C | 151 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(148): Show |
153 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(150): Show |
intron_variant | MODIFIER | c.257+5898T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853829 | |||||||
chr18:2853872 | C | G | 15 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0005g0257 others(12): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.257+5941C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853872 | |||||||
chr18:2853890 | C | T | 123 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(120): Show |
124 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.257+5959C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853890 | |||||||
chr18:2853915 | G | A | 5 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+5984G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2853915 | |||||||
chr18:2854004 | T | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(112): Show |
116 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.257+6073T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854004 | |||||||
chr18:2854009 | G | A | 1 | a0008c0017t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.257+6078G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854009 | |||||||
chr18:2854141 | C | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(105): Show |
109 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.257+6210C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854141 | |||||||
chr18:2854190 | A | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(112): Show |
116 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.257+6259A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854190 | |||||||
chr18:2854250 | C | T | 5 | a0001c0001t0009g0041 a0001c0013t0001g0009 a0002c0005t0004g0011 others(2): Show |
5 | HG01192.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+6319C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854250 | |||||||
chr18:2854285 | G | A | 5 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+6354G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854285 | |||||||
chr18:2854287 | G | C | 1 | a0002c0007t0004g0049 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.257+6356G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854287 | |||||||
chr18:2854383 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0038 others(190): Show |
196 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.257+6452G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854383 | |||||||
chr18:2854387 | C | A | 1 | a0001c0006t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.257+6456C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854387 | |||||||
chr18:2854426 | G | T | 7 | a0001c0001t0001g0255 a0001c0001t0009g0045 a0001c0001t0018g0026 others(4): Show |
7 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+6495G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854426 | |||||||
chr18:2854448 | CTTA | C | 5 | a0001c0001t0009g0041 a0001c0013t0001g0009 a0002c0005t0004g0011 others(2): Show |
5 | HG01192.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+6521_257+6523d others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2854448 | ||||||
chr18:2854487 | A | AAC | 5 | a0001c0001t0001g0255 a0001c0001t0009g0045 a0001c0014t0004g0006 others(2): Show |
5 | HG02257.hp1 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+6570_257+6571d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2854487 | ||||||
chr18:2854487 | A | AACAC | 5 | a0001c0001t0009g0041 a0001c0013t0001g0009 a0002c0005t0004g0011 others(2): Show |
5 | HG01192.hp1 HG02572.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+6568_257+6571d others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2854487 | ||||||
chr18:2854487 | A | AACACAC | 4 | a0001c0001t0018g0026 a0001c0001t0018g0027 a0003c0012t0001g0025 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+6566_257+6571d others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2854487 | ||||||
chr18:2854579 | A | G | 9 | a0001c0001t0001g0255 a0001c0001t0009g0045 a0001c0001t0018g0026 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+6648A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854579 | |||||||
chr18:2854626 | T | C | 140 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(137): Show |
142 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.257+6695T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854626 | |||||||
chr18:2854629 | C | CA | 5 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+6704dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2854629 | ||||||
chr18:2854665 | G | A | 1 | a0001c0002t0002g0082 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.257+6734G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854665 | |||||||
chr18:2854802 | A | T | 5 | a0001c0001t0009g0045 a0001c0001t0018g0026 a0001c0001t0018g0027 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+6871A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854802 | |||||||
chr18:2854835 | C | T | 1 | a0002c0005t0004g0056 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.257+6904C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854835 | |||||||
chr18:2854940 | G | A | 3 | a0001c0001t0005g0439 a0001c0003t0005g0380 a0001c0003t0057g0346 |
3 | NA18952.hp2 NA18973.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.257+7009G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854940 | |||||||
chr18:2854988 | A | G | 1 | a0002c0005t0026g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.257+7057A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854988 | |||||||
chr18:2854992 | A | G | 1 | a0001c0001t0005g0241 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.257+7061A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2854992 | |||||||
chr18:2855014 | C | G | 2 | a0001c0003t0001g0282 a0001c0003t0001g0283 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.257+7083C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855014 | |||||||
chr18:2855025 | G | A | 130 | a0001c0001t0001g0002 a0001c0001t0001g0057 a0001c0001t0001g0254 others(127): Show |
131 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.257+7094G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855025 | |||||||
chr18:2855100 | C | T | 23 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0005g0257 others(20): Show |
24 | HG01884.hp1 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.257+7169C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855100 | |||||||
chr18:2855163 | C | T | 32 | a0001c0001t0001g0220 a0001c0001t0002g0081 a0001c0001t0002g0217 others(29): Show |
33 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.257+7232C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855163 | |||||||
chr18:2855222 | T | C | 15 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0005g0257 others(12): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.257+7291T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855222 | |||||||
chr18:2855227 | C | G | 1 | a0001c0001t0005g0241 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.257+7296C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855227 | |||||||
chr18:2855328 | C | T | 16 | a0001c0001t0001g0057 a0001c0001t0001g0254 a0001c0001t0001g0255 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.257+7397C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855328 | |||||||
chr18:2855378 | A | G | 1 | a0002c0047t0004g0379 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.257+7447A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855378 | |||||||
chr18:2855545 | G | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0038 others(232): Show |
238 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.257+7614G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855545 | |||||||
chr18:2855605 | C | G | 160 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(157): Show |
162 | HG00099.hp2 HG00423.hp1 HG00597.hp2 others(159): Show |
intron_variant | MODIFIER | c.257+7674C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855605 | |||||||
chr18:2855621 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0021g0253 a0019c0048t0004g0252 |
3 | HG03225.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.257+7690G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855621 | |||||||
chr18:2855753 | C | T | 1 | a0001c0002t0003g0324 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.257+7822C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855753 | |||||||
chr18:2855754 | G | A | 33 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0005g0048 others(30): Show |
34 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+7823G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855754 | |||||||
chr18:2855787 | A | C | 1 | a0002c0025t0004g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.257+7856A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855787 | |||||||
chr18:2855847 | G | A | 1 | a0004c0039t0056g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.257+7916G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2855847 | |||||||
chr18:2856026 | C | T | 1 | a0001c0004t0005g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.257+8095C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856026 | |||||||
chr18:2856080 | T | C | 6 | a0001c0001t0014g0033 a0001c0014t0004g0006 a0001c0016t0017g0259 others(3): Show |
6 | HG02615.hp1 HG02717.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+8149T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856080 | |||||||
chr18:2856096 | C | T | 1 | a0001c0001t0002g0435 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.257+8165C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856096 | |||||||
chr18:2856140 | T | G | 41 | a0001c0001t0001g0220 a0001c0001t0001g0255 a0001c0001t0002g0081 others(38): Show |
42 | HG00423.hp2 HG00639.hp1 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.257+8209T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856140 | |||||||
chr18:2856177 | C | A | 1 | a0001c0001t0001g0083 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.257+8246C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856177 | |||||||
chr18:2856212 | AAAAAT | A | 3 | a0001c0001t0005g0044 a0001c0002t0014g0243 a0001c0014t0001g0043 |
3 | HG02055.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.257+8292_257+8296d others(7): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2856212 | ||||||
chr18:2856484 | C | A | 352 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(349): Show |
355 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(352): Show |
intron_variant | MODIFIER | c.257+8553C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856484 | |||||||
chr18:2856488 | A | G | 2 | a0001c0001t0010g0323 a0001c0001t0010g0420 |
2 | HG01515.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.257+8557A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856488 | |||||||
chr18:2856538 | A | C | 169 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0172 others(166): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.257+8607A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856538 | |||||||
chr18:2856621 | C | T | 26 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0208 others(23): Show |
27 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.257+8690C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856621 | |||||||
chr18:2856715 | C | A | 1 | a0001c0016t0017g0259 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.257+8784C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856715 | |||||||
chr18:2856754 | G | A | 79 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0002g0091 others(76): Show |
79 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.257+8823G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856754 | |||||||
chr18:2856934 | A | C | 11 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0005g0065 others(8): Show |
11 | HG02647.hp2 HG02723.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.257+9003A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856934 | |||||||
chr18:2856974 | G | A | 185 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(182): Show |
187 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.257+9043G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856974 | |||||||
chr18:2856975 | A | G | 185 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(182): Show |
187 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(184): Show |
intron_variant | MODIFIER | c.257+9044A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2856975 | |||||||
chr18:2857045 | G | A | 2 | a0003c0010t0001g0007 a0003c0045t0062g0005 |
2 | HG01106.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.257+9114G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857045 | |||||||
chr18:2857120 | G | T | 1 | a0001c0001t0011g0123 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.257+9189G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857120 | |||||||
chr18:2857235 | A | G | 8 | a0001c0001t0001g0207 a0001c0001t0009g0045 a0001c0016t0016g0029 others(5): Show |
8 | HG01192.hp1 HG02615.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+9304A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857235 | |||||||
chr18:2857261 | G | GACTTTGC others(22): Show |
1 | a0003c0046t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.257+9331_257+9359d others(31): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2857261 | ||||||
chr18:2857447 | G | A | 1 | a0001c0003t0004g0375 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.257+9516G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857447 | |||||||
chr18:2857547 | C | G | 1 | a0001c0001t0002g0435 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.257+9616C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857547 | |||||||
chr18:2857661 | G | T | 2 | a0001c0001t0022g0122 a0001c0002t0006g0204 |
2 | NA18981.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.257+9730G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857661 | |||||||
chr18:2857672 | G | A | 91 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0254 others(88): Show |
91 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.257+9741G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857672 | |||||||
chr18:2857985 | G | A | 2 | a0010c0019t0001g0034 a0010c0019t0001g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.257+10054G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2857985 | |||||||
chr18:2858017 | C | T | 3 | a0001c0001t0030g0143 a0001c0001t0030g0144 a0002c0020t0004g0131 |
3 | HG03491.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.257+10086C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858017 | |||||||
chr18:2858064 | CAA | C | 10 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0005g0065 others(7): Show |
10 | HG02647.hp2 HG02723.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+10135_257+1013 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858064 | ||||||
chr18:2858109 | C | T | 2 | a0005c0021t0004g0069 a0005c0021t0004g0070 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.257+10178C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858109 | |||||||
chr18:2858522 | C | CAT | 9 | a0001c0001t0002g0170 a0001c0001t0002g0328 a0001c0001t0002g0390 others(6): Show |
9 | HG00280.hp2 HG01358.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+10638_257+1063 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | C | CATAT | 11 | a0001c0001t0002g0372 a0001c0001t0003g0376 a0001c0001t0005g0235 others(8): Show |
11 | HG01069.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.257+10636_257+1063 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | C | CATATAT | 19 | a0001c0001t0002g0081 a0001c0001t0002g0364 a0001c0001t0002g0368 others(16): Show |
19 | HG00733.hp2 HG01123.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.257+10634_257+1063 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | C | CATATATA others(1): Show |
7 | a0001c0001t0003g0342 a0001c0001t0005g0065 a0001c0001t0018g0274 others(4): Show |
7 | HG02258.hp1 HG02647.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+10632_257+1063 others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | C | CATATATA others(3): Show |
6 | a0001c0001t0007g0386 a0001c0002t0002g0082 a0001c0003t0002g0291 others(3): Show |
6 | HG02040.hp2 HG03831.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+10630_257+1063 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | C | CATATATA others(7): Show |
1 | a0023c0044t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.257+10626_257+1063 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | C | CATATATA others(9): Show |
1 | a0001c0001t0001g0384 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.257+10624_257+1063 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CAT | C | 33 | a0001c0001t0001g0040 a0001c0001t0001g0254 a0001c0001t0001g0402 others(30): Show |
34 | HG00597.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.257+10638_257+1063 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATAT | C | 24 | a0001c0001t0002g0217 a0001c0001t0002g0421 a0001c0001t0002g0428 others(21): Show |
24 | HG00642.hp1 HG00738.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.257+10636_257+1063 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATAT | C | 11 | a0001c0001t0002g0321 a0001c0001t0003g0269 a0001c0001t0003g0410 others(8): Show |
11 | HG00558.hp1 HG00609.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.257+10634_257+1063 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(3): Show |
C | 4 | a0001c0001t0016g0344 a0001c0001t0018g0026 a0001c0001t0018g0027 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+10630_257+1063 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(5): Show |
C | 1 | a0001c0002t0002g0337 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.257+10628_257+1063 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(7): Show |
C | 1 | a0001c0004t0010g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.257+10626_257+1063 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(9): Show |
C | 2 | a0001c0014t0004g0047 a0005c0036t0004g0046 |
2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.257+10624_257+1063 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(11): Show |
C | 2 | a0002c0005t0029g0231 a0004c0011t0003g0148 |
2 | HG01109.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.257+10622_257+1063 others(22): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(13): Show |
C | 3 | a0001c0001t0002g0182 a0001c0001t0002g0233 a0001c0001t0032g0232 |
3 | HG00140.hp1 HG00323.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.257+10620_257+1063 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(15): Show |
C | 2 | a0001c0003t0003g0325 a0001c0014t0004g0006 |
2 | HG02717.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.257+10618_257+1063 others(26): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(17): Show |
C | 8 | a0001c0001t0002g0159 a0001c0001t0006g0436 a0001c0001t0014g0033 others(5): Show |
8 | HG00438.hp1 HG01943.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.257+10616_257+1063 others(28): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858522 | CATATATA others(19): Show |
C | 88 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(85): Show |
88 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.257+10614_257+1063 others(30): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858522 | ||||||
chr18:2858549 | A | ATATATAT others(23): Show |
1 | a0001c0002t0006g0134 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.257+10639_257+1064 others(34): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858549 | ||||||
chr18:2858549 | A | G | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.257+10618A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858549 | |||||||
chr18:2858551 | A | G | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.257+10620A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858551 | |||||||
chr18:2858551 | ATATATAT others(25): Show |
A | 1 | a0001c0002t0005g0434 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.257+10644_257+1067 others(36): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858551 | ||||||
chr18:2858553 | A | ATATATAT others(15): Show |
1 | a0001c0001t0017g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.257+10631_257+1063 others(26): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858553 | ||||||
chr18:2858553 | A | G | 2 | a0001c0001t0001g0057 a0001c0016t0016g0029 |
2 | HG02622.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.257+10622A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858553 | |||||||
chr18:2858555 | A | ATATATAT others(13): Show |
2 | a0012c0051t0019g0076 a0015c0050t0001g0077 |
2 | HG01891.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.257+10631_257+1063 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858555 | ||||||
chr18:2858555 | A | ATATATGT others(9): Show |
1 | a0001c0001t0034g0426 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.257+10629_257+1063 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858555 | ||||||
chr18:2858555 | A | G | 5 | a0001c0001t0001g0057 a0001c0001t0037g0374 a0001c0016t0016g0029 others(2): Show |
5 | HG02486.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+10624A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858555 | |||||||
chr18:2858555 | ATATATAT others(9): Show |
A | 2 | a0001c0001t0001g0255 a0001c0008t0003g0226 |
2 | HG01943.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.257+10626_257+1064 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858555 | ||||||
chr18:2858557 | A | G | 16 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0005g0257 others(13): Show |
17 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.257+10626A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858557 | |||||||
chr18:2858557 | ATATATAT others(7): Show |
A | 7 | a0001c0001t0001g0181 a0001c0002t0003g0178 a0001c0008t0040g0176 others(4): Show |
7 | HG01952.hp1 HG01993.hp2 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+10628_257+1064 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858557 | ||||||
chr18:2858559 | A | G | 19 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0005g0257 others(16): Show |
20 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.257+10628A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858559 | |||||||
chr18:2858559 | ATATATAT others(5): Show |
A | 1 | a0001c0003t0003g0175 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.257+10630_257+1064 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858559 | ||||||
chr18:2858560 | T | G | 8 | a0001c0001t0007g0089 a0001c0001t0011g0084 a0001c0001t0011g0158 others(5): Show |
8 | HG02155.hp1 NA18949.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.257+10629T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858560 | |||||||
chr18:2858561 | A | G | 25 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0005g0257 others(22): Show |
26 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.257+10630A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858561 | |||||||
chr18:2858561 | ATATATAT others(3): Show |
A | 2 | a0001c0001t0002g0294 a0001c0001t0005g0413 |
2 | HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.257+10632_257+1064 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858561 | ||||||
chr18:2858563 | A | G | 32 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0057 others(29): Show |
33 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.257+10632A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858563 | |||||||
chr18:2858563 | ATATATAT others(13): Show |
A | 1 | a0001c0001t0005g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.257+10640_257+1065 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858563 | ||||||
chr18:2858565 | A | G | 42 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0057 others(39): Show |
43 | HG01192.hp1 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.257+10634A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858565 | |||||||
chr18:2858567 | A | ATATATAT others(9): Show |
1 | a0001c0001t0003g0273 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.257+10639_257+1064 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858567 | ||||||
chr18:2858567 | A | ATATATAT others(7): Show |
2 | a0001c0002t0002g0195 a0001c0002t0002g0360 |
2 | HG00673.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.257+10639_257+1064 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858567 | ||||||
chr18:2858567 | A | ATG | 3 | a0001c0001t0009g0041 a0001c0003t0012g0311 a0002c0005t0004g0011 |
3 | HG00597.hp1 HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.257+10637_257+1063 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858567 | ||||||
chr18:2858567 | A | G | 65 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0057 others(62): Show |
66 | HG00597.hp2 HG00673.hp2 HG01192.hp1 others(63): Show |
intron_variant | MODIFIER | c.257+10636A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858567 | |||||||
chr18:2858567 | ATATG | A | 3 | a0001c0003t0002g0338 a0001c0003t0002g0339 a0001c0042t0002g0149 |
3 | NA18948.hp2 NA18962.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.257+10638_257+1064 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858567 | ||||||
chr18:2858569 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.257+10639_257+1064 others(38): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(13): Show |
1 | a0001c0003t0006g0326 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.257+10639_257+1064 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0133 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.257+10639_257+1064 others(26): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(9): Show |
1 | a0001c0001t0012g0299 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.257+10639_257+1064 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(15): Show |
1 | a0001c0002t0024g0385 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.257+10639_257+1064 others(26): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(7): Show |
1 | a0001c0002t0005g0021 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.257+10639_257+1064 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(5): Show |
1 | a0001c0001t0038g0300 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.257+10639_257+1064 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(3): Show |
1 | a0001c0003t0002g0301 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.257+10639_257+1064 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(5): Show |
2 | a0001c0002t0003g0050 a0002c0007t0004g0345 |
2 | HG02602.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.257+10639_257+1064 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(21): Show |
1 | a0003c0010t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.257+10639_257+1064 others(32): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(1): Show |
7 | a0001c0001t0003g0389 a0001c0001t0010g0323 a0001c0001t0010g0420 others(4): Show |
7 | HG01515.hp1 HG01981.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+10639_257+1064 others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATAT others(3): Show |
2 | a0002c0005t0004g0136 a0020c0029t0006g0135 |
2 | NA18970.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.257+10639_257+1064 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATG | 6 | a0001c0001t0001g0303 a0001c0001t0001g0362 a0001c0001t0005g0439 others(3): Show |
6 | HG00558.hp2 HG00741.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+10639_257+1064 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATATATGT others(1): Show |
3 | a0001c0001t0002g0382 a0001c0001t0025g0051 a0002c0020t0004g0010 |
3 | HG02698.hp1 HG03471.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.257+10639_257+1064 others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | ATG | 9 | a0001c0001t0001g0172 a0001c0001t0002g0173 a0001c0001t0002g0307 others(6): Show |
9 | HG01168.hp1 HG02735.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+10652_257+1065 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858569 | A | G | 231 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0040 others(228): Show |
233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.257+10638A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858569 | |||||||
chr18:2858569 | ATG | A | 5 | a0001c0001t0030g0143 a0001c0001t0030g0144 a0001c0002t0001g0352 others(2): Show |
5 | HG00323.hp2 HG02145.hp2 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+10652_257+1065 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858569 | ||||||
chr18:2858570 | T | TATATATA others(3): Show |
2 | a0005c0021t0004g0069 a0005c0021t0004g0070 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.257+10639_257+1064 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858570 | |||||||
chr18:2858571 | G | A | 29 | a0001c0001t0001g0220 a0001c0001t0001g0363 a0001c0001t0002g0170 others(26): Show |
29 | HG00280.hp2 HG00423.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.257+10640G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858571 | |||||||
chr18:2858573 | G | A | 7 | a0001c0001t0006g0219 a0001c0002t0004g0192 a0001c0002t0005g0351 others(4): Show |
7 | HG00423.hp2 HG02970.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.257+10642G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858573 | |||||||
chr18:2858573 | G | GTATATAT others(43): Show |
1 | a0001c0001t0003g0281 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.257+10643_257+1064 others(54): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858573 | ||||||
chr18:2858573 | G | GTGTATAT others(19): Show |
1 | a0001c0003t0001g0171 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.257+10645_257+1064 others(30): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858573 | ||||||
chr18:2858573 | GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0005g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.257+10648_257+1067 others(32): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858573 | ||||||
chr18:2858575 | G | A | 5 | a0001c0001t0001g0014 a0001c0002t0004g0192 a0001c0002t0005g0351 others(2): Show |
5 | HG03579.hp1 HG03834.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+10644G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858575 | |||||||
chr18:2858577 | G | A | 7 | a0001c0001t0001g0014 a0001c0002t0002g0082 a0001c0002t0004g0192 others(4): Show |
7 | HG01256.hp1 HG02040.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+10646G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858577 | |||||||
chr18:2858577 | G | GTATATAT others(5): Show |
1 | a0001c0003t0016g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.257+10647_257+1064 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858577 | ||||||
chr18:2858579 | G | A | 47 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0181 others(44): Show |
47 | HG00280.hp2 HG00323.hp2 HG01256.hp1 others(44): Show |
intron_variant | MODIFIER | c.257+10648G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858579 | |||||||
chr18:2858579 | G | GTA | 3 | a0001c0001t0006g0147 a0001c0023t0002g0221 a0002c0009t0004g0223 |
3 | HG02004.hp1 HG02602.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.257+10649_257+1065 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858579 | ||||||
chr18:2858579 | G | GTATATA | 3 | a0001c0001t0001g0277 a0001c0001t0005g0044 a0001c0001t0059g0276 |
3 | HG01243.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.257+10649_257+1065 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858579 | ||||||
chr18:2858579 | G | GTATATAT others(3): Show |
1 | a0001c0006t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.257+10649_257+1065 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858579 | ||||||
chr18:2858579 | G | GTATATAT others(7): Show |
1 | a0002c0005t0026g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.257+10649_257+1065 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858579 | ||||||
chr18:2858579 | GTGTGTAT others(15): Show |
G | 1 | a0001c0001t0003g0292 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.257+10666_257+1068 others(26): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858579 | ||||||
chr18:2858581 | G | A | 70 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0181 others(67): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.257+10650G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858581 | |||||||
chr18:2858581 | G | GTATA | 12 | a0001c0001t0002g0081 a0001c0001t0003g0001 a0001c0001t0003g0190 others(9): Show |
13 | HG01074.hp1 HG01192.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+10651_257+1065 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858581 | ||||||
chr18:2858581 | G | GTATATA | 5 | a0001c0001t0017g0228 a0001c0004t0002g0340 a0001c0006t0001g0062 others(2): Show |
5 | HG00733.hp2 HG01081.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.257+10651_257+1065 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858581 | ||||||
chr18:2858581 | G | GTATATAT others(1): Show |
11 | a0001c0001t0003g0273 a0001c0001t0018g0274 a0001c0001t0033g0215 others(8): Show |
11 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.257+10651_257+1065 others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858581 | ||||||
chr18:2858581 | G | GTATATAT others(3): Show |
1 | a0002c0007t0004g0016 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.257+10651_257+1065 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858581 | ||||||
chr18:2858583 | G | A | 189 | a0001c0001t0001g0014 a0001c0001t0001g0040 a0001c0001t0001g0181 others(186): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.257+10652G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858583 | |||||||
chr18:2858583 | G | GTA | 9 | a0001c0001t0001g0002 a0001c0002t0001g0266 a0001c0003t0006g0429 others(6): Show |
10 | HG00642.hp2 HG00741.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+10670_257+1067 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTATA | 3 | a0001c0001t0001g0363 a0001c0002t0005g0280 a0002c0007t0004g0049 |
3 | HG01106.hp2 NA18964.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.257+10668_257+1067 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTATATA | 7 | a0001c0001t0015g0296 a0001c0001t0017g0075 a0001c0006t0002g0240 others(4): Show |
7 | HG00639.hp1 HG01109.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+10666_257+1067 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTATATAT others(3): Show |
7 | a0001c0001t0002g0364 a0001c0002t0014g0243 a0001c0004t0054g0194 others(4): Show |
7 | HG01069.hp1 HG01168.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+10662_257+1067 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTATATAT others(5): Show |
1 | a0001c0004t0002g0055 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.257+10660_257+1067 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0030 a0001c0004t0002g0019 |
2 | HG04115.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.257+10658_257+1067 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTATATAT others(9): Show |
1 | a0001c0013t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.257+10656_257+1067 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTATATAT others(51): Show |
1 | a0002c0005t0004g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.257+10671_257+1067 others(62): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTA | 5 | a0001c0002t0001g0400 a0001c0002t0003g0398 a0001c0002t0008g0399 others(2): Show |
5 | NA18946.hp1 NA18966.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+10653_257+1065 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTATAT others(1): Show |
4 | a0001c0001t0001g0220 a0001c0001t0006g0219 a0001c0001t0034g0426 others(1): Show |
4 | HG00423.hp2 HG01081.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+10653_257+1065 others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTATAT others(5): Show |
1 | a0001c0006t0005g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.257+10653_257+1065 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTATAT others(7): Show |
1 | a0001c0014t0001g0043 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.257+10653_257+1065 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTAT others(9): Show |
1 | a0004c0039t0056g0017 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(5): Show |
1 | a0003c0012t0001g0025 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(7): Show |
2 | a0001c0001t0037g0374 a0001c0004t0013g0004 |
3 | HG01884.hp1 HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.257+10653_257+1065 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(5): Show |
1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(11): Show |
4 | a0001c0001t0005g0257 a0001c0001t0014g0213 a0001c0001t0035g0214 others(1): Show |
4 | HG02109.hp1 HG02895.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+10653_257+1065 others(22): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(13): Show |
3 | a0001c0013t0009g0211 a0002c0005t0004g0256 a0003c0010t0009g0262 |
3 | HG02630.hp1 HG03540.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.257+10653_257+1065 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0037g0212 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.257+10653_257+1065 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(15): Show |
1 | a0001c0001t0001g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(26): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0052g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.257+10653_257+1065 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(17): Show |
1 | a0001c0008t0021g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(28): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(19): Show |
4 | a0001c0004t0009g0068 a0002c0005t0072g0258 a0005c0021t0004g0069 others(1): Show |
4 | HG02723.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.257+10653_257+1065 others(30): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(21): Show |
2 | a0001c0001t0001g0066 a0001c0004t0005g0067 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.257+10653_257+1065 others(32): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(17): Show |
1 | a0002c0009t0004g0260 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.257+10653_257+1065 others(28): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(21): Show |
1 | a0001c0001t0005g0065 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.257+10653_257+1065 others(32): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(15): Show |
1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.257+10653_257+1065 others(26): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(21): Show |
1 | a0001c0001t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(32): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(25): Show |
1 | a0003c0012t0001g0437 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(36): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(21): Show |
1 | a0024c0030t0004g0438 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(32): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | G | GTGTGTGT others(29): Show |
1 | a0001c0001t0005g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.257+10653_257+1065 others(40): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858583 | GTATATAT others(11): Show |
G | 2 | a0001c0001t0002g0294 a0001c0001t0005g0413 |
2 | HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.257+10654_257+1067 others(22): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858583 | ||||||
chr18:2858585 | A | G | 8 | a0001c0001t0001g0057 a0001c0001t0002g0173 a0001c0001t0002g0217 others(5): Show |
8 | HG00642.hp1 HG01192.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.257+10654A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858585 | |||||||
chr18:2858587 | A | G | 5 | a0001c0001t0001g0057 a0001c0016t0016g0029 a0003c0010t0019g0216 others(2): Show |
5 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+10656A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858587 | |||||||
chr18:2858589 | A | G | 5 | a0001c0001t0001g0057 a0001c0016t0016g0029 a0003c0010t0019g0216 others(2): Show |
5 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+10658A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858589 | |||||||
chr18:2858591 | A | G | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+10660A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858591 | |||||||
chr18:2858593 | A | G | 1 | a0003c0012t0048g0008 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.257+10662A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858593 | |||||||
chr18:2858597 | A | G | 1 | a0001c0001t0005g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.257+10666A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858597 | |||||||
chr18:2858599 | A | ATG | 87 | a0001c0001t0001g0245 a0001c0001t0001g0415 a0001c0001t0001g0418 others(84): Show |
87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.257+10669_257+1067 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858599 | ||||||
chr18:2858599 | A | ATGTGTG | 5 | a0001c0001t0002g0368 a0001c0001t0002g0369 a0001c0001t0002g0370 others(2): Show |
5 | NA18960.hp1 NA18977.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.257+10669_257+1067 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858599 | ||||||
chr18:2858599 | A | G | 6 | a0001c0001t0001g0083 a0001c0001t0005g0166 a0001c0016t0016g0029 others(3): Show |
6 | HG01192.hp1 HG02622.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.257+10668A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858599 | |||||||
chr18:2858601 | A | G | 99 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(96): Show |
99 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.257+10670A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858601 | |||||||
chr18:2858603 | G | A | 1 | a0001c0023t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.257+10672G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858603 | |||||||
chr18:2858605 | G | GTATA | 31 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0066 others(28): Show |
32 | HG01884.hp1 HG02109.hp1 HG02258.hp2 others(29): Show |
intron_variant | MODIFIER | c.257+10684_257+1068 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858605 | ||||||
chr18:2858605 | G | GTATATA | 9 | a0001c0001t0001g0040 a0001c0001t0001g0207 a0001c0041t0014g0263 others(6): Show |
9 | HG01106.hp1 HG01891.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.257+10682_257+1068 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2858605 | ||||||
chr18:2858696 | C | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0005g0065 others(4): Show |
7 | HG02647.hp2 HG02723.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+10765C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858696 | |||||||
chr18:2858710 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.257+10779A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858710 | |||||||
chr18:2858826 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.257+10895G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858826 | |||||||
chr18:2858856 | G | A | 88 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(85): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.257+10925G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2858856 | |||||||
chr18:2859006 | C | T | 7 | a0001c0001t0009g0041 a0001c0001t0047g0064 a0001c0013t0001g0009 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.257+11075C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859006 | |||||||
chr18:2859101 | T | C | 92 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(89): Show |
92 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.257+11170T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859101 | |||||||
chr18:2859152 | C | T | 1 | a0001c0004t0064g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.257+11221C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859152 | |||||||
chr18:2859174 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.257+11243G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859174 | |||||||
chr18:2859266 | G | A | 1 | a0002c0007t0004g0053 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.257+11335G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859266 | |||||||
chr18:2859474 | T | C | 10 | a0001c0001t0009g0041 a0001c0001t0016g0344 a0001c0001t0018g0026 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+11543T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859474 | |||||||
chr18:2859484 | T | C | 16 | a0001c0001t0002g0328 a0001c0001t0003g0334 a0001c0001t0005g0333 others(13): Show |
16 | HG02132.hp2 NA18943.hp1 NA18944.hp2 others(13): Show |
intron_variant | MODIFIER | c.257+11553T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859484 | |||||||
chr18:2859588 | T | C | 2 | a0001c0001t0001g0255 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.257+11657T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859588 | |||||||
chr18:2859652 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.257+11721T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859652 | |||||||
chr18:2859762 | G | A | 1 | a0005c0038t0004g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.257+11831G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859762 | |||||||
chr18:2859860 | A | G | 2 | a0001c0001t0001g0255 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.257+11929A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859860 | |||||||
chr18:2859923 | G | A | 1 | a0002c0005t0004g0256 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.257+11992G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2859923 | |||||||
chr18:2860225 | A | T | 38 | a0001c0001t0001g0014 a0001c0001t0001g0277 a0001c0001t0002g0364 others(35): Show |
38 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.257+12294A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860225 | |||||||
chr18:2860249 | T | A | 3 | a0001c0004t0009g0068 a0005c0021t0004g0069 a0005c0021t0004g0070 |
3 | HG02723.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.257+12318T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860249 | |||||||
chr18:2860295 | G | A | 10 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0005g0065 others(7): Show |
10 | HG02647.hp2 HG02723.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.257+12364G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860295 | |||||||
chr18:2860303 | G | C | 1 | a0001c0004t0003g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.257+12372G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860303 | |||||||
chr18:2860331 | C | T | 38 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(35): Show |
39 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.257+12400C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860331 | |||||||
chr18:2860359 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0021g0253 a0019c0048t0004g0252 |
3 | HG03225.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.257+12428G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860359 | |||||||
chr18:2860395 | A | G | 1 | a0001c0001t0007g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.257+12464A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860395 | |||||||
chr18:2860458 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.257+12527A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860458 | |||||||
chr18:2860608 | G | A | 1 | a0001c0001t0007g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.257+12677G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860608 | |||||||
chr18:2860612 | C | T | 2 | a0001c0001t0001g0255 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.257+12681C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860612 | |||||||
chr18:2860861 | A | C | 3 | a0001c0001t0005g0235 a0003c0012t0001g0437 a0024c0030t0004g0438 |
3 | HG02922.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.257+12930A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860861 | |||||||
chr18:2860873 | A | G | 2 | a0001c0001t0009g0041 a0002c0005t0004g0011 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.257+12942A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860873 | |||||||
chr18:2860881 | A | G | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+12950A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860881 | |||||||
chr18:2860893 | G | A | 133 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(130): Show |
134 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.257+12962G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860893 | |||||||
chr18:2860938 | T | C | 2 | a0010c0019t0001g0034 a0010c0019t0001g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.257+13007T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860938 | |||||||
chr18:2860949 | A | G | 42 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(39): Show |
43 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.257+13018A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2860949 | |||||||
chr18:2860966 | A | AT | 4 | a0001c0001t0012g0299 a0001c0002t0003g0324 a0002c0007t0004g0305 others(1): Show |
4 | HG01123.hp1 NA18997.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+13037dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2860966 | ||||||
chr18:2861081 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.257+13150T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861081 | |||||||
chr18:2861087 | G | GT | 12 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0005g0065 others(9): Show |
12 | HG02647.hp2 HG02723.hp2 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.257+13164dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2861087 | ||||||
chr18:2861191 | C | G | 2 | a0001c0006t0001g0062 a0001c0006t0001g0063 |
2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.257+13260C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861191 | |||||||
chr18:2861199 | C | T | 3 | a0001c0001t0001g0255 a0001c0006t0001g0316 a0008c0017t0001g0074 |
3 | HG01928.hp1 HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.257+13268C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861199 | |||||||
chr18:2861200 | G | A | 3 | a0003c0010t0009g0155 a0009c0018t0001g0012 a0009c0018t0001g0156 |
3 | HG02109.hp2 HG02257.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.257+13269G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861200 | |||||||
chr18:2861490 | A | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0348 a0001c0001t0001g0362 others(108): Show |
113 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.257+13559A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861490 | |||||||
chr18:2861504 | G | T | 2 | a0001c0002t0003g0120 a0002c0005t0004g0078 |
2 | HG02071.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.257+13573G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861504 | |||||||
chr18:2861543 | A | G | 92 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(89): Show |
92 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.257+13612A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861543 | |||||||
chr18:2861551 | A | G | 44 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(41): Show |
45 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.257+13620A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861551 | |||||||
chr18:2861714 | A | G | 1 | a0001c0014t0004g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.257+13783A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861714 | |||||||
chr18:2861913 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.257+13982C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861913 | |||||||
chr18:2861960 | G | A | 2 | a0001c0001t0030g0143 a0001c0001t0030g0144 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.257+14029G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2861960 | |||||||
chr18:2862061 | G | T | 1 | a0001c0002t0003g0335 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.257+14130G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862061 | |||||||
chr18:2862112 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0022g0122 a0001c0002t0006g0204 |
3 | NA18942.hp1 NA18981.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.257+14181A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862112 | |||||||
chr18:2862117 | C | T | 4 | a0001c0001t0002g0294 a0001c0001t0005g0295 a0001c0001t0005g0350 others(1): Show |
4 | HG01361.hp2 HG03688.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+14186C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862117 | |||||||
chr18:2862188 | A | G | 1 | a0002c0005t0004g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.257+14257A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862188 | |||||||
chr18:2862190 | T | G | 92 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(89): Show |
92 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.257+14259T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862190 | |||||||
chr18:2862240 | C | G | 308 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(305): Show |
310 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(307): Show |
intron_variant | MODIFIER | c.257+14309C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862240 | |||||||
chr18:2862281 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.257+14350G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862281 | |||||||
chr18:2862686 | T | C | 44 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(41): Show |
45 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.257+14755T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862686 | |||||||
chr18:2862688 | T | C | 1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.257+14757T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862688 | |||||||
chr18:2862691 | T | G | 3 | a0001c0001t0001g0254 a0001c0001t0021g0253 a0019c0048t0004g0252 |
3 | HG03225.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.257+14760T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862691 | |||||||
chr18:2862856 | T | G | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.257+14925T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862856 | |||||||
chr18:2862878 | A | G | 1 | a0001c0002t0002g0218 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.257+14947A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2862878 | |||||||
chr18:2863006 | C | T | 88 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(85): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.257+15075C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863006 | |||||||
chr18:2863024 | A | G | 1 | a0008c0017t0001g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.257+15093A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863024 | |||||||
chr18:2863057 | C | G | 1 | a0001c0001t0002g0435 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.257+15126C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863057 | |||||||
chr18:2863341 | T | C | 4 | a0001c0001t0001g0220 a0001c0003t0001g0224 a0002c0009t0004g0223 others(1): Show |
4 | HG01081.hp2 HG01975.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+15410T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863341 | |||||||
chr18:2863432 | T | C | 1 | a0001c0001t0006g0308 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.257+15501T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863432 | |||||||
chr18:2863498 | A | T | 1 | a0002c0007t0004g0313 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.257+15567A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863498 | |||||||
chr18:2863538 | GT | G | 87 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(84): Show |
87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.257+15610delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2863538 | ||||||
chr18:2863541 | TC | T | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.257+15611delC | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863541 | |||||||
chr18:2863669 | TGTG | T | 91 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(88): Show |
91 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.257+15742_257+1574 others(7): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2863669 | ||||||
chr18:2863706 | G | C | 44 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(41): Show |
45 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(42): Show |
intron_variant | MODIFIER | c.257+15775G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863706 | |||||||
chr18:2863707 | G | T | 13 | a0001c0001t0001g0254 a0001c0001t0009g0041 a0001c0001t0016g0344 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+15776G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863707 | |||||||
chr18:2863759 | A | T | 2 | a0001c0001t0003g0203 a0002c0005t0004g0165 |
2 | NA18975.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.257+15828A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863759 | |||||||
chr18:2863791 | C | T | 42 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(39): Show |
43 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.257+15860C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863791 | |||||||
chr18:2863891 | A | C | 1 | a0001c0001t0002g0233 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.257+15960A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863891 | |||||||
chr18:2863933 | G | C | 1 | a0001c0037t0063g0361 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.257+16002G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2863933 | |||||||
chr18:2864074 | T | C | 3 | a0001c0001t0005g0235 a0003c0012t0001g0437 a0024c0030t0004g0438 |
3 | HG02922.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.257+16143T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864074 | |||||||
chr18:2864121 | C | T | 9 | a0001c0001t0001g0172 a0001c0001t0001g0303 a0001c0001t0002g0307 others(6): Show |
9 | HG01168.hp1 HG01261.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.257+16190C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864121 | |||||||
chr18:2864251 | C | G | 2 | a0003c0010t0019g0216 a0003c0012t0048g0008 |
2 | HG01192.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.257+16320C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864251 | |||||||
chr18:2864265 | G | T | 2 | a0003c0010t0019g0216 a0003c0012t0048g0008 |
2 | HG01192.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.257+16334G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864265 | |||||||
chr18:2864266 | T | A | 2 | a0003c0010t0019g0216 a0003c0012t0048g0008 |
2 | HG01192.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.257+16335T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864266 | |||||||
chr18:2864278 | T | A | 1 | a0002c0007t0004g0313 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.257+16347T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864278 | |||||||
chr18:2864279 | A | T | 1 | a0002c0007t0004g0313 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.257+16348A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864279 | |||||||
chr18:2864378 | T | G | 3 | a0001c0001t0030g0143 a0001c0001t0030g0144 a0002c0020t0004g0131 |
3 | HG03491.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.257+16447T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864378 | |||||||
chr18:2864399 | C | G | 20 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0208 others(17): Show |
21 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.257+16468C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864399 | |||||||
chr18:2864461 | A | G | 92 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(89): Show |
92 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.257+16530A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864461 | |||||||
chr18:2864468 | C | A | 1 | a0001c0001t0002g0372 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.257+16537C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864468 | |||||||
chr18:2864763 | T | C | 3 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 |
3 | HG01192.hp1 HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.257+16832T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864763 | |||||||
chr18:2864857 | T | C | 13 | a0001c0001t0001g0254 a0001c0001t0009g0041 a0001c0001t0016g0344 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+16926T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864857 | |||||||
chr18:2864863 | G | A | 1 | a0006c0027t0001g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.257+16932G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2864863 | |||||||
chr18:2865004 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.257+17073C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865004 | |||||||
chr18:2865005 | G | A | 1 | a0001c0001t0009g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.257+17074G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865005 | |||||||
chr18:2865032 | G | A | 87 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(84): Show |
87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.257+17101G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865032 | |||||||
chr18:2865050 | T | C | 313 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(310): Show |
315 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.257+17119T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865050 | |||||||
chr18:2865069 | A | T | 1 | a0001c0001t0002g0372 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.257+17138A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865069 | |||||||
chr18:2865124 | T | A | 1 | a0001c0001t0002g0372 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.257+17193T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865124 | |||||||
chr18:2865157 | T | TTTGAA | 13 | a0001c0001t0001g0254 a0001c0001t0009g0041 a0001c0001t0016g0344 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.257+17227_257+1723 others(9): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2865157 | ||||||
chr18:2865202 | C | CT | 11 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0005g0065 others(8): Show |
11 | HG02647.hp2 HG02723.hp2 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.257+17273dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2865202 | ||||||
chr18:2865288 | G | C | 91 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(88): Show |
91 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.257+17357G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865288 | |||||||
chr18:2865437 | C | G | 1 | a0001c0001t0003g0269 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.257+17506C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865437 | |||||||
chr18:2865490 | G | T | 1 | a0001c0001t0003g0297 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.257+17559G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865490 | |||||||
chr18:2865507 | G | A | 15 | a0001c0001t0009g0041 a0001c0001t0014g0033 a0001c0001t0016g0344 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.257+17576G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865507 | |||||||
chr18:2865705 | T | C | 312 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(309): Show |
314 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.257+17774T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865705 | |||||||
chr18:2865831 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0021g0253 a0019c0048t0004g0252 |
3 | HG03225.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.257+17900G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865831 | |||||||
chr18:2865905 | A | C | 70 | a0001c0001t0001g0181 a0001c0001t0001g0220 a0001c0001t0002g0081 others(67): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.257+17974A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865905 | |||||||
chr18:2865979 | G | A | 6 | a0001c0001t0009g0041 a0001c0001t0047g0064 a0001c0013t0001g0009 others(3): Show |
6 | HG02486.hp2 HG02572.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.257+18048G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865979 | |||||||
chr18:2865995 | A | G | 1 | a0001c0002t0002g0118 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.257+18064A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2865995 | |||||||
chr18:2866005 | G | A | 69 | a0001c0001t0001g0181 a0001c0001t0001g0220 a0001c0001t0002g0081 others(66): Show |
70 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.257+18074G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866005 | |||||||
chr18:2866175 | G | A | 1 | a0005c0038t0004g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.257+18244G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866175 | |||||||
chr18:2866213 | G | C | 92 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(89): Show |
92 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.257+18282G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866213 | |||||||
chr18:2866216 | C | T | 2 | a0003c0010t0019g0216 a0003c0012t0048g0008 |
2 | HG01192.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.257+18285C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866216 | |||||||
chr18:2866228 | G | T | 1 | a0001c0001t0005g0241 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.257+18297G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866228 | |||||||
chr18:2866372 | A | G | 70 | a0001c0001t0001g0181 a0001c0001t0001g0220 a0001c0001t0002g0081 others(67): Show |
71 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.257+18441A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866372 | |||||||
chr18:2866422 | T | G | 1 | a0001c0001t0002g0372 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.257+18491T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866422 | |||||||
chr18:2866449 | A | T | 2 | a0001c0001t0001g0255 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.258-18515A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866449 | |||||||
chr18:2866492 | T | C | 31 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0207 others(28): Show |
32 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.258-18472T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866492 | |||||||
chr18:2866503 | G | A | 301 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(298): Show |
303 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.258-18461G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866503 | |||||||
chr18:2866619 | G | A | 1 | a0001c0003t0003g0411 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.258-18345G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866619 | |||||||
chr18:2866669 | A | G | 20 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0208 others(17): Show |
21 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.258-18295A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866669 | |||||||
chr18:2866704 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-18260T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866704 | |||||||
chr18:2866720 | TC | T | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-18242delC | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2866720 | ||||||
chr18:2866729 | A | G | 1 | a0001c0001t0002g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.258-18235A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2866729 | |||||||
chr18:2867006 | C | G | 1 | a0001c0001t0006g0219 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.258-17958C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867006 | |||||||
chr18:2867244 | C | G | 4 | a0001c0001t0003g0269 a0001c0001t0003g0314 a0001c0001t0006g0309 others(1): Show |
4 | NA18948.hp1 NA18980.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-17720C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867244 | |||||||
chr18:2867346 | CTTTA | C | 6 | a0001c0002t0002g0244 a0001c0016t0016g0029 a0002c0007t0004g0053 others(3): Show |
6 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-17595_258-1759 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2867346 | ||||||
chr18:2867346 | CTTTATTT others(1): Show |
C | 88 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(85): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.258-17599_258-1759 others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2867346 | ||||||
chr18:2867369 | T | G | 2 | a0001c0001t0001g0255 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.258-17595T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867369 | |||||||
chr18:2867394 | G | A | 1 | a0001c0001t0038g0300 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.258-17570G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867394 | |||||||
chr18:2867395 | C | G | 1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.258-17569C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867395 | |||||||
chr18:2867419 | A | G | 1 | a0001c0002t0002g0304 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.258-17545A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867419 | |||||||
chr18:2867495 | C | T | 14 | a0001c0001t0001g0254 a0001c0001t0009g0041 a0001c0001t0016g0344 others(11): Show |
14 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.258-17469C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867495 | |||||||
chr18:2867503 | C | T | 1 | a0001c0003t0006g0429 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.258-17461C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867503 | |||||||
chr18:2867522 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-17442G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867522 | |||||||
chr18:2867599 | T | G | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-17365T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867599 | |||||||
chr18:2867667 | G | A | 5 | a0001c0001t0002g0446 a0001c0001t0005g0238 a0001c0001t0005g0445 others(2): Show |
5 | HG00639.hp1 HG00733.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-17297G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867667 | |||||||
chr18:2867746 | ACTT | A | 29 | a0001c0001t0001g0220 a0001c0001t0002g0081 a0001c0001t0002g0368 others(26): Show |
30 | HG00423.hp2 HG00733.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.258-17214_258-1721 others(7): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2867746 | ||||||
chr18:2867777 | G | A | 1 | a0001c0001t0052g0210 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.258-17187G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867777 | |||||||
chr18:2867787 | T | G | 4 | a0001c0001t0017g0075 a0001c0001t0034g0426 a0012c0051t0019g0076 others(1): Show |
4 | HG01891.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-17177T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867787 | |||||||
chr18:2867826 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.258-17138C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867826 | |||||||
chr18:2867864 | G | A | 1 | a0001c0004t0064g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.258-17100G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867864 | |||||||
chr18:2867883 | GTGGT | G | 3 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 |
3 | HG01192.hp1 HG02622.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.258-17080_258-1707 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867883 | |||||||
chr18:2867884 | T | TGGTGGCC others(70): Show |
1 | a0001c0001t0002g0390 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.258-17077_258-1700 others(81): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2867884 | ||||||
chr18:2867895 | C | CAG | 6 | a0001c0001t0001g0415 a0001c0001t0001g0418 a0001c0001t0002g0239 others(3): Show |
6 | HG01261.hp1 HG01934.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-17066_258-1706 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2867895 | ||||||
chr18:2867924 | C | T | 1 | a0003c0010t0020g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258-17040C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867924 | |||||||
chr18:2867938 | C | T | 2 | a0001c0006t0001g0357 a0001c0006t0032g0358 |
2 | HG00733.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.258-17026C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867938 | |||||||
chr18:2867939 | G | A | 3 | a0001c0001t0005g0235 a0003c0012t0001g0437 a0024c0030t0004g0438 |
3 | HG02922.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.258-17025G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867939 | |||||||
chr18:2867948 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-17016C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867948 | |||||||
chr18:2867974 | A | G | 135 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(132): Show |
136 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.258-16990A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2867974 | |||||||
chr18:2867980 | C | CTGACCCC others(42): Show |
1 | a0002c0009t0004g0223 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.258-16955_258-1695 others(53): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2867980 | ||||||
chr18:2868021 | C | G | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16943C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868021 | |||||||
chr18:2868027 | T | C | 136 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(133): Show |
137 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.258-16937T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868027 | |||||||
chr18:2868055 | G | A | 88 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0415 others(85): Show |
88 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.258-16909G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868055 | |||||||
chr18:2868085 | A | G | 150 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(147): Show |
151 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.258-16879A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868085 | |||||||
chr18:2868095 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16869G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868095 | |||||||
chr18:2868122 | T | C | 4 | a0001c0001t0003g0132 a0001c0001t0011g0298 a0001c0002t0003g0167 others(1): Show |
4 | NA18969.hp2 NA18995.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-16842T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868122 | |||||||
chr18:2868128 | G | A | 163 | a0001c0001t0001g0014 a0001c0001t0001g0181 a0001c0001t0001g0220 others(160): Show |
164 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.258-16836G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868128 | |||||||
chr18:2868182 | G | T | 1 | a0001c0001t0059g0276 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.258-16782G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868182 | |||||||
chr18:2868204 | C | T | 1 | a0001c0001t0018g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.258-16760C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868204 | |||||||
chr18:2868274 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16690A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868274 | |||||||
chr18:2868283 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0009g0045 a0003c0012t0001g0025 others(1): Show |
4 | HG02615.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-16681C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868283 | |||||||
chr18:2868287 | G | A | 40 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(37): Show |
41 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.258-16677G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868287 | |||||||
chr18:2868287 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16677G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868287 | |||||||
chr18:2868291 | A | C | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16673A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868291 | |||||||
chr18:2868292 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16672A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868292 | |||||||
chr18:2868296 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16668G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868296 | |||||||
chr18:2868298 | G | A | 3 | a0001c0001t0005g0439 a0001c0003t0005g0380 a0001c0003t0057g0346 |
3 | NA18952.hp2 NA18973.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.258-16666G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868298 | |||||||
chr18:2868343 | C | T | 1 | a0001c0008t0001g0249 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.258-16621C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868343 | |||||||
chr18:2868359 | C | T | 87 | a0001c0001t0001g0083 a0001c0001t0001g0418 a0001c0001t0002g0091 others(84): Show |
87 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.258-16605C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868359 | |||||||
chr18:2868366 | G | A | 2 | a0003c0010t0019g0216 a0003c0012t0048g0008 |
2 | HG01192.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.258-16598G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868366 | |||||||
chr18:2868412 | A | G | 1 | a0002c0005t0004g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.258-16552A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868412 | |||||||
chr18:2868426 | T | A | 1 | a0002c0005t0004g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.258-16538T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868426 | |||||||
chr18:2868434 | A | C | 1 | a0002c0005t0004g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.258-16530A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868434 | |||||||
chr18:2868445 | G | C | 1 | a0001c0001t0039g0229 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.258-16519G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868445 | |||||||
chr18:2868449 | G | A | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-16515G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868449 | |||||||
chr18:2868464 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.258-16500C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868464 | |||||||
chr18:2868468 | C | G | 1 | a0001c0001t0001g0362 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.258-16496C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868468 | |||||||
chr18:2868523 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-16441C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868523 | |||||||
chr18:2868527 | G | C | 1 | a0002c0005t0026g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.258-16437G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868527 | |||||||
chr18:2868543 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.258-16421C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868543 | |||||||
chr18:2868568 | C | T | 1 | a0002c0005t0043g0440 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.258-16396C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868568 | |||||||
chr18:2868577 | C | T | 35 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0066 others(32): Show |
36 | HG01106.hp1 HG01884.hp1 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.258-16387C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868577 | |||||||
chr18:2868614 | C | T | 1 | a0001c0002t0067g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.258-16350C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868614 | |||||||
chr18:2868625 | C | T | 2 | a0001c0001t0030g0143 a0001c0001t0030g0144 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.258-16339C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868625 | |||||||
chr18:2868641 | C | T | 3 | a0001c0001t0005g0235 a0003c0012t0001g0437 a0024c0030t0004g0438 |
3 | HG02922.hp1 HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.258-16323C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868641 | |||||||
chr18:2868661 | G | C | 21 | a0001c0001t0001g0057 a0001c0001t0001g0348 a0001c0001t0002g0446 others(18): Show |
21 | HG00423.hp1 HG00733.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.258-16303G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868661 | |||||||
chr18:2868661 | G | T | 1 | a0001c0002t0067g0013 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.258-16303G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868661 | |||||||
chr18:2868668 | C | T | 20 | a0001c0001t0001g0348 a0001c0001t0002g0446 a0001c0001t0003g0278 others(17): Show |
20 | HG00423.hp1 HG00733.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.258-16296C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868668 | |||||||
chr18:2868688 | C | G | 1 | a0001c0001t0001g0030 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.258-16276C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868688 | |||||||
chr18:2868689 | G | A | 4 | a0001c0002t0002g0391 a0001c0003t0005g0380 a0001c0003t0005g0392 others(1): Show |
4 | NA18955.hp1 NA18973.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-16275G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868689 | |||||||
chr18:2868702 | A | G | 2 | a0001c0001t0002g0321 a0001c0001t0002g0421 |
2 | HG00609.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.258-16262A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868702 | |||||||
chr18:2868708 | A | T | 3 | a0001c0014t0004g0006 a0001c0016t0017g0259 a0005c0038t0004g0023 |
3 | HG02258.hp2 HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.258-16256A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868708 | |||||||
chr18:2868722 | C | T | 1 | a0002c0005t0004g0206 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.258-16242C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868722 | |||||||
chr18:2868761 | G | C | 1 | a0001c0002t0002g0337 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.258-16203G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868761 | |||||||
chr18:2868766 | G | A | 172 | a0001c0001t0001g0014 a0001c0001t0001g0181 a0001c0001t0001g0220 others(169): Show |
173 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.258-16198G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868766 | |||||||
chr18:2868775 | C | G | 305 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(302): Show |
307 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.258-16189C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868775 | |||||||
chr18:2868791 | A | AGGAGAGG others(11): Show |
8 | a0001c0001t0044g0442 a0001c0001t0045g0443 a0001c0002t0042g0444 others(5): Show |
8 | HG00738.hp1 HG01433.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-16167_258-1615 others(22): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2868791 | ||||||
chr18:2868850 | G | A | 1 | a0001c0001t0005g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.258-16114G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868850 | |||||||
chr18:2868955 | GT | G | 295 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(292): Show |
297 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(294): Show |
intron_variant | MODIFIER | c.258-15995delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2868955 | ||||||
chr18:2868959 | T | G | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-16005T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2868959 | |||||||
chr18:2869063 | A | G | 4 | a0001c0001t0005g0048 a0003c0010t0009g0155 a0009c0018t0001g0012 others(1): Show |
4 | HG02109.hp2 HG02257.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-15901A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869063 | |||||||
chr18:2869101 | A | T | 2 | a0001c0001t0003g0290 a0001c0002t0002g0118 |
2 | HG02083.hp2 NA18941.hp1 |
intron_variant | MODIFIER | c.258-15863A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869101 | |||||||
chr18:2869141 | A | T | 2 | a0002c0007t0004g0312 a0002c0007t0004g0313 |
2 | NA18949.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.258-15823A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869141 | |||||||
chr18:2869280 | TA | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0001g0066 others(14): Show |
17 | HG02257.hp1 HG02486.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.258-15672delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869280 | ||||||
chr18:2869280 | TAA | T | 145 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0181 others(142): Show |
147 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.258-15673_258-1567 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869280 | ||||||
chr18:2869322 | A | G | 3 | a0001c0001t0003g0269 a0001c0001t0006g0309 a0001c0001t0038g0300 |
3 | NA18948.hp1 NA18980.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.258-15642A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869322 | |||||||
chr18:2869379 | A | G | 1 | a0001c0004t0040g0113 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.258-15585A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869379 | |||||||
chr18:2869422 | T | C | 1 | a0001c0001t0001g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.258-15542T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869422 | |||||||
chr18:2869437 | C | A | 87 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0208 others(84): Show |
88 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.258-15527C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869437 | |||||||
chr18:2869446 | G | C | 89 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0208 others(86): Show |
90 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.258-15518G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869446 | |||||||
chr18:2869537 | A | T | 2 | a0001c0001t0002g0321 a0001c0001t0002g0421 |
2 | HG00609.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.258-15427A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869537 | |||||||
chr18:2869591 | G | A | 173 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(170): Show |
175 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.258-15373G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869591 | |||||||
chr18:2869604 | AT | A | 7 | a0001c0001t0005g0235 a0001c0001t0014g0033 a0001c0016t0061g0058 others(4): Show |
7 | HG02809.hp1 HG02922.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-15349delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869604 | ||||||
chr18:2869619 | A | G | 1 | a0001c0002t0024g0385 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.258-15345A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869619 | |||||||
chr18:2869670 | T | C | 156 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0001g0066 others(153): Show |
157 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.258-15294T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869670 | |||||||
chr18:2869726 | C | T | 7 | a0001c0001t0005g0235 a0001c0001t0014g0033 a0001c0016t0061g0058 others(4): Show |
7 | HG02809.hp1 HG02922.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-15238C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869726 | |||||||
chr18:2869768 | C | G | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-15196C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869768 | |||||||
chr18:2869768 | CTGTGTGT others(17): Show |
C | 122 | a0001c0001t0001g0181 a0001c0001t0001g0220 a0001c0001t0001g0415 others(119): Show |
123 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.258-15178_258-1515 others(28): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869768 | ||||||
chr18:2869774 | GTGTGTGT others(5): Show |
G | 11 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0208 others(8): Show |
11 | HG01106.hp1 HG01891.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.258-15178_258-1516 others(16): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869774 | ||||||
chr18:2869776 | GTGTGTGT others(3): Show |
G | 10 | a0001c0001t0001g0057 a0001c0001t0005g0257 a0001c0001t0014g0213 others(7): Show |
11 | HG01884.hp1 HG02109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.258-15178_258-1516 others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869776 | ||||||
chr18:2869780 | GTGTGTT | G | 15 | a0001c0001t0001g0030 a0001c0001t0005g0065 a0001c0001t0005g0235 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.258-15178_258-1517 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869780 | ||||||
chr18:2869782 | G | GTGTGTT | 37 | a0001c0001t0001g0014 a0001c0001t0001g0277 a0001c0001t0002g0364 others(34): Show |
37 | HG00609.hp1 HG00673.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.258-15179_258-1517 others(10): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869782 | ||||||
chr18:2869782 | GTGTT | G | 4 | a0001c0001t0001g0255 a0001c0014t0004g0006 a0008c0017t0001g0074 others(1): Show |
4 | HG02257.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-15178_258-1517 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869782 | ||||||
chr18:2869786 | T | G | 46 | a0001c0001t0001g0014 a0001c0001t0001g0277 a0001c0001t0002g0364 others(43): Show |
46 | HG00609.hp1 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.258-15178T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869786 | |||||||
chr18:2869786 | T | TTG | 9 | a0001c0001t0002g0110 a0001c0001t0002g0428 a0001c0001t0003g0388 others(6): Show |
9 | HG01257.hp1 HG01496.hp1 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-15152_258-1515 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869786 | ||||||
chr18:2869786 | T | TTGTGTGT others(7): Show |
3 | a0001c0001t0001g0207 a0003c0012t0001g0025 a0016c0028t0001g0024 |
3 | HG02970.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.258-15164_258-1515 others(18): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869786 | ||||||
chr18:2869786 | T | TTGTGTGT others(13): Show |
1 | a0001c0001t0009g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.258-15170_258-1515 others(24): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2869786 | ||||||
chr18:2869805 | T | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-15159T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869805 | |||||||
chr18:2869815 | C | G | 170 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(167): Show |
172 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.258-15149C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869815 | |||||||
chr18:2869840 | C | CAT | 165 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(162): Show |
167 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.258-15124_258-1512 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869840 | |||||||
chr18:2869841 | G | A | 216 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(213): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.258-15123G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869841 | |||||||
chr18:2869918 | T | G | 161 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0057 others(158): Show |
163 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.258-15046T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2869918 | |||||||
chr18:2870163 | C | G | 1 | a0002c0005t0004g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.258-14801C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870163 | |||||||
chr18:2870195 | T | C | 22 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0009g0041 others(19): Show |
22 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.258-14769T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870195 | |||||||
chr18:2870268 | T | C | 3 | a0001c0001t0001g0254 a0001c0001t0021g0253 a0019c0048t0004g0252 |
3 | HG03225.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.258-14696T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870268 | |||||||
chr18:2870385 | A | G | 1 | a0001c0001t0005g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.258-14579A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870385 | |||||||
chr18:2870423 | T | A | 27 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(24): Show |
27 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.258-14541T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870423 | |||||||
chr18:2870494 | A | G | 150 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0181 others(147): Show |
152 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.258-14470A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870494 | |||||||
chr18:2870522 | G | C | 29 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-14442G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870522 | |||||||
chr18:2870541 | G | A | 6 | a0001c0001t0001g0207 a0001c0001t0009g0045 a0001c0014t0004g0006 others(3): Show |
6 | HG02615.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-14423G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870541 | |||||||
chr18:2870550 | G | T | 29 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-14414G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870550 | |||||||
chr18:2870567 | T | C | 29 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-14397T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870567 | |||||||
chr18:2870660 | C | T | 29 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-14304C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870660 | |||||||
chr18:2870833 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.258-14131T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870833 | |||||||
chr18:2870863 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.258-14101T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870863 | |||||||
chr18:2870879 | G | T | 89 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0002g0091 others(86): Show |
89 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.258-14085G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870879 | |||||||
chr18:2870893 | A | C | 29 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-14071A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870893 | |||||||
chr18:2870913 | T | C | 24 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0254 others(21): Show |
24 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.258-14051T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2870913 | |||||||
chr18:2871006 | T | G | 4 | a0001c0001t0047g0064 a0001c0013t0001g0009 a0002c0020t0004g0010 others(1): Show |
4 | HG02486.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-13958T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871006 | |||||||
chr18:2871030 | T | C | 29 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(26): Show |
29 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.258-13934T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871030 | |||||||
chr18:2871044 | T | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0254 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-13920T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871044 | |||||||
chr18:2871218 | T | C | 5 | a0001c0001t0001g0207 a0001c0001t0009g0045 a0001c0014t0004g0006 others(2): Show |
5 | HG02615.hp2 HG02717.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-13746T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871218 | |||||||
chr18:2871297 | G | C | 6 | a0001c0001t0001g0207 a0001c0001t0009g0045 a0001c0014t0004g0006 others(3): Show |
6 | HG02615.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-13667G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871297 | |||||||
chr18:2871297 | G | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0255 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.258-13667G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871297 | |||||||
chr18:2871339 | A | G | 5 | a0001c0001t0002g0368 a0001c0001t0002g0369 a0001c0001t0002g0370 others(2): Show |
5 | NA18960.hp1 NA18977.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-13625A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871339 | |||||||
chr18:2871414 | G | A | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-13550G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871414 | |||||||
chr18:2871415 | C | A | 4 | a0001c0016t0016g0029 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02622.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-13549C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871415 | |||||||
chr18:2871463 | G | T | 3 | a0001c0001t0003g0290 a0001c0001t0011g0123 a0001c0002t0002g0118 |
3 | HG02083.hp2 NA18941.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.258-13501G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871463 | |||||||
chr18:2871498 | G | A | 4 | a0001c0003t0005g0392 a0003c0010t0019g0216 a0003c0012t0048g0008 others(1): Show |
4 | HG01192.hp1 HG02717.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-13466G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871498 | |||||||
chr18:2871538 | T | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-13426T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871538 | |||||||
chr18:2871559 | C | T | 2 | a0001c0006t0001g0357 a0001c0006t0032g0358 |
2 | HG00733.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.258-13405C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871559 | |||||||
chr18:2871560 | G | A | 2 | a0001c0001t0001g0402 a0001c0001t0001g0403 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.258-13404G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871560 | |||||||
chr18:2871638 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-13326G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871638 | |||||||
chr18:2871669 | A | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-13295A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871669 | |||||||
chr18:2871768 | G | A | 23 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-13196G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871768 | |||||||
chr18:2871813 | A | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0066 a0001c0001t0001g0207 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.258-13151A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871813 | |||||||
chr18:2871815 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.258-13149G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871815 | |||||||
chr18:2871938 | C | G | 2 | a0001c0001t0001g0255 a0008c0017t0001g0074 |
2 | HG02257.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.258-13026C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2871938 | |||||||
chr18:2872050 | A | C | 4 | a0001c0002t0001g0400 a0001c0002t0001g0425 a0001c0002t0003g0398 others(1): Show |
4 | NA18946.hp1 NA18966.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-12914A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872050 | |||||||
chr18:2872093 | A | T | 186 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(183): Show |
188 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.258-12871A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872093 | |||||||
chr18:2872273 | C | T | 4 | a0001c0001t0047g0064 a0001c0013t0001g0009 a0002c0020t0004g0010 others(1): Show |
4 | HG02486.hp2 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-12691C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872273 | |||||||
chr18:2872333 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.258-12631C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872333 | |||||||
chr18:2872370 | T | C | 91 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0040 others(88): Show |
92 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(89): Show |
intron_variant | MODIFIER | c.258-12594T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872370 | |||||||
chr18:2872417 | C | T | 217 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(214): Show |
220 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.258-12547C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872417 | |||||||
chr18:2872451 | T | A | 146 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0207 others(143): Show |
148 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.258-12513T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872451 | |||||||
chr18:2872525 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.258-12439A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872525 | |||||||
chr18:2872543 | G | A | 1 | a0003c0010t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.258-12421G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872543 | |||||||
chr18:2872588 | G | A | 209 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(206): Show |
210 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(207): Show |
intron_variant | MODIFIER | c.258-12376G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872588 | |||||||
chr18:2872617 | G | A | 73 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0040 others(70): Show |
73 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(70): Show |
intron_variant | MODIFIER | c.258-12347G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872617 | |||||||
chr18:2872681 | G | C | 37 | a0001c0001t0001g0014 a0001c0001t0001g0277 a0001c0001t0002g0364 others(34): Show |
37 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.258-12283G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872681 | |||||||
chr18:2872689 | T | A | 1 | a0001c0003t0003g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.258-12275T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872689 | |||||||
chr18:2872723 | C | T | 1 | a0001c0001t0032g0232 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.258-12241C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872723 | |||||||
chr18:2872737 | A | T | 1 | a0001c0001t0045g0443 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.258-12227A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872737 | |||||||
chr18:2872738 | C | T | 3 | a0001c0001t0045g0443 a0001c0002t0042g0444 a0001c0035t0001g0250 |
3 | HG01433.hp1 HG01978.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.258-12226C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872738 | |||||||
chr18:2872823 | C | T | 56 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0066 others(53): Show |
56 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.258-12141C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872823 | |||||||
chr18:2872831 | G | GA | 56 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0066 others(53): Show |
56 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.258-12131dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2872831 | ||||||
chr18:2872853 | G | A | 1 | a0001c0001t0010g0393 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.258-12111G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2872853 | |||||||
chr18:2873050 | A | T | 40 | a0001c0001t0001g0014 a0001c0001t0001g0277 a0001c0001t0002g0364 others(37): Show |
40 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.258-11914A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873050 | |||||||
chr18:2873060 | AAC | A | 8 | a0001c0001t0001g0057 a0001c0001t0005g0257 a0001c0001t0014g0213 others(5): Show |
8 | HG02109.hp1 HG02895.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.258-11902_258-1190 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2873060 | ||||||
chr18:2873061 | AC | A | 77 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0040 others(74): Show |
78 | HG00609.hp1 HG00673.hp1 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.258-11902delC | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873061 | |||||||
chr18:2873062 | C | A | 140 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0220 others(137): Show |
141 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.258-11902C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873062 | |||||||
chr18:2873085 | A | G | 81 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0040 others(78): Show |
82 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(79): Show |
intron_variant | MODIFIER | c.258-11879A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873085 | |||||||
chr18:2873106 | T | C | 1 | a0001c0014t0004g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.258-11858T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873106 | |||||||
chr18:2873121 | C | T | 82 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0040 others(79): Show |
83 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(80): Show |
intron_variant | MODIFIER | c.258-11843C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873121 | |||||||
chr18:2873133 | G | A | 82 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0040 others(79): Show |
83 | HG00609.hp1 HG00673.hp1 HG01109.hp2 others(80): Show |
intron_variant | MODIFIER | c.258-11831G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873133 | |||||||
chr18:2873147 | A | G | 1 | a0022c0034t0002g0347 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.258-11817A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873147 | |||||||
chr18:2873198 | G | A | 1 | a0001c0013t0009g0211 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.258-11766G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873198 | |||||||
chr18:2873258 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.258-11706A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873258 | |||||||
chr18:2873266 | C | A | 1 | a0001c0002t0012g0412 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.258-11698C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873266 | |||||||
chr18:2873270 | C | A | 3 | a0003c0010t0001g0007 a0003c0045t0062g0005 a0005c0036t0004g0046 |
3 | HG01106.hp1 HG02572.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.258-11694C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873270 | |||||||
chr18:2873280 | C | T | 2 | a0001c0016t0016g0029 a0008c0017t0001g0073 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.258-11684C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873280 | |||||||
chr18:2873397 | A | G | 23 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0057 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.258-11567A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873397 | |||||||
chr18:2873401 | T | C | 23 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0057 others(20): Show |
23 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.258-11563T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873401 | |||||||
chr18:2873450 | A | G | 150 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(147): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.258-11514A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873450 | |||||||
chr18:2873482 | T | C | 1 | a0001c0001t0009g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.258-11482T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873482 | |||||||
chr18:2873489 | C | T | 18 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0057 others(15): Show |
18 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.258-11475C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873489 | |||||||
chr18:2873492 | G | C | 7 | a0001c0001t0005g0257 a0001c0001t0014g0213 a0001c0001t0035g0214 others(4): Show |
7 | HG02109.hp1 HG02895.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.258-11472G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873492 | |||||||
chr18:2873508 | C | T | 8 | a0001c0001t0001g0040 a0001c0001t0009g0045 a0001c0014t0004g0006 others(5): Show |
8 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-11456C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873508 | |||||||
chr18:2873513 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0009g0045 a0001c0014t0004g0006 others(6): Show |
9 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-11451C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873513 | |||||||
chr18:2873515 | G | A | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-11449G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873515 | |||||||
chr18:2873535 | A | G | 10 | a0001c0001t0001g0040 a0001c0001t0009g0045 a0001c0014t0004g0006 others(7): Show |
10 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-11429A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873535 | |||||||
chr18:2873558 | T | A | 9 | a0001c0001t0001g0040 a0001c0001t0009g0045 a0001c0014t0004g0006 others(6): Show |
9 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-11406T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873558 | |||||||
chr18:2873563 | C | T | 9 | a0001c0001t0001g0040 a0001c0001t0009g0045 a0001c0014t0004g0006 others(6): Show |
9 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-11401C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873563 | |||||||
chr18:2873569 | T | C | 9 | a0001c0001t0001g0040 a0001c0001t0009g0045 a0001c0014t0004g0006 others(6): Show |
9 | HG01192.hp1 HG01891.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-11395T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873569 | |||||||
chr18:2873570 | G | A | 29 | a0001c0001t0001g0038 a0001c0001t0001g0220 a0001c0001t0002g0081 others(26): Show |
30 | HG00423.hp2 HG01074.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.258-11394G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873570 | |||||||
chr18:2873573 | G | A | 1 | a0003c0046t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.258-11391G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873573 | |||||||
chr18:2873575 | C | T | 1 | a0001c0001t0003g0289 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.258-11389C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873575 | |||||||
chr18:2873576 | G | A | 5 | a0001c0001t0001g0040 a0001c0001t0009g0045 a0001c0041t0014g0263 others(2): Show |
5 | HG01891.hp1 HG02615.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-11388G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873576 | |||||||
chr18:2873579 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0001g0066 others(3): Show |
6 | HG02257.hp1 HG02886.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-11385C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873579 | |||||||
chr18:2873623 | C | T | 4 | a0001c0014t0004g0006 a0003c0010t0001g0007 a0003c0045t0062g0005 others(1): Show |
4 | HG01106.hp1 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-11341C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873623 | |||||||
chr18:2873632 | G | A | 317 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0038 others(314): Show |
319 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.258-11332G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873632 | |||||||
chr18:2873664 | G | A | 10 | a0001c0001t0001g0348 a0001c0001t0003g0278 a0001c0002t0024g0385 others(7): Show |
10 | NA18959.hp2 NA18964.hp2 NA18991.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-11300G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873664 | |||||||
chr18:2873665 | T | C | 4 | a0001c0001t0005g0404 a0001c0001t0005g0439 a0001c0002t0005g0280 others(1): Show |
4 | HG01192.hp1 NA18952.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-11299T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873665 | |||||||
chr18:2873694 | A | G | 15 | a0001c0001t0001g0172 a0001c0001t0001g0303 a0001c0001t0002g0405 others(12): Show |
15 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(12): Show |
intron_variant | MODIFIER | c.258-11270A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873694 | |||||||
chr18:2873702 | A | G | 1 | a0001c0001t0006g0147 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.258-11262A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873702 | |||||||
chr18:2873707 | AAAAT | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0277 a0001c0001t0001g0348 others(91): Show |
95 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(92): Show |
intron_variant | MODIFIER | c.258-11237_258-1123 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2873707 | ||||||
chr18:2873850 | C | G | 96 | a0001c0001t0001g0083 a0001c0001t0001g0181 a0001c0001t0001g0418 others(93): Show |
96 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.258-11114C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873850 | |||||||
chr18:2873902 | G | C | 299 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0083 others(296): Show |
301 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(298): Show |
intron_variant | MODIFIER | c.258-11062G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873902 | |||||||
chr18:2873908 | G | A | 1 | a0001c0004t0064g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.258-11056G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873908 | |||||||
chr18:2873941 | C | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0040 others(97): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.258-11023C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2873941 | |||||||
chr18:2874080 | G | A | 2 | a0001c0004t0064g0196 a0001c0006t0002g0240 |
2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.258-10884G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874080 | |||||||
chr18:2874123 | AC | A | 410 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(407): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.258-10836delC | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2874123 | ||||||
chr18:2874129 | G | T | 410 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(407): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.258-10835G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874129 | |||||||
chr18:2874145 | C | T | 2 | a0001c0001t0016g0344 a0003c0012t0013g0343 |
2 | HG02055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.258-10819C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874145 | |||||||
chr18:2874158 | G | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0057 others(215): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.258-10806G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874158 | |||||||
chr18:2874228 | G | GT | 10 | a0001c0001t0001g0208 a0001c0001t0047g0064 a0001c0002t0003g0168 others(7): Show |
10 | HG01256.hp2 HG01258.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-10728dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2874228 | ||||||
chr18:2874249 | C | G | 2 | a0001c0016t0016g0029 a0008c0017t0001g0073 |
2 | HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.258-10715C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874249 | |||||||
chr18:2874331 | A | G | 5 | a0001c0006t0001g0062 a0001c0006t0001g0063 a0001c0014t0004g0047 others(2): Show |
5 | HG01081.hp1 HG01167.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-10633A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874331 | |||||||
chr18:2874366 | C | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0083 others(148): Show |
153 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.258-10598C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874366 | |||||||
chr18:2874388 | CTG | C | 6 | a0001c0001t0001g0172 a0001c0001t0003g0389 a0001c0001t0070g0137 others(3): Show |
6 | HG02257.hp1 HG02258.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-10562_258-1056 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2874388 | ||||||
chr18:2874410 | A | G | 361 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(358): Show |
364 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(361): Show |
intron_variant | MODIFIER | c.258-10554A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874410 | |||||||
chr18:2874433 | A | G | 43 | a0001c0001t0001g0057 a0001c0001t0001g0208 a0001c0001t0005g0044 others(40): Show |
44 | HG01192.hp1 HG01884.hp1 HG01891.hp2 others(41): Show |
intron_variant | MODIFIER | c.258-10531A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874433 | |||||||
chr18:2874554 | T | C | 267 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(264): Show |
269 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.258-10410T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874554 | |||||||
chr18:2874569 | T | C | 6 | a0001c0001t0001g0057 a0001c0004t0064g0196 a0001c0014t0004g0047 others(3): Show |
6 | HG01192.hp1 HG02622.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-10395T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874569 | |||||||
chr18:2874619 | T | C | 1 | a0002c0005t0028g0401 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.258-10345T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874619 | |||||||
chr18:2874652 | T | C | 3 | a0001c0006t0001g0357 a0001c0006t0005g0191 a0001c0006t0032g0358 |
3 | HG00733.hp2 HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.258-10312T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874652 | |||||||
chr18:2874771 | A | AT | 156 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(153): Show |
157 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.258-10187dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2874771 | ||||||
chr18:2874856 | G | C | 1 | a0001c0002t0024g0162 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.258-10108G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2874856 | |||||||
chr18:2875014 | G | A | 1 | a0001c0002t0001g0285 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.258-9950G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875014 | |||||||
chr18:2875103 | G | A | 1 | a0002c0005t0004g0018 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.258-9861G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875103 | |||||||
chr18:2875257 | G | A | 92 | a0001c0001t0001g0181 a0001c0001t0001g0303 a0001c0001t0001g0363 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.258-9707G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875257 | |||||||
chr18:2875329 | T | C | 1 | a0001c0003t0002g0431 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.258-9635T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875329 | |||||||
chr18:2875346 | C | T | 4 | a0001c0001t0010g0393 a0001c0002t0067g0013 a0007c0022t0001g0197 others(1): Show |
4 | HG01168.hp2 HG01169.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-9618C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875346 | |||||||
chr18:2875434 | T | A | 361 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(358): Show |
365 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(362): Show |
intron_variant | MODIFIER | c.258-9530T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875434 | |||||||
chr18:2875611 | C | T | 1 | a0003c0010t0009g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.258-9353C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875611 | |||||||
chr18:2875671 | C | CGA | 284 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(281): Show |
287 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.258-9293_258-9292i others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875671 | |||||||
chr18:2875692 | G | A | 1 | a0001c0014t0004g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.258-9272G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875692 | |||||||
chr18:2875895 | A | G | 442 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(439): Show |
446 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(443): Show |
intron_variant | MODIFIER | c.258-9069A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875895 | |||||||
chr18:2875915 | A | G | 1 | a0003c0010t0020g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258-9049A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2875915 | |||||||
chr18:2875979 | AT | A | 235 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(232): Show |
238 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.258-8965delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2875979 | ||||||
chr18:2875979 | ATT | A | 7 | a0001c0001t0003g0188 a0001c0001t0005g0333 a0001c0002t0005g0021 others(4): Show |
7 | HG00639.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-8966_258-8965d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2875979 | ||||||
chr18:2875979 | ATTT | A | 83 | a0001c0001t0001g0172 a0001c0001t0001g0208 a0001c0001t0001g0254 others(80): Show |
83 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.258-8967_258-8965d others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2875979 | ||||||
chr18:2876012 | C | T | 32 | a0001c0001t0001g0245 a0001c0001t0001g0348 a0001c0001t0001g0362 others(29): Show |
32 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.258-8952C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876012 | |||||||
chr18:2876037 | A | C | 2 | a0001c0002t0005g0021 a0002c0005t0004g0193 |
2 | HG00639.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.258-8927A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876037 | |||||||
chr18:2876044 | C | T | 1 | a0001c0001t0003g0100 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.258-8920C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876044 | |||||||
chr18:2876064 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8900C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876064 | |||||||
chr18:2876070 | C | G | 1 | a0001c0001t0002g0428 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.258-8894C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876070 | |||||||
chr18:2876084 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8880C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876084 | |||||||
chr18:2876127 | G | A | 87 | a0001c0001t0001g0172 a0001c0001t0001g0208 a0001c0001t0001g0254 others(84): Show |
87 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.258-8837G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876127 | |||||||
chr18:2876273 | G | A | 1 | a0001c0004t0054g0194 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.258-8691G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876273 | |||||||
chr18:2876440 | C | T | 103 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0303 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.258-8524C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876440 | |||||||
chr18:2876450 | G | C | 2 | a0001c0006t0001g0062 a0001c0006t0001g0063 |
2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.258-8514G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876450 | |||||||
chr18:2876495 | GGTGGCTC others(140): Show |
G | 44 | a0001c0001t0001g0172 a0001c0001t0001g0362 a0001c0001t0002g0405 others(41): Show |
44 | HG00558.hp1 HG00609.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.258-8466_258-8320d others(2): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2876495 | ||||||
chr18:2876582 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8382C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876582 | |||||||
chr18:2876583 | G | A | 1 | a0001c0013t0001g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.258-8381G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876583 | |||||||
chr18:2876591 | C | T | 3 | a0001c0001t0014g0033 a0001c0037t0063g0361 a0003c0010t0019g0216 |
3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.258-8373C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876591 | |||||||
chr18:2876593 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8371C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876593 | |||||||
chr18:2876594 | G | A | 344 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(341): Show |
348 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(345): Show |
intron_variant | MODIFIER | c.258-8370G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876594 | |||||||
chr18:2876622 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8342C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876622 | |||||||
chr18:2876626 | T | C | 347 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(344): Show |
351 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.258-8338T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876626 | |||||||
chr18:2876627 | G | A | 221 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(218): Show |
224 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.258-8337G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876627 | |||||||
chr18:2876628 | T | A | 347 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(344): Show |
351 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.258-8336T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876628 | |||||||
chr18:2876634 | C | T | 347 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(344): Show |
351 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.258-8330C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876634 | |||||||
chr18:2876639 | G | A | 347 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(344): Show |
351 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.258-8325G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876639 | |||||||
chr18:2876642 | T | C | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8322T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876642 | |||||||
chr18:2876661 | G | A | 26 | a0001c0001t0001g0245 a0001c0001t0001g0348 a0001c0001t0001g0433 others(23): Show |
26 | HG00642.hp1 HG00733.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.258-8303G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876661 | |||||||
chr18:2876679 | T | C | 1 | a0001c0001t0002g0405 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.258-8285T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876679 | |||||||
chr18:2876685 | G | A | 346 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(343): Show |
350 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.258-8279G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876685 | |||||||
chr18:2876687 | A | G | 346 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(343): Show |
350 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.258-8277A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876687 | |||||||
chr18:2876690 | C | T | 101 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0303 others(98): Show |
102 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.258-8274C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876690 | |||||||
chr18:2876715 | A | G | 1 | a0003c0010t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.258-8249A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876715 | |||||||
chr18:2876723 | G | A | 1 | a0002c0007t0004g0367 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.258-8241G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876723 | |||||||
chr18:2876760 | T | C | 348 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(345): Show |
352 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.258-8204T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876760 | |||||||
chr18:2876771 | A | C | 1 | a0003c0010t0020g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258-8193A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876771 | |||||||
chr18:2876772 | T | A | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8192T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876772 | |||||||
chr18:2876778 | G | T | 349 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(346): Show |
353 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.258-8186G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876778 | |||||||
chr18:2876785 | G | A | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-8179G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876785 | |||||||
chr18:2876796 | C | T | 1 | a0001c0002t0002g0268 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.258-8168C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876796 | |||||||
chr18:2876798 | T | C | 348 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(345): Show |
352 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.258-8166T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876798 | |||||||
chr18:2876823 | C | T | 348 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(345): Show |
352 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.258-8141C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876823 | |||||||
chr18:2876842 | C | T | 349 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(346): Show |
353 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.258-8122C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876842 | |||||||
chr18:2876854 | T | G | 102 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0303 others(99): Show |
103 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.258-8110T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876854 | |||||||
chr18:2876877 | C | T | 348 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(345): Show |
352 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(349): Show |
intron_variant | MODIFIER | c.258-8087C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876877 | |||||||
chr18:2876936 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-8028C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876936 | |||||||
chr18:2876978 | A | G | 2 | a0001c0037t0063g0361 a0003c0010t0019g0216 |
2 | HG02717.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.258-7986A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2876978 | |||||||
chr18:2877172 | T | C | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-7792T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877172 | |||||||
chr18:2877200 | A | T | 26 | a0001c0001t0005g0257 a0001c0006t0001g0015 a0001c0006t0001g0316 others(23): Show |
26 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(23): Show |
intron_variant | MODIFIER | c.258-7764A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877200 | |||||||
chr18:2877201 | T | A | 1 | a0003c0010t0020g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258-7763T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877201 | |||||||
chr18:2877225 | G | A | 1 | a0002c0009t0004g0223 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.258-7739G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877225 | |||||||
chr18:2877273 | CT | C | 13 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(10): Show |
13 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.258-7687delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2877273 | ||||||
chr18:2877283 | G | A | 13 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(10): Show |
13 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.258-7681G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877283 | |||||||
chr18:2877328 | A | C | 9 | a0001c0001t0052g0210 a0001c0013t0001g0009 a0001c0016t0061g0058 others(6): Show |
9 | HG01884.hp2 HG01891.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-7636A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877328 | |||||||
chr18:2877380 | T | C | 33 | a0001c0001t0005g0257 a0001c0001t0014g0033 a0001c0002t0005g0021 others(30): Show |
33 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(30): Show |
intron_variant | MODIFIER | c.258-7584T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877380 | |||||||
chr18:2877431 | T | A | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-7533T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877431 | |||||||
chr18:2877436 | G | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-7528G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877436 | |||||||
chr18:2877436 | GT | G | 317 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(314): Show |
320 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.258-7510delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2877436 | ||||||
chr18:2877436 | GTT | G | 103 | a0001c0001t0001g0038 a0001c0001t0001g0181 a0001c0001t0001g0303 others(100): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.258-7511_258-7510d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2877436 | ||||||
chr18:2877436 | GTTT | G | 8 | a0001c0001t0001g0040 a0001c0001t0034g0426 a0001c0001t0052g0210 others(5): Show |
8 | HG01891.hp1 HG01891.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-7512_258-7510d others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2877436 | ||||||
chr18:2877509 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.258-7455C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877509 | |||||||
chr18:2877512 | G | A | 1 | a0001c0002t0014g0243 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.258-7452G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877512 | |||||||
chr18:2877519 | T | A | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-7445T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877519 | |||||||
chr18:2877552 | C | T | 4 | a0001c0001t0009g0045 a0001c0013t0009g0211 a0001c0014t0001g0043 others(1): Show |
4 | HG02615.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.258-7412C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877552 | |||||||
chr18:2877556 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-7408C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877556 | |||||||
chr18:2877686 | G | A | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-7278G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877686 | |||||||
chr18:2877733 | G | A | 335 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(332): Show |
339 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.258-7231G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877733 | |||||||
chr18:2877777 | C | CA | 9 | a0001c0001t0001g0038 a0001c0001t0002g0081 a0001c0001t0003g0121 others(6): Show |
9 | HG00621.hp2 HG01106.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-7172dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2877777 | ||||||
chr18:2877777 | CA | C | 8 | a0001c0001t0002g0133 a0001c0001t0025g0365 a0001c0002t0011g0087 others(5): Show |
8 | HG00639.hp2 HG02451.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-7172delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2877777 | ||||||
chr18:2877790 | AAAG | A | 10 | a0001c0001t0001g0057 a0001c0001t0014g0213 a0001c0001t0017g0075 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-7171_258-7169d others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2877790 | ||||||
chr18:2877926 | C | T | 12 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(9): Show |
12 | HG02257.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.258-7038C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2877926 | |||||||
chr18:2878011 | G | A | 220 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(217): Show |
223 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.258-6953G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878011 | |||||||
chr18:2878061 | A | T | 19 | a0001c0001t0001g0057 a0001c0001t0014g0213 a0001c0001t0017g0075 others(16): Show |
19 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.258-6903A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878061 | |||||||
chr18:2878144 | GT | G | 442 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(439): Show |
446 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(443): Show |
intron_variant | MODIFIER | c.258-6818delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2878144 | ||||||
chr18:2878212 | G | A | 3 | a0001c0001t0014g0033 a0001c0037t0063g0361 a0003c0010t0019g0216 |
3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.258-6752G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878212 | |||||||
chr18:2878228 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0034g0426 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258-6736A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878228 | |||||||
chr18:2878262 | G | A | 1 | a0001c0008t0021g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-6702G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878262 | |||||||
chr18:2878295 | G | C | 3 | a0005c0038t0004g0023 a0010c0019t0001g0034 a0010c0019t0001g0035 |
3 | HG02258.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.258-6669G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878295 | |||||||
chr18:2878389 | T | C | 355 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(352): Show |
359 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.258-6575T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878389 | |||||||
chr18:2878421 | T | G | 11 | a0001c0001t0001g0057 a0001c0001t0014g0213 a0001c0001t0017g0075 others(8): Show |
11 | HG02109.hp1 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.258-6543T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878421 | |||||||
chr18:2878439 | G | A | 1 | a0001c0001t0006g0308 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.258-6525G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878439 | |||||||
chr18:2878480 | AC | A | 5 | a0001c0002t0005g0021 a0001c0002t0014g0243 a0001c0004t0064g0196 others(2): Show |
5 | HG00639.hp1 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-6483delC | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878480 | |||||||
chr18:2878483 | CT | C | 5 | a0001c0002t0005g0021 a0001c0002t0014g0243 a0001c0004t0064g0196 others(2): Show |
5 | HG00639.hp1 HG02280.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-6480delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878483 | |||||||
chr18:2878615 | G | A | 326 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(323): Show |
330 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.258-6349G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878615 | |||||||
chr18:2878649 | T | C | 355 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(352): Show |
359 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(356): Show |
intron_variant | MODIFIER | c.258-6315T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878649 | |||||||
chr18:2878701 | C | A | 327 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(324): Show |
331 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(328): Show |
intron_variant | MODIFIER | c.258-6263C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878701 | |||||||
chr18:2878914 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0220 a0001c0003t0023g0248 others(1): Show |
5 | HG00642.hp2 HG00741.hp2 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.258-6050G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878914 | |||||||
chr18:2878935 | G | A | 2 | a0001c0006t0001g0062 a0001c0006t0001g0063 |
2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.258-6029G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878935 | |||||||
chr18:2878936 | G | A | 1 | a0001c0003t0001g0270 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.258-6028G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878936 | |||||||
chr18:2878980 | C | T | 1 | a0003c0046t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.258-5984C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2878980 | |||||||
chr18:2879007 | A | T | 2 | a0001c0001t0001g0040 a0001c0001t0034g0426 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258-5957A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879007 | |||||||
chr18:2879161 | C | T | 1 | a0001c0006t0002g0240 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.258-5803C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879161 | |||||||
chr18:2879247 | A | G | 1 | a0001c0008t0021g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-5717A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879247 | |||||||
chr18:2879303 | T | C | 3 | a0001c0002t0014g0243 a0001c0004t0064g0196 a0002c0005t0026g0036 |
3 | HG02976.hp2 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.258-5661T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879303 | |||||||
chr18:2879430 | G | A | 1 | a0001c0002t0005g0378 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.258-5534G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879430 | |||||||
chr18:2879433 | C | T | 1 | a0003c0010t0020g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.258-5531C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879433 | |||||||
chr18:2879450 | G | A | 125 | a0001c0001t0001g0057 a0001c0001t0001g0181 a0001c0001t0001g0208 others(122): Show |
126 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.258-5514G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879450 | |||||||
chr18:2879656 | G | A | 1 | a0002c0009t0029g0355 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.258-5308G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879656 | |||||||
chr18:2879675 | C | A | 110 | a0001c0001t0001g0040 a0001c0001t0001g0181 a0001c0001t0001g0208 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.258-5289C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879675 | |||||||
chr18:2879743 | C | T | 23 | a0001c0002t0014g0243 a0001c0006t0001g0015 a0001c0006t0001g0316 others(20): Show |
23 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(20): Show |
intron_variant | MODIFIER | c.258-5221C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879743 | |||||||
chr18:2879839 | G | T | 1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.258-5125G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2879839 | |||||||
chr18:2880322 | C | T | 3 | a0001c0001t0014g0033 a0001c0037t0063g0361 a0003c0010t0019g0216 |
3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.258-4642C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880322 | |||||||
chr18:2880342 | C | G | 1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.258-4622C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880342 | |||||||
chr18:2880421 | G | C | 125 | a0001c0001t0001g0245 a0001c0001t0001g0348 a0001c0001t0001g0433 others(122): Show |
126 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.258-4543G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880421 | |||||||
chr18:2880453 | C | A | 2 | a0001c0002t0005g0021 a0002c0005t0004g0193 |
2 | HG00639.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.258-4511C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880453 | |||||||
chr18:2880488 | G | T | 4 | a0001c0001t0002g0328 a0001c0001t0003g0334 a0004c0011t0003g0148 others(1): Show |
4 | NA18944.hp2 NA18945.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.258-4476G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880488 | |||||||
chr18:2880497 | C | T | 1 | a0001c0001t0001g0362 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.258-4467C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880497 | |||||||
chr18:2880514 | C | G | 434 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(431): Show |
438 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(435): Show |
intron_variant | MODIFIER | c.258-4450C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880514 | |||||||
chr18:2880627 | G | T | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-4337G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880627 | |||||||
chr18:2880676 | A | G | 1 | a0001c0002t0003g0151 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.258-4288A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880676 | |||||||
chr18:2880807 | G | A | 8 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-4157G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880807 | |||||||
chr18:2880842 | G | C | 1 | a0001c0001t0009g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.258-4122G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880842 | |||||||
chr18:2880848 | T | C | 4 | a0001c0004t0013g0004 a0001c0016t0016g0029 a0003c0045t0062g0005 others(1): Show |
5 | HG01884.hp1 HG02622.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-4116T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2880848 | |||||||
chr18:2881060 | T | C | 10 | a0001c0001t0001g0038 a0001c0001t0009g0041 a0001c0001t0014g0033 others(7): Show |
10 | HG01081.hp1 HG01167.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.258-3904T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881060 | |||||||
chr18:2881073 | C | T | 6 | a0001c0001t0002g0368 a0001c0001t0002g0369 a0001c0001t0002g0370 others(3): Show |
6 | NA18960.hp1 NA18977.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-3891C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881073 | |||||||
chr18:2881084 | G | A | 1 | a0001c0003t0001g0416 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.258-3880G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881084 | |||||||
chr18:2881108 | G | C | 1 | a0001c0001t0009g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.258-3856G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881108 | |||||||
chr18:2881243 | G | A | 6 | a0001c0001t0001g0362 a0001c0001t0010g0393 a0001c0002t0067g0013 others(3): Show |
6 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-3721G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881243 | |||||||
chr18:2881245 | A | G | 1 | a0001c0001t0010g0420 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.258-3719A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881245 | |||||||
chr18:2881382 | G | T | 1 | a0001c0008t0021g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-3582G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881382 | |||||||
chr18:2881424 | GGGCTCCA | G | 8 | a0001c0001t0001g0040 a0001c0001t0034g0426 a0001c0001t0052g0210 others(5): Show |
8 | HG01891.hp1 HG02809.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-3530_258-3524d others(9): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2881424 | ||||||
chr18:2881460 | G | A | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-3504G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881460 | |||||||
chr18:2881543 | G | C | 1 | a0002c0007t0008g0177 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.258-3421G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881543 | |||||||
chr18:2881563 | G | A | 2 | a0001c0001t0003g0116 a0004c0043t0003g0164 |
2 | NA18950.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.258-3401G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881563 | |||||||
chr18:2881566 | C | T | 1 | a0002c0007t0008g0177 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.258-3398C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881566 | |||||||
chr18:2881590 | G | A | 2 | a0001c0004t0013g0004 a0008c0017t0001g0073 |
3 | HG01884.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.258-3374G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881590 | |||||||
chr18:2881641 | C | G | 1 | a0001c0006t0005g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.258-3323C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881641 | |||||||
chr18:2881796 | G | A | 2 | a0001c0002t0005g0021 a0002c0005t0004g0193 |
2 | HG00639.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.258-3168G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881796 | |||||||
chr18:2881841 | T | C | 212 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0066 others(209): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.258-3123T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881841 | |||||||
chr18:2881931 | T | TTGGCCG | 3 | a0001c0001t0014g0033 a0001c0037t0063g0361 a0003c0010t0019g0216 |
3 | HG02717.hp2 HG02809.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.258-3032_258-3027d others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2881931 | ||||||
chr18:2881989 | C | T | 1 | a0001c0001t0002g0435 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.258-2975C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2881989 | |||||||
chr18:2882003 | G | A | 1 | a0001c0004t0031g0109 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.258-2961G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882003 | |||||||
chr18:2882137 | T | C | 229 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0066 others(226): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.258-2827T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882137 | |||||||
chr18:2882212 | G | A | 9 | a0001c0001t0003g0101 a0001c0001t0003g0114 a0001c0001t0006g0436 others(6): Show |
9 | HG01433.hp1 HG01978.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-2752G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882212 | |||||||
chr18:2882241 | A | G | 2 | a0001c0002t0005g0021 a0002c0005t0004g0193 |
2 | HG00639.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.258-2723A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882241 | |||||||
chr18:2882247 | C | T | 2 | a0001c0001t0001g0040 a0001c0001t0034g0426 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258-2717C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882247 | |||||||
chr18:2882291 | A | G | 1 | a0001c0002t0003g0120 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.258-2673A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882291 | |||||||
chr18:2882377 | G | GGGT | 6 | a0006c0026t0053g0059 a0006c0026t0055g0032 a0006c0027t0001g0039 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.258-2585_258-2583d others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2882377 | ||||||
chr18:2882414 | C | T | 3 | a0001c0001t0001g0245 a0001c0001t0005g0238 a0001c0006t0003g0230 |
3 | HG00733.hp1 HG01070.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.258-2550C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882414 | |||||||
chr18:2882583 | A | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0034g0426 others(6): Show |
9 | HG01891.hp1 HG02809.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.258-2381A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882583 | |||||||
chr18:2882584 | A | G | 1 | a0001c0008t0021g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.258-2380A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882584 | |||||||
chr18:2882620 | A | T | 1 | a0019c0048t0004g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.258-2344A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882620 | |||||||
chr18:2882751 | T | G | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-2213T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882751 | |||||||
chr18:2882753 | G | A | 2 | a0001c0006t0002g0240 a0001c0006t0035g0174 |
2 | HG01109.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.258-2211G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882753 | |||||||
chr18:2882798 | G | A | 8 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-2166G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882798 | |||||||
chr18:2882832 | G | A | 1 | a0001c0001t0011g0158 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.258-2132G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882832 | |||||||
chr18:2882840 | G | A | 8 | a0001c0001t0014g0213 a0001c0001t0017g0075 a0001c0001t0035g0214 others(5): Show |
8 | HG01891.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-2124G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882840 | |||||||
chr18:2882883 | CA | C | 234 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0066 others(231): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.258-2068delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2882883 | ||||||
chr18:2882904 | C | A | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-2060C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882904 | |||||||
chr18:2882987 | C | T | 112 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0172 others(109): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.258-1977C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2882987 | |||||||
chr18:2883018 | C | T | 15 | a0001c0001t0001g0057 a0001c0001t0014g0213 a0001c0001t0017g0075 others(12): Show |
15 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.258-1946C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883018 | |||||||
chr18:2883103 | A | G | 1 | a0003c0010t0020g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.258-1861A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883103 | |||||||
chr18:2883191 | C | T | 1 | a0002c0005t0043g0440 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.258-1773C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883191 | |||||||
chr18:2883227 | G | GATGTCAA others(11): Show |
233 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0066 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.258-1724_258-1723i others(20): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2883227 | ||||||
chr18:2883290 | C | A | 1 | a0001c0003t0006g0429 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.258-1674C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883290 | |||||||
chr18:2883352 | C | T | 2 | a0001c0002t0005g0021 a0002c0005t0004g0193 |
2 | HG00639.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.258-1612C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883352 | |||||||
chr18:2883393 | G | A | 12 | a0001c0001t0001g0057 a0001c0001t0014g0213 a0001c0001t0017g0075 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.258-1571G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883393 | |||||||
chr18:2883518 | T | C | 2 | a0001c0001t0001g0040 a0001c0001t0034g0426 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.258-1446T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883518 | |||||||
chr18:2883528 | G | A | 2 | a0001c0002t0005g0021 a0002c0005t0004g0193 |
2 | HG00639.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.258-1436G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883528 | |||||||
chr18:2883626 | G | A | 3 | a0001c0001t0009g0041 a0001c0006t0001g0062 a0001c0006t0001g0063 |
3 | HG01081.hp1 HG01167.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.258-1338G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883626 | |||||||
chr18:2883753 | G | A | 1 | a0001c0023t0002g0221 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.258-1211G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883753 | |||||||
chr18:2883841 | G | A | 12 | a0001c0001t0001g0057 a0001c0001t0014g0213 a0001c0001t0017g0075 others(9): Show |
12 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.258-1123G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883841 | |||||||
chr18:2883869 | G | C | 8 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-1095G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883869 | |||||||
chr18:2883904 | G | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(6): Show |
9 | HG02257.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.258-1060G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883904 | |||||||
chr18:2883976 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.258-988G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2883976 | |||||||
chr18:2884019 | G | A | 6 | a0001c0001t0009g0041 a0001c0001t0014g0033 a0001c0006t0001g0062 others(3): Show |
6 | HG01081.hp1 HG01167.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.258-945G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884019 | |||||||
chr18:2884025 | G | C | 110 | a0001c0001t0001g0040 a0001c0001t0001g0066 a0001c0001t0001g0172 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.258-939G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884025 | |||||||
chr18:2884056 | C | T | 1 | a0001c0001t0009g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.258-908C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884056 | |||||||
chr18:2884094 | T | C | 90 | a0001c0001t0001g0066 a0001c0001t0001g0172 a0001c0001t0001g0207 others(87): Show |
90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.258-870T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884094 | |||||||
chr18:2884100 | C | T | 1 | a0002c0025t0004g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.258-864C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884100 | |||||||
chr18:2884103 | A | C | 33 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0006g0308 others(30): Show |
33 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.258-861A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884103 | |||||||
chr18:2884104 | C | T | 1 | a0001c0001t0009g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.258-860C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884104 | |||||||
chr18:2884106 | C | G | 1 | a0002c0005t0004g0193 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.258-858C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884106 | |||||||
chr18:2884109 | T | C | 24 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0014g0213 others(21): Show |
24 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.258-855T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884109 | |||||||
chr18:2884147 | G | A | 27 | a0001c0006t0001g0015 a0001c0006t0001g0316 a0001c0006t0001g0357 others(24): Show |
27 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(24): Show |
intron_variant | MODIFIER | c.258-817G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884147 | |||||||
chr18:2884199 | G | A | 1 | a0003c0046t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.258-765G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884199 | |||||||
chr18:2884202 | T | C | 1 | a0003c0046t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.258-762T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884202 | |||||||
chr18:2884208 | G | A | 8 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(5): Show |
8 | HG02257.hp1 HG02451.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.258-756G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884208 | |||||||
chr18:2884224 | C | G | 7 | a0003c0046t0001g0028 a0006c0026t0053g0059 a0006c0026t0055g0032 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-740C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884224 | |||||||
chr18:2884225 | A | G | 7 | a0003c0046t0001g0028 a0006c0026t0053g0059 a0006c0026t0055g0032 others(4): Show |
7 | HG01884.hp2 HG02486.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.258-739A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884225 | |||||||
chr18:2884235 | C | A | 2 | a0001c0004t0013g0004 a0008c0017t0001g0073 |
3 | HG01884.hp1 HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.258-729C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884235 | |||||||
chr18:2884252 | A | G | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.258-712A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884252 | |||||||
chr18:2884338 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.258-626G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884338 | |||||||
chr18:2884420 | AT | A | 196 | a0001c0001t0001g0066 a0001c0001t0001g0172 a0001c0001t0001g0181 others(193): Show |
198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.258-538delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr18 | 2884420 | ||||||
chr18:2884561 | A | G | 2 | a0001c0008t0021g0209 a0003c0045t0062g0005 |
2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.258-403A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884561 | |||||||
chr18:2884669 | A | G | 17 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(14): Show |
18 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.258-295A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884669 | |||||||
chr18:2884733 | G | A | 1 | a0002c0024t0008g0179 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.258-231G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884733 | |||||||
chr18:2884786 | CTGAGTTA others(6): Show |
C | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.258-177_258-165del others(13): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884786 | |||||||
chr18:2884896 | G | C | 1 | a0001c0001t0005g0238 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.258-68G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884896 | |||||||
chr18:2884905 | G | A | 1 | a0001c0001t0034g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.258-59G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884905 | |||||||
chr18:2884932 | G | A | 4 | a0001c0004t0013g0004 a0001c0008t0021g0209 a0003c0045t0062g0005 others(1): Show |
5 | HG01884.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.258-32G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 2/7 | chr18 | 2884932 | |||||||
chr18:2885243 | T | C | 3 | a0001c0002t0005g0021 a0001c0014t0004g0006 a0002c0005t0004g0193 |
3 | HG00639.hp1 HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.433+104T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885243 | |||||||
chr18:2885338 | T | C | 1 | a0006c0026t0055g0032 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.433+199T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885338 | |||||||
chr18:2885401 | A | G | 73 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0208 others(70): Show |
74 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(71): Show |
intron_variant | MODIFIER | c.433+262A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885401 | |||||||
chr18:2885439 | G | A | 101 | a0001c0001t0001g0066 a0001c0001t0001g0172 a0001c0001t0001g0207 others(98): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.433+300G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885439 | |||||||
chr18:2885475 | T | C | 64 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(61): Show |
65 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.433+336T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885475 | |||||||
chr18:2885578 | G | A | 64 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(61): Show |
65 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.433+439G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885578 | |||||||
chr18:2885580 | G | A | 2 | a0001c0001t0002g0307 a0001c0001t0002g0390 |
2 | HG01168.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.433+441G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885580 | |||||||
chr18:2885583 | A | G | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.433+444A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885583 | |||||||
chr18:2885593 | A | G | 2 | a0001c0001t0039g0229 a0002c0020t0004g0131 |
2 | HG03491.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.433+454A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885593 | |||||||
chr18:2885679 | G | A | 32 | a0001c0001t0001g0066 a0001c0006t0001g0015 a0001c0006t0001g0316 others(29): Show |
32 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(29): Show |
intron_variant | MODIFIER | c.433+540G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885679 | |||||||
chr18:2885729 | G | A | 1 | a0002c0009t0029g0355 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.433+590G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885729 | |||||||
chr18:2885769 | C | T | 4 | a0001c0013t0001g0009 a0002c0020t0004g0010 a0015c0050t0001g0077 others(1): Show |
4 | HG03453.hp2 HG03471.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+630C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885769 | |||||||
chr18:2885797 | C | T | 2 | a0001c0001t0002g0294 a0001c0001t0005g0350 |
2 | HG01361.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.433+658C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885797 | |||||||
chr18:2885852 | T | C | 6 | a0001c0001t0001g0362 a0001c0001t0010g0393 a0001c0002t0067g0013 others(3): Show |
6 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.433+713T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2885852 | |||||||
chr18:2886035 | C | T | 6 | a0006c0026t0053g0059 a0006c0026t0055g0032 a0006c0027t0001g0039 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.433+896C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886035 | |||||||
chr18:2886164 | A | G | 4 | a0001c0001t0014g0033 a0001c0003t0001g0199 a0001c0037t0063g0361 others(1): Show |
4 | HG02717.hp2 HG02809.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+1025A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886164 | |||||||
chr18:2886214 | A | C | 12 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(9): Show |
12 | HG00639.hp1 HG01081.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.433+1075A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886214 | |||||||
chr18:2886308 | C | G | 36 | a0001c0001t0001g0066 a0001c0001t0052g0210 a0001c0006t0001g0015 others(33): Show |
36 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.433+1169C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886308 | |||||||
chr18:2886493 | G | C | 62 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(59): Show |
63 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.433+1354G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886493 | |||||||
chr18:2886503 | G | A | 4 | a0001c0001t0005g0044 a0001c0001t0005g0065 a0001c0001t0005g0235 others(1): Show |
4 | HG02055.hp1 HG02559.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+1364G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886503 | |||||||
chr18:2886544 | G | A | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.433+1405G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886544 | |||||||
chr18:2886721 | A | G | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.433+1582A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886721 | |||||||
chr18:2886722 | C | T | 13 | a0001c0001t0014g0213 a0001c0001t0017g0075 a0001c0001t0021g0253 others(10): Show |
13 | HG01081.hp1 HG01167.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.433+1583C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886722 | |||||||
chr18:2886723 | G | A | 105 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0172 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.433+1584G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886723 | |||||||
chr18:2886778 | G | C | 1 | a0001c0001t0006g0147 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.433+1639G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886778 | |||||||
chr18:2886903 | C | G | 4 | a0001c0006t0001g0316 a0001c0008t0001g0249 a0001c0008t0003g0226 others(1): Show |
4 | HG01361.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+1764C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886903 | |||||||
chr18:2886910 | G | T | 4 | a0001c0002t0005g0021 a0001c0006t0001g0062 a0001c0006t0001g0063 others(1): Show |
4 | HG00639.hp1 HG01081.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+1771G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886910 | |||||||
chr18:2886935 | T | A | 105 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0001g0172 others(102): Show |
106 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.433+1796T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886935 | |||||||
chr18:2886940 | C | T | 2 | a0007c0022t0001g0197 a0007c0022t0001g0198 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.433+1801C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886940 | |||||||
chr18:2886968 | T | C | 63 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(60): Show |
64 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.433+1829T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886968 | |||||||
chr18:2886990 | C | T | 1 | a0003c0046t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.433+1851C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886990 | |||||||
chr18:2886992 | C | T | 1 | a0008c0017t0001g0074 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.433+1853C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2886992 | |||||||
chr18:2887000 | C | G | 1 | a0001c0002t0001g0352 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.433+1861C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887000 | |||||||
chr18:2887040 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.433+1901C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887040 | |||||||
chr18:2887096 | TA | T | 2 | a0001c0001t0003g0003 a0001c0001t0025g0365 |
3 | HG00639.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.433+1958delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887096 | |||||||
chr18:2887204 | T | TA | 63 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(60): Show |
64 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.433+2072dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2887204 | ||||||
chr18:2887210 | A | G | 6 | a0001c0001t0052g0210 a0001c0002t0014g0243 a0001c0013t0001g0009 others(3): Show |
6 | HG02809.hp2 HG02976.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.433+2071A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887210 | |||||||
chr18:2887300 | G | A | 6 | a0006c0026t0053g0059 a0006c0026t0055g0032 a0006c0027t0001g0039 others(3): Show |
6 | HG02486.hp2 HG02630.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.433+2161G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887300 | |||||||
chr18:2887332 | T | A | 81 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0172 others(78): Show |
82 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.433+2193T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887332 | |||||||
chr18:2887471 | C | T | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.433+2332C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887471 | |||||||
chr18:2887474 | TAATA | T | 63 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(60): Show |
64 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(61): Show |
intron_variant | MODIFIER | c.433+2339_433+2342d others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2887474 | ||||||
chr18:2887504 | C | CAT | 246 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0057 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.433+2365_433+2366i others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887504 | |||||||
chr18:2887561 | C | T | 6 | a0001c0001t0052g0210 a0001c0013t0001g0009 a0002c0020t0004g0010 others(3): Show |
6 | HG01884.hp2 HG02809.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.433+2422C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887561 | |||||||
chr18:2887562 | G | A | 1 | a0003c0045t0062g0005 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.433+2423G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887562 | |||||||
chr18:2887567 | C | T | 4 | a0001c0002t0005g0021 a0001c0006t0001g0062 a0001c0006t0001g0063 others(1): Show |
4 | HG00639.hp1 HG01081.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+2428C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887567 | |||||||
chr18:2887593 | C | T | 29 | a0001c0001t0001g0066 a0001c0006t0001g0015 a0001c0006t0001g0316 others(26): Show |
29 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(26): Show |
intron_variant | MODIFIER | c.433+2454C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887593 | |||||||
chr18:2887767 | C | T | 61 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(58): Show |
61 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.433+2628C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887767 | |||||||
chr18:2887783 | T | C | 1 | a0003c0010t0020g0275 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.433+2644T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887783 | |||||||
chr18:2887786 | T | TA | 65 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(62): Show |
66 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.433+2655dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2887786 | ||||||
chr18:2887888 | G | A | 241 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0057 others(238): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.434-2673G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887888 | |||||||
chr18:2887900 | C | G | 9 | a0001c0001t0014g0033 a0001c0037t0063g0361 a0003c0010t0019g0216 others(6): Show |
9 | HG02486.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.434-2661C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887900 | |||||||
chr18:2887962 | G | C | 2 | a0001c0006t0001g0062 a0001c0006t0001g0063 |
2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.434-2599G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2887962 | |||||||
chr18:2888217 | A | G | 5 | a0001c0001t0052g0210 a0001c0013t0001g0009 a0002c0020t0004g0010 others(2): Show |
5 | HG02809.hp2 HG03453.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-2344A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888217 | |||||||
chr18:2888278 | A | G | 1 | a0001c0001t0003g0410 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.434-2283A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888278 | |||||||
chr18:2888279 | C | T | 67 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(64): Show |
68 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.434-2282C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888279 | |||||||
chr18:2888331 | C | G | 75 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(72): Show |
76 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.434-2230C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888331 | |||||||
chr18:2888331 | C | T | 8 | a0001c0004t0005g0067 a0001c0004t0009g0068 a0003c0012t0001g0025 others(5): Show |
8 | HG02572.hp2 HG02723.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.434-2230C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888331 | |||||||
chr18:2888338 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0034g0426 |
3 | HG01891.hp1 HG03098.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.434-2223C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888338 | |||||||
chr18:2888385 | C | T | 67 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(64): Show |
68 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(65): Show |
intron_variant | MODIFIER | c.434-2176C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888385 | |||||||
chr18:2888401 | G | A | 2 | a0001c0006t0001g0062 a0001c0006t0001g0063 |
2 | HG01081.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.434-2160G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888401 | |||||||
chr18:2888433 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0034g0426 others(2): Show |
5 | HG01257.hp2 HG01258.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.434-2128C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888433 | |||||||
chr18:2888453 | C | T | 66 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(63): Show |
67 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.434-2108C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888453 | |||||||
chr18:2888485 | G | A | 12 | a0001c0001t0001g0362 a0001c0001t0005g0044 a0001c0001t0005g0065 others(9): Show |
12 | HG00741.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.434-2076G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888485 | |||||||
chr18:2888532 | A | G | 1 | a0001c0004t0064g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.434-2029A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888532 | |||||||
chr18:2888538 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.434-2023A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888538 | |||||||
chr18:2888571 | C | T | 9 | a0001c0001t0001g0348 a0001c0001t0001g0433 a0001c0002t0006g0287 others(6): Show |
9 | HG00735.hp1 NA18944.hp1 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.434-1990C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888571 | |||||||
chr18:2888572 | G | A | 1 | a0001c0002t0003g0050 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.434-1989G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888572 | |||||||
chr18:2888576 | A | G | 3 | a0001c0001t0002g0119 a0001c0001t0003g0200 a0001c0002t0002g0320 |
3 | HG02523.hp1 NA18942.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.434-1985A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888576 | |||||||
chr18:2888583 | T | C | 3 | a0001c0001t0002g0119 a0001c0001t0003g0200 a0001c0002t0002g0320 |
3 | HG02523.hp1 NA18942.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.434-1978T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888583 | |||||||
chr18:2888588 | A | G | 66 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(63): Show |
67 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.434-1973A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888588 | |||||||
chr18:2888639 | C | T | 3 | a0001c0001t0002g0081 a0005c0036t0004g0046 a0024c0030t0004g0438 |
3 | HG02572.hp2 HG04184.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.434-1922C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888639 | |||||||
chr18:2888640 | A | G | 443 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(440): Show |
447 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(444): Show |
intron_variant | MODIFIER | c.434-1921A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888640 | |||||||
chr18:2888641 | A | G | 1 | a0001c0004t0031g0161 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.434-1920A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888641 | |||||||
chr18:2888663 | C | T | 3 | a0001c0001t0001g0066 a0001c0016t0017g0259 a0002c0005t0004g0011 |
3 | HG02572.hp1 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.434-1898C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888663 | |||||||
chr18:2888664 | G | A | 1 | a0001c0001t0044g0442 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.434-1897G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888664 | |||||||
chr18:2888694 | A | G | 2 | a0001c0001t0001g0433 a0002c0005t0004g0430 |
2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.434-1867A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888694 | |||||||
chr18:2888714 | C | CA | 22 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(19): Show |
23 | HG01074.hp1 HG01169.hp2 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.434-1830dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2888714 | ||||||
chr18:2888714 | C | CAA | 57 | a0001c0001t0001g0172 a0001c0001t0001g0362 a0001c0001t0002g0405 others(54): Show |
58 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.434-1831_434-1830d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2888714 | ||||||
chr18:2888730 | A | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0066 a0001c0001t0003g0410 others(4): Show |
7 | HG01358.hp1 HG02055.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-1831A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888730 | |||||||
chr18:2888732 | G | A | 65 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(62): Show |
66 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.434-1829G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888732 | |||||||
chr18:2888839 | G | C | 4 | a0001c0001t0003g0100 a0001c0001t0003g0150 a0001c0001t0003g0290 others(1): Show |
4 | HG00544.hp1 HG02083.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-1722G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888839 | |||||||
chr18:2888871 | AGCT | A | 66 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(63): Show |
67 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(64): Show |
intron_variant | MODIFIER | c.434-1686_434-1684d others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2888871 | ||||||
chr18:2888910 | A | G | 1 | a0001c0001t0005g0404 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.434-1651A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888910 | |||||||
chr18:2888917 | A | G | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.434-1644A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888917 | |||||||
chr18:2888922 | C | T | 2 | a0001c0002t0006g0287 a0004c0011t0003g0286 |
2 | NA18944.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.434-1639C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888922 | |||||||
chr18:2888963 | A | C | 1 | a0001c0006t0033g0279 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.434-1598A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888963 | |||||||
chr18:2888971 | C | T | 1 | a0001c0001t0015g0332 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.434-1590C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888971 | |||||||
chr18:2888984 | T | A | 4 | a0001c0001t0001g0038 a0003c0012t0013g0343 a0009c0018t0001g0012 others(1): Show |
4 | HG02055.hp2 HG02257.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-1577T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2888984 | |||||||
chr18:2889023 | T | C | 72 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0362 others(69): Show |
73 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.434-1538T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889023 | |||||||
chr18:2889048 | A | G | 1 | a0001c0001t0002g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.434-1513A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889048 | |||||||
chr18:2889120 | A | ATTTC | 81 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0245 others(78): Show |
82 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.434-1433_434-1430d others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889120 | ||||||
chr18:2889128 | C | CTTTCTTT others(8): Show |
2 | a0003c0045t0062g0005 a0023c0044t0001g0272 |
2 | HG02976.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.434-1430_434-1429i others(17): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889128 | ||||||
chr18:2889128 | CTTTTCTT others(5): Show |
C | 1 | a0001c0013t0001g0009 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.434-1428_434-1417d others(14): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889128 | ||||||
chr18:2889128 | CTTTTCTT others(6): Show |
C | 3 | a0001c0001t0052g0210 a0002c0020t0004g0010 a0015c0050t0001g0077 |
3 | HG02809.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.434-1428_434-1416d others(15): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889128 | ||||||
chr18:2889129 | T | TTTC | 5 | a0001c0001t0002g0081 a0001c0001t0015g0296 a0001c0002t0005g0378 others(2): Show |
5 | HG04184.hp1 NA18968.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.434-1430_434-1429i others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889129 | ||||||
chr18:2889133 | C | CT | 15 | a0001c0001t0003g0289 a0001c0001t0011g0158 a0001c0002t0003g0151 others(12): Show |
15 | HG01070.hp2 HG01884.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.434-1406dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889133 | ||||||
chr18:2889133 | C | CTT | 26 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0066 others(23): Show |
26 | HG00733.hp2 HG01074.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.434-1407_434-1406d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889133 | ||||||
chr18:2889133 | C | T | 7 | a0001c0001t0002g0081 a0001c0001t0015g0296 a0001c0002t0005g0378 others(4): Show |
7 | HG02976.hp1 HG04184.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-1428C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889133 | |||||||
chr18:2889133 | CT | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(166): Show |
172 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.434-1406delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889133 | ||||||
chr18:2889133 | CTT | C | 25 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(22): Show |
25 | HG01070.hp1 HG01071.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.434-1407_434-1406d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889133 | ||||||
chr18:2889134 | T | C | 5 | a0001c0001t0002g0081 a0001c0001t0015g0296 a0001c0002t0005g0378 others(2): Show |
5 | HG04184.hp1 NA18968.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.434-1427T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889134 | |||||||
chr18:2889137 | T | TC | 77 | a0001c0001t0001g0172 a0001c0001t0001g0207 a0001c0001t0001g0245 others(74): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.434-1424_434-1423i others(3): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889137 | |||||||
chr18:2889138 | T | C | 4 | a0001c0001t0003g0190 a0001c0001t0003g0389 a0001c0001t0038g0300 others(1): Show |
4 | HG02683.hp2 HG02735.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.434-1423T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889138 | |||||||
chr18:2889142 | T | C | 1 | a0001c0004t0013g0004 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.434-1419T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889142 | |||||||
chr18:2889333 | A | T | 3 | a0001c0001t0001g0066 a0001c0013t0009g0211 a0003c0010t0020g0275 |
3 | HG02630.hp1 HG03486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.434-1228A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889333 | |||||||
chr18:2889376 | A | G | 2 | a0001c0003t0001g0282 a0001c0003t0001g0283 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.434-1185A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889376 | |||||||
chr18:2889433 | T | C | 425 | a0001c0001t0001g0038 a0001c0001t0001g0040 a0001c0001t0001g0057 others(422): Show |
428 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(425): Show |
intron_variant | MODIFIER | c.434-1128T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889433 | |||||||
chr18:2889434 | G | A | 1 | a0001c0001t0002g0435 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.434-1127G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889434 | |||||||
chr18:2889579 | C | T | 10 | a0001c0001t0001g0208 a0001c0001t0001g0277 a0001c0001t0014g0213 others(7): Show |
10 | HG01243.hp1 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.434-982C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889579 | |||||||
chr18:2889606 | C | G | 69 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0057 others(66): Show |
70 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.434-955C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889606 | |||||||
chr18:2889617 | A | AT | 5 | a0001c0001t0001g0277 a0001c0001t0018g0274 a0001c0001t0059g0276 others(2): Show |
5 | HG01243.hp1 HG02258.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-938dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889617 | ||||||
chr18:2889692 | C | CT | 135 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0181 others(132): Show |
136 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.434-847dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889692 | ||||||
chr18:2889692 | C | CTT | 11 | a0001c0001t0001g0303 a0001c0001t0003g0128 a0001c0001t0003g0188 others(8): Show |
11 | HG01123.hp2 HG01175.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.434-848_434-847dup others(2): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889692 | ||||||
chr18:2889692 | C | CTTT | 7 | a0001c0014t0001g0043 a0002c0009t0004g0260 a0006c0026t0053g0059 others(4): Show |
7 | HG02486.hp2 HG02630.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-849_434-847dup others(3): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889692 | ||||||
chr18:2889692 | CT | C | 84 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0172 others(81): Show |
85 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(82): Show |
intron_variant | MODIFIER | c.434-847delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889692 | ||||||
chr18:2889692 | CTT | C | 21 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0255 others(18): Show |
21 | HG01167.hp2 HG01169.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.434-848_434-847del others(2): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr18 | 2889692 | ||||||
chr18:2889697 | T | C | 1 | a0001c0001t0070g0137 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.434-864T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889697 | |||||||
chr18:2889698 | T | C | 5 | a0001c0004t0013g0004 a0001c0004t0013g0261 a0001c0006t0001g0062 others(2): Show |
6 | HG01081.hp1 HG01167.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.434-863T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889698 | |||||||
chr18:2889715 | A | T | 3 | a0002c0005t0004g0011 a0002c0005t0026g0071 a0005c0038t0004g0023 |
3 | HG02258.hp2 HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.434-846A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889715 | |||||||
chr18:2889795 | T | C | 1 | a0003c0010t0001g0007 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.434-766T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889795 | |||||||
chr18:2889828 | G | A | 67 | a0001c0001t0001g0066 a0001c0001t0001g0083 a0001c0001t0001g0181 others(64): Show |
68 | HG00323.hp1 HG00621.hp2 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.434-733G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889828 | |||||||
chr18:2889882 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.434-679G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889882 | |||||||
chr18:2889947 | T | C | 1 | a0001c0006t0001g0316 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.434-614T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889947 | |||||||
chr18:2889994 | T | A | 10 | a0001c0001t0001g0277 a0001c0001t0018g0274 a0001c0001t0059g0276 others(7): Show |
10 | HG01192.hp1 HG01243.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.434-567T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2889994 | |||||||
chr18:2890113 | C | T | 1 | a0001c0016t0016g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.434-448C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2890113 | |||||||
chr18:2890197 | G | A | 2 | a0001c0016t0061g0058 a0023c0044t0001g0272 |
2 | HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.434-364G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2890197 | |||||||
chr18:2890402 | A | C | 4 | a0001c0001t0017g0075 a0001c0014t0004g0006 a0001c0014t0004g0047 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-159A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 3/7 | chr18 | 2890402 | |||||||
chr18:2892564 | A | C | 38 | a0001c0004t0001g0383 a0001c0004t0002g0019 a0001c0004t0002g0042 others(35): Show |
39 | HG00280.hp1 HG00544.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.2359+78A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2892564 | |||||||
chr18:2892728 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2359+242T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2892728 | |||||||
chr18:2892762 | A | T | 1 | a0002c0047t0004g0379 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2359+276A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2892762 | |||||||
chr18:2892821 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(81): Show |
85 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.2359+335G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2892821 | |||||||
chr18:2892869 | T | G | 1 | a0001c0001t0003g0389 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2359+383T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2892869 | |||||||
chr18:2892976 | T | C | 20 | a0001c0001t0001g0066 a0001c0001t0047g0064 a0001c0006t0001g0062 others(17): Show |
20 | HG00099.hp1 HG00639.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.2359+490T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2892976 | |||||||
chr18:2893099 | T | A | 1 | a0001c0004t0002g0340 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2359+613T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893099 | |||||||
chr18:2893110 | A | C | 1 | a0003c0010t0009g0155 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2359+624A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893110 | |||||||
chr18:2893129 | T | C | 15 | a0001c0001t0001g0057 a0001c0001t0001g0208 a0001c0001t0001g0255 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2359+643T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893129 | |||||||
chr18:2893174 | C | A | 387 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(384): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.2359+688C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893174 | |||||||
chr18:2893263 | C | T | 1 | a0001c0014t0004g0006 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2359+777C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893263 | |||||||
chr18:2893274 | G | C | 1 | a0001c0001t0001g0002 | 2 | HG00642.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2359+788G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893274 | |||||||
chr18:2893380 | C | CACAG | 404 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(401): Show |
407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2359+895_2359+898d others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2893380 | ||||||
chr18:2893415 | A | T | 174 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0083 others(171): Show |
176 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.2359+929A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893415 | |||||||
chr18:2893559 | T | C | 2 | a0003c0010t0020g0031 a0003c0010t0020g0275 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2359+1073T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893559 | |||||||
chr18:2893581 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2359+1095G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893581 | |||||||
chr18:2893641 | C | A | 445 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(442): Show |
449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.2359+1155C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893641 | |||||||
chr18:2893665 | C | T | 1 | a0001c0001t0005g0333 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2359+1179C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893665 | |||||||
chr18:2893720 | A | G | 1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2359+1234A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2893720 | |||||||
chr18:2894166 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(93): Show |
97 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.2359+1680G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894166 | |||||||
chr18:2894227 | C | T | 1 | a0011c0052t0001g0242 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2359+1741C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894227 | |||||||
chr18:2894235 | C | T | 2 | a0001c0002t0003g0097 a0001c0002t0003g0098 |
2 | NA18946.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2359+1749C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894235 | |||||||
chr18:2894257 | G | A | 5 | a0001c0014t0004g0047 a0003c0012t0001g0025 a0003c0012t0001g0437 others(2): Show |
5 | HG02486.hp2 HG02922.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2359+1771G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894257 | |||||||
chr18:2894418 | C | T | 1 | a0002c0005t0008g0251 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2359+1932C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894418 | |||||||
chr18:2894527 | C | T | 4 | a0001c0013t0001g0009 a0001c0013t0001g0060 a0001c0013t0009g0211 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+2041C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894527 | |||||||
chr18:2894603 | G | A | 77 | a0001c0001t0001g0418 a0001c0001t0001g0433 a0001c0001t0002g0110 others(74): Show |
77 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.2359+2117G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894603 | |||||||
chr18:2894670 | T | G | 1 | a0001c0004t0009g0068 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2359+2184T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894670 | |||||||
chr18:2894761 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(92): Show |
96 | HG00323.hp2 HG00544.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.2359+2275G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894761 | |||||||
chr18:2894999 | C | A | 31 | a0001c0001t0001g0362 a0001c0001t0002g0233 a0001c0001t0002g0239 others(28): Show |
31 | HG00140.hp1 HG00621.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2359+2513C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2894999 | |||||||
chr18:2895200 | G | A | 2 | a0001c0003t0001g0282 a0001c0003t0001g0283 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2359+2714G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895200 | |||||||
chr18:2895276 | C | T | 1 | a0001c0003t0016g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2359+2790C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895276 | |||||||
chr18:2895301 | G | T | 1 | a0001c0001t0003g0234 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2359+2815G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895301 | |||||||
chr18:2895554 | C | T | 2 | a0001c0006t0010g0322 a0002c0020t0004g0010 |
2 | HG00140.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2359+3068C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895554 | |||||||
chr18:2895621 | T | C | 1 | a0001c0008t0021g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2359+3135T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895621 | |||||||
chr18:2895687 | C | T | 2 | a0001c0002t0002g0244 a0001c0002t0024g0385 |
2 | NA18953.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.2359+3201C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895687 | |||||||
chr18:2895759 | C | T | 1 | a0023c0044t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2359+3273C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895759 | |||||||
chr18:2895790 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2359+3304A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895790 | |||||||
chr18:2895822 | C | T | 445 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(442): Show |
449 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(446): Show |
intron_variant | MODIFIER | c.2359+3336C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895822 | |||||||
chr18:2895865 | C | T | 1 | a0005c0038t0004g0023 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2359+3379C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895865 | |||||||
chr18:2895905 | A | G | 26 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0001g0066 others(23): Show |
27 | HG01081.hp1 HG01167.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.2359+3419A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895905 | |||||||
chr18:2895937 | G | T | 1 | a0001c0001t0002g0390 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2359+3451G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895937 | |||||||
chr18:2895961 | G | C | 248 | a0001c0001t0001g0030 a0001c0001t0001g0038 a0001c0001t0001g0040 others(245): Show |
248 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.2359+3475G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2895961 | |||||||
chr18:2896182 | A | G | 1 | a0001c0008t0036g0141 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2359+3696A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896182 | |||||||
chr18:2896232 | G | A | 4 | a0001c0013t0001g0009 a0001c0013t0001g0060 a0001c0013t0009g0211 others(1): Show |
4 | HG02145.hp1 HG02572.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+3746G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896232 | |||||||
chr18:2896247 | C | T | 1 | a0001c0001t0002g0435 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2359+3761C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896247 | |||||||
chr18:2896250 | A | G | 3 | a0001c0006t0001g0062 a0001c0006t0001g0063 a0001c0014t0001g0043 |
3 | HG01081.hp1 HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2359+3764A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896250 | |||||||
chr18:2896278 | C | T | 2 | a0001c0001t0015g0296 a0002c0005t0004g0056 |
2 | NA18968.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2359+3792C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896278 | |||||||
chr18:2896279 | G | A | 121 | a0001c0001t0001g0014 a0001c0001t0001g0038 a0001c0001t0001g0040 others(118): Show |
122 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.2359+3793G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896279 | |||||||
chr18:2896290 | C | T | 52 | a0001c0001t0001g0030 a0001c0001t0001g0303 a0001c0001t0001g0362 others(49): Show |
52 | HG00140.hp1 HG00621.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.2359+3804C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896290 | |||||||
chr18:2896322 | T | C | 74 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0303 others(71): Show |
74 | HG00140.hp1 HG00621.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.2359+3836T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896322 | |||||||
chr18:2896477 | G | GAT | 4 | a0001c0001t0001g0255 a0001c0014t0004g0047 a0003c0012t0001g0025 others(1): Show |
4 | HG02886.hp2 HG02922.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+4002_2359+400 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2896477 | ||||||
chr18:2896599 | C | T | 4 | a0001c0001t0017g0228 a0010c0019t0001g0034 a0010c0019t0001g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2359+4113C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896599 | |||||||
chr18:2896619 | C | T | 4 | a0001c0001t0017g0228 a0010c0019t0001g0034 a0010c0019t0001g0035 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2359+4133C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896619 | |||||||
chr18:2896622 | G | A | 2 | a0001c0001t0017g0075 a0002c0005t0004g0256 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2359+4136G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896622 | |||||||
chr18:2896648 | G | GTTAT | 82 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0057 others(79): Show |
83 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.2359+4177_2359+418 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2896648 | ||||||
chr18:2896721 | C | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0057 others(194): Show |
200 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.2359+4235C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896721 | |||||||
chr18:2896817 | T | C | 4 | a0001c0002t0042g0444 a0001c0003t0003g0127 a0001c0008t0003g0226 others(1): Show |
4 | HG00738.hp1 HG01943.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+4331T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896817 | |||||||
chr18:2896980 | T | C | 1 | a0001c0006t0010g0322 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2359+4494T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2896980 | |||||||
chr18:2897194 | G | A | 2 | a0001c0001t0018g0026 a0001c0001t0018g0027 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2359+4708G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2897194 | |||||||
chr18:2897288 | T | C | 1 | a0001c0004t0003g0102 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2359+4802T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2897288 | |||||||
chr18:2897394 | T | A | 3 | a0001c0001t0014g0033 a0001c0014t0004g0006 a0003c0046t0001g0028 |
3 | HG01884.hp2 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2359+4908T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2897394 | |||||||
chr18:2897861 | C | CT | 9 | a0001c0001t0001g0208 a0001c0001t0001g0254 a0001c0001t0001g0277 others(6): Show |
9 | HG01243.hp1 HG02258.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.2359+5378dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2897861 | ||||||
chr18:2897864 | T | TA | 121 | a0001c0001t0001g0014 a0001c0001t0001g0433 a0001c0001t0002g0091 others(118): Show |
121 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.2359+5393dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2897864 | ||||||
chr18:2897864 | T | TTA | 20 | a0001c0001t0001g0040 a0001c0001t0001g0057 a0001c0001t0001g0255 others(17): Show |
20 | HG00673.hp2 HG01106.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.2359+5378_2359+537 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2897864 | |||||||
chr18:2897864 | TA | T | 56 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0303 others(53): Show |
56 | HG00140.hp1 HG00621.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2359+5393delA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2897864 | ||||||
chr18:2897995 | T | C | 110 | a0001c0001t0001g0172 a0001c0001t0001g0245 a0001c0001t0001g0384 others(107): Show |
112 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.2359+5509T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2897995 | |||||||
chr18:2898133 | T | C | 439 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(436): Show |
443 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(440): Show |
intron_variant | MODIFIER | c.2359+5647T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898133 | |||||||
chr18:2898303 | A | G | 434 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(431): Show |
438 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(435): Show |
intron_variant | MODIFIER | c.2359+5817A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898303 | |||||||
chr18:2898308 | G | A | 1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2359+5822G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898308 | |||||||
chr18:2898318 | C | G | 1 | a0001c0001t0023g0099 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2359+5832C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898318 | |||||||
chr18:2898364 | C | T | 1 | a0001c0002t0008g0399 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2359+5878C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898364 | |||||||
chr18:2898492 | G | A | 1 | a0001c0008t0021g0209 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2359+6006G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898492 | |||||||
chr18:2898522 | G | C | 3 | a0001c0001t0014g0213 a0001c0001t0035g0214 a0001c0001t0037g0212 |
3 | HG02109.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2359+6036G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898522 | |||||||
chr18:2898537 | A | G | 100 | a0001c0001t0001g0040 a0001c0001t0001g0066 a0001c0001t0001g0433 others(97): Show |
100 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2359+6051A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898537 | |||||||
chr18:2898648 | C | T | 1 | a0001c0004t0002g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2359+6162C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898648 | |||||||
chr18:2898679 | G | A | 438 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(435): Show |
442 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(439): Show |
intron_variant | MODIFIER | c.2359+6193G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898679 | |||||||
chr18:2898863 | T | C | 161 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0040 others(158): Show |
161 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2359+6377T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898863 | |||||||
chr18:2898868 | A | T | 1 | a0001c0002t0002g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2359+6382A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2898868 | |||||||
chr18:2899030 | C | T | 16 | a0001c0001t0002g0133 a0001c0001t0002g0368 a0001c0001t0002g0369 others(13): Show |
16 | HG00423.hp1 HG00438.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2359+6544C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899030 | |||||||
chr18:2899050 | G | A | 2 | a0001c0003t0002g0330 a0002c0009t0004g0331 |
2 | NA18943.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2359+6564G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899050 | |||||||
chr18:2899081 | T | TA | 269 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0066 others(266): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.2359+6603dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2899081 | ||||||
chr18:2899081 | T | TAA | 79 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0001g0208 others(76): Show |
80 | HG00639.hp1 HG00738.hp2 HG01106.hp1 others(77): Show |
intron_variant | MODIFIER | c.2359+6602_2359+660 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2899081 | ||||||
chr18:2899186 | A | G | 82 | a0001c0001t0001g0030 a0001c0001t0001g0083 a0001c0001t0001g0255 others(79): Show |
82 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.2359+6700A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899186 | |||||||
chr18:2899258 | G | A | 8 | a0001c0001t0002g0368 a0001c0001t0002g0369 a0001c0001t0002g0370 others(5): Show |
8 | NA18946.hp1 NA18960.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.2359+6772G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899258 | |||||||
chr18:2899284 | G | A | 3 | a0001c0001t0034g0426 a0003c0012t0013g0343 a0003c0045t0062g0005 |
3 | HG02055.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.2359+6798G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899284 | |||||||
chr18:2899326 | C | T | 100 | a0001c0001t0001g0402 a0001c0001t0001g0403 a0001c0001t0002g0081 others(97): Show |
101 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2359+6840C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899326 | |||||||
chr18:2899327 | G | A | 2 | a0001c0001t0003g0389 a0001c0004t0002g0042 |
2 | HG02683.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.2359+6841G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899327 | |||||||
chr18:2899430 | G | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0254 others(118): Show |
123 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2359+6944G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899430 | |||||||
chr18:2899445 | A | G | 1 | a0001c0002t0049g0157 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2359+6959A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899445 | |||||||
chr18:2899485 | A | T | 17 | a0001c0001t0001g0038 a0001c0001t0001g0418 a0001c0001t0003g0290 others(14): Show |
17 | HG00738.hp1 HG01928.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.2359+6999A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899485 | |||||||
chr18:2899528 | G | A | 4 | a0001c0001t0003g0200 a0001c0002t0003g0080 a0001c0002t0003g0324 others(1): Show |
4 | HG02074.hp2 NA18954.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.2359+7042G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899528 | |||||||
chr18:2899535 | T | C | 1 | a0001c0001t0006g0309 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2359+7049T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899535 | |||||||
chr18:2899536 | G | A | 1 | a0001c0001t0006g0309 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2359+7050G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899536 | |||||||
chr18:2899557 | T | G | 8 | a0001c0001t0001g0254 a0001c0001t0001g0277 a0001c0001t0052g0210 others(5): Show |
8 | HG01243.hp1 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2359+7071T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899557 | |||||||
chr18:2899626 | A | T | 1 | a0001c0001t0001g0363 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2359+7140A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899626 | |||||||
chr18:2899630 | G | A | 87 | a0001c0001t0001g0083 a0001c0001t0001g0245 a0001c0001t0001g0303 others(84): Show |
88 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.2359+7144G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899630 | |||||||
chr18:2899739 | G | A | 2 | a0001c0001t0001g0362 a0001c0001t0001g0363 |
2 | HG00741.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.2360-7044G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899739 | |||||||
chr18:2899755 | C | A | 1 | a0008c0017t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-7028C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899755 | |||||||
chr18:2899756 | A | G | 1 | a0008c0017t0001g0073 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2360-7027A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899756 | |||||||
chr18:2899776 | T | C | 2 | a0001c0001t0003g0289 a0002c0005t0004g0430 |
2 | NA18747.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2360-7007T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899776 | |||||||
chr18:2899798 | G | A | 2 | a0001c0001t0001g0030 a0001c0014t0004g0006 |
2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2360-6985G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899798 | |||||||
chr18:2899976 | G | C | 3 | a0005c0036t0004g0046 a0005c0038t0004g0023 a0019c0048t0004g0252 |
3 | HG02258.hp2 HG02572.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2360-6807G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2899976 | |||||||
chr18:2900030 | C | T | 363 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(360): Show |
366 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(363): Show |
intron_variant | MODIFIER | c.2360-6753C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900030 | |||||||
chr18:2900132 | G | GT | 67 | a0001c0001t0001g0057 a0001c0001t0001g0207 a0001c0001t0001g0363 others(64): Show |
68 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2360-6641dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2900132 | ||||||
chr18:2900132 | GT | G | 361 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(358): Show |
364 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(361): Show |
intron_variant | MODIFIER | c.2360-6641delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2900132 | ||||||
chr18:2900195 | C | T | 204 | a0001c0001t0001g0172 a0001c0001t0001g0245 a0001c0001t0001g0303 others(201): Show |
206 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.2360-6588C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900195 | |||||||
chr18:2900235 | T | C | 1 | a0002c0005t0072g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2360-6548T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900235 | |||||||
chr18:2900288 | T | C | 365 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(362): Show |
368 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(365): Show |
intron_variant | MODIFIER | c.2360-6495T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900288 | |||||||
chr18:2900589 | G | C | 434 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(431): Show |
438 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(435): Show |
intron_variant | MODIFIER | c.2360-6194G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900589 | |||||||
chr18:2900600 | G | T | 1 | a0001c0001t0003g0273 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2360-6183G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900600 | |||||||
chr18:2900618 | C | A | 12 | a0001c0001t0001g0030 a0001c0001t0001g0208 a0001c0001t0001g0254 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-6165C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900618 | |||||||
chr18:2900641 | T | C | 350 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0040 others(347): Show |
353 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(350): Show |
intron_variant | MODIFIER | c.2360-6142T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900641 | |||||||
chr18:2900673 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0181 a0001c0001t0001g0220 others(47): Show |
51 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.2360-6110G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900673 | |||||||
chr18:2900679 | A | ACAAGCGA others(4): Show |
1 | a0001c0001t0034g0186 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2360-6104_2360-610 others(15): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900679 | |||||||
chr18:2900679 | A | AT | 348 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0040 others(345): Show |
351 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(348): Show |
intron_variant | MODIFIER | c.2360-6101dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2900679 | ||||||
chr18:2900703 | C | T | 1 | a0001c0001t0005g0166 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2360-6080C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900703 | |||||||
chr18:2900727 | C | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0208 a0001c0001t0001g0254 others(10): Show |
13 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2360-6056C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900727 | |||||||
chr18:2900756 | T | G | 2 | a0003c0012t0013g0343 a0003c0045t0062g0005 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2360-6027T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900756 | |||||||
chr18:2900805 | A | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0181 others(100): Show |
104 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.2360-5978A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900805 | |||||||
chr18:2900831 | G | A | 2 | a0001c0001t0027g0406 a0001c0001t0027g0407 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2360-5952G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900831 | |||||||
chr18:2900837 | C | T | 2 | a0010c0019t0001g0034 a0010c0019t0001g0035 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2360-5946C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900837 | |||||||
chr18:2900870 | A | T | 2 | a0003c0012t0013g0343 a0003c0045t0062g0005 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2360-5913A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900870 | |||||||
chr18:2900871 | A | T | 2 | a0003c0012t0013g0343 a0003c0045t0062g0005 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2360-5912A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2900871 | |||||||
chr18:2901009 | T | C | 347 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0040 others(344): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(347): Show |
intron_variant | MODIFIER | c.2360-5774T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901009 | |||||||
chr18:2901081 | A | C | 1 | a0001c0001t0017g0228 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2360-5702A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901081 | |||||||
chr18:2901082 | A | G | 12 | a0001c0001t0001g0030 a0001c0001t0001g0208 a0001c0001t0001g0254 others(9): Show |
12 | HG01243.hp1 HG01891.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2360-5701A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901082 | |||||||
chr18:2901205 | A | G | 2 | a0003c0012t0013g0343 a0003c0045t0062g0005 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2360-5578A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901205 | |||||||
chr18:2901298 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2360-5485C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901298 | |||||||
chr18:2901358 | G | A | 1 | a0001c0001t0002g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2360-5425G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901358 | |||||||
chr18:2901568 | G | A | 1 | a0001c0016t0061g0058 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2360-5215G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901568 | |||||||
chr18:2901572 | C | T | 1 | a0002c0009t0008g0225 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.2360-5211C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901572 | |||||||
chr18:2901574 | T | G | 74 | a0001c0001t0001g0057 a0001c0001t0001g0207 a0001c0001t0001g0363 others(71): Show |
74 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(71): Show |
intron_variant | MODIFIER | c.2360-5209T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901574 | |||||||
chr18:2901823 | G | A | 3 | a0001c0001t0001g0254 a0001c0001t0001g0277 a0006c0027t0001g0039 |
3 | HG01243.hp1 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2360-4960G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901823 | |||||||
chr18:2901845 | A | T | 1 | a0004c0011t0003g0397 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2360-4938A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901845 | |||||||
chr18:2901887 | C | T | 1 | a0001c0006t0001g0015 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2360-4896C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2901887 | |||||||
chr18:2902001 | T | C | 2 | a0001c0001t0017g0075 a0002c0005t0004g0256 |
2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2360-4782T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902001 | |||||||
chr18:2902314 | C | A | 1 | a0001c0004t0003g0020 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2360-4469C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902314 | |||||||
chr18:2902404 | T | C | 305 | a0001c0001t0001g0014 a0001c0001t0001g0057 a0001c0001t0001g0066 others(302): Show |
307 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.2360-4379T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902404 | |||||||
chr18:2902479 | T | C | 2 | a0003c0012t0013g0343 a0003c0045t0062g0005 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2360-4304T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902479 | |||||||
chr18:2902545 | T | C | 1 | a0001c0016t0017g0259 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2360-4238T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902545 | |||||||
chr18:2902571 | G | A | 1 | a0001c0004t0002g0019 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2360-4212G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902571 | |||||||
chr18:2902658 | G | A | 407 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(404): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.2360-4125G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902658 | |||||||
chr18:2902816 | A | G | 114 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0057 others(111): Show |
115 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.2360-3967A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902816 | |||||||
chr18:2902871 | C | T | 215 | a0001c0001t0001g0002 a0001c0001t0001g0038 a0001c0001t0001g0040 others(212): Show |
217 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.2360-3912C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902871 | |||||||
chr18:2902905 | C | T | 3 | a0001c0004t0005g0067 a0002c0005t0004g0011 a0002c0005t0004g0193 |
3 | HG00639.hp1 HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.2360-3878C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902905 | |||||||
chr18:2902934 | G | A | 3 | a0001c0001t0003g0100 a0001c0001t0003g0388 a0001c0002t0002g0090 |
3 | HG02155.hp2 NA19079.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.2360-3849G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902934 | |||||||
chr18:2902961 | A | G | 1 | a0023c0044t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2360-3822A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2902961 | |||||||
chr18:2903068 | TAGAG | T | 15 | a0001c0001t0002g0321 a0001c0001t0003g0100 a0001c0001t0003g0111 others(12): Show |
15 | HG00408.hp1 HG00609.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.2360-3711_2360-370 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2903068 | ||||||
chr18:2903080 | C | T | 1 | a0002c0009t0004g0318 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2360-3703C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903080 | |||||||
chr18:2903099 | A | C | 4 | a0001c0001t0001g0172 a0001c0004t0001g0383 a0001c0004t0003g0227 others(1): Show |
4 | HG00280.hp1 HG00735.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-3684A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903099 | |||||||
chr18:2903109 | G | A | 1 | a0001c0001t0003g0334 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2360-3674G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903109 | |||||||
chr18:2903171 | G | GA | 3 | a0001c0001t0047g0064 a0003c0012t0013g0343 a0003c0045t0062g0005 |
3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2360-3611dupA | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2903171 | ||||||
chr18:2903182 | G | T | 1 | a0001c0003t0006g0153 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2360-3601G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903182 | |||||||
chr18:2903183 | T | G | 1 | a0001c0003t0006g0153 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2360-3600T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903183 | |||||||
chr18:2903208 | T | A | 1 | a0001c0001t0002g0294 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2360-3575T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903208 | |||||||
chr18:2903240 | A | G | 13 | a0001c0001t0003g0200 a0001c0001t0003g0273 a0001c0001t0003g0278 others(10): Show |
13 | HG00609.hp1 HG02071.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.2360-3543A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903240 | |||||||
chr18:2903333 | G | C | 16 | a0001c0001t0001g0030 a0001c0001t0001g0208 a0001c0001t0018g0026 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.2360-3450G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903333 | |||||||
chr18:2903394 | A | G | 1 | a0023c0044t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2360-3389A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903394 | |||||||
chr18:2903497 | C | T | 2 | a0001c0004t0002g0340 a0001c0004t0002g0341 |
2 | NA18955.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.2360-3286C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903497 | |||||||
chr18:2903775 | A | AT | 67 | a0001c0001t0001g0030 a0001c0001t0001g0415 a0001c0001t0002g0382 others(64): Show |
67 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.2360-3000dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2903775 | ||||||
chr18:2903783 | T | A | 4 | a0001c0001t0001g0208 a0002c0009t0004g0260 a0012c0051t0019g0076 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-3000T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903783 | |||||||
chr18:2903976 | A | C | 9 | a0001c0001t0005g0044 a0001c0001t0005g0065 a0001c0001t0005g0185 others(6): Show |
9 | HG02055.hp1 HG02280.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2360-2807A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2903976 | |||||||
chr18:2904007 | C | T | 4 | a0001c0001t0001g0208 a0002c0009t0004g0260 a0012c0051t0019g0076 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-2776C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904007 | |||||||
chr18:2904067 | A | C | 1 | a0001c0003t0006g0153 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2360-2716A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904067 | |||||||
chr18:2904116 | C | A | 3 | a0001c0001t0047g0064 a0003c0012t0013g0343 a0003c0045t0062g0005 |
3 | HG02055.hp2 HG02976.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2360-2667C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904116 | |||||||
chr18:2904134 | G | A | 164 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0083 others(161): Show |
164 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2360-2649G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904134 | |||||||
chr18:2904192 | T | C | 1 | a0001c0016t0017g0259 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2360-2591T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904192 | |||||||
chr18:2904327 | C | G | 4 | a0001c0001t0001g0208 a0002c0009t0004g0260 a0012c0051t0019g0076 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-2456C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904327 | |||||||
chr18:2904480 | T | C | 2 | a0001c0001t0001g0014 a0001c0001t0021g0253 |
2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2360-2303T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904480 | |||||||
chr18:2904491 | T | C | 1 | a0001c0001t0005g0423 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2360-2292T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904491 | |||||||
chr18:2904596 | T | C | 204 | a0001c0001t0001g0172 a0001c0001t0001g0245 a0001c0001t0001g0303 others(201): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.2360-2187T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904596 | |||||||
chr18:2904601 | G | C | 223 | a0001c0001t0001g0040 a0001c0001t0001g0172 a0001c0001t0001g0208 others(220): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.2360-2182G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904601 | |||||||
chr18:2904655 | A | C | 4 | a0001c0001t0001g0208 a0002c0009t0004g0260 a0012c0051t0019g0076 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-2128A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904655 | |||||||
chr18:2904875 | A | G | 4 | a0001c0001t0001g0208 a0002c0009t0004g0260 a0012c0051t0019g0076 others(1): Show |
4 | HG01891.hp2 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2360-1908A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2904875 | |||||||
chr18:2905057 | C | A | 15 | a0001c0001t0001g0040 a0001c0001t0001g0208 a0001c0001t0014g0213 others(12): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2360-1726C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905057 | |||||||
chr18:2905100 | T | C | 1 | a0009c0018t0001g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2360-1683T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905100 | |||||||
chr18:2905140 | TAGAATGG others(40): Show |
T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2360-1641_2360-159 others(51): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905140 | ||||||
chr18:2905237 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2360-1546G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905237 | |||||||
chr18:2905293 | G | C | 5 | a0001c0001t0071g0319 a0001c0003t0002g0302 a0002c0005t0004g0206 others(2): Show |
5 | HG00558.hp1 HG02080.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-1490G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905293 | |||||||
chr18:2905300 | C | CG | 175 | a0001c0001t0001g0014 a0001c0001t0001g0083 a0001c0001t0001g0245 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2360-1473dupG | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905300 | ||||||
chr18:2905300 | C | CGG | 78 | a0001c0001t0001g0038 a0001c0001t0001g0172 a0001c0001t0001g0303 others(75): Show |
78 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.2360-1474_2360-147 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905300 | ||||||
chr18:2905300 | C | G | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2360-1483C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905300 | |||||||
chr18:2905301 | G | C | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2360-1482G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905301 | |||||||
chr18:2905322 | T | C | 4 | a0001c0002t0002g0105 a0001c0002t0002g0391 a0001c0003t0002g0431 others(1): Show |
4 | HG00597.hp2 HG02074.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.2360-1461T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905322 | |||||||
chr18:2905381 | G | GAT | 7 | a0001c0001t0002g0119 a0001c0001t0002g0159 a0001c0001t0002g0421 others(4): Show |
7 | HG00438.hp1 HG02040.hp2 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.2360-1389_2360-138 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905381 | ||||||
chr18:2905402 | C | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2360-1381C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905402 | |||||||
chr18:2905465 | C | G | 187 | a0001c0001t0001g0172 a0001c0001t0001g0303 a0001c0001t0001g0348 others(184): Show |
189 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.2360-1318C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905465 | |||||||
chr18:2905476 | C | T | 323 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(320): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.2360-1307C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905476 | |||||||
chr18:2905775 | G | GT | 15 | a0001c0001t0002g0110 a0001c0001t0012g0299 a0001c0001t0044g0442 others(12): Show |
15 | HG00408.hp2 HG00544.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.2360-1001dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905775 | ||||||
chr18:2905775 | G | T | 2 | a0001c0001t0002g0081 a0001c0001t0002g0371 |
2 | HG04184.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.2360-1008G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905775 | |||||||
chr18:2905775 | GTTTTTTT others(3): Show |
G | 1 | a0014c0054t0019g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2360-1000_2360-991 others(13): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905775 | ||||||
chr18:2905778 | TTTTTG | T | 24 | a0001c0001t0001g0040 a0001c0001t0001g0208 a0001c0001t0001g0254 others(21): Show |
24 | HG00738.hp1 HG01081.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.2360-1000_2360-996 others(8): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905778 | ||||||
chr18:2905779 | T | G | 1 | a0001c0002t0002g0320 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2360-1004T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905779 | |||||||
chr18:2905780 | TTTG | T | 28 | a0001c0001t0001g0348 a0001c0001t0001g0362 a0001c0001t0001g0363 others(25): Show |
28 | HG00099.hp2 HG00741.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.2360-1000_2360-998 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905780 | ||||||
chr18:2905781 | TTG | T | 107 | a0001c0001t0001g0172 a0001c0001t0002g0119 a0001c0001t0002g0159 others(104): Show |
108 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.2360-1000_2360-999 others(5): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr18 | 2905781 | ||||||
chr18:2905782 | TG | T | 100 | a0001c0001t0001g0030 a0001c0001t0002g0091 a0001c0001t0003g0273 others(97): Show |
100 | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.2360-1000delG | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905782 | |||||||
chr18:2905783 | G | T | 99 | a0001c0001t0001g0083 a0001c0001t0001g0303 a0001c0001t0002g0081 others(96): Show |
100 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.2360-1000G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905783 | |||||||
chr18:2905784 | T | TG | 4 | a0001c0004t0013g0004 a0001c0004t0013g0261 a0001c0004t0064g0196 others(1): Show |
5 | HG01884.hp1 HG02055.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.2360-999_2360-998i others(3): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905784 | |||||||
chr18:2905785 | T | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0181 a0001c0001t0001g0220 others(52): Show |
56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.2360-998T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905785 | |||||||
chr18:2905786 | T | G | 1 | a0001c0001t0006g0147 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2360-997T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905786 | |||||||
chr18:2905854 | G | A | 1 | a0014c0054t0019g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2360-929G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905854 | |||||||
chr18:2905873 | G | C | 425 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0040 others(422): Show |
429 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(426): Show |
intron_variant | MODIFIER | c.2360-910G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905873 | |||||||
chr18:2905975 | C | T | 23 | a0001c0001t0001g0040 a0001c0001t0001g0254 a0001c0001t0001g0277 others(20): Show |
23 | HG01081.hp1 HG01167.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.2360-808C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2905975 | |||||||
chr18:2906079 | C | A | 1 | a0001c0002t0002g0337 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2360-704C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906079 | |||||||
chr18:2906088 | C | T | 266 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0057 others(263): Show |
267 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.2360-695C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906088 | |||||||
chr18:2906095 | C | A | 1 | a0001c0001t0007g0089 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2360-688C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906095 | |||||||
chr18:2906104 | G | C | 1 | a0001c0002t0005g0378 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2360-679G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906104 | |||||||
chr18:2906197 | G | C | 2 | a0001c0001t0006g0309 a0003c0010t0019g0216 |
2 | HG02717.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.2360-586G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906197 | |||||||
chr18:2906281 | G | A | 2 | a0003c0010t0020g0031 a0003c0010t0020g0275 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2360-502G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906281 | |||||||
chr18:2906342 | G | A | 1 | a0001c0037t0063g0361 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2360-441G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906342 | |||||||
chr18:2906529 | C | G | 1 | a0001c0002t0002g0356 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2360-254C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906529 | |||||||
chr18:2906671 | A | G | 2 | a0001c0001t0006g0219 a0001c0001t0006g0436 |
2 | HG00423.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2360-112A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 4/7 | chr18 | 2906671 | |||||||
chr18:2907190 | G | T | 1 | a0004c0043t0003g0164 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2662+105G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907190 | |||||||
chr18:2907303 | C | T | 17 | a0001c0001t0001g0348 a0001c0001t0001g0362 a0001c0001t0001g0363 others(14): Show |
17 | HG00741.hp1 HG01106.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.2662+218C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907303 | |||||||
chr18:2907371 | C | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2662+286C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907371 | |||||||
chr18:2907400 | T | C | 150 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0207 others(147): Show |
151 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.2662+315T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907400 | |||||||
chr18:2907480 | T | G | 88 | a0001c0001t0006g0103 a0001c0001t0006g0104 a0001c0001t0006g0147 others(85): Show |
88 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.2662+395T>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907480 | |||||||
chr18:2907610 | C | G | 1 | a0001c0001t0010g0420 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2662+525C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907610 | |||||||
chr18:2907611 | A | G | 1 | a0023c0044t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2662+526A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907611 | |||||||
chr18:2907755 | C | G | 5 | a0001c0001t0003g0188 a0001c0001t0003g0189 a0001c0003t0001g0199 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.2662+670C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907755 | |||||||
chr18:2907757 | A | G | 3 | a0001c0001t0001g0083 a0001c0001t0001g0303 a0001c0006t0001g0015 |
3 | HG01261.hp2 HG01496.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2662+672A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2907757 | |||||||
chr18:2908001 | C | T | 89 | a0001c0001t0006g0103 a0001c0001t0006g0104 a0001c0001t0006g0147 others(86): Show |
89 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2662+916C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908001 | |||||||
chr18:2908133 | AT | A | 3 | a0001c0001t0016g0344 a0001c0003t0016g0061 a0001c0016t0016g0029 |
3 | HG02622.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2663-806delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr18 | 2908133 | ||||||
chr18:2908166 | C | T | 2 | a0001c0004t0002g0019 a0001c0004t0002g0055 |
2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2663-777C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908166 | |||||||
chr18:2908285 | C | T | 258 | a0001c0001t0002g0081 a0001c0001t0002g0091 a0001c0001t0002g0096 others(255): Show |
261 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.2663-658C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908285 | |||||||
chr18:2908467 | C | G | 1 | a0001c0001t0002g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2663-476C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908467 | |||||||
chr18:2908484 | T | C | 436 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(433): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.2663-459T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908484 | |||||||
chr18:2908497 | A | G | 1 | a0001c0001t0014g0213 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2663-446A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908497 | |||||||
chr18:2908512 | C | T | 1 | a0006c0026t0053g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2663-431C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908512 | |||||||
chr18:2908776 | T | C | 1 | a0001c0004t0002g0042 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2663-167T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908776 | |||||||
chr18:2908845 | G | A | 1 | a0023c0044t0001g0272 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2663-98G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 5/7 | chr18 | 2908845 | |||||||
chr18:2909010 | G | C | 3 | a0001c0001t0017g0075 a0001c0001t0017g0228 a0001c0016t0017g0259 |
3 | HG02451.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2695+35G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909010 | |||||||
chr18:2909117 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2695+142G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909117 | |||||||
chr18:2909137 | T | C | 2 | a0003c0010t0020g0031 a0003c0010t0020g0275 |
2 | NA19043.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2695+162T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909137 | |||||||
chr18:2909139 | G | A | 1 | a0001c0001t0009g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2695+164G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909139 | |||||||
chr18:2909338 | G | A | 1 | a0001c0003t0066g0353 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2696-353G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909338 | |||||||
chr18:2909410 | G | A | 16 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0207 others(13): Show |
16 | HG01106.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.2696-281G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909410 | |||||||
chr18:2909482 | G | A | 16 | a0001c0001t0009g0041 a0001c0001t0009g0045 a0001c0001t0037g0212 others(13): Show |
16 | HG01123.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.2696-209G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909482 | |||||||
chr18:2909512 | G | GTCATTTC others(3): Show |
1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-179_2696-178i others(12): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909512 | |||||||
chr18:2909513 | C | T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-178C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909513 | |||||||
chr18:2909515 | G | C | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-176G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909515 | |||||||
chr18:2909518 | C | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-173C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909518 | |||||||
chr18:2909519 | C | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-172C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909519 | |||||||
chr18:2909523 | G | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-168G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909523 | |||||||
chr18:2909524 | A | T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-167A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909524 | |||||||
chr18:2909526 | A | T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-165A>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909526 | |||||||
chr18:2909527 | G | T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-164G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909527 | |||||||
chr18:2909529 | G | C | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-162G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909529 | |||||||
chr18:2909533 | C | G | 4 | a0001c0037t0063g0361 a0003c0045t0062g0005 a0012c0051t0019g0076 others(1): Show |
4 | HG01891.hp2 HG02976.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-158C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909533 | |||||||
chr18:2909535 | T | C | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-156T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909535 | |||||||
chr18:2909537 | T | C | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-154T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909537 | |||||||
chr18:2909538 | G | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-153G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909538 | |||||||
chr18:2909539 | G | T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-152G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909539 | |||||||
chr18:2909540 | C | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-151C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909540 | |||||||
chr18:2909542 | G | T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-149G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909542 | |||||||
chr18:2909545 | G | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-146G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909545 | |||||||
chr18:2909546 | G | T | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-145G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909546 | |||||||
chr18:2909547 | G | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-144G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909547 | |||||||
chr18:2909548 | C | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-143C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909548 | |||||||
chr18:2909550 | T | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-141T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909550 | |||||||
chr18:2909551 | G | C | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-140G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909551 | |||||||
chr18:2909552 | A | C | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-139A>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909552 | |||||||
chr18:2909553 | G | A | 1 | a0021c0040t0001g0163 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.2696-138G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909553 | |||||||
chr18:2909610 | C | T | 3 | a0001c0001t0003g0001 a0001c0001t0027g0406 a0001c0001t0027g0407 |
4 | HG01074.hp1 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2696-81C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909610 | |||||||
chr18:2909645 | G | A | 56 | a0001c0014t0004g0006 a0001c0014t0004g0047 a0002c0005t0004g0011 others(53): Show |
56 | HG00558.hp1 HG00639.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.2696-46G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 6/7 | chr18 | 2909645 | |||||||
chr18:2909833 | C | G | 299 | a0001c0001t0001g0002 a0001c0001t0001g0083 a0001c0001t0001g0172 others(296): Show |
303 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.2824+14C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2909833 | |||||||
chr18:2910014 | G | A | 5 | a0001c0001t0002g0233 a0001c0004t0002g0019 a0001c0004t0002g0042 others(2): Show |
5 | HG01109.hp2 HG01952.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.2824+195G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910014 | |||||||
chr18:2910051 | C | T | 1 | a0001c0001t0001g0363 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2824+232C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910051 | |||||||
chr18:2910179 | C | CCT | 170 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0003g0001 others(167): Show |
173 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.2824+366_2824+367d others(4): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2910179 | ||||||
chr18:2910197 | A | G | 1 | a0001c0001t0003g0003 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2824+378A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910197 | |||||||
chr18:2910200 | C | T | 2 | a0001c0001t0001g0303 a0001c0006t0001g0015 |
2 | HG01261.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2824+381C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910200 | |||||||
chr18:2910230 | G | A | 1 | a0001c0004t0003g0227 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2824+411G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910230 | |||||||
chr18:2910359 | G | A | 1 | a0006c0026t0053g0059 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2824+540G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910359 | |||||||
chr18:2910471 | G | C | 1 | a0001c0001t0002g0428 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2824+652G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910471 | |||||||
chr18:2910474 | C | T | 1 | a0001c0001t0071g0319 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2824+655C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910474 | |||||||
chr18:2910475 | G | A | 1 | a0001c0004t0060g0306 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2824+656G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910475 | |||||||
chr18:2910580 | G | A | 121 | a0001c0001t0002g0170 a0001c0001t0002g0173 a0001c0001t0003g0001 others(118): Show |
123 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.2824+761G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910580 | |||||||
chr18:2910586 | C | T | 3 | a0001c0004t0009g0068 a0001c0016t0061g0058 a0003c0010t0009g0262 |
3 | HG02723.hp2 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2824+767C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2910586 | |||||||
chr18:2911097 | C | CTG | 12 | a0001c0001t0009g0041 a0001c0001t0009g0045 a0001c0001t0037g0212 others(9): Show |
12 | HG01123.hp1 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2824+1279_2824+128 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2911097 | ||||||
chr18:2911101 | G | A | 1 | a0001c0001t0003g0359 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2824+1282G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911101 | |||||||
chr18:2911134 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2824+1315G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911134 | |||||||
chr18:2911180 | C | T | 2 | a0012c0051t0019g0076 a0014c0054t0019g0037 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2824+1361C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911180 | |||||||
chr18:2911189 | T | A | 2 | a0001c0002t0006g0204 a0001c0003t0006g0326 |
2 | NA19005.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2824+1370T>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911189 | |||||||
chr18:2911309 | C | G | 4 | a0001c0001t0018g0026 a0001c0001t0018g0027 a0001c0001t0018g0274 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2824+1490C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911309 | |||||||
chr18:2911331 | C | T | 3 | a0001c0001t0017g0075 a0001c0001t0017g0228 a0001c0016t0017g0259 |
3 | HG02451.hp2 HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2824+1512C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911331 | |||||||
chr18:2911569 | T | C | 4 | a0001c0001t0002g0217 a0001c0001t0002g0294 a0001c0001t0002g0307 others(1): Show |
4 | HG00642.hp1 HG01168.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.2825-1498T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911569 | |||||||
chr18:2911723 | G | T | 1 | a0002c0005t0072g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2825-1344G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2911723 | |||||||
chr18:2911889 | T | TGGTGCTG others(11): Show |
20 | a0001c0001t0001g0245 a0001c0001t0001g0348 a0001c0001t0001g0362 others(17): Show |
20 | HG00099.hp2 HG00741.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.2825-1177_2825-116 others(22): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2911889 | ||||||
chr18:2912032 | C | CT | 47 | a0001c0001t0001g0207 a0001c0001t0017g0075 a0001c0001t0034g0426 others(44): Show |
47 | HG00558.hp1 HG01109.hp1 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.2825-1011dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2912032 | ||||||
chr18:2912032 | CT | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0030 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.2825-1011delT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2912032 | ||||||
chr18:2912032 | CTT | C | 36 | a0001c0001t0001g0403 a0001c0001t0001g0415 a0001c0001t0002g0371 others(33): Show |
37 | HG00597.hp2 HG00609.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.2825-1012_2825-101 others(6): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2912032 | ||||||
chr18:2912032 | CTTT | C | 97 | a0001c0001t0003g0001 a0001c0001t0003g0100 a0001c0001t0003g0101 others(94): Show |
98 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.2825-1013_2825-101 others(7): Show |
EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2912032 | ||||||
chr18:2912044 | T | C | 1 | a0001c0001t0003g0003 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.2825-1023T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912044 | |||||||
chr18:2912205 | A | AT | 12 | a0001c0001t0009g0041 a0001c0001t0009g0045 a0001c0001t0037g0212 others(9): Show |
12 | HG01123.hp1 HG02109.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.2825-854dupT | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr18 | 2912205 | ||||||
chr18:2912284 | G | C | 1 | a0001c0003t0002g0431 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2825-783G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912284 | |||||||
chr18:2912414 | A | G | 347 | a0001c0001t0002g0081 a0001c0001t0002g0091 a0001c0001t0002g0096 others(344): Show |
350 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(347): Show |
intron_variant | MODIFIER | c.2825-653A>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912414 | |||||||
chr18:2912419 | T | C | 339 | a0001c0001t0002g0081 a0001c0001t0002g0091 a0001c0001t0002g0096 others(336): Show |
342 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(339): Show |
intron_variant | MODIFIER | c.2825-648T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912419 | |||||||
chr18:2912424 | C | T | 1 | a0001c0001t0005g0238 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2825-643C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912424 | |||||||
chr18:2912432 | G | T | 1 | a0001c0006t0005g0237 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2825-635G>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912432 | |||||||
chr18:2912453 | C | T | 1 | a0001c0001t0003g0334 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2825-614C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912453 | |||||||
chr18:2912516 | C | T | 1 | a0001c0001t0014g0213 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2825-551C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912516 | |||||||
chr18:2912593 | G | A | 3 | a0001c0001t0011g0084 a0001c0001t0011g0298 a0001c0002t0011g0087 |
3 | NA18949.hp1 NA18962.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.2825-474G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912593 | |||||||
chr18:2912666 | C | T | 1 | a0001c0002t0006g0287 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2825-401C>T | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912666 | |||||||
chr18:2912758 | C | A | 236 | a0001c0001t0002g0081 a0001c0001t0002g0091 a0001c0001t0002g0110 others(233): Show |
237 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.2825-309C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912758 | |||||||
chr18:2912760 | G | A | 1 | a0001c0001t0009g0045 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2825-307G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912760 | |||||||
chr18:2912884 | T | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0030 a0001c0001t0001g0057 others(96): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.2825-183T>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912884 | |||||||
chr18:2912885 | G | A | 2 | a0002c0025t0004g0140 a0002c0025t0004g0145 |
2 | HG00735.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2825-182G>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912885 | |||||||
chr18:2912922 | C | A | 137 | a0001c0001t0001g0245 a0001c0001t0001g0348 a0001c0001t0001g0362 others(134): Show |
138 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(135): Show |
intron_variant | MODIFIER | c.2825-145C>A | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912922 | |||||||
chr18:2912938 | C | G | 2 | a0001c0001t0014g0033 a0001c0002t0014g0243 |
2 | HG02809.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2825-129C>G | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2912938 | |||||||
chr18:2913028 | G | C | 2 | a0001c0014t0004g0006 a0001c0014t0004g0047 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2825-39G>C | EMILIN2 | ENSG00000132205.11 | transcript | ENST00000254528.4 | protein_coding | 7/7 | chr18 | 2913028 |