Item | Value |
---|---|
geneid | 5837 |
ensemblid | ENSG00000068976.14 |
hgncid | 9726 |
symbol | PYGM |
name | glycogen phosphorylase, muscle associated |
refseq_nuc | NM_005609.4 |
refseq_prot | NP_005600.1 |
ensembl_nuc | ENST00000164139.4 |
ensembl_prot | ENSP00000164139.3 |
mane_status | MANE Select |
chr | chr11 |
start | 64746398 |
end | 64759974 |
strand | - |
ver | v1.2 |
region | chr11:64746398-64759974 |
region5000 | chr11:64741398-64764974 |
regionname0 | PYGM_chr11_64746398_64759974 |
regionname5000 | PYGM_chr11_64741398_64764974 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 842 | 315 | 65 | 59 | 144 | 11 | 34 | 102 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
a0002 | 0/0 | 842 | 22 | 21 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
a0003 | 0/0 | 842 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
a0004 | 0/0 | 842 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
a0005 | 0/0 | 842 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
a0006 | 0/0 | 842 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
a0007 | 0/0 | 842 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
a0008 | 0/0 | 842 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PYGM_chr11_64741398_64764974 | PYGM | MSRPL others(837): Show |
chr11 | 64741398 | 64764974 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2526 | 310 | 64 | 57 | 142 | 11 | 34 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0001c0005 | 0/0 | 2526 | 2 | 0 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0001c0006 | 0/0 | 2526 | 2 | 0 | 0 | 2 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0001c0011 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0002c0002 | 0/0 | 2526 | 11 | 11 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0002c0003 | 0/0 | 2526 | 11 | 10 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0003c0004 | 0/0 | 2526 | 8 | 6 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0004c0007 | 0/0 | 2526 | 1 | 0 | 0 | 0 | 1 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0005c0009 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0006c0010 | 0/0 | 2526 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0007c0012 | 0/0 | 2526 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 | ||
a0008c0008 | 0/0 | 2526 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | ATGTC others(2521): Show |
chr11 | 64741398 | 64764974 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2866 | 305 | 63 | 57 | 138 | 11 | 34 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0001c0001t0002 | 0/0 | 2866 | 4 | 0 | 0 | 4 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | GCTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0001c0001t0004 | 0/0 | 2866 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0001c0005t0001 | 0/0 | 2866 | 2 | 0 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0001c0006t0001 | 0/0 | 2866 | 2 | 0 | 0 | 2 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0001c0011t0001 | 0/0 | 2866 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0002c0002t0001 | 0/0 | 2866 | 10 | 10 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0002c0002t0003 | 0/0 | 2866 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0002c0003t0001 | 0/0 | 2866 | 11 | 10 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0003c0004t0001 | 0/0 | 2866 | 8 | 6 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0004c0007t0001 | 0/0 | 2866 | 1 | 0 | 0 | 0 | 1 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0005c0009t0001 | 0/0 | 2866 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0006c0010t0001 | 0/0 | 2866 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0007c0012t0001 | 0/0 | 2866 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
a0008c0008t0001 | 0/0 | 2866 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | ACTCC others(2861): Show |
chr11 | 64741398 | 64764974 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 80 | 6 | 16 | 40 | 5 | 12 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0002 | 0/0 | 46 | 0 | 8 | 32 | 1 | 5 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0003 | 0/0 | 8 | 1 | 4 | 1 | 1 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0006 | 1/0 | 7 | 6 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0012 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0014 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0032 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0005t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0001c0011t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0003t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0003t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0003t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0002c0003t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0003c0004t0001g0005 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0003c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0004c0007t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0005c0009t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0006c0010t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0007c0012t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
a0008c0008t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00280 | hp1 | a0004 | c0007 | t0001 | g0061 | EUR | FIN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00673 | hp2 | a0001 | c0006 | t0001 | g0046 | EAS | CHS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01074 | hp2 | a0001 | c0005 | t0001 | g0027 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01081 | hp2 | a0001 | c0005 | t0001 | g0027 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01106 | hp2 | a0003 | c0004 | t0001 | g0005 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0100 | AMR | PUR | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01884 | hp1 | a0002 | c0002 | t0003 | g0041 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0089 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01934 | hp1 | a0003 | c0004 | t0001 | g0005 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02132 | hp1 | a0001 | c0006 | t0001 | g0081 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02145 | hp1 | a0003 | c0004 | t0001 | g0077 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02280 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02615 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02630 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02647 | hp1 | a0002 | c0003 | t0001 | g0020 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02717 | hp1 | a0002 | c0003 | t0001 | g0020 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02717 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0125 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02896 | hp1 | a0002 | c0003 | t0001 | g0020 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0122 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0088 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02970 | hp2 | a0005 | c0009 | t0001 | g0092 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03139 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03209 | hp1 | a0002 | c0003 | t0001 | g0015 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03486 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03516 | hp1 | a0006 | c0010 | t0001 | g0095 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03540 | hp2 | a0003 | c0004 | t0001 | g0005 | AFR | GWD | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04199 | hp2 | a0007 | c0012 | t0001 | g0071 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04228 | hp1 | a0008 | c0008 | t0001 | g0066 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18522 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | YRI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | LWK | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | LWK | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | YRI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA19240 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | YRI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20129 | hp2 | a0002 | c0003 | t0001 | g0015 | AFR | ASW | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | GIH | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02486 | hp2 | a0001 | c0011 | t0001 | g0121 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02559 | hp1 | a0003 | c0004 | t0001 | g0005 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | USA | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | USA | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | USA | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | PYGM_chr11_64741398_64764974 | PYGM | chr11 | 64741398 | 64764974 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64747281 | G | A | 1 | a0005 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.2255C>T | p.Ser752Phe | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 18/20 | 2331/2866 | 2255/2529 | 752/842 | chr11 | 64747281 | |||
chr11:64750544 | G | A | 1 | a0004 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.2009C>T | p.Ala670Val | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/20 | 2085/2866 | 2009/2529 | 670/842 | chr11 | 64750544 | |||
chr11:64753583 | T | G | 1 | a0008 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.1339A>C | p.Ile447Leu | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/20 | 1415/2866 | 1339/2529 | 447/842 | chr11 | 64753583 | |||
chr11:64753682 | G | C | 2 | a0002 a0005 |
23 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(20): Show |
missense_variant&splice_region_variant | MODERATE | c.1240C>G | p.Arg414Gly | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/20 | 1316/2866 | 1240/2529 | 414/842 | chr11 | 64753682 | |||
chr11:64753881 | T | A | 1 | a0006 | 1 | HG03516.hp1 | missense_variant&splice_region_variant | MODERATE | c.1237A>T | p.Asn413Tyr | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 10/20 | 1313/2866 | 1237/2529 | 413/842 | chr11 | 64753881 | |||
chr11:64753934 | G | A | 1 | a0003 | 8 | HG01106.hp2 HG01934.hp1 HG02145.hp1 others(5): Show |
missense_variant | MODERATE | c.1184C>T | p.Thr395Met | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 10/20 | 1260/2866 | 1184/2529 | 395/842 | chr11 | 64753934 | |||
chr11:64757862 | C | A | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.577G>T | p.Ala193Ser | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/20 | 653/2866 | 577/2529 | 193/842 | chr11 | 64757862 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64752454 | G | C | 1 | a0001c0005 | 2 | HG01074.hp2 HG01081.hp2 |
synonymous_variant | LOW | c.1569C>G | p.Leu523Leu | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 13/20 | 1645/2866 | 1569/2529 | 523/842 | chr11 | 64752454 | |||
chr11:64752496 | C | A | 1 | a0001c0006 | 2 | HG00673.hp2 HG02132.hp1 |
synonymous_variant | LOW | c.1527G>T | p.Gly509Gly | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 13/20 | 1603/2866 | 1527/2529 | 509/842 | chr11 | 64752496 | |||
chr11:64753097 | G | A | 1 | a0002c0003 | 11 | HG01243.hp2 HG02280.hp1 HG02615.hp2 others(8): Show |
synonymous_variant | LOW | c.1494C>T | p.Pro498Pro | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 12/20 | 1570/2866 | 1494/2529 | 498/842 | chr11 | 64753097 | |||
chr11:64754262 | G | A | 1 | a0001c0011 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1083C>T | p.Asp361Asp | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 9/20 | 1159/2866 | 1083/2529 | 361/842 | chr11 | 64754262 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64746628 | C | T | 1 | a0002c0002t0003 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 20/20 | 31 | chr11 | 64746628 | ||||||
chr11:64759946 | G | A | 1 | a0001c0001t0004 | 1 | HG02895.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/20 | chr11 | 64759946 | |||||||
chr11:64759974 | T | C | 1 | a0001c0001t0002 | 4 | NA18944.hp2 NA18954.hp1 NA18971.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-76A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/20 | 76 | chr11 | 64759974 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:64746878 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2379+43C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 19/19 | chr11 | 64746878 | |||||||
chr11:64747034 | A | G | 25 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(22): Show |
85 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.2313-47T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 18/19 | chr11 | 64747034 | |||||||
chr11:64747175 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2312+49C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 18/19 | chr11 | 64747175 | |||||||
chr11:64747813 | C | G | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2178-455G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64747813 | |||||||
chr11:64747814 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2178-456C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64747814 | |||||||
chr11:64747989 | C | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2178-631G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64747989 | |||||||
chr11:64748040 | CA | C | 9 | a0001c0001t0001g0011 a0001c0001t0001g0058 a0001c0001t0001g0079 others(6): Show |
13 | HG00609.hp1 HG01167.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.2178-683delT | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64748040 | |||||||
chr11:64748091 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2178-733G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64748091 | |||||||
chr11:64748150 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2178-792C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64748150 | |||||||
chr11:64748784 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2178-1426A>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64748784 | |||||||
chr11:64748821 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2178-1463C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64748821 | |||||||
chr11:64748836 | G | A | 9 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0036 others(6): Show |
19 | HG01106.hp2 HG01175.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.2178-1478C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64748836 | |||||||
chr11:64748990 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2177+1386T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64748990 | |||||||
chr11:64749005 | T | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2177+1371A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749005 | |||||||
chr11:64749176 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2177+1200C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749176 | |||||||
chr11:64749208 | G | A | 1 | a0001c0001t0001g0033 | 2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2177+1168C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749208 | |||||||
chr11:64749273 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2177+1103C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749273 | |||||||
chr11:64749276 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG01167.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.2177+1100C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749276 | |||||||
chr11:64749503 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2177+873C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749503 | |||||||
chr11:64749567 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(114): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.2177+809T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749567 | |||||||
chr11:64749575 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(68): Show |
211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.2177+801C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749575 | |||||||
chr11:64749597 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2177+779C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749597 | |||||||
chr11:64749637 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2177+739C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749637 | |||||||
chr11:64749793 | A | AT | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(50): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.2177+582dupA | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749793 | |||||||
chr11:64749793 | A | ATT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0051 a0001c0001t0001g0054 others(6): Show |
19 | HG02055.hp1 HG02074.hp1 HG02129.hp1 others(16): Show |
intron_variant | MODIFIER | c.2177+581_2177+582d others(4): Show |
PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749793 | |||||||
chr11:64749793 | AT | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(26): Show |
87 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.2177+582delA | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749793 | |||||||
chr11:64749845 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2177+531G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749845 | |||||||
chr11:64749854 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0124 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2177+522C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64749854 | |||||||
chr11:64750081 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2177+295G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64750081 | |||||||
chr11:64750088 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0124 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2177+288C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64750088 | |||||||
chr11:64750187 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2177+189A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64750187 | |||||||
chr11:64750191 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2177+185A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64750191 | |||||||
chr11:64750192 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2177+184G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 17/19 | chr11 | 64750192 | |||||||
chr11:64750692 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1970-109T>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64750692 | |||||||
chr11:64750873 | G | A | 2 | a0002c0002t0001g0088 a0002c0002t0001g0089 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1970-290C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64750873 | |||||||
chr11:64750961 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1969+364C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64750961 | |||||||
chr11:64751032 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1969+293A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64751032 | |||||||
chr11:64751039 | C | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1969+286G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64751039 | |||||||
chr11:64751045 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1969+280A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64751045 | |||||||
chr11:64751048 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1969+277G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64751048 | |||||||
chr11:64751053 | A | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1969+272T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64751053 | |||||||
chr11:64751058 | A | ATG | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
92 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1969+266_1969+267i others(4): Show |
PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64751058 | |||||||
chr11:64751071 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0034 |
4 | NA18747.hp1 NA18957.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.1969+254A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 16/19 | chr11 | 64751071 | |||||||
chr11:64751590 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(18): Show |
76 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(73): Show |
splice_region_variant&intron_variant | LOW | c.1827+7A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 15/19 | chr11 | 64751590 | |||||||
chr11:64751784 | T | C | 1 | a0001c0001t0001g0063 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1769-129A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 14/19 | chr11 | 64751784 | |||||||
chr11:64751873 | G | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(16): Show |
74 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1768+51C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 14/19 | chr11 | 64751873 | |||||||
chr11:64752195 | C | T | 1 | a0001c0001t0001g0040 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1621-124G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 13/19 | chr11 | 64752195 | |||||||
chr11:64752198 | G | C | 1 | a0001c0001t0001g0040 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1621-127C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 13/19 | chr11 | 64752198 | |||||||
chr11:64752245 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1620+158C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 13/19 | chr11 | 64752245 | |||||||
chr11:64752288 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1620+115G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 13/19 | chr11 | 64752288 | |||||||
chr11:64752330 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1620+73C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 13/19 | chr11 | 64752330 | |||||||
chr11:64752777 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1519-273C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 12/19 | chr11 | 64752777 | |||||||
chr11:64752783 | C | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0025 others(7): Show |
23 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1519-279G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 12/19 | chr11 | 64752783 | |||||||
chr11:64752805 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1518+268G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 12/19 | chr11 | 64752805 | |||||||
chr11:64752902 | T | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(105): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.1518+171A>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 12/19 | chr11 | 64752902 | |||||||
chr11:64753355 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1403+164G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753355 | |||||||
chr11:64753356 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1403+163C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753356 | |||||||
chr11:64753391 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1403+128G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753391 | |||||||
chr11:64753408 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1403+111C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753408 | |||||||
chr11:64753444 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1403+75C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753444 | |||||||
chr11:64753470 | G | T | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(58): Show |
200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.1403+49C>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753470 | |||||||
chr11:64753477 | G | A | 1 | a0002c0002t0003g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1403+42C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753477 | |||||||
chr11:64753495 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0049 |
3 | HG01168.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1403+24G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 11/19 | chr11 | 64753495 | |||||||
chr11:64753759 | C | G | 1 | a0001c0001t0001g0025 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1240-77G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 10/19 | chr11 | 64753759 | |||||||
chr11:64753807 | C | T | 1 | a0002c0003t0001g0021 | 3 | HG02280.hp1 HG02615.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1239+72G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 10/19 | chr11 | 64753807 | |||||||
chr11:64753813 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1239+66C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 10/19 | chr11 | 64753813 | |||||||
chr11:64754107 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1093-82G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 9/19 | chr11 | 64754107 | |||||||
chr11:64754108 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1093-83G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 9/19 | chr11 | 64754108 | |||||||
chr11:64754208 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1092+45G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 9/19 | chr11 | 64754208 | |||||||
chr11:64754219 | G | C | 1 | a0001c0001t0001g0068 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1092+34C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 9/19 | chr11 | 64754219 | |||||||
chr11:64754246 | A | AG | 4 | a0001c0001t0001g0078 a0001c0001t0001g0087 a0001c0001t0001g0093 others(1): Show |
4 | HG01109.hp1 HG02976.hp1 HG03225.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1092+6dupC | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 9/19 | chr11 | 64754246 | |||||||
chr11:64754495 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1000-150C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 8/19 | chr11 | 64754495 | |||||||
chr11:64754594 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.999+99T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 8/19 | chr11 | 64754594 | |||||||
chr11:64754894 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.856-58C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 7/19 | chr11 | 64754894 | |||||||
chr11:64755083 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.855+190C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 7/19 | chr11 | 64755083 | |||||||
chr11:64755170 | C | T | 1 | a0006c0010t0001g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.855+103G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 7/19 | chr11 | 64755170 | |||||||
chr11:64755226 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.855+47G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 7/19 | chr11 | 64755226 | |||||||
chr11:64755563 | G | C | 3 | a0001c0001t0001g0101 a0002c0003t0001g0015 a0002c0003t0001g0020 |
8 | HG02572.hp1 HG02630.hp1 HG02647.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.661-5C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64755563 | |||||||
chr11:64755687 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.661-129T>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64755687 | |||||||
chr11:64755718 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.661-160A>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64755718 | |||||||
chr11:64755828 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.661-270C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64755828 | |||||||
chr11:64755872 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.661-314C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64755872 | |||||||
chr11:64756022 | C | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(18): Show |
77 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.661-464G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756022 | |||||||
chr11:64756109 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.661-551T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756109 | |||||||
chr11:64756112 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.661-554G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756112 | |||||||
chr11:64756164 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.661-606A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756164 | |||||||
chr11:64756272 | C | T | 1 | a0003c0004t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.661-714G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756272 | |||||||
chr11:64756401 | G | A | 1 | a0001c0001t0001g0028 | 2 | HG00741.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.661-843C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756401 | |||||||
chr11:64756536 | C | T | 1 | a0001c0001t0001g0024 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.661-978G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756536 | |||||||
chr11:64756686 | C | T | 1 | a0001c0006t0001g0046 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.660+1093G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64756686 | |||||||
chr11:64757069 | C | T | 1 | a0001c0001t0001g0018 | 3 | HG02976.hp2 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.660+710G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757069 | |||||||
chr11:64757112 | G | A | 1 | a0001c0001t0001g0001 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.660+667C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757112 | |||||||
chr11:64757119 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.660+660G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757119 | |||||||
chr11:64757280 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0101 a0002c0002t0001g0023 others(11): Show |
27 | HG01243.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.660+499T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757280 | |||||||
chr11:64757309 | C | T | 25 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0019 others(22): Show |
82 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.660+470G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757309 | |||||||
chr11:64757321 | G | T | 1 | a0002c0003t0001g0020 | 3 | HG02647.hp1 HG02717.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.660+458C>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757321 | |||||||
chr11:64757337 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.660+442G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757337 | |||||||
chr11:64757439 | C | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(66): Show |
210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.660+340G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757439 | |||||||
chr11:64757604 | T | A | 1 | a0001c0001t0001g0069 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.660+175A>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757604 | |||||||
chr11:64757744 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.660+35G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 5/19 | chr11 | 64757744 | |||||||
chr11:64757967 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.529-57C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64757967 | |||||||
chr11:64757973 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG00597.hp2 HG00621.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.529-63C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64757973 | |||||||
chr11:64757992 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(53): Show |
185 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.529-82G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64757992 | |||||||
chr11:64758009 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.529-99A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64758009 | |||||||
chr11:64758032 | T | C | 1 | a0001c0001t0001g0031 | 2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.529-122A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64758032 | |||||||
chr11:64758063 | C | G | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.529-153G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64758063 | |||||||
chr11:64758172 | G | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(70): Show |
217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.528+74C>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64758172 | |||||||
chr11:64758195 | G | A | 1 | a0001c0001t0001g0040 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.528+51C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 4/19 | chr11 | 64758195 | |||||||
chr11:64758371 | G | A | 1 | a0001c0001t0001g0008 | 6 | HG00280.hp2 HG01192.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-22C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 3/19 | chr11 | 64758371 | |||||||
chr11:64758566 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.345+37G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 2/19 | chr11 | 64758566 | |||||||
chr11:64758869 | A | C | 1 | a0001c0001t0001g0044 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.244-165T>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64758869 | |||||||
chr11:64758880 | C | T | 1 | a0001c0001t0001g0012 | 4 | HG00735.hp1 HG01192.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-176G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64758880 | |||||||
chr11:64759012 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.244-308G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759012 | |||||||
chr11:64759013 | C | CCCCCCCG others(69): Show |
2 | a0001c0001t0001g0019 a0001c0001t0001g0043 |
4 | NA18972.hp2 NA18981.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.244-310_244-309ins others(76): Show |
PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759013 | |||||||
chr11:64759013 | C | CCCCCCGC others(68): Show |
116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(113): Show |
329 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.244-310_244-309ins others(75): Show |
PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759013 | |||||||
chr11:64759159 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.244-455A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759159 | |||||||
chr11:64759214 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.243+442C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759214 | |||||||
chr11:64759317 | G | C | 1 | a0002c0002t0001g0122 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.243+339C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759317 | |||||||
chr11:64759333 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.243+323C>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759333 | |||||||
chr11:64759334 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+322G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759334 | |||||||
chr11:64759336 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+320G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759336 | |||||||
chr11:64759337 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+319T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759337 | |||||||
chr11:64759338 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+318A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759338 | |||||||
chr11:64759339 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+317T>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759339 | |||||||
chr11:64759340 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+316G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759340 | |||||||
chr11:64759341 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+315T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759341 | |||||||
chr11:64759351 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+305A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759351 | |||||||
chr11:64759353 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+303T>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759353 | |||||||
chr11:64759354 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+302A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759354 | |||||||
chr11:64759356 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+300A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759356 | |||||||
chr11:64759358 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+298A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759358 | |||||||
chr11:64759359 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+297G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759359 | |||||||
chr11:64759360 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+296G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759360 | |||||||
chr11:64759361 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+295A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759361 | |||||||
chr11:64759362 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+294A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759362 | |||||||
chr11:64759363 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+293G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759363 | |||||||
chr11:64759366 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+290G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759366 | |||||||
chr11:64759372 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+284G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759372 | |||||||
chr11:64759378 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+278G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759378 | |||||||
chr11:64759381 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+275C>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759381 | |||||||
chr11:64759382 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+274G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759382 | |||||||
chr11:64759383 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+273G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759383 | |||||||
chr11:64759384 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+272T>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759384 | |||||||
chr11:64759386 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+270T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759386 | |||||||
chr11:64759388 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+268C>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759388 | |||||||
chr11:64759391 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+265G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759391 | |||||||
chr11:64759392 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+264G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759392 | |||||||
chr11:64759399 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+257G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759399 | |||||||
chr11:64759401 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+255G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759401 | |||||||
chr11:64759409 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+247G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759409 | |||||||
chr11:64759412 | A | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+244T>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759412 | |||||||
chr11:64759413 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+243G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759413 | |||||||
chr11:64759414 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+242A>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759414 | |||||||
chr11:64759416 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+240G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759416 | |||||||
chr11:64759417 | A | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+239T>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759417 | |||||||
chr11:64759418 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+238T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759418 | |||||||
chr11:64759422 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+234A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759422 | |||||||
chr11:64759424 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+232A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759424 | |||||||
chr11:64759434 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+222G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759434 | |||||||
chr11:64759435 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+221T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759435 | |||||||
chr11:64759436 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+220G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759436 | |||||||
chr11:64759437 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+219A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759437 | |||||||
chr11:64759439 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+217T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759439 | |||||||
chr11:64759440 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+216G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759440 | |||||||
chr11:64759444 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+212A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759444 | |||||||
chr11:64759445 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+211A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759445 | |||||||
chr11:64759450 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+206G>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759450 | |||||||
chr11:64759452 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+204T>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759452 | |||||||
chr11:64759465 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+191A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759465 | |||||||
chr11:64759473 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+183G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759473 | |||||||
chr11:64759474 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+182A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759474 | |||||||
chr11:64759480 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+176G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759480 | |||||||
chr11:64759481 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+175G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759481 | |||||||
chr11:64759484 | T | A | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+172A>T | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759484 | |||||||
chr11:64759489 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+167G>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759489 | |||||||
chr11:64759489 | C | T | 2 | a0002c0002t0001g0023 a0002c0002t0003g0041 |
3 | HG01884.hp1 HG02109.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.243+167G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759489 | |||||||
chr11:64759507 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+149C>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759507 | |||||||
chr11:64759509 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+147A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759509 | |||||||
chr11:64759512 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+144A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759512 | |||||||
chr11:64759520 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+136G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759520 | |||||||
chr11:64759528 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+128C>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759528 | |||||||
chr11:64759537 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+119G>A | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759537 | |||||||
chr11:64759544 | T | G | 1 | a0001c0001t0001g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.243+112A>C | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759544 | |||||||
chr11:64759608 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0010 others(47): Show |
132 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.243+48A>G | PYGM | ENSG00000068976.14 | transcript | ENST00000164139.4 | protein_coding | 1/19 | chr11 | 64759608 |