Item | Value |
---|---|
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 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0002 | 0/0 | 1606 | 11 | 0 | 0 | 11 | 0 | 0 | 10 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0003 | 0/0 | 1606 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0004 | 0/0 | 1606 | 4 | 0 | 3 | 1 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0005 | 0/0 | 1606 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0006 | 0/0 | 1606 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0007 | 0/0 | 1606 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0008 | 0/0 | 1606 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0009 | 0/0 | 1606 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0010 | 0/0 | 1606 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0011 | 0/0 | 1606 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0012 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0013 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0014 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0015 | 0/0 | 1606 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0016 | 0/0 | 1606 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0017 | 0/0 | 1606 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
a0018 | 0/0 | 1606 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | MVVFI others(1601): Show |
chr6 | 138417043 | 138504494 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4818 | 179 | 20 | 33 | 102 | 4 | 19 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0002 | 1/0 | 4818 | 37 | 2 | 16 | 11 | 2 | 5 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0003 | 0/0 | 4818 | 19 | 15 | 3 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0004 | 0/0 | 4818 | 16 | 13 | 3 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0007 | 0/0 | 4818 | 6 | 3 | 1 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0008 | 0/0 | 4818 | 5 | 0 | 0 | 5 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0010 | 0/0 | 4818 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0015 | 0/0 | 4818 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0016 | 0/0 | 4818 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0017 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0020 | 0/0 | 4818 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0021 | 0/0 | 4818 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0024 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0028 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0029 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0030 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0031 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0034 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0037 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0039 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0041 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0001c0042 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0002c0005 | 0/0 | 4818 | 11 | 0 | 0 | 11 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0003c0006 | 0/0 | 4818 | 8 | 8 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0003c0033 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0004c0009 | 0/0 | 4818 | 4 | 0 | 3 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0005c0012 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0005c0013 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0006c0019 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0006c0038 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0007c0011 | 0/0 | 4818 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0008c0018 | 0/0 | 4818 | 2 | 0 | 0 | 0 | 0 | 2 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0009c0014 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0010c0032 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0011c0022 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0012c0026 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0013c0025 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0014c0023 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0015c0036 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0016c0040 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0017c0027 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
chr6 | 138417043 | 138504494 | ||
a0018c0035 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | ATGGT others(4813): Show |
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 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0002 | 0/0 | 7065 | 21 | 3 | 5 | 7 | 2 | 4 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0003 | 0/0 | 7064 | 30 | 2 | 4 | 22 | 1 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0004 | 0/0 | 7061 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0005 | 0/0 | 7065 | 5 | 0 | 0 | 5 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0006 | 0/0 | 7065 | 13 | 0 | 1 | 9 | 0 | 3 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0008 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0009 | 0/0 | 7066 | 4 | 1 | 2 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0010 | 0/0 | 7063 | 3 | 1 | 1 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0012 | 0/0 | 7066 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0013 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0014 | 0/0 | 7064 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0015 | 0/0 | 7065 | 2 | 0 | 0 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0018 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7054): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0019 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0024 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0027 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0029 | 0/0 | 7060 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7055): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0032 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0033 | 0/0 | 7063 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0034 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0035 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0036 | 0/0 | 7066 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0045 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7054): Show |
chr6 | 138417043 | 138504494 |
a0001c0001t0051 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0001 | 0/0 | 7064 | 20 | 2 | 6 | 5 | 2 | 5 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0002 | 0/0 | 7065 | 8 | 0 | 4 | 4 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0003 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0005 | 0/0 | 7065 | 2 | 0 | 1 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0009 | 0/0 | 7066 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0010 | 1/0 | 7063 | 2 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0023 | 0/0 | 7062 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0001c0002t0026 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0003t0004 | 0/0 | 7061 | 4 | 0 | 3 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0001c0003t0007 | 0/0 | 7062 | 12 | 12 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0001c0003t0021 | 0/0 | 7063 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0003t0040 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0001c0004t0002 | 0/0 | 7065 | 4 | 3 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0004t0004 | 0/0 | 7061 | 7 | 5 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0001c0004t0009 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0001c0004t0011 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0004t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0001c0004t0028 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0004t0030 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0001c0007t0001 | 0/0 | 7064 | 3 | 0 | 1 | 2 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0007t0011 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0007t0020 | 0/0 | 7074 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7069): Show |
chr6 | 138417043 | 138504494 |
a0001c0008t0008 | 0/0 | 7062 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0001c0008t0011 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0008t0046 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0010t0016 | 0/0 | 7063 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0015t0001 | 0/0 | 7064 | 2 | 1 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0016t0001 | 0/0 | 7064 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0016t0003 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0017t0001 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0017t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0001c0020t0048 | 0/0 | 7075 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7070): Show |
chr6 | 138417043 | 138504494 |
a0001c0020t0049 | 0/0 | 7076 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7071): Show |
chr6 | 138417043 | 138504494 |
a0001c0021t0001 | 0/0 | 7064 | 2 | 0 | 2 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0024t0004 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0001c0028t0043 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0029t0047 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0030t0025 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0031t0041 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0001c0034t0031 | 0/0 | 7076 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7071): Show |
chr6 | 138417043 | 138504494 |
a0001c0037t0003 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0001c0039t0018 | 0/0 | 7059 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7054): Show |
chr6 | 138417043 | 138504494 |
a0001c0041t0008 | 0/0 | 7062 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0001c0042t0011 | 0/0 | 7063 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0002c0005t0001 | 0/0 | 7064 | 6 | 0 | 0 | 6 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0002c0005t0002 | 0/0 | 7065 | 3 | 0 | 0 | 3 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0002c0005t0003 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0002c0005t0019 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0003c0006t0005 | 0/0 | 7065 | 5 | 5 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0003c0006t0012 | 0/0 | 7066 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7061): Show |
chr6 | 138417043 | 138504494 |
a0003c0006t0017 | 0/0 | 7064 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0003c0033t0005 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0004c0009t0001 | 0/0 | 7064 | 3 | 0 | 3 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0004c0009t0015 | 0/0 | 7065 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0005c0012t0042 | 0/0 | 7061 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0005c0012t0044 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0005c0013t0001 | 0/0 | 7064 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0005c0013t0011 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0006c0019t0038 | 0/0 | 7076 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7071): Show |
chr6 | 138417043 | 138504494 |
a0006c0019t0039 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7072): Show |
chr6 | 138417043 | 138504494 |
a0006c0038t0050 | 0/0 | 7077 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7072): Show |
chr6 | 138417043 | 138504494 |
a0007c0011t0008 | 0/0 | 7062 | 3 | 3 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0008c0018t0002 | 0/0 | 7065 | 2 | 0 | 0 | 0 | 0 | 2 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0009c0014t0008 | 0/0 | 7062 | 2 | 2 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7057): Show |
chr6 | 138417043 | 138504494 |
a0010c0032t0001 | 0/0 | 7064 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
a0011c0022t0004 | 0/0 | 7061 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0012c0026t0037 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0013c0025t0013 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0014c0023t0002 | 0/0 | 7065 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7060): Show |
chr6 | 138417043 | 138504494 |
a0015c0036t0013 | 0/0 | 7063 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0016c0040t0010 | 0/0 | 7063 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7058): Show |
chr6 | 138417043 | 138504494 |
a0017c0027t0022 | 0/0 | 7061 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7056): Show |
chr6 | 138417043 | 138504494 |
a0018c0035t0001 | 0/0 | 7064 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | AGGTT others(7059): Show |
chr6 | 138417043 | 138504494 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0041 | 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 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0310 | 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 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0202 | 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 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0002g0324 | 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 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0199 | 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 |
a0001c0001t0003g0264 | 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 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0003g0274 | 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 |
a0001c0001t0003g0283 | 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 |
a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0200 | 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 |
a0001c0001t0006g0228 | 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 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0006g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0008g0321 | 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 |
a0001c0001t0009g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0009g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0010g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0010g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0012g0159 | 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 |
a0001c0001t0014g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0015g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0015g0279 | 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 |
a0001c0001t0019g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0024g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0027g0254 | 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 |
a0001c0001t0032g0229 | 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 |
a0001c0001t0036g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0001t0045g0130 | 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 |
a0001c0002t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0158 | 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 |
a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0002g0134 | 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 |
a0001c0002t0002g0326 | 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 |
a0001c0002t0005g0057 | 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 |
a0001c0002t0009g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0009g0093 | 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 |
a0001c0002t0010g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0023g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0002t0026g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0004g0032 | 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 |
a0001c0003t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0161 | 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 |
a0001c0003t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0007g0259 | 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 |
a0001c0003t0021g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0021g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0003t0040g0177 | 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 |
a0001c0004t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0004t0004g0140 | 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 |
a0001c0004t0030g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0011g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0007t0020g0138 | 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 |
a0001c0008t0008g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0008t0008g0109 | 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 |
a0001c0008t0046g0108 | 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 |
a0001c0010t0016g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0010t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0015t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0015t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0016t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0016t0003g0083 | 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 |
a0001c0020t0048g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0020t0049g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0021t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0021t0001g0305 | 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 |
a0001c0028t0043g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0029t0047g0235 | 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 |
a0001c0034t0031g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0037t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0039t0018g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0001c0041t0008g0136 | 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 |
a0002c0005t0001g0074 | 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 |
a0002c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0002c0005t0002g0078 | 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 |
a0003c0006t0005g0132 | 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 |
a0003c0006t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0006t0012g0113 | 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 |
a0003c0006t0017g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0003c0033t0005g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0004c0009t0015g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0005c0012t0042g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0005c0012t0044g0250 | 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 |
a0006c0019t0038g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0006c0019t0039g0248 | 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 |
a0007c0011t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0007c0011t0008g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0008c0018t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0008c0018t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0009c0014t0008g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
a0010c0032t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0011c0022t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0012c0026t0037g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0013c0025t0013g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0014c0023t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0015c0036t0013g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0016c0040t0010g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0017c0027t0022g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
a0018c0035t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | g0262 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0070 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00140 | hp1 | a0001 | c0002 | t0001 | g0034 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0275 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00423 | hp1 | a0010 | c0032 | t0001 | g0196 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0134 | 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 | g0081 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0008 | 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 | g0074 | 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 | g0131 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0073 | 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 | g0084 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0092 | 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 | g0236 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0022 | 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 | g0051 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01074 | hp2 | a0001 | c0007 | t0001 | g0315 | 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 | g0310 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0276 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01106 | hp1 | a0001 | c0002 | t0002 | g0326 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01106 | hp2 | a0001 | c0004 | t0004 | g0127 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01167 | hp1 | a0001 | c0002 | t0023 | g0327 | 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 | g0284 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01169 | hp1 | a0001 | c0001 | t0010 | g0288 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01169 | hp2 | a0001 | c0002 | t0010 | g0328 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01192 | hp1 | a0011 | c0022 | t0004 | g0002 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0308 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0260 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0309 | AMR | PUR | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01255 | hp1 | a0001 | c0002 | t0026 | g0261 | 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 | g0102 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01258 | hp1 | a0001 | c0021 | t0001 | g0305 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01258 | hp2 | a0004 | c0009 | t0001 | g0100 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01261 | hp1 | a0001 | c0002 | t0001 | g0097 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01261 | hp2 | a0001 | c0002 | t0001 | g0013 | 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 | g0302 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01361 | hp1 | a0004 | c0009 | t0001 | g0101 | AMR | CLM | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0068 | 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 | g0087 | 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 | g0052 | 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 | g0325 | 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 | g0137 | 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 | g0030 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01943 | hp1 | a0001 | c0003 | t0004 | g0032 | 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 | g0049 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01978 | hp2 | a0001 | c0002 | t0009 | g0093 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0015 | 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 | g0047 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0057 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02040 | hp1 | a0001 | c0001 | t0014 | g0277 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02040 | hp2 | a0001 | c0001 | t0006 | g0268 | 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 | g0235 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02056 | hp2 | a0001 | c0001 | t0015 | g0279 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0025 | 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 | g0019 | EAS | KHV | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0103 | 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 | g0010 | 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 | g0094 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02148 | hp2 | a0001 | c0020 | t0049 | g0031 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | CDX | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02257 | hp1 | a0001 | c0007 | t0020 | g0138 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0069 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02258 | hp1 | a0001 | c0001 | t0045 | g0130 | 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 | g0239 | AMR | PEL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0283 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02300 | hp1 | a0001 | c0016 | t0001 | g0085 | 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 | g0176 | 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 | g0278 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02615 | hp1 | a0012 | c0026 | t0037 | g0238 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02615 | hp2 | a0013 | c0025 | t0013 | g0173 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02622 | hp1 | a0001 | c0003 | t0007 | g0323 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02622 | hp2 | a0006 | c0019 | t0039 | g0248 | 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 | g0140 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02647 | hp1 | a0001 | c0003 | t0007 | g0161 | 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 | g0317 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0054 | 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 | g0035 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02723 | hp1 | a0001 | c0003 | t0007 | g0128 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02723 | hp2 | a0001 | c0028 | t0043 | g0258 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02809 | hp1 | a0001 | c0015 | t0001 | g0129 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02809 | hp2 | a0001 | c0010 | t0016 | g0313 | 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 | g0292 | 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 | g0112 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02895 | hp2 | a0005 | c0012 | t0044 | g0250 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02896 | hp1 | a0001 | c0001 | t0024 | g0255 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02896 | hp2 | a0001 | c0004 | t0004 | g0111 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02897 | hp1 | a0001 | c0001 | t0027 | g0254 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02897 | hp2 | a0005 | c0012 | t0042 | g0249 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02922 | hp1 | a0001 | c0004 | t0030 | g0246 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0257 | 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 | g0243 | 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 | g0174 | 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 | g0295 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03041 | hp2 | a0014 | c0023 | t0002 | g0263 | 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 | g0195 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03130 | hp1 | a0009 | c0014 | t0008 | g0175 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03130 | hp2 | a0001 | c0003 | t0007 | g0163 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03139 | hp1 | a0001 | c0003 | t0007 | g0234 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03139 | hp2 | a0001 | c0003 | t0007 | g0259 | AFR | ESN | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03195 | hp1 | a0003 | c0006 | t0005 | g0286 | 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 | g0126 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03209 | hp2 | a0001 | c0004 | t0002 | g0237 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03453 | hp1 | a0001 | c0003 | t0021 | g0114 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03453 | hp2 | a0001 | c0003 | t0021 | g0245 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03486 | hp1 | a0001 | c0003 | t0007 | g0244 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0016 | 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 | g0296 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0301 | AFR | GWD | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03579 | hp1 | a0007 | c0011 | t0008 | g0133 | 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 | g0298 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0028 | SAS | PJL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0027 | 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 | g0023 | 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 | g0303 | 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 | g0077 | SAS | BEB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0285 | SAS | BEB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0159 | SAS | STU | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0271 | 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 | g0136 | 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 | g0273 | EAS | CHB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18906 | hp1 | a0003 | c0006 | t0012 | g0113 | 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 | g0280 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18942 | hp2 | a0002 | c0005 | t0001 | g0270 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18947 | hp1 | a0001 | c0008 | t0008 | g0109 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18954 | hp2 | a0001 | c0008 | t0046 | g0108 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18957 | hp2 | a0001 | c0007 | t0001 | g0160 | 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 | g0039 | 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 | g0044 | 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 | g0107 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18968 | hp1 | a0001 | c0001 | t0005 | g0291 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18968 | hp2 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0199 | 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 | g0078 | 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 | g0036 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18974 | hp1 | a0001 | c0001 | t0009 | g0198 | 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 | g0063 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18978 | hp1 | a0001 | c0007 | t0001 | g0253 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18979 | hp1 | a0001 | c0001 | t0015 | g0061 | 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 | g0086 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18982 | hp1 | a0001 | c0002 | t0002 | g0037 | 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 | g0274 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0329 | 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 | g0088 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0038 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0090 | 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 | g0229 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18998 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18998 | hp2 | a0001 | c0001 | t0019 | g0072 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0065 | 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 | g0267 | 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 | g0106 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19005 | hp2 | a0001 | c0001 | t0005 | g0055 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19006 | hp1 | a0001 | c0001 | t0036 | g0075 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19006 | hp2 | a0004 | c0009 | t0015 | g0099 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0158 | 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 | g0230 | 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 | g0242 | 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 | g0297 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19068 | hp1 | a0001 | c0001 | t0006 | g0269 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0202 | 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 | g0287 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19077 | hp2 | a0001 | c0001 | t0006 | g0082 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19081 | hp1 | a0001 | c0001 | t0006 | g0228 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19081 | hp2 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19082 | hp1 | a0001 | c0001 | t0006 | g0200 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0046 | 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 | g0330 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0011 | 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 | g0307 | 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 | g0045 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0265 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19091 | hp2 | a0015 | c0036 | t0013 | g0289 | EAS | JPT | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19240 | hp1 | a0001 | c0004 | t0002 | g0139 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA19240 | hp2 | a0006 | c0019 | t0038 | g0251 | AFR | YRI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20129 | hp1 | a0016 | 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 | a0017 | c0027 | t0022 | g0020 | 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 | g0009 | EUR | TSI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20805 | hp2 | a0018 | c0035 | t0001 | g0282 | EUR | TSI | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | GIH | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20905 | hp2 | a0008 | c0018 | t0002 | g0318 | 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 | g0247 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0290 | AFR | ACB | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0321 | 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 | g0241 | 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 | g0322 | AFR | MSL | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG06807 | hp1 | a0001 | c0003 | t0040 | g0177 | AFR | USA | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
HG06807 | hp2 | a0003 | c0006 | t0005 | g0132 | AFR | USA | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20300 | hp1 | a0001 | c0016 | t0003 | g0083 | AFR | USA | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0135 | 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 | a0001 | c0001 | t0001 | g0252 | REF | REF | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
homoSapiens | grch38p0 | a0001 | c0002 | t0010 | g0233 | REF | REF | NHSL1_chr6_138417043_138504494 | NHSL1 | chr6 | 138417043 | 138504494 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138424158 | G | C | 2 | a0006 a0012 |
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 | a0003 a0013 |
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 | a0012 | 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 | a0018 | 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 | a0018 | 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 | a0015 | 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 | a0014 | 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 | a0010 | 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 | a0015 | 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 | a0017 | 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 | a0016 | 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 | a0012 | 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 | a0007 a0009 |
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 | a0005 a0009 a0013 |
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 | a0011 | 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 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138424162 | G | A | 8 | a0001c0003 a0001c0004 a0001c0008 others(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 | a0001c0016 a0001c0037 |
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 | a0001c0020 a0001c0034 |
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 | a0001c0015 a0001c0024 a0001c0028 others(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 | a0001c0001 a0001c0004 a0001c0016 others(17): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): 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 | a0001c0030 a0001c0031 a0001c0042 |
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 | a0001c0015 a0001c0024 a0001c0028 others(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 | a0001c0001 a0001c0003 a0001c0004 others(35): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): 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 | a0003c0006 a0013c0025 |
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 | a0014c0023 | 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 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138422055 | T | C | 2 | a0005c0012t0042 a0005c0012t0044 |
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 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0024 others(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 | a0001c0001t0034 a0001c0002t0026 |
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 | a0001c0007t0020 a0001c0028t0043 a0005c0012t0042 others(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 | a0001c0001t0019 a0001c0010t0016 a0001c0020t0048 others(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 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): 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 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0015 others(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 | a0001c0007t0020 a0001c0020t0048 a0001c0020t0049 others(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 | a0001c0020t0048 a0001c0020t0049 a0001c0034t0031 |
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 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(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 | a0001c0001t0009 a0001c0002t0009 a0001c0004t0009 |
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 | a0001c0007t0020 a0006c0019t0039 a0006c0038t0050 |
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 | a0001c0020t0049 a0001c0034t0031 |
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 | a0001c0001t0013 a0001c0001t0024 a0001c0001t0032 others(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 | a0001c0001t0004 a0001c0001t0008 a0001c0003t0004 others(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 | a0006c0019t0038 a0006c0019t0039 a0006c0038t0050 |
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 | a0001c0007t0020 a0006c0019t0038 a0006c0019t0039 others(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 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0015 others(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 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0045 others(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 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:138424997 | C | T | 3 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0001c0001t0001g0201 | 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 | a0001c0007t0011g0292 a0001c0030t0025g0006 a0001c0031t0041g0149 others(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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0020t0048g0030 others(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 | a0001c0001t0008g0321 a0001c0003t0004g0032 a0001c0003t0004g0181 others(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 | a0001c0001t0008g0321 a0001c0003t0004g0032 a0001c0003t0004g0181 others(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 | a0001c0001t0001g0239 a0001c0002t0002g0052 a0001c0002t0002g0232 others(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 | a0012c0026t0037g0238 | 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 | a0001c0007t0011g0292 a0001c0007t0020g0138 a0001c0007t0020g0148 others(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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0020t0048g0030 others(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 | a0001c0001t0006g0082 a0001c0001t0036g0075 |
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 | a0001c0001t0002g0197 | 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 | a0001c0007t0011g0292 a0001c0030t0025g0006 a0001c0031t0041g0149 others(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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0001c0001t0008g0321 a0001c0003t0004g0032 a0001c0003t0004g0181 others(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 | a0001c0001t0012g0159 | 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 | a0001c0001t0008g0321 a0005c0013t0011g0007 |
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 | a0001c0001t0001g0281 a0001c0001t0001g0294 a0001c0001t0009g0309 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0020t0048g0030 others(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 | a0001c0002t0001g0025 | 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 | a0001c0001t0008g0321 a0001c0003t0004g0032 a0001c0003t0004g0181 others(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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0020t0048g0030 others(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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0001c0001t0001g0208 a0001c0001t0001g0221 a0010c0032t0001g0196 |
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 | a0001c0001t0001g0298 | 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 | a0001c0001t0001g0330 | 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 | a0014c0023t0002g0263 | 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 | a0001c0007t0011g0292 a0001c0030t0025g0006 a0001c0031t0041g0149 others(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 | 252 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(249): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0008g0321 a0001c0003t0004g0032 a0001c0003t0004g0181 others(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 | a0001c0003t0007g0126 | 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 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0005c0012t0042g0249 a0005c0012t0044g0250 |
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 | a0001c0001t0001g0060 | 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 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0201 a0001c0001t0001g0299 others(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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | a0001c0001t0002g0015 | 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 | a0001c0001t0003g0042 a0001c0007t0011g0292 a0001c0030t0025g0006 others(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 | a0006c0019t0038g0251 a0006c0019t0039g0248 a0006c0038t0050g0122 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0006c0019t0038g0251 a0006c0019t0039g0248 a0006c0038t0050g0122 |
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 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0001c0004t0002g0237 | 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 | a0001c0028t0043g0258 a0005c0012t0042g0249 a0005c0012t0044g0250 |
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 | a0001c0001t0008g0321 a0001c0003t0004g0032 a0001c0003t0004g0181 others(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 | a0007c0011t0008g0322 | 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 | a0001c0001t0014g0207 a0001c0001t0014g0222 a0001c0001t0014g0277 |
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 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0010t0016g0145 others(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 | a0001c0007t0011g0292 a0001c0007t0020g0138 a0001c0007t0020g0148 others(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 | a0001c0016t0001g0085 a0001c0016t0003g0083 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0010t0016g0145 others(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 | a0001c0020t0048g0030 a0001c0020t0049g0031 a0001c0034t0031g0077 |
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 | a0001c0001t0006g0082 a0001c0001t0036g0075 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0010t0016g0145 others(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 | a0001c0007t0001g0315 | 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 | a0001c0001t0002g0308 | 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 | a0001c0003t0040g0177 | 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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0012c0026t0037g0238 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0010t0016g0145 others(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 | a0001c0001t0001g0019 | 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0010t0016g0145 others(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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0028t0043g0258 a0005c0012t0042g0249 a0005c0012t0044g0250 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0002g0324 | 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 | a0001c0030t0025g0006 a0001c0031t0041g0149 a0001c0042t0011g0116 |
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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | a0001c0001t0001g0080 | 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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 others(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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0030t0025g0006 a0001c0031t0041g0149 a0001c0042t0011g0116 |
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 | a0001c0001t0003g0001 a0001c0001t0003g0154 a0001c0001t0003g0213 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0001g0155 a0001c0007t0001g0253 a0001c0007t0011g0292 others(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 | 261 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(258): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.665-1797C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138435477 | |||||||
chr6:138435656 | A | T | 56 | a0001c0001t0001g0029 a0001c0001t0001g0040 a0001c0001t0001g0041 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(53): 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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 others(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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | a0001c0001t0001g0089 a0001c0007t0001g0160 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0020t0048g0030 a0001c0020t0049g0031 |
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 | a0001c0028t0043g0258 a0005c0012t0042g0249 a0005c0012t0044g0250 others(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 | a0001c0001t0008g0321 a0005c0013t0011g0007 |
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 | a0001c0030t0025g0006 a0001c0031t0041g0149 a0001c0042t0011g0116 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0001g0304 a0001c0001t0002g0018 |
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 | a0001c0015t0001g0236 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0006c0019t0038g0251 a0006c0019t0039g0248 a0006c0038t0050g0122 |
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 | a0001c0001t0002g0260 | 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 | a0001c0002t0001g0189 a0001c0002t0009g0049 a0001c0002t0009g0093 others(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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0002g0162 a0001c0004t0002g0237 a0001c0030t0025g0006 others(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 | a0001c0001t0001g0096 a0001c0001t0002g0015 a0013c0025t0013g0173 |
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 | a0001c0002t0001g0290 | 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 | 226 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(223): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(224): Show |
intron_variant | MODIFIER | c.665-3635A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437315 | |||||||
chr6:138437317 | T | C | 233 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(230): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.665-3637A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437317 | |||||||
chr6:138437319 | T | C | 236 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(234): 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 | a0001c0028t0043g0258 a0006c0019t0038g0251 a0006c0019t0039g0248 others(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 | a0006c0019t0039g0248 | 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 | a0001c0041t0008g0136 | 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 | a0001c0002t0001g0025 | 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 | 220 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(217): Show |
221 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(218): 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 | a0001c0003t0004g0032 a0001c0003t0004g0181 a0001c0003t0004g0182 others(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 | 240 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(237): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(238): 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 | a0001c0010t0016g0242 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0313 a0001c0020t0048g0030 others(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 | a0001c0010t0016g0145 a0001c0010t0016g0313 |
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 | a0006c0019t0038g0251 a0006c0038t0050g0122 a0012c0026t0037g0238 |
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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | a0001c0028t0043g0258 a0005c0012t0042g0249 a0005c0012t0044g0250 |
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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | 228 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(225): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): 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 | a0001c0010t0016g0145 a0001c0010t0016g0313 |
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 | a0001c0007t0011g0292 a0001c0029t0047g0235 |
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 | a0001c0020t0048g0030 a0001c0020t0049g0031 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0096 a0001c0001t0002g0015 others(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 | 227 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(224): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(225): 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 | a0001c0007t0011g0292 a0001c0029t0047g0235 |
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 | a0001c0007t0011g0292 a0001c0029t0047g0235 |
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 | a0001c0007t0011g0292 a0001c0029t0047g0235 |
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 | a0006c0019t0039g0248 | 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 | a0001c0004t0002g0237 a0003c0006t0017g0176 |
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 | a0001c0004t0002g0237 a0003c0006t0017g0176 |
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 | a0001c0004t0004g0111 a0001c0004t0004g0112 a0001c0004t0004g0143 others(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 |
156 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(153): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): 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 | a0001c0028t0043g0258 a0005c0012t0042g0249 a0005c0012t0044g0250 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0001c0028t0043g0258 a0005c0012t0042g0249 a0005c0012t0044g0250 |
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 | a0001c0030t0025g0006 a0001c0031t0041g0149 a0001c0042t0011g0116 |
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 | a0001c0028t0043g0258 a0005c0012t0042g0249 a0005c0012t0044g0250 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0239 others(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 | a0001c0003t0007g0126 a0001c0003t0007g0161 a0001c0003t0007g0163 others(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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 |
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 | a0006c0019t0039g0248 | 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 | a0006c0019t0038g0251 a0006c0038t0050g0122 a0012c0026t0037g0238 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0239 others(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 | a0001c0003t0004g0032 a0001c0003t0004g0181 a0001c0003t0004g0183 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0239 others(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 | a0001c0003t0007g0124 a0001c0003t0007g0244 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0010t0016g0242 | 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 | a0001c0029t0047g0235 | 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 | a0001c0003t0004g0182 a0001c0007t0011g0292 |
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 | a0001c0010t0016g0242 a0001c0029t0047g0235 |
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 | a0001c0029t0047g0235 | 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 | a0001c0003t0004g0182 a0001c0007t0011g0292 a0001c0010t0016g0145 others(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 | a0001c0001t0002g0015 a0001c0003t0004g0182 a0001c0003t0021g0114 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0053 a0001c0001t0001g0058 others(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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0029t0047g0235 |
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 | a0001c0007t0020g0138 a0001c0007t0020g0148 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0298 a0001c0001t0001g0311 others(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 | a0001c0001t0003g0069 a0001c0001t0006g0269 a0001c0001t0036g0075 others(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 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0066 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0215 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0298 others(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 | a0001c0001t0003g0204 a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | 54 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0040 others(51): Show |
54 | HG00544.hp2 HG00558.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.665-3763delG | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 5/7 | chr6 | 138437442 | |||||||
chr6:138437443 | C | A | 116 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0051 others(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 | 219 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(216): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): 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 | a0001c0001t0001g0121 a0001c0003t0007g0128 a0001c0003t0007g0179 others(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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0001c0010t0016g0145 a0001c0010t0016g0313 |
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 | a0001c0010t0016g0242 | 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 | a0001c0002t0001g0023 a0001c0002t0001g0097 a0001c0002t0001g0290 others(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 | a0001c0003t0007g0128 a0001c0003t0007g0179 a0001c0003t0007g0180 others(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 | a0001c0003t0004g0182 a0001c0003t0007g0124 a0001c0003t0007g0126 others(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 | a0001c0003t0007g0128 a0001c0003t0007g0179 a0001c0003t0007g0180 others(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 | a0001c0003t0007g0124 a0001c0003t0007g0126 a0001c0003t0007g0163 others(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 | a0001c0028t0043g0258 | 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 | a0001c0003t0007g0234 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0313 |
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 | a0001c0030t0025g0006 a0001c0031t0041g0149 a0001c0042t0011g0116 |
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 | a0012c0026t0037g0238 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0016t0001g0085 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0020t0048g0030 a0001c0020t0049g0031 |
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 | a0001c0002t0001g0013 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0004c0009t0001g0100 a0004c0009t0001g0101 a0004c0009t0001g0102 |
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 | a0001c0003t0040g0177 | 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 | a0012c0026t0037g0238 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0312 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0001g0008 | 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 | a0001c0002t0001g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0002g0162 a0001c0008t0008g0107 |
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 | a0001c0001t0003g0110 | 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 | a0012c0026t0037g0238 | 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 | a0001c0004t0002g0115 a0001c0004t0002g0139 a0001c0004t0009g0004 others(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 | a0001c0003t0004g0032 a0001c0003t0004g0181 a0001c0003t0004g0182 others(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 | a0001c0002t0001g0013 a0001c0002t0001g0278 |
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 | a0001c0001t0002g0015 | 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 | a0001c0003t0004g0032 a0001c0003t0004g0181 a0001c0003t0004g0182 others(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 | a0001c0001t0001g0312 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0001g0195 a0001c0001t0010g0296 |
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 | a0001c0021t0001g0302 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0006g0028 | 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 | a0001c0041t0008g0136 | 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 | a0001c0001t0015g0061 | 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 | a0001c0010t0016g0145 a0001c0010t0016g0242 a0001c0010t0016g0313 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0005g0055 |
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 | a0001c0004t0004g0111 a0001c0004t0004g0112 a0001c0004t0004g0127 |
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 | a0001c0029t0047g0235 | 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 | a0001c0003t0007g0170 a0001c0030t0025g0006 a0001c0042t0011g0116 |
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 | a0001c0003t0007g0170 a0001c0003t0007g0323 a0001c0007t0011g0292 others(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 | a0001c0001t0004g0186 a0001c0001t0018g0141 a0001c0001t0029g0117 others(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 | a0001c0001t0002g0320 | 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 | a0001c0001t0002g0162 | 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 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0150 others(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 | a0001c0001t0004g0186 a0001c0001t0018g0141 a0001c0001t0029g0117 others(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 | a0001c0003t0007g0170 a0001c0003t0007g0323 a0001c0007t0011g0292 others(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 | a0001c0015t0001g0129 a0001c0028t0043g0258 a0005c0012t0042g0249 others(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 | a0001c0001t0002g0015 a0001c0001t0009g0187 a0001c0001t0009g0309 |
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 | a0001c0001t0004g0186 a0001c0004t0004g0111 a0001c0004t0004g0112 others(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 | a0006c0019t0038g0251 a0006c0019t0039g0248 a0006c0038t0050g0122 |
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 | a0001c0001t0018g0141 a0001c0001t0029g0117 a0001c0017t0012g0146 others(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 | a0001c0001t0001g0284 a0001c0001t0010g0288 |
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 | a0001c0015t0001g0129 a0001c0015t0001g0236 a0001c0024t0004g0123 others(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 | a0001c0007t0011g0292 | 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 | a0001c0007t0011g0292 | 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 | a0013c0025t0013g0173 | 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 | a0001c0001t0001g0125 a0001c0024t0004g0123 a0001c0028t0043g0258 others(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 | a0001c0021t0001g0302 a0001c0021t0001g0305 |
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 | a0001c0001t0001g0092 | 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 | a0001c0015t0001g0129 | 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 | a0001c0007t0020g0138 a0001c0007t0020g0148 |
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 | a0001c0003t0007g0170 a0001c0003t0007g0323 a0001c0030t0025g0006 others(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 | a0001c0001t0001g0125 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0287 a0001c0001t0005g0291 others(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 | a0001c0001t0004g0186 a0001c0001t0006g0276 |
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 | a0001c0001t0002g0197 a0001c0001t0009g0198 |
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 | a0001c0003t0007g0126 a0001c0007t0011g0292 a0001c0007t0020g0148 |
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 | a0001c0001t0001g0226 | 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0058 a0001c0001t0001g0089 a0001c0001t0001g0287 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0029g0117 a0001c0004t0011g0152 a0001c0010t0016g0145 others(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 | a0001c0001t0003g0264 | 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 | 153 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0043 others(150): Show |
154 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(151): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0029 | 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 | 68 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(65): Show |
69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0002g0324 | 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 | a0001c0001t0001g0240 a0001c0001t0003g0274 |
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 | a0014c0023t0002g0263 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 63 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): 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 | 63 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): 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 | a0001c0001t0001g0156 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0002t0001g0172 a0001c0002t0001g0325 a0001c0002t0002g0326 others(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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0015t0001g0129 others(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 | a0001c0001t0036g0075 | 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 | a0001c0007t0020g0138 | 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | 63 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): 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 | a0001c0001t0001g0103 | 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0015t0001g0129 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 63 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): 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 | 63 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.532+957A>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 4/7 | chr6 | 138446044 | |||||||
chr6:138446061 | T | C | 63 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(60): Show |
64 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(61): 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 | a0001c0001t0002g0073 a0001c0001t0006g0082 a0001c0001t0036g0075 |
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 | a0001c0028t0043g0258 | 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 | 127 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0043 others(124): Show |
128 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(125): 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 | a0001c0001t0019g0072 | 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 | a0001c0008t0008g0211 a0001c0008t0011g0212 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0003t0007g0124 others(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 | a0001c0001t0002g0135 a0001c0001t0009g0165 a0001c0001t0018g0141 others(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 | a0001c0001t0001g0298 | 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 | 66 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(63): Show |
67 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(64): 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0053 a0001c0001t0003g0231 a0001c0001t0005g0300 others(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 | a0001c0001t0001g0156 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | a0001c0001t0001g0310 | 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 | a0001c0001t0002g0073 | 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 | a0001c0001t0018g0141 a0001c0004t0002g0139 |
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 | a0001c0001t0001g0215 a0001c0001t0001g0307 |
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 | a0001c0001t0029g0117 a0001c0003t0007g0323 a0001c0004t0002g0119 others(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 | 68 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(65): Show |
69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): 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 | a0001c0001t0029g0117 a0001c0004t0004g0111 a0001c0004t0004g0112 others(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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0003t0007g0179 a0001c0003t0007g0180 |
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 | 328 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(325): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): 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 | a0001c0015t0001g0129 a0001c0024t0004g0123 |
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 | a0001c0001t0003g0267 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0002g0162 a0001c0001t0003g0095 a0001c0001t0006g0205 others(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 | 57 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(54): Show |
58 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(55): 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 | 62 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(59): Show |
63 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.340-1945G>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138449138 | |||||||
chr6:138449162 | G | A | 89 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(86): Show |
90 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(87): 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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0002g0202 | 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 | a0001c0002t0001g0172 a0001c0002t0001g0325 a0001c0002t0002g0326 others(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 | a0001c0001t0001g0153 a0001c0001t0035g0206 |
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 | a0005c0012t0042g0249 a0005c0012t0044g0250 a0005c0013t0001g0178 others(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 | a0001c0001t0003g0081 a0001c0001t0006g0088 |
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 | a0001c0001t0001g0156 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0001t0003g0081 a0001c0001t0006g0088 |
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 | a0001c0001t0001g0156 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | a0001c0001t0002g0260 | 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 | a0001c0003t0007g0323 a0001c0004t0002g0119 a0001c0007t0011g0292 |
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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0006g0268 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0156 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | a0001c0001t0001g0156 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | a0001c0001t0002g0135 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0003t0007g0323 a0001c0004t0002g0119 a0001c0007t0011g0292 |
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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0156 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | a0001c0003t0007g0179 a0001c0003t0007g0180 |
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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0002g0162 a0001c0003t0007g0161 a0001c0003t0007g0163 |
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 | a0001c0001t0029g0117 a0001c0004t0004g0111 a0001c0004t0004g0112 others(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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0007t0001g0315 |
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 | a0001c0004t0004g0140 | 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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0281 a0001c0001t0001g0294 |
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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0008 | 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 | 147 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(144): Show |
148 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(145): 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0003t0007g0244 a0001c0003t0007g0323 a0001c0003t0021g0245 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0002g0015 | 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 | a0001c0002t0001g0172 a0001c0002t0001g0325 a0001c0002t0002g0326 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0003t0007g0124 a0001c0003t0007g0126 a0001c0004t0002g0115 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0003t0007g0179 a0001c0003t0007g0180 |
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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0007t0020g0138 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0003t0007g0179 a0001c0003t0007g0180 |
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 | a0001c0001t0010g0296 a0001c0039t0018g0295 |
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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0004t0002g0139 | 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 | 65 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(62): Show |
66 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.340-5628dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138452820 | |||||||
chr6:138452820 | C | CTTT | 82 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0103 a0001c0001t0002g0024 |
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 | a0001c0001t0001g0215 a0001c0001t0001g0306 a0001c0001t0001g0307 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0156 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0004t0004g0143 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0121 a0001c0001t0029g0117 a0005c0012t0042g0249 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0007t0011g0292 | 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 | a0001c0002t0001g0084 a0001c0016t0001g0085 a0001c0016t0003g0083 |
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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0001t0027g0254 | 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 | a0001c0001t0024g0255 | 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | 162 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(159): Show |
163 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(160): 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0003t0021g0114 others(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 | a0001c0001t0002g0162 a0001c0002t0001g0172 a0001c0002t0001g0325 others(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 | a0001c0001t0005g0062 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | 162 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(159): Show |
163 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(160): 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0003t0021g0245 a0003c0006t0012g0113 |
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 | a0001c0001t0014g0277 | 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 | a0001c0001t0001g0121 a0001c0001t0029g0117 a0001c0003t0007g0124 others(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 | 162 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(159): Show |
163 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(160): 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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0004t0004g0143 others(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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0004t0004g0143 others(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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0004t0004g0143 others(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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0004t0004g0143 others(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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0004t0004g0143 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0311 a0001c0001t0002g0059 others(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 | a0001c0002t0001g0023 | 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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0002t0001g0158 a0001c0007t0001g0160 |
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 | 167 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(164): Show |
168 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(165): 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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0002t0001g0158 | 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 | a0001c0001t0006g0285 | 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 | a0001c0002t0001g0035 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0051 a0001c0001t0001g0053 others(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 | a0001c0001t0001g0029 | 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 |
68 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(65): Show |
69 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(66): 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 | a0001c0001t0001g0169 a0001c0001t0002g0209 a0001c0001t0013g0214 others(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 | a0001c0007t0011g0292 | 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | 80 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0096 others(77): Show |
81 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(78): 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 | a0001c0001t0001g0026 a0001c0001t0001g0221 a0001c0002t0003g0003 |
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 | a0003c0006t0005g0286 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0156 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0008g0321 a0001c0031t0041g0149 a0007c0011t0008g0322 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0002t0001g0023 a0001c0003t0007g0234 a0001c0004t0002g0119 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0004t0009g0004 a0001c0004t0028g0005 |
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 | 253 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.340-8562C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455755 | |||||||
chr6:138455756 | C | A | 253 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.340-8563G>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455756 | |||||||
chr6:138455758 | A | C | 253 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.340-8565T>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455758 | |||||||
chr6:138455760 | A | T | 253 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.340-8567T>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138455760 | |||||||
chr6:138455761 | G | GTT | 253 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): 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 | a0001c0001t0001g0011 a0001c0001t0001g0053 a0001c0001t0001g0125 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0092 | 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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0284 a0001c0001t0010g0288 |
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 | a0001c0001t0001g0125 a0003c0033t0005g0241 |
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 | a0008c0018t0002g0317 a0008c0018t0002g0318 |
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 | 131 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(128): Show |
132 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(129): 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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0281 a0001c0001t0001g0294 |
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 | a0001c0004t0002g0139 | 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 | a0001c0002t0001g0035 | 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 | a0001c0001t0001g0156 a0001c0001t0002g0162 a0001c0001t0010g0296 others(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 | a0004c0009t0001g0100 a0004c0009t0001g0102 |
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 | a0001c0001t0001g0027 a0001c0001t0006g0028 |
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 | a0001c0001t0002g0197 a0001c0001t0009g0198 |
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 | a0001c0003t0040g0177 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0002t0002g0232 a0001c0020t0048g0030 a0001c0020t0049g0031 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0185 a0001c0001t0001g0221 a0001c0001t0003g0267 others(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 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0156 a0001c0001t0001g0256 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0036g0075 | 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 | 128 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(125): Show |
129 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(126): 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0004t0004g0127 | 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 | 136 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(133): Show |
137 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(134): 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 | a0001c0004t0002g0115 a0001c0004t0009g0004 a0001c0004t0028g0005 others(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 | a0001c0002t0001g0023 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(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 | 232 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(229): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.340-11636delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138458828 | |||||||
chr6:138458841 | A | C | 1 | a0001c0001t0001g0041 | 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 | a0001c0001t0001g0041 a0001c0007t0020g0148 a0001c0024t0004g0123 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0007t0020g0138 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0032g0229 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0003g0068 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0002t0001g0036 | 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 | a0001c0001t0001g0051 a0001c0001t0002g0135 |
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 | a0001c0002t0001g0325 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+12911C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460395 | |||||||
chr6:138460400 | A | C | 122 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(119): Show |
123 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(120): 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 | a0001c0001t0005g0291 | 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 | a0001c0003t0007g0128 a0001c0003t0007g0259 |
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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0001c0008t0008g0107 a0001c0008t0008g0109 a0001c0008t0008g0211 others(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 | 119 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(116): Show |
120 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.339+12422T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138460884 | |||||||
chr6:138461006 | G | A | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): 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 | a0001c0001t0001g0089 a0001c0001t0001g0103 a0001c0001t0002g0024 |
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 | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.339+12150dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461155 | |||||||
chr6:138461156 | T | G | 45 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(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 | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): 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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0001c0001t0002g0094 | 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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.339+11790delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138461515 | |||||||
chr6:138461544 | G | A | 3 | a0001c0003t0021g0114 a0003c0006t0005g0132 a0007c0011t0008g0133 |
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 | a0001c0001t0010g0296 a0001c0002t0001g0172 a0001c0002t0001g0325 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0001t0024g0255 others(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 | a0005c0012t0042g0249 a0005c0012t0044g0250 a0005c0013t0001g0178 others(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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0266 | 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 | a0001c0028t0043g0258 | 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 | a0001c0002t0001g0056 | 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0001t0010g0296 a0001c0003t0040g0177 a0001c0039t0018g0295 |
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 | a0001c0001t0001g0087 a0001c0001t0002g0014 a0001c0001t0002g0015 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0066 a0001c0001t0001g0096 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0016c0040t0010g0191 | 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 | a0005c0012t0042g0249 a0005c0012t0044g0250 a0005c0013t0001g0178 others(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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0010g0296 a0001c0002t0001g0172 a0001c0002t0001g0325 others(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 | a0001c0003t0007g0124 a0001c0003t0007g0126 a0001c0003t0007g0323 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0240 a0001c0001t0001g0287 others(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 | a0001c0001t0003g0091 | 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 | a0001c0034t0031g0077 | 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0007t0011g0292 a0001c0015t0001g0129 |
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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0104 a0001c0001t0001g0167 |
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 | a0001c0001t0003g0105 a0001c0001t0003g0106 |
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 | a0001c0004t0004g0144 a0001c0004t0011g0152 a0001c0010t0016g0145 others(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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0002t0001g0301 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0004t0004g0144 a0001c0004t0011g0152 a0001c0010t0016g0145 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0001t0002g0135 a0001c0001t0003g0081 a0001c0001t0009g0165 others(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 | a0001c0001t0001g0239 a0001c0001t0002g0162 a0001c0001t0006g0230 others(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 | 55 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(52): Show |
56 | HG00423.hp1 HG00558.hp2 HG00597.hp1 others(53): 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 | a0001c0001t0001g0029 a0001c0001t0001g0045 a0001c0001t0001g0192 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0003t0007g0124 a0001c0003t0007g0323 a0001c0004t0030g0246 |
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 | a0001c0001t0001g0104 a0001c0001t0001g0167 |
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 | 57 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(54): Show |
58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): 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 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | a0001c0003t0007g0124 a0001c0003t0007g0126 a0001c0003t0007g0323 others(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 | a0001c0001t0001g0121 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 87 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(84): Show |
88 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.339+8251delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465054 | |||||||
chr6:138465144 | C | T | 1 | a0001c0001t0001g0029 | 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 | a0001c0003t0007g0234 a0001c0015t0001g0236 a0001c0029t0047g0235 |
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 | a0001c0003t0007g0179 a0001c0003t0007g0180 a0001c0003t0007g0244 others(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 | 134 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(131): Show |
135 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.339+7912A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138465394 | |||||||
chr6:138465446 | G | C | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0003t0021g0114 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0015g0279 others(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 | 90 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(87): Show |
91 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(88): 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 | a0001c0003t0007g0179 a0001c0003t0007g0180 a0001c0003t0007g0244 others(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 | a0001c0001t0001g0011 a0001c0001t0001g0215 a0001c0001t0001g0307 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0002t0001g0301 others(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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0053 a0001c0001t0001g0067 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(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 | 36 | a0001c0001t0001g0045 a0001c0001t0001g0193 a0001c0001t0001g0201 others(33): Show |
36 | HG00423.hp1 HG00558.hp2 HG00738.hp1 others(33): 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 | a0001c0001t0001g0029 a0001c0001t0001g0092 a0001c0001t0001g0153 others(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 | 121 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(118): Show |
122 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(119): 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 119 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(116): Show |
120 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(117): 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 | a0001c0001t0003g0081 a0001c0001t0006g0088 |
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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0002t0001g0301 others(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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0002t0001g0325 | 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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0002t0001g0301 others(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 | 119 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(116): Show |
120 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.339+6531dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138466774 | |||||||
chr6:138466807 | G | A | 6 | a0005c0012t0042g0249 a0005c0012t0044g0250 a0005c0013t0001g0178 others(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 | 121 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(118): Show |
122 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(119): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0004t0004g0140 | 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0002t0001g0301 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | 119 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(116): Show |
120 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(117): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | 124 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(121): Show |
125 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(122): 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 | a0001c0002t0001g0035 | 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 | a0001c0001t0001g0121 a0001c0001t0029g0117 a0005c0013t0011g0007 |
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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0003t0007g0124 |
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 | a0001c0003t0021g0114 a0001c0031t0041g0149 a0003c0006t0005g0132 others(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 | a0001c0001t0001g0195 | 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 | a0001c0001t0009g0309 | 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 | a0001c0003t0007g0124 a0001c0003t0007g0323 a0001c0004t0004g0140 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0272 a0001c0001t0001g0293 |
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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0002g0014 a0001c0001t0002g0015 |
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 | a0001c0003t0007g0124 a0001c0003t0007g0323 a0001c0004t0004g0140 others(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 | a0001c0010t0016g0313 | 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 | a0001c0001t0001g0053 a0001c0001t0003g0231 a0001c0002t0002g0052 others(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 | a0001c0001t0045g0130 a0001c0003t0007g0170 a0001c0004t0004g0171 others(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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0005c0012t0042g0249 a0005c0012t0044g0250 a0005c0013t0001g0178 others(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 | a0001c0001t0010g0296 a0001c0002t0001g0172 a0001c0002t0001g0325 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0003t0007g0179 others(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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0156 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | a0001c0001t0010g0296 a0001c0002t0001g0172 a0001c0002t0001g0325 others(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 | a0001c0002t0001g0301 | 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 | a0001c0003t0007g0124 a0001c0003t0007g0323 a0001c0004t0004g0140 others(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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+3549G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138469757 | |||||||
chr6:138469855 | A | C | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0004t0030g0246 | 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 | a0001c0001t0010g0296 a0001c0002t0001g0172 a0001c0002t0001g0325 others(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 | 93 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(90): Show |
94 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(91): 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 | a0001c0001t0002g0059 | 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 | 105 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(102): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): 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 | a0001c0004t0004g0111 a0001c0004t0004g0112 |
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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0287 a0001c0001t0005g0291 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0040 a0001c0001t0001g0041 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | 91 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(88): Show |
92 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.339+2457T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138470849 | |||||||
chr6:138470924 | G | A | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): 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 | a0001c0007t0020g0138 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0003t0007g0161 | 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 | a0001c0001t0001g0121 a0001c0001t0029g0117 a0005c0013t0011g0007 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0001c0003t0007g0124 a0001c0003t0007g0323 a0001c0004t0004g0140 others(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 | a0001c0001t0015g0061 | 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 | 98 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(95): Show |
99 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(96): 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 | a0001c0001t0002g0135 a0001c0001t0009g0165 |
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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.339+1122delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138472183 | |||||||
chr6:138473099 | G | C | 2 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0001t0001g0303 | 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 | 103 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(100): Show |
104 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.339+146C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 3/7 | chr6 | 138473160 | |||||||
chr6:138473491 | A | G | 104 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(101): Show |
105 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(102): 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 | a0001c0001t0002g0135 | 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 | a0001c0001t0002g0162 a0001c0001t0010g0296 a0001c0002t0001g0172 others(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 | 102 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(99): Show |
103 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(100): Show |
intron_variant | MODIFIER | c.212-315T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473748 | |||||||
chr6:138473843 | T | TA | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.212-411dupT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138473843 | |||||||
chr6:138473872 | C | T | 2 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | a0001c0001t0003g0081 | 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 | a0001c0001t0003g0267 a0001c0001t0006g0265 |
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 | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0048 others(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 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0001t0002g0162 others(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 | a0001c0001t0002g0202 | 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 | a0001c0002t0009g0093 | 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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.212-1596A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475029 | |||||||
chr6:138475041 | G | A | 130 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(127): Show |
131 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(128): 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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(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 | 56 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0048 others(53): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.212-1717delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475149 | |||||||
chr6:138475163 | A | G | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0007t0020g0148 |
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 | a0001c0001t0001g0208 a0001c0001t0003g0267 a0001c0001t0003g0280 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.212-1893C>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475326 | |||||||
chr6:138475395 | A | AT | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.212-1963dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138475395 | |||||||
chr6:138475455 | T | C | 1 | a0015c0036t0013g0289 | 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 | a0001c0001t0001g0121 a0001c0001t0024g0255 a0001c0001t0027g0254 others(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 | 292 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0012 others(289): Show |
293 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(290): 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 | a0001c0010t0016g0313 | 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 | a0001c0001t0002g0320 | 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 | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | 137 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(134): Show |
138 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(135): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0007t0020g0138 others(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 | a0001c0004t0002g0115 a0001c0004t0009g0004 a0001c0004t0028g0005 others(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 | 57 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(54): Show |
58 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(55): 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 | a0001c0001t0001g0050 a0001c0001t0001g0064 a0001c0001t0001g0065 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0104 a0001c0001t0001g0256 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0284 a0001c0001t0003g0098 others(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 | 55 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(52): Show |
56 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(53): 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 | a0001c0001t0001g0155 a0001c0001t0003g0154 a0001c0007t0001g0253 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0024g0255 a0001c0001t0027g0254 a0001c0002t0001g0301 others(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 | a0001c0001t0001g0155 a0001c0001t0003g0154 a0001c0007t0001g0253 |
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 | a0001c0010t0016g0313 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.212-4149C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138477582 | |||||||
chr6:138477754 | C | T | 1 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0153 a0001c0001t0001g0167 a0001c0001t0001g0294 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(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 | 21 | a0001c0001t0002g0162 a0001c0001t0002g0271 a0001c0001t0003g0105 others(18): Show |
21 | HG00438.hp1 HG00597.hp2 HG01081.hp1 others(18): 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 | a0001c0002t0001g0325 a0001c0002t0002g0184 a0001c0002t0002g0326 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0046 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0019 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0014 a0001c0001t0002g0015 others(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 | a0001c0003t0007g0124 a0001c0003t0007g0323 a0001c0003t0021g0114 others(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 | a0001c0001t0002g0324 | 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 | 105 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(102): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.212-4634G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478067 | |||||||
chr6:138478117 | G | A | 91 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(88): Show |
92 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.212-4684C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138478117 | |||||||
chr6:138478220 | A | G | 106 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(103): Show |
107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): 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 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0003t0007g0179 others(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 | 108 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(105): Show |
109 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(106): 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 | a0001c0002t0001g0033 a0001c0002t0001g0034 |
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 | a0001c0001t0002g0197 a0001c0001t0009g0198 |
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 | 106 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(103): Show |
107 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(104): 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0298 | 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 | a0001c0010t0016g0313 | 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 | a0001c0001t0002g0324 | 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 | 54 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(51): Show |
55 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(52): 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 | a0001c0001t0010g0296 a0001c0002t0001g0172 a0001c0002t0001g0325 others(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 | 56 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(53): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): 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 | a0001c0001t0003g0199 | 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 | 56 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(53): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): 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 | 56 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(53): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): Show |
intron_variant | MODIFIER | c.212-7228C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138480661 | |||||||
chr6:138481194 | C | T | 56 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(53): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): 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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | 56 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(53): Show |
57 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(54): 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 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | a0001c0001t0001g0047 a0001c0001t0001g0096 a0001c0001t0002g0094 others(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 | a0012c0026t0037g0238 | 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 | a0001c0001t0006g0028 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0002t0001g0016 | 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 | a0001c0001t0005g0300 | 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 | a0001c0001t0001g0226 | 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 | 76 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0092 others(73): Show |
77 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(74): 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 | a0001c0001t0024g0255 a0001c0001t0027g0254 |
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 | a0001c0002t0001g0084 a0001c0016t0001g0085 a0001c0016t0003g0083 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0299 a0001c0001t0001g0330 others(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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | 138 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(135): Show |
139 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.212-9013delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138482445 | |||||||
chr6:138482445 | CAA | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0155 a0001c0001t0003g0154 others(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 | a0001c0001t0001g0155 a0001c0001t0002g0223 a0001c0001t0003g0154 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0221 a0001c0001t0014g0222 a0001c0002t0003g0003 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0002t0001g0022 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0003t0007g0179 a0001c0003t0007g0180 a0001c0003t0007g0244 others(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 | a0001c0001t0010g0296 | 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 | a0001c0002t0001g0023 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0293 |
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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0001t0006g0200 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0028t0043g0258 | 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 | a0001c0001t0001g0256 a0001c0001t0001g0257 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0087 a0001c0001t0001g0294 others(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 | 81 | a0001c0001t0001g0029 a0001c0001t0001g0047 a0001c0001t0001g0048 others(78): Show |
82 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.211+10772delT | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138485446 | |||||||
chr6:138485446 | TAA | T | 15 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0001t0001g0026 | 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 | a0001c0037t0003g0009 | 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 | a0001c0001t0001g0221 a0001c0001t0014g0222 a0001c0002t0003g0003 |
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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0001t0002g0271 | 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 | a0001c0001t0002g0131 a0001c0001t0003g0105 a0001c0001t0003g0106 others(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 | a0001c0001t0001g0089 | 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 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | 137 | a0001c0001t0001g0029 a0001c0001t0001g0043 a0001c0001t0001g0044 others(134): Show |
138 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(135): 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0001c0001t0003g0273 | 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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0005c0012t0042g0249 a0005c0012t0044g0250 a0005c0013t0001g0178 others(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 | a0001c0001t0001g0155 a0001c0001t0003g0154 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0190 a0001c0001t0002g0260 a0001c0001t0033g0188 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0024g0255 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0003g0154 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0003g0154 others(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 | a0001c0001t0001g0190 a0001c0001t0002g0260 a0001c0001t0033g0188 others(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 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | a0001c0001t0001g0156 a0001c0003t0007g0179 a0001c0003t0007g0180 others(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 | a0001c0002t0001g0035 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0002g0260 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0190 others(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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | 53 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0047 others(50): Show |
54 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(51): 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 | a0001c0001t0003g0264 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0002g0260 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0002g0260 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0003t0007g0179 a0001c0003t0007g0180 a0001c0003t0007g0244 others(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 | a0001c0001t0001g0156 a0003c0006t0017g0151 |
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 | a0004c0009t0001g0100 a0004c0009t0001g0101 a0004c0009t0001g0102 others(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 | a0001c0001t0001g0190 a0001c0001t0002g0260 a0001c0001t0033g0188 others(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 | a0001c0001t0001g0155 a0001c0001t0003g0154 |
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 | a0001c0001t0001g0299 | 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 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0002g0260 others(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 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0103 a0001c0001t0001g0156 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0155 a0001c0001t0003g0154 a0001c0004t0004g0143 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0215 a0001c0001t0001g0272 others(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 | 3 | a0001c0001t0001g0193 a0001c0001t0002g0271 a0001c0001t0051g0331 |
3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.211+6453T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138489766 | |||||||
chr6:138489777 | A | G | 2 | a0001c0001t0008g0321 a0001c0024t0004g0123 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0043 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0190 a0001c0001t0002g0260 a0001c0002t0001g0189 others(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 | a0001c0001t0001g0155 a0001c0001t0003g0154 |
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 | a0001c0003t0007g0179 a0001c0003t0007g0180 a0001c0003t0007g0244 others(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 | a0001c0001t0001g0155 a0001c0001t0003g0154 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | a0001c0001t0001g0046 a0003c0006t0017g0151 |
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 | a0001c0001t0001g0104 a0001c0001t0001g0167 a0001c0001t0034g0168 |
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 | a0001c0001t0001g0155 a0001c0001t0003g0154 a0001c0004t0004g0111 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0156 a0001c0001t0001g0256 others(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 | a0001c0003t0007g0124 a0001c0003t0007g0323 |
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 | a0001c0003t0007g0179 a0001c0003t0007g0180 a0001c0003t0007g0244 others(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 | a0001c0001t0001g0041 a0001c0001t0002g0059 a0001c0002t0001g0036 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0003g0231 a0001c0002t0002g0232 a0001c0020t0048g0030 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0226 | 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 | a0001c0001t0008g0321 a0007c0011t0008g0322 |
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 | a0001c0001t0001g0155 a0001c0001t0001g0190 a0001c0001t0002g0260 others(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 | a0001c0001t0008g0321 | 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 | 105 | a0001c0001t0001g0027 a0001c0001t0001g0029 a0001c0001t0001g0047 others(102): Show |
106 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(103): 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 | a0001c0001t0008g0321 a0001c0003t0007g0179 a0001c0003t0007g0180 others(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 | a0007c0011t0008g0322 | 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 | a0001c0001t0001g0156 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0190 a0001c0001t0002g0260 a0001c0001t0033g0188 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0121 a0001c0001t0029g0117 |
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 | a0001c0001t0005g0300 a0001c0008t0008g0107 a0001c0008t0008g0109 others(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 | a0001c0001t0018g0141 a0001c0017t0001g0142 |
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 | 324 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(321): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): 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 | a0001c0001t0001g0121 a0001c0001t0003g0042 a0001c0001t0003g0203 |
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 | a0001c0001t0001g0155 a0001c0001t0003g0154 a0001c0001t0008g0321 others(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 | a0001c0002t0001g0301 | 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 | a0001c0001t0001g0155 a0001c0001t0003g0154 |
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 | 49 | a0001c0001t0001g0150 a0001c0001t0001g0167 a0001c0001t0001g0185 others(46): Show |
50 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(47): 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 | a0001c0001t0029g0117 a0001c0002t0005g0118 a0001c0004t0002g0115 others(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 | a0001c0004t0004g0111 a0001c0004t0004g0112 a0003c0033t0005g0241 |
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 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
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 | a0001c0004t0004g0143 a0001c0004t0004g0144 a0001c0004t0011g0152 others(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 | 308 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(305): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.211+4826T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138491393 | |||||||
chr6:138491480 | G | T | 297 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(294): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0012c0026t0037g0238 | 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 | a0001c0001t0001g0190 a0001c0001t0033g0188 a0001c0002t0001g0189 others(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 | a0001c0008t0008g0107 a0001c0008t0008g0109 a0001c0008t0046g0108 |
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 | a0001c0001t0006g0268 a0001c0001t0006g0269 a0002c0005t0001g0270 |
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 | 315 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(312): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0169 a0001c0001t0001g0256 a0001c0001t0001g0257 others(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 | a0001c0003t0007g0234 a0001c0004t0002g0237 a0001c0015t0001g0236 others(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 | a0001c0003t0007g0244 a0001c0003t0021g0245 a0001c0004t0030g0246 others(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 | a0001c0001t0029g0117 a0001c0002t0005g0118 a0001c0004t0002g0115 others(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 | a0001c0001t0029g0117 a0001c0002t0005g0118 a0001c0004t0002g0115 others(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 | 148 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0150 others(145): Show |
149 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.211+3226dupA | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 2/7 | chr6 | 138492992 | |||||||
chr6:138493051 | A | G | 16 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0008g0321 others(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 | a0001c0001t0001g0312 | 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 | a0001c0010t0016g0313 | 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 | 315 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(312): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | 109 | a0001c0001t0001g0185 a0001c0001t0001g0190 a0001c0001t0001g0192 others(106): Show |
110 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(107): 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 | a0001c0002t0002g0326 a0001c0002t0010g0328 a0001c0002t0023g0327 |
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 | a0001c0001t0003g0042 | 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 | a0001c0001t0001g0167 a0001c0001t0001g0240 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0240 a0001c0001t0002g0162 others(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 | a0001c0003t0007g0170 a0001c0004t0004g0171 |
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 | a0001c0003t0007g0179 a0001c0003t0007g0180 |
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 | a0001c0001t0001g0167 a0001c0001t0001g0240 a0001c0001t0002g0162 others(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 | a0001c0001t0029g0117 a0001c0002t0005g0118 a0001c0004t0002g0115 others(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 | a0001c0001t0003g0267 | 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 | a0001c0002t0001g0172 a0001c0003t0007g0170 a0001c0004t0004g0171 |
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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0208 a0001c0001t0001g0215 a0001c0001t0002g0209 others(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 | a0001c0001t0001g0167 a0001c0001t0001g0240 a0001c0001t0002g0162 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0002t0001g0172 a0001c0003t0007g0170 a0001c0003t0040g0177 others(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 | a0001c0003t0040g0177 a0003c0006t0017g0176 a0005c0013t0001g0178 others(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 | 316 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): 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 | a0001c0001t0001g0314 a0001c0001t0001g0316 a0001c0007t0001g0315 |
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 | 63 | a0001c0001t0001g0266 a0001c0001t0001g0272 a0001c0001t0001g0281 others(60): Show |
63 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(60): 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 | a0001c0001t0004g0186 a0001c0001t0009g0187 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0003g0154 |
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 | a0001c0001t0002g0262 | 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 | a0001c0001t0001g0215 a0002c0005t0001g0216 a0002c0005t0001g0217 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0167 a0001c0001t0001g0240 others(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 | a0001c0002t0001g0036 a0001c0002t0002g0037 a0001c0002t0002g0038 others(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 | a0008c0018t0002g0317 a0008c0018t0002g0318 |
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 | 316 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): 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 | a0001c0001t0001g0185 a0001c0001t0002g0260 a0001c0001t0004g0186 others(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 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0002g0223 a0001c0001t0014g0222 others(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 | G | A | 1 | a0001c0001t0003g0110 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.59-1031C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497402 | |||||||
chr6:138497464 | G | A | 24 | a0001c0001t0001g0167 a0001c0001t0001g0240 a0001c0001t0002g0162 others(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 | A | G | 173 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0150 others(170): Show |
174 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.59-1329T>C | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138497700 | |||||||
chr6:138498032 | AACTATCA others(5): Show |
A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0041 |
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 | C | G | 3 | a0001c0001t0008g0321 a0001c0003t0007g0323 a0007c0011t0008g0322 |
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 | G | A | 4 | a0001c0001t0029g0117 a0001c0002t0005g0118 a0001c0004t0002g0115 others(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 | G | A | 1 | a0006c0019t0038g0251 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.58+1040C>T | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498193 | |||||||
chr6:138498359 | G | C | 4 | a0001c0003t0021g0114 a0001c0004t0004g0111 a0001c0004t0004g0112 others(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 | 153 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0150 others(150): Show |
154 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.58+860G>A | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498373 | |||||||
chr6:138498474 | C | T | 2 | a0001c0003t0007g0170 a0001c0004t0004g0171 |
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 | A | G | 9 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0024g0255 others(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 | 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 | a0001c0001t0008g0321 a0001c0003t0007g0323 a0007c0011t0008g0322 |
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 | C | T | 4 | a0001c0001t0029g0117 a0001c0002t0005g0118 a0001c0004t0002g0115 others(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 | A | G | 1 | a0001c0007t0001g0253 | 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 | a0001c0001t0002g0324 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.58+234A>G | NHSL1 | ENSG00000135540.12 | transcript | ENST00000343505.10 | protein_coding | 1/7 | chr6 | 138498999 | |||||||
chr6:138499134 | G | GAC | 72 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0266 others(69): Show |
72 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(69): 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 | a0001c0001t0001g0329 a0001c0001t0001g0330 a0001c0002t0001g0325 others(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 | a0001c0002t0001g0172 a0001c0003t0007g0170 a0001c0003t0040g0177 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0150 others(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 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0001t0008g0321 a0001c0003t0007g0323 a0007c0011t0008g0322 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(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 | a0001c0004t0009g0004 a0001c0004t0028g0005 a0001c0030t0025g0006 others(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 |