Item | Value |
---|---|
geneid | 348938 |
ensemblid | ENSG00000172548.15 |
hgncid | 28018 |
symbol | NIPAL4 |
name | NIPA like domain containing 4 |
refseq_nuc | NM_001099287.2 |
refseq_prot | NP_001092757.2 |
ensembl_nuc | ENST00000311946.8 |
ensembl_prot | ENSP00000311687.8 |
mane_status | MANE Select |
chr | chr5 |
start | 157460213 |
end | 157474722 |
strand | + |
ver | v1.2 |
region | chr5:157460213-157474722 |
region5000 | chr5:157455213-157479722 |
regionname0 | NIPAL4_chr5_157460213_157474722 |
regionname5000 | NIPAL4_chr5_157455213_157479722 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 404 | 190 | 37 | 38 | 93 | 7 | 14 | 70 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
a0002 | 1/0 | 404 | 160 | 36 | 38 | 60 | 7 | 18 | 47 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
a0003 | 0/0 | 404 | 37 | 19 | 8 | 0 | 2 | 8 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
a0004 | 0/0 | 404 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
a0005 | 0/0 | 404 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
a0006 | 0/0 | 404 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
a0007 | 0/0 | 404 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
a0008 | 0/0 | 404 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | MELRV others(399): Show |
chr5 | 157455213 | 157479722 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1215 | 188 | 37 | 38 | 91 | 7 | 14 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0001c0010 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0001c0011 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0002c0002 | 0/0 | 1215 | 157 | 35 | 37 | 60 | 7 | 18 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0002c0004 | 1/0 | 1215 | 2 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0002c0007 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0003c0003 | 0/0 | 1215 | 37 | 19 | 8 | 0 | 2 | 8 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0004c0005 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0005c0006 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0006c0008 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0007c0009 | 0/0 | 1215 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 | ||
a0008c0012 | 0/0 | 1215 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | ATGGA others(1210): Show |
chr5 | 157455213 | 157479722 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 3085 | 134 | 17 | 17 | 86 | 2 | 11 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0004 | 0/0 | 3085 | 23 | 2 | 12 | 3 | 3 | 3 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0005 | 0/0 | 3082 | 11 | 10 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3077): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0007 | 0/0 | 3085 | 8 | 1 | 5 | 0 | 2 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0009 | 0/0 | 3085 | 4 | 1 | 3 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0010 | 0/0 | 3085 | 3 | 3 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0014 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0017 | 0/0 | 3085 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0018 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0019 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3077): Show |
chr5 | 157455213 | 157479722 |
a0001c0001t0020 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3077): Show |
chr5 | 157455213 | 157479722 |
a0001c0010t0002 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0001c0011t0002 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0001 | 0/0 | 3085 | 110 | 29 | 14 | 55 | 2 | 10 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0003 | 0/0 | 3085 | 28 | 1 | 21 | 1 | 3 | 2 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0006 | 0/0 | 3085 | 9 | 0 | 1 | 0 | 2 | 6 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0008 | 0/0 | 3085 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0011 | 0/0 | 3085 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0012 | 0/0 | 3085 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0015 | 0/0 | 3085 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0002t0016 | 0/0 | 3085 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0004t0003 | 1/0 | 3085 | 2 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0002c0007t0001 | 0/0 | 3085 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0003c0003t0001 | 0/0 | 3085 | 34 | 16 | 8 | 0 | 2 | 8 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0003c0003t0013 | 0/0 | 3085 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0003c0003t0021 | 0/0 | 3085 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0004c0005t0002 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0005c0006t0005 | 0/0 | 3082 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3077): Show |
chr5 | 157455213 | 157479722 |
a0006c0008t0001 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0007c0009t0001 | 0/0 | 3085 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
a0008c0012t0002 | 0/0 | 3085 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | GGCTT others(3080): Show |
chr5 | 157455213 | 157479722 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 79 | 9 | 14 | 46 | 2 | 8 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0008 | 0/1 | 14 | 0 | 0 | 13 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0015 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0016 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0004g0006 | 0/0 | 20 | 2 | 9 | 3 | 3 | 3 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0005g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0005g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0007g0012 | 0/0 | 6 | 0 | 4 | 0 | 2 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0007g0035 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0009g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0009g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0010g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0014g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0017g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0018g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0019g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0001t0020g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0010t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0001c0011t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0002 | 0/0 | 33 | 4 | 5 | 22 | 0 | 2 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0004 | 0/0 | 25 | 0 | 0 | 21 | 0 | 4 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0005 | 0/0 | 13 | 1 | 3 | 4 | 2 | 3 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0009 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0003g0003 | 0/0 | 24 | 1 | 18 | 1 | 2 | 2 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0003g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0006g0005 | 0/0 | 9 | 0 | 1 | 0 | 2 | 6 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0008g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0011g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0011g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0015g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0002t0016g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0004t0003g0028 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0002c0007t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0007 | 0/0 | 11 | 10 | 1 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0010 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0011 | 0/0 | 7 | 0 | 0 | 0 | 0 | 7 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0013g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0003c0003t0021g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0004c0005t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0005c0006t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0006c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0007c0009t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
a0008c0012t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | GBR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00140 | hp2 | a0003 | c0003 | t0001 | g0010 | EUR | GBR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00280 | hp1 | a0001 | c0001 | t0007 | g0012 | EUR | FIN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | FIN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | FIN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00544 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00544 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00558 | hp2 | a0004 | c0005 | t0002 | g0001 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00642 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00738 | hp1 | a0002 | c0002 | t0006 | g0005 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00738 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0079 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01070 | hp1 | a0003 | c0003 | t0001 | g0023 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01070 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0020 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01074 | hp1 | a0002 | c0004 | t0003 | g0028 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01074 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01081 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01106 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01109 | hp2 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0023 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01168 | hp1 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01169 | hp1 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01169 | hp2 | a0003 | c0003 | t0001 | g0023 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01175 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01175 | hp2 | a0003 | c0003 | t0001 | g0010 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01192 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01256 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0005 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01258 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01346 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0035 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01358 | hp2 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01361 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0012 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01433 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0021 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01515 | hp1 | a0002 | c0002 | t0006 | g0005 | EUR | IBS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0010 | EUR | IBS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01516 | hp1 | a0002 | c0002 | t0003 | g0062 | EUR | IBS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01516 | hp2 | a0002 | c0002 | t0003 | g0003 | EUR | IBS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01517 | hp1 | a0002 | c0002 | t0003 | g0003 | EUR | IBS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01517 | hp2 | a0002 | c0002 | t0006 | g0005 | EUR | IBS | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01884 | hp2 | a0005 | c0006 | t0005 | g0063 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01891 | hp1 | a0003 | c0003 | t0001 | g0007 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01928 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01934 | hp1 | a0003 | c0003 | t0001 | g0010 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01943 | hp1 | a0001 | c0001 | t0009 | g0020 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01952 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01978 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01981 | hp1 | a0003 | c0003 | t0001 | g0007 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01993 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0021 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02056 | hp2 | a0006 | c0008 | t0001 | g0002 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02083 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02145 | hp1 | a0001 | c0001 | t0019 | g0040 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0049 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0005 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CDX | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0013 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02273 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02273 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02280 | hp2 | a0002 | c0002 | t0003 | g0003 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02293 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02300 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02451 | hp2 | a0003 | c0003 | t0001 | g0007 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02622 | hp1 | a0001 | c0001 | t0020 | g0041 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02622 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02647 | hp2 | a0002 | c0002 | t0012 | g0003 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02683 | hp1 | a0002 | c0002 | t0006 | g0005 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02683 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02698 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02717 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02723 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0010 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02738 | hp1 | a0002 | c0002 | t0006 | g0005 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02896 | hp2 | a0002 | c0002 | t0012 | g0003 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02970 | hp1 | a0003 | c0003 | t0013 | g0007 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02970 | hp2 | a0003 | c0003 | t0001 | g0060 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0007 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0013 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03098 | hp1 | a0003 | c0003 | t0021 | g0007 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03130 | hp1 | a0002 | c0002 | t0015 | g0003 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03195 | hp1 | a0003 | c0003 | t0001 | g0007 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0018 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03225 | hp1 | a0001 | c0001 | t0010 | g0036 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03225 | hp2 | a0002 | c0002 | t0011 | g0002 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03453 | hp1 | a0003 | c0003 | t0001 | g0007 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0017 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03486 | hp2 | a0001 | c0001 | t0017 | g0001 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03492 | hp2 | a0002 | c0002 | t0006 | g0005 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0007 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0059 | AFR | GWD | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03579 | hp1 | a0008 | c0012 | t0002 | g0069 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03579 | hp2 | a0003 | c0003 | t0001 | g0007 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03654 | hp1 | a0002 | c0002 | t0006 | g0005 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03834 | hp2 | a0002 | c0002 | t0006 | g0005 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0011 | SAS | STU | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | STU | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04184 | hp2 | a0002 | c0002 | t0003 | g0003 | SAS | BEB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04199 | hp1 | a0002 | c0002 | t0006 | g0005 | SAS | STU | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | STU | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0005 | SAS | STU | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0006 | SAS | STU | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | YRI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | YRI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | CHB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0030 | AFR | YRI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18942 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18944 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18947 | hp2 | a0002 | c0002 | t0003 | g0003 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18950 | hp1 | a0001 | c0001 | t0018 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18963 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18972 | hp2 | a0001 | c0001 | t0014 | g0024 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18977 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18981 | hp2 | a0002 | c0002 | t0008 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18986 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19000 | hp1 | a0001 | c0010 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19004 | hp1 | a0002 | c0002 | t0008 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19006 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19007 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19030 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | LWK | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19030 | hp2 | a0003 | c0003 | t0001 | g0007 | AFR | LWK | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0007 | AFR | LWK | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19043 | hp2 | a0003 | c0003 | t0013 | g0007 | AFR | LWK | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19056 | hp1 | a0002 | c0002 | t0008 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19058 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19066 | hp1 | a0001 | c0011 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19076 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19087 | hp1 | a0002 | c0002 | t0008 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0009 | AFR | YRI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA19240 | hp2 | a0002 | c0007 | t0001 | g0013 | AFR | YRI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ASW | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | ASW | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20805 | hp1 | a0001 | c0001 | t0007 | g0012 | EUR | TSI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0005 | EUR | TSI | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | GIH | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01123 | hp1 | a0002 | c0002 | t0016 | g0002 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG01123 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0025 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02109 | hp2 | a0002 | c0002 | t0011 | g0056 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | ACB | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03471 | hp1 | a0003 | c0003 | t0001 | g0055 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0025 | AFR | MSL | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG06807 | hp1 | a0003 | c0003 | t0001 | g0007 | AFR | USA | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | USA | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | USA | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | USA | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA21309 | hp1 | a0001 | c0001 | t0009 | g0043 | AFR | LWK | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | LWK | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0008 | REF | REF | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
homoSapiens_grch38 | hp1 | a0002 | c0004 | t0003 | g0028 | REF | REF | NIPAL4_chr5_157455213_157479722 | NIPAL4 | chr5 | 157455213 | 157479722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157463111 | T | G | 1 | a0004 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.55T>G | p.Tyr19Asp | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/6 | 163/3085 | 55/1215 | 19/404 | chr5 | 157463111 | |||
chr5:157463173 | C | A | 1 | a0005 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.117C>A | p.Ser39Arg | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/6 | 225/3085 | 117/1215 | 39/404 | chr5 | 157463173 | |||
chr5:157463266 | C | G | 1 | a0008 | 1 | HG03579.hp1 | missense_variant | MODERATE | c.210C>G | p.Ile70Met | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/6 | 318/3085 | 210/1215 | 70/404 | chr5 | 157463266 | |||
chr5:157471682 | A | G | 4 | a0001 a0004 a0005 others(1): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
missense_variant | MODERATE | c.451A>G | p.Arg151Gly | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/6 | 559/3085 | 451/1215 | 151/404 | chr5 | 157471682 | |||
chr5:157472340 | G | A | 1 | a0006 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.595G>A | p.Val199Met | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 703/3085 | 595/1215 | 199/404 | chr5 | 157472340 | |||
chr5:157472364 | T | A | 1 | a0007 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.619T>A | p.Ser207Thr | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 727/3085 | 619/1215 | 207/404 | chr5 | 157472364 | |||
chr5:157472917 | C | T | 1 | a0003 | 37 | HG00140.hp2 HG01070.hp1 HG01106.hp1 others(34): Show |
missense_variant | MODERATE | c.1172C>T | p.Ser391Leu | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1280/3085 | 1172/1215 | 391/404 | chr5 | 157472917 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157468771 | A | G | 1 | a0001c0011 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.384A>G | p.Ala128Ala | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/6 | 492/3085 | 384/1215 | 128/404 | chr5 | 157468771 | |||
chr5:157468783 | G | A | 1 | a0002c0007 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.396G>A | p.Thr132Thr | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/6 | 504/3085 | 396/1215 | 132/404 | chr5 | 157468783 | |||
chr5:157471666 | C | T | 1 | a0001c0010 | 1 | NA19000.hp1 | synonymous_variant | LOW | c.435C>T | p.Leu145Leu | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/6 | 543/3085 | 435/1215 | 145/404 | chr5 | 157471666 | |||
chr5:157472861 | T | C | 11 | a0001c0001 a0001c0010 a0001c0011 others(8): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
synonymous_variant | LOW | c.1116T>C | p.Val372Val | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1224/3085 | 1116/1215 | 372/404 | chr5 | 157472861 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157460250 | G | A | 1 | a0001c0001t0014 | 1 | NA18972.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/6 | 71 | chr5 | 157460250 | ||||||
chr5:157460301 | G | A | 1 | a0002c0002t0015 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-20G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/6 | 20 | chr5 | 157460301 | ||||||
chr5:157473039 | C | T | 2 | a0001c0001t0007 a0001c0001t0010 |
11 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*79C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 79 | chr5 | 157473039 | ||||||
chr5:157473041 | A | G | 1 | a0003c0003t0021 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 81 | chr5 | 157473041 | ||||||
chr5:157473057 | A | G | 1 | a0003c0003t0013 | 2 | HG02970.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*97A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 97 | chr5 | 157473057 | ||||||
chr5:157473187 | T | A | 1 | a0002c0002t0016 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227T>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 227 | chr5 | 157473187 | ||||||
chr5:157473188 | C | G | 1 | a0002c0002t0016 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*228C>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 228 | chr5 | 157473188 | ||||||
chr5:157473364 | CGTT | C | 4 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0020 others(1): Show |
14 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*423_*425delGTT | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 423 | INFO_REALIGN_3_PRIME | chr5 | 157473364 | |||||
chr5:157473405 | T | C | 1 | a0001c0001t0014 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*445T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 445 | chr5 | 157473405 | ||||||
chr5:157473526 | C | A | 2 | a0001c0001t0007 a0001c0001t0010 |
11 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*566C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 566 | chr5 | 157473526 | ||||||
chr5:157473562 | T | C | 1 | a0002c0002t0011 | 2 | HG02109.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*602T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 602 | chr5 | 157473562 | ||||||
chr5:157473583 | T | C | 2 | a0002c0002t0012 a0002c0002t0015 |
3 | HG02647.hp2 HG02896.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*623T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 623 | chr5 | 157473583 | ||||||
chr5:157473702 | C | T | 1 | a0001c0001t0020 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 742 | chr5 | 157473702 | ||||||
chr5:157473742 | T | C | 8 | a0001c0001t0002 a0001c0001t0014 a0001c0001t0017 others(5): Show |
141 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*782T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 782 | chr5 | 157473742 | ||||||
chr5:157473764 | T | A | 1 | a0001c0001t0017 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804T>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 804 | chr5 | 157473764 | ||||||
chr5:157473870 | A | T | 16 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(13): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*910A>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 910 | chr5 | 157473870 | ||||||
chr5:157473972 | A | G | 1 | a0001c0001t0019 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1012A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1012 | chr5 | 157473972 | ||||||
chr5:157474100 | G | T | 1 | a0002c0002t0006 | 9 | HG00738.hp1 HG01515.hp1 HG01517.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1140G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1140 | chr5 | 157474100 | ||||||
chr5:157474181 | C | T | 1 | a0001c0001t0010 | 3 | HG02109.hp1 HG03225.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1221C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1221 | chr5 | 157474181 | ||||||
chr5:157474208 | C | T | 1 | a0002c0002t0008 | 4 | NA18981.hp2 NA19004.hp1 NA19056.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1248C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1248 | chr5 | 157474208 | ||||||
chr5:157474316 | T | C | 29 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(26): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
3_prime_UTR_variant | MODIFIER | c.*1356T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1356 | chr5 | 157474316 | ||||||
chr5:157474375 | T | C | 1 | a0001c0001t0018 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1415T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1415 | chr5 | 157474375 | ||||||
chr5:157474607 | T | C | 3 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0010 |
15 | HG00280.hp1 HG01069.hp1 HG01071.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1647T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1647 | chr5 | 157474607 | ||||||
chr5:157474693 | G | T | 1 | a0001c0001t0007 | 8 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1733G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 6/6 | 1733 | chr5 | 157474693 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:157460453 | G | C | 2 | a0001c0001t0010g0025 a0001c0001t0010g0036 |
3 | HG02109.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.37+96G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157460453 | |||||||
chr5:157460465 | G | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0037 a0002c0002t0001g0005 others(2): Show |
27 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.37+108G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157460465 | |||||||
chr5:157460483 | G | T | 1 | a0002c0002t0001g0079 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.37+126G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157460483 | |||||||
chr5:157460500 | G | A | 1 | a0001c0001t0004g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.37+143G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157460500 | |||||||
chr5:157460645 | T | C | 5 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0026 others(2): Show |
12 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.37+288T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157460645 | |||||||
chr5:157460978 | C | A | 3 | a0001c0001t0005g0017 a0001c0001t0005g0026 a0001c0001t0019g0040 |
7 | HG01243.hp1 HG02145.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.37+621C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157460978 | |||||||
chr5:157461093 | TG | T | 7 | a0001c0001t0004g0006 a0001c0001t0004g0039 a0001c0001t0004g0044 others(4): Show |
28 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(25): Show |
intron_variant | MODIFIER | c.37+738delG | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr5 | 157461093 | ||||||
chr5:157461250 | T | C | 6 | a0002c0002t0001g0004 a0002c0002t0001g0021 a0002c0002t0001g0046 others(3): Show |
35 | HG00544.hp2 HG01167.hp1 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.37+893T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157461250 | |||||||
chr5:157461367 | A | G | 1 | a0002c0002t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.37+1010A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157461367 | |||||||
chr5:157461379 | C | G | 47 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(44): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.37+1022C>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157461379 | |||||||
chr5:157461443 | C | A | 1 | a0002c0002t0001g0048 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.37+1086C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157461443 | |||||||
chr5:157461870 | C | G | 1 | a0002c0002t0001g0038 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.38-1224C>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157461870 | |||||||
chr5:157461965 | G | A | 1 | a0001c0001t0019g0040 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.38-1129G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157461965 | |||||||
chr5:157462089 | C | A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(34): Show |
151 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.38-1005C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462089 | |||||||
chr5:157462211 | C | T | 31 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(28): Show |
138 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.38-883C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462211 | |||||||
chr5:157462241 | A | G | 1 | a0001c0001t0002g0078 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.38-853A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462241 | |||||||
chr5:157462242 | G | T | 1 | a0001c0001t0002g0016 | 5 | HG02280.hp1 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.38-852G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462242 | |||||||
chr5:157462247 | T | C | 2 | a0001c0001t0009g0020 a0001c0001t0009g0043 |
4 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-847T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462247 | |||||||
chr5:157462258 | G | C | 2 | a0002c0002t0001g0027 a0002c0002t0001g0049 |
3 | HG01243.hp2 HG02145.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.38-836G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462258 | |||||||
chr5:157462391 | G | A | 2 | a0002c0002t0001g0050 a0002c0002t0001g0051 |
2 | NA19001.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.38-703G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462391 | |||||||
chr5:157462477 | C | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0037 a0002c0002t0001g0005 others(2): Show |
27 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.38-617C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462477 | |||||||
chr5:157462690 | C | T | 30 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(27): Show |
137 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(134): Show |
intron_variant | MODIFIER | c.38-404C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462690 | |||||||
chr5:157462711 | T | C | 1 | a0001c0001t0004g0044 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.38-383T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462711 | |||||||
chr5:157462797 | T | C | 1 | a0002c0002t0003g0022 | 3 | HG01109.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.38-297T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462797 | |||||||
chr5:157462881 | C | T | 1 | a0001c0001t0020g0041 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.38-213C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462881 | |||||||
chr5:157462955 | T | C | 2 | a0001c0001t0009g0020 a0001c0001t0009g0043 |
4 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-139T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462955 | |||||||
chr5:157462999 | G | C | 1 | a0001c0001t0002g0064 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.38-95G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 1/5 | chr5 | 157462999 | |||||||
chr5:157463391 | C | T | 2 | a0001c0001t0007g0012 a0001c0001t0007g0035 |
8 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+58C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463391 | |||||||
chr5:157463392 | G | A | 3 | a0002c0002t0001g0009 a0002c0002t0001g0052 a0002c0002t0001g0053 |
10 | HG01884.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.277+59G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463392 | |||||||
chr5:157463515 | G | T | 1 | a0001c0001t0009g0020 | 3 | HG01069.hp1 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.277+182G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463515 | |||||||
chr5:157463547 | C | T | 1 | a0002c0002t0001g0047 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.277+214C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463547 | |||||||
chr5:157463734 | A | G | 1 | a0005c0006t0005g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.277+401A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463734 | |||||||
chr5:157463847 | G | A | 2 | a0001c0001t0010g0025 a0001c0001t0010g0036 |
3 | HG02109.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.277+514G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463847 | |||||||
chr5:157463853 | C | T | 1 | a0001c0001t0004g0045 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.277+520C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463853 | |||||||
chr5:157463889 | C | G | 43 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(40): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.277+556C>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157463889 | |||||||
chr5:157464059 | A | C | 1 | a0002c0002t0003g0062 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.277+726A>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464059 | |||||||
chr5:157464318 | G | A | 2 | a0001c0001t0007g0012 a0001c0001t0007g0035 |
8 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.277+985G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464318 | |||||||
chr5:157464345 | T | C | 47 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(44): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.277+1012T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464345 | |||||||
chr5:157464449 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.277+1116C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464449 | |||||||
chr5:157464516 | G | A | 1 | a0002c0002t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.277+1183G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464516 | |||||||
chr5:157464523 | G | A | 31 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(28): Show |
138 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(135): Show |
intron_variant | MODIFIER | c.277+1190G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464523 | |||||||
chr5:157464531 | G | A | 1 | a0002c0002t0001g0054 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.277+1198G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464531 | |||||||
chr5:157464534 | T | C | 1 | a0002c0002t0001g0050 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.277+1201T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464534 | |||||||
chr5:157464582 | C | T | 1 | a0002c0002t0001g0061 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.277+1249C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464582 | |||||||
chr5:157464780 | T | C | 4 | a0001c0001t0004g0006 a0001c0001t0004g0039 a0001c0001t0004g0044 others(1): Show |
23 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(20): Show |
intron_variant | MODIFIER | c.277+1447T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464780 | |||||||
chr5:157464844 | T | C | 1 | a0001c0001t0002g0065 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.277+1511T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464844 | |||||||
chr5:157464945 | T | C | 4 | a0001c0001t0007g0012 a0001c0001t0007g0035 a0001c0001t0010g0025 others(1): Show |
11 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.277+1612T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157464945 | |||||||
chr5:157465131 | T | C | 1 | a0001c0001t0002g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.277+1798T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465131 | |||||||
chr5:157465301 | C | T | 3 | a0001c0001t0002g0076 a0001c0001t0009g0020 a0001c0001t0009g0043 |
5 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.278-1748C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465301 | |||||||
chr5:157465302 | A | G | 47 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(44): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.278-1747A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465302 | |||||||
chr5:157465395 | T | C | 2 | a0001c0001t0002g0032 a0001c0001t0002g0067 |
3 | HG00741.hp1 HG02132.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.278-1654T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465395 | |||||||
chr5:157465423 | G | T | 1 | a0002c0002t0001g0031 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.278-1626G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465423 | |||||||
chr5:157465554 | T | G | 1 | a0003c0003t0001g0055 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.278-1495T>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465554 | |||||||
chr5:157465782 | G | A | 1 | a0005c0006t0005g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.278-1267G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465782 | |||||||
chr5:157465792 | G | C | 1 | a0002c0002t0001g0031 | 2 | HG02717.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.278-1257G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465792 | |||||||
chr5:157465802 | G | A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(34): Show |
151 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.278-1247G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465802 | |||||||
chr5:157465849 | G | T | 1 | a0001c0001t0009g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.278-1200G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465849 | |||||||
chr5:157465927 | A | G | 1 | a0001c0001t0002g0075 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.278-1122A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157465927 | |||||||
chr5:157466051 | AAG | A | 39 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(36): Show |
155 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(152): Show |
intron_variant | MODIFIER | c.278-988_278-987del others(2): Show |
NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr5 | 157466051 | ||||||
chr5:157466111 | A | G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0065 a0001c0001t0002g0074 |
16 | HG00558.hp1 HG02135.hp1 NA18943.hp2 others(13): Show |
intron_variant | MODIFIER | c.278-938A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157466111 | |||||||
chr5:157466122 | T | G | 1 | a0001c0001t0005g0017 | 4 | HG01243.hp1 HG02630.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-927T>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157466122 | |||||||
chr5:157466360 | G | A | 1 | a0001c0001t0002g0033 | 2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.278-689G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157466360 | |||||||
chr5:157466414 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(29): Show |
141 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.278-635G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157466414 | |||||||
chr5:157466448 | C | T | 1 | a0002c0002t0001g0021 | 3 | HG01167.hp1 HG01496.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.278-601C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157466448 | |||||||
chr5:157466576 | G | A | 2 | a0001c0001t0002g0014 a0001c0001t0002g0068 |
6 | NA18941.hp2 NA18957.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-473G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157466576 | |||||||
chr5:157466644 | G | A | 1 | a0001c0001t0020g0041 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278-405G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 2/5 | chr5 | 157466644 | |||||||
chr5:157467335 | C | A | 2 | a0001c0001t0009g0020 a0001c0001t0009g0043 |
4 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.334+230C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467335 | |||||||
chr5:157467335 | C | G | 43 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(40): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.334+230C>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467335 | |||||||
chr5:157467396 | G | A | 1 | a0001c0001t0009g0020 | 3 | HG01069.hp1 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.334+291G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467396 | |||||||
chr5:157467459 | G | A | 1 | a0001c0001t0004g0044 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.334+354G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467459 | |||||||
chr5:157467486 | AG | A | 1 | a0003c0003t0001g0010 | 7 | HG00140.hp2 HG01106.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.334+382delG | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467486 | |||||||
chr5:157467543 | C | T | 1 | a0005c0006t0005g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+438C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467543 | |||||||
chr5:157467733 | A | C | 1 | a0005c0006t0005g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.334+628A>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467733 | |||||||
chr5:157467734 | C | T | 1 | a0003c0003t0001g0011 | 7 | HG02683.hp2 HG02698.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.334+629C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467734 | |||||||
chr5:157467771 | G | T | 10 | a0003c0003t0001g0007 a0003c0003t0001g0010 a0003c0003t0001g0011 others(7): Show |
36 | HG00140.hp2 HG01070.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.334+666G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467771 | |||||||
chr5:157467910 | A | T | 84 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(81): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.334+805A>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157467910 | |||||||
chr5:157468005 | A | G | 1 | a0001c0001t0009g0043 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.335-717A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468005 | |||||||
chr5:157468062 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0014g0024 |
3 | HG00609.hp2 HG02523.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.335-660G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468062 | |||||||
chr5:157468071 | A | AT | 15 | a0001c0001t0004g0006 a0001c0001t0004g0039 a0001c0001t0004g0044 others(12): Show |
44 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(41): Show |
intron_variant | MODIFIER | c.335-636dupT | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 157468071 | ||||||
chr5:157468071 | AT | A | 4 | a0001c0001t0002g0068 a0001c0001t0010g0025 a0001c0001t0010g0036 others(1): Show |
6 | HG02109.hp1 HG02818.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.335-636delT | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr5 | 157468071 | ||||||
chr5:157468103 | C | T | 1 | a0001c0001t0002g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.335-619C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468103 | |||||||
chr5:157468115 | G | A | 33 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(30): Show |
142 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.335-607G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468115 | |||||||
chr5:157468294 | G | C | 6 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0026 others(3): Show |
13 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.335-428G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468294 | |||||||
chr5:157468307 | A | T | 1 | a0003c0003t0001g0059 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.335-415A>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468307 | |||||||
chr5:157468410 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.335-312G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468410 | |||||||
chr5:157468492 | G | A | 1 | a0008c0012t0002g0069 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.335-230G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468492 | |||||||
chr5:157468591 | G | C | 1 | a0003c0003t0001g0060 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.335-131G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468591 | |||||||
chr5:157468649 | A | G | 1 | a0002c0002t0001g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.335-73A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 3/5 | chr5 | 157468649 | |||||||
chr5:157469036 | C | T | 1 | a0001c0001t0007g0035 | 2 | HG01358.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.425+224C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469036 | |||||||
chr5:157469093 | T | C | 3 | a0002c0002t0001g0005 a0002c0002t0001g0038 a0002c0002t0006g0005 |
23 | HG00323.hp2 HG00544.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.425+281T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469093 | |||||||
chr5:157469146 | T | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(46): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.425+334T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469146 | |||||||
chr5:157469196 | T | C | 1 | a0001c0001t0005g0018 | 4 | HG02055.hp1 HG02717.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.425+384T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469196 | |||||||
chr5:157469702 | A | G | 1 | a0002c0002t0001g0027 | 2 | HG01243.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.425+890A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469702 | |||||||
chr5:157469728 | G | A | 1 | a0002c0002t0011g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.425+916G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469728 | |||||||
chr5:157469772 | C | T | 1 | a0002c0002t0001g0058 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.425+960C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469772 | |||||||
chr5:157469777 | C | A | 1 | a0001c0001t0002g0074 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.425+965C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469777 | |||||||
chr5:157469797 | T | C | 1 | a0001c0001t0009g0020 | 3 | HG01069.hp1 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.425+985T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469797 | |||||||
chr5:157469848 | T | A | 6 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0026 others(3): Show |
13 | HG01243.hp1 HG02055.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.425+1036T>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469848 | |||||||
chr5:157469949 | G | A | 1 | a0003c0003t0001g0030 | 2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.425+1137G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157469949 | |||||||
chr5:157470275 | C | G | 49 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(46): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.426-1382C>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470275 | |||||||
chr5:157470312 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.426-1345C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470312 | |||||||
chr5:157470625 | G | A | 1 | a0005c0006t0005g0063 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.426-1032G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470625 | |||||||
chr5:157470711 | T | C | 1 | a0001c0001t0002g0067 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.426-946T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470711 | |||||||
chr5:157470778 | C | T | 3 | a0002c0002t0001g0009 a0002c0002t0001g0052 a0002c0002t0001g0053 |
10 | HG01884.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.426-879C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470778 | |||||||
chr5:157470849 | T | G | 1 | a0001c0001t0010g0025 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.426-808T>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470849 | |||||||
chr5:157470850 | G | A | 1 | a0002c0002t0001g0057 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.426-807G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470850 | |||||||
chr5:157470928 | C | T | 2 | a0001c0001t0009g0020 a0001c0001t0009g0043 |
4 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.426-729C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470928 | |||||||
chr5:157470938 | A | G | 1 | a0002c0002t0001g0079 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.426-719A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157470938 | |||||||
chr5:157471125 | G | T | 49 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(46): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.426-532G>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471125 | |||||||
chr5:157471221 | G | C | 7 | a0001c0001t0005g0017 a0001c0001t0005g0018 a0001c0001t0005g0026 others(4): Show |
14 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.426-436G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471221 | |||||||
chr5:157471237 | T | C | 42 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(39): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.426-420T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471237 | |||||||
chr5:157471321 | C | A | 2 | a0001c0001t0002g0015 a0001c0001t0002g0066 |
6 | HG00621.hp1 HG02165.hp1 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.426-336C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471321 | |||||||
chr5:157471428 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.426-229C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471428 | |||||||
chr5:157471524 | A | G | 1 | a0001c0001t0009g0020 | 3 | HG01069.hp1 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.426-133A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471524 | |||||||
chr5:157471575 | G | C | 2 | a0001c0001t0009g0020 a0001c0001t0009g0043 |
4 | HG01069.hp1 HG01071.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.426-82G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471575 | |||||||
chr5:157471650 | C | T | 1 | a0001c0001t0009g0043 | 1 | NA21309.hp1 | splice_region_variant&intron_variant | LOW | c.426-7C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 4/5 | chr5 | 157471650 | |||||||
chr5:157471866 | C | A | 4 | a0001c0001t0007g0012 a0001c0001t0007g0035 a0001c0001t0010g0025 others(1): Show |
11 | HG00280.hp1 HG01074.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+49C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157471866 | |||||||
chr5:157471878 | C | T | 1 | a0001c0001t0002g0034 | 2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.586+61C>T | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157471878 | |||||||
chr5:157471891 | G | A | 97 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(94): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.586+74G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157471891 | |||||||
chr5:157471933 | G | C | 1 | a0003c0003t0001g0023 | 3 | HG01070.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.586+116G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157471933 | |||||||
chr5:157471959 | G | A | 32 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(29): Show |
141 | HG00099.hp2 HG00140.hp1 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.586+142G>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157471959 | |||||||
chr5:157471991 | G | C | 1 | a0001c0001t0010g0036 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.586+174G>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157471991 | |||||||
chr5:157472165 | A | C | 49 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(46): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.587-167A>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157472165 | |||||||
chr5:157472265 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.587-67A>G | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157472265 | |||||||
chr5:157472282 | T | C | 69 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0014 others(66): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.587-50T>C | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157472282 | |||||||
chr5:157472327 | C | A | 1 | a0001c0001t0002g0071 | 1 | NA19000.hp2 | splice_region_variant&intron_variant | LOW | c.587-5C>A | NIPAL4 | ENSG00000172548.15 | transcript | ENST00000311946.8 | protein_coding | 5/5 | chr5 | 157472327 |