Item | Value |
---|---|
geneid | 89781 |
ensemblid | ENSG00000100099.22 |
hgncid | 15844 |
symbol | HPS4 |
name | HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 |
refseq_nuc | NM_022081.6 |
refseq_prot | NP_071364.4 |
ensembl_nuc | ENST00000398145.7 |
ensembl_prot | ENSP00000381213.2 |
mane_status | MANE Select |
chr | chr22 |
start | 26450882 |
end | 26483783 |
strand | - |
ver | v1.2 |
region | chr22:26450882-26483783 |
region5000 | chr22:26445882-26488783 |
regionname0 | HPS4_chr22_26450882_26483783 |
regionname5000 | HPS4_chr22_26445882_26488783 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 708 | 165 | 30 | 34 | 76 | 5 | 19 | 61 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0002 | 0/0 | 708 | 127 | 27 | 17 | 60 | 8 | 15 | 49 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0003 | 1/0 | 708 | 85 | 20 | 17 | 41 | 1 | 5 | 35 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0004 | 0/0 | 708 | 8 | 5 | 3 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0005 | 0/0 | 708 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0006 | 0/0 | 708 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0007 | 0/0 | 708 | 2 | 0 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0008 | 0/0 | 708 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0009 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0010 | 0/0 | 708 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0011 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0012 | 0/0 | 708 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0013 | 0/0 | 708 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
a0014 | 0/0 | 708 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | MATST others(703): Show |
chr22 | 26445882 | 26488783 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2124 | 156 | 26 | 34 | 71 | 5 | 19 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0001c0007 | 0/0 | 2124 | 5 | 0 | 0 | 5 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0001c0010 | 0/0 | 2124 | 4 | 4 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0002c0002 | 0/0 | 2124 | 114 | 18 | 16 | 58 | 8 | 14 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0002c0005 | 0/0 | 2124 | 10 | 9 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0002c0018 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0002c0019 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0002c0021 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0003c0003 | 1/0 | 2124 | 61 | 18 | 17 | 21 | 1 | 3 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0003c0004 | 0/0 | 2124 | 21 | 0 | 0 | 20 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0003c0014 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0003c0015 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0003c0016 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0004c0008 | 0/0 | 2124 | 4 | 1 | 3 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0004c0009 | 0/0 | 2124 | 4 | 4 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0005c0006 | 0/0 | 2124 | 6 | 6 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0006c0011 | 0/0 | 2124 | 3 | 1 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0007c0013 | 0/0 | 2124 | 2 | 0 | 0 | 0 | 2 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0008c0012 | 0/0 | 2124 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0009c0017 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0010c0024 | 0/0 | 2124 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0011c0022 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0012c0023 | 0/0 | 2124 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0013c0025 | 0/0 | 2124 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 | ||
a0014c0020 | 0/0 | 2124 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | ATGGC others(2119): Show |
chr22 | 26445882 | 26488783 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5062 | 45 | 3 | 9 | 27 | 0 | 6 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0004 | 0/0 | 5060 | 40 | 7 | 11 | 15 | 1 | 6 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0005 | 0/0 | 5058 | 28 | 9 | 4 | 6 | 3 | 6 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5053): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0006 | 0/0 | 5056 | 20 | 1 | 5 | 13 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0013 | 0/0 | 5066 | 7 | 2 | 2 | 3 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0015 | 0/0 | 5064 | 6 | 1 | 1 | 3 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5059): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0027 | 0/0 | 5066 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0034 | 0/0 | 5060 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0045 | 0/1 | 5056 | 1 | 0 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0046 | 0/0 | 5064 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5059): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0048 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0050 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0051 | 0/0 | 5066 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0001c0001t0058 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0001c0007t0005 | 0/0 | 5058 | 5 | 0 | 0 | 5 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5053): Show |
chr22 | 26445882 | 26488783 |
a0001c0010t0003 | 0/0 | 5066 | 4 | 4 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0002 | 0/0 | 5056 | 44 | 2 | 4 | 25 | 7 | 6 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0003 | 0/0 | 5066 | 25 | 13 | 4 | 4 | 0 | 4 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0010 | 0/0 | 5058 | 11 | 0 | 1 | 8 | 0 | 2 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5053): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0011 | 0/0 | 5060 | 5 | 0 | 0 | 5 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0014 | 0/0 | 5066 | 7 | 0 | 5 | 0 | 1 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0017 | 0/0 | 5058 | 6 | 0 | 0 | 6 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5053): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0021 | 0/0 | 5062 | 3 | 0 | 0 | 3 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0026 | 0/0 | 5060 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0032 | 0/0 | 5066 | 2 | 1 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0033 | 0/0 | 5056 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0035 | 0/0 | 5066 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCGC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0036 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCGC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0037 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0047 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0049 | 0/0 | 5056 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0052 | 0/0 | 5058 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5053): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0057 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0002t0059 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5059): Show |
chr22 | 26445882 | 26488783 |
a0002c0005t0003 | 0/0 | 5066 | 10 | 9 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0018t0010 | 0/0 | 5058 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5053): Show |
chr22 | 26445882 | 26488783 |
a0002c0019t0003 | 0/0 | 5066 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0002c0021t0002 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0008 | 0/0 | 5066 | 9 | 9 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0009 | 1/0 | 5066 | 15 | 0 | 5 | 7 | 0 | 2 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0016 | 0/0 | 5066 | 6 | 0 | 2 | 3 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0018 | 0/0 | 5060 | 4 | 0 | 3 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0019 | 0/0 | 5062 | 4 | 0 | 0 | 4 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0022 | 0/0 | 5064 | 3 | 0 | 1 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5059): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0023 | 0/0 | 5046 | 2 | 0 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5041): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0024 | 0/0 | 5062 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0025 | 0/0 | 5060 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0028 | 0/0 | 5046 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5041): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0029 | 0/0 | 5062 | 2 | 0 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0030 | 0/0 | 5066 | 2 | 1 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0031 | 0/0 | 5064 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5059): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0038 | 0/0 | 5048 | 1 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5043): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0039 | 0/0 | 5046 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5041): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0041 | 0/0 | 5062 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0044 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0053 | 0/0 | 5066 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0054 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0055 | 0/0 | 5066 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0003t0056 | 0/0 | 5062 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0003c0004t0007 | 0/0 | 5050 | 18 | 0 | 0 | 17 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5045): Show |
chr22 | 26445882 | 26488783 |
a0003c0004t0040 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5047): Show |
chr22 | 26445882 | 26488783 |
a0003c0004t0042 | 0/0 | 5066 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0004t0043 | 0/0 | 5052 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5047): Show |
chr22 | 26445882 | 26488783 |
a0003c0014t0025 | 0/0 | 5060 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0003c0015t0008 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0003c0016t0031 | 0/0 | 5064 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5059): Show |
chr22 | 26445882 | 26488783 |
a0004c0008t0012 | 0/0 | 5066 | 4 | 1 | 3 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0004c0009t0012 | 0/0 | 5066 | 4 | 4 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0005c0006t0008 | 0/0 | 5066 | 6 | 6 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0006c0011t0020 | 0/0 | 5066 | 3 | 1 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0007c0013t0002 | 0/0 | 5056 | 2 | 0 | 0 | 0 | 2 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0008c0012t0011 | 0/0 | 5060 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0009c0017t0011 | 0/0 | 5060 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5055): Show |
chr22 | 26445882 | 26488783 |
a0010c0024t0003 | 0/0 | 5066 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0011c0022t0033 | 0/0 | 5056 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5051): Show |
chr22 | 26445882 | 26488783 |
a0012c0023t0001 | 0/0 | 5062 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
a0013c0025t0003 | 0/0 | 5066 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5061): Show |
chr22 | 26445882 | 26488783 |
a0014c0020t0001 | 0/0 | 5062 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | CTCTC others(5057): Show |
chr22 | 26445882 | 26488783 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 14 | 0 | 3 | 7 | 0 | 4 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0004 | 0/0 | 6 | 1 | 3 | 1 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0015 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0023 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0027 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0005 | 0/0 | 6 | 1 | 1 | 2 | 2 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0016 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0005g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0013g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0013g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0013g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0013g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0013g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0013g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0013g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0015g0026 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0015g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0015g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0027g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0027g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0034g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0034g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0045g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0046g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0048g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0050g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0051g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0001t0058g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0007t0005g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0007t0005g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0007t0005g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0010t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0010t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0001c0010t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0002 | 0/0 | 11 | 0 | 2 | 8 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0014 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0048 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0010g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0010g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0010g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0010g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0010g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0010g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0010g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0011g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0011g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0011g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0014g0051 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0014g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0014g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0014g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0014g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0017g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0017g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0017g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0017g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0017g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0021g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0021g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0021g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0026g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0032g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0032g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0033g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0035g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0036g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0037g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0047g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0049g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0052g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0057g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0002t0059g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0005t0003g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0005t0003g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0005t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0005t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0005t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0018t0010g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0019t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0002c0021t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0008g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0008g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0008g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0008g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0007 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0009g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0016g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0016g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0016g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0016g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0016g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0018g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0018g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0019g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0019g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0019g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0022g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0022g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0022g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0023g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0024g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0024g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0025g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0028g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0028g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0029g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0029g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0030g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0030g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0031g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0038g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0039g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0041g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0044g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0053g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0054g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0055g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0003t0056g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0003 | 0/0 | 8 | 0 | 0 | 7 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0040g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0042g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0004t0043g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0014t0025g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0015t0008g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0003c0016t0031g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0004c0008t0012g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0004c0008t0012g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0004c0008t0012g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0004c0009t0012g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0004c0009t0012g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0004c0009t0012g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0004c0009t0012g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0005c0006t0008g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0005c0006t0008g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0006c0011t0020g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0006c0011t0020g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0007c0013t0002g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0008c0012t0011g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0009c0017t0011g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0010c0024t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0011c0022t0033g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0012c0023t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0013c0025t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
a0014c0020t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0002 | g0014 | EUR | GBR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0016 | EUR | GBR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00140 | hp1 | a0002 | c0002 | t0002 | g0048 | EUR | GBR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00140 | hp2 | a0002 | c0002 | t0014 | g0051 | EUR | GBR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00323 | hp1 | a0001 | c0001 | t0006 | g0244 | EUR | FIN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00323 | hp2 | a0002 | c0002 | t0002 | g0192 | EUR | FIN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00423 | hp1 | a0009 | c0017 | t0011 | g0180 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00423 | hp2 | a0001 | c0001 | t0013 | g0241 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00438 | hp1 | a0002 | c0002 | t0003 | g0199 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00544 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00597 | hp1 | a0003 | c0004 | t0007 | g0019 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00597 | hp2 | a0003 | c0003 | t0016 | g0081 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00609 | hp2 | a0003 | c0004 | t0007 | g0102 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0121 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00639 | hp2 | a0003 | c0003 | t0009 | g0082 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00642 | hp2 | a0002 | c0002 | t0002 | g0198 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00673 | hp1 | a0001 | c0001 | t0006 | g0141 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00673 | hp2 | a0002 | c0019 | t0003 | g0225 | EAS | CHS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00733 | hp1 | a0002 | c0002 | t0010 | g0112 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00733 | hp2 | a0002 | c0002 | t0002 | g0214 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00735 | hp1 | a0001 | c0001 | t0005 | g0257 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00735 | hp2 | a0003 | c0003 | t0009 | g0011 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00738 | hp1 | a0002 | c0002 | t0033 | g0275 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00738 | hp2 | a0001 | c0001 | t0015 | g0254 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00741 | hp1 | a0003 | c0003 | t0039 | g0264 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG00741 | hp2 | a0002 | c0002 | t0003 | g0219 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01069 | hp1 | a0003 | c0003 | t0009 | g0011 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01069 | hp2 | a0001 | c0001 | t0013 | g0181 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01070 | hp1 | a0001 | c0001 | t0048 | g0247 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01070 | hp2 | a0002 | c0002 | t0014 | g0276 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01071 | hp1 | a0003 | c0003 | t0009 | g0011 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01071 | hp2 | a0002 | c0002 | t0014 | g0051 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0016 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0005 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01099 | hp2 | a0003 | c0003 | t0023 | g0034 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01106 | hp1 | a0001 | c0001 | t0006 | g0110 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0027 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01167 | hp1 | a0003 | c0003 | t0016 | g0030 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01167 | hp2 | a0003 | c0003 | t0023 | g0034 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01168 | hp2 | a0004 | c0008 | t0012 | g0086 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01175 | hp1 | a0004 | c0008 | t0012 | g0032 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01175 | hp2 | a0010 | c0024 | t0003 | g0217 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0004 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01192 | hp2 | a0003 | c0003 | t0016 | g0030 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01243 | hp1 | a0002 | c0005 | t0003 | g0020 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0163 | AMR | PUR | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0164 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01256 | hp1 | a0006 | c0011 | t0020 | g0035 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01256 | hp2 | a0002 | c0002 | t0014 | g0277 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01257 | hp1 | a0002 | c0002 | t0014 | g0052 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0123 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01258 | hp1 | a0002 | c0002 | t0014 | g0052 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01258 | hp2 | a0006 | c0011 | t0020 | g0035 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01261 | hp2 | a0001 | c0001 | t0046 | g0246 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01358 | hp1 | a0003 | c0003 | t0018 | g0018 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01358 | hp2 | a0003 | c0003 | t0022 | g0078 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01361 | hp1 | a0001 | c0001 | t0006 | g0109 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01496 | hp1 | a0002 | c0002 | t0032 | g0266 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01515 | hp1 | a0002 | c0002 | t0002 | g0215 | EUR | IBS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01515 | hp2 | a0001 | c0001 | t0005 | g0005 | EUR | IBS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01516 | hp1 | a0007 | c0013 | t0002 | g0037 | EUR | IBS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01516 | hp2 | a0002 | c0002 | t0002 | g0231 | EUR | IBS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01517 | hp1 | a0007 | c0013 | t0002 | g0037 | EUR | IBS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01517 | hp2 | a0001 | c0001 | t0005 | g0005 | EUR | IBS | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01884 | hp1 | a0002 | c0005 | t0003 | g0020 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01884 | hp2 | a0002 | c0002 | t0057 | g0233 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01891 | hp1 | a0002 | c0005 | t0003 | g0131 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01891 | hp2 | a0002 | c0002 | t0003 | g0021 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01934 | hp1 | a0002 | c0002 | t0003 | g0195 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01934 | hp2 | a0003 | c0003 | t0056 | g0091 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0004 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01975 | hp2 | a0003 | c0003 | t0018 | g0018 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01981 | hp1 | a0003 | c0003 | t0018 | g0018 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01981 | hp2 | a0002 | c0002 | t0003 | g0036 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0148 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01993 | hp2 | a0001 | c0001 | t0005 | g0170 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02004 | hp1 | a0001 | c0001 | t0013 | g0146 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02004 | hp2 | a0004 | c0008 | t0012 | g0032 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02015 | hp1 | a0001 | c0001 | t0050 | g0248 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02015 | hp2 | a0002 | c0002 | t0026 | g0046 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02055 | hp1 | a0002 | c0005 | t0003 | g0012 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02055 | hp2 | a0002 | c0002 | t0002 | g0116 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02056 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02056 | hp2 | a0003 | c0004 | t0043 | g0105 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02071 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02071 | hp2 | a0003 | c0003 | t0009 | g0007 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02074 | hp1 | a0011 | c0022 | t0033 | g0273 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02074 | hp2 | a0001 | c0001 | t0015 | g0026 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02132 | hp2 | a0002 | c0002 | t0010 | g0009 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02135 | hp1 | a0002 | c0002 | t0003 | g0149 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02145 | hp2 | a0005 | c0006 | t0008 | g0006 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02148 | hp1 | a0002 | c0002 | t0003 | g0210 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02148 | hp2 | a0003 | c0003 | t0029 | g0097 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0203 | EAS | CDX | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02155 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | CDX | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02165 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | CDX | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02165 | hp2 | a0003 | c0003 | t0019 | g0031 | EAS | CDX | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02257 | hp1 | a0003 | c0003 | t0008 | g0029 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02257 | hp2 | a0002 | c0002 | t0003 | g0115 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0125 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02280 | hp2 | a0002 | c0002 | t0003 | g0137 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02293 | hp1 | a0003 | c0003 | t0029 | g0090 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02293 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02300 | hp2 | a0003 | c0003 | t0009 | g0011 | AMR | PEL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02451 | hp1 | a0002 | c0002 | t0003 | g0111 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02451 | hp2 | a0003 | c0003 | t0054 | g0085 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02523 | hp1 | a0002 | c0002 | t0011 | g0024 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02523 | hp2 | a0002 | c0002 | t0010 | g0009 | EAS | KHV | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02615 | hp1 | a0001 | c0010 | t0003 | g0117 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02615 | hp2 | a0004 | c0009 | t0012 | g0087 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02622 | hp1 | a0001 | c0001 | t0034 | g0279 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02622 | hp2 | a0002 | c0002 | t0003 | g0189 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02630 | hp1 | a0006 | c0011 | t0020 | g0107 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0157 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0177 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02647 | hp2 | a0003 | c0003 | t0008 | g0028 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02683 | hp1 | a0002 | c0002 | t0003 | g0229 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02683 | hp2 | a0002 | c0002 | t0002 | g0113 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02698 | hp1 | a0002 | c0002 | t0002 | g0048 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0176 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02717 | hp1 | a0003 | c0015 | t0008 | g0067 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02717 | hp2 | a0004 | c0009 | t0012 | g0098 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02723 | hp1 | a0003 | c0014 | t0025 | g0059 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02723 | hp2 | a0001 | c0001 | t0013 | g0156 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02735 | hp1 | a0012 | c0023 | t0001 | g0256 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0154 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0184 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0016 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02818 | hp1 | a0003 | c0003 | t0024 | g0062 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02818 | hp2 | a0002 | c0005 | t0003 | g0012 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02886 | hp1 | a0003 | c0003 | t0008 | g0017 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02886 | hp2 | a0002 | c0005 | t0003 | g0012 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02895 | hp1 | a0003 | c0003 | t0008 | g0017 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0161 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02896 | hp2 | a0003 | c0003 | t0028 | g0259 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02897 | hp1 | a0003 | c0003 | t0028 | g0260 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02922 | hp2 | a0001 | c0010 | t0003 | g0038 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02965 | hp1 | a0001 | c0010 | t0003 | g0038 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02965 | hp2 | a0003 | c0003 | t0008 | g0066 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02970 | hp2 | a0005 | c0006 | t0008 | g0006 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02976 | hp2 | a0003 | c0003 | t0025 | g0061 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03017 | hp2 | a0003 | c0003 | t0009 | g0007 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03041 | hp1 | a0003 | c0003 | t0044 | g0060 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03041 | hp2 | a0002 | c0002 | t0002 | g0230 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03098 | hp1 | a0002 | c0002 | t0047 | g0190 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03098 | hp2 | a0001 | c0010 | t0003 | g0118 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03130 | hp1 | a0013 | c0025 | t0003 | g0232 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03130 | hp2 | a0003 | c0003 | t0008 | g0028 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03195 | hp1 | a0002 | c0002 | t0003 | g0136 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03209 | hp1 | a0005 | c0006 | t0008 | g0065 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03209 | hp2 | a0002 | c0002 | t0003 | g0021 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0152 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03239 | hp2 | a0002 | c0018 | t0010 | g0211 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03453 | hp1 | a0001 | c0001 | t0004 | g0158 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03453 | hp2 | a0003 | c0003 | t0041 | g0106 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03486 | hp1 | a0003 | c0003 | t0008 | g0017 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03486 | hp2 | a0001 | c0001 | t0015 | g0159 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03490 | hp2 | a0001 | c0001 | t0005 | g0119 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03516 | hp1 | a0001 | c0001 | t0058 | g0234 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03516 | hp2 | a0003 | c0003 | t0008 | g0029 | AFR | ESN | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0004 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03540 | hp2 | a0002 | c0005 | t0003 | g0020 | AFR | GWD | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03579 | hp1 | a0002 | c0002 | t0003 | g0021 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03579 | hp2 | a0002 | c0005 | t0003 | g0130 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03654 | hp1 | a0002 | c0002 | t0002 | g0178 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03654 | hp2 | a0003 | c0016 | t0031 | g0079 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03669 | hp1 | a0002 | c0002 | t0003 | g0200 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03669 | hp2 | a0001 | c0001 | t0015 | g0026 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0036 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03704 | hp1 | a0002 | c0002 | t0002 | g0201 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03704 | hp2 | a0002 | c0002 | t0010 | g0179 | SAS | PJL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03831 | hp1 | a0003 | c0003 | t0009 | g0007 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0191 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0128 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03927 | hp2 | a0002 | c0002 | t0049 | g0220 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0185 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03942 | hp2 | a0001 | c0001 | t0005 | g0016 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04115 | hp2 | a0002 | c0002 | t0010 | g0197 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04184 | hp1 | a0003 | c0004 | t0007 | g0003 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0047 | SAS | BEB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04199 | hp1 | a0003 | c0003 | t0016 | g0096 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04199 | hp2 | a0002 | c0002 | t0014 | g0274 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04204 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | STU | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0160 | AFR | YRI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18522 | hp2 | a0001 | c0001 | t0034 | g0278 | AFR | YRI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18612 | hp1 | a0002 | c0002 | t0010 | g0009 | EAS | CHB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | CHB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | CHB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0167 | EAS | CHB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18906 | hp2 | a0002 | c0002 | t0032 | g0267 | AFR | YRI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18939 | hp1 | a0003 | c0003 | t0009 | g0080 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18939 | hp2 | a0014 | c0020 | t0001 | g0150 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18940 | hp1 | a0003 | c0003 | t0055 | g0094 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18942 | hp1 | a0003 | c0004 | t0007 | g0003 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18942 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18945 | hp2 | a0002 | c0002 | t0010 | g0009 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18946 | hp2 | a0003 | c0003 | t0019 | g0083 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18949 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18950 | hp2 | a0003 | c0003 | t0018 | g0075 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18951 | hp1 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18951 | hp2 | a0003 | c0004 | t0007 | g0003 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18953 | hp1 | a0002 | c0002 | t0017 | g0050 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18953 | hp2 | a0002 | c0002 | t0010 | g0213 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18954 | hp1 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18956 | hp2 | a0003 | c0004 | t0007 | g0033 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18959 | hp1 | a0001 | c0007 | t0005 | g0043 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18959 | hp2 | a0002 | c0002 | t0026 | g0046 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18960 | hp2 | a0003 | c0003 | t0009 | g0071 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18962 | hp1 | a0001 | c0007 | t0005 | g0040 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18963 | hp1 | a0001 | c0001 | t0051 | g0249 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18963 | hp2 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18965 | hp1 | a0003 | c0003 | t0022 | g0058 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0005 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18967 | hp2 | a0003 | c0004 | t0042 | g0101 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18968 | hp1 | a0002 | c0002 | t0011 | g0024 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18969 | hp2 | a0002 | c0002 | t0037 | g0055 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18970 | hp2 | a0002 | c0002 | t0052 | g0258 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18971 | hp1 | a0002 | c0021 | t0002 | g0235 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18971 | hp2 | a0001 | c0001 | t0015 | g0026 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18972 | hp1 | a0003 | c0003 | t0031 | g0074 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18972 | hp2 | a0002 | c0002 | t0059 | g0272 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18973 | hp2 | a0002 | c0002 | t0002 | g0196 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18974 | hp2 | a0003 | c0003 | t0009 | g0076 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18975 | hp1 | a0003 | c0004 | t0007 | g0099 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18975 | hp2 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18976 | hp1 | a0003 | c0004 | t0007 | g0103 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18976 | hp2 | a0001 | c0001 | t0027 | g0151 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18978 | hp1 | a0003 | c0003 | t0030 | g0072 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18978 | hp2 | a0002 | c0002 | t0011 | g0194 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18981 | hp1 | a0003 | c0003 | t0009 | g0092 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18982 | hp1 | a0008 | c0012 | t0011 | g0044 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18982 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18983 | hp1 | a0003 | c0003 | t0009 | g0007 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18983 | hp2 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18984 | hp1 | a0003 | c0003 | t0009 | g0007 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18984 | hp2 | a0001 | c0001 | t0006 | g0142 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18985 | hp1 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18985 | hp2 | a0002 | c0002 | t0017 | g0050 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18988 | hp2 | a0002 | c0002 | t0010 | g0226 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0171 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18989 | hp2 | a0002 | c0002 | t0011 | g0024 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18990 | hp1 | a0001 | c0001 | t0013 | g0240 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18990 | hp2 | a0001 | c0007 | t0005 | g0043 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18991 | hp1 | a0003 | c0004 | t0007 | g0033 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18991 | hp2 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18992 | hp1 | a0003 | c0003 | t0016 | g0093 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18993 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18993 | hp2 | a0003 | c0003 | t0022 | g0073 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18994 | hp1 | a0003 | c0003 | t0019 | g0069 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18994 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18997 | hp1 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18997 | hp2 | a0003 | c0003 | t0019 | g0031 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18998 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18999 | hp1 | a0001 | c0001 | t0013 | g0236 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA18999 | hp2 | a0002 | c0002 | t0017 | g0268 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19000 | hp2 | a0002 | c0002 | t0010 | g0224 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19002 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19002 | hp2 | a0003 | c0004 | t0007 | g0019 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19003 | hp1 | a0002 | c0002 | t0003 | g0212 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19003 | hp2 | a0002 | c0002 | t0017 | g0269 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19004 | hp1 | a0002 | c0002 | t0021 | g0204 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19007 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19009 | hp2 | a0008 | c0012 | t0011 | g0044 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19010 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19012 | hp2 | a0002 | c0002 | t0003 | g0221 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19030 | hp1 | a0005 | c0006 | t0008 | g0006 | AFR | LWK | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19030 | hp2 | a0003 | c0003 | t0008 | g0064 | AFR | LWK | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19043 | hp1 | a0003 | c0003 | t0030 | g0084 | AFR | LWK | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19043 | hp2 | a0004 | c0009 | t0012 | g0089 | AFR | LWK | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19054 | hp2 | a0003 | c0004 | t0007 | g0003 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19055 | hp1 | a0003 | c0003 | t0053 | g0077 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19055 | hp2 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19056 | hp1 | a0001 | c0007 | t0005 | g0040 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0242 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19057 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19057 | hp2 | a0001 | c0001 | t0006 | g0049 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19058 | hp1 | a0003 | c0004 | t0007 | g0003 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19060 | hp1 | a0001 | c0001 | t0027 | g0168 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19060 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19062 | hp2 | a0003 | c0004 | t0007 | g0019 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19064 | hp1 | a0002 | c0002 | t0010 | g0009 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19066 | hp1 | a0002 | c0002 | t0017 | g0270 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19066 | hp2 | a0003 | c0004 | t0007 | g0003 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19067 | hp1 | a0003 | c0003 | t0016 | g0095 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19067 | hp2 | a0002 | c0002 | t0021 | g0222 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19076 | hp2 | a0002 | c0002 | t0035 | g0053 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19079 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19080 | hp2 | a0003 | c0004 | t0007 | g0003 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19082 | hp2 | a0003 | c0004 | t0007 | g0104 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19084 | hp1 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19084 | hp2 | a0003 | c0004 | t0007 | g0108 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19085 | hp1 | a0002 | c0002 | t0017 | g0271 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19085 | hp2 | a0003 | c0004 | t0040 | g0100 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19086 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19087 | hp2 | a0001 | c0007 | t0005 | g0144 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19088 | hp1 | a0002 | c0002 | t0011 | g0208 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19089 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19090 | hp1 | a0002 | c0002 | t0021 | g0223 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19090 | hp2 | a0003 | c0004 | t0007 | g0003 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19091 | hp2 | a0002 | c0002 | t0036 | g0054 | EAS | JPT | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0126 | AFR | YRI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA19240 | hp2 | a0002 | c0005 | t0003 | g0129 | AFR | YRI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20129 | hp1 | a0002 | c0005 | t0003 | g0012 | AFR | ASW | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ASW | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20752 | hp1 | a0002 | c0002 | t0002 | g0114 | EUR | TSI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20752 | hp2 | a0003 | c0003 | t0038 | g0265 | EUR | TSI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0014 | EUR | TSI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0015 | EUR | TSI | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA20905 | hp2 | a0002 | c0002 | t0003 | g0202 | SAS | GIH | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0023 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG01123 | hp2 | a0001 | c0001 | t0006 | g0182 | AMR | CLM | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0135 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02109 | hp2 | a0005 | c0006 | t0008 | g0006 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02486 | hp1 | a0001 | c0001 | t0013 | g0120 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02486 | hp2 | a0003 | c0003 | t0024 | g0063 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02559 | hp1 | a0004 | c0009 | t0012 | g0088 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG02559 | hp2 | a0002 | c0002 | t0003 | g0262 | AFR | ACB | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03471 | hp1 | a0002 | c0002 | t0003 | g0132 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG03471 | hp2 | a0005 | c0006 | t0008 | g0006 | AFR | MSL | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG06807 | hp1 | a0004 | c0008 | t0012 | g0068 | AFR | USA | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0140 | AFR | USA | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA21309 | hp1 | a0002 | c0002 | t0003 | g0263 | AFR | LWK | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
homoSapiens | chm13v2 | a0001 | c0001 | t0045 | g0057 | REF | REF | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
homoSapiens | grch38p0 | a0003 | c0003 | t0009 | g0070 | REF | REF | HPS4_chr22_26445882_26488783 | HPS4 | chr22 | 26445882 | 26488783 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:26457867 | C | T | 2 | a0008 a0009 |
3 | HG00423.hp1 NA18982.hp1 NA19009.hp2 |
missense_variant | MODERATE | c.1947G>A | p.Met649Ile | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/14 | 2535/5066 | 1947/2127 | 649/708 | chr22 | 26457867 | |||
chr22:26457939 | C | A | 11 | a0001 a0002 a0004 others(8): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
missense_variant | MODERATE | c.1875G>T | p.Gln625His | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/14 | 2463/5066 | 1875/2127 | 625/708 | chr22 | 26457939 | |||
chr22:26458475 | G | A | 11 | a0001 a0002 a0004 others(8): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
missense_variant | MODERATE | c.1816C>T | p.His606Tyr | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 12/14 | 2404/5066 | 1816/2127 | 606/708 | chr22 | 26458475 | |||
chr22:26463930 | G | A | 1 | a0006 | 3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
missense_variant | MODERATE | c.1700C>T | p.Ala567Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 2288/5066 | 1700/2127 | 567/708 | chr22 | 26463930 | |||
chr22:26463976 | C | T | 10 | a0001 a0002 a0007 others(7): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
missense_variant | MODERATE | c.1654G>A | p.Val552Met | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 2242/5066 | 1654/2127 | 552/708 | chr22 | 26463976 | |||
chr22:26463990 | C | G | 1 | a0008 | 2 | NA18982.hp1 NA19009.hp2 |
missense_variant | MODERATE | c.1640G>C | p.Cys547Ser | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 2228/5066 | 1640/2127 | 547/708 | chr22 | 26463990 | |||
chr22:26464303 | G | C | 7 | a0002 a0007 a0008 others(4): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
missense_variant | MODERATE | c.1327C>G | p.Leu443Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 1915/5066 | 1327/2127 | 443/708 | chr22 | 26464303 | |||
chr22:26464569 | G | C | 1 | a0001 | 4 | HG02615.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.1061C>G | p.Ser354Cys | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 1649/5066 | 1061/2127 | 354/708 | chr22 | 26464569 | |||
chr22:26464570 | A | T | 1 | a0001 | 4 | HG02615.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.1060T>A | p.Ser354Thr | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 1648/5066 | 1060/2127 | 354/708 | chr22 | 26464570 | |||
chr22:26464646 | C | G | 1 | a0013 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.984G>C | p.Leu328Phe | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 1572/5066 | 984/2127 | 328/708 | chr22 | 26464646 | |||
chr22:26465507 | T | A | 1 | a0007 | 2 | HG01516.hp1 HG01517.hp1 |
missense_variant | MODERATE | c.751A>T | p.Thr251Ser | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/14 | 1339/5066 | 751/2127 | 251/708 | chr22 | 26465507 | |||
chr22:26465548 | G | A | 1 | a0005 | 6 | HG02109.hp2 HG02145.hp2 HG02970.hp2 others(3): Show |
missense_variant | MODERATE | c.710C>T | p.Ala237Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/14 | 1298/5066 | 710/2127 | 237/708 | chr22 | 26465548 | |||
chr22:26466246 | T | C | 10 | a0001 a0002 a0007 others(7): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
missense_variant | MODERATE | c.686A>G | p.Glu229Gly | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/14 | 1274/5066 | 686/2127 | 229/708 | chr22 | 26466246 | |||
chr22:26466252 | G | A | 1 | a0014 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.680C>T | p.Thr227Met | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/14 | 1268/5066 | 680/2127 | 227/708 | chr22 | 26466252 | |||
chr22:26472843 | G | C | 1 | a0011 | 1 | HG02074.hp1 | missense_variant | MODERATE | c.373C>G | p.Leu125Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 5/14 | 961/5066 | 373/2127 | 125/708 | chr22 | 26472843 | |||
chr22:26477003 | T | A | 1 | a0012 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.266A>T | p.Asp89Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/14 | 854/5066 | 266/2127 | 89/708 | chr22 | 26477003 | |||
chr22:26477019 | T | C | 1 | a0010 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.250A>G | p.Ile84Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/14 | 838/5066 | 250/2127 | 84/708 | chr22 | 26477019 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:26453281 | G | A | 1 | a0002c0018 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.2079C>T | p.Ser693Ser | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 2667/5066 | 2079/2127 | 693/708 | chr22 | 26453281 | |||
chr22:26457915 | G | A | 2 | a0002c0005 a0013c0025 |
11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
synonymous_variant | LOW | c.1899C>T | p.Val633Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/14 | 2487/5066 | 1899/2127 | 633/708 | chr22 | 26457915 | |||
chr22:26464538 | T | C | 1 | a0003c0015 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1092A>G | p.Gln364Gln | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 1680/5066 | 1092/2127 | 364/708 | chr22 | 26464538 | |||
chr22:26464547 | G | C | 1 | a0003c0016 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.1083C>G | p.Val361Val | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 1671/5066 | 1083/2127 | 361/708 | chr22 | 26464547 | |||
chr22:26464685 | G | A | 1 | a0002c0019 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.945C>T | p.Asp315Asp | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/14 | 1533/5066 | 945/2127 | 315/708 | chr22 | 26464685 | |||
chr22:26465517 | A | T | 1 | a0001c0007 | 5 | NA18959.hp1 NA18962.hp1 NA18990.hp2 others(2): Show |
synonymous_variant | LOW | c.741T>A | p.Pro247Pro | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/14 | 1329/5066 | 741/2127 | 247/708 | chr22 | 26465517 | |||
chr22:26466236 | C | T | 1 | a0003c0004 | 21 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(18): Show |
synonymous_variant | LOW | c.696G>A | p.Pro232Pro | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/14 | 1284/5066 | 696/2127 | 232/708 | chr22 | 26466236 | |||
chr22:26470745 | G | A | 1 | a0002c0021 | 1 | NA18971.hp1 | synonymous_variant | LOW | c.570C>T | p.Leu190Leu | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/14 | 1158/5066 | 570/2127 | 190/708 | chr22 | 26470745 | |||
chr22:26470757 | C | T | 1 | a0004c0008 | 4 | HG01168.hp2 HG01175.hp1 HG02004.hp2 others(1): Show |
synonymous_variant | LOW | c.558G>A | p.Ser186Ser | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/14 | 1146/5066 | 558/2127 | 186/708 | chr22 | 26470757 | |||
chr22:26472371 | C | T | 1 | a0003c0014 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.432G>A | p.Glu144Glu | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/14 | 1020/5066 | 432/2127 | 144/708 | chr22 | 26472371 | |||
chr22:26481748 | G | A | 1 | a0013c0025 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.15C>T | p.Thr5Thr | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/14 | 603/5066 | 15/2127 | 5/708 | chr22 | 26481748 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:26450964 | T | C | 1 | a0002c0002t0032 | 2 | HG01496.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2269A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 2269 | chr22 | 26450964 | ||||||
chr22:26451024 | A | G | 1 | a0006c0011t0020 | 3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2209T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 2209 | chr22 | 26451024 | ||||||
chr22:26451207 | C | T | 1 | a0003c0003t0041 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2026G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 2026 | chr22 | 26451207 | ||||||
chr22:26451210 | T | C | 1 | a0003c0003t0023 | 2 | HG01099.hp2 HG01167.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2023A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 2023 | chr22 | 26451210 | ||||||
chr22:26451217 | G | A | 1 | a0002c0002t0049 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2016C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 2016 | chr22 | 26451217 | ||||||
chr22:26451271 | G | A | 16 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(13): Show |
162 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*1962C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1962 | chr22 | 26451271 | ||||||
chr22:26451471 | C | T | 2 | a0001c0001t0046 a0001c0001t0048 |
2 | HG01070.hp1 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1762G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1762 | chr22 | 26451471 | ||||||
chr22:26451546 | T | C | 2 | a0002c0002t0021 a0002c0002t0026 |
5 | HG02015.hp2 NA18959.hp2 NA19004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1687A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1687 | chr22 | 26451546 | ||||||
chr22:26451620 | G | T | 56 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(53): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
3_prime_UTR_variant | MODIFIER | c.*1613C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1613 | chr22 | 26451620 | ||||||
chr22:26451644 | G | T | 4 | a0003c0004t0007 a0003c0004t0040 a0003c0004t0042 others(1): Show |
21 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1589C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1589 | chr22 | 26451644 | ||||||
chr22:26451684 | C | T | 1 | a0002c0002t0047 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1549 | chr22 | 26451684 | ||||||
chr22:26451705 | A | C | 4 | a0003c0003t0024 a0003c0003t0025 a0003c0003t0044 others(1): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1528T>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1528 | chr22 | 26451705 | ||||||
chr22:26451734 | T | C | 1 | a0001c0001t0050 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1499A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1499 | chr22 | 26451734 | ||||||
chr22:26451846 | A | T | 2 | a0002c0002t0021 a0002c0002t0026 |
5 | HG02015.hp2 NA18959.hp2 NA19004.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1387T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1387 | chr22 | 26451846 | ||||||
chr22:26451980 | C | T | 1 | a0006c0011t0020 | 3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1253G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1253 | chr22 | 26451980 | ||||||
chr22:26451983 | G | A | 4 | a0003c0003t0024 a0003c0003t0025 a0003c0003t0044 others(1): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1250C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1250 | chr22 | 26451983 | ||||||
chr22:26451986 | ACG | A | 3 | a0001c0001t0015 a0001c0001t0046 a0002c0002t0059 |
8 | HG00738.hp2 HG01261.hp2 HG02074.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1245_*1246delCG | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1245 | chr22 | 26451986 | ||||||
chr22:26451986 | ACGCG | A | 7 | a0001c0001t0001 a0001c0001t0048 a0002c0002t0021 others(4): Show |
53 | HG00609.hp1 HG00642.hp1 HG01070.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1243_*1246delCGCG | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1243 | chr22 | 26451986 | ||||||
chr22:26451986 | ACGCGCG | A | 7 | a0001c0001t0004 a0001c0001t0034 a0002c0002t0011 others(4): Show |
53 | HG00423.hp1 HG01099.hp1 HG01106.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1241_*1246delCGCG others(2): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1241 | chr22 | 26451986 | ||||||
chr22:26451986 | ACGCGCGC others(1): Show |
A | 6 | a0001c0001t0005 a0001c0007t0005 a0002c0002t0010 others(3): Show |
52 | HG00099.hp2 HG00544.hp1 HG00733.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1239_*1246delCGCG others(4): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1239 | chr22 | 26451986 | ||||||
chr22:26451986 | ACGCGCGC others(3): Show |
A | 9 | a0001c0001t0006 a0001c0001t0050 a0002c0002t0002 others(6): Show |
72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1237_*1246delCGCG others(6): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1237 | chr22 | 26451986 | ||||||
chr22:26451992 | GCGCGCGC others(9): Show |
G | 1 | a0010c0024t0003 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225_*1240delTGTG others(12): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1225 | chr22 | 26451992 | ||||||
chr22:26451994 | GCGCGCGC others(5): Show |
G | 8 | a0001c0001t0013 a0001c0001t0058 a0001c0010t0003 others(5): Show |
29 | HG00140.hp2 HG01069.hp2 HG01070.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1227_*1238delTGCG others(8): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1227 | chr22 | 26451994 | ||||||
chr22:26451994 | GCGCGCGC others(7): Show |
G | 5 | a0001c0001t0013 a0001c0010t0003 a0002c0002t0003 others(2): Show |
17 | HG01168.hp2 HG01243.hp1 HG01884.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1225_*1238delTGTG others(10): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1225 | chr22 | 26451994 | ||||||
chr22:26451994 | GCGCGCGC others(9): Show |
G | 3 | a0001c0001t0013 a0002c0005t0003 a0004c0008t0012 |
5 | HG01175.hp1 HG02004.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1223_*1238delTGTG others(12): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1223 | chr22 | 26451994 | ||||||
chr22:26451994 | GCGCGCGC others(11): Show |
G | 1 | a0001c0001t0013 | 3 | HG00423.hp2 NA18990.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1221_*1238delTGTG others(14): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1221 | chr22 | 26451994 | ||||||
chr22:26451994 | GCGCGCGC others(13): Show |
G | 1 | a0004c0009t0012 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219_*1238delTGTG others(16): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1219 | chr22 | 26451994 | ||||||
chr22:26451995 | C | A | 1 | a0001c0001t0051 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1238G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1238 | chr22 | 26451995 | ||||||
chr22:26451995 | C | T | 1 | a0003c0003t0030 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1238G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1238 | chr22 | 26451995 | ||||||
chr22:26451996 | G | A | 1 | a0001c0001t0027 | 2 | NA18976.hp2 NA19060.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1237C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1237 | chr22 | 26451996 | ||||||
chr22:26451996 | GCGCGCGC others(3): Show |
G | 2 | a0002c0002t0003 a0002c0019t0003 |
3 | HG00438.hp1 HG00673.hp2 HG00741.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1227_*1236delTGCG others(6): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1227 | chr22 | 26451996 | ||||||
chr22:26451996 | GCGCGCGC others(5): Show |
G | 2 | a0002c0002t0032 a0004c0009t0012 |
4 | HG01496.hp1 HG02559.hp1 HG02615.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1225_*1236delTGTG others(8): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1225 | chr22 | 26451996 | ||||||
chr22:26451996 | GCGCGCGC others(7): Show |
G | 3 | a0002c0002t0003 a0002c0002t0032 a0002c0002t0057 |
6 | HG01884.hp2 HG01891.hp2 HG03209.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1223_*1236delTGTG others(10): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1223 | chr22 | 26451996 | ||||||
chr22:26451996 | GCGCGCGC others(11): Show |
G | 3 | a0003c0003t0008 a0003c0015t0008 a0005c0006t0008 |
11 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1219_*1236delTGTG others(14): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1219 | chr22 | 26451996 | ||||||
chr22:26451997 | C | A | 1 | a0003c0004t0042 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1236G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1236 | chr22 | 26451997 | ||||||
chr22:26451998 | G | A | 3 | a0001c0001t0015 a0001c0001t0027 a0002c0002t0059 |
5 | HG00738.hp2 NA18972.hp2 NA18975.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1235C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1235 | chr22 | 26451998 | ||||||
chr22:26451998 | G | T | 1 | a0003c0003t0053 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1235C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1235 | chr22 | 26451998 | ||||||
chr22:26451998 | GCGCGCGC others(9): Show |
G | 2 | a0003c0003t0008 a0006c0011t0020 |
6 | HG01256.hp1 HG01258.hp2 HG02630.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1219_*1234delTGTG others(12): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1219 | chr22 | 26451998 | ||||||
chr22:26451998 | GCGCGCGC others(11): Show |
G | 1 | a0003c0003t0008 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1217_*1234delTGTG others(14): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1217 | chr22 | 26451998 | ||||||
chr22:26451998 | GCGCGCGC others(13): Show |
G | 1 | a0003c0003t0008 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1215_*1234delTGTG others(16): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1215 | chr22 | 26451998 | ||||||
chr22:26451999 | C | T | 1 | a0003c0003t0055 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1234G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1234 | chr22 | 26451999 | ||||||
chr22:26452000 | G | A | 9 | a0001c0001t0001 a0001c0001t0015 a0001c0001t0027 others(6): Show |
48 | HG00609.hp1 HG00642.hp1 HG00738.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1233C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1233 | chr22 | 26452000 | ||||||
chr22:26452000 | GCGCGCAC others(7): Show |
G | 1 | a0003c0004t0040 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1219_*1232delTGTG others(10): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1219 | chr22 | 26452000 | ||||||
chr22:26452000 | GCGCGCAC others(9): Show |
G | 1 | a0003c0004t0007 | 18 | HG00597.hp1 HG00609.hp2 HG04184.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1217_*1232delTGTG others(12): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1217 | chr22 | 26452000 | ||||||
chr22:26452000 | GCGCGCAC others(13): Show |
G | 2 | a0003c0003t0023 a0003c0003t0028 |
4 | HG01099.hp2 HG01167.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1213_*1232delTGTG others(16): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1213 | chr22 | 26452000 | ||||||
chr22:26452002 | G | A | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0015 others(14): Show |
108 | HG00423.hp1 HG00609.hp1 HG00642.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1231C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1231 | chr22 | 26452002 | ||||||
chr22:26452002 | GCGCACAC others(7): Show |
G | 1 | a0003c0004t0043 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1217_*1230delTGTG others(10): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1217 | chr22 | 26452002 | ||||||
chr22:26452003 | C | A | 1 | a0002c0002t0059 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1230G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1230 | chr22 | 26452003 | ||||||
chr22:26452004 | G | A | 24 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(21): Show |
167 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*1229C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1229 | chr22 | 26452004 | ||||||
chr22:26452004 | GCA | G | 3 | a0003c0003t0022 a0003c0003t0031 a0003c0016t0031 |
5 | HG01358.hp2 HG03654.hp2 NA18965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1227_*1228delTG | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1227 | chr22 | 26452004 | ||||||
chr22:26452004 | GCACA | G | 4 | a0003c0003t0019 a0003c0003t0024 a0003c0003t0029 others(1): Show |
9 | HG01934.hp2 HG02148.hp2 HG02165.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1225_*1228delTGTG | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1225 | chr22 | 26452004 | ||||||
chr22:26452004 | GCACACA | G | 3 | a0003c0003t0018 a0003c0003t0025 a0003c0014t0025 |
6 | HG01358.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1223_*1228delTGTG others(2): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1223 | chr22 | 26452004 | ||||||
chr22:26452004 | GCACACAC others(7): Show |
G | 1 | a0003c0004t0042 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1215_*1228delTGTG others(10): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1215 | chr22 | 26452004 | ||||||
chr22:26452004 | GCACACAC others(11): Show |
G | 1 | a0003c0003t0038 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1211_*1228delTGTG others(14): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1211 | chr22 | 26452004 | ||||||
chr22:26452004 | GCACACAC others(13): Show |
G | 1 | a0003c0003t0039 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1209_*1228delTGTG others(16): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1209 | chr22 | 26452004 | ||||||
chr22:26452006 | A | G | 4 | a0003c0003t0016 a0003c0003t0030 a0003c0003t0054 others(1): Show |
10 | HG00597.hp2 HG01167.hp1 HG01192.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1227T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1227 | chr22 | 26452006 | ||||||
chr22:26452008 | A | G | 4 | a0003c0003t0030 a0003c0003t0031 a0003c0003t0054 others(1): Show |
5 | HG02451.hp2 HG03654.hp2 NA18972.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1225T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1225 | chr22 | 26452008 | ||||||
chr22:26452010 | A | G | 4 | a0003c0003t0024 a0003c0003t0029 a0003c0003t0054 others(1): Show |
6 | HG01934.hp2 HG02148.hp2 HG02293.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1223T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1223 | chr22 | 26452010 | ||||||
chr22:26452012 | A | G | 5 | a0003c0003t0024 a0003c0003t0025 a0003c0003t0041 others(2): Show |
6 | HG02451.hp2 HG02486.hp2 HG02723.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1221T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1221 | chr22 | 26452012 | ||||||
chr22:26452014 | A | G | 1 | a0003c0003t0044 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1219T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1219 | chr22 | 26452014 | ||||||
chr22:26452024 | A | G | 1 | a0003c0003t0038 | 1 | NA20752.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1209T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1209 | chr22 | 26452024 | ||||||
chr22:26452026 | A | G | 2 | a0003c0003t0038 a0003c0003t0039 |
2 | HG00741.hp1 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1207T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1207 | chr22 | 26452026 | ||||||
chr22:26452044 | T | A | 1 | a0003c0003t0028 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1189A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 1189 | chr22 | 26452044 | ||||||
chr22:26452753 | G | A | 1 | a0003c0004t0043 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 480 | chr22 | 26452753 | ||||||
chr22:26452756 | G | A | 4 | a0003c0003t0024 a0003c0003t0025 a0003c0003t0044 others(1): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*477C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 477 | chr22 | 26452756 | ||||||
chr22:26452987 | G | A | 1 | a0003c0003t0056 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*246C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 246 | chr22 | 26452987 | ||||||
chr22:26453005 | T | C | 1 | a0002c0002t0052 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*228A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 228 | chr22 | 26453005 | ||||||
chr22:26453164 | C | T | 1 | a0003c0003t0053 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*69G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 14/14 | 69 | chr22 | 26453164 | ||||||
chr22:26481947 | T | C | 1 | a0006c0011t0020 | 3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
5_prime_UTR_variant | MODIFIER | c.-185A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/14 | 185 | chr22 | 26481947 | ||||||
chr22:26482015 | G | A | 45 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(42): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-253C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/14 | chr22 | 26482015 | |||||||
chr22:26482058 | A | G | 61 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(58): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
5_prime_UTR_variant | MODIFIER | c.-296T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/14 | 296 | chr22 | 26482058 | ||||||
chr22:26482067 | T | C | 1 | a0002c0002t0057 | 1 | HG01884.hp2 | 5_prime_UTR_variant | MODIFIER | c.-305A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/14 | 305 | chr22 | 26482067 | ||||||
chr22:26482182 | T | C | 1 | a0001c0001t0058 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-420A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/14 | 420 | chr22 | 26482182 | ||||||
chr22:26483725 | T | C | 6 | a0002c0002t0014 a0002c0002t0017 a0002c0002t0032 others(3): Show |
18 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-530A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/14 | 1963 | chr22 | 26483725 | ||||||
chr22:26483749 | G | A | 1 | a0001c0001t0034 | 2 | HG02622.hp1 NA18522.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-554C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/14 | chr22 | 26483749 | |||||||
chr22:26483777 | C | T | 1 | a0002c0002t0037 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-582G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/14 | 2015 | chr22 | 26483777 | ||||||
chr22:26483780 | A | C | 2 | a0002c0002t0035 a0002c0002t0036 |
2 | NA19076.hp2 NA19091.hp2 |
5_prime_UTR_variant | MODIFIER | c.-585T>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/14 | 2018 | chr22 | 26483780 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:26453436 | A | G | 1 | a0002c0002t0002g0198 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1956-32T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26453436 | |||||||
chr22:26453645 | G | A | 1 | a0002c0002t0010g0179 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1956-241C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26453645 | |||||||
chr22:26453660 | C | G | 1 | a0008c0012t0011g0044 | 2 | NA18982.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1956-256G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26453660 | |||||||
chr22:26453700 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(229): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1956-296A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26453700 | |||||||
chr22:26453855 | C | T | 8 | a0002c0002t0003g0021 a0002c0002t0003g0132 a0002c0002t0003g0135 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1956-451G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26453855 | |||||||
chr22:26453907 | G | C | 1 | a0001c0001t0004g0169 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1956-503C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26453907 | |||||||
chr22:26453939 | C | A | 2 | a0002c0002t0032g0266 a0002c0002t0032g0267 |
2 | HG01496.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1956-535G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26453939 | |||||||
chr22:26454015 | C | T | 1 | a0004c0009t0012g0087 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1956-611G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26454015 | |||||||
chr22:26454016 | G | A | 1 | a0003c0003t0008g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1956-612C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26454016 | |||||||
chr22:26454271 | G | A | 1 | a0001c0001t0004g0148 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1956-867C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26454271 | |||||||
chr22:26454527 | T | A | 5 | a0003c0003t0024g0062 a0003c0003t0024g0063 a0003c0003t0025g0061 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1956-1123A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26454527 | |||||||
chr22:26454555 | C | T | 1 | a0002c0002t0002g0206 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1956-1151G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26454555 | |||||||
chr22:26454924 | T | C | 2 | a0002c0002t0014g0052 a0002c0002t0014g0277 |
3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1956-1520A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26454924 | |||||||
chr22:26454974 | T | C | 4 | a0004c0008t0012g0032 a0004c0008t0012g0068 a0004c0008t0012g0086 others(1): Show |
5 | HG01168.hp2 HG01175.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1956-1570A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26454974 | |||||||
chr22:26455115 | C | T | 1 | a0001c0001t0004g0167 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1956-1711G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455115 | |||||||
chr22:26455175 | G | A | 6 | a0002c0005t0003g0012 a0002c0005t0003g0020 a0002c0005t0003g0129 others(3): Show |
11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1956-1771C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455175 | |||||||
chr22:26455254 | A | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(227): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.1956-1850T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455254 | |||||||
chr22:26455346 | C | T | 1 | a0001c0001t0006g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1956-1942G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455346 | |||||||
chr22:26455482 | A | G | 9 | a0001c0001t0001g0145 a0001c0001t0001g0165 a0001c0001t0004g0023 others(6): Show |
11 | HG01123.hp1 HG01255.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1956-2078T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455482 | |||||||
chr22:26455578 | G | T | 1 | a0003c0003t0023g0034 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1956-2174C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455578 | |||||||
chr22:26455596 | G | T | 1 | a0003c0003t0008g0064 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1956-2192C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455596 | |||||||
chr22:26455743 | T | TAA | 6 | a0004c0008t0012g0032 a0004c0008t0012g0068 a0004c0008t0012g0086 others(3): Show |
7 | HG01168.hp2 HG01175.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.1955+2114_1955+211 others(6): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455743 | |||||||
chr22:26455744 | A | T | 1 | a0001c0001t0004g0164 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1955+2115T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455744 | |||||||
chr22:26455862 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(212): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1955+1997T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26455862 | |||||||
chr22:26456113 | G | C | 1 | a0003c0003t0023g0034 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1955+1746C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456113 | |||||||
chr22:26456191 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(212): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1955+1668T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456191 | |||||||
chr22:26456368 | A | T | 1 | a0001c0001t0001g0253 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1955+1491T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456368 | |||||||
chr22:26456417 | T | C | 4 | a0003c0003t0018g0018 a0003c0003t0029g0090 a0003c0003t0029g0097 others(1): Show |
6 | HG01358.hp1 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1955+1442A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456417 | |||||||
chr22:26456617 | C | T | 3 | a0004c0008t0012g0032 a0004c0008t0012g0068 a0004c0008t0012g0086 |
4 | HG01168.hp2 HG01175.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1955+1242G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456617 | |||||||
chr22:26456664 | T | G | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1955+1195A>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456664 | |||||||
chr22:26456711 | GACTAATA others(1): Show |
G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(212): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1955+1140_1955+114 others(12): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456711 | |||||||
chr22:26456891 | G | A | 3 | a0004c0009t0012g0087 a0004c0009t0012g0088 a0004c0009t0012g0098 |
3 | HG02559.hp1 HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1955+968C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456891 | |||||||
chr22:26456960 | C | A | 3 | a0001c0001t0001g0243 a0001c0001t0004g0015 a0001c0001t0006g0244 |
6 | HG00323.hp1 HG01099.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1955+899G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26456960 | |||||||
chr22:26457203 | C | T | 1 | a0003c0003t0041g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1955+656G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457203 | |||||||
chr22:26457209 | A | AC | 195 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(192): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1955+649dupG | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457209 | |||||||
chr22:26457210 | C | CCT | 26 | a0001c0001t0001g0186 a0001c0001t0001g0237 a0001c0001t0001g0239 others(23): Show |
28 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.1955+648_1955+649i others(4): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457210 | |||||||
chr22:26457210 | C | CCTT | 6 | a0001c0001t0006g0109 a0002c0002t0003g0135 a0003c0003t0023g0034 others(3): Show |
7 | HG01099.hp2 HG01167.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.1955+648_1955+649i others(5): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457210 | |||||||
chr22:26457210 | CT | C | 17 | a0003c0003t0008g0017 a0003c0003t0008g0028 a0003c0003t0008g0029 others(14): Show |
25 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.1955+648delA | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457210 | |||||||
chr22:26457211 | T | C | 3 | a0001c0001t0001g0173 a0001c0007t0005g0144 a0002c0002t0014g0277 |
3 | HG01256.hp2 NA19087.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1955+648A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457211 | |||||||
chr22:26457232 | T | C | 1 | a0001c0001t0005g0170 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1955+627A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457232 | |||||||
chr22:26457631 | T | C | 2 | a0003c0003t0023g0034 a0003c0003t0041g0106 |
3 | HG01099.hp2 HG01167.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1955+228A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457631 | |||||||
chr22:26457650 | A | G | 1 | a0002c0002t0002g0116 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1955+209T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457650 | |||||||
chr22:26457657 | G | T | 1 | a0001c0001t0005g0039 | 2 | HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1955+202C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457657 | |||||||
chr22:26457709 | G | A | 8 | a0002c0002t0003g0021 a0002c0002t0003g0132 a0002c0002t0003g0135 others(5): Show |
10 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1955+150C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457709 | |||||||
chr22:26457782 | G | A | 1 | a0003c0003t0038g0265 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1955+77C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457782 | |||||||
chr22:26457788 | T | C | 2 | a0003c0003t0028g0259 a0003c0003t0028g0260 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1955+71A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457788 | |||||||
chr22:26457821 | G | A | 1 | a0002c0002t0047g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1955+38C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457821 | |||||||
chr22:26457832 | G | A | 1 | a0003c0003t0023g0034 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1955+27C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457832 | |||||||
chr22:26457841 | C | T | 2 | a0002c0002t0032g0266 a0002c0002t0032g0267 |
2 | HG01496.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1955+18G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 13/13 | chr22 | 26457841 | |||||||
chr22:26458000 | A | G | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1847-33T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 12/13 | chr22 | 26458000 | |||||||
chr22:26458014 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(229): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1847-47A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 12/13 | chr22 | 26458014 | |||||||
chr22:26458087 | C | T | 2 | a0002c0002t0002g0201 a0002c0002t0003g0200 |
2 | HG03669.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1847-120G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 12/13 | chr22 | 26458087 | |||||||
chr22:26458106 | C | T | 1 | a0002c0002t0003g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1847-139G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 12/13 | chr22 | 26458106 | |||||||
chr22:26458150 | C | T | 1 | a0002c0002t0017g0269 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1847-183G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 12/13 | chr22 | 26458150 | |||||||
chr22:26458716 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(212): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1714-139A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458716 | |||||||
chr22:26458750 | G | A | 7 | a0004c0008t0012g0032 a0004c0008t0012g0068 a0004c0008t0012g0086 others(4): Show |
8 | HG01168.hp2 HG01175.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1714-173C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458750 | |||||||
chr22:26458794 | C | T | 3 | a0001c0001t0001g0243 a0001c0001t0004g0015 a0001c0001t0006g0244 |
6 | HG00323.hp1 HG01099.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1714-217G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458794 | |||||||
chr22:26458797 | G | A | 1 | a0002c0002t0002g0203 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1714-220C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458797 | |||||||
chr22:26458820 | C | CG | 7 | a0001c0001t0001g0188 a0001c0001t0001g0250 a0001c0001t0001g0252 others(4): Show |
8 | HG02895.hp2 HG02897.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1714-244dupC | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458820 | |||||||
chr22:26458821 | G | GA | 10 | a0002c0002t0002g0116 a0002c0002t0002g0207 a0002c0002t0003g0132 others(7): Show |
11 | HG01099.hp2 HG01167.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1714-245dupT | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458821 | |||||||
chr22:26458822 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(105): Show |
164 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.1714-245T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458822 | |||||||
chr22:26458965 | GA | G | 2 | a0003c0003t0023g0034 a0003c0003t0041g0106 |
3 | HG01099.hp2 HG01167.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1714-389delT | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26458965 | |||||||
chr22:26459071 | G | T | 1 | a0002c0002t0003g0199 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1714-494C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459071 | |||||||
chr22:26459110 | C | T | 2 | a0003c0003t0023g0034 a0003c0003t0041g0106 |
3 | HG01099.hp2 HG01167.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1714-533G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459110 | |||||||
chr22:26459190 | C | T | 2 | a0003c0003t0023g0034 a0003c0003t0041g0106 |
3 | HG01099.hp2 HG01167.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1714-613G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459190 | |||||||
chr22:26459274 | C | T | 11 | a0003c0004t0007g0003 a0003c0004t0007g0019 a0003c0004t0007g0033 others(8): Show |
21 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.1714-697G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459274 | |||||||
chr22:26459717 | C | A | 1 | a0002c0002t0021g0204 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1714-1140G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459717 | |||||||
chr22:26459797 | C | G | 1 | a0004c0009t0012g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1714-1220G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459797 | |||||||
chr22:26459820 | C | T | 2 | a0002c0002t0003g0189 a0002c0002t0003g0263 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1714-1243G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459820 | |||||||
chr22:26459949 | A | T | 1 | a0003c0004t0007g0103 | 1 | NA18976.hp1 | intron_variant | MODIFIER | c.1714-1372T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26459949 | |||||||
chr22:26460111 | C | T | 1 | a0003c0003t0031g0074 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1714-1534G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460111 | |||||||
chr22:26460118 | T | C | 2 | a0003c0003t0008g0017 a0003c0003t0008g0064 |
4 | HG02886.hp1 HG02895.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1714-1541A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460118 | |||||||
chr22:26460165 | T | G | 1 | a0001c0001t0034g0279 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1714-1588A>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460165 | |||||||
chr22:26460393 | C | T | 1 | a0001c0001t0005g0119 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1714-1816G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460393 | |||||||
chr22:26460404 | C | T | 1 | a0003c0003t0041g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1714-1827G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460404 | |||||||
chr22:26460474 | C | T | 16 | a0002c0002t0003g0021 a0002c0002t0003g0132 a0002c0002t0003g0135 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1714-1897G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460474 | |||||||
chr22:26460496 | A | G | 2 | a0002c0002t0002g0230 a0002c0002t0002g0231 |
2 | HG01516.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1714-1919T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460496 | |||||||
chr22:26460541 | G | A | 1 | a0003c0003t0016g0093 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1714-1964C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460541 | |||||||
chr22:26460551 | A | G | 1 | a0002c0002t0010g0197 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1714-1974T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460551 | |||||||
chr22:26460772 | C | T | 16 | a0002c0002t0002g0113 a0002c0002t0002g0114 a0002c0002t0002g0116 others(13): Show |
21 | HG00423.hp1 HG00733.hp1 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.1714-2195G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460772 | |||||||
chr22:26460974 | C | A | 1 | a0004c0008t0012g0086 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1714-2397G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26460974 | |||||||
chr22:26461009 | T | C | 1 | a0003c0003t0041g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1714-2432A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26461009 | |||||||
chr22:26461160 | C | T | 1 | a0003c0003t0024g0063 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1714-2583G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26461160 | |||||||
chr22:26461309 | G | A | 2 | a0003c0003t0008g0028 a0003c0003t0008g0066 |
3 | HG02647.hp2 HG02965.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1713+2608C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26461309 | |||||||
chr22:26461621 | G | A | 1 | a0002c0002t0003g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1713+2296C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26461621 | |||||||
chr22:26461633 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(206): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1713+2284C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26461633 | |||||||
chr22:26461649 | G | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1713+2268C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26461649 | |||||||
chr22:26461692 | A | G | 1 | a0003c0003t0041g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1713+2225T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26461692 | |||||||
chr22:26462126 | CA | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(212): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.1713+1790delT | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462126 | |||||||
chr22:26462129 | A | G | 1 | a0003c0003t0023g0034 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1713+1788T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462129 | |||||||
chr22:26462142 | A | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1713+1775T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462142 | |||||||
chr22:26462371 | G | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1713+1546C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462371 | |||||||
chr22:26462441 | T | C | 1 | a0002c0002t0003g0137 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1713+1476A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462441 | |||||||
chr22:26462779 | A | G | 4 | a0003c0003t0028g0259 a0003c0003t0028g0260 a0003c0003t0030g0084 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1713+1138T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462779 | |||||||
chr22:26462850 | A | G | 1 | a0001c0001t0004g0158 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1713+1067T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462850 | |||||||
chr22:26462868 | G | A | 10 | a0002c0002t0002g0002 a0002c0002t0002g0205 a0002c0002t0002g0206 others(7): Show |
20 | HG00438.hp2 HG01934.hp1 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.1713+1049C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462868 | |||||||
chr22:26462911 | T | C | 1 | a0003c0003t0023g0034 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1713+1006A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26462911 | |||||||
chr22:26463120 | T | C | 98 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0025 others(95): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1713+797A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463120 | |||||||
chr22:26463441 | C | T | 6 | a0002c0005t0003g0012 a0002c0005t0003g0020 a0002c0005t0003g0129 others(3): Show |
11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1713+476G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463441 | |||||||
chr22:26463499 | G | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1713+418C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463499 | |||||||
chr22:26463558 | A | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1713+359T>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463558 | |||||||
chr22:26463610 | A | G | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1713+307T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463610 | |||||||
chr22:26463643 | T | C | 1 | a0002c0002t0047g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1713+274A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463643 | |||||||
chr22:26463736 | C | G | 10 | a0003c0004t0007g0003 a0003c0004t0007g0019 a0003c0004t0007g0033 others(7): Show |
20 | HG00597.hp1 HG02056.hp2 HG04184.hp1 others(17): Show |
intron_variant | MODIFIER | c.1713+181G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463736 | |||||||
chr22:26463834 | G | A | 2 | a0001c0001t0034g0278 a0001c0001t0034g0279 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1713+83C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 11/13 | chr22 | 26463834 | |||||||
chr22:26464971 | A | G | 2 | a0003c0003t0023g0034 a0003c0003t0041g0106 |
3 | HG01099.hp2 HG01167.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.804-145T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/13 | chr22 | 26464971 | |||||||
chr22:26465239 | A | G | 7 | a0004c0008t0012g0032 a0004c0008t0012g0068 a0004c0008t0012g0086 others(4): Show |
8 | HG01168.hp2 HG01175.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.803+216T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/13 | chr22 | 26465239 | |||||||
chr22:26465320 | C | A | 1 | a0003c0003t0016g0081 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.803+135G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/13 | chr22 | 26465320 | |||||||
chr22:26465350 | G | A | 1 | a0007c0013t0002g0037 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.803+105C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/13 | chr22 | 26465350 | |||||||
chr22:26465426 | C | A | 1 | a0003c0003t0024g0062 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.803+29G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 10/13 | chr22 | 26465426 | |||||||
chr22:26465579 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.707-28T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26465579 | |||||||
chr22:26465605 | C | T | 1 | a0002c0002t0017g0268 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.707-54G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26465605 | |||||||
chr22:26465755 | T | C | 38 | a0002c0002t0002g0002 a0002c0002t0002g0025 a0002c0002t0002g0047 others(35): Show |
56 | HG00438.hp1 HG00438.hp2 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.707-204A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26465755 | |||||||
chr22:26466004 | G | A | 3 | a0001c0001t0005g0045 a0001c0001t0006g0182 a0001c0001t0013g0181 |
4 | HG01069.hp2 HG01123.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+222C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26466004 | |||||||
chr22:26466075 | G | A | 50 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0025 others(47): Show |
72 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.706+151C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26466075 | |||||||
chr22:26466187 | C | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.706+39G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26466187 | |||||||
chr22:26466190 | C | T | 3 | a0001c0010t0003g0038 a0001c0010t0003g0117 a0001c0010t0003g0118 |
4 | HG02615.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.706+36G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26466190 | |||||||
chr22:26466218 | C | G | 5 | a0003c0003t0009g0071 a0003c0003t0009g0076 a0003c0003t0009g0092 others(2): Show |
5 | NA18950.hp2 NA18960.hp2 NA18972.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.706+8G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 9/13 | chr22 | 26466218 | |||||||
chr22:26466433 | T | A | 1 | a0007c0013t0002g0037 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.670-171A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26466433 | |||||||
chr22:26466471 | C | A | 5 | a0002c0002t0011g0024 a0002c0002t0011g0208 a0002c0002t0037g0055 others(2): Show |
8 | HG00423.hp1 HG02523.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-209G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26466471 | |||||||
chr22:26466659 | C | T | 1 | a0002c0005t0003g0129 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.670-397G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26466659 | |||||||
chr22:26466719 | A | AATGCTAT others(20): Show |
5 | a0002c0002t0002g0113 a0002c0002t0002g0114 a0002c0002t0003g0036 others(2): Show |
7 | HG00733.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-484_670-458dup others(27): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26466719 | |||||||
chr22:26466806 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(246): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.670-544A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26466806 | |||||||
chr22:26466839 | A | C | 1 | a0001c0001t0005g0126 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.670-577T>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26466839 | |||||||
chr22:26466846 | C | A | 3 | a0001c0001t0001g0041 a0001c0001t0004g0160 a0001c0001t0004g0177 |
4 | HG02647.hp1 HG03195.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-584G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26466846 | |||||||
chr22:26467066 | G | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.670-804C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467066 | |||||||
chr22:26467127 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(203): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.670-865G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467127 | |||||||
chr22:26467175 | A | G | 4 | a0003c0003t0023g0034 a0003c0003t0038g0265 a0003c0003t0039g0264 others(1): Show |
5 | HG00741.hp1 HG01099.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-913T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467175 | |||||||
chr22:26467280 | T | C | 13 | a0001c0001t0004g0153 a0001c0001t0006g0141 a0003c0004t0007g0003 others(10): Show |
23 | HG00597.hp1 HG00609.hp2 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.670-1018A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467280 | |||||||
chr22:26467516 | G | A | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.669+1035C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467516 | |||||||
chr22:26467593 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(207): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.669+958A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467593 | |||||||
chr22:26467673 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.669+878T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467673 | |||||||
chr22:26467697 | C | T | 5 | a0003c0003t0024g0062 a0003c0003t0024g0063 a0003c0003t0025g0061 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+854G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467697 | |||||||
chr22:26467893 | A | T | 3 | a0002c0002t0003g0212 a0002c0002t0003g0221 a0002c0002t0010g0213 |
3 | NA18953.hp2 NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.669+658T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467893 | |||||||
chr22:26467965 | C | T | 3 | a0003c0003t0038g0265 a0003c0003t0039g0264 a0003c0003t0041g0106 |
3 | HG00741.hp1 HG03453.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.669+586G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26467965 | |||||||
chr22:26468001 | C | G | 4 | a0003c0003t0016g0081 a0003c0003t0022g0058 a0003c0003t0022g0073 others(1): Show |
4 | HG00597.hp2 NA18965.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+550G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468001 | |||||||
chr22:26468005 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0005g0152 a0001c0001t0027g0151 |
3 | HG03239.hp1 NA18976.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.669+546G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468005 | |||||||
chr22:26468101 | T | C | 4 | a0001c0001t0006g0141 a0003c0003t0009g0080 a0003c0003t0016g0095 others(1): Show |
4 | HG00673.hp1 NA18939.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+450A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468101 | |||||||
chr22:26468108 | G | A | 4 | a0002c0002t0002g0113 a0002c0002t0002g0114 a0002c0002t0003g0036 others(1): Show |
5 | HG00733.hp1 HG01981.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+443C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468108 | |||||||
chr22:26468163 | A | C | 1 | a0004c0008t0012g0032 | 2 | HG01175.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.669+388T>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468163 | |||||||
chr22:26468190 | ACCGTG | A | 24 | a0001c0001t0006g0123 a0002c0002t0032g0266 a0002c0002t0032g0267 others(21): Show |
36 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.669+356_669+360del others(5): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468190 | |||||||
chr22:26468235 | G | A | 1 | a0002c0002t0011g0208 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.669+316C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468235 | |||||||
chr22:26468429 | T | C | 15 | a0002c0002t0002g0113 a0002c0002t0002g0114 a0002c0002t0002g0116 others(12): Show |
20 | HG00423.hp1 HG00733.hp1 HG01516.hp1 others(17): Show |
intron_variant | MODIFIER | c.669+122A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468429 | |||||||
chr22:26468431 | C | T | 2 | a0002c0002t0003g0189 a0002c0002t0003g0263 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.669+120G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 8/13 | chr22 | 26468431 | |||||||
chr22:26468692 | A | G | 213 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(210): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.597-69T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26468692 | |||||||
chr22:26468763 | A | G | 10 | a0002c0002t0003g0021 a0002c0002t0003g0132 a0002c0002t0003g0135 others(7): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.597-140T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26468763 | |||||||
chr22:26468950 | A | T | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.597-327T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26468950 | |||||||
chr22:26469051 | C | T | 4 | a0001c0001t0005g0039 a0001c0001t0005g0125 a0001c0001t0005g0126 others(1): Show |
5 | HG02258.hp1 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.597-428G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469051 | |||||||
chr22:26469074 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.597-451A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469074 | |||||||
chr22:26469088 | A | G | 225 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.597-465T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469088 | |||||||
chr22:26469092 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.597-469C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469092 | |||||||
chr22:26469264 | T | G | 3 | a0001c0010t0003g0038 a0001c0010t0003g0117 a0001c0010t0003g0118 |
4 | HG02615.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-641A>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469264 | |||||||
chr22:26469272 | T | C | 214 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(211): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.597-649A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469272 | |||||||
chr22:26469283 | C | CA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(178): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.597-661dupT | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469283 | |||||||
chr22:26469283 | C | CAA | 31 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0004g0183 others(28): Show |
35 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.597-662_597-661dup others(2): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469283 | |||||||
chr22:26469283 | C | CAAA | 7 | a0001c0001t0001g0134 a0001c0001t0004g0153 a0001c0001t0005g0152 others(4): Show |
7 | HG00673.hp1 HG03239.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.597-663_597-661dup others(3): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469283 | |||||||
chr22:26469486 | G | A | 2 | a0001c0001t0034g0278 a0001c0001t0034g0279 |
2 | HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.597-863C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469486 | |||||||
chr22:26469500 | C | T | 1 | a0003c0003t0023g0034 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.597-877G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469500 | |||||||
chr22:26469560 | G | A | 1 | a0002c0002t0003g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.597-937C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469560 | |||||||
chr22:26469670 | G | A | 2 | a0003c0003t0008g0017 a0003c0003t0008g0064 |
4 | HG02886.hp1 HG02895.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.597-1047C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469670 | |||||||
chr22:26469680 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0004g0154 a0001c0001t0004g0185 |
3 | HG02735.hp2 HG03492.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.596+1039C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469680 | |||||||
chr22:26469694 | A | G | 1 | a0002c0002t0049g0220 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.596+1025T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469694 | |||||||
chr22:26469701 | AG | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0239 a0001c0001t0001g0253 others(9): Show |
17 | HG00423.hp2 HG02135.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+1017delC | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469701 | |||||||
chr22:26469704 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0239 a0001c0001t0001g0253 others(9): Show |
17 | HG00423.hp2 HG02135.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+1015T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469704 | |||||||
chr22:26469710 | A | T | 2 | a0003c0003t0009g0071 a0004c0008t0012g0068 |
2 | HG06807.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.596+1009T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469710 | |||||||
chr22:26469710 | AAT | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0041 others(208): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.596+1007_596+1008d others(4): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469710 | |||||||
chr22:26469712 | T | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0239 a0001c0001t0001g0253 others(9): Show |
17 | HG00423.hp2 HG02135.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.596+1007A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469712 | |||||||
chr22:26469837 | G | A | 13 | a0002c0002t0014g0051 a0002c0002t0014g0052 a0002c0002t0014g0274 others(10): Show |
16 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.596+882C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469837 | |||||||
chr22:26469974 | C | T | 10 | a0002c0002t0003g0021 a0002c0002t0003g0132 a0002c0002t0003g0135 others(7): Show |
12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.596+745G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26469974 | |||||||
chr22:26470007 | G | A | 97 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0025 others(94): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.596+712C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26470007 | |||||||
chr22:26470022 | A | G | 1 | a0002c0002t0047g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.596+697T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26470022 | |||||||
chr22:26470089 | C | T | 4 | a0001c0001t0005g0133 a0001c0001t0005g0143 a0001c0001t0006g0008 others(1): Show |
8 | HG00544.hp2 HG02165.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.596+630G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26470089 | |||||||
chr22:26470117 | C | G | 1 | a0003c0003t0041g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.596+602G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26470117 | |||||||
chr22:26470206 | C | T | 1 | a0001c0001t0004g0163 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.596+513G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26470206 | |||||||
chr22:26470463 | G | A | 1 | a0004c0009t0012g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.596+256C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26470463 | |||||||
chr22:26470570 | G | A | 2 | a0002c0002t0003g0195 a0002c0002t0003g0210 |
2 | HG01934.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.596+149C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 7/13 | chr22 | 26470570 | |||||||
chr22:26470934 | G | A | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.502-121C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26470934 | |||||||
chr22:26471113 | G | C | 1 | a0001c0001t0006g0124 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.502-300C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471113 | |||||||
chr22:26471148 | C | T | 2 | a0005c0006t0008g0006 a0005c0006t0008g0065 |
6 | HG02109.hp2 HG02145.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-335G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471148 | |||||||
chr22:26471149 | G | T | 1 | a0001c0001t0006g0141 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.502-336C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471149 | |||||||
chr22:26471255 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.502-442A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471255 | |||||||
chr22:26471492 | C | T | 1 | a0001c0001t0006g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.502-679G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471492 | |||||||
chr22:26471524 | G | A | 98 | a0001c0001t0001g0253 a0002c0002t0002g0002 a0002c0002t0002g0014 others(95): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.502-711C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471524 | |||||||
chr22:26471658 | T | C | 2 | a0002c0002t0003g0189 a0002c0002t0003g0263 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.501+644A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471658 | |||||||
chr22:26471689 | C | T | 225 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.501+613G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471689 | |||||||
chr22:26471844 | A | T | 1 | a0002c0002t0002g0196 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.501+458T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26471844 | |||||||
chr22:26472171 | G | A | 1 | a0001c0001t0015g0254 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.501+131C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26472171 | |||||||
chr22:26472188 | G | A | 1 | a0002c0018t0010g0211 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501+114C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26472188 | |||||||
chr22:26472266 | T | C | 1 | a0004c0009t0012g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.501+36A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 6/13 | chr22 | 26472266 | |||||||
chr22:26472524 | C | T | 8 | a0002c0002t0002g0113 a0002c0002t0002g0114 a0002c0002t0002g0116 others(5): Show |
10 | HG00733.hp1 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.385-106G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 5/13 | chr22 | 26472524 | |||||||
chr22:26472577 | C | T | 6 | a0002c0005t0003g0012 a0002c0005t0003g0020 a0002c0005t0003g0129 others(3): Show |
11 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-159G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 5/13 | chr22 | 26472577 | |||||||
chr22:26472580 | G | T | 1 | a0001c0001t0005g0162 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.385-162C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 5/13 | chr22 | 26472580 | |||||||
chr22:26472740 | G | A | 11 | a0003c0004t0007g0003 a0003c0004t0007g0019 a0003c0004t0007g0033 others(8): Show |
21 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.384+92C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 5/13 | chr22 | 26472740 | |||||||
chr22:26472782 | G | A | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.384+50C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 5/13 | chr22 | 26472782 | |||||||
chr22:26473373 | T | C | 2 | a0003c0003t0008g0029 a0003c0015t0008g0067 |
3 | HG02257.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.277-434A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26473373 | |||||||
chr22:26473417 | G | A | 7 | a0001c0010t0003g0038 a0001c0010t0003g0117 a0001c0010t0003g0118 others(4): Show |
9 | HG00733.hp1 HG01981.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-478C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26473417 | |||||||
chr22:26473467 | C | T | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.277-528G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26473467 | |||||||
chr22:26473604 | G | A | 1 | a0002c0002t0003g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.277-665C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26473604 | |||||||
chr22:26473686 | C | T | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.277-747G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26473686 | |||||||
chr22:26473708 | A | C | 3 | a0001c0001t0005g0157 a0001c0001t0013g0156 a0001c0001t0058g0234 |
3 | HG02630.hp2 HG02723.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.277-769T>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26473708 | |||||||
chr22:26473868 | T | C | 5 | a0003c0003t0024g0062 a0003c0003t0024g0063 a0003c0003t0025g0061 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-929A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26473868 | |||||||
chr22:26474023 | T | C | 5 | a0003c0003t0024g0062 a0003c0003t0024g0063 a0003c0003t0025g0061 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.277-1084A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474023 | |||||||
chr22:26474032 | T | C | 1 | a0002c0002t0032g0267 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.277-1093A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474032 | |||||||
chr22:26474046 | A | G | 6 | a0002c0002t0002g0178 a0002c0002t0010g0179 a0002c0002t0011g0024 others(3): Show |
9 | HG00423.hp1 HG02523.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.277-1107T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474046 | |||||||
chr22:26474254 | A | G | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.277-1315T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474254 | |||||||
chr22:26474288 | A | T | 1 | a0002c0002t0003g0195 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.277-1349T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474288 | |||||||
chr22:26474380 | GA | G | 100 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0025 others(97): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.277-1442delT | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474380 | |||||||
chr22:26474381 | A | G | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.277-1442T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474381 | |||||||
chr22:26474515 | A | T | 1 | a0003c0003t0023g0034 | 2 | HG01099.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.277-1576T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474515 | |||||||
chr22:26474536 | T | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(105): Show |
163 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.277-1597A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474536 | |||||||
chr22:26474579 | T | C | 25 | a0003c0003t0009g0007 a0003c0003t0009g0071 a0003c0003t0009g0076 others(22): Show |
32 | HG00597.hp2 HG01358.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.277-1640A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474579 | |||||||
chr22:26474643 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.277-1704G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474643 | |||||||
chr22:26474713 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.277-1774A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474713 | |||||||
chr22:26474820 | A | G | 7 | a0002c0002t0017g0050 a0002c0002t0017g0268 a0002c0002t0017g0269 others(4): Show |
8 | HG02074.hp1 NA18953.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.277-1881T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474820 | |||||||
chr22:26474949 | G | GTT | 8 | a0001c0001t0001g0041 a0001c0001t0004g0158 a0001c0001t0004g0160 others(5): Show |
9 | HG02630.hp2 HG02647.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.277-2011_277-2010i others(4): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26474949 | |||||||
chr22:26475019 | A | G | 44 | a0001c0001t0001g0022 a0001c0001t0001g0122 a0001c0001t0001g0134 others(41): Show |
63 | HG00544.hp1 HG00544.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.276+1974T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475019 | |||||||
chr22:26475102 | C | T | 210 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(207): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.276+1891G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475102 | |||||||
chr22:26475347 | C | CT | 49 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0025 others(46): Show |
74 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.276+1645dupA | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475347 | |||||||
chr22:26475347 | C | CTT | 8 | a0002c0002t0002g0193 a0002c0002t0003g0219 a0002c0002t0011g0194 others(5): Show |
13 | HG00741.hp2 HG01243.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.276+1644_276+1645d others(4): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475347 | |||||||
chr22:26475347 | CT | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(103): Show |
161 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.276+1645delA | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475347 | |||||||
chr22:26475347 | CTT | C | 5 | a0001c0001t0004g0175 a0001c0001t0005g0125 a0001c0001t0005g0126 others(2): Show |
6 | HG02258.hp1 HG02280.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.276+1644_276+1645d others(4): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475347 | |||||||
chr22:26475352 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.276+1641A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475352 | |||||||
chr22:26475353 | T | C | 1 | a0002c0002t0047g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.276+1640A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475353 | |||||||
chr22:26475420 | T | A | 1 | a0003c0004t0007g0104 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.276+1573A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475420 | |||||||
chr22:26475422 | A | G | 1 | a0001c0010t0003g0117 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.276+1571T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475422 | |||||||
chr22:26475478 | G | A | 1 | a0001c0001t0004g0176 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.276+1515C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475478 | |||||||
chr22:26475560 | C | T | 1 | a0003c0003t0030g0084 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.276+1433G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475560 | |||||||
chr22:26475686 | TAGAG | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.276+1303_276+1306d others(6): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475686 | |||||||
chr22:26475740 | C | T | 8 | a0003c0003t0008g0017 a0003c0003t0008g0028 a0003c0003t0008g0029 others(5): Show |
16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.276+1253G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26475740 | |||||||
chr22:26476138 | T | A | 8 | a0003c0003t0008g0017 a0003c0003t0008g0028 a0003c0003t0008g0029 others(5): Show |
16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.276+855A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476138 | |||||||
chr22:26476253 | A | G | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.276+740T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476253 | |||||||
chr22:26476307 | A | G | 1 | a0001c0001t0005g0128 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.276+686T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476307 | |||||||
chr22:26476313 | G | C | 1 | a0002c0002t0002g0114 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.276+680C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476313 | |||||||
chr22:26476468 | T | A | 2 | a0006c0011t0020g0035 a0006c0011t0020g0107 |
3 | HG01256.hp1 HG01258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.276+525A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476468 | |||||||
chr22:26476644 | T | C | 1 | a0007c0013t0002g0037 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.276+349A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476644 | |||||||
chr22:26476681 | G | A | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.276+312C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476681 | |||||||
chr22:26476690 | A | T | 11 | a0003c0004t0007g0003 a0003c0004t0007g0019 a0003c0004t0007g0033 others(8): Show |
21 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.276+303T>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476690 | |||||||
chr22:26476696 | T | C | 1 | a0002c0002t0003g0262 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.276+297A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476696 | |||||||
chr22:26476800 | T | C | 1 | a0001c0001t0004g0177 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.276+193A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476800 | |||||||
chr22:26476888 | G | A | 4 | a0003c0003t0028g0259 a0003c0003t0028g0260 a0003c0003t0030g0084 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.276+105C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 4/13 | chr22 | 26476888 | |||||||
chr22:26477148 | G | A | 1 | a0002c0002t0047g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.133-12C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477148 | |||||||
chr22:26477241 | C | T | 1 | a0003c0003t0041g0106 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.133-105G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477241 | |||||||
chr22:26477431 | C | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.133-295G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477431 | |||||||
chr22:26477449 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.133-313C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477449 | |||||||
chr22:26477523 | T | C | 7 | a0004c0008t0012g0032 a0004c0008t0012g0068 a0004c0008t0012g0086 others(4): Show |
8 | HG01168.hp2 HG01175.hp1 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.133-387A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477523 | |||||||
chr22:26477530 | T | C | 4 | a0003c0003t0018g0018 a0003c0003t0029g0090 a0003c0003t0029g0097 others(1): Show |
6 | HG01358.hp1 HG01934.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.133-394A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477530 | |||||||
chr22:26477629 | G | A | 2 | a0001c0010t0003g0038 a0001c0010t0003g0117 |
3 | HG02615.hp1 HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.133-493C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477629 | |||||||
chr22:26477649 | A | G | 3 | a0001c0010t0003g0038 a0001c0010t0003g0117 a0001c0010t0003g0118 |
4 | HG02615.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-513T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477649 | |||||||
chr22:26477835 | C | G | 2 | a0003c0003t0008g0017 a0003c0003t0008g0064 |
4 | HG02886.hp1 HG02895.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.133-699G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477835 | |||||||
chr22:26477877 | T | G | 2 | a0001c0001t0005g0126 a0001c0001t0005g0127 |
2 | HG02258.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.133-741A>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477877 | |||||||
chr22:26477980 | A | G | 2 | a0002c0002t0003g0189 a0002c0002t0003g0263 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.133-844T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26477980 | |||||||
chr22:26478138 | C | T | 13 | a0002c0002t0014g0051 a0002c0002t0014g0052 a0002c0002t0014g0274 others(10): Show |
16 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.133-1002G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478138 | |||||||
chr22:26478231 | G | A | 1 | a0002c0002t0002g0218 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.132+1034C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478231 | |||||||
chr22:26478299 | G | A | 2 | a0003c0003t0023g0034 a0003c0003t0041g0106 |
3 | HG01099.hp2 HG01167.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.132+966C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478299 | |||||||
chr22:26478332 | G | T | 1 | a0002c0002t0002g0192 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.132+933C>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478332 | |||||||
chr22:26478388 | T | C | 5 | a0003c0003t0024g0062 a0003c0003t0024g0063 a0003c0003t0025g0061 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.132+877A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478388 | |||||||
chr22:26478443 | C | T | 2 | a0002c0002t0032g0266 a0002c0002t0032g0267 |
2 | HG01496.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.132+822G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478443 | |||||||
chr22:26478496 | G | A | 14 | a0002c0002t0002g0113 a0002c0002t0002g0114 a0002c0002t0002g0116 others(11): Show |
19 | HG00423.hp1 HG00733.hp1 HG01516.hp1 others(16): Show |
intron_variant | MODIFIER | c.132+769C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478496 | |||||||
chr22:26478556 | G | C | 3 | a0001c0001t0005g0045 a0001c0001t0006g0182 a0001c0001t0013g0181 |
4 | HG01069.hp2 HG01123.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.132+709C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478556 | |||||||
chr22:26478570 | C | CA | 194 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(191): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.132+694dupT | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478570 | |||||||
chr22:26478570 | C | CAA | 28 | a0001c0001t0001g0186 a0001c0001t0001g0188 a0001c0001t0004g0183 others(25): Show |
31 | HG00597.hp1 HG00673.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.132+693_132+694dup others(2): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478570 | |||||||
chr22:26478648 | T | C | 15 | a0002c0002t0014g0051 a0002c0002t0014g0052 a0002c0002t0014g0274 others(12): Show |
18 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.132+617A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478648 | |||||||
chr22:26478695 | T | C | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.132+570A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478695 | |||||||
chr22:26478765 | A | AC | 225 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.132+499dupG | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478765 | |||||||
chr22:26478794 | G | A | 1 | a0006c0011t0020g0035 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.132+471C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26478794 | |||||||
chr22:26479018 | A | C | 8 | a0003c0003t0008g0017 a0003c0003t0008g0028 a0003c0003t0008g0029 others(5): Show |
16 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.132+247T>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26479018 | |||||||
chr22:26479073 | C | T | 1 | a0001c0001t0006g0123 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.132+192G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 3/13 | chr22 | 26479073 | |||||||
chr22:26479404 | C | T | 4 | a0001c0001t0001g0122 a0001c0001t0005g0119 a0001c0001t0006g0121 others(1): Show |
4 | HG00639.hp1 HG01975.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-49G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26479404 | |||||||
chr22:26479607 | G | C | 1 | a0002c0002t0003g0229 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.42-252C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26479607 | |||||||
chr22:26479687 | G | A | 1 | a0004c0009t0012g0098 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.42-332C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26479687 | |||||||
chr22:26479752 | C | T | 3 | a0001c0010t0003g0038 a0001c0010t0003g0117 a0001c0010t0003g0118 |
4 | HG02615.hp1 HG02922.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.42-397G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26479752 | |||||||
chr22:26479838 | C | T | 1 | a0003c0004t0007g0099 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.42-483G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26479838 | |||||||
chr22:26479839 | G | A | 2 | a0002c0002t0003g0189 a0002c0002t0003g0263 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.42-484C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26479839 | |||||||
chr22:26480179 | G | C | 2 | a0003c0003t0008g0029 a0003c0015t0008g0067 |
3 | HG02257.hp1 HG02717.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.42-824C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480179 | |||||||
chr22:26480203 | T | C | 4 | a0003c0003t0008g0028 a0003c0003t0008g0029 a0003c0003t0008g0066 others(1): Show |
6 | HG02257.hp1 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.42-848A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480203 | |||||||
chr22:26480237 | T | C | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.42-882A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480237 | |||||||
chr22:26480328 | T | G | 1 | a0002c0002t0047g0190 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.42-973A>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480328 | |||||||
chr22:26480339 | T | A | 1 | a0001c0001t0005g0191 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.42-984A>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480339 | |||||||
chr22:26480430 | C | T | 5 | a0003c0003t0024g0062 a0003c0003t0024g0063 a0003c0003t0025g0061 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.42-1075G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480430 | |||||||
chr22:26480864 | C | T | 8 | a0002c0002t0002g0113 a0002c0002t0002g0114 a0002c0002t0002g0116 others(5): Show |
10 | HG00733.hp1 HG01516.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.41+858G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480864 | |||||||
chr22:26480915 | C | G | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.41+807G>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26480915 | |||||||
chr22:26481135 | G | GAAAGAAA others(341): Show |
1 | a0002c0002t0002g0230 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.41+586_41+587insTT others(346): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481135 | |||||||
chr22:26481135 | G | GAAAGAAA others(353): Show |
1 | a0002c0002t0002g0231 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.41+586_41+587insTT others(358): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481135 | |||||||
chr22:26481136 | A | G | 1 | a0004c0008t0012g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.41+586T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481136 | |||||||
chr22:26481185 | CATAA | C | 7 | a0002c0002t0017g0050 a0002c0002t0017g0268 a0002c0002t0017g0269 others(4): Show |
8 | HG02074.hp1 NA18953.hp1 NA18972.hp2 others(5): Show |
intron_variant | MODIFIER | c.41+533_41+536delTT others(2): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481185 | |||||||
chr22:26481343 | C | T | 11 | a0003c0004t0007g0003 a0003c0004t0007g0019 a0003c0004t0007g0033 others(8): Show |
21 | HG00597.hp1 HG00609.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.41+379G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481343 | |||||||
chr22:26481497 | G | A | 51 | a0002c0002t0002g0002 a0002c0002t0002g0014 a0002c0002t0002g0025 others(48): Show |
73 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.41+225C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481497 | |||||||
chr22:26481573 | C | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.41+149G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481573 | |||||||
chr22:26481643 | G | C | 1 | a0002c0002t0002g0048 | 2 | HG00140.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.41+79C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 2/13 | chr22 | 26481643 | |||||||
chr22:26482317 | A | G | 2 | a0001c0001t0006g0109 a0001c0001t0006g0110 |
2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-478-77T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482317 | |||||||
chr22:26482372 | G | A | 1 | a0003c0004t0007g0108 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-478-132C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482372 | |||||||
chr22:26482528 | AACCCAAA others(47): Show |
A | 1 | a0003c0003t0022g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-478-342_-478-289d others(56): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482528 | |||||||
chr22:26482847 | C | A | 1 | a0003c0003t0022g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-478-607G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482847 | |||||||
chr22:26482901 | A | ATTGTTTC others(45): Show |
1 | a0003c0003t0022g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-478-662_-478-661i others(54): Show |
HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482901 | |||||||
chr22:26482904 | C | T | 1 | a0003c0003t0022g0058 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-478-664G>A | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482904 | |||||||
chr22:26482940 | T | C | 1 | a0002c0021t0002g0235 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-478-700A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482940 | |||||||
chr22:26482991 | G | A | 2 | a0002c0002t0014g0052 a0002c0002t0014g0277 |
3 | HG01256.hp2 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-479+683C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26482991 | |||||||
chr22:26483001 | T | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(205): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.-479+673A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483001 | |||||||
chr22:26483125 | G | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0237 others(28): Show |
59 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.-479+549C>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483125 | |||||||
chr22:26483331 | G | C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0022 others(222): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.-479+343C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483331 | |||||||
chr22:26483453 | C | A | 1 | a0002c0002t0052g0258 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-479+221G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483453 | |||||||
chr22:26483518 | A | G | 1 | a0001c0001t0004g0056 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-479+156T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483518 | |||||||
chr22:26483529 | C | A | 2 | a0003c0003t0028g0259 a0003c0003t0028g0260 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-479+145G>T | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483529 | |||||||
chr22:26483534 | G | C | 13 | a0002c0002t0014g0051 a0002c0002t0014g0052 a0002c0002t0014g0274 others(10): Show |
16 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.-479+140C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483534 | |||||||
chr22:26483535 | G | C | 1 | a0001c0001t0015g0261 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-479+139C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483535 | |||||||
chr22:26483565 | G | C | 1 | a0002c0002t0003g0262 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-479+109C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483565 | |||||||
chr22:26483576 | T | C | 1 | a0002c0002t0003g0263 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-479+98A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483576 | |||||||
chr22:26483596 | A | G | 15 | a0002c0002t0014g0051 a0002c0002t0014g0052 a0002c0002t0014g0274 others(12): Show |
18 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-479+78T>C | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483596 | |||||||
chr22:26483597 | T | C | 15 | a0002c0002t0014g0051 a0002c0002t0014g0052 a0002c0002t0014g0274 others(12): Show |
18 | HG00140.hp2 HG00738.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-479+77A>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483597 | |||||||
chr22:26483628 | G | C | 2 | a0003c0003t0038g0265 a0003c0003t0039g0264 |
2 | HG00741.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-479+46C>G | HPS4 | ENSG00000100099.22 | transcript | ENST00000398145.7 | protein_coding | 1/13 | chr22 | 26483628 |