geneid | 57224 |
---|---|
ensemblid | ENSG00000135540.12 |
hgncid | 21021 |
symbol | NHSL1 |
name | NHS like 1 |
refseq_nuc | NM_001144060.2 |
refseq_prot | NP_001137532.1 |
ensembl_nuc | ENST00000343505.10 |
ensembl_prot | ENSP00000344672.5 |
mane_status | MANE Select |
chr | chr6 |
start | 138422043 |
end | 138499494 |
strand | - |
ver | v1.2 |
region | chr6:138422043-138499494 |
region5000 | chr6:138417043-138504494 |
regionname0 | NHSL1_chr6_138422043_138499494 |
regionname5000 | NHSL1_chr6_138417043_138504494 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1606 | 285 | 67 | 62 | 120 | 8 | 26 | 84 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0002 | 0/0 | 1606 | 11 | 0 | 0 | 11 | 0 | 0 | 10 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0003 | 0/0 | 1606 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0004 | 0/0 | 1606 | 4 | 0 | 3 | 1 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0005 | 0/0 | 1606 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0006 | 0/0 | 1606 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0007 | 0/0 | 1606 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0008 | 0/0 | 1606 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0009 | 0/0 | 1606 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0010 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0011 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0012 | 0/0 | 1606 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0013 | 0/0 | 1606 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0014 | 0/0 | 1606 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0015 | 0/0 | 1606 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0016 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0017 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0018 | 0/0 | 1606 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 4821 | 179 | 20 | 33 | 102 | 4 | 19 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0002 | 1/0 | 4821 | 37 | 2 | 16 | 11 | 2 | 5 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0003 | 0/0 | 4821 | 19 | 15 | 3 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0004 | 0/0 | 4821 | 16 | 13 | 3 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0005 | 0/0 | 4821 | 11 | 0 | 0 | 11 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0006 | 0/0 | 4821 | 8 | 8 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0007 | 0/0 | 4821 | 6 | 3 | 1 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0008 | 0/0 | 4821 | 5 | 0 | 0 | 5 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0009 | 0/0 | 4821 | 4 | 0 | 3 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0010 | 0/0 | 4821 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0011 | 0/0 | 4821 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0012 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0013 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0014 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0015 | 0/0 | 4821 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0016 | 0/0 | 4821 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0017 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0018 | 0/0 | 4821 | 2 | 0 | 0 | 0 | 0 | 2 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0019 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0020 | 0/0 | 4821 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0021 | 0/0 | 4821 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0022 | 0/0 | 4821 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0023 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0024 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0025 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0026 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0027 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0028 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0029 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0030 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0031 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0032 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0033 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0034 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0035 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0036 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0037 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0038 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0039 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0040 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0041 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
c0042 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2244 | 123 | 12 | 31 | 61 | 4 | 14 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0002 | 0/0 | 2245 | 39 | 7 | 10 | 14 | 2 | 6 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0003 | 0/0 | 2244 | 34 | 3 | 4 | 24 | 2 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0004 | 0/0 | 2241 | 14 | 6 | 7 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0005 | 0/0 | 2245 | 13 | 6 | 1 | 6 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0006 | 0/0 | 2245 | 13 | 0 | 1 | 9 | 0 | 3 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0007 | 0/0 | 2242 | 12 | 12 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0008 | 0/0 | 2242 | 10 | 7 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0009 | 0/0 | 2246 | 7 | 2 | 4 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0010 | 1/0 | 2243 | 6 | 2 | 2 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0011 | 0/0 | 2243 | 5 | 3 | 0 | 1 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0012 | 0/0 | 2246 | 4 | 3 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0013 | 0/0 | 2243 | 3 | 1 | 0 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0014 | 0/0 | 2244 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0015 | 0/0 | 2245 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0016 | 0/0 | 2243 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0017 | 0/0 | 2244 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0018 | 0/0 | 2239 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0019 | 0/0 | 2244 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0020 | 0/0 | 2254 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0021 | 0/0 | 2243 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0022 | 0/0 | 2241 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0023 | 0/0 | 2242 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0024 | 0/0 | 2242 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0025 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0026 | 0/0 | 2244 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0027 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0028 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0029 | 0/0 | 2240 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0030 | 0/0 | 2245 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0031 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0032 | 0/0 | 2243 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0033 | 0/0 | 2243 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0034 | 0/0 | 2244 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0035 | 0/0 | 2245 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0036 | 0/0 | 2246 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0037 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0038 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0039 | 0/0 | 2257 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0040 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0041 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0042 | 0/0 | 2241 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0043 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0044 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0045 | 0/0 | 2239 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0046 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0047 | 0/0 | 2243 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0048 | 0/0 | 2255 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0049 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0050 | 0/0 | 2257 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
t0051 | 0/0 | 2244 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4821 | 179 | 20 | 33 | 102 | 4 | 19 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002 | 1/0 | 4821 | 37 | 2 | 16 | 11 | 2 | 5 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0003 | 0/0 | 4821 | 19 | 15 | 3 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004 | 0/0 | 4821 | 16 | 13 | 3 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0007 | 0/0 | 4821 | 6 | 3 | 1 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0008 | 0/0 | 4821 | 5 | 0 | 0 | 5 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0010 | 0/0 | 4821 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0015 | 0/0 | 4821 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0016 | 0/0 | 4821 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0017 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0020 | 0/0 | 4821 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0021 | 0/0 | 4821 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0024 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0028 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0029 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0030 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0031 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0034 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0037 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0039 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0041 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0042 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0002c0005 | 0/0 | 4821 | 11 | 0 | 0 | 11 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0003c0006 | 0/0 | 4821 | 8 | 8 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0003c0033 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0004c0009 | 0/0 | 4821 | 4 | 0 | 3 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0005c0012 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0005c0013 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0006c0019 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0006c0038 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0007c0011 | 0/0 | 4821 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0008c0018 | 0/0 | 4821 | 2 | 0 | 0 | 0 | 0 | 2 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0009c0014 | 0/0 | 4821 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0010c0040 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0011c0023 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0012c0035 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0013c0032 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0014c0036 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0015c0027 | 0/0 | 4821 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0016c0026 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0017c0025 | 0/0 | 4821 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0018c0022 | 0/0 | 4821 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7064 | 82 | 7 | 17 | 47 | 1 | 9 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0002 | 0/0 | 7065 | 21 | 3 | 5 | 7 | 2 | 4 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0003 | 0/0 | 7064 | 30 | 2 | 4 | 22 | 1 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0004 | 0/0 | 7061 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0005 | 0/0 | 7065 | 5 | 0 | 0 | 5 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0006 | 0/0 | 7065 | 13 | 0 | 1 | 9 | 0 | 3 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0008 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0009 | 0/0 | 7066 | 4 | 1 | 2 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0010 | 0/0 | 7063 | 3 | 1 | 1 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0012 | 0/0 | 7066 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0013 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0014 | 0/0 | 7064 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0015 | 0/0 | 7065 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0018 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0019 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0024 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0027 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0029 | 0/0 | 7060 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0032 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0033 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0034 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0035 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0036 | 0/0 | 7066 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0045 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0001t0051 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0001 | 0/0 | 7064 | 20 | 2 | 6 | 5 | 2 | 5 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0002 | 0/0 | 7065 | 8 | 0 | 4 | 4 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0003 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0005 | 0/0 | 7065 | 2 | 0 | 1 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0009 | 0/0 | 7066 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0010 | 1/0 | 7063 | 2 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0023 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0002t0026 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0003t0004 | 0/0 | 7061 | 4 | 0 | 3 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0003t0007 | 0/0 | 7062 | 12 | 12 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0003t0021 | 0/0 | 7063 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0003t0040 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004t0002 | 0/0 | 7065 | 4 | 3 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004t0004 | 0/0 | 7061 | 7 | 5 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004t0009 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004t0011 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004t0028 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0004t0030 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0007t0001 | 0/0 | 7064 | 3 | 0 | 1 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0007t0011 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0007t0020 | 0/0 | 7074 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0008t0008 | 0/0 | 7062 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0008t0011 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0008t0046 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0010t0016 | 0/0 | 7063 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0015t0001 | 0/0 | 7064 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0016t0001 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0016t0003 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0017t0001 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0017t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0020t0048 | 0/0 | 7075 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0020t0049 | 0/0 | 7076 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0021t0001 | 0/0 | 7064 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0024t0004 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0028t0043 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0029t0047 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0030t0025 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0031t0041 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0034t0031 | 0/0 | 7076 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0037t0003 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0039t0018 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0041t0008 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0001c0042t0011 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0002c0005t0001 | 0/0 | 7064 | 6 | 0 | 0 | 6 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0002c0005t0002 | 0/0 | 7065 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0002c0005t0003 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0002c0005t0019 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0003c0006t0005 | 0/0 | 7065 | 5 | 5 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0003c0006t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0003c0006t0017 | 0/0 | 7064 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0003c0033t0005 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0004c0009t0001 | 0/0 | 7064 | 3 | 0 | 3 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0004c0009t0015 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0005c0012t0042 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0005c0012t0044 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0005c0013t0001 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0005c0013t0011 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0006c0019t0038 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0006c0019t0039 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0006c0038t0050 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0007c0011t0008 | 0/0 | 7062 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0008c0018t0002 | 0/0 | 7065 | 2 | 0 | 0 | 0 | 0 | 2 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0009c0014t0008 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0010c0040t0010 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0011c0023t0002 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0012c0035t0001 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0013c0032t0001 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0014c0036t0013 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0015c0027t0022 | 0/0 | 7061 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0016c0026t0037 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0017c0025t0013 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
a0018c0022t0004 | 0/0 | 7061 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | copy fasta | chr6 | 138417043 | 138504494 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0009g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0009g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0009g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0010g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0010g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0013g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0014g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0014g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0014g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0015g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0015g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0019g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0024g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0027g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0029g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0032g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0033g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0034g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0035g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0036g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0045g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0051g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0009g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0009g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0010g0233 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0010g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0023g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0026g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0004g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0021g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0021g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0040g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0011g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0012g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0028g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0030g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0020g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0020g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0008t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0008t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0008t0008g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0008t0011g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0008t0046g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0010t0016g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0010t0016g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0010t0016g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0015t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0015t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0016t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0016t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0017t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0017t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0020t0048g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0020t0049g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0021t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0021t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0024t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0028t0043g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0029t0047g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0030t0025g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0031t0041g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0034t0031g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0037t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0039t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0041t0008g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0042t0011g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0019g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0012g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0017g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0017g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0033t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0015g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0005c0012t0042g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0005c0012t0044g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0005c0013t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0005c0013t0011g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0006c0019t0038g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0006c0019t0039g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0006c0038t0050g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0007c0011t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0007c0011t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0007c0011t0008g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0008c0018t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0008c0018t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0009c0014t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0009c0014t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0010c0040t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0011c0023t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0012c0035t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0013c0032t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0014c0036t0013g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0015c0027t0022g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0016c0026t0037g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0017c0025t0013g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0018c0022t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0257 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0047 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0107 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0093 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0281 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00423 | hp1 | a0013 | c0032 | t0001 | g0195 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0135 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00438 | hp1 | a0001 | c0001 | t0013 | g0214 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00609 | hp1 | a0002 | c0005 | t0001 | g0052 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00639 | hp1 | a0001 | c0004 | t0004 | g0143 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00738 | hp1 | a0001 | c0015 | t0001 | g0325 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00741 | hp1 | a0001 | c0001 | t0009 | g0187 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00741 | hp2 | a0001 | c0002 | t0005 | g0118 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01069 | hp1 | a0001 | c0001 | t0033 | g0188 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01074 | hp2 | a0001 | c0007 | t0001 | g0310 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01081 | hp1 | a0001 | c0004 | t0002 | g0115 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0282 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0318 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01106 | hp2 | a0001 | c0004 | t0004 | g0130 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01167 | hp1 | a0001 | c0002 | t0023 | g0319 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0290 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01169 | hp2 | a0001 | c0002 | t0010 | g0320 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01192 | hp1 | a0018 | c0022 | t0004 | g0002 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0304 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01255 | hp1 | a0001 | c0002 | t0026 | g0256 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01257 | hp1 | a0001 | c0003 | t0004 | g0182 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01257 | hp2 | a0004 | c0009 | t0001 | g0070 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01258 | hp1 | a0001 | c0021 | t0001 | g0300 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01258 | hp2 | a0004 | c0009 | t0001 | g0068 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01346 | hp1 | a0001 | c0002 | t0002 | g0184 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01346 | hp2 | a0001 | c0021 | t0001 | g0297 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01361 | hp1 | a0004 | c0009 | t0001 | g0069 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01433 | hp1 | a0001 | c0003 | t0004 | g0183 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01496 | hp1 | a0001 | c0001 | t0051 | g0331 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0031 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0317 | EUR | IBS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01884 | hp1 | a0001 | c0007 | t0020 | g0148 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01884 | hp2 | a0001 | c0004 | t0012 | g0194 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01891 | hp2 | a0001 | c0004 | t0002 | g0119 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01934 | hp1 | a0001 | c0020 | t0048 | g0103 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01943 | hp1 | a0001 | c0003 | t0004 | g0105 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01978 | hp1 | a0001 | c0002 | t0009 | g0028 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01978 | hp2 | a0001 | c0002 | t0009 | g0020 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0036 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02040 | hp1 | a0001 | c0001 | t0014 | g0274 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0264 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0165 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02055 | hp2 | a0001 | c0029 | t0047 | g0324 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02056 | hp2 | a0001 | c0001 | t0015 | g0275 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0101 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02083 | hp1 | a0001 | c0001 | t0035 | g0206 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02132 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02148 | hp2 | a0001 | c0020 | t0049 | g0104 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0054 | EAS | CDX | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02257 | hp1 | a0001 | c0007 | t0020 | g0139 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02258 | hp1 | a0001 | c0001 | t0045 | g0128 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02258 | hp2 | a0001 | c0003 | t0007 | g0180 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0231 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0286 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02300 | hp1 | a0001 | c0016 | t0001 | g0062 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02572 | hp1 | a0003 | c0006 | t0017 | g0177 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02572 | hp2 | a0001 | c0017 | t0012 | g0146 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0283 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02615 | hp1 | a0016 | c0026 | t0037 | g0327 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02615 | hp2 | a0017 | c0025 | t0013 | g0174 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02622 | hp1 | a0001 | c0003 | t0007 | g0330 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02622 | hp2 | a0006 | c0019 | t0039 | g0243 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02630 | hp1 | a0001 | c0001 | t0029 | g0117 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02630 | hp2 | a0001 | c0004 | t0004 | g0131 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02647 | hp1 | a0001 | c0003 | t0007 | g0163 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02647 | hp2 | a0003 | c0006 | t0005 | g0147 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02683 | hp1 | a0008 | c0018 | t0002 | g0312 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02698 | hp1 | a0001 | c0001 | t0034 | g0168 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02698 | hp2 | a0001 | c0002 | t0001 | g0108 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02723 | hp1 | a0001 | c0003 | t0007 | g0126 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02723 | hp2 | a0001 | c0028 | t0043 | g0253 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02809 | hp1 | a0001 | c0015 | t0001 | g0127 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02809 | hp2 | a0001 | c0010 | t0016 | g0308 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02818 | hp1 | a0001 | c0031 | t0041 | g0149 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02818 | hp2 | a0001 | c0010 | t0016 | g0145 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02886 | hp1 | a0001 | c0007 | t0011 | g0278 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02886 | hp2 | a0001 | c0004 | t0011 | g0152 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02895 | hp1 | a0001 | c0004 | t0004 | g0081 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02895 | hp2 | a0005 | c0012 | t0044 | g0245 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02896 | hp1 | a0001 | c0001 | t0024 | g0250 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02896 | hp2 | a0001 | c0004 | t0004 | g0080 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02897 | hp1 | a0001 | c0001 | t0027 | g0249 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02897 | hp2 | a0005 | c0012 | t0042 | g0244 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02922 | hp1 | a0001 | c0004 | t0030 | g0241 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02965 | hp2 | a0001 | c0024 | t0004 | g0123 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02970 | hp1 | a0003 | c0006 | t0005 | g0238 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02970 | hp2 | a0005 | c0013 | t0001 | g0178 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02976 | hp1 | a0009 | c0014 | t0008 | g0175 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02976 | hp2 | a0001 | c0004 | t0004 | g0144 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03041 | hp1 | a0001 | c0039 | t0018 | g0270 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03041 | hp2 | a0011 | c0023 | t0002 | g0258 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03098 | hp1 | a0003 | c0006 | t0017 | g0151 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03130 | hp1 | a0009 | c0014 | t0008 | g0176 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03130 | hp2 | a0001 | c0003 | t0007 | g0159 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03139 | hp1 | a0001 | c0003 | t0007 | g0323 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03139 | hp2 | a0001 | c0003 | t0007 | g0254 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03195 | hp1 | a0003 | c0006 | t0005 | g0289 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03195 | hp2 | a0001 | c0003 | t0007 | g0179 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03209 | hp1 | a0001 | c0003 | t0007 | g0129 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03209 | hp2 | a0001 | c0004 | t0002 | g0326 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03453 | hp1 | a0001 | c0003 | t0021 | g0083 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03453 | hp2 | a0001 | c0003 | t0021 | g0240 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03486 | hp1 | a0001 | c0003 | t0007 | g0239 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03516 | hp1 | a0001 | c0001 | t0018 | g0141 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03516 | hp2 | a0001 | c0003 | t0007 | g0124 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0271 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0296 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03579 | hp1 | a0007 | c0011 | t0008 | g0134 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03579 | hp2 | a0006 | c0038 | t0050 | g0122 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0085 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03704 | hp2 | a0001 | c0042 | t0011 | g0116 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0298 | SAS | BEB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03831 | hp2 | a0001 | c0001 | t0006 | g0205 | SAS | BEB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03834 | hp1 | a0001 | c0034 | t0031 | g0026 | SAS | BEB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0288 | SAS | BEB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0161 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18522 | hp1 | a0001 | c0004 | t0028 | g0005 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18522 | hp2 | a0001 | c0041 | t0008 | g0137 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18612 | hp1 | a0001 | c0001 | t0014 | g0222 | EAS | CHB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | CHB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18906 | hp1 | a0003 | c0006 | t0012 | g0082 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18906 | hp2 | a0001 | c0004 | t0004 | g0171 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18942 | hp2 | a0002 | c0005 | t0001 | g0263 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18947 | hp1 | a0001 | c0008 | t0008 | g0078 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18954 | hp2 | a0001 | c0008 | t0046 | g0077 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18957 | hp2 | a0001 | c0007 | t0001 | g0162 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18960 | hp2 | a0002 | c0005 | t0001 | g0216 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18964 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18965 | hp1 | a0001 | c0008 | t0008 | g0076 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0269 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0295 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18970 | hp1 | a0002 | c0005 | t0002 | g0225 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18970 | hp2 | a0002 | c0005 | t0002 | g0055 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18971 | hp1 | a0002 | c0005 | t0003 | g0220 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18974 | hp1 | a0001 | c0001 | t0009 | g0197 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18974 | hp2 | a0002 | c0005 | t0001 | g0217 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18975 | hp1 | a0001 | c0008 | t0011 | g0212 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18978 | hp1 | a0001 | c0007 | t0001 | g0248 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18979 | hp1 | a0001 | c0001 | t0015 | g0039 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18982 | hp2 | a0001 | c0008 | t0008 | g0211 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18985 | hp1 | a0002 | c0005 | t0002 | g0219 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18985 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18994 | hp1 | a0002 | c0005 | t0001 | g0218 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18994 | hp2 | a0001 | c0001 | t0032 | g0228 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18998 | hp2 | a0001 | c0001 | t0019 | g0049 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19006 | hp1 | a0001 | c0001 | t0036 | g0053 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19006 | hp2 | a0004 | c0009 | t0015 | g0067 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19010 | hp1 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19030 | hp1 | a0001 | c0010 | t0016 | g0237 | AFR | LWK | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19030 | hp2 | a0001 | c0017 | t0001 | g0142 | AFR | LWK | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19043 | hp1 | a0001 | c0003 | t0007 | g0170 | AFR | LWK | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | LWK | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19054 | hp1 | a0002 | c0005 | t0001 | g0272 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19070 | hp1 | a0002 | c0005 | t0019 | g0210 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0230 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19081 | hp2 | a0001 | c0001 | t0010 | g0095 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19082 | hp1 | a0001 | c0001 | t0006 | g0199 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19083 | hp1 | a0001 | c0001 | t0014 | g0207 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0260 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19091 | hp2 | a0014 | c0036 | t0013 | g0277 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19240 | hp1 | a0001 | c0004 | t0002 | g0140 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19240 | hp2 | a0006 | c0019 | t0038 | g0246 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20129 | hp1 | a0010 | c0040 | t0010 | g0191 | AFR | ASW | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20129 | hp2 | a0005 | c0013 | t0011 | g0007 | AFR | ASW | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20752 | hp1 | a0015 | c0027 | t0022 | g0097 | EUR | TSI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20752 | hp2 | a0001 | c0003 | t0004 | g0181 | EUR | TSI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20805 | hp1 | a0001 | c0037 | t0003 | g0088 | EUR | TSI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20805 | hp2 | a0012 | c0035 | t0001 | g0285 | EUR | TSI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0316 | SAS | GIH | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20905 | hp2 | a0008 | c0018 | t0002 | g0313 | SAS | GIH | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02109 | hp1 | a0001 | c0004 | t0009 | g0004 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02109 | hp2 | a0003 | c0006 | t0005 | g0242 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0291 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0328 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02559 | hp2 | a0003 | c0033 | t0005 | g0236 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03471 | hp1 | a0007 | c0011 | t0008 | g0120 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03471 | hp2 | a0007 | c0011 | t0008 | g0329 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG06807 | hp1 | a0001 | c0003 | t0040 | g0173 | AFR | USA | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG06807 | hp2 | a0003 | c0006 | t0005 | g0133 | AFR | USA | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20300 | hp1 | a0001 | c0016 | t0003 | g0060 | AFR | USA | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | USA | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA21309 | hp1 | a0001 | c0030 | t0025 | g0006 | AFR | LWK | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0247 | REF | REF | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0010 | g0233 | REF | REF | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138424158
|
G | C | 2 | a0006a0016 | 4 | HG02615.hp1 HG02622.hp2 HG03579.hp2 others(1): Show |
missense_variant | MODERATE | c.4744C>G | p.Pro1582Ala | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 4948/7063 | 4744/4821 | 1582/1606 | chr6 | 138424158 | ||
chr6:138424185
|
C | G | 2 | a0003a0017 | 10 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(7): Show |
missense_variant | MODERATE | c.4717G>C | p.Ala1573Pro | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 4921/7063 | 4717/4821 | 1573/1606 | chr6 | 138424185 | ||
chr6:138430429
|
C | T | 1 | a0016 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.3916G>A | p.Asp1306Asn | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 4120/7063 | 3916/4821 | 1306/1606 | chr6 | 138430429 | ||
chr6:138430861
|
G | A | 1 | a0012 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.3484C>T | p.Arg1162Cys | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 3688/7063 | 3484/4821 | 1162/1606 | chr6 | 138430861 | ||
chr6:138430914
|
C | G | 1 | a0004 | 4 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(1): Show |
missense_variant | MODERATE | c.3431G>C | p.Ser1144Thr | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 3635/7063 | 3431/4821 | 1144/1606 | chr6 | 138430914 | ||
chr6:138431079
|
G | A | 1 | a0012 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.3266C>T | p.Ala1089Val | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 3470/7063 | 3266/4821 | 1089/1606 | chr6 | 138431079 | ||
chr6:138431104
|
C | T | 1 | a0014 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.3241G>A | p.Val1081Met | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 3445/7063 | 3241/4821 | 1081/1606 | chr6 | 138431104 | ||
chr6:138431238
|
G | A | 1 | a0011 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.3107C>T | p.Pro1036Leu | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 3311/7063 | 3107/4821 | 1036/1606 | chr6 | 138431238 | ||
chr6:138432064
|
C | T | 1 | a0013 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.2281G>A | p.Gly761Arg | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2485/7063 | 2281/4821 | 761/1606 | chr6 | 138432064 | ||
chr6:138432084
|
G | C | 1 | a0008 | 2 | HG02683.hp1 NA20905.hp2 |
missense_variant | MODERATE | c.2261C>G | p.Pro754Arg | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2465/7063 | 2261/4821 | 754/1606 | chr6 | 138432084 | ||
chr6:138432145
|
G | A | 1 | a0014 | 1 | NA19091.hp2 | missense_variant | MODERATE | c.2200C>T | p.Pro734Ser | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2404/7063 | 2200/4821 | 734/1606 | chr6 | 138432145 | ||
chr6:138432919
|
C | T | 1 | a0015 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1426G>A | p.Ala476Thr | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1630/7063 | 1426/4821 | 476/1606 | chr6 | 138432919 | ||
chr6:138433086
|
G | A | 1 | a0010 | 1 | NA20129.hp1 | missense_variant | MODERATE | c.1259C>T | p.Ser420Phe | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1463/7063 | 1259/4821 | 420/1606 | chr6 | 138433086 | ||
chr6:138433175
|
G | T | 1 | a0016 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1170C>A | p.Phe390Leu | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1374/7063 | 1170/4821 | 390/1606 | chr6 | 138433175 | ||
chr6:138433444
|
T | C | 2 | a0007a0009 | 5 | HG02976.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
missense_variant | MODERATE | c.901A>G | p.Met301Val | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1105/7063 | 901/4821 | 301/1606 | chr6 | 138433444 | ||
chr6:138433578
|
C | T | 1 | a0002 | 11 | HG00609.hp1 NA18942.hp2 NA18960.hp2 others(8): Show |
missense_variant | MODERATE | c.767G>A | p.Arg256His | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 971/7063 | 767/4821 | 256/1606 | chr6 | 138433578 | ||
chr6:138447163
|
A | C | 3 | a0005a0009a0017 | 7 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
missense_variant | MODERATE | c.370T>G | p.Phe124Val | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/8 | 574/7063 | 370/4821 | 124/1606 | chr6 | 138447163 | ||
chr6:138499244
|
A | G | 1 | a0018 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.47T>C | p.Phe16Ser | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/8 | 251/7063 | 47/4821 | 16/1606 | chr6 | 138499244 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138424162
|
G | A | 8 | a0001c0003a0001c0004a0001c0008others(5): Show | 48 | HG00639.hp1 HG01081.hp1 HG01106.hp2 others(45): Show |
synonymous_variant | LOW | c.4740C>T | p.Pro1580Pro | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 4944/7063 | 4740/4821 | 1580/1606 | chr6 | 138424162 | ||
chr6:138424420
|
G | C | 1 | a0001c0017 | 2 | HG02572.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.4482C>G | p.Gly1494Gly | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 4686/7063 | 4482/4821 | 1494/1606 | chr6 | 138424420 | ||
chr6:138424759
|
A | G | 2 | a0001c0016a0001c0037 | 3 | HG02300.hp1 NA20300.hp1 NA20805.hp1 |
synonymous_variant | LOW | c.4143T>C | p.His1381His | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 4347/7063 | 4143/4821 | 1381/1606 | chr6 | 138424759 | ||
chr6:138424771
|
G | A | 2 | a0001c0020a0001c0034 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
synonymous_variant | LOW | c.4131C>T | p.His1377His | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 4335/7063 | 4131/4821 | 1377/1606 | chr6 | 138424771 | ||
chr6:138429818
|
G | A | 1 | a0001c0028 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.3978C>T | p.Ala1326Ala | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/8 | 4182/7063 | 3978/4821 | 1326/1606 | chr6 | 138429818 | ||
chr6:138430526
|
G | A | 1 | a0001c0031 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.3819C>T | p.Pro1273Pro | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 4023/7063 | 3819/4821 | 1273/1606 | chr6 | 138430526 | ||
chr6:138431105
|
G | A | 1 | a0001c0010 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.3240C>T | p.Pro1080Pro | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 3444/7063 | 3240/4821 | 1080/1606 | chr6 | 138431105 | ||
chr6:138431135
|
C | T | 1 | a0001c0008 | 5 | NA18947.hp1 NA18954.hp2 NA18965.hp1 others(2): Show |
synonymous_variant | LOW | c.3210G>A | p.Thr1070Thr | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 3414/7063 | 3210/4821 | 1070/1606 | chr6 | 138431135 | ||
chr6:138432050
|
C | T | 4 | a0001c0015a0001c0024a0001c0028others(1): Show | 6 | HG00738.hp1 HG02723.hp2 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.2295G>A | p.Ser765Ser | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2499/7063 | 2295/4821 | 765/1606 | chr6 | 138432050 | ||
chr6:138432200
|
C | T | 20 | a0001c0001a0001c0004a0001c0016others(17): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
synonymous_variant | LOW | c.2145G>A | p.Lys715Lys | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2349/7063 | 2145/4821 | 715/1606 | chr6 | 138432200 | ||
chr6:138432242
|
G | A | 1 | a0006c0038 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.2103C>T | p.Ile701Ile | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2307/7063 | 2103/4821 | 701/1606 | chr6 | 138432242 | ||
chr6:138432413
|
A | G | 3 | a0001c0030a0001c0031a0001c0042 | 3 | HG02818.hp1 HG03704.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.1932T>C | p.Ala644Ala | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2136/7063 | 1932/4821 | 644/1606 | chr6 | 138432413 | ||
chr6:138432425
|
A | G | 1 | a0001c0029 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.1920T>C | p.Phe640Phe | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 2124/7063 | 1920/4821 | 640/1606 | chr6 | 138432425 | ||
chr6:138432596
|
G | A | 1 | a0001c0039 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.1749C>T | p.Ser583Ser | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1953/7063 | 1749/4821 | 583/1606 | chr6 | 138432596 | ||
chr6:138432794
|
C | T | 4 | a0001c0015a0001c0024a0001c0028others(1): Show | 6 | HG00738.hp1 HG02723.hp2 HG02809.hp1 others(3): Show |
synonymous_variant | LOW | c.1551G>A | p.Pro517Pro | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1755/7063 | 1551/4821 | 517/1606 | chr6 | 138432794 | ||
chr6:138432944
|
G | A | 1 | a0001c0021 | 2 | HG01258.hp1 HG01346.hp2 |
synonymous_variant | LOW | c.1401C>T | p.Pro467Pro | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1605/7063 | 1401/4821 | 467/1606 | chr6 | 138432944 | ||
chr6:138433186
|
A | G | 38 | a0001c0001a0001c0003a0001c0004others(35): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(286): Show |
synonymous_variant | LOW | c.1159T>C | p.Leu387Leu | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1363/7063 | 1159/4821 | 387/1606 | chr6 | 138433186 | ||
chr6:138433415
|
G | A | 2 | a0003c0006a0017c0025 | 9 | HG02109.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
synonymous_variant | LOW | c.930C>T | p.Ile310Ile | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1134/7063 | 930/4821 | 310/1606 | chr6 | 138433415 | ||
chr6:138433532
|
G | A | 1 | a0001c0042 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.813C>T | p.Val271Val | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/8 | 1017/7063 | 813/4821 | 271/1606 | chr6 | 138433532 | ||
chr6:138473342
|
A | G | 1 | a0001c0008 | 5 | NA18947.hp1 NA18954.hp2 NA18965.hp1 others(2): Show |
synonymous_variant | LOW | c.303T>C | p.Asp101Asp | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/8 | 507/7063 | 303/4821 | 101/1606 | chr6 | 138473342 | ||
chr6:138473417
|
C | T | 1 | a0001c0024 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.228G>A | p.Arg76Arg | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/8 | 432/7063 | 228/4821 | 76/1606 | chr6 | 138473417 | ||
chr6:138496319
|
C | T | 1 | a0011c0023 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.111G>A | p.Pro37Pro | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/8 | 315/7063 | 111/4821 | 37/1606 | chr6 | 138496319 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138422055
|
T | C | 2 | a0005c0012t0042a0005c0012t0044 | 2 | HG02895.hp2 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2026A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 2026 | chr6 | 138422055 | |||||
chr6:138422070
|
G | C | 36 | a0001c0001t0004a0001c0001t0008a0001c0001t0024others(33): Show | 65 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*2011C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 2011 | chr6 | 138422070 | |||||
chr6:138422088
|
A | G | 2 | a0001c0001t0034a0001c0002t0026 | 2 | HG01255.hp1 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1993T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1993 | chr6 | 138422088 | |||||
chr6:138422125
|
T | C | 1 | a0001c0010t0016 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1956A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1956 | chr6 | 138422125 | |||||
chr6:138422424
|
C | T | 1 | a0001c0001t0035 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1657G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1657 | chr6 | 138422424 | |||||
chr6:138422521
|
C | T | 5 | a0001c0007t0020a0001c0028t0043a0005c0012t0042others(2): Show | 6 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1560G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1560 | chr6 | 138422521 | |||||
chr6:138422573
|
T | G | 1 | a0001c0001t0014 | 3 | HG02040.hp1 NA18612.hp1 NA19083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1508A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1508 | chr6 | 138422573 | |||||
chr6:138422677
|
G | C | 1 | a0001c0003t0040 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1404C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1404 | chr6 | 138422677 | |||||
chr6:138422778
|
T | C | 6 | a0001c0001t0019a0001c0010t0016a0001c0020t0048others(3): Show | 8 | HG01934.hp1 HG02148.hp2 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1303A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1303 | chr6 | 138422778 | |||||
chr6:138422898
|
A | G | 1 | a0001c0010t0016 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1183T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 1183 | chr6 | 138422898 | |||||
chr6:138423094
|
T | TA | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(56): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*986dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 986 | chr6 | 138423094 | |||||
chr6:138423094
|
T | TAA | 12 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(9): Show | 23 | HG00408.hp1 HG00741.hp2 HG01884.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*985_*986dupTT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 986 | chr6 | 138423094 | |||||
chr6:138423094
|
TAA | T | 5 | a0001c0007t0020a0001c0020t0048a0001c0020t0049others(2): Show | 6 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*985_*986delTT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 985 | chr6 | 138423094 | |||||
chr6:138423116
|
C | A | 1 | a0001c0004t0030 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*965G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 965 | chr6 | 138423116 | |||||
chr6:138423276
|
C | G | 1 | a0001c0001t0035 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*805G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 805 | chr6 | 138423276 | |||||
chr6:138423505
|
C | T | 1 | a0001c0007t0020 | 2 | HG01884.hp1 HG02257.hp1 |
3_prime_UTR_variant | MODIFIER | c.*576G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 576 | chr6 | 138423505 | |||||
chr6:138423566
|
G | A | 3 | a0001c0020t0048a0001c0020t0049a0001c0034t0031 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*515C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 515 | chr6 | 138423566 | |||||
chr6:138423723
|
T | G | 1 | a0001c0029t0047 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*358A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 358 | chr6 | 138423723 | |||||
chr6:138423815
|
C | CA | 16 | a0001c0001t0002a0001c0001t0006a0001c0001t0012others(13): Show | 61 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*265dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 265 | chr6 | 138423815 | |||||
chr6:138423815
|
C | CAA | 3 | a0001c0001t0009a0001c0002t0009a0001c0004t0009 | 7 | HG00741.hp1 HG01243.hp2 HG01978.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*264_*265dupTT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 265 | chr6 | 138423815 | |||||
chr6:138423815
|
C | CAAAAAAA others(5): Show |
1 | a0006c0019t0038 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*254_*265dupTTTTTT others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 265 | chr6 | 138423815 | |||||
chr6:138423815
|
C | CAAAAAAA others(6): Show |
3 | a0001c0007t0020a0006c0019t0039a0006c0038t0050 | 4 | HG01884.hp1 HG02257.hp1 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*253_*265dupTTTTTT others(7): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 265 | chr6 | 138423815 | |||||
chr6:138423815
|
C | CAAAAAAA others(7): Show |
1 | a0001c0020t0048 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*252_*265dupTTTTTT others(8): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 265 | chr6 | 138423815 | |||||
chr6:138423815
|
C | CAAAAAAA others(8): Show |
2 | a0001c0020t0049a0001c0034t0031 | 2 | HG02148.hp2 HG03834.hp1 |
3_prime_UTR_variant | MODIFIER | c.*251_*265dupTTTTTT others(9): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 265 | chr6 | 138423815 | |||||
chr6:138423815
|
CA | C | 14 | a0001c0001t0013a0001c0001t0024a0001c0001t0032others(11): Show | 26 | HG00438.hp1 HG01167.hp1 HG02258.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*265delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 265 | chr6 | 138423815 | |||||
chr6:138423815
|
CAA | C | 12 | a0001c0001t0004a0001c0001t0008a0001c0003t0004others(9): Show | 26 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*264_*265delTT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 264 | chr6 | 138423815 | |||||
chr6:138423840
|
T | A | 3 | a0006c0019t0038a0006c0019t0039a0006c0038t0050 | 3 | HG02622.hp2 HG03579.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*241A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 241 | chr6 | 138423840 | |||||
chr6:138423924
|
C | G | 4 | a0001c0007t0020a0006c0019t0038a0006c0019t0039others(1): Show | 5 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*157G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 157 | chr6 | 138423924 | |||||
chr6:138423955
|
G | A | 13 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(10): Show | 55 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*126C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 126 | chr6 | 138423955 | |||||
chr6:138424041
|
G | A | 33 | a0001c0001t0004a0001c0001t0008a0001c0001t0045others(30): Show | 62 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*40C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 8/8 | 40 | chr6 | 138424041 | |||||
chr6:138499355
|
G | A | 1 | a0001c0001t0051 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-65C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/8 | 65 | chr6 | 138499355 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138424997
|
C | T | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4086-181G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138424997 | ||||||
chr6:138425017
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.4086-201G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425017 | ||||||
chr6:138425021
|
G | GGAGTCC | 4 | a0001c0007t0011g0278a0001c0030t0025g0006a0001c0031t0041g0149others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.4086-206_4086-205i others(8): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425021 | ||||||
chr6:138425040
|
G | A | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.4086-224C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425040 | ||||||
chr6:138425194
|
G | C | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.4086-378C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425194 | ||||||
chr6:138425232
|
C | T | 5 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0020t0048g0103others(2): Show | 5 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.4086-416G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425232 | ||||||
chr6:138425248
|
T | C | 57 | a0001c0001t0008g0328a0001c0003t0004g0105a0001c0003t0004g0181others(54): Show | 57 | HG00738.hp1 HG01192.hp1 HG01257.hp1 others(54): Show |
intron_variant | MODIFIER | c.4086-432A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425248 | ||||||
chr6:138425249
|
G | A | 38 | a0001c0001t0008g0328a0001c0003t0004g0105a0001c0003t0004g0181others(35): Show | 38 | HG00738.hp1 HG01192.hp1 HG01257.hp1 others(35): Show |
intron_variant | MODIFIER | c.4086-433C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425249 | ||||||
chr6:138425269
|
G | T | 1 | a0001c0004t0002g0115 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4086-453C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425269 | ||||||
chr6:138425372
|
T | C | 5 | a0001c0001t0001g0234a0001c0002t0002g0031a0001c0002t0002g0232others(2): Show | 5 | HG01255.hp2 HG01496.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.4086-556A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425372 | ||||||
chr6:138425432
|
C | T | 1 | a0016c0026t0037g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4086-616G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425432 | ||||||
chr6:138425555
|
C | CTG | 9 | a0001c0007t0011g0278a0001c0007t0020g0139a0001c0007t0020g0148others(6): Show | 9 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(6): Show |
intron_variant | MODIFIER | c.4086-740_4086-739i others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425555 | ||||||
chr6:138425563
|
T | C | 5 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0020t0048g0103others(2): Show | 5 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.4086-747A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425563 | ||||||
chr6:138425596
|
G | A | 2 | a0001c0001t0006g0059a0001c0001t0036g0053 | 2 | NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.4086-780C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425596 | ||||||
chr6:138425633
|
G | A | 1 | a0003c0006t0017g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4086-817C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425633 | ||||||
chr6:138425660
|
T | C | 1 | a0001c0001t0002g0196 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.4086-844A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425660 | ||||||
chr6:138425670
|
T | C | 4 | a0001c0007t0011g0278a0001c0030t0025g0006a0001c0031t0041g0149others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.4086-854A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425670 | ||||||
chr6:138425753
|
C | T | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.4086-937G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425753 | ||||||
chr6:138425781
|
G | A | 57 | a0001c0001t0008g0328a0001c0003t0004g0105a0001c0003t0004g0181others(54): Show | 57 | HG00738.hp1 HG01192.hp1 HG01257.hp1 others(54): Show |
intron_variant | MODIFIER | c.4086-965C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425781 | ||||||
chr6:138425995
|
T | A | 1 | a0001c0001t0012g0161 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4086-1179A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138425995 | ||||||
chr6:138426212
|
G | C | 2 | a0001c0001t0008g0328a0005c0013t0011g0007 | 2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4086-1396C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426212 | ||||||
chr6:138426230
|
A | G | 3 | a0001c0001t0001g0284a0001c0001t0001g0293a0001c0001t0009g0304 | 3 | HG00642.hp2 HG01074.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.4086-1414T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426230 | ||||||
chr6:138426350
|
A | C | 5 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0020t0048g0103others(2): Show | 5 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.4086-1534T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426350 | ||||||
chr6:138426420
|
G | T | 1 | a0001c0002t0001g0101 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4086-1604C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426420 | ||||||
chr6:138426481
|
C | A | 57 | a0001c0001t0008g0328a0001c0003t0004g0105a0001c0003t0004g0181others(54): Show | 57 | HG00738.hp1 HG01192.hp1 HG01257.hp1 others(54): Show |
intron_variant | MODIFIER | c.4086-1665G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426481 | ||||||
chr6:138426523
|
T | A | 5 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0020t0048g0103others(2): Show | 5 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.4086-1707A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426523 | ||||||
chr6:138426854
|
C | T | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.4086-2038G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426854 | ||||||
chr6:138426942
|
G | A | 3 | a0001c0001t0001g0208a0001c0001t0001g0221a0013c0032t0001g0195 | 3 | HG00423.hp1 NA18969.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.4086-2126C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426942 | ||||||
chr6:138426952
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4086-2136C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138426952 | ||||||
chr6:138427078
|
C | A | 1 | a0001c0001t0001g0322 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.4086-2262G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427078 | ||||||
chr6:138427141
|
G | A | 1 | a0011c0023t0002g0258 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4086-2325C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427141 | ||||||
chr6:138427198
|
G | A | 4 | a0001c0007t0011g0278a0001c0030t0025g0006a0001c0031t0041g0149others(1): Show | 4 | HG02818.hp1 HG02886.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.4086-2382C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427198 | ||||||
chr6:138427273
|
G | C | 253 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(250): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.4085+2438C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427273 | ||||||
chr6:138427297
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4085+2414C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427297 | ||||||
chr6:138427312
|
C | T | 35 | a0001c0001t0008g0328a0001c0003t0004g0105a0001c0003t0004g0181others(32): Show | 35 | HG01192.hp1 HG01257.hp1 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.4085+2399G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427312 | ||||||
chr6:138427395
|
G | A | 1 | a0001c0003t0007g0129 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4085+2316C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427395 | ||||||
chr6:138427775
|
A | C | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4085+1936T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427775 | ||||||
chr6:138427843
|
T | C | 1 | a0001c0004t0002g0115 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4085+1868A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427843 | ||||||
chr6:138427879
|
C | T | 2 | a0005c0012t0042g0244a0005c0012t0044g0245 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4085+1832G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427879 | ||||||
chr6:138427883
|
A | G | 1 | a0001c0001t0001g0038 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.4085+1828T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427883 | ||||||
chr6:138427970
|
G | A | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4085+1741C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138427970 | ||||||
chr6:138428004
|
C | T | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4085+1707G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428004 | ||||||
chr6:138428005
|
G | A | 4 | a0001c0001t0001g0016a0001c0001t0001g0200a0001c0001t0001g0273others(1): Show | 4 | HG00673.hp2 HG02004.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.4085+1706C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428005 | ||||||
chr6:138428032
|
C | T | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.4085+1679G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428032 | ||||||
chr6:138428056
|
G | T | 1 | a0001c0004t0011g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4085+1655C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428056 | ||||||
chr6:138428073
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4085+1638C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428073 | ||||||
chr6:138428077
|
C | A | 5 | a0001c0001t0003g0011a0001c0007t0011g0278a0001c0030t0025g0006others(2): Show | 5 | HG02818.hp1 HG02886.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.4085+1634G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428077 | ||||||
chr6:138428134
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4085+1577A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428134 | ||||||
chr6:138428175
|
G | A | 3 | a0006c0019t0038g0246a0006c0019t0039g0243a0006c0038t0050g0122 | 3 | HG02622.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4085+1536C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428175 | ||||||
chr6:138428247
|
A | C | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.4085+1464T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428247 | ||||||
chr6:138428310
|
G | A | 3 | a0006c0019t0038g0246a0006c0019t0039g0243a0006c0038t0050g0122 | 3 | HG02622.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4085+1401C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428310 | ||||||
chr6:138428360
|
G | A | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4085+1351C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428360 | ||||||
chr6:138428400
|
T | C | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4085+1311A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428400 | ||||||
chr6:138428438
|
C | A | 1 | a0001c0004t0002g0326 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4085+1273G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428438 | ||||||
chr6:138428457
|
T | C | 3 | a0001c0028t0043g0253a0005c0012t0042g0244a0005c0012t0044g0245 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.4085+1254A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428457 | ||||||
chr6:138428557
|
G | A | 34 | a0001c0001t0008g0328a0001c0003t0004g0105a0001c0003t0004g0181others(31): Show | 34 | HG01192.hp1 HG01257.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.4085+1154C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428557 | ||||||
chr6:138428717
|
G | C | 1 | a0007c0011t0008g0329 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4085+994C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428717 | ||||||
chr6:138428851
|
T | G | 3 | a0001c0001t0014g0207a0001c0001t0014g0222a0001c0001t0014g0274 | 3 | HG02040.hp1 NA18612.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.4085+860A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428851 | ||||||
chr6:138428864
|
C | G | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4085+847G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138428864 | ||||||
chr6:138429180
|
G | A | 15 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0010t0016g0145others(12): Show | 15 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.4085+531C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429180 | ||||||
chr6:138429209
|
G | A | 1 | a0001c0017t0012g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4085+502C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429209 | ||||||
chr6:138429260
|
T | C | 19 | a0001c0007t0011g0278a0001c0007t0020g0139a0001c0007t0020g0148others(16): Show | 19 | HG01884.hp1 HG01934.hp1 HG02148.hp2 others(16): Show |
intron_variant | MODIFIER | c.4085+451A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429260 | ||||||
chr6:138429374
|
C | T | 2 | a0001c0016t0001g0062a0001c0016t0003g0060 | 2 | HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4085+337G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429374 | ||||||
chr6:138429417
|
A | G | 12 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0010t0016g0145others(9): Show | 12 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.4085+294T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429417 | ||||||
chr6:138429466
|
C | T | 3 | a0001c0020t0048g0103a0001c0020t0049g0104a0001c0034t0031g0026 | 3 | HG01934.hp1 HG02148.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.4085+245G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429466 | ||||||
chr6:138429476
|
C | T | 2 | a0001c0001t0006g0059a0001c0001t0036g0053 | 2 | NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.4085+235G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429476 | ||||||
chr6:138429572
|
A | C | 12 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0010t0016g0145others(9): Show | 12 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.4085+139T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 7/7 | chr6 | 138429572 | ||||||
chr6:138429905
|
A | G | 1 | a0001c0007t0001g0310 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3953-62T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/7 | chr6 | 138429905 | ||||||
chr6:138429966
|
G | A | 1 | a0001c0001t0002g0303 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.3953-123C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/7 | chr6 | 138429966 | ||||||
chr6:138430022
|
G | A | 1 | a0001c0003t0040g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3953-179C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/7 | chr6 | 138430022 | ||||||
chr6:138430126
|
T | C | 3 | a0001c0007t0020g0139a0001c0007t0020g0148a0016c0026t0037g0327 | 3 | HG01884.hp1 HG02257.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.3952+267A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/7 | chr6 | 138430126 | ||||||
chr6:138430157
|
A | T | 12 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0010t0016g0145others(9): Show | 12 | HG01884.hp1 HG02257.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.3952+236T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/7 | chr6 | 138430157 | ||||||
chr6:138430243
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3952+150A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 6/7 | chr6 | 138430243 | ||||||
chr6:138433766
|
T | A | 8 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0010t0016g0145others(5): Show | 8 | HG02809.hp2 HG02818.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.665-86A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138433766 | ||||||
chr6:138433959
|
C | T | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-279G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138433959 | ||||||
chr6:138434030
|
G | A | 3 | a0001c0028t0043g0253a0005c0012t0042g0244a0005c0012t0044g0245 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665-350C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434030 | ||||||
chr6:138434047
|
G | A | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-367C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434047 | ||||||
chr6:138434087
|
T | C | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-407A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434087 | ||||||
chr6:138434325
|
T | C | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-645A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434325 | ||||||
chr6:138434386
|
A | G | 1 | a0001c0001t0002g0316 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.665-706T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434386 | ||||||
chr6:138434435
|
A | G | 3 | a0001c0030t0025g0006a0001c0031t0041g0149a0001c0042t0011g0116 | 3 | HG02818.hp1 HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.665-755T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434435 | ||||||
chr6:138434472
|
C | T | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.665-792G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434472 | ||||||
chr6:138434473
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.665-793C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434473 | ||||||
chr6:138434740
|
T | C | 6 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123others(3): Show | 6 | HG00738.hp1 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-1060A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434740 | ||||||
chr6:138434758
|
T | A | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-1078A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434758 | ||||||
chr6:138434770
|
A | G | 3 | a0001c0030t0025g0006a0001c0031t0041g0149a0001c0042t0011g0116 | 3 | HG02818.hp1 HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.665-1090T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434770 | ||||||
chr6:138434901
|
A | T | 3 | a0001c0001t0003g0001a0001c0001t0003g0154a0001c0001t0003g0213 | 4 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(1): Show |
intron_variant | MODIFIER | c.665-1221T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434901 | ||||||
chr6:138434971
|
A | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-1291T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138434971 | ||||||
chr6:138435173
|
T | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-1493A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435173 | ||||||
chr6:138435438
|
T | TA | 9 | a0001c0001t0001g0155a0001c0007t0001g0248a0001c0007t0011g0278others(6): Show | 9 | HG00738.hp1 HG02723.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.665-1759dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435438 | ||||||
chr6:138435477
|
G | C | 262 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.665-1797C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435477 | ||||||
chr6:138435656
|
A | T | 57 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(54): Show | 57 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.665-1976T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435656 | ||||||
chr6:138435689
|
A | C | 6 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123others(3): Show | 6 | HG00738.hp1 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-2009T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435689 | ||||||
chr6:138435710
|
G | GT | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-2031_665-2030i others(3): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435710 | ||||||
chr6:138435711
|
G | T | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-2031C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435711 | ||||||
chr6:138435712
|
G | T | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-2032C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435712 | ||||||
chr6:138435713
|
T | G | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.665-2033A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435713 | ||||||
chr6:138435717
|
T | A | 2 | a0001c0001t0001g0066a0001c0007t0001g0162 | 2 | HG00544.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.665-2037A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435717 | ||||||
chr6:138435811
|
A | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-2131T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435811 | ||||||
chr6:138435931
|
A | G | 2 | a0001c0020t0048g0103a0001c0020t0049g0104 | 2 | HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.665-2251T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435931 | ||||||
chr6:138435956
|
C | A | 6 | a0001c0028t0043g0253a0005c0012t0042g0244a0005c0012t0044g0245others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-2276G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435956 | ||||||
chr6:138436007
|
T | C | 2 | a0001c0001t0008g0328a0005c0013t0011g0007 | 2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.665-2327A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138436007 | ||||||
chr6:138436202
|
G | A | 3 | a0001c0030t0025g0006a0001c0031t0041g0149a0001c0042t0011g0116 | 3 | HG02818.hp1 HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.665-2522C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138436202 | ||||||
chr6:138436317
|
C | T | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-2637G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138436317 | ||||||
chr6:138436532
|
T | C | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-2852A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138436532 | ||||||
chr6:138436666
|
T | C | 2 | a0001c0001t0001g0299a0001c0001t0002g0009 | 2 | HG03654.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.665-2986A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138436666 | ||||||
chr6:138436744
|
G | T | 1 | a0001c0001t0003g0204 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.665-3064C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138436744 | ||||||
chr6:138436931
|
C | T | 1 | a0001c0015t0001g0325 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.665-3251G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138436931 | ||||||
chr6:138437025
|
A | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-3345T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437025 | ||||||
chr6:138437089
|
T | A | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-3409A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437089 | ||||||
chr6:138437143
|
A | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-3463T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437143 | ||||||
chr6:138437234
|
A | G | 3 | a0006c0019t0038g0246a0006c0019t0039g0243a0006c0038t0050g0122 | 3 | HG02622.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.665-3554T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437234 | ||||||
chr6:138437235
|
T | C | 1 | a0001c0001t0002g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.665-3555A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437235 | ||||||
chr6:138437296
|
G | GTA | 6 | a0001c0002t0001g0189a0001c0002t0009g0020a0001c0002t0009g0028others(3): Show | 6 | HG01934.hp1 HG01978.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-3618_665-3617d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437296 | ||||||
chr6:138437296
|
G | GTGTA | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-3617_665-3616i others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437296 | ||||||
chr6:138437296
|
GTA | G | 7 | a0001c0001t0002g0158a0001c0004t0002g0326a0001c0030t0025g0006others(4): Show | 7 | HG02280.hp1 HG02572.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.665-3618_665-3617d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437296 | ||||||
chr6:138437296
|
GTATA | G | 3 | a0001c0001t0001g0023a0001c0001t0002g0094a0017c0025t0013g0174 | 3 | HG01993.hp1 HG01993.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.665-3620_665-3617d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437296 | ||||||
chr6:138437309
|
T | TATATATA others(29): Show |
1 | a0001c0002t0001g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.665-3665_665-3630d others(38): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437309 | ||||||
chr6:138437315
|
T | C | 227 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(224): Show | 228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.665-3635A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437315 | ||||||
chr6:138437317
|
T | C | 234 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.665-3637A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437317 | ||||||
chr6:138437319
|
T | C | 237 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(234): Show | 238 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(235): Show |
intron_variant | MODIFIER | c.665-3639A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437319 | ||||||
chr6:138437321
|
C | T | 5 | a0001c0028t0043g0253a0006c0019t0038g0246a0006c0019t0039g0243others(2): Show | 5 | HG02615.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-3641G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437321 | ||||||
chr6:138437323
|
C | T | 1 | a0006c0019t0039g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.665-3643G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437323 | ||||||
chr6:138437325
|
C | CACACATA others(23): Show |
1 | a0001c0041t0008g0137 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.665-3675_665-3646d others(32): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437325 | ||||||
chr6:138437325
|
CACACATA others(23): Show |
C | 1 | a0001c0002t0001g0101 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.665-3675_665-3646d others(32): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437325 | ||||||
chr6:138437327
|
C | T | 221 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(218): Show | 222 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(219): Show |
intron_variant | MODIFIER | c.665-3647G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437327 | ||||||
chr6:138437329
|
C | CAT | 21 | a0001c0003t0004g0105a0001c0003t0004g0181a0001c0003t0004g0182others(18): Show | 21 | HG01257.hp1 HG01433.hp1 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.665-3651_665-3650d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437329 | ||||||
chr6:138437329
|
C | T | 241 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(238): Show | 242 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.665-3649G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437329 | ||||||
chr6:138437329
|
CATATATA others(49): Show |
C | 1 | a0001c0010t0016g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665-3705_665-3650d others(58): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437329 | ||||||
chr6:138437331
|
T | C | 5 | a0001c0010t0016g0145a0001c0010t0016g0308a0001c0020t0048g0103others(2): Show | 5 | HG01934.hp1 HG02148.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-3651A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437331 | ||||||
chr6:138437333
|
T | C | 2 | a0001c0010t0016g0145a0001c0010t0016g0308 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665-3653A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437333 | ||||||
chr6:138437333
|
TATATATA others(19): Show |
T | 3 | a0006c0019t0038g0246a0006c0038t0050g0122a0016c0026t0037g0327 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.665-3679_665-3654d others(28): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437333 | ||||||
chr6:138437335
|
T | C | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.665-3655A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437335 | ||||||
chr6:138437335
|
TATATATA others(17): Show |
T | 3 | a0001c0028t0043g0253a0005c0012t0042g0244a0005c0012t0044g0245 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665-3679_665-3656d others(26): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437335 | ||||||
chr6:138437337
|
T | C | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.665-3657A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437337 | ||||||
chr6:138437339
|
T | C | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.665-3659A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437339 | ||||||
chr6:138437341
|
T | C | 229 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(226): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.665-3661A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437341 | ||||||
chr6:138437341
|
TACACATA others(57): Show |
T | 2 | a0001c0010t0016g0145a0001c0010t0016g0308 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665-3725_665-3662d others(66): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437341 | ||||||
chr6:138437343
|
C | T | 2 | a0001c0007t0011g0278a0001c0029t0047g0324 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.665-3663G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437343 | ||||||
chr6:138437345
|
C | CACATATA others(103): Show |
2 | a0001c0020t0048g0103a0001c0020t0049g0104 | 2 | HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.665-3666_665-3665i others(112): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437345 | ||||||
chr6:138437345
|
C | CAT | 7 | a0001c0001t0001g0023a0001c0001t0001g0042a0001c0001t0002g0094others(4): Show | 7 | HG01993.hp1 HG01993.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.665-3667_665-3666d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437345 | ||||||
chr6:138437345
|
C | T | 228 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(225): Show | 229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.665-3665G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437345 | ||||||
chr6:138437347
|
T | C | 2 | a0001c0007t0011g0278a0001c0029t0047g0324 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.665-3667A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437347 | ||||||
chr6:138437357
|
C | T | 2 | a0001c0007t0011g0278a0001c0029t0047g0324 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.665-3677G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437357 | ||||||
chr6:138437361
|
T | C | 2 | a0001c0007t0011g0278a0001c0029t0047g0324 | 2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.665-3681A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437361 | ||||||
chr6:138437361
|
TATATATA others(7): Show |
T | 1 | a0006c0019t0039g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.665-3695_665-3682d others(16): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437361 | ||||||
chr6:138437363
|
T | C | 2 | a0001c0004t0002g0326a0003c0006t0017g0177 | 2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.665-3683A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437363 | ||||||
chr6:138437365
|
T | C | 2 | a0001c0004t0002g0326a0003c0006t0017g0177 | 2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.665-3685A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437365 | ||||||
chr6:138437365
|
T | TATATACA others(1): Show |
6 | a0001c0004t0004g0080a0001c0004t0004g0081a0001c0004t0004g0143others(3): Show | 6 | HG00639.hp1 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.665-3686_665-3685i others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437365 | ||||||
chr6:138437365
|
T | TATATATA others(3): Show |
157 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(154): Show | 157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.665-3695_665-3686d others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437365 | ||||||
chr6:138437369
|
T | C | 3 | a0001c0028t0043g0253a0005c0012t0042g0244a0005c0012t0044g0245 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665-3689A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437369 | ||||||
chr6:138437369
|
TATACACA others(33): Show |
T | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.665-3729_665-3690d others(42): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437369 | ||||||
chr6:138437371
|
T | C | 3 | a0001c0028t0043g0253a0005c0012t0042g0244a0005c0012t0044g0245 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665-3691A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437371 | ||||||
chr6:138437373
|
CACATATA others(23): Show |
C | 3 | a0001c0030t0025g0006a0001c0031t0041g0149a0001c0042t0011g0116 | 3 | HG02818.hp1 HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.665-3723_665-3694d others(32): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437373 | ||||||
chr6:138437375
|
C | T | 3 | a0001c0028t0043g0253a0005c0012t0042g0244a0005c0012t0044g0245 | 3 | HG02723.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.665-3695G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437375 | ||||||
chr6:138437377
|
T | TATATACA others(1): Show |
72 | a0001c0001t0001g0029a0001c0001t0001g0087a0001c0001t0001g0234others(69): Show | 73 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.665-3698_665-3697i others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437377 | ||||||
chr6:138437377
|
T | TATATATA others(19): Show |
7 | a0001c0003t0007g0129a0001c0003t0007g0159a0001c0003t0007g0163others(4): Show | 7 | HG02622.hp1 HG02647.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.665-3698_665-3697i others(28): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437377 | ||||||
chr6:138437381
|
TATATACA others(1): Show |
T | 3 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123 | 3 | HG00738.hp1 HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.665-3709_665-3702d others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437381 | ||||||
chr6:138437385
|
T | C | 1 | a0006c0019t0039g0243 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.665-3705A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437385 | ||||||
chr6:138437385
|
T | TAC | 3 | a0006c0019t0038g0246a0006c0038t0050g0122a0016c0026t0037g0327 | 3 | HG02615.hp1 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.665-3707_665-3706d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437385 | ||||||
chr6:138437387
|
C | T | 79 | a0001c0001t0001g0029a0001c0001t0001g0087a0001c0001t0001g0234others(76): Show | 80 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.665-3707G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437387 | ||||||
chr6:138437389
|
CAT | C | 17 | a0001c0003t0004g0105a0001c0003t0004g0181a0001c0003t0004g0183others(14): Show | 17 | HG01192.hp1 HG01433.hp1 HG01943.hp1 others(14): Show |
intron_variant | MODIFIER | c.665-3711_665-3710d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437389 | ||||||
chr6:138437391
|
T | C | 82 | a0001c0001t0001g0029a0001c0001t0001g0087a0001c0001t0001g0234others(79): Show | 83 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.665-3711A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437391 | ||||||
chr6:138437391
|
T | TATATATA others(21): Show |
2 | a0001c0003t0007g0124a0001c0003t0007g0239 | 2 | HG03486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.665-3712_665-3711i others(30): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437391 | ||||||
chr6:138437393
|
T | C | 3 | a0001c0001t0001g0156a0001c0001t0001g0251a0001c0001t0001g0252 | 3 | HG02922.hp2 HG02965.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.665-3713A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437393 | ||||||
chr6:138437399
|
T | C | 1 | a0001c0010t0016g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665-3719A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437399 | ||||||
chr6:138437401
|
T | C | 1 | a0001c0029t0047g0324 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.665-3721A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437401 | ||||||
chr6:138437403
|
T | C | 2 | a0001c0003t0004g0182a0001c0007t0011g0278 | 2 | HG01257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.665-3723A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437403 | ||||||
chr6:138437405
|
C | T | 2 | a0001c0010t0016g0237a0001c0029t0047g0324 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.665-3725G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437405 | ||||||
chr6:138437407
|
C | T | 1 | a0001c0029t0047g0324 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.665-3727G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437407 | ||||||
chr6:138437409
|
C | T | 5 | a0001c0003t0004g0182a0001c0007t0011g0278a0001c0010t0016g0145others(2): Show | 5 | HG01257.hp1 HG02055.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-3729G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437409 | ||||||
chr6:138437413
|
T | C | 4 | a0001c0001t0002g0094a0001c0003t0004g0182a0001c0003t0021g0083others(1): Show | 4 | HG01257.hp1 HG01993.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-3733A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437413 | ||||||
chr6:138437413
|
TAC | T | 28 | a0001c0001t0001g0032a0001c0001t0001g0037a0001c0001t0001g0056others(25): Show | 28 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(25): Show |
intron_variant | MODIFIER | c.665-3735_665-3734d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437413 | ||||||
chr6:138437421
|
C | T | 3 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0029t0047g0324 | 3 | HG01884.hp1 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.665-3741G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437421 | ||||||
chr6:138437423
|
C | T | 3 | a0001c0007t0020g0139a0001c0007t0020g0148a0001c0029t0047g0324 | 3 | HG01884.hp1 HG02055.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.665-3743G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437423 | ||||||
chr6:138437438
|
AC | A | 15 | a0001c0001t0001g0014a0001c0001t0001g0294a0001c0001t0001g0306others(12): Show | 15 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.665-3759delG | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437438 | ||||||
chr6:138437439
|
C | A | 4 | a0001c0001t0003g0048a0001c0001t0006g0265a0001c0001t0036g0053others(1): Show | 4 | HG02257.hp2 HG02559.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-3759G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437439 | ||||||
chr6:138437440
|
AC | A | 75 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0044others(72): Show | 75 | HG00408.hp1 HG00438.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.665-3761delG | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437440 | ||||||
chr6:138437440
|
ACAC | A | 12 | a0001c0001t0001g0012a0001c0001t0001g0084a0001c0001t0001g0215others(9): Show | 12 | HG01993.hp2 HG02258.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.665-3763_665-3761d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437440 | ||||||
chr6:138437441
|
C | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0294others(24): Show | 27 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.665-3761G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437441 | ||||||
chr6:138437441
|
C | CA | 3 | a0001c0001t0003g0204a0001c0001t0024g0250a0001c0001t0027g0249 | 3 | HG02896.hp1 HG02897.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.665-3762dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437441 | ||||||
chr6:138437442
|
AC | A | 55 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0016others(52): Show | 55 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.665-3763delG | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437442 | ||||||
chr6:138437443
|
C | A | 116 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0029others(113): Show | 117 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.665-3763G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437443 | ||||||
chr6:138437443
|
C | CA | 4 | a0001c0001t0001g0089a0001c0001t0001g0096a0001c0001t0001g0102others(1): Show | 4 | HG00408.hp2 HG02083.hp2 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.665-3764dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437443 | ||||||
chr6:138437444
|
AC | A | 19 | a0001c0001t0001g0030a0001c0001t0001g0072a0001c0001t0001g0086others(16): Show | 19 | HG00639.hp1 HG00733.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.665-3765delG | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437444 | ||||||
chr6:138437445
|
C | A | 220 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(217): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.665-3765G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437445 | ||||||
chr6:138437445
|
CA | C | 7 | a0001c0001t0001g0121a0001c0003t0007g0126a0001c0003t0007g0179others(4): Show | 7 | HG02258.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.665-3766delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437445 | ||||||
chr6:138437445
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.665-3775_665-3766d others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437445 | ||||||
chr6:138437445
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0010t0016g0145a0001c0010t0016g0308 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665-3777_665-3766d others(14): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437445 | ||||||
chr6:138437445
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0010t0016g0237 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.665-3780_665-3766d others(17): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437445 | ||||||
chr6:138437447
|
A | C | 30 | a0001c0002t0001g0024a0001c0002t0001g0100a0001c0002t0001g0291others(27): Show | 30 | HG00423.hp2 HG01192.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.665-3767T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437447 | ||||||
chr6:138437448
|
A | C | 5 | a0001c0003t0007g0126a0001c0003t0007g0179a0001c0003t0007g0180others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-3768T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437448 | ||||||
chr6:138437449
|
A | C | 19 | a0001c0003t0004g0182a0001c0003t0007g0124a0001c0003t0007g0129others(16): Show | 19 | HG01257.hp1 HG01934.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.665-3769T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437449 | ||||||
chr6:138437450
|
A | C | 5 | a0001c0003t0007g0126a0001c0003t0007g0179a0001c0003t0007g0180others(2): Show | 5 | HG02258.hp2 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.665-3770T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437450 | ||||||
chr6:138437451
|
A | C | 6 | a0001c0003t0007g0124a0001c0003t0007g0129a0001c0003t0007g0159others(3): Show | 6 | HG03130.hp2 HG03139.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.665-3771T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437451 | ||||||
chr6:138437452
|
A | C | 1 | a0001c0028t0043g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.665-3772T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437452 | ||||||
chr6:138437453
|
A | C | 1 | a0001c0003t0007g0323 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.665-3773T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437453 | ||||||
chr6:138437459
|
A | C | 2 | a0001c0010t0016g0145a0001c0010t0016g0308 | 2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.665-3779T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437459 | ||||||
chr6:138437680
|
A | G | 3 | a0001c0030t0025g0006a0001c0031t0041g0149a0001c0042t0011g0116 | 3 | HG02818.hp1 HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.665-4000T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437680 | ||||||
chr6:138437703
|
T | G | 1 | a0016c0026t0037g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.665-4023A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437703 | ||||||
chr6:138437889
|
T | C | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.664+4094A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437889 | ||||||
chr6:138437940
|
A | G | 1 | a0001c0016t0001g0062 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.664+4043T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437940 | ||||||
chr6:138438295
|
C | A | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.664+3688G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138438295 | ||||||
chr6:138438328
|
C | T | 2 | a0001c0020t0048g0103a0001c0020t0049g0104 | 2 | HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.664+3655G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138438328 | ||||||
chr6:138438416
|
T | C | 1 | a0001c0002t0001g0092 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.664+3567A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138438416 | ||||||
chr6:138438477
|
T | C | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.664+3506A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138438477 | ||||||
chr6:138438529
|
A | G | 3 | a0004c0009t0001g0068a0004c0009t0001g0069a0004c0009t0001g0070 | 3 | HG01257.hp2 HG01258.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.664+3454T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138438529 | ||||||
chr6:138438612
|
G | A | 1 | a0001c0003t0040g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.664+3371C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138438612 | ||||||
chr6:138439233
|
G | A | 1 | a0016c0026t0037g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.664+2750C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439233 | ||||||
chr6:138439240
|
A | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.664+2743T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439240 | ||||||
chr6:138439275
|
C | A | 4 | a0001c0001t0001g0156a0001c0001t0001g0251a0001c0001t0001g0252others(1): Show | 4 | HG01891.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+2708G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439275 | ||||||
chr6:138439459
|
C | T | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.664+2524G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439459 | ||||||
chr6:138439498
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.664+2485T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439498 | ||||||
chr6:138439537
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.664+2446A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439537 | ||||||
chr6:138439679
|
C | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.664+2304G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439679 | ||||||
chr6:138439749
|
C | G | 1 | a0006c0038t0050g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.664+2234G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439749 | ||||||
chr6:138439751
|
GTCTCGTG others(868): Show |
G | 1 | a0006c0038t0050g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.664+1357_664+2231d others(2): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439751 | ||||||
chr6:138439815
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.664+2168T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439815 | ||||||
chr6:138439853
|
G | A | 4 | a0001c0002t0001g0109a0001c0002t0002g0110a0001c0002t0002g0111others(1): Show | 4 | NA18959.hp2 NA18971.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.664+2130C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439853 | ||||||
chr6:138439878
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.664+2105C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138439878 | ||||||
chr6:138440123
|
G | T | 2 | a0001c0001t0002g0158a0001c0008t0008g0076 | 2 | HG02280.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.664+1860C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440123 | ||||||
chr6:138440154
|
G | C | 1 | a0001c0001t0003g0079 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.664+1829C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440154 | ||||||
chr6:138440418
|
T | C | 1 | a0016c0026t0037g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.664+1565A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440418 | ||||||
chr6:138440490
|
T | C | 5 | a0001c0004t0002g0115a0001c0004t0002g0140a0001c0004t0009g0004others(2): Show | 5 | HG01081.hp1 HG02109.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.664+1493A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440490 | ||||||
chr6:138440563
|
C | T | 16 | a0001c0003t0004g0105a0001c0003t0004g0181a0001c0003t0004g0182others(13): Show | 16 | HG01192.hp1 HG01257.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.664+1420G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440563 | ||||||
chr6:138440593
|
T | C | 2 | a0001c0002t0001g0092a0001c0002t0001g0283 | 2 | HG01261.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.664+1390A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440593 | ||||||
chr6:138440823
|
T | A | 1 | a0001c0001t0002g0094 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.664+1160A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440823 | ||||||
chr6:138440877
|
G | C | 46 | a0001c0003t0004g0105a0001c0003t0004g0181a0001c0003t0004g0182others(43): Show | 46 | HG00738.hp1 HG01192.hp1 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.664+1106C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440877 | ||||||
chr6:138440883
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.664+1100G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138440883 | ||||||
chr6:138441096
|
T | C | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.664+887A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138441096 | ||||||
chr6:138441154
|
C | T | 2 | a0001c0001t0001g0202a0001c0001t0010g0271 | 2 | HG03098.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.664+829G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138441154 | ||||||
chr6:138441453
|
G | T | 1 | a0001c0021t0001g0297 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.664+530C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138441453 | ||||||
chr6:138441460
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.664+523A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138441460 | ||||||
chr6:138441486
|
T | A | 1 | a0001c0001t0001g0305 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.664+497A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138441486 | ||||||
chr6:138441625
|
A | G | 1 | a0001c0001t0006g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.664+358T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138441625 | ||||||
chr6:138441879
|
C | T | 1 | a0001c0041t0008g0137 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.664+104G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138441879 | ||||||
chr6:138442169
|
C | A | 1 | a0001c0001t0015g0039 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.533-55G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442169 | ||||||
chr6:138442269
|
A | G | 3 | a0001c0010t0016g0145a0001c0010t0016g0237a0001c0010t0016g0308 | 3 | HG02809.hp2 HG02818.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.533-155T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442269 | ||||||
chr6:138442413
|
A | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0063a0001c0001t0005g0034 | 3 | NA18981.hp1 NA18990.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.533-299T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442413 | ||||||
chr6:138442591
|
C | T | 3 | a0001c0004t0004g0080a0001c0004t0004g0081a0001c0004t0004g0130 | 3 | HG01106.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.533-477G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442591 | ||||||
chr6:138442628
|
A | T | 1 | a0001c0029t0047g0324 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.533-514T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442628 | ||||||
chr6:138442633
|
G | A | 3 | a0001c0003t0007g0170a0001c0030t0025g0006a0001c0042t0011g0116 | 3 | HG03704.hp2 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.533-519C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442633 | ||||||
chr6:138442844
|
T | C | 6 | a0001c0003t0007g0170a0001c0003t0007g0330a0001c0007t0011g0278others(3): Show | 6 | HG02622.hp1 HG02818.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-730A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442844 | ||||||
chr6:138442952
|
C | T | 74 | a0001c0001t0004g0186a0001c0001t0018g0141a0001c0001t0029g0117others(71): Show | 74 | HG00639.hp1 HG00735.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.533-838G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138442952 | ||||||
chr6:138443020
|
TACATATA others(7): Show |
T | 1 | a0001c0001t0002g0315 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.533-920_533-907del others(14): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443020 | ||||||
chr6:138443023
|
A | T | 1 | a0001c0001t0002g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.533-909T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443023 | ||||||
chr6:138443036
|
C | CAT | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0150others(6): Show | 9 | HG00544.hp1 HG00621.hp2 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.533-924_533-923dup others(2): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443036 | ||||||
chr6:138443052
|
TAC | T | 24 | a0001c0001t0004g0186a0001c0001t0018g0141a0001c0001t0029g0117others(21): Show | 24 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.533-940_533-939del others(2): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443052 | ||||||
chr6:138443062
|
C | CAT | 12 | a0001c0003t0007g0170a0001c0003t0007g0330a0001c0007t0011g0278others(9): Show | 12 | HG01934.hp1 HG02148.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.533-950_533-949dup others(2): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443062 | ||||||
chr6:138443062
|
CAT | C | 4 | a0001c0015t0001g0127a0001c0028t0043g0253a0005c0012t0042g0244others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-950_533-949del others(2): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443062 | ||||||
chr6:138443074
|
T | C | 3 | a0001c0001t0002g0094a0001c0001t0009g0187a0001c0001t0009g0304 | 3 | HG00741.hp1 HG01243.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.533-960A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443074 | ||||||
chr6:138443150
|
CAT | C | 8 | a0001c0001t0004g0186a0001c0004t0004g0080a0001c0004t0004g0081others(5): Show | 8 | HG00639.hp1 HG00735.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.533-1038_533-1037d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443150 | ||||||
chr6:138443327
|
G | A | 3 | a0006c0019t0038g0246a0006c0019t0039g0243a0006c0038t0050g0122 | 3 | HG02622.hp2 HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.533-1213C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443327 | ||||||
chr6:138443345
|
A | G | 4 | a0001c0001t0018g0141a0001c0001t0029g0117a0001c0017t0012g0146others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-1231T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443345 | ||||||
chr6:138443348
|
T | C | 2 | a0001c0001t0001g0287a0001c0001t0010g0290 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.533-1234A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443348 | ||||||
chr6:138443399
|
T | G | 6 | a0001c0015t0001g0127a0001c0015t0001g0325a0001c0024t0004g0123others(3): Show | 6 | HG00738.hp1 HG02723.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-1285A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443399 | ||||||
chr6:138443745
|
G | C | 1 | a0001c0007t0011g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.533-1631C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443745 | ||||||
chr6:138443747
|
T | G | 1 | a0001c0007t0011g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.533-1633A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443747 | ||||||
chr6:138443753
|
C | G | 1 | a0017c0025t0013g0174 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.533-1639G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443753 | ||||||
chr6:138443778
|
C | T | 6 | a0001c0001t0001g0125a0001c0024t0004g0123a0001c0028t0043g0253others(3): Show | 6 | HG02723.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.533-1664G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443778 | ||||||
chr6:138443786
|
C | T | 2 | a0001c0021t0001g0297a0001c0021t0001g0300 | 2 | HG01258.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.533-1672G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443786 | ||||||
chr6:138443796
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.533-1682A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443796 | ||||||
chr6:138443832
|
AAAAATAA others(3): Show |
A | 1 | a0001c0015t0001g0127 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.533-1728_533-1719d others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443832 | ||||||
chr6:138443899
|
A | G | 2 | a0001c0007t0020g0139a0001c0007t0020g0148 | 2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.533-1785T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138443899 | ||||||
chr6:138444017
|
T | C | 5 | a0001c0003t0007g0170a0001c0003t0007g0330a0001c0030t0025g0006others(2): Show | 5 | HG02622.hp1 HG02818.hp1 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.533-1903A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444017 | ||||||
chr6:138444131
|
C | G | 28 | a0001c0001t0001g0125a0001c0001t0024g0250a0001c0001t0027g0249others(25): Show | 28 | HG01934.hp1 HG02109.hp2 HG02148.hp2 others(25): Show |
intron_variant | MODIFIER | c.533-2017G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444131 | ||||||
chr6:138444483
|
C | T | 7 | a0001c0001t0001g0066a0001c0001t0001g0268a0001c0001t0005g0269others(4): Show | 7 | HG00544.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.533-2369G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444483 | ||||||
chr6:138444519
|
A | G | 2 | a0001c0001t0004g0186a0001c0001t0006g0282 | 2 | HG00735.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.533-2405T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444519 | ||||||
chr6:138444524
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0009g0197 | 2 | NA18974.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.533-2410C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444524 | ||||||
chr6:138444536
|
C | G | 3 | a0001c0003t0007g0129a0001c0007t0011g0278a0001c0007t0020g0148 | 3 | HG01884.hp1 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.533-2422G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444536 | ||||||
chr6:138444537
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.533-2423G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444537 | ||||||
chr6:138444574
|
G | A | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.532+2427C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444574 | ||||||
chr6:138444577
|
A | AT | 10 | a0001c0001t0001g0037a0001c0001t0001g0066a0001c0001t0001g0268others(7): Show | 10 | HG00544.hp2 HG00741.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.532+2423dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444577 | ||||||
chr6:138444577
|
AT | A | 49 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(46): Show | 49 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(46): Show |
intron_variant | MODIFIER | c.532+2423delA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444577 | ||||||
chr6:138444693
|
T | C | 6 | a0001c0001t0029g0117a0001c0004t0011g0152a0001c0010t0016g0145others(3): Show | 6 | HG02572.hp2 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+2308A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444693 | ||||||
chr6:138444702
|
T | C | 1 | a0001c0001t0003g0259 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.532+2299A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444702 | ||||||
chr6:138444884
|
C | T | 154 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(151): Show | 155 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.532+2117G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444884 | ||||||
chr6:138444930
|
A | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 22 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.532+2071T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444930 | ||||||
chr6:138444937
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.532+2064C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138444937 | ||||||
chr6:138445010
|
C | A | 1 | a0001c0003t0004g0183 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.532+1991G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445010 | ||||||
chr6:138445110
|
A | G | 69 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(66): Show | 70 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.532+1891T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445110 | ||||||
chr6:138445220
|
T | C | 1 | a0001c0001t0001g0014 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.532+1781A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445220 | ||||||
chr6:138445230
|
C | T | 1 | a0001c0001t0002g0316 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.532+1771G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445230 | ||||||
chr6:138445243
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0003g0280 | 2 | HG02165.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.532+1758A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445243 | ||||||
chr6:138445246
|
T | C | 1 | a0011c0023t0002g0258 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.532+1755A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445246 | ||||||
chr6:138445261
|
T | C | 22 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(19): Show | 22 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(19): Show |
intron_variant | MODIFIER | c.532+1740A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445261 | ||||||
chr6:138445289
|
A | G | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.532+1712T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445289 | ||||||
chr6:138445309
|
C | A | 1 | a0001c0003t0007g0124 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.532+1692G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445309 | ||||||
chr6:138445437
|
C | A | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.532+1564G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445437 | ||||||
chr6:138445484
|
AG | A | 13 | a0001c0001t0001g0156a0001c0001t0001g0251a0001c0001t0001g0252others(10): Show | 13 | HG01081.hp1 HG01106.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.532+1516delC | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445484 | ||||||
chr6:138445510
|
T | G | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.532+1491A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445510 | ||||||
chr6:138445627
|
C | A | 12 | a0001c0002t0001g0172a0001c0002t0001g0317a0001c0002t0002g0318others(9): Show | 12 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.532+1374G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445627 | ||||||
chr6:138445663
|
TG | T | 4 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0015t0001g0127others(1): Show | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+1337delC | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445663 | ||||||
chr6:138445708
|
T | C | 1 | a0001c0001t0036g0053 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.532+1293A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445708 | ||||||
chr6:138445736
|
C | T | 1 | a0001c0007t0020g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.532+1265G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445736 | ||||||
chr6:138445873
|
C | T | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.532+1128G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445873 | ||||||
chr6:138445875
|
A | G | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.532+1126T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445875 | ||||||
chr6:138445949
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.532+1052C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445949 | ||||||
chr6:138445956
|
TTGCACTT others(2): Show |
T | 4 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0015t0001g0127others(1): Show | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.532+1036_532+1044d others(11): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138445956 | ||||||
chr6:138446033
|
A | AT | 39 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(36): Show | 39 | HG00438.hp2 HG00639.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.532+967dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138446033 | ||||||
chr6:138446033
|
ATTT | A | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.532+965_532+967del others(3): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138446033 | ||||||
chr6:138446044
|
T | A | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.532+957A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138446044 | ||||||
chr6:138446061
|
T | C | 64 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(61): Show | 65 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.532+940A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138446061 | ||||||
chr6:138446131
|
G | A | 3 | a0001c0001t0002g0051a0001c0001t0006g0059a0001c0001t0036g0053 | 3 | HG00621.hp2 NA19006.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.532+870C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138446131 | ||||||
chr6:138446159
|
T | C | 1 | a0001c0028t0043g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.532+842A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138446159 | ||||||
chr6:138447271
|
A | T | 128 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(125): Show | 129 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.340-78T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447271 | ||||||
chr6:138447482
|
G | A | 1 | a0001c0001t0019g0049 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.340-289C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447482 | ||||||
chr6:138447484
|
T | C | 2 | a0001c0008t0008g0211a0001c0008t0011g0212 | 2 | NA18975.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.340-291A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447484 | ||||||
chr6:138447523
|
C | T | 22 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0003t0007g0124others(19): Show | 22 | HG01081.hp1 HG01106.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-330G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447523 | ||||||
chr6:138447784
|
A | T | 14 | a0001c0001t0002g0136a0001c0001t0009g0165a0001c0001t0018g0141others(11): Show | 14 | HG00140.hp1 HG01099.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.340-591T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447784 | ||||||
chr6:138447881
|
G | A | 1 | a0001c0001t0001g0294 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.340-688C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447881 | ||||||
chr6:138447939
|
T | C | 67 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(64): Show | 68 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.340-746A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447939 | ||||||
chr6:138447961
|
G | A | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-768C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138447961 | ||||||
chr6:138448249
|
T | C | 5 | a0001c0001t0001g0032a0001c0001t0003g0231a0001c0001t0005g0295others(2): Show | 5 | HG01496.hp2 HG01934.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-1056A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448249 | ||||||
chr6:138448354
|
T | C | 5 | a0001c0001t0001g0156a0001c0001t0024g0250a0001c0001t0027g0249others(2): Show | 5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-1161A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448354 | ||||||
chr6:138448389
|
A | C | 1 | a0001c0001t0001g0305 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.340-1196T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448389 | ||||||
chr6:138448391
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.340-1198G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448391 | ||||||
chr6:138448484
|
C | T | 2 | a0001c0001t0018g0141a0001c0004t0002g0140 | 2 | HG03516.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.340-1291G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448484 | ||||||
chr6:138448505
|
C | T | 2 | a0001c0001t0001g0215a0001c0001t0001g0302 | 2 | NA19086.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.340-1312G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448505 | ||||||
chr6:138448527
|
C | G | 19 | a0001c0001t0029g0117a0001c0003t0007g0330a0001c0004t0002g0119others(16): Show | 19 | HG00639.hp1 HG01891.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.340-1334G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448527 | ||||||
chr6:138448549
|
T | C | 69 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(66): Show | 70 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.340-1356A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448549 | ||||||
chr6:138448664
|
G | T | 16 | a0001c0001t0029g0117a0001c0004t0004g0080a0001c0004t0004g0081others(13): Show | 16 | HG00639.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.340-1471C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448664 | ||||||
chr6:138448666
|
T | C | 22 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(19): Show | 22 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-1473A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448666 | ||||||
chr6:138448709
|
A | C | 22 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(19): Show | 22 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-1516T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448709 | ||||||
chr6:138448843
|
G | A | 2 | a0001c0003t0007g0179a0001c0003t0007g0180 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.340-1650C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448843 | ||||||
chr6:138448850
|
T | C | 329 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(326): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.340-1657A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138448850 | ||||||
chr6:138449000
|
C | T | 2 | a0001c0015t0001g0127a0001c0024t0004g0123 | 2 | HG02809.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.340-1807G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449000 | ||||||
chr6:138449014
|
T | C | 1 | a0001c0001t0001g0155 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.340-1821A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449014 | ||||||
chr6:138449017
|
G | A | 1 | a0001c0001t0003g0262 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.340-1824C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449017 | ||||||
chr6:138449052
|
CA | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(59): Show | 62 | HG00639.hp1 HG01081.hp1 HG01106.hp2 others(59): Show |
intron_variant | MODIFIER | c.340-1860delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449052 | ||||||
chr6:138449052
|
CAA | C | 26 | a0001c0001t0002g0158a0001c0001t0003g0022a0001c0001t0006g0205others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-1861_340-1860d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449052 | ||||||
chr6:138449052
|
CAAA | C | 58 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(55): Show | 59 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.340-1862_340-1860d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449052 | ||||||
chr6:138449138
|
C | G | 63 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(60): Show | 64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.340-1945G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449138 | ||||||
chr6:138449162
|
G | A | 90 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(87): Show | 91 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.340-1969C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449162 | ||||||
chr6:138449222
|
T | C | 22 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(19): Show | 22 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-2029A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449222 | ||||||
chr6:138449240
|
A | T | 1 | a0001c0001t0002g0201 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.340-2047T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449240 | ||||||
chr6:138449403
|
G | A | 12 | a0001c0002t0001g0172a0001c0002t0001g0317a0001c0002t0002g0318others(9): Show | 12 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-2210C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449403 | ||||||
chr6:138449419
|
G | A | 2 | a0001c0001t0001g0153a0001c0001t0035g0206 | 2 | HG02083.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.340-2226C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449419 | ||||||
chr6:138449448
|
G | A | 7 | a0005c0012t0042g0244a0005c0012t0044g0245a0005c0013t0001g0178others(4): Show | 7 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-2255C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449448 | ||||||
chr6:138449468
|
A | C | 2 | a0001c0001t0003g0058a0001c0001t0006g0065 | 2 | HG00438.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.340-2275T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449468 | ||||||
chr6:138449469
|
C | G | 27 | a0001c0001t0001g0156a0001c0001t0001g0251a0001c0001t0001g0252others(24): Show | 27 | HG01081.hp1 HG01106.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.340-2276G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449469 | ||||||
chr6:138449469
|
C | T | 2 | a0001c0001t0003g0058a0001c0001t0006g0065 | 2 | HG00438.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.340-2276G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449469 | ||||||
chr6:138449503
|
C | T | 5 | a0001c0001t0001g0156a0001c0001t0024g0250a0001c0001t0027g0249others(2): Show | 5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-2310G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449503 | ||||||
chr6:138449537
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.340-2344G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449537 | ||||||
chr6:138449538
|
G | A | 3 | a0001c0003t0007g0330a0001c0004t0002g0119a0001c0007t0011g0278 | 3 | HG01891.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.340-2345C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449538 | ||||||
chr6:138449555
|
T | C | 22 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(19): Show | 22 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-2362A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449555 | ||||||
chr6:138449602
|
G | T | 1 | a0001c0001t0006g0264 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.340-2409C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449602 | ||||||
chr6:138449675
|
C | CA | 27 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(24): Show | 27 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.340-2483dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449675 | ||||||
chr6:138449690
|
A | T | 5 | a0001c0001t0001g0156a0001c0001t0024g0250a0001c0001t0027g0249others(2): Show | 5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-2497T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449690 | ||||||
chr6:138449764
|
C | CT | 5 | a0001c0001t0001g0156a0001c0001t0024g0250a0001c0001t0027g0249others(2): Show | 5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-2572dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449764 | ||||||
chr6:138449769
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.340-2576A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449769 | ||||||
chr6:138449782
|
G | A | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.340-2589C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449782 | ||||||
chr6:138449791
|
CAAT | C | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 23 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.340-2601_340-2599d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449791 | ||||||
chr6:138449924
|
T | C | 3 | a0001c0003t0007g0330a0001c0004t0002g0119a0001c0007t0011g0278 | 3 | HG01891.hp2 HG02622.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.340-2731A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449924 | ||||||
chr6:138450013
|
T | C | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-2820A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450013 | ||||||
chr6:138450104
|
T | G | 5 | a0001c0001t0001g0156a0001c0001t0024g0250a0001c0001t0027g0249others(2): Show | 5 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.340-2911A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450104 | ||||||
chr6:138450130
|
C | A | 2 | a0001c0003t0007g0179a0001c0003t0007g0180 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.340-2937G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450130 | ||||||
chr6:138450192
|
G | GCACA | 24 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(21): Show | 24 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.340-3003_340-3000d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450192 | ||||||
chr6:138450221
|
A | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.340-3028T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450221 | ||||||
chr6:138450222
|
T | C | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-3029A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450222 | ||||||
chr6:138450332
|
A | G | 3 | a0001c0001t0002g0158a0001c0003t0007g0159a0001c0003t0007g0163 | 3 | HG02280.hp1 HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.340-3139T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450332 | ||||||
chr6:138450482
|
G | A | 16 | a0001c0001t0029g0117a0001c0004t0004g0080a0001c0004t0004g0081others(13): Show | 16 | HG00639.hp1 HG02572.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.340-3289C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450482 | ||||||
chr6:138450631
|
C | T | 22 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(19): Show | 22 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-3438G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450631 | ||||||
chr6:138450658
|
C | A | 3 | a0001c0001t0001g0309a0001c0001t0001g0311a0001c0007t0001g0310 | 3 | HG01074.hp2 HG01168.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.340-3465G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450658 | ||||||
chr6:138450704
|
A | C | 1 | a0001c0004t0004g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.340-3511T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450704 | ||||||
chr6:138450815
|
A | G | 25 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(22): Show | 25 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.340-3622T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450815 | ||||||
chr6:138450828
|
C | G | 1 | a0001c0004t0002g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.340-3635G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450828 | ||||||
chr6:138450836
|
C | T | 80 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(77): Show | 80 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.340-3643G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450836 | ||||||
chr6:138450870
|
A | G | 22 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(19): Show | 22 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.340-3677T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450870 | ||||||
chr6:138450874
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0293 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.340-3681G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450874 | ||||||
chr6:138450879
|
A | G | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-3686T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450879 | ||||||
chr6:138450904
|
G | A | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340-3711C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450904 | ||||||
chr6:138450932
|
G | T | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340-3739C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450932 | ||||||
chr6:138450984
|
T | C | 18 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(15): Show | 18 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.340-3791A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138450984 | ||||||
chr6:138451008
|
A | G | 1 | a0001c0001t0003g0204 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.340-3815T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451008 | ||||||
chr6:138451032
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.340-3839G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451032 | ||||||
chr6:138451038
|
A | G | 148 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(145): Show | 149 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.340-3845T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451038 | ||||||
chr6:138451111
|
C | A | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340-3918G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451111 | ||||||
chr6:138451307
|
A | G | 13 | a0001c0003t0007g0239a0001c0003t0007g0330a0001c0003t0021g0240others(10): Show | 13 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.340-4114T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451307 | ||||||
chr6:138451359
|
A | G | 87 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(84): Show | 87 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.340-4166T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451359 | ||||||
chr6:138451422
|
T | C | 1 | a0001c0001t0002g0094 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.340-4229A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451422 | ||||||
chr6:138451540
|
T | C | 12 | a0001c0002t0001g0172a0001c0002t0001g0317a0001c0002t0002g0318others(9): Show | 12 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.340-4347A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451540 | ||||||
chr6:138451763
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.340-4570G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451763 | ||||||
chr6:138451870
|
T | G | 9 | a0001c0003t0007g0124a0001c0003t0007g0129a0001c0004t0002g0115others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-4677A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451870 | ||||||
chr6:138451934
|
G | C | 86 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(83): Show | 86 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.340-4741C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138451934 | ||||||
chr6:138452062
|
C | G | 1 | a0001c0024t0004g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.340-4869G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452062 | ||||||
chr6:138452268
|
T | C | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-5075A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452268 | ||||||
chr6:138452281
|
C | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.340-5088G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452281 | ||||||
chr6:138452354
|
T | C | 2 | a0001c0003t0007g0179a0001c0003t0007g0180 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.340-5161A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452354 | ||||||
chr6:138452455
|
TTTTGA | T | 10 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0007t0020g0139others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.340-5267_340-5263d others(7): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452455 | ||||||
chr6:138452599
|
T | C | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-5406A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452599 | ||||||
chr6:138452606
|
A | G | 2 | a0001c0003t0007g0179a0001c0003t0007g0180 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.340-5413T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452606 | ||||||
chr6:138452663
|
C | A | 2 | a0001c0001t0010g0271a0001c0039t0018g0270 | 2 | HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.340-5470G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452663 | ||||||
chr6:138452721
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.340-5528C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452721 | ||||||
chr6:138452723
|
G | A | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-5530C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452723 | ||||||
chr6:138452732
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.340-5539G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452732 | ||||||
chr6:138452733
|
G | A | 1 | a0001c0004t0002g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.340-5540C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452733 | ||||||
chr6:138452820
|
C | CT | 66 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(63): Show | 67 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.340-5628dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452820 | ||||||
chr6:138452820
|
C | CTTT | 82 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(79): Show | 82 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(79): Show |
intron_variant | MODIFIER | c.340-5630_340-5628d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452820 | ||||||
chr6:138452839
|
G | A | 1 | a0001c0024t0004g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.340-5646C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452839 | ||||||
chr6:138452982
|
T | G | 1 | a0006c0038t0050g0122 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.340-5789A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452982 | ||||||
chr6:138453009
|
C | T | 3 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0002g0010 | 3 | HG00544.hp2 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.340-5816G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453009 | ||||||
chr6:138453064
|
TC | T | 3 | a0001c0001t0001g0215a0001c0001t0001g0301a0001c0001t0001g0302 | 3 | NA18954.hp1 NA19086.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.340-5872delG | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453064 | ||||||
chr6:138453218
|
G | A | 27 | a0001c0001t0001g0030a0001c0001t0001g0156a0001c0001t0002g0158others(24): Show | 27 | HG00738.hp1 HG00741.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.340-6025C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453218 | ||||||
chr6:138453252
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.340-6059C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453252 | ||||||
chr6:138453264
|
A | G | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-6071T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453264 | ||||||
chr6:138453389
|
C | G | 16 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0004t0004g0143others(13): Show | 16 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-6196G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453389 | ||||||
chr6:138453492
|
G | C | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-6299C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453492 | ||||||
chr6:138453494
|
A | G | 1 | a0001c0024t0004g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.340-6301T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453494 | ||||||
chr6:138453509
|
C | T | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-6316G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453509 | ||||||
chr6:138453514
|
C | T | 58 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(55): Show | 58 | HG00639.hp1 HG01255.hp2 HG01257.hp2 others(55): Show |
intron_variant | MODIFIER | c.340-6321G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453514 | ||||||
chr6:138453553
|
T | C | 84 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(81): Show | 84 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.340-6360A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453553 | ||||||
chr6:138453585
|
T | C | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-6392A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453585 | ||||||
chr6:138453596
|
G | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.340-6403C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453596 | ||||||
chr6:138453637
|
C | A | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-6444G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453637 | ||||||
chr6:138453672
|
G | A | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-6479C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453672 | ||||||
chr6:138453688
|
C | T | 9 | a0001c0001t0001g0121a0001c0001t0029g0117a0005c0012t0042g0244others(6): Show | 9 | HG02559.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.340-6495G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453688 | ||||||
chr6:138453751
|
T | C | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-6558A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453751 | ||||||
chr6:138453771
|
C | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.340-6578G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453771 | ||||||
chr6:138453897
|
C | A | 1 | a0001c0007t0011g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.340-6704G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453897 | ||||||
chr6:138453919
|
A | T | 3 | a0001c0002t0001g0061a0001c0016t0001g0062a0001c0016t0003g0060 | 3 | HG00639.hp2 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.340-6726T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453919 | ||||||
chr6:138453936
|
A | G | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340-6743T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453936 | ||||||
chr6:138453938
|
G | GCTGCCAT others(11818): Show |
1 | a0001c0001t0027g0249 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.340-6746_340-6745i others(11827): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453938 | ||||||
chr6:138453938
|
G | GCTGCCAT others(11821): Show |
1 | a0001c0001t0024g0250 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.340-6746_340-6745i others(11830): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453938 | ||||||
chr6:138453940
|
A | T | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340-6747T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138453940 | ||||||
chr6:138454088
|
A | T | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(160): Show | 164 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.340-6895T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454088 | ||||||
chr6:138454188
|
T | TGCGC | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-6996_340-6995i others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454188 | ||||||
chr6:138454190
|
C | CGCGCGTG others(1): Show |
7 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0003t0021g0083others(4): Show | 7 | HG02965.hp1 HG03041.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.340-6998_340-6997i others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454190 | ||||||
chr6:138454190
|
C | CGCGCGTG others(3): Show |
16 | a0001c0001t0002g0158a0001c0002t0001g0172a0001c0002t0001g0317others(13): Show | 16 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-6998_340-6997i others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454190 | ||||||
chr6:138454190
|
C | CGT | 4 | a0001c0001t0005g0040a0001c0001t0024g0250a0001c0001t0027g0249others(1): Show | 4 | HG02886.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.340-6999_340-6998d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454190 | ||||||
chr6:138454204
|
C | T | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(160): Show | 164 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.340-7011G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454204 | ||||||
chr6:138454214
|
T | A | 1 | a0001c0001t0001g0016 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.340-7021A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454214 | ||||||
chr6:138454220
|
T | A | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(21): Show |
intron_variant | MODIFIER | c.340-7027A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454220 | ||||||
chr6:138454301
|
T | C | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340-7108A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454301 | ||||||
chr6:138454374
|
T | C | 2 | a0001c0003t0021g0240a0003c0006t0012g0082 | 2 | HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.340-7181A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454374 | ||||||
chr6:138454400
|
G | A | 1 | a0001c0001t0014g0274 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.340-7207C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454400 | ||||||
chr6:138454456
|
G | C | 40 | a0001c0001t0001g0121a0001c0001t0029g0117a0001c0003t0007g0124others(37): Show | 40 | HG00639.hp1 HG01081.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.340-7263C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454456 | ||||||
chr6:138454466
|
A | G | 163 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(160): Show | 164 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.340-7273T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454466 | ||||||
chr6:138454497
|
CATTACTG others(5): Show |
C | 16 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0004t0004g0143others(13): Show | 16 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-7316_340-7305d others(14): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454497 | ||||||
chr6:138454510
|
A | C | 16 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0004t0004g0143others(13): Show | 16 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-7317T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454510 | ||||||
chr6:138454511
|
A | C | 16 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0004t0004g0143others(13): Show | 16 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-7318T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454511 | ||||||
chr6:138454512
|
A | C | 16 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0004t0004g0143others(13): Show | 16 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-7319T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454512 | ||||||
chr6:138454513
|
A | C | 16 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0004t0004g0143others(13): Show | 16 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.340-7320T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454513 | ||||||
chr6:138454530
|
G | A | 30 | a0001c0001t0001g0156a0001c0001t0001g0306a0001c0001t0002g0073others(27): Show | 30 | HG00099.hp2 HG00642.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.340-7337C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454530 | ||||||
chr6:138454642
|
GTATACTT others(3): Show |
G | 1 | a0001c0002t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.340-7459_340-7450d others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454642 | ||||||
chr6:138454697
|
G | A | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-7504C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454697 | ||||||
chr6:138454713
|
A | T | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-7520T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454713 | ||||||
chr6:138454852
|
C | T | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-7659G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454852 | ||||||
chr6:138454993
|
T | C | 26 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.340-7800A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138454993 | ||||||
chr6:138455021
|
A | T | 2 | a0001c0002t0001g0160a0001c0007t0001g0162 | 2 | NA18957.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.340-7828T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455021 | ||||||
chr6:138455225
|
T | C | 168 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(165): Show | 169 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.340-8032A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455225 | ||||||
chr6:138455226
|
G | A | 23 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(20): Show | 23 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.340-8033C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455226 | ||||||
chr6:138455277
|
T | C | 27 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(24): Show | 27 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.340-8084A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455277 | ||||||
chr6:138455457
|
G | GCTGCAAG others(22): Show |
1 | a0001c0003t0007g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.340-8293_340-8265d others(31): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455457
|
G | GCTGCAAG others(51): Show |
1 | a0001c0001t0001g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.340-8265_340-8264i others(60): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455457
|
G | GCTGCAAG others(138): Show |
2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.340-8265_340-8264i others(147): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455457
|
G | GCTGCAAG others(196): Show |
1 | a0001c0002t0001g0160 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.340-8265_340-8264i others(205): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455457
|
G | GCTGCAAG others(109): Show |
1 | a0001c0001t0006g0288 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.340-8265_340-8264i others(118): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455457
|
G | GCTGCAAG others(80): Show |
1 | a0001c0002t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.340-8351_340-8265d others(89): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455457
|
GCTGCAAG others(22): Show |
G | 175 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.340-8293_340-8265d others(31): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455457
|
GCTGCAAG others(51): Show |
G | 44 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0090others(41): Show | 44 | HG00673.hp1 HG00741.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.340-8322_340-8265d others(60): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455457 | ||||||
chr6:138455460
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.340-8267C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455460 | ||||||
chr6:138455465
|
G | GAGCCCCG others(22): Show |
69 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(66): Show | 70 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.340-8273_340-8272i others(31): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455465 | ||||||
chr6:138455465
|
G | GAGCCCCG others(51): Show |
6 | a0001c0001t0001g0169a0001c0001t0002g0209a0001c0001t0013g0214others(3): Show | 6 | HG00438.hp1 HG01258.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-8273_340-8272i others(60): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455465 | ||||||
chr6:138455472
|
G | GCCTTCAC others(22): Show |
1 | a0001c0007t0011g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.340-8280_340-8279i others(31): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455472 | ||||||
chr6:138455489
|
G | C | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-8296C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455489 | ||||||
chr6:138455494
|
G | A | 81 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0086others(78): Show | 82 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.340-8301C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455494 | ||||||
chr6:138455494
|
G | GAGCCCCG others(22): Show |
3 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0002t0003g0003 | 3 | HG00408.hp2 HG02132.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.340-8302_340-8301i others(31): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455494 | ||||||
chr6:138455494
|
G | GAGCCCCG others(80): Show |
1 | a0001c0001t0014g0222 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.340-8302_340-8301i others(89): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455494 | ||||||
chr6:138455494
|
G | GAGCCCCG others(80): Show |
1 | a0003c0006t0005g0289 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.340-8302_340-8301i others(89): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455494 | ||||||
chr6:138455518
|
G | C | 25 | a0001c0001t0001g0030a0001c0001t0001g0156a0001c0001t0001g0190others(22): Show | 25 | HG00741.hp2 HG01069.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.340-8325C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455518 | ||||||
chr6:138455523
|
G | A | 77 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(74): Show | 77 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.340-8330C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455523 | ||||||
chr6:138455523
|
G | GAGCCCCG others(51): Show |
3 | a0001c0001t0008g0328a0001c0031t0041g0149a0007c0011t0008g0329 | 3 | HG02486.hp2 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.340-8331_340-8330i others(60): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455523 | ||||||
chr6:138455530
|
G | A | 61 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(58): Show | 61 | HG00609.hp1 HG00621.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.340-8337C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455530 | ||||||
chr6:138455536
|
A | ACATGCTC others(167): Show |
1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.340-8344_340-8343i others(176): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455536 | ||||||
chr6:138455536
|
A | G | 6 | a0001c0002t0001g0100a0001c0003t0007g0323a0001c0004t0002g0119others(3): Show | 6 | HG00738.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-8343T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455536 | ||||||
chr6:138455552
|
G | A | 24 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(21): Show | 24 | HG00738.hp1 HG00741.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.340-8359C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455552 | ||||||
chr6:138455744
|
T | C | 2 | a0001c0004t0009g0004a0001c0004t0028g0005 | 2 | HG02109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.340-8551A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455744 | ||||||
chr6:138455755
|
G | A | 254 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.340-8562C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455755 | ||||||
chr6:138455756
|
C | A | 254 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.340-8563G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455756 | ||||||
chr6:138455758
|
A | C | 254 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.340-8565T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455758 | ||||||
chr6:138455760
|
A | T | 254 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.340-8567T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455760 | ||||||
chr6:138455761
|
G | GTT | 254 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(251): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.340-8569_340-8568i others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455761 | ||||||
chr6:138455810
|
A | G | 14 | a0001c0001t0001g0032a0001c0001t0001g0090a0001c0001t0001g0125others(11): Show | 14 | HG00673.hp1 HG01496.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.340-8617T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455810 | ||||||
chr6:138455962
|
G | A | 26 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(23): Show | 26 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(23): Show |
intron_variant | MODIFIER | c.340-8769C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455962 | ||||||
chr6:138456248
|
A | C | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG00639.hp1 HG01255.hp2 HG01257.hp2 others(59): Show |
intron_variant | MODIFIER | c.340-9055T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456248 | ||||||
chr6:138456318
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.340-9125G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456318 | ||||||
chr6:138456426
|
A | T | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.340-9233T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456426 | ||||||
chr6:138456450
|
C | T | 31 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(28): Show | 31 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.340-9257G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456450 | ||||||
chr6:138456466
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0010g0290 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.340-9273G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456466 | ||||||
chr6:138456469
|
G | A | 2 | a0001c0001t0001g0125a0003c0033t0005g0236 | 2 | HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.340-9276C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456469 | ||||||
chr6:138456648
|
C | T | 2 | a0008c0018t0002g0312a0008c0018t0002g0313 | 2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.340-9455G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456648 | ||||||
chr6:138456649
|
G | A | 132 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(129): Show | 133 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(130): Show |
intron_variant | MODIFIER | c.340-9456C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456649 | ||||||
chr6:138456794
|
G | GA | 31 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(28): Show | 31 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.340-9602dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456794 | ||||||
chr6:138456833
|
CTT | C | 31 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(28): Show | 31 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.340-9642_340-9641d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456833 | ||||||
chr6:138456883
|
C | CT | 29 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(26): Show | 29 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.340-9691dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456883 | ||||||
chr6:138456923
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0293 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.340-9730C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456923 | ||||||
chr6:138456946
|
C | T | 1 | a0001c0004t0002g0140 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.340-9753G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456946 | ||||||
chr6:138456972
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.340-9779G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138456972 | ||||||
chr6:138457223
|
T | C | 31 | a0001c0001t0001g0156a0001c0001t0002g0158a0001c0001t0010g0271others(28): Show | 31 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.340-10030A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457223 | ||||||
chr6:138457346
|
G | A | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.340-10153C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457346 | ||||||
chr6:138457460
|
C | T | 2 | a0004c0009t0001g0068a0004c0009t0001g0070 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.340-10267G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457460 | ||||||
chr6:138457479
|
T | C | 1 | a0002c0005t0002g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.340-10286A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457479 | ||||||
chr6:138457605
|
T | C | 2 | a0001c0001t0001g0084a0001c0001t0006g0085 | 2 | HG03669.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.340-10412A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457605 | ||||||
chr6:138457611
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0009g0197 | 2 | NA18974.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.340-10418C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457611 | ||||||
chr6:138457713
|
G | A | 1 | a0001c0003t0040g0173 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.340-10520C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457713 | ||||||
chr6:138457804
|
C | T | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 67 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.340-10611G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457804 | ||||||
chr6:138457814
|
C | T | 3 | a0001c0002t0002g0232a0001c0020t0048g0103a0001c0020t0049g0104 | 3 | HG01255.hp2 HG01934.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.340-10621G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457814 | ||||||
chr6:138457958
|
A | G | 1 | a0001c0002t0002g0184 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.340-10765T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457958 | ||||||
chr6:138457959
|
G | T | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-10766C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138457959 | ||||||
chr6:138458007
|
G | GA | 7 | a0001c0001t0001g0185a0001c0001t0001g0221a0001c0001t0003g0262others(4): Show | 7 | NA18612.hp1 NA18975.hp1 NA19000.hp2 others(4): Show |
intron_variant | MODIFIER | c.340-10815dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458007 | ||||||
chr6:138458007
|
GA | G | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00423.hp2 HG00639.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.340-10815delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458007 | ||||||
chr6:138458007
|
GAA | G | 34 | a0001c0001t0001g0121a0001c0001t0001g0156a0001c0001t0001g0251others(31): Show | 34 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.340-10816_340-1081 others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458007 | ||||||
chr6:138458186
|
T | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-10993A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458186 | ||||||
chr6:138458219
|
T | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-11026A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458219 | ||||||
chr6:138458317
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.340-11124G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458317 | ||||||
chr6:138458324
|
G | C | 1 | a0001c0001t0036g0053 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.340-11131C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458324 | ||||||
chr6:138458345
|
C | T | 129 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(126): Show | 130 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(127): Show |
intron_variant | MODIFIER | c.340-11152G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458345 | ||||||
chr6:138458369
|
T | C | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-11176A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458369 | ||||||
chr6:138458374
|
G | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-11181C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458374 | ||||||
chr6:138458390
|
C | A | 67 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(64): Show | 67 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.340-11197G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458390 | ||||||
chr6:138458392
|
T | C | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-11199A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458392 | ||||||
chr6:138458397
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.340-11204G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458397 | ||||||
chr6:138458482
|
C | A | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-11289G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458482 | ||||||
chr6:138458530
|
T | C | 1 | a0001c0004t0004g0130 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.340-11337A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458530 | ||||||
chr6:138458567
|
A | G | 137 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(134): Show | 138 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.340-11374T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458567 | ||||||
chr6:138458689
|
G | C | 4 | a0001c0004t0002g0115a0001c0004t0009g0004a0001c0004t0028g0005others(1): Show | 4 | HG01081.hp1 HG02109.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.340-11496C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458689 | ||||||
chr6:138458806
|
C | G | 1 | a0001c0002t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.340-11613G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458806 | ||||||
chr6:138458820
|
A | C | 64 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(61): Show | 64 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.340-11627T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458820 | ||||||
chr6:138458828
|
C | CAA | 29 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(26): Show | 29 | HG00639.hp1 HG01255.hp2 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.340-11637_340-1163 others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458828 | ||||||
chr6:138458828
|
CA | C | 233 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(230): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.340-11636delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458828 | ||||||
chr6:138458841
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.340-11648T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458841 | ||||||
chr6:138458842
|
C | A | 3 | a0001c0001t0001g0114a0001c0007t0020g0148a0001c0024t0004g0123 | 3 | HG01884.hp1 HG02965.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.340-11649G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458842 | ||||||
chr6:138458853
|
A | C | 34 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(31): Show | 34 | HG00639.hp1 HG01255.hp2 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.340-11660T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458853 | ||||||
chr6:138458970
|
G | A | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.340-11777C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458970 | ||||||
chr6:138459258
|
T | G | 65 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(62): Show | 65 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.340-12065A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459258 | ||||||
chr6:138459312
|
C | T | 10 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0007t0020g0139others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.340-12119G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459312 | ||||||
chr6:138459440
|
C | A | 36 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(33): Show | 36 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.340-12247G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459440 | ||||||
chr6:138459447
|
A | G | 1 | a0001c0001t0032g0228 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.340-12254T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459447 | ||||||
chr6:138459448
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.340-12255G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459448 | ||||||
chr6:138459453
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.340-12260G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459453 | ||||||
chr6:138459500
|
T | G | 1 | a0001c0001t0003g0046 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.340-12307A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459500 | ||||||
chr6:138459601
|
C | G | 39 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(36): Show | 39 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.340-12408G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459601 | ||||||
chr6:138459784
|
T | A | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-12591A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459784 | ||||||
chr6:138459925
|
T | A | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.340-12732A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138459925 | ||||||
chr6:138460017
|
C | G | 1 | a0001c0001t0003g0166 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.340-12824G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460017 | ||||||
chr6:138460024
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.340-12831C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460024 | ||||||
chr6:138460081
|
C | T | 25 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0002t0001g0172others(22): Show | 25 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.340-12888G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460081 | ||||||
chr6:138460135
|
A | C | 1 | a0001c0002t0001g0109 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.340-12942T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460135 | ||||||
chr6:138460154
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0002g0136 | 2 | HG01069.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.340-12961G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460154 | ||||||
chr6:138460250
|
C | T | 1 | a0001c0002t0001g0317 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.339+13056G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460250 | ||||||
chr6:138460326
|
C | T | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+12980G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460326 | ||||||
chr6:138460378
|
TG | T | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.339+12927delC | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460378 | ||||||
chr6:138460395
|
G | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+12911C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460395 | ||||||
chr6:138460400
|
A | C | 123 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(120): Show | 124 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.339+12906T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460400 | ||||||
chr6:138460500
|
C | T | 1 | a0001c0001t0005g0269 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.339+12806G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460500 | ||||||
chr6:138460510
|
T | A | 2 | a0001c0003t0007g0126a0001c0003t0007g0254 | 2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.339+12796A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460510 | ||||||
chr6:138460588
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.339+12718A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460588 | ||||||
chr6:138460612
|
C | T | 29 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+12694G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460612 | ||||||
chr6:138460772
|
T | A | 5 | a0001c0008t0008g0076a0001c0008t0008g0078a0001c0008t0008g0211others(2): Show | 5 | NA18947.hp1 NA18954.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+12534A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460772 | ||||||
chr6:138460884
|
A | G | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 121 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.339+12422T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460884 | ||||||
chr6:138461006
|
G | A | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+12300C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461006 | ||||||
chr6:138461040
|
A | C | 3 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0001t0002g0010 | 3 | HG00544.hp2 HG02074.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.339+12266T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461040 | ||||||
chr6:138461155
|
G | GT | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+12150dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461155 | ||||||
chr6:138461156
|
T | G | 45 | a0001c0001t0001g0030a0001c0001t0001g0032a0001c0001t0001g0064others(42): Show | 45 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.339+12150A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461156 | ||||||
chr6:138461232
|
G | T | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+12074C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461232 | ||||||
chr6:138461248
|
A | G | 29 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+12058T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461248 | ||||||
chr6:138461294
|
A | G | 1 | a0001c0001t0002g0021 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.339+12012T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461294 | ||||||
chr6:138461313
|
T | A | 29 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+11993A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461313 | ||||||
chr6:138461323
|
G | A | 29 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+11983C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461323 | ||||||
chr6:138461345
|
A | C | 29 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+11961T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461345 | ||||||
chr6:138461349
|
C | T | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.339+11957G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461349 | ||||||
chr6:138461382
|
C | T | 29 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+11924G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461382 | ||||||
chr6:138461394
|
A | C | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+11912T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461394 | ||||||
chr6:138461399
|
T | C | 32 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(29): Show | 32 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+11907A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461399 | ||||||
chr6:138461453
|
A | T | 29 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.339+11853T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461453 | ||||||
chr6:138461515
|
GA | G | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+11790delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461515 | ||||||
chr6:138461544
|
G | A | 3 | a0001c0003t0021g0083a0003c0006t0005g0133a0007c0011t0008g0134 | 3 | HG03453.hp1 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.339+11762C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461544 | ||||||
chr6:138461701
|
T | G | 23 | a0001c0001t0010g0271a0001c0002t0001g0172a0001c0002t0001g0317others(20): Show | 23 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.339+11605A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461701 | ||||||
chr6:138461937
|
T | C | 1 | a0001c0004t0002g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.339+11369A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461937 | ||||||
chr6:138462171
|
A | G | 30 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0001t0024g0250others(27): Show | 30 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.339+11135T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462171 | ||||||
chr6:138462190
|
G | A | 6 | a0005c0012t0042g0244a0005c0012t0044g0245a0005c0013t0001g0178others(3): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+11116C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462190 | ||||||
chr6:138462205
|
T | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+11101A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462205 | ||||||
chr6:138462223
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.339+11083C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462223 | ||||||
chr6:138462237
|
T | C | 1 | a0001c0028t0043g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.339+11069A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462237 | ||||||
chr6:138462580
|
C | T | 1 | a0001c0002t0001g0035 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.339+10726G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462580 | ||||||
chr6:138462759
|
T | C | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.339+10547A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462759 | ||||||
chr6:138462861
|
G | C | 3 | a0001c0001t0010g0271a0001c0003t0040g0173a0001c0039t0018g0270 | 3 | HG03041.hp1 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.339+10445C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138462861 | ||||||
chr6:138463425
|
C | T | 7 | a0001c0001t0001g0064a0001c0001t0002g0093a0001c0001t0002g0094others(4): Show | 7 | HG00140.hp1 HG00140.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.339+9881G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463425 | ||||||
chr6:138463457
|
G | A | 25 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0002t0001g0172others(22): Show | 25 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.339+9849C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463457 | ||||||
chr6:138463504
|
C | CT | 38 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(35): Show | 38 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.339+9801dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463504 | ||||||
chr6:138463504
|
CT | C | 24 | a0001c0001t0001g0023a0001c0001t0001g0030a0001c0001t0001g0044others(21): Show | 24 | HG00639.hp2 HG01069.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.339+9801delA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463504 | ||||||
chr6:138463504
|
CTTT | C | 24 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0002t0001g0172others(21): Show | 24 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.339+9799_339+9801d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463504 | ||||||
chr6:138463589
|
T | C | 1 | a0010c0040t0010g0191 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.339+9717A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463589 | ||||||
chr6:138463615
|
G | C | 6 | a0005c0012t0042g0244a0005c0012t0044g0245a0005c0013t0001g0178others(3): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+9691C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463615 | ||||||
chr6:138463623
|
T | C | 25 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0002t0001g0172others(22): Show | 25 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.339+9683A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463623 | ||||||
chr6:138463716
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+9590G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463716 | ||||||
chr6:138463729
|
T | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+9577A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463729 | ||||||
chr6:138463764
|
A | G | 1 | a0001c0024t0004g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.339+9542T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463764 | ||||||
chr6:138463780
|
C | T | 23 | a0001c0001t0010g0271a0001c0002t0001g0172a0001c0002t0001g0317others(20): Show | 23 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.339+9526G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463780 | ||||||
chr6:138463813
|
T | C | 6 | a0001c0003t0007g0124a0001c0003t0007g0129a0001c0003t0007g0330others(3): Show | 6 | HG01106.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+9493A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463813 | ||||||
chr6:138463816
|
T | C | 26 | a0001c0001t0001g0125a0001c0001t0001g0235a0001c0001t0001g0268others(23): Show | 26 | HG00673.hp1 HG01884.hp2 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+9490A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463816 | ||||||
chr6:138463829
|
C | A | 1 | a0001c0001t0003g0018 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.339+9477G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138463829 | ||||||
chr6:138464087
|
G | A | 1 | a0001c0034t0031g0026 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.339+9219C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464087 | ||||||
chr6:138464191
|
CAGCCTGA others(11): Show |
C | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.339+9097_339+9114d others(20): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464191 | ||||||
chr6:138464193
|
G | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+9113C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464193 | ||||||
chr6:138464284
|
C | A | 2 | a0001c0007t0011g0278a0001c0015t0001g0127 | 2 | HG02809.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.339+9022G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464284 | ||||||
chr6:138464363
|
G | A | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+8943C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464363 | ||||||
chr6:138464385
|
A | G | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+8921T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464385 | ||||||
chr6:138464416
|
G | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+8890C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464416 | ||||||
chr6:138464526
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0167 | 2 | HG01167.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.339+8780C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464526 | ||||||
chr6:138464666
|
A | T | 2 | a0001c0001t0003g0074a0001c0001t0003g0075 | 2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.339+8640T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464666 | ||||||
chr6:138464705
|
T | TTTTC | 6 | a0001c0004t0004g0144a0001c0004t0011g0152a0001c0010t0016g0145others(3): Show | 6 | HG02572.hp2 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+8600_339+8601i others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464705 | ||||||
chr6:138464707
|
T | TTCTTTTC | 16 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0002t0001g0296others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.339+8598_339+8599i others(9): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464707 | ||||||
chr6:138464708
|
T | TCTTTTC | 8 | a0001c0001t0001g0121a0001c0001t0001g0251a0001c0001t0001g0252others(5): Show | 8 | HG00639.hp1 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.339+8597_339+8598i others(8): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464708 | ||||||
chr6:138464710
|
C | CT | 5 | a0001c0004t0004g0144a0001c0004t0011g0152a0001c0010t0016g0145others(2): Show | 5 | HG02572.hp2 HG02647.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.339+8595dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464710 | ||||||
chr6:138464710
|
C | T | 27 | a0001c0001t0001g0121a0001c0001t0001g0251a0001c0001t0001g0252others(24): Show | 27 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.339+8596G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464710 | ||||||
chr6:138464715
|
C | CT | 11 | a0001c0001t0002g0136a0001c0001t0003g0058a0001c0001t0009g0165others(8): Show | 11 | HG00438.hp2 HG01099.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.339+8590dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464715 | ||||||
chr6:138464715
|
C | CTTTTTT | 26 | a0001c0001t0001g0234a0001c0001t0002g0158a0001c0001t0006g0229others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+8585_339+8590d others(8): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464715 | ||||||
chr6:138464715
|
C | CTTTTTTT | 56 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(53): Show | 57 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.339+8584_339+8590d others(9): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464715 | ||||||
chr6:138464715
|
C | CTTTTTTT others(1): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0086a0001c0001t0001g0192others(10): Show | 13 | HG00438.hp1 HG01978.hp2 HG02148.hp1 others(10): Show |
intron_variant | MODIFIER | c.339+8583_339+8590d others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464715 | ||||||
chr6:138464715
|
C | T | 32 | a0001c0001t0001g0121a0001c0001t0001g0251a0001c0001t0001g0252others(29): Show | 32 | HG00639.hp1 HG01884.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.339+8591G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464715 | ||||||
chr6:138464859
|
C | T | 3 | a0001c0003t0007g0124a0001c0003t0007g0330a0001c0004t0030g0241 | 3 | HG02622.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.339+8447G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464859 | ||||||
chr6:138464925
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0167 | 2 | HG01167.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.339+8381A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138464925 | ||||||
chr6:138465021
|
T | C | 58 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(55): Show | 59 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.339+8285A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465021 | ||||||
chr6:138465054
|
C | A | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.339+8252G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465054 | ||||||
chr6:138465054
|
C | CA | 18 | a0001c0003t0007g0124a0001c0003t0007g0129a0001c0003t0007g0330others(15): Show | 18 | HG00639.hp1 HG01106.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.339+8251dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465054 | ||||||
chr6:138465054
|
C | CAA | 19 | a0001c0001t0001g0121a0001c0001t0024g0250a0001c0001t0027g0249others(16): Show | 19 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.339+8250_339+8251d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465054 | ||||||
chr6:138465054
|
C | CAAAA | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG01255.hp2 HG01934.hp1 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.339+8248_339+8251d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465054 | ||||||
chr6:138465054
|
CA | C | 88 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(85): Show | 89 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.339+8251delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465054 | ||||||
chr6:138465144
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.339+8162G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465144 | ||||||
chr6:138465315
|
T | TCCAC | 3 | a0001c0003t0007g0323a0001c0015t0001g0325a0001c0029t0047g0324 | 3 | HG00738.hp1 HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.339+7990_339+7991i others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465315 | ||||||
chr6:138465388
|
A | C | 18 | a0001c0003t0007g0179a0001c0003t0007g0180a0001c0003t0007g0239others(15): Show | 18 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.339+7918T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465388 | ||||||
chr6:138465394
|
T | C | 135 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(132): Show | 136 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.339+7912A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465394 | ||||||
chr6:138465446
|
G | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+7860C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465446 | ||||||
chr6:138465724
|
C | CT | 6 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0003t0021g0083others(3): Show | 6 | HG01884.hp1 HG02922.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+7581dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465724 | ||||||
chr6:138465724
|
CT | C | 12 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0015g0275others(9): Show | 12 | HG01069.hp1 HG01069.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+7581delA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465724 | ||||||
chr6:138465724
|
CTT | C | 91 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(88): Show | 92 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.339+7580_339+7581d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465724 | ||||||
chr6:138465724
|
CTTTTT | C | 12 | a0001c0003t0007g0179a0001c0003t0007g0180a0001c0003t0007g0239others(9): Show | 12 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+7577_339+7581d others(7): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465724 | ||||||
chr6:138465729
|
T | C | 3 | a0001c0001t0001g0090a0001c0001t0001g0215a0001c0001t0001g0302 | 3 | NA19086.hp1 NA19086.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.339+7577A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465729 | ||||||
chr6:138465855
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.339+7451G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465855 | ||||||
chr6:138465882
|
C | T | 6 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0002t0001g0296others(3): Show | 6 | HG01891.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+7424G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465882 | ||||||
chr6:138466023
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+7283G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466023 | ||||||
chr6:138466037
|
T | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+7269A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466037 | ||||||
chr6:138466041
|
T | TG | 26 | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0063others(23): Show | 26 | HG01074.hp1 HG01192.hp2 HG01261.hp2 others(23): Show |
intron_variant | MODIFIER | c.339+7264dupC | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466041 | ||||||
chr6:138466041
|
T | TGG | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(21): Show | 24 | HG00673.hp2 HG01255.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.339+7263_339+7264d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466041 | ||||||
chr6:138466041
|
T | TGGG | 37 | a0001c0001t0001g0014a0001c0001t0001g0193a0001c0001t0001g0200others(34): Show | 37 | HG00423.hp1 HG00558.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.339+7262_339+7264d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466041 | ||||||
chr6:138466041
|
T | TGGGG | 32 | a0001c0001t0001g0019a0001c0001t0001g0086a0001c0001t0001g0153others(29): Show | 33 | HG00438.hp1 HG00597.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.339+7261_339+7264d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466041 | ||||||
chr6:138466052
|
C | G | 1 | a0001c0004t0002g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.339+7254G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466052 | ||||||
chr6:138466053
|
A | C | 1 | a0001c0004t0002g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.339+7253T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466053 | ||||||
chr6:138466068
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.339+7238G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466068 | ||||||
chr6:138466078
|
T | C | 122 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(119): Show | 123 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.339+7228A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466078 | ||||||
chr6:138466127
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.339+7179G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466127 | ||||||
chr6:138466134
|
G | A | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+7172C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466134 | ||||||
chr6:138466165
|
G | A | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 121 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.339+7141C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466165 | ||||||
chr6:138466291
|
T | G | 2 | a0001c0001t0003g0058a0001c0001t0006g0065 | 2 | HG00438.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.339+7015A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466291 | ||||||
chr6:138466333
|
G | A | 6 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0002t0001g0296others(3): Show | 6 | HG01891.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.339+6973C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466333 | ||||||
chr6:138466471
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.339+6835G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466471 | ||||||
chr6:138466524
|
G | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+6782C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466524 | ||||||
chr6:138466587
|
C | T | 1 | a0001c0002t0001g0317 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.339+6719G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466587 | ||||||
chr6:138466650
|
A | G | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+6656T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466650 | ||||||
chr6:138466756
|
A | T | 5 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0002t0001g0296others(2): Show | 5 | HG02809.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+6550T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466756 | ||||||
chr6:138466774
|
T | TA | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 121 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.339+6531dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466774 | ||||||
chr6:138466807
|
G | A | 6 | a0005c0012t0042g0244a0005c0012t0044g0245a0005c0013t0001g0178others(3): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+6499C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466807 | ||||||
chr6:138467001
|
C | G | 122 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(119): Show | 123 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(120): Show |
intron_variant | MODIFIER | c.339+6305G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467001 | ||||||
chr6:138467156
|
T | C | 11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(8): Show | 11 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.339+6150A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467156 | ||||||
chr6:138467161
|
A | G | 1 | a0001c0004t0004g0131 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.339+6145T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467161 | ||||||
chr6:138467222
|
G | A | 5 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0002t0001g0296others(2): Show | 5 | HG02809.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+6084C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467222 | ||||||
chr6:138467232
|
C | T | 62 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(59): Show | 62 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.339+6074G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467232 | ||||||
chr6:138467255
|
C | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+6051G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467255 | ||||||
chr6:138467318
|
A | G | 120 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(117): Show | 121 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.339+5988T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467318 | ||||||
chr6:138467327
|
T | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+5979A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467327 | ||||||
chr6:138467350
|
T | C | 125 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(122): Show | 126 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(123): Show |
intron_variant | MODIFIER | c.339+5956A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467350 | ||||||
chr6:138467373
|
C | T | 1 | a0001c0002t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.339+5933G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467373 | ||||||
chr6:138467399
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0029g0117a0005c0013t0011g0007 | 3 | HG02559.hp1 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.339+5907C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467399 | ||||||
chr6:138467434
|
A | G | 3 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0003t0007g0124 | 3 | HG02896.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.339+5872T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467434 | ||||||
chr6:138467713
|
A | G | 4 | a0001c0003t0021g0083a0001c0031t0041g0149a0003c0006t0005g0133others(1): Show | 4 | HG02818.hp1 HG03453.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+5593T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467713 | ||||||
chr6:138467748
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.339+5558A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467748 | ||||||
chr6:138467918
|
A | G | 1 | a0001c0001t0009g0304 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.339+5388T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467918 | ||||||
chr6:138467930
|
TAG | T | 4 | a0001c0003t0007g0124a0001c0003t0007g0330a0001c0004t0004g0131others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+5374_339+5375d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467930 | ||||||
chr6:138467987
|
A | G | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+5319T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138467987 | ||||||
chr6:138468056
|
T | G | 1 | a0001c0001t0013g0214 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.339+5250A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138468056 | ||||||
chr6:138468197
|
T | G | 2 | a0001c0001t0001g0279a0001c0001t0001g0292 | 2 | NA18965.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.339+5109A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138468197 | ||||||
chr6:138468200
|
T | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+5106A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138468200 | ||||||
chr6:138468887
|
C | G | 59 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(56): Show | 59 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.339+4419G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138468887 | ||||||
chr6:138468994
|
A | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0094 | 2 | HG00140.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.339+4312T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138468994 | ||||||
chr6:138469090
|
T | C | 4 | a0001c0003t0007g0124a0001c0003t0007g0330a0001c0004t0004g0131others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+4216A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469090 | ||||||
chr6:138469204
|
A | C | 1 | a0001c0010t0016g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.339+4102T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469204 | ||||||
chr6:138469258
|
A | T | 4 | a0001c0001t0001g0032a0001c0001t0003g0231a0001c0002t0002g0031others(1): Show | 4 | HG01496.hp2 HG01934.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+4048T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469258 | ||||||
chr6:138469312
|
G | A | 4 | a0001c0001t0045g0128a0001c0003t0007g0170a0001c0004t0004g0171others(1): Show | 4 | HG02258.hp1 HG02572.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.339+3994C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469312 | ||||||
chr6:138469332
|
C | T | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.339+3974G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469332 | ||||||
chr6:138469443
|
G | T | 6 | a0005c0012t0042g0244a0005c0012t0044g0245a0005c0013t0001g0178others(3): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.339+3863C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469443 | ||||||
chr6:138469451
|
C | T | 23 | a0001c0001t0010g0271a0001c0002t0001g0172a0001c0002t0001g0317others(20): Show | 23 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.339+3855G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469451 | ||||||
chr6:138469461
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+3845G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469461 | ||||||
chr6:138469462
|
G | A | 21 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0003t0007g0179others(18): Show | 21 | HG00639.hp1 HG01884.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.339+3844C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469462 | ||||||
chr6:138469559
|
A | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+3747T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469559 | ||||||
chr6:138469577
|
C | T | 33 | a0001c0001t0001g0156a0001c0001t0010g0271a0001c0002t0001g0172others(30): Show | 33 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.339+3729G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469577 | ||||||
chr6:138469585
|
C | T | 23 | a0001c0001t0010g0271a0001c0002t0001g0172a0001c0002t0001g0317others(20): Show | 23 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.339+3721G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469585 | ||||||
chr6:138469588
|
G | T | 1 | a0001c0002t0001g0296 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.339+3718C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469588 | ||||||
chr6:138469617
|
C | T | 4 | a0001c0003t0007g0124a0001c0003t0007g0330a0001c0004t0004g0131others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+3689G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469617 | ||||||
chr6:138469757
|
C | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+3549G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469757 | ||||||
chr6:138469855
|
A | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+3451T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469855 | ||||||
chr6:138469857
|
G | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+3449C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469857 | ||||||
chr6:138469896
|
G | C | 1 | a0001c0004t0030g0241 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.339+3410C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469896 | ||||||
chr6:138470098
|
C | A | 23 | a0001c0001t0010g0271a0001c0002t0001g0172a0001c0002t0001g0317others(20): Show | 23 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.339+3208G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470098 | ||||||
chr6:138470189
|
T | A | 94 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(91): Show | 95 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.339+3117A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470189 | ||||||
chr6:138470285
|
C | A | 1 | a0001c0001t0002g0073 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.339+3021G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470285 | ||||||
chr6:138470312
|
A | C | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.339+2994T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470312 | ||||||
chr6:138470358
|
C | T | 2 | a0001c0004t0004g0080a0001c0004t0004g0081 | 2 | HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.339+2948G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470358 | ||||||
chr6:138470460
|
G | T | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+2846C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470460 | ||||||
chr6:138470540
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+2766G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470540 | ||||||
chr6:138470583
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0005g0269 | 2 | NA18968.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.339+2723C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470583 | ||||||
chr6:138470657
|
G | C | 11 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0056others(8): Show | 11 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.339+2649C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470657 | ||||||
chr6:138470671
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.339+2635G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470671 | ||||||
chr6:138470735
|
G | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+2571C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470735 | ||||||
chr6:138470776
|
C | A | 26 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.339+2530G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470776 | ||||||
chr6:138470849
|
A | G | 92 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(89): Show | 93 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.339+2457T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470849 | ||||||
chr6:138470924
|
G | A | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+2382C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470924 | ||||||
chr6:138471003
|
C | G | 1 | a0001c0007t0020g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.339+2303G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471003 | ||||||
chr6:138471135
|
T | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+2171A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471135 | ||||||
chr6:138471186
|
C | T | 1 | a0001c0003t0007g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.339+2120G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471186 | ||||||
chr6:138471242
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0029g0117a0005c0013t0011g0007 | 3 | HG02559.hp1 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.339+2064C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471242 | ||||||
chr6:138471252
|
T | C | 17 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(14): Show | 17 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.339+2054A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471252 | ||||||
chr6:138471464
|
G | A | 4 | a0001c0003t0007g0124a0001c0003t0007g0330a0001c0004t0004g0131others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.339+1842C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471464 | ||||||
chr6:138471791
|
C | T | 1 | a0001c0001t0015g0039 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.339+1515G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471791 | ||||||
chr6:138471845
|
T | C | 1 | a0001c0001t0009g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.339+1461A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471845 | ||||||
chr6:138471979
|
GACC | G | 99 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(96): Show | 100 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.339+1324_339+1326d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138471979 | ||||||
chr6:138472020
|
G | A | 1 | a0001c0001t0009g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.339+1286C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472020 | ||||||
chr6:138472051
|
G | A | 2 | a0001c0001t0002g0136a0001c0001t0009g0165 | 2 | HG02055.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.339+1255C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472051 | ||||||
chr6:138472076
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.339+1230C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472076 | ||||||
chr6:138472118
|
T | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.339+1188A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472118 | ||||||
chr6:138472183
|
C | CA | 61 | a0001c0001t0001g0032a0001c0001t0001g0064a0001c0001t0001g0087others(58): Show | 61 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.339+1122dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472183 | ||||||
chr6:138472183
|
C | CAAA | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.339+1120_339+1122d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472183 | ||||||
chr6:138472183
|
CA | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.339+1122delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472183 | ||||||
chr6:138473099
|
G | C | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.339+207C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138473099 | ||||||
chr6:138473142
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.339+164G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138473142 | ||||||
chr6:138473160
|
G | A | 104 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(101): Show | 105 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.339+146C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138473160 | ||||||
chr6:138473491
|
A | G | 105 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(102): Show | 106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.212-58T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473491 | ||||||
chr6:138473567
|
T | C | 1 | a0001c0001t0002g0136 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.212-134A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473567 | ||||||
chr6:138473606
|
C | T | 26 | a0001c0001t0002g0158a0001c0001t0010g0271a0001c0002t0001g0172others(23): Show | 26 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.212-173G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473606 | ||||||
chr6:138473748
|
A | G | 103 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(100): Show | 104 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.212-315T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473748 | ||||||
chr6:138473843
|
T | TA | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-411dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473843 | ||||||
chr6:138473872
|
C | T | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.212-439G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473872 | ||||||
chr6:138473952
|
A | G | 1 | a0001c0024t0004g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.212-519T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473952 | ||||||
chr6:138474076
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.212-643G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474076 | ||||||
chr6:138474080
|
G | C | 2 | a0001c0001t0003g0262a0001c0001t0006g0260 | 2 | NA19000.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.212-647C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474080 | ||||||
chr6:138474145
|
C | T | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-712G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474145 | ||||||
chr6:138474286
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-853G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474286 | ||||||
chr6:138474312
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.212-879G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474312 | ||||||
chr6:138474379
|
C | A | 10 | a0001c0001t0001g0027a0001c0001t0001g0038a0001c0001t0001g0056others(7): Show | 10 | HG00544.hp2 HG00621.hp1 HG02074.hp1 others(7): Show |
intron_variant | MODIFIER | c.212-946G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474379 | ||||||
chr6:138474646
|
A | G | 29 | a0001c0001t0001g0309a0001c0001t0001g0311a0001c0001t0002g0158others(26): Show | 29 | HG00738.hp1 HG00741.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.212-1213T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474646 | ||||||
chr6:138474769
|
A | G | 1 | a0001c0001t0002g0201 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.212-1336T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474769 | ||||||
chr6:138474941
|
G | C | 1 | a0001c0002t0009g0020 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.212-1508C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138474941 | ||||||
chr6:138475029
|
T | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.212-1596A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475029 | ||||||
chr6:138475041
|
G | A | 131 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(128): Show | 132 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(129): Show |
intron_variant | MODIFIER | c.212-1608C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475041 | ||||||
chr6:138475149
|
C | CA | 28 | a0001c0001t0001g0014a0001c0001t0001g0032a0001c0001t0001g0064others(25): Show | 28 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(25): Show |
intron_variant | MODIFIER | c.212-1717dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475149 | ||||||
chr6:138475149
|
CA | C | 57 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(54): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.212-1717delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475149 | ||||||
chr6:138475163
|
A | G | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-1730T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475163 | ||||||
chr6:138475175
|
T | C | 1 | a0001c0003t0004g0182 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.212-1742A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475175 | ||||||
chr6:138475194
|
A | C | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0007t0020g0148 | 3 | HG01884.hp1 HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.212-1761T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475194 | ||||||
chr6:138475197
|
T | C | 6 | a0001c0001t0001g0208a0001c0001t0003g0262a0001c0001t0003g0276others(3): Show | 6 | HG02056.hp2 HG03831.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-1764A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475197 | ||||||
chr6:138475315
|
T | G | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-1882A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475315 | ||||||
chr6:138475326
|
G | C | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-1893C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475326 | ||||||
chr6:138475395
|
A | AT | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-1963dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475395 | ||||||
chr6:138475455
|
T | C | 1 | a0014c0036t0013g0277 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.212-2022A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475455 | ||||||
chr6:138475524
|
G | A | 30 | a0001c0001t0001g0121a0001c0001t0024g0250a0001c0001t0027g0249others(27): Show | 30 | HG00639.hp1 HG02109.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.212-2091C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475524 | ||||||
chr6:138475732
|
C | G | 293 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(290): Show | 294 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.212-2299G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475732 | ||||||
chr6:138475771
|
C | T | 1 | a0001c0010t0016g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.212-2338G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475771 | ||||||
chr6:138475797
|
A | G | 1 | a0001c0001t0002g0315 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.212-2364T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475797 | ||||||
chr6:138475817
|
G | A | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-2384C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475817 | ||||||
chr6:138476035
|
C | A | 1 | a0001c0001t0001g0045 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.212-2602G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476035 | ||||||
chr6:138476092
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-2659G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476092 | ||||||
chr6:138476193
|
T | C | 138 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(135): Show | 139 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.212-2760A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476193 | ||||||
chr6:138476222
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-2789G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476222 | ||||||
chr6:138476230
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-2797G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476230 | ||||||
chr6:138476266
|
T | C | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.212-2833A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476266 | ||||||
chr6:138476377
|
G | A | 10 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0007t0020g0139others(7): Show | 10 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.212-2944C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476377 | ||||||
chr6:138476685
|
G | A | 4 | a0001c0004t0002g0115a0001c0004t0009g0004a0001c0004t0028g0005others(1): Show | 4 | HG01081.hp1 HG02109.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.212-3252C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476685 | ||||||
chr6:138476789
|
T | C | 58 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(55): Show | 59 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.212-3356A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476789 | ||||||
chr6:138476831
|
A | T | 18 | a0001c0001t0001g0029a0001c0001t0001g0042a0001c0001t0001g0043others(15): Show | 18 | HG00544.hp1 HG01257.hp2 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-3398T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476831 | ||||||
chr6:138476957
|
T | TA | 29 | a0001c0001t0001g0072a0001c0001t0001g0084a0001c0001t0001g0251others(26): Show | 29 | HG00438.hp2 HG00544.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.212-3525dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476957 | ||||||
chr6:138476957
|
TA | T | 11 | a0001c0001t0001g0038a0001c0001t0001g0287a0001c0001t0003g0025others(8): Show | 11 | HG00639.hp1 HG00639.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-3525delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476957 | ||||||
chr6:138476957
|
TAAAAAAA others(3): Show |
T | 56 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(53): Show | 57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.212-3534_212-3525d others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476957 | ||||||
chr6:138476957
|
TAAAAAAA others(4): Show |
T | 3 | a0001c0001t0001g0155a0001c0001t0003g0154a0001c0007t0001g0248 | 3 | NA18959.hp1 NA18960.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.212-3535_212-3525d others(13): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476957 | ||||||
chr6:138476957
|
TAAAAAAA others(5): Show |
T | 50 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(47): Show | 50 | HG00738.hp1 HG00741.hp2 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.212-3536_212-3525d others(14): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138476957 | ||||||
chr6:138477244
|
A | C | 6 | a0001c0001t0024g0250a0001c0001t0027g0249a0001c0002t0001g0296others(3): Show | 6 | HG01891.hp2 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-3811T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477244 | ||||||
chr6:138477426
|
C | T | 1 | a0001c0024t0004g0123 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.212-3993G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477426 | ||||||
chr6:138477530
|
G | C | 3 | a0001c0001t0001g0155a0001c0001t0003g0154a0001c0007t0001g0248 | 3 | NA18959.hp1 NA18960.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.212-4097C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477530 | ||||||
chr6:138477582
|
G | A | 1 | a0001c0010t0016g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.212-4149C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477582 | ||||||
chr6:138477712
|
G | T | 1 | a0001c0001t0001g0247 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.212-4279C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477712 | ||||||
chr6:138477754
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.212-4321G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477754 | ||||||
chr6:138477962
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.212-4529C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477962 | ||||||
chr6:138478007
|
T | C | 12 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(9): Show | 12 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.212-4574A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478007 | ||||||
chr6:138478012
|
C | CT | 18 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0001t0001g0293others(15): Show | 18 | HG00408.hp1 HG00642.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.212-4580dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478012
|
C | CTT | 43 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(40): Show | 44 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.212-4581_212-4580d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478012
|
C | CTTT | 22 | a0001c0001t0001g0247a0001c0001t0002g0158a0001c0001t0002g0266others(19): Show | 22 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.212-4582_212-4580d others(5): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478012
|
C | CTTTT | 12 | a0001c0002t0001g0317a0001c0002t0002g0184a0001c0002t0002g0318others(9): Show | 12 | HG00741.hp2 HG01074.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.212-4583_212-4580d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478012
|
C | CTTTTTTT others(1): Show |
11 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(8): Show | 11 | HG00738.hp1 HG01255.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.212-4587_212-4580d others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478012
|
CT | C | 126 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(123): Show | 126 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.212-4580delA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478012
|
CTT | C | 9 | a0001c0001t0001g0156a0001c0001t0002g0093a0001c0001t0002g0094others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.212-4581_212-4580d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478012
|
CTTTT | C | 8 | a0001c0003t0007g0124a0001c0003t0007g0330a0001c0003t0021g0083others(5): Show | 8 | HG02622.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.212-4583_212-4580d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478012 | ||||||
chr6:138478014
|
T | C | 1 | a0001c0001t0002g0316 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.212-4581A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478014 | ||||||
chr6:138478067
|
C | T | 106 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(103): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.212-4634G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478067 | ||||||
chr6:138478117
|
G | A | 92 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(89): Show | 93 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.212-4684C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478117 | ||||||
chr6:138478220
|
A | G | 107 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(104): Show | 108 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.212-4787T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478220 | ||||||
chr6:138478270
|
C | T | 33 | a0001c0001t0001g0309a0001c0001t0001g0311a0001c0001t0002g0158others(30): Show | 33 | HG00597.hp2 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.212-4837G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478270 | ||||||
chr6:138478271
|
G | A | 19 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0003t0007g0179others(16): Show | 19 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.212-4838C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478271 | ||||||
chr6:138478318
|
G | A | 109 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(106): Show | 110 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.212-4885C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478318 | ||||||
chr6:138478437
|
A | G | 2 | a0001c0002t0001g0106a0001c0002t0001g0107 | 2 | HG00140.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.212-5004T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478437 | ||||||
chr6:138478534
|
G | A | 2 | a0001c0001t0002g0196a0001c0001t0009g0197 | 2 | NA18974.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.212-5101C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478534 | ||||||
chr6:138478722
|
A | T | 107 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(104): Show | 108 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.212-5289T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478722 | ||||||
chr6:138478880
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-5447G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478880 | ||||||
chr6:138479066
|
G | T | 1 | a0001c0001t0001g0294 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.212-5633C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138479066 | ||||||
chr6:138479154
|
T | C | 1 | a0001c0010t0016g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.212-5721A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138479154 | ||||||
chr6:138479465
|
C | A | 1 | a0001c0001t0002g0316 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.212-6032G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138479465 | ||||||
chr6:138479509
|
G | A | 55 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(52): Show | 56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-6076C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138479509 | ||||||
chr6:138479553
|
C | A | 27 | a0001c0001t0010g0271a0001c0002t0001g0172a0001c0002t0001g0317others(24): Show | 27 | HG00738.hp1 HG01081.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.212-6120G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138479553 | ||||||
chr6:138479824
|
T | C | 1 | a0001c0002t0002g0184 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.212-6391A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138479824 | ||||||
chr6:138480131
|
C | A | 57 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(54): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.212-6698G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138480131 | ||||||
chr6:138480444
|
G | C | 1 | a0001c0001t0003g0198 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.212-7011C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138480444 | ||||||
chr6:138480485
|
C | A | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.212-7052G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138480485 | ||||||
chr6:138480513
|
C | A | 57 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(54): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.212-7080G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138480513 | ||||||
chr6:138480539
|
G | A | 1 | a0003c0006t0005g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.212-7106C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138480539 | ||||||
chr6:138480661
|
G | A | 57 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(54): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.212-7228C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138480661 | ||||||
chr6:138481194
|
C | T | 57 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(54): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.212-7761G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481194 | ||||||
chr6:138481249
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(42): Show | 45 | HG00738.hp1 HG00741.hp2 HG01074.hp2 others(42): Show |
intron_variant | MODIFIER | c.212-7816A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481249 | ||||||
chr6:138481264
|
C | T | 57 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(54): Show | 58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): Show |
intron_variant | MODIFIER | c.212-7831G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481264 | ||||||
chr6:138481351
|
A | G | 30 | a0001c0001t0001g0309a0001c0001t0001g0311a0001c0001t0002g0158others(27): Show | 30 | HG00738.hp1 HG00741.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.212-7918T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481351 | ||||||
chr6:138481379
|
T | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.212-7946A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481379 | ||||||
chr6:138481397
|
C | T | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.212-7964G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481397 | ||||||
chr6:138481398
|
G | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0002g0021others(4): Show | 7 | HG01261.hp1 HG01978.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.212-7965C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481398 | ||||||
chr6:138481502
|
T | C | 1 | a0016c0026t0037g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.212-8069A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481502 | ||||||
chr6:138481774
|
C | A | 1 | a0001c0001t0006g0085 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.212-8341G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481774 | ||||||
chr6:138481820
|
G | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-8387C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481820 | ||||||
chr6:138481870
|
T | G | 1 | a0001c0002t0001g0008 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.212-8437A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481870 | ||||||
chr6:138481978
|
T | C | 1 | a0001c0001t0005g0295 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.212-8545A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138481978 | ||||||
chr6:138482223
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.212-8790C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482223 | ||||||
chr6:138482312
|
G | A | 77 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(74): Show | 78 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.212-8879C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482312 | ||||||
chr6:138482371
|
G | A | 2 | a0001c0001t0024g0250a0001c0001t0027g0249 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.212-8938C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482371 | ||||||
chr6:138482433
|
G | A | 3 | a0001c0002t0001g0061a0001c0016t0001g0062a0001c0016t0003g0060 | 3 | HG00639.hp2 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.212-9000C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482433 | ||||||
chr6:138482445
|
C | CA | 19 | a0001c0001t0001g0063a0001c0001t0001g0273a0001c0001t0001g0322others(16): Show | 19 | HG00423.hp2 HG00673.hp2 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.212-9013dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482445 | ||||||
chr6:138482445
|
C | CAA | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-9014_212-9013d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482445 | ||||||
chr6:138482445
|
CA | C | 139 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0019others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.212-9013delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482445 | ||||||
chr6:138482445
|
CAA | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0155a0001c0001t0003g0154others(3): Show | 6 | HG01069.hp1 HG01255.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.212-9014_212-9013d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482445 | ||||||
chr6:138482625
|
T | G | 5 | a0001c0001t0001g0155a0001c0001t0002g0223a0001c0001t0003g0154others(2): Show | 5 | HG00597.hp2 NA18957.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.212-9192A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482625 | ||||||
chr6:138482662
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-9229G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482662 | ||||||
chr6:138482749
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-9316G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482749 | ||||||
chr6:138482771
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.212-9338C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482771 | ||||||
chr6:138482902
|
T | A | 3 | a0001c0001t0001g0221a0001c0001t0014g0222a0001c0002t0003g0003 | 3 | HG02132.hp2 NA18612.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.212-9469A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482902 | ||||||
chr6:138482969
|
A | G | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-9536T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482969 | ||||||
chr6:138483033
|
A | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-9600T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483033 | ||||||
chr6:138483052
|
G | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-9619C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483052 | ||||||
chr6:138483153
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.212-9720C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483153 | ||||||
chr6:138483199
|
C | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-9766G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483199 | ||||||
chr6:138483528
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10095G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483528 | ||||||
chr6:138483544
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10111G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483544 | ||||||
chr6:138483547
|
C | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10114G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483547 | ||||||
chr6:138483630
|
A | T | 24 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | HG01069.hp1 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.212-10197T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483630 | ||||||
chr6:138483631
|
T | C | 1 | a0001c0004t0004g0171 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.212-10198A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483631 | ||||||
chr6:138483638
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10205G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483638 | ||||||
chr6:138483679
|
G | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10246C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483679 | ||||||
chr6:138483686
|
T | C | 1 | a0002c0005t0019g0210 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.212-10253A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483686 | ||||||
chr6:138483736
|
C | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10303G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483736 | ||||||
chr6:138483881
|
G | T | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.212-10448C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483881 | ||||||
chr6:138483928
|
T | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10495A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483928 | ||||||
chr6:138483958
|
T | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10525A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138483958 | ||||||
chr6:138484009
|
C | T | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.212-10576G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484009 | ||||||
chr6:138484105
|
G | A | 1 | a0001c0002t0001g0099 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.212-10672C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484105 | ||||||
chr6:138484186
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.212-10753C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484186 | ||||||
chr6:138484273
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-10840G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484273 | ||||||
chr6:138484526
|
G | A | 1 | a0002c0005t0003g0220 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.212-11093C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484526 | ||||||
chr6:138484593
|
T | G | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.212-11160A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484593 | ||||||
chr6:138484679
|
C | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.212-11246G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484679 | ||||||
chr6:138484679
|
C | T | 13 | a0001c0003t0007g0179a0001c0003t0007g0180a0001c0003t0007g0239others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.212-11246G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484679 | ||||||
chr6:138484711
|
T | C | 1 | a0001c0001t0010g0271 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.212-11278A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484711 | ||||||
chr6:138484853
|
T | C | 1 | a0001c0002t0001g0100 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.211+11366A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484853 | ||||||
chr6:138484936
|
T | C | 2 | a0001c0001t0001g0279a0001c0001t0001g0292 | 2 | NA18965.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.211+11283A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484936 | ||||||
chr6:138484963
|
G | T | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+11256C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484963 | ||||||
chr6:138484964
|
A | T | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+11255T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138484964 | ||||||
chr6:138485167
|
C | G | 1 | a0001c0001t0006g0199 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.211+11052G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485167 | ||||||
chr6:138485174
|
G | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.211+11045C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485174 | ||||||
chr6:138485183
|
C | T | 1 | a0001c0028t0043g0253 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.211+11036G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485183 | ||||||
chr6:138485314
|
A | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | HG02922.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.211+10905T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485314 | ||||||
chr6:138485337
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.211+10882T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485337 | ||||||
chr6:138485446
|
T | TA | 23 | a0001c0001t0001g0064a0001c0001t0001g0084a0001c0001t0001g0293others(20): Show | 23 | HG00099.hp1 HG00642.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.211+10772dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485446 | ||||||
chr6:138485446
|
TA | T | 82 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(79): Show | 83 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.211+10772delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485446 | ||||||
chr6:138485446
|
TAA | T | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01255.hp2 HG01934.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.211+10771_211+1077 others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485446 | ||||||
chr6:138485446
|
TAAAA | T | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+10769_211+1077 others(8): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485446 | ||||||
chr6:138485655
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.211+10564A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485655 | ||||||
chr6:138485669
|
T | C | 1 | a0001c0037t0003g0088 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.211+10550A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485669 | ||||||
chr6:138485670
|
A | C | 3 | a0001c0001t0001g0221a0001c0001t0014g0222a0001c0002t0003g0003 | 3 | HG02132.hp2 NA18612.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.211+10549T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485670 | ||||||
chr6:138485727
|
T | C | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+10492A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485727 | ||||||
chr6:138485733
|
T | C | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+10486A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485733 | ||||||
chr6:138485754
|
G | A | 1 | a0001c0001t0002g0266 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.211+10465C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485754 | ||||||
chr6:138485841
|
TTAA | T | 9 | a0001c0001t0002g0132a0001c0001t0003g0074a0001c0001t0003g0075others(6): Show | 9 | HG00423.hp2 HG00621.hp1 HG03453.hp1 others(6): Show |
intron_variant | MODIFIER | c.211+10375_211+1037 others(7): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485841 | ||||||
chr6:138485894
|
G | A | 1 | a0001c0001t0009g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.211+10325C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485894 | ||||||
chr6:138486012
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.211+10207C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486012 | ||||||
chr6:138486081
|
C | T | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.211+10138G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486081 | ||||||
chr6:138486093
|
C | T | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.211+10126G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486093 | ||||||
chr6:138486144
|
T | C | 138 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(135): Show | 139 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.211+10075A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486144 | ||||||
chr6:138486179
|
C | T | 1 | a0001c0031t0041g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+10040G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486179 | ||||||
chr6:138486235
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.211+9984C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486235 | ||||||
chr6:138486272
|
T | C | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.211+9947A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486272 | ||||||
chr6:138486373
|
T | C | 1 | a0001c0001t0003g0267 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.211+9846A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486373 | ||||||
chr6:138486398
|
C | T | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.211+9821G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486398 | ||||||
chr6:138486418
|
C | T | 6 | a0005c0012t0042g0244a0005c0012t0044g0245a0005c0013t0001g0178others(3): Show | 6 | HG02615.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+9801G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486418 | ||||||
chr6:138486428
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0003g0154 | 2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.211+9791G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486428 | ||||||
chr6:138486440
|
T | C | 29 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0190others(26): Show | 29 | HG00639.hp1 HG01069.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.211+9779A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486440 | ||||||
chr6:138486488
|
A | C | 5 | a0001c0001t0001g0190a0001c0001t0002g0255a0001c0001t0033g0188others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+9731T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486488 | ||||||
chr6:138486591
|
C | G | 5 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0024g0250others(2): Show | 5 | HG01891.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+9628G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486591 | ||||||
chr6:138486768
|
A | G | 26 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0003g0154others(23): Show | 26 | HG00639.hp1 HG02109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.211+9451T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486768 | ||||||
chr6:138486865
|
C | T | 26 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0003g0154others(23): Show | 26 | HG00639.hp1 HG02109.hp2 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.211+9354G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138486865 | ||||||
chr6:138487110
|
C | G | 5 | a0001c0001t0001g0190a0001c0001t0002g0255a0001c0001t0033g0188others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+9109G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487110 | ||||||
chr6:138487110
|
C | T | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.211+9109G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487110 | ||||||
chr6:138487125
|
T | TA | 22 | a0001c0001t0001g0156a0001c0003t0007g0179a0001c0003t0007g0180others(19): Show | 22 | HG00639.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.211+9093dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487125 | ||||||
chr6:138487244
|
T | C | 1 | a0001c0002t0001g0108 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.211+8975A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487244 | ||||||
chr6:138487263
|
C | T | 29 | a0001c0001t0001g0155a0001c0001t0001g0190a0001c0001t0002g0255others(26): Show | 29 | HG00639.hp1 HG01069.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.211+8956G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487263 | ||||||
chr6:138487323
|
T | G | 31 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0190others(28): Show | 31 | HG00639.hp1 HG01069.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.211+8896A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487323 | ||||||
chr6:138487391
|
T | C | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+8828A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487391 | ||||||
chr6:138487698
|
T | C | 54 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(51): Show | 55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.211+8521A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487698 | ||||||
chr6:138487705
|
T | C | 1 | a0001c0031t0041g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+8514A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487705 | ||||||
chr6:138487784
|
C | T | 1 | a0001c0001t0003g0259 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.211+8435G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487784 | ||||||
chr6:138487936
|
C | T | 7 | a0001c0001t0001g0155a0001c0001t0001g0190a0001c0001t0002g0255others(4): Show | 7 | HG01069.hp1 HG01243.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+8283G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138487936 | ||||||
chr6:138488180
|
C | T | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+8039G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138488180 | ||||||
chr6:138488277
|
CAA | C | 26 | a0001c0001t0001g0155a0001c0001t0001g0190a0001c0001t0002g0255others(23): Show | 26 | HG00639.hp1 HG01069.hp1 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.211+7940_211+7941d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138488277 | ||||||
chr6:138488339
|
A | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG01255.hp2 HG01934.hp1 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.211+7880T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138488339 | ||||||
chr6:138488354
|
T | G | 20 | a0001c0003t0007g0179a0001c0003t0007g0180a0001c0003t0007g0239others(17): Show | 20 | HG00639.hp1 HG02109.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.211+7865A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138488354 | ||||||
chr6:138488376
|
G | A | 2 | a0001c0001t0001g0156a0003c0006t0017g0151 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.211+7843C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138488376 | ||||||
chr6:138488560
|
T | C | 4 | a0004c0009t0001g0068a0004c0009t0001g0069a0004c0009t0001g0070others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+7659A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138488560 | ||||||
chr6:138488706
|
T | C | 5 | a0001c0001t0001g0190a0001c0001t0002g0255a0001c0001t0033g0188others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+7513A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138488706 | ||||||
chr6:138489054
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0003g0154 | 2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.211+7165G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489054 | ||||||
chr6:138489068
|
T | C | 1 | a0001c0001t0001g0273 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.211+7151A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489068 | ||||||
chr6:138489390
|
C | T | 27 | a0001c0001t0001g0155a0001c0001t0001g0190a0001c0001t0002g0255others(24): Show | 27 | HG00639.hp1 HG01069.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.211+6829G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489390 | ||||||
chr6:138489731
|
T | C | 29 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0190others(26): Show | 29 | HG00639.hp1 HG01069.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.211+6488A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489731 | ||||||
chr6:138489761
|
C | CA | 28 | a0001c0001t0001g0071a0001c0001t0001g0156a0001c0001t0001g0190others(25): Show | 28 | HG00438.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.211+6457dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489761 | ||||||
chr6:138489761
|
C | CAA | 8 | a0001c0001t0001g0155a0001c0001t0003g0154a0001c0004t0004g0143others(5): Show | 8 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+6456_211+6457d others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489761 | ||||||
chr6:138489761
|
CA | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0215a0001c0001t0001g0279others(5): Show | 8 | HG01168.hp2 HG01884.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.211+6457delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489761 | ||||||
chr6:138489766
|
A | G | 4 | a0001c0001t0001g0193a0001c0001t0001g0247a0001c0001t0002g0266others(1): Show | 4 | HG01496.hp1 HG01943.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+6453T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489766 | ||||||
chr6:138489777
|
A | G | 2 | a0001c0001t0008g0328a0001c0024t0004g0123 | 2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.211+6442T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489777 | ||||||
chr6:138489781
|
GAGAA | G | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(13): Show | 16 | HG00558.hp1 HG01255.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.211+6434_211+6437d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489781 | ||||||
chr6:138489809
|
GGAGAGAG others(21): Show |
G | 4 | a0001c0001t0001g0190a0001c0001t0002g0255a0001c0002t0001g0189others(1): Show | 4 | HG01243.hp1 HG01515.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+6382_211+6409d others(30): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489809 | ||||||
chr6:138489825
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0003g0154 | 2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.211+6394C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489825 | ||||||
chr6:138489825
|
GGAGAGAG others(23): Show |
G | 1 | a0001c0001t0033g0188 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.211+6364_211+6393d others(32): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489825 | ||||||
chr6:138489835
|
AGAGAGAG others(11): Show |
A | 12 | a0001c0003t0007g0179a0001c0003t0007g0180a0001c0003t0007g0239others(9): Show | 12 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.211+6366_211+6383d others(20): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489835 | ||||||
chr6:138489837
|
A | G | 3 | a0001c0001t0001g0155a0001c0001t0003g0154a0003c0006t0017g0151 | 3 | HG03098.hp1 NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.211+6382T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489837 | ||||||
chr6:138489843
|
A | G | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+6376T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489843 | ||||||
chr6:138489845
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01255.hp2 HG01884.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.211+6374C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489845 | ||||||
chr6:138489845
|
GGAGAGAG others(13): Show |
G | 6 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(3): Show | 6 | HG00639.hp1 HG02572.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+6354_211+6373d others(22): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489845 | ||||||
chr6:138489851
|
A | G | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+6368T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489851 | ||||||
chr6:138489853
|
G | A | 2 | a0001c0001t0001g0015a0003c0006t0017g0151 | 2 | HG03098.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.211+6366C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489853 | ||||||
chr6:138489853
|
G | GGAGAGA | 3 | a0001c0001t0001g0072a0001c0001t0001g0167a0001c0001t0034g0168 | 3 | HG01167.hp2 HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.211+6360_211+6365d others(8): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489853 | ||||||
chr6:138489853
|
GGAGAGAG others(5): Show |
G | 4 | a0001c0001t0001g0155a0001c0001t0003g0154a0001c0004t0004g0080others(1): Show | 4 | HG02895.hp1 HG02896.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+6354_211+6365d others(14): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489853 | ||||||
chr6:138489861
|
A | G | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01255.hp2 HG01934.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+6358T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489861 | ||||||
chr6:138489865
|
A | AGAGAGAG others(1): Show |
20 | a0001c0001t0001g0125a0001c0001t0001g0156a0001c0001t0001g0251others(17): Show | 20 | HG02040.hp1 HG02056.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.211+6346_211+6353d others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489865 | ||||||
chr6:138489865
|
A | AGAGAGAG others(9): Show |
2 | a0001c0003t0007g0124a0001c0003t0007g0330 | 2 | HG02622.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.211+6338_211+6353d others(18): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489865 | ||||||
chr6:138489865
|
A | AGAGAGGG others(7): Show |
1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+6353_211+6354i others(16): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489865 | ||||||
chr6:138489865
|
A | G | 13 | a0001c0003t0007g0179a0001c0003t0007g0180a0001c0003t0007g0239others(10): Show | 13 | HG02109.hp2 HG02258.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+6354T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489865 | ||||||
chr6:138489865
|
AGAGAGAG others(1): Show |
A | 7 | a0001c0001t0001g0114a0001c0001t0002g0073a0001c0002t0001g0109others(4): Show | 7 | HG02809.hp2 HG03492.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+6346_211+6353d others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489865 | ||||||
chr6:138489873
|
G | A | 14 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(11): Show | 14 | HG01255.hp2 HG01934.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.211+6346C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489873 | ||||||
chr6:138489896
|
GGGAGAGA others(49): Show |
G | 4 | a0001c0001t0003g0231a0001c0002t0002g0232a0001c0020t0048g0103others(1): Show | 4 | HG01255.hp2 HG01934.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.211+6267_211+6322d others(58): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489896 | ||||||
chr6:138489904
|
GCGAGAGG others(41): Show |
G | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(7): Show | 10 | HG02132.hp2 NA18612.hp1 NA18947.hp2 others(7): Show |
intron_variant | MODIFIER | c.211+6267_211+6314d others(50): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489904 | ||||||
chr6:138489905
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.211+6314G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489905 | ||||||
chr6:138489935
|
G | A | 2 | a0001c0001t0008g0328a0007c0011t0008g0329 | 2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.211+6284C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489935 | ||||||
chr6:138489944
|
GGGAGAGA others(1): Show |
G | 10 | a0001c0001t0001g0155a0001c0001t0001g0190a0001c0001t0002g0255others(7): Show | 10 | HG01069.hp1 HG01243.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.211+6267_211+6274d others(10): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489944 | ||||||
chr6:138489951
|
A | G | 1 | a0001c0001t0008g0328 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.211+6268T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489951 | ||||||
chr6:138489952
|
A | G | 106 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0023others(103): Show | 107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.211+6267T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489952 | ||||||
chr6:138489959
|
A | G | 23 | a0001c0001t0008g0328a0001c0003t0007g0179a0001c0003t0007g0180others(20): Show | 23 | HG00639.hp1 HG00738.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.211+6260T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489959 | ||||||
chr6:138489985
|
G | GGAGAGGG others(3): Show |
1 | a0007c0011t0008g0329 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.211+6233_211+6234i others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489985 | ||||||
chr6:138489985
|
GGAGA | G | 7 | a0001c0001t0001g0156a0001c0001t0001g0251a0001c0001t0001g0252others(4): Show | 7 | HG02622.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+6230_211+6233d others(6): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489985 | ||||||
chr6:138490066
|
T | C | 1 | a0001c0007t0020g0148 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.211+6153A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490066 | ||||||
chr6:138490150
|
A | C | 5 | a0001c0001t0001g0190a0001c0001t0002g0255a0001c0001t0033g0188others(2): Show | 5 | HG01069.hp1 HG01243.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+6069T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490150 | ||||||
chr6:138490191
|
C | T | 40 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(37): Show | 40 | HG00639.hp1 HG01255.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.211+6028G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490191 | ||||||
chr6:138490288
|
T | C | 1 | a0001c0001t0003g0164 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.211+5931A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490288 | ||||||
chr6:138490364
|
C | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(12): Show | 15 | HG01255.hp2 HG01934.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.211+5855G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490364 | ||||||
chr6:138490371
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0029g0117 | 2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.211+5848C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490371 | ||||||
chr6:138490376
|
A | G | 1 | a0003c0006t0017g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+5843T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490376 | ||||||
chr6:138490498
|
T | C | 6 | a0001c0001t0005g0295a0001c0008t0008g0076a0001c0008t0008g0078others(3): Show | 6 | NA18947.hp1 NA18954.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.211+5721A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490498 | ||||||
chr6:138490591
|
T | C | 2 | a0001c0001t0018g0141a0001c0017t0001g0142 | 2 | HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.211+5628A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490591 | ||||||
chr6:138490761
|
A | T | 325 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(322): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.211+5458T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490761 | ||||||
chr6:138490846
|
A | C | 3 | a0001c0001t0001g0121a0001c0001t0003g0011a0001c0001t0003g0203 | 3 | HG02559.hp1 HG04115.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.211+5373T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490846 | ||||||
chr6:138490851
|
A | C | 7 | a0001c0001t0001g0155a0001c0001t0003g0154a0001c0001t0008g0328others(4): Show | 7 | HG02486.hp2 HG02615.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.211+5368T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490851 | ||||||
chr6:138490854
|
T | G | 1 | a0001c0002t0001g0296 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.211+5365A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490854 | ||||||
chr6:138490891
|
C | A | 2 | a0001c0001t0001g0155a0001c0001t0003g0154 | 2 | NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.211+5328G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490891 | ||||||
chr6:138490912
|
G | A | 50 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0185others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.211+5307C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490912 | ||||||
chr6:138490964
|
T | C | 4 | a0001c0001t0029g0117a0001c0002t0005g0118a0001c0004t0002g0115others(1): Show | 4 | HG00741.hp2 HG01081.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+5255A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138490964 | ||||||
chr6:138491063
|
A | C | 3 | a0001c0004t0004g0080a0001c0004t0004g0081a0003c0033t0005g0236 | 3 | HG02559.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.211+5156T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491063 | ||||||
chr6:138491111
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | NA18991.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.211+5108C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491111 | ||||||
chr6:138491248
|
C | T | 1 | a0003c0006t0017g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+4971G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491248 | ||||||
chr6:138491270
|
C | T | 1 | a0003c0006t0017g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+4949G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491270 | ||||||
chr6:138491336
|
C | G | 7 | a0001c0004t0004g0143a0001c0004t0004g0144a0001c0004t0011g0152others(4): Show | 7 | HG00639.hp1 HG01884.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.211+4883G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491336 | ||||||
chr6:138491393
|
A | G | 309 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(306): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.211+4826T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491393 | ||||||
chr6:138491480
|
G | T | 298 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(295): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.211+4739C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491480 | ||||||
chr6:138491501
|
T | C | 1 | a0016c0026t0037g0327 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.211+4718A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491501 | ||||||
chr6:138491590
|
A | G | 1 | a0001c0001t0004g0186 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.211+4629T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491590 | ||||||
chr6:138491682
|
G | T | 4 | a0001c0001t0001g0190a0001c0001t0033g0188a0001c0002t0001g0189others(1): Show | 4 | HG01069.hp1 HG01515.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+4537C>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491682 | ||||||
chr6:138491692
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.211+4527A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491692 | ||||||
chr6:138491698
|
T | C | 3 | a0001c0008t0008g0076a0001c0008t0008g0078a0001c0008t0046g0077 | 3 | NA18947.hp1 NA18954.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.211+4521A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491698 | ||||||
chr6:138491744
|
A | G | 3 | a0001c0001t0006g0264a0001c0001t0006g0265a0002c0005t0001g0263 | 3 | HG02040.hp2 NA18942.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.211+4475T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491744 | ||||||
chr6:138492034
|
T | C | 316 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.211+4185A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492034 | ||||||
chr6:138492204
|
C | G | 22 | a0001c0001t0001g0169a0001c0001t0001g0251a0001c0001t0001g0252others(19): Show | 22 | HG00738.hp1 HG00741.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.211+4015G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492204 | ||||||
chr6:138492340
|
C | T | 5 | a0001c0003t0007g0323a0001c0004t0002g0326a0001c0015t0001g0325others(2): Show | 5 | HG00738.hp1 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.211+3879G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492340 | ||||||
chr6:138492381
|
C | G | 11 | a0001c0003t0007g0239a0001c0003t0021g0240a0001c0004t0030g0241others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.211+3838G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492381 | ||||||
chr6:138492427
|
G | A | 4 | a0001c0001t0029g0117a0001c0002t0005g0118a0001c0004t0002g0115others(1): Show | 4 | HG00741.hp2 HG01081.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3792C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492427 | ||||||
chr6:138492659
|
A | C | 4 | a0001c0001t0029g0117a0001c0002t0005g0118a0001c0004t0002g0115others(1): Show | 4 | HG00741.hp2 HG01081.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+3560T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492659 | ||||||
chr6:138492992
|
A | AT | 149 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0150others(146): Show | 150 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.211+3226dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492992 | ||||||
chr6:138493051
|
A | G | 16 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0008g0328others(13): Show | 16 | HG00738.hp1 HG02055.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.211+3168T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493051 | ||||||
chr6:138493099
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.211+3120A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493099 | ||||||
chr6:138493126
|
G | A | 1 | a0001c0010t0016g0308 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.211+3093C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493126 | ||||||
chr6:138493174
|
A | T | 316 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(313): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.211+3045T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493174 | ||||||
chr6:138493186
|
T | C | 1 | a0001c0001t0013g0214 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.211+3033A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493186 | ||||||
chr6:138493280
|
T | C | 110 | a0001c0001t0001g0185a0001c0001t0001g0190a0001c0001t0001g0192others(107): Show | 111 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.211+2939A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493280 | ||||||
chr6:138493591
|
C | T | 3 | a0001c0002t0002g0318a0001c0002t0010g0320a0001c0002t0023g0319 | 3 | HG01106.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.211+2628G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493591 | ||||||
chr6:138493700
|
A | G | 1 | a0001c0001t0003g0011 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.211+2519T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493700 | ||||||
chr6:138493761
|
A | G | 13 | a0001c0001t0001g0167a0001c0001t0001g0235a0001c0001t0002g0158others(10): Show | 13 | HG00597.hp2 HG00673.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+2458T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493761 | ||||||
chr6:138493892
|
C | T | 1 | a0001c0002t0001g0172 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.211+2327G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493892 | ||||||
chr6:138493976
|
C | T | 13 | a0001c0001t0001g0167a0001c0001t0001g0235a0001c0001t0002g0158others(10): Show | 13 | HG00597.hp2 HG00673.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+2243G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138493976 | ||||||
chr6:138494192
|
C | T | 2 | a0001c0003t0007g0170a0001c0004t0004g0171 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.211+2027G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138494192 | ||||||
chr6:138494521
|
C | T | 2 | a0001c0003t0007g0179a0001c0003t0007g0180 | 2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.211+1698G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138494521 | ||||||
chr6:138494779
|
G | A | 12 | a0001c0001t0001g0167a0001c0001t0001g0235a0001c0001t0002g0158others(9): Show | 12 | HG00597.hp2 HG01167.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.211+1440C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138494779 | ||||||
chr6:138494870
|
C | A | 4 | a0001c0001t0029g0117a0001c0002t0005g0118a0001c0004t0002g0115others(1): Show | 4 | HG00741.hp2 HG01081.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.211+1349G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138494870 | ||||||
chr6:138494969
|
G | A | 1 | a0001c0031t0041g0149 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.211+1250C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138494969 | ||||||
chr6:138495023
|
A | C | 1 | a0001c0001t0003g0262 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.211+1196T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495023 | ||||||
chr6:138495141
|
G | A | 3 | a0001c0002t0001g0172a0001c0003t0007g0170a0001c0004t0004g0171 | 3 | HG03704.hp1 NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.211+1078C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495141 | ||||||
chr6:138495482
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.211+737T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495482 | ||||||
chr6:138495515
|
G | C | 20 | a0001c0001t0001g0208a0001c0001t0001g0215a0001c0001t0002g0209others(17): Show | 21 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(18): Show |
intron_variant | MODIFIER | c.211+704C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495515 | ||||||
chr6:138495759
|
A | G | 13 | a0001c0001t0001g0167a0001c0001t0001g0235a0001c0001t0002g0158others(10): Show | 13 | HG00597.hp2 HG00673.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.211+460T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495759 | ||||||
chr6:138495810
|
C | T | 1 | a0001c0001t0001g0224 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.211+409G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495810 | ||||||
chr6:138495830
|
T | C | 145 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(142): Show | 145 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.211+389A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495830 | ||||||
chr6:138495851
|
C | T | 8 | a0001c0002t0001g0172a0001c0003t0007g0170a0001c0003t0040g0173others(5): Show | 8 | HG02572.hp1 HG02615.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.211+368G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495851 | ||||||
chr6:138495879
|
G | C | 6 | a0001c0003t0040g0173a0003c0006t0017g0177a0005c0013t0001g0178others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.211+340C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495879 | ||||||
chr6:138495917
|
T | A | 1 | a0003c0006t0017g0151 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.211+302A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495917 | ||||||
chr6:138495926
|
T | A | 1 | a0001c0001t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.211+293A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495926 | ||||||
chr6:138495936
|
T | C | 317 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(314): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.211+283A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495936 | ||||||
chr6:138495959
|
G | A | 3 | a0001c0001t0001g0309a0001c0001t0001g0311a0001c0007t0001g0310 | 3 | HG01074.hp2 HG01168.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.211+260C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495959 | ||||||
chr6:138495968
|
T | C | 64 | a0001c0001t0001g0247a0001c0001t0001g0261a0001c0001t0001g0268others(61): Show | 64 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.211+251A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138495968 | ||||||
chr6:138496007
|
G | A | 2 | a0001c0001t0004g0186a0001c0001t0009g0187 | 2 | HG00735.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.211+212C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138496007 | ||||||
chr6:138496095
|
G | A | 1 | a0001c0004t0011g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.211+124C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138496095 | ||||||
chr6:138496197
|
C | A | 3 | a0001c0001t0001g0153a0001c0001t0001g0155a0001c0001t0003g0154 | 3 | HG02129.hp2 NA18959.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.211+22G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138496197 | ||||||
chr6:138496804
|
C | G | 1 | a0001c0001t0002g0257 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.59-433G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138496804 | ||||||
chr6:138496839
|
ATTAT | A | 6 | a0001c0001t0001g0215a0002c0005t0001g0216a0002c0005t0001g0217others(3): Show | 6 | NA18960.hp2 NA18971.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-472_59-469delAT others(2): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138496839 | ||||||
chr6:138496893
|
C | T | 24 | a0001c0001t0001g0156a0001c0001t0001g0167a0001c0001t0001g0235others(21): Show | 24 | HG00597.hp2 HG01167.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.59-522G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138496893 | ||||||
chr6:138496946
|
T | C | 4 | a0001c0002t0001g0109a0001c0002t0002g0110a0001c0002t0002g0111others(1): Show | 4 | NA18959.hp2 NA18971.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-575A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138496946 | ||||||
chr6:138496946
|
T | G | 2 | a0008c0018t0002g0312a0008c0018t0002g0313 | 2 | HG02683.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.59-575A>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138496946 | ||||||
chr6:138497049
|
G | A | 317 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(314): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.59-678C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497049 | ||||||
chr6:138497173
|
C | T | 11 | a0001c0001t0001g0185a0001c0001t0002g0255a0001c0001t0004g0186others(8): Show | 11 | HG00735.hp2 HG00741.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-802G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497173 | ||||||
chr6:138497200
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C | T | 4 | a0001c0001t0001g0221a0001c0001t0002g0223a0001c0001t0014g0222others(1): Show | 4 | HG02132.hp2 NA18612.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-829G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497200 | ||||||
chr6:138497402
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G | A | 1 | a0001c0001t0003g0079 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.59-1031C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497402 | ||||||
chr6:138497464
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G | A | 24 | a0001c0001t0001g0167a0001c0001t0001g0235a0001c0001t0002g0158others(21): Show | 24 | HG00597.hp2 HG00673.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.59-1093C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497464 | ||||||
chr6:138497700
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A | G | 174 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0150others(171): Show | 175 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.59-1329T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497700 | ||||||
chr6:138498032
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AACTATCA others(5): Show |
A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | NA18991.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.58+1189_58+1200del others(12): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498032 | ||||||
chr6:138498049
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C | G | 3 | a0001c0001t0008g0328a0001c0003t0007g0330a0007c0011t0008g0329 | 3 | HG02486.hp2 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.58+1184G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498049 | ||||||
chr6:138498173
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G | A | 4 | a0001c0001t0029g0117a0001c0002t0005g0118a0001c0004t0002g0115others(1): Show | 4 | HG00741.hp2 HG01081.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+1060C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498173 | ||||||
chr6:138498193
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G | A | 1 | a0006c0019t0038g0246 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.58+1040C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498193 | ||||||
chr6:138498359
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G | C | 4 | a0001c0003t0021g0083a0001c0004t0004g0080a0001c0004t0004g0081others(1): Show | 4 | HG02895.hp1 HG02896.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+874C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498359 | ||||||
chr6:138498373
|
C | T | 154 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0150others(151): Show | 155 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.58+860G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498373 | ||||||
chr6:138498474
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C | T | 2 | a0001c0003t0007g0170a0001c0004t0004g0171 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.58+759G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498474 | ||||||
chr6:138498513
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A | G | 9 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0024g0250others(6): Show | 9 | HG01891.hp2 HG02258.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+720T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498513 | ||||||
chr6:138498648
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C | A | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.58+585G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498648 | ||||||
chr6:138498712
|
G | C | 3 | a0001c0001t0008g0328a0001c0003t0007g0330a0007c0011t0008g0329 | 3 | HG02486.hp2 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.58+521C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498712 | ||||||
chr6:138498730
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C | T | 4 | a0001c0001t0029g0117a0001c0002t0005g0118a0001c0004t0002g0115others(1): Show | 4 | HG00741.hp2 HG01081.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.58+503G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498730 | ||||||
chr6:138498858
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A | G | 1 | a0001c0007t0001g0248 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.58+375T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498858 | ||||||
chr6:138498999
|
T | C | 1 | a0001c0001t0002g0316 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+234A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498999 | ||||||
chr6:138499039
|
C | T | 1 | a0001c0001t0001g0247 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.58+194G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499039 | ||||||
chr6:138499134
|
G | GAC | 73 | a0001c0001t0001g0247a0001c0001t0001g0251a0001c0001t0001g0252others(70): Show | 73 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.58+97_58+98dupGT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499134 | ||||||
chr6:138499134
|
G | GACAC | 6 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0002t0001g0317others(3): Show | 6 | HG01106.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+95_58+98dupGTGT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499134 | ||||||
chr6:138499134
|
GAC | G | 9 | a0001c0002t0001g0172a0001c0003t0007g0170a0001c0003t0040g0173others(6): Show | 9 | HG02572.hp1 HG02615.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+97_58+98delGT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499134 | ||||||
chr6:138499134
|
GACAC | G | 59 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0150others(56): Show | 59 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.58+95_58+98delGTGT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499134 | ||||||
chr6:138499152
|
CACACACA others(1): Show |
C | 73 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(70): Show | 73 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.58+73_58+80delCTGT others(4): Show |
NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499152 | ||||||
chr6:138499156
|
CACAG | C | 37 | a0001c0001t0001g0084a0001c0001t0001g0086a0001c0001t0001g0087others(34): Show | 37 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.58+73_58+76delCTGT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499156 | ||||||
chr6:138499160
|
G | C | 3 | a0001c0001t0008g0328a0001c0003t0007g0330a0007c0011t0008g0329 | 3 | HG02486.hp2 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.58+73C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499160 | ||||||
chr6:138499187
|
A | G | 108 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(105): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.58+46T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499187 | ||||||
chr6:138499223
|
A | G | 4 | a0001c0004t0009g0004a0001c0004t0028g0005a0001c0030t0025g0006others(1): Show | 4 | HG02109.hp1 NA18522.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+10T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499223 | ||||||
chr6:138499224
|
A | G | 1 | a0001c0002t0003g0003 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.58+9T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138499224 |