Item | Value |
---|---|
geneid | 6667 |
ensemblid | ENSG00000185591.10 |
hgncid | 11205 |
symbol | SP1 |
name | Sp1 transcription factor |
refseq_nuc | NM_138473.3 |
refseq_prot | NP_612482.2 |
ensembl_nuc | ENST00000327443.9 |
ensembl_prot | ENSP00000329357.4 |
mane_status | MANE Select |
chr | chr12 |
start | 53380176 |
end | 53416446 |
strand | + |
ver | v1.2 |
region | chr12:53380176-53416446 |
region5000 | chr12:53375176-53421446 |
regionname0 | SP1_chr12_53380176_53416446 |
regionname5000 | SP1_chr12_53375176_53421446 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 785 | 320 | 78 | 65 | 121 | 16 | 38 | 97 | SP1_chr12_53375176_53421446 | SP1 | MSDQD others(780): Show |
chr12 | 53375176 | 53421446 |
a0002 | 0/0 | 785 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SP1_chr12_53375176_53421446 | SP1 | MSDQD others(780): Show |
chr12 | 53375176 | 53421446 |
a0003 | 0/0 | 785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | MSDQD others(780): Show |
chr12 | 53375176 | 53421446 |
a0004 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | MSDQD others(780): Show |
chr12 | 53375176 | 53421446 |
a0005 | 0/0 | 790 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | MSDQD others(785): Show |
chr12 | 53375176 | 53421446 |
a0006 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | MSDQD others(780): Show |
chr12 | 53375176 | 53421446 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2355 | 217 | 52 | 50 | 71 | 14 | 28 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0001c0002 | 0/0 | 2355 | 96 | 21 | 14 | 49 | 2 | 10 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0001c0003 | 0/0 | 2355 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0001c0006 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0001c0008 | 0/0 | 2355 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0001c0010 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0002c0004 | 0/0 | 2355 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0003c0011 | 0/0 | 2355 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0004c0009 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 | ||
a0005c0005 | 0/0 | 2370 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2365): Show |
chr12 | 53375176 | 53421446 | ||
a0006c0007 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ATGAG others(2350): Show |
chr12 | 53375176 | 53421446 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7677 | 55 | 1 | 14 | 28 | 1 | 10 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0003 | 1/0 | 7680 | 28 | 4 | 5 | 8 | 3 | 7 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0004 | 0/0 | 7679 | 25 | 2 | 9 | 11 | 2 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0005 | 0/0 | 7674 | 12 | 11 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7669): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0007 | 0/0 | 7678 | 8 | 1 | 4 | 2 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0008 | 0/0 | 7681 | 6 | 1 | 2 | 3 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7676): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0010 | 0/0 | 7672 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7667): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0011 | 0/0 | 7677 | 4 | 4 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0012 | 0/0 | 7681 | 4 | 0 | 1 | 2 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7676): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0013 | 0/0 | 7680 | 4 | 2 | 1 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0014 | 0/0 | 7679 | 4 | 0 | 0 | 3 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0015 | 0/0 | 7678 | 3 | 0 | 1 | 1 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0017 | 0/0 | 7682 | 3 | 0 | 0 | 1 | 1 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7677): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0019 | 0/0 | 7680 | 2 | 1 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0020 | 0/0 | 7681 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7676): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0024 | 0/0 | 7679 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0025 | 0/0 | 7680 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0026 | 0/0 | 7682 | 2 | 0 | 1 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7677): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0030 | 0/0 | 7674 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7669): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0032 | 0/0 | 7681 | 2 | 1 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7676): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0034 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7669): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0035 | 0/0 | 7679 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0036 | 0/0 | 7683 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7678): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0037 | 0/0 | 7682 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7677): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0038 | 0/0 | 7684 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7679): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0042 | 0/0 | 7672 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7667): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0045 | 0/0 | 7673 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7668): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0046 | 0/0 | 7675 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7670): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0047 | 0/0 | 7676 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7671): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0048 | 0/0 | 7675 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7670): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0049 | 0/0 | 7676 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7671): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0050 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0051 | 0/0 | 7678 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0053 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0054 | 0/0 | 7678 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0055 | 0/0 | 7678 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0056 | 0/0 | 7679 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0057 | 0/0 | 7676 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7671): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0058 | 0/0 | 7676 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7671): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0059 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0061 | 0/0 | 7678 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0062 | 0/0 | 7679 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0063 | 0/0 | 7679 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0064 | 0/0 | 7678 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0065 | 0/0 | 7679 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0066 | 0/0 | 7682 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7677): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0067 | 0/0 | 7684 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7679): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0068 | 0/0 | 7683 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7678): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0069 | 0/0 | 7678 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0070 | 0/0 | 7677 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0071 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7669): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0072 | 0/0 | 7675 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7670): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0073 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0078 | 0/0 | 7675 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7670): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0079 | 0/0 | 7673 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7668): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0080 | 0/0 | 7674 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7669): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0082 | 0/0 | 7677 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0084 | 0/0 | 7680 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0086 | 0/0 | 7683 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7678): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0089 | 0/0 | 7683 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7678): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0090 | 0/0 | 7685 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7680): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0091 | 0/0 | 7676 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7671): Show |
chr12 | 53375176 | 53421446 |
a0001c0001t0092 | 0/0 | 7677 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0002 | 0/0 | 7669 | 53 | 4 | 5 | 35 | 1 | 8 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7664): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0006 | 0/0 | 7671 | 9 | 3 | 4 | 1 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7666): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0009 | 0/0 | 7670 | 4 | 0 | 2 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7665): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0018 | 0/0 | 7671 | 3 | 0 | 0 | 3 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7666): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0021 | 0/0 | 7672 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7667): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0022 | 0/0 | 7674 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7669): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0023 | 0/0 | 7678 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0027 | 0/0 | 7669 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7664): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0028 | 0/0 | 7670 | 2 | 0 | 1 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7665): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0029 | 0/0 | 7670 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7665): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0031 | 0/0 | 7670 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7665): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0033 | 0/0 | 7678 | 2 | 2 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0039 | 0/0 | 7673 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7668): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0040 | 0/0 | 7670 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7665): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0041 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7664): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0044 | 0/0 | 7667 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7662): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0074 | 0/0 | 7669 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7664): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0075 | 0/0 | 7671 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7666): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0077 | 0/0 | 7668 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7663): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0081 | 0/0 | 7673 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7668): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0085 | 0/0 | 7678 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0087 | 0/0 | 7679 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0002t0088 | 0/0 | 7680 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0001c0003t0016 | 0/0 | 7679 | 3 | 3 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7674): Show |
chr12 | 53375176 | 53421446 |
a0001c0003t0052 | 0/0 | 7678 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0001c0006t0043 | 0/0 | 7666 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7661): Show |
chr12 | 53375176 | 53421446 |
a0001c0008t0001 | 0/0 | 7677 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7672): Show |
chr12 | 53375176 | 53421446 |
a0001c0010t0060 | 0/0 | 7680 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0002c0004t0002 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7664): Show |
chr12 | 53375176 | 53421446 |
a0002c0004t0076 | 0/0 | 7672 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7667): Show |
chr12 | 53375176 | 53421446 |
a0003c0011t0003 | 0/0 | 7680 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7675): Show |
chr12 | 53375176 | 53421446 |
a0004c0009t0083 | 0/0 | 7678 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7673): Show |
chr12 | 53375176 | 53421446 |
a0005c0005t0004 | 0/0 | 7694 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7689): Show |
chr12 | 53375176 | 53421446 |
a0006c0007t0002 | 0/0 | 7669 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | ACCCC others(7664): Show |
chr12 | 53375176 | 53421446 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0011 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0007g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0008g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0008g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0008g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0010g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0011g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0011g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0012g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0012g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0012g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0013g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0013g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0013g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0013g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0014g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0014g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0014g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0014g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0015g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0015g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0015g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0017g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0017g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0017g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0019g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0019g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0020g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0020g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0024g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0024g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0025g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0025g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0026g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0026g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0030g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0030g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0032g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0032g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0034g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0035g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0036g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0037g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0038g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0042g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0045g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0046g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0047g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0048g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0049g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0050g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0051g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0053g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0054g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0055g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0056g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0057g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0058g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0059g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0061g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0062g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0063g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0064g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0065g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0066g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0067g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0068g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0069g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0070g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0071g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0072g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0073g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0078g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0079g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0080g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0082g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0084g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0086g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0089g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0090g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0091g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0001t0092g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0006g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0009g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0018g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0018g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0018g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0021g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0021g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0022g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0022g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0023g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0023g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0027g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0027g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0028g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0028g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0029g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0029g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0031g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0031g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0033g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0033g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0039g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0040g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0041g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0044g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0074g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0075g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0077g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0081g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0085g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0087g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0002t0088g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0003t0016g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0003t0016g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0003t0016g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0003t0052g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0006t0043g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0008t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0001c0010t0060g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0002c0004t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0002c0004t0076g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0003c0011t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0004c0009t0083g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0005c0005t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
a0006c0007t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00099 | hp2 | a0001 | c0001 | t0012 | g0005 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00140 | hp1 | a0001 | c0001 | t0048 | g0190 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00280 | hp1 | a0001 | c0001 | t0013 | g0144 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00280 | hp2 | a0001 | c0002 | t0006 | g0244 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0175 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00323 | hp2 | a0001 | c0001 | t0061 | g0038 | EUR | FIN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00438 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00597 | hp1 | a0001 | c0002 | t0022 | g0220 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0018 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0202 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0125 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00639 | hp1 | a0001 | c0001 | t0004 | g0138 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00639 | hp2 | a0001 | c0001 | t0013 | g0004 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0295 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0123 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00673 | hp2 | a0001 | c0001 | t0024 | g0099 | EAS | CHS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0104 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00733 | hp2 | a0001 | c0002 | t0006 | g0245 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00738 | hp1 | a0001 | c0001 | t0054 | g0060 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00741 | hp1 | a0001 | c0001 | t0084 | g0147 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG00741 | hp2 | a0003 | c0011 | t0003 | g0158 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0080 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01070 | hp2 | a0001 | c0001 | t0045 | g0007 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01099 | hp1 | a0001 | c0001 | t0032 | g0268 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0106 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01106 | hp2 | a0001 | c0001 | t0058 | g0089 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01109 | hp1 | a0001 | c0001 | t0005 | g0272 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0296 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01167 | hp1 | a0001 | c0008 | t0001 | g0073 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01167 | hp2 | a0001 | c0002 | t0023 | g0041 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01168 | hp2 | a0001 | c0002 | t0006 | g0259 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01169 | hp1 | a0001 | c0002 | t0006 | g0243 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01169 | hp2 | a0001 | c0002 | t0023 | g0040 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01175 | hp1 | a0001 | c0001 | t0008 | g0157 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01175 | hp2 | a0001 | c0002 | t0028 | g0234 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01192 | hp1 | a0001 | c0001 | t0020 | g0292 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0179 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01243 | hp1 | a0001 | c0001 | t0069 | g0154 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0105 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01257 | hp2 | a0001 | c0001 | t0026 | g0034 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01346 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01358 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01361 | hp2 | a0001 | c0001 | t0068 | g0153 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01433 | hp1 | a0001 | c0001 | t0015 | g0101 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01496 | hp1 | a0001 | c0002 | t0006 | g0246 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01496 | hp2 | a0001 | c0002 | t0009 | g0003 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0005 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0177 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01516 | hp1 | a0001 | c0001 | t0026 | g0067 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0108 | EUR | IBS | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0293 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01884 | hp2 | a0001 | c0006 | t0043 | g0270 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01891 | hp1 | a0001 | c0002 | t0033 | g0045 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01891 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01934 | hp1 | a0001 | c0001 | t0020 | g0004 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01934 | hp2 | a0001 | c0001 | t0012 | g0133 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01943 | hp2 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01952 | hp2 | a0001 | c0002 | t0002 | g0229 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01978 | hp1 | a0001 | c0001 | t0053 | g0134 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0139 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01981 | hp1 | a0001 | c0001 | t0059 | g0170 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01993 | hp1 | a0001 | c0002 | t0009 | g0211 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0084 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02015 | hp1 | a0001 | c0001 | t0050 | g0162 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02015 | hp2 | a0001 | c0001 | t0012 | g0078 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0066 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02055 | hp2 | a0001 | c0001 | t0078 | g0262 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02074 | hp1 | a0001 | c0001 | t0012 | g0151 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0251 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02135 | hp1 | a0001 | c0001 | t0008 | g0168 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02135 | hp2 | a0001 | c0001 | t0008 | g0002 | EAS | KHV | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02145 | hp1 | a0001 | c0001 | t0042 | g0265 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02145 | hp2 | a0001 | c0002 | t0021 | g0029 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | CDX | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | CDX | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02257 | hp2 | a0001 | c0002 | t0088 | g0043 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0297 | AMR | PEL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02451 | hp1 | a0001 | c0001 | t0011 | g0109 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02451 | hp2 | a0001 | c0002 | t0031 | g0223 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0273 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02572 | hp2 | a0001 | c0001 | t0025 | g0187 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02602 | hp2 | a0001 | c0001 | t0036 | g0167 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02615 | hp1 | a0001 | c0001 | t0019 | g0117 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02622 | hp1 | a0001 | c0001 | t0079 | g0284 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02622 | hp2 | a0001 | c0002 | t0006 | g0027 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02630 | hp1 | a0001 | c0001 | t0090 | g0172 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02630 | hp2 | a0001 | c0001 | t0030 | g0277 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02647 | hp1 | a0001 | c0001 | t0037 | g0269 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02683 | hp2 | a0001 | c0002 | t0075 | g0003 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02723 | hp1 | a0001 | c0002 | t0087 | g0044 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02723 | hp2 | a0001 | c0002 | t0085 | g0042 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0130 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0178 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02809 | hp1 | a0001 | c0001 | t0034 | g0298 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02809 | hp2 | a0001 | c0002 | t0021 | g0025 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02818 | hp1 | a0001 | c0001 | t0080 | g0185 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02818 | hp2 | a0001 | c0001 | t0072 | g0184 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02886 | hp1 | a0001 | c0002 | t0006 | g0031 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02886 | hp2 | a0001 | c0001 | t0071 | g0183 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02896 | hp1 | a0001 | c0001 | t0091 | g0016 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02896 | hp2 | a0001 | c0003 | t0016 | g0287 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02897 | hp2 | a0001 | c0003 | t0016 | g0289 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02922 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02922 | hp2 | a0001 | c0002 | t0027 | g0214 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02965 | hp1 | a0001 | c0001 | t0005 | g0016 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02965 | hp2 | a0001 | c0003 | t0052 | g0288 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0209 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0276 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03017 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0186 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03041 | hp2 | a0001 | c0001 | t0011 | g0161 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03130 | hp1 | a0001 | c0002 | t0027 | g0213 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03130 | hp2 | a0001 | c0001 | t0038 | g0271 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03195 | hp1 | a0001 | c0001 | t0065 | g0128 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03195 | hp2 | a0001 | c0002 | t0033 | g0046 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03209 | hp1 | a0001 | c0001 | t0010 | g0017 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0071 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03225 | hp1 | a0001 | c0002 | t0031 | g0224 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03225 | hp2 | a0001 | c0001 | t0064 | g0166 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03453 | hp1 | a0001 | c0001 | t0089 | g0072 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03453 | hp2 | a0001 | c0002 | t0077 | g0210 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0283 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0241 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0237 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0249 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0242 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03516 | hp1 | a0001 | c0002 | t0006 | g0030 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03516 | hp2 | a0001 | c0001 | t0025 | g0286 | AFR | ESN | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03540 | hp2 | a0001 | c0001 | t0032 | g0264 | AFR | GWD | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0266 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0282 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03669 | hp2 | a0001 | c0001 | t0046 | g0110 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03688 | hp1 | a0001 | c0001 | t0070 | g0116 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03688 | hp2 | a0001 | c0001 | t0082 | g0126 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03704 | hp1 | a0001 | c0001 | t0014 | g0114 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0248 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0240 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0181 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0092 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04115 | hp1 | a0001 | c0002 | t0040 | g0193 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04184 | hp1 | a0001 | c0001 | t0035 | g0160 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0068 | SAS | BEB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04199 | hp1 | a0001 | c0001 | t0015 | g0142 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04228 | hp1 | a0001 | c0001 | t0049 | g0113 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG04228 | hp2 | a0001 | c0001 | t0047 | g0112 | SAS | STU | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18522 | hp1 | a0001 | c0002 | t0074 | g0212 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18612 | hp1 | a0001 | c0002 | t0018 | g0003 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18747 | hp1 | a0001 | c0001 | t0014 | g0077 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18747 | hp2 | a0001 | c0001 | t0014 | g0093 | EAS | CHB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18945 | hp2 | a0001 | c0001 | t0017 | g0002 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18947 | hp1 | a0001 | c0002 | t0039 | g0294 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18947 | hp2 | a0001 | c0002 | t0018 | g0208 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18951 | hp1 | a0001 | c0002 | t0018 | g0203 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18954 | hp1 | a0002 | c0004 | t0076 | g0257 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18959 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18959 | hp2 | a0001 | c0001 | t0092 | g0036 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18961 | hp1 | a0001 | c0001 | t0062 | g0091 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18961 | hp2 | a0001 | c0002 | t0041 | g0236 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18962 | hp1 | a0001 | c0002 | t0009 | g0228 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18968 | hp1 | a0001 | c0001 | t0019 | g0191 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18968 | hp2 | a0001 | c0002 | t0022 | g0225 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18970 | hp1 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18970 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18971 | hp2 | a0001 | c0002 | t0002 | g0258 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18972 | hp1 | a0001 | c0002 | t0029 | g0204 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18972 | hp2 | a0001 | c0001 | t0057 | g0189 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18975 | hp1 | a0001 | c0001 | t0055 | g0159 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18978 | hp2 | a0001 | c0002 | t0002 | g0219 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0205 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18981 | hp2 | a0001 | c0001 | t0073 | g0019 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18982 | hp1 | a0004 | c0009 | t0083 | g0163 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18982 | hp2 | a0001 | c0002 | t0029 | g0195 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18987 | hp2 | a0002 | c0004 | t0002 | g0247 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18992 | hp1 | a0005 | c0005 | t0004 | g0056 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18994 | hp2 | a0001 | c0002 | t0006 | g0226 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18998 | hp1 | a0001 | c0002 | t0009 | g0013 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0261 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19000 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19000 | hp2 | a0001 | c0002 | t0028 | g0235 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19002 | hp2 | a0001 | c0002 | t0002 | g0260 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19005 | hp2 | a0006 | c0007 | t0002 | g0253 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19010 | hp2 | a0001 | c0001 | t0024 | g0063 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19011 | hp1 | a0001 | c0001 | t0063 | g0146 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19043 | hp1 | a0001 | c0001 | t0067 | g0291 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0252 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19062 | hp2 | a0001 | c0001 | t0051 | g0140 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19063 | hp1 | a0001 | c0002 | t0044 | g0218 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19067 | hp2 | a0001 | c0001 | t0007 | g0051 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19068 | hp2 | a0001 | c0010 | t0060 | g0079 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19070 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0014 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19081 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0256 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19082 | hp2 | a0001 | c0001 | t0014 | g0086 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19086 | hp2 | a0001 | c0001 | t0056 | g0098 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19089 | hp1 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19240 | hp1 | a0001 | c0001 | t0011 | g0022 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA19240 | hp2 | a0001 | c0001 | t0011 | g0115 | AFR | YRI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20129 | hp1 | a0001 | c0001 | t0030 | g0285 | AFR | ASW | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | ASW | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20752 | hp1 | a0001 | c0001 | t0066 | g0155 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20752 | hp2 | a0001 | c0001 | t0017 | g0124 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20805 | hp2 | a0001 | c0001 | t0007 | g0076 | EUR | TSI | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | CLM | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02486 | hp1 | a0001 | c0003 | t0016 | g0290 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02486 | hp2 | a0001 | c0002 | t0081 | g0026 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02559 | hp1 | a0001 | c0001 | t0086 | g0263 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | ACB | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0267 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
HG03471 | hp2 | a0001 | c0001 | t0010 | g0278 | AFR | MSL | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0215 | AFR | USA | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0107 | AFR | USA | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA21309 | hp1 | a0001 | c0001 | t0013 | g0145 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0275 | AFR | LWK | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0100 | REF | REF | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0011 | REF | REF | SP1_chr12_53375176_53421446 | SP1 | chr12 | 53375176 | 53421446 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53382438 | T | TACCTGGA others(8): Show |
1 | a0005 | 1 | NA18992.hp1 | disruptive_inframe_insertion | MODERATE | c.492_506dupACCTGGAG others(7): Show |
p.Pro169_Asn170insPr others(13): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 623/7680 | 507/2358 | 169/785 | INFO_REALIGN_3_PRIME | chr12 | 53382438 | ||
chr12:53382543 | A | G | 1 | a0003 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.596A>G | p.Asp199Gly | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 712/7680 | 596/2358 | 199/785 | chr12 | 53382543 | |||
chr12:53382597 | A | G | 1 | a0002 | 2 | NA18954.hp1 NA18987.hp2 |
missense_variant | MODERATE | c.650A>G | p.Asn217Ser | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 766/7680 | 650/2358 | 217/785 | chr12 | 53382597 | |||
chr12:53383036 | G | C | 1 | a0006 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.1089G>C | p.Gln363His | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 1205/7680 | 1089/2358 | 363/785 | chr12 | 53383036 | |||
chr12:53409367 | C | T | 1 | a0004 | 1 | NA18982.hp1 | missense_variant | MODERATE | c.1850C>T | p.Ser617Leu | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/6 | 1966/7680 | 1850/2358 | 617/785 | chr12 | 53409367 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53382190 | C | G | 1 | a0001c0003 | 4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.243C>G | p.Ser81Ser | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 359/7680 | 243/2358 | 81/785 | chr12 | 53382190 | |||
chr12:53382766 | T | C | 1 | a0001c0006 | 1 | HG01884.hp2 | synonymous_variant | LOW | c.819T>C | p.Ser273Ser | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 935/7680 | 819/2358 | 273/785 | chr12 | 53382766 | |||
chr12:53383387 | A | G | 3 | a0001c0002 a0002c0004 a0006c0007 |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
synonymous_variant | LOW | c.1440A>G | p.Gln480Gln | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/6 | 1556/7680 | 1440/2358 | 480/785 | chr12 | 53383387 | |||
chr12:53406706 | C | T | 1 | a0001c0010 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.1797C>T | p.Thr599Thr | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/6 | 1913/7680 | 1797/2358 | 599/785 | chr12 | 53406706 | |||
chr12:53409443 | C | T | 1 | a0001c0008 | 1 | HG01167.hp1 | synonymous_variant | LOW | c.1926C>T | p.His642His | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/6 | 2042/7680 | 1926/2358 | 642/785 | chr12 | 53409443 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53380176 | A | AC | 13 | a0001c0001t0008 a0001c0001t0015 a0001c0001t0019 others(10): Show |
27 | HG00597.hp1 HG00597.hp2 HG01175.hp1 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-108dupC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/6 | 107 | INFO_REALIGN_3_PRIME | chr12 | 53380176 | |||||
chr12:53380185 | T | C | 1 | a0001c0001t0034 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-107T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/6 | 107 | chr12 | 53380185 | ||||||
chr12:53380240 | C | T | 1 | a0001c0002t0040 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-52C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/6 | 52 | chr12 | 53380240 | ||||||
chr12:53411253 | G | A | 1 | a0001c0002t0023 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*13G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 13 | chr12 | 53411253 | ||||||
chr12:53411518 | C | G | 1 | a0001c0001t0092 | 1 | NA18959.hp2 | 3_prime_UTR_variant | MODIFIER | c.*278C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 278 | chr12 | 53411518 | ||||||
chr12:53411575 | C | A | 1 | a0001c0002t0041 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*335C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 335 | chr12 | 53411575 | ||||||
chr12:53411654 | T | TTA | 40 | a0001c0001t0005 a0001c0001t0014 a0001c0001t0017 others(37): Show |
129 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(126): Show |
3_prime_UTR_variant | MODIFIER | c.*435_*436dupTA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 437 | INFO_REALIGN_3_PRIME | chr12 | 53411654 | |||||
chr12:53411654 | T | TTATA | 3 | a0001c0001t0091 a0001c0002t0018 a0001c0002t0039 |
5 | HG02896.hp1 NA18612.hp1 NA18947.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*433_*436dupTATA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 437 | INFO_REALIGN_3_PRIME | chr12 | 53411654 | |||||
chr12:53412076 | T | C | 1 | a0001c0001t0042 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 836 | chr12 | 53412076 | ||||||
chr12:53412152 | G | T | 1 | a0001c0001t0073 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*912G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 912 | chr12 | 53412152 | ||||||
chr12:53412344 | C | T | 2 | a0001c0001t0071 a0001c0001t0072 |
2 | HG02818.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1104C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1104 | chr12 | 53412344 | ||||||
chr12:53412350 | C | G | 1 | a0001c0001t0026 | 2 | HG01257.hp2 HG01516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1110C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1110 | chr12 | 53412350 | ||||||
chr12:53412453 | A | G | 1 | a0001c0001t0070 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1213 | chr12 | 53412453 | ||||||
chr12:53412871 | C | T | 3 | a0001c0001t0013 a0001c0001t0020 a0001c0001t0069 |
7 | HG00280.hp1 HG00639.hp2 HG01192.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1631C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1631 | chr12 | 53412871 | ||||||
chr12:53412930 | C | CTG | 8 | a0001c0001t0012 a0001c0001t0026 a0001c0001t0036 others(5): Show |
12 | HG00099.hp2 HG01257.hp2 HG01516.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1727dupGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1728 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | |||||
chr12:53412930 | C | CTGTG | 3 | a0001c0001t0067 a0001c0001t0068 a0001c0001t0090 |
3 | HG01361.hp2 HG02630.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1724_*1727dupGTGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1728 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | |||||
chr12:53412930 | CTG | C | 25 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0014 others(22): Show |
93 | HG00140.hp2 HG00438.hp1 HG00597.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1727delGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1726 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | |||||
chr12:53412930 | CTGTG | C | 7 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0048 others(4): Show |
8 | HG00140.hp1 HG00597.hp1 HG02486.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1724_*1727delGTGT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1724 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | |||||
chr12:53412930 | CTGTGTG | C | 6 | a0001c0001t0045 a0001c0001t0071 a0001c0001t0072 others(3): Show |
16 | HG00280.hp2 HG00733.hp2 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1722_*1727delGTGT others(2): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1722 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | |||||
chr12:53412930 | CTGTGTGT others(1): Show |
C | 25 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0030 others(22): Show |
100 | HG00323.hp1 HG00609.hp1 HG00673.hp1 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1720_*1727delGTGT others(4): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1720 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | |||||
chr12:53412930 | CTGTGTGT others(7): Show |
C | 1 | a0001c0006t0043 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1714_*1727delGTGT others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1714 | INFO_REALIGN_3_PRIME | chr12 | 53412930 | |||||
chr12:53413133 | C | T | 1 | a0001c0001t0080 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1893C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1893 | chr12 | 53413133 | ||||||
chr12:53413227 | C | G | 1 | a0001c0001t0064 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1987C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 1987 | chr12 | 53413227 | ||||||
chr12:53413297 | T | G | 2 | a0001c0002t0023 a0001c0002t0085 |
3 | HG01167.hp2 HG01169.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2057T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2057 | chr12 | 53413297 | ||||||
chr12:53413299 | T | C | 1 | a0001c0002t0027 | 2 | HG02922.hp2 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2059T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2059 | chr12 | 53413299 | ||||||
chr12:53413571 | A | G | 1 | a0001c0001t0063 | 1 | NA19011.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2331 | chr12 | 53413571 | ||||||
chr12:53413812 | G | A | 1 | a0001c0001t0024 | 2 | HG00673.hp2 NA19010.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2572G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2572 | chr12 | 53413812 | ||||||
chr12:53414123 | CAG | C | 26 | a0001c0002t0002 a0001c0002t0006 a0001c0002t0009 others(23): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886delGA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2885 | INFO_REALIGN_3_PRIME | chr12 | 53414123 | |||||
chr12:53414197 | G | C | 1 | a0001c0001t0050 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 2957 | chr12 | 53414197 | ||||||
chr12:53414275 | T | C | 2 | a0001c0001t0046 a0001c0001t0047 |
2 | HG03669.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3035T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3035 | chr12 | 53414275 | ||||||
chr12:53414362 | C | G | 1 | a0001c0001t0059 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3122C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3122 | chr12 | 53414362 | ||||||
chr12:53414373 | G | A | 2 | a0001c0001t0051 a0001c0002t0074 |
2 | NA18522.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3133G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3133 | chr12 | 53414373 | ||||||
chr12:53414580 | T | C | 4 | a0001c0001t0025 a0001c0001t0067 a0001c0003t0016 others(1): Show |
7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3340T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3340 | chr12 | 53414580 | ||||||
chr12:53414808 | T | C | 1 | a0001c0001t0053 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3568T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3568 | chr12 | 53414808 | ||||||
chr12:53415177 | C | T | 5 | a0001c0002t0023 a0001c0002t0033 a0001c0002t0085 others(2): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3937C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3937 | chr12 | 53415177 | ||||||
chr12:53415178 | G | A | 1 | a0001c0001t0054 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3938G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 3938 | chr12 | 53415178 | ||||||
chr12:53415582 | A | G | 1 | a0001c0001t0064 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4342A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4342 | chr12 | 53415582 | ||||||
chr12:53415639 | G | GA | 6 | a0001c0001t0051 a0001c0001t0055 a0001c0001t0056 others(3): Show |
7 | HG01175.hp2 NA18947.hp1 NA18975.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4416dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4417 | INFO_REALIGN_3_PRIME | chr12 | 53415639 | |||||
chr12:53415639 | GA | G | 5 | a0001c0001t0058 a0001c0001t0079 a0001c0002t0031 others(2): Show |
6 | HG01106.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4416delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4416 | INFO_REALIGN_3_PRIME | chr12 | 53415639 | |||||
chr12:53415640 | A | G | 4 | a0001c0002t0023 a0001c0002t0033 a0001c0002t0085 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4400A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4400 | chr12 | 53415640 | ||||||
chr12:53415961 | A | G | 1 | a0001c0001t0062 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4721A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4721 | chr12 | 53415961 | ||||||
chr12:53415987 | G | C | 1 | a0001c0002t0041 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4747G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4747 | chr12 | 53415987 | ||||||
chr12:53416080 | T | C | 1 | a0001c0001t0030 | 2 | HG02630.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4840T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4840 | chr12 | 53416080 | ||||||
chr12:53416136 | C | G | 2 | a0001c0001t0025 a0001c0001t0067 |
3 | HG02572.hp2 HG03516.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4896C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4896 | chr12 | 53416136 | ||||||
chr12:53416235 | C | G | 5 | a0001c0001t0067 a0001c0002t0023 a0001c0002t0033 others(2): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4995C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 4995 | chr12 | 53416235 | ||||||
chr12:53416349 | C | CT | 7 | a0001c0001t0032 a0001c0001t0037 a0001c0001t0038 others(4): Show |
10 | HG01099.hp1 HG02055.hp2 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*5127dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5128 | INFO_REALIGN_3_PRIME | chr12 | 53416349 | |||||
chr12:53416349 | CT | C | 29 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0012 others(26): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*5127delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5127 | INFO_REALIGN_3_PRIME | chr12 | 53416349 | |||||
chr12:53416349 | CTT | C | 10 | a0001c0001t0057 a0001c0001t0061 a0001c0001t0064 others(7): Show |
13 | HG00323.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*5126_*5127delTT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5126 | INFO_REALIGN_3_PRIME | chr12 | 53416349 | |||||
chr12:53416349 | CTTT | C | 20 | a0001c0001t0011 a0001c0001t0065 a0001c0002t0002 others(17): Show |
93 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*5125_*5127delTTT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 6/6 | 5125 | INFO_REALIGN_3_PRIME | chr12 | 53416349 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53380395 | G | A | 1 | a0001c0001t0010g0017 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.7+97G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380395 | |||||||
chr12:53380427 | C | T | 1 | a0001c0001t0034g0298 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.7+129C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380427 | |||||||
chr12:53380457 | G | C | 2 | a0001c0001t0015g0018 a0001c0001t0073g0019 |
2 | HG00597.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.7+159G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380457 | |||||||
chr12:53380494 | C | A | 3 | a0001c0001t0003g0021 a0001c0001t0007g0020 a0001c0001t0011g0022 |
3 | HG02559.hp2 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.7+196C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380494 | |||||||
chr12:53380494 | CCGCCCGC others(25): Show |
C | 1 | a0001c0001t0001g0023 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.7+207_7+238delGGGG others(28): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53380494 | ||||||
chr12:53380536 | C | T | 3 | a0001c0001t0007g0295 a0001c0001t0007g0296 a0001c0001t0007g0297 |
3 | HG00642.hp1 HG01109.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.7+238C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380536 | |||||||
chr12:53380555 | G | T | 1 | a0001c0002t0039g0294 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.7+257G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380555 | |||||||
chr12:53380711 | C | T | 1 | a0001c0001t0004g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.7+413C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380711 | |||||||
chr12:53380716 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.7+418C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380716 | |||||||
chr12:53380841 | G | T | 1 | a0001c0001t0020g0292 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.7+543G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380841 | |||||||
chr12:53380854 | G | A | 7 | a0001c0002t0002g0028 a0001c0002t0006g0027 a0001c0002t0006g0030 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.7+556G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380854 | |||||||
chr12:53380924 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.7+626T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380924 | |||||||
chr12:53380946 | C | CT | 124 | a0001c0001t0001g0188 a0001c0001t0005g0016 a0001c0001t0005g0272 others(121): Show |
127 | HG00140.hp1 HG00280.hp2 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.7+669dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53380946 | ||||||
chr12:53380946 | CT | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0033 a0001c0001t0001g0035 others(13): Show |
16 | HG00140.hp2 HG00323.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.7+669delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53380946 | ||||||
chr12:53380985 | C | G | 39 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.8-674C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380985 | |||||||
chr12:53380992 | C | T | 7 | a0001c0001t0025g0187 a0001c0001t0025g0286 a0001c0001t0067g0291 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.8-667C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380992 | |||||||
chr12:53380995 | A | G | 95 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(92): Show |
98 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.8-664A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53380995 | |||||||
chr12:53381042 | C | G | 5 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0180 others(2): Show |
5 | HG01192.hp2 HG01515.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.8-617C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53381042 | |||||||
chr12:53381363 | GA | G | 42 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0028 others(39): Show |
44 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.8-293delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chr12 | 53381363 | ||||||
chr12:53381490 | G | C | 1 | a0001c0002t0002g0232 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.8-169G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53381490 | |||||||
chr12:53381539 | T | C | 1 | a0001c0001t0001g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.8-120T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 1/5 | chr12 | 53381539 | |||||||
chr12:53381837 | G | C | 2 | a0001c0002t0002g0175 a0001c0002t0002g0233 |
2 | HG00323.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.162+24G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 2/5 | chr12 | 53381837 | |||||||
chr12:53381958 | CAA | C | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.162+147_162+148del others(2): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 2/5 | INFO_REALIGN_3_PRIME | chr12 | 53381958 | ||||||
chr12:53382012 | C | T | 1 | a0001c0002t0002g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163-98C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 2/5 | chr12 | 53382012 | |||||||
chr12:53383807 | C | T | 2 | a0001c0001t0004g0012 a0001c0001t0004g0174 |
3 | HG01943.hp1 NA18612.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1675+185C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53383807 | |||||||
chr12:53383963 | ATTTTC | A | 20 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(17): Show |
20 | HG01109.hp1 HG01891.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.1675+351_1675+355d others(7): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53383963 | ||||||
chr12:53383973 | C | CT | 94 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0003g0070 others(91): Show |
97 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1675+365dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53383973 | ||||||
chr12:53384030 | C | T | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+408C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384030 | |||||||
chr12:53384098 | T | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0049 others(3): Show |
6 | NA18949.hp1 NA18987.hp1 NA18992.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+476T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384098 | |||||||
chr12:53384190 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1675+568C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384190 | |||||||
chr12:53384220 | C | T | 1 | a0001c0001t0004g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1675+598C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384220 | |||||||
chr12:53384258 | C | T | 1 | a0001c0001t0090g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1675+636C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384258 | |||||||
chr12:53384468 | A | G | 2 | a0001c0002t0002g0260 a0001c0002t0002g0261 |
2 | NA18999.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1675+846A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384468 | |||||||
chr12:53384725 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1675+1103G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384725 | |||||||
chr12:53384866 | G | T | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+1244G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384866 | |||||||
chr12:53384980 | GA | G | 136 | a0001c0001t0001g0169 a0001c0001t0001g0171 a0001c0001t0005g0016 others(133): Show |
139 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.1675+1372delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53384980 | ||||||
chr12:53384995 | T | A | 2 | a0001c0001t0004g0054 a0001c0001t0004g0055 |
2 | NA18970.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1675+1373T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384995 | |||||||
chr12:53384996 | A | G | 1 | a0001c0001t0001g0052 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1675+1374A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53384996 | |||||||
chr12:53385356 | G | A | 1 | a0005c0005t0004g0056 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1734G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385356 | |||||||
chr12:53385357 | A | G | 1 | a0005c0005t0004g0056 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1735A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385357 | |||||||
chr12:53385358 | G | A | 1 | a0005c0005t0004g0056 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1736G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385358 | |||||||
chr12:53385511 | CTT | C | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+1890_1675+189 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385511 | |||||||
chr12:53385537 | A | G | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+1915A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385537 | |||||||
chr12:53385581 | C | T | 1 | a0001c0001t0008g0168 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1675+1959C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385581 | |||||||
chr12:53385594 | C | CA | 6 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG00738.hp1 HG01243.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+1986dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53385594 | ||||||
chr12:53385603 | A | T | 1 | a0005c0005t0004g0056 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+1981A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385603 | |||||||
chr12:53385605 | A | AT | 89 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(86): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1675+1983_1675+198 others(5): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385605 | |||||||
chr12:53385605 | A | T | 2 | a0001c0001t0036g0167 a0001c0001t0038g0271 |
2 | HG02602.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1675+1983A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385605 | |||||||
chr12:53385606 | A | AT | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+1984_1675+198 others(5): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385606 | |||||||
chr12:53385612 | A | G | 1 | a0001c0001t0067g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1675+1990A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385612 | |||||||
chr12:53385625 | T | C | 2 | a0001c0001t0025g0187 a0001c0001t0025g0286 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1675+2003T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385625 | |||||||
chr12:53385686 | G | A | 3 | a0001c0001t0005g0272 a0001c0001t0005g0273 a0001c0001t0005g0274 |
3 | HG01109.hp1 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1675+2064G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385686 | |||||||
chr12:53385912 | C | CA | 97 | a0001c0001t0001g0048 a0001c0001t0001g0065 a0001c0001t0005g0275 others(94): Show |
100 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1675+2306dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53385912 | ||||||
chr12:53385912 | CA | C | 6 | a0001c0001t0001g0033 a0001c0001t0001g0039 a0001c0001t0001g0164 others(3): Show |
6 | HG03225.hp2 NA18948.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+2306delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53385912 | ||||||
chr12:53385991 | T | C | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+2369T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53385991 | |||||||
chr12:53386038 | C | T | 2 | a0001c0002t0033g0045 a0001c0002t0033g0046 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1675+2416C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386038 | |||||||
chr12:53386046 | G | A | 2 | a0001c0001t0003g0176 a0001c0001t0003g0177 |
2 | HG01515.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1675+2424G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386046 | |||||||
chr12:53386082 | C | CT | 5 | a0001c0002t0002g0254 a0001c0002t0002g0255 a0001c0002t0002g0256 others(2): Show |
5 | NA18945.hp1 NA18999.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675+2461dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386082 | ||||||
chr12:53386175 | A | T | 1 | a0001c0001t0050g0162 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1675+2553A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386175 | |||||||
chr12:53386300 | T | G | 1 | a0005c0005t0004g0056 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1675+2678T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386300 | |||||||
chr12:53386358 | T | C | 7 | a0001c0001t0025g0187 a0001c0001t0025g0286 a0001c0001t0067g0291 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+2736T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386358 | |||||||
chr12:53386479 | C | CT | 13 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0053 others(10): Show |
13 | HG00741.hp2 HG01175.hp1 HG01975.hp1 others(10): Show |
intron_variant | MODIFIER | c.1675+2876dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386479 | ||||||
chr12:53386479 | C | CTT | 92 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(89): Show |
95 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1675+2875_1675+287 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386479 | ||||||
chr12:53386498 | T | TC | 4 | a0001c0003t0016g0287 a0001c0003t0016g0289 a0001c0003t0016g0290 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675+2877dupC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386498 | ||||||
chr12:53386522 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1675+2900C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386522 | |||||||
chr12:53386537 | TAGTG | T | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+2920_1675+292 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386537 | ||||||
chr12:53386609 | A | G | 7 | a0001c0001t0025g0187 a0001c0001t0025g0286 a0001c0001t0067g0291 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+2987A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386609 | |||||||
chr12:53386891 | C | T | 1 | a0001c0001t0066g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1675+3269C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386891 | |||||||
chr12:53386908 | T | C | 6 | a0001c0001t0003g0005 a0001c0001t0003g0068 a0001c0001t0008g0157 others(3): Show |
6 | HG00099.hp2 HG01175.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+3286T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386908 | |||||||
chr12:53386936 | G | GT | 14 | a0001c0002t0002g0182 a0001c0002t0002g0227 a0001c0002t0002g0229 others(11): Show |
14 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1675+3317dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386936 | ||||||
chr12:53386940 | G | GT | 49 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(46): Show |
49 | HG00741.hp1 HG01099.hp1 HG01192.hp1 others(46): Show |
intron_variant | MODIFIER | c.1675+3334dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386940 | ||||||
chr12:53386940 | G | T | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+3318G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53386940 | |||||||
chr12:53386940 | GT | G | 13 | a0001c0001t0001g0039 a0001c0001t0001g0164 a0001c0001t0003g0021 others(10): Show |
13 | HG01192.hp2 HG01515.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+3334delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53386940 | ||||||
chr12:53387097 | C | T | 9 | a0001c0001t0003g0004 a0001c0001t0003g0143 a0001c0001t0013g0004 others(6): Show |
9 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675+3475C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387097 | |||||||
chr12:53387139 | G | T | 1 | a0001c0001t0064g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1675+3517G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387139 | |||||||
chr12:53387150 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1675+3528A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387150 | |||||||
chr12:53387243 | G | A | 1 | a0001c0002t0002g0192 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1675+3621G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387243 | |||||||
chr12:53387414 | T | G | 1 | a0003c0011t0003g0158 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1675+3792T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387414 | |||||||
chr12:53387544 | T | G | 1 | a0004c0009t0083g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1675+3922T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387544 | |||||||
chr12:53387558 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0008t0001g0073 |
4 | HG00140.hp2 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1675+3936G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387558 | |||||||
chr12:53387761 | G | A | 3 | a0001c0001t0032g0264 a0001c0001t0038g0271 a0001c0001t0086g0263 |
3 | HG02559.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1675+4139G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387761 | |||||||
chr12:53387919 | G | T | 1 | a0001c0001t0030g0285 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1675+4297G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53387919 | |||||||
chr12:53388282 | C | G | 1 | a0001c0001t0004g0055 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1675+4660C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388282 | |||||||
chr12:53388609 | C | T | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+4987C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388609 | |||||||
chr12:53388779 | A | G | 1 | a0001c0001t0015g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1675+5157A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388779 | |||||||
chr12:53388844 | G | T | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5222G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53388844 | |||||||
chr12:53388977 | C | CAAAAAAA others(1): Show |
83 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(80): Show |
86 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1675+5359_1675+536 others(12): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53388977 | ||||||
chr12:53388977 | C | CAAAAAAA others(2): Show |
8 | a0001c0002t0002g0194 a0001c0002t0028g0235 a0001c0002t0029g0195 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.1675+5358_1675+536 others(13): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53388977 | ||||||
chr12:53388977 | C | CAAAAAAA others(3): Show |
3 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0085g0042 |
3 | HG01167.hp2 HG01169.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1675+5357_1675+536 others(14): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53388977 | ||||||
chr12:53389151 | G | T | 1 | a0001c0001t0004g0141 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1675+5529G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389151 | |||||||
chr12:53389175 | G | A | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5553G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389175 | |||||||
chr12:53389216 | C | CT | 20 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0135 others(17): Show |
20 | HG00639.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1675+5614dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | ||||||
chr12:53389216 | C | CTT | 7 | a0001c0002t0002g0237 a0001c0002t0002g0238 a0001c0002t0023g0040 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+5613_1675+561 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | ||||||
chr12:53389216 | C | CTTT | 68 | a0001c0002t0002g0003 a0001c0002t0002g0014 a0001c0002t0002g0028 others(65): Show |
70 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.1675+5612_1675+561 others(7): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | ||||||
chr12:53389216 | C | CTTTT | 18 | a0001c0002t0002g0013 a0001c0002t0002g0015 a0001c0002t0002g0194 others(15): Show |
19 | HG00597.hp1 HG01168.hp2 HG01952.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675+5611_1675+561 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53389216 | ||||||
chr12:53389232 | T | C | 1 | a0001c0001t0003g0074 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1675+5610T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389232 | |||||||
chr12:53389302 | A | G | 1 | a0001c0001t0079g0284 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1675+5680A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389302 | |||||||
chr12:53389390 | A | G | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5768A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389390 | |||||||
chr12:53389392 | C | A | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5770C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389392 | |||||||
chr12:53389398 | T | G | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+5776T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389398 | |||||||
chr12:53389409 | A | G | 19 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(16): Show |
19 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1675+5787A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389409 | |||||||
chr12:53389602 | C | T | 1 | a0001c0001t0004g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1675+5980C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389602 | |||||||
chr12:53389612 | C | T | 133 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(130): Show |
136 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.1675+5990C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53389612 | |||||||
chr12:53390264 | T | C | 1 | a0001c0006t0043g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1675+6642T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390264 | |||||||
chr12:53390409 | G | A | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+6787G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390409 | |||||||
chr12:53390463 | G | T | 39 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1675+6841G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390463 | |||||||
chr12:53390682 | C | CA | 7 | a0001c0001t0008g0157 a0001c0002t0002g0196 a0001c0002t0002g0219 others(4): Show |
7 | HG01175.hp1 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+7072dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53390682 | ||||||
chr12:53390684 | A | G | 5 | a0001c0001t0032g0264 a0001c0001t0032g0268 a0001c0001t0037g0269 others(2): Show |
5 | HG01099.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1675+7062A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390684 | |||||||
chr12:53390767 | T | C | 5 | a0001c0002t0002g0197 a0001c0002t0002g0198 a0001c0002t0002g0221 others(2): Show |
5 | HG00597.hp1 NA18959.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1675+7145T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390767 | |||||||
chr12:53390885 | G | C | 1 | a0001c0001t0003g0075 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1675+7263G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53390885 | |||||||
chr12:53391129 | G | A | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+7507G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391129 | |||||||
chr12:53391153 | C | G | 4 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0085g0042 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1675+7531C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391153 | |||||||
chr12:53391160 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1675+7538A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391160 | |||||||
chr12:53391171 | A | G | 2 | a0001c0001t0003g0130 a0001c0001t0054g0060 |
2 | HG00738.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1675+7549A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391171 | |||||||
chr12:53391221 | A | G | 1 | a0001c0006t0043g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1675+7599A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391221 | |||||||
chr12:53391244 | A | G | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+7622A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391244 | |||||||
chr12:53391346 | C | CT | 10 | a0001c0001t0003g0021 a0001c0001t0003g0129 a0001c0001t0003g0180 others(7): Show |
10 | HG01109.hp2 HG02055.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1675+7745dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | ||||||
chr12:53391346 | C | CTTTT | 69 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(66): Show |
72 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1675+7742_1675+774 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | ||||||
chr12:53391346 | C | CTTTTT | 13 | a0001c0002t0002g0182 a0001c0002t0002g0198 a0001c0002t0002g0219 others(10): Show |
13 | HG01361.hp1 HG01952.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1675+7741_1675+774 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | ||||||
chr12:53391346 | C | CTTTTTT | 8 | a0001c0002t0002g0028 a0001c0002t0006g0027 a0001c0002t0021g0029 others(5): Show |
8 | HG01167.hp2 HG02145.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1675+7740_1675+774 others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | ||||||
chr12:53391346 | CT | C | 82 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(79): Show |
90 | HG00438.hp1 HG00597.hp2 HG00673.hp2 others(87): Show |
intron_variant | MODIFIER | c.1675+7745delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53391346 | ||||||
chr12:53391372 | C | T | 1 | a0001c0002t0002g0217 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1675+7750C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391372 | |||||||
chr12:53391427 | C | T | 2 | a0001c0001t0026g0034 a0001c0001t0026g0067 |
2 | HG01257.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1675+7805C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391427 | |||||||
chr12:53391645 | T | G | 1 | a0001c0002t0002g0240 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1675+8023T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391645 | |||||||
chr12:53391719 | G | A | 1 | a0001c0001t0015g0018 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1675+8097G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391719 | |||||||
chr12:53391814 | A | G | 3 | a0001c0001t0003g0021 a0001c0001t0007g0020 a0001c0001t0011g0022 |
3 | HG02559.hp2 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1675+8192A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391814 | |||||||
chr12:53391860 | C | T | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+8238C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391860 | |||||||
chr12:53391903 | A | G | 1 | a0001c0002t0002g0216 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1675+8281A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391903 | |||||||
chr12:53391953 | C | G | 2 | a0001c0001t0003g0180 a0001c0001t0008g0179 |
2 | HG01192.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1675+8331C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53391953 | |||||||
chr12:53392007 | T | A | 1 | a0001c0002t0002g0200 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1675+8385T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392007 | |||||||
chr12:53392013 | C | T | 1 | a0001c0002t0087g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1675+8391C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392013 | |||||||
chr12:53392035 | T | C | 1 | a0001c0001t0090g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1675+8413T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392035 | |||||||
chr12:53392077 | G | A | 9 | a0001c0002t0002g0240 a0001c0002t0002g0241 a0001c0002t0002g0242 others(6): Show |
9 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675+8455G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392077 | |||||||
chr12:53392249 | C | T | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+8627C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392249 | |||||||
chr12:53392347 | A | AT | 33 | a0001c0001t0001g0009 a0001c0001t0001g0035 a0001c0001t0001g0050 others(30): Show |
34 | HG00140.hp2 HG00609.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1675+8752dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | ||||||
chr12:53392347 | AT | A | 34 | a0001c0001t0005g0274 a0001c0001t0005g0283 a0001c0001t0071g0183 others(31): Show |
36 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.1675+8752delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | ||||||
chr12:53392347 | ATT | A | 97 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(94): Show |
98 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1675+8751_1675+875 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | ||||||
chr12:53392347 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0064g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1675+8741_1675+875 others(16): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53392347 | ||||||
chr12:53392376 | A | G | 1 | a0001c0001t0003g0121 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1675+8754A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392376 | |||||||
chr12:53392458 | G | A | 89 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(86): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1675+8836G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392458 | |||||||
chr12:53392556 | A | C | 89 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(86): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1675+8934A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392556 | |||||||
chr12:53392601 | C | T | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+8979C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392601 | |||||||
chr12:53392606 | C | T | 1 | a0001c0001t0008g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1675+8984C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392606 | |||||||
chr12:53392697 | G | C | 1 | a0001c0001t0065g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1675+9075G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392697 | |||||||
chr12:53392836 | T | G | 1 | a0001c0002t0031g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1675+9214T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392836 | |||||||
chr12:53392909 | C | T | 1 | a0001c0002t0002g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1675+9287C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53392909 | |||||||
chr12:53393028 | G | A | 2 | a0001c0002t0002g0254 a0001c0002t0002g0256 |
2 | NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1675+9406G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393028 | |||||||
chr12:53393247 | G | A | 1 | a0001c0001t0005g0276 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1675+9625G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393247 | |||||||
chr12:53393345 | C | A | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+9723C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393345 | |||||||
chr12:53393362 | G | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0102 others(1): Show |
4 | HG00738.hp2 HG01975.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1675+9740G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393362 | |||||||
chr12:53393449 | A | G | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1675+9827A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393449 | |||||||
chr12:53393511 | G | C | 1 | a0001c0001t0003g0103 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1675+9889G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393511 | |||||||
chr12:53393592 | C | CT | 7 | a0001c0001t0019g0191 a0001c0001t0032g0264 a0001c0001t0032g0268 others(4): Show |
7 | HG01099.hp1 HG02602.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+9985dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53393592 | ||||||
chr12:53393592 | CT | C | 96 | a0001c0001t0030g0277 a0001c0002t0002g0003 a0001c0002t0002g0013 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+9985delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53393592 | ||||||
chr12:53393610 | A | G | 1 | a0001c0001t0003g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1675+9988A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393610 | |||||||
chr12:53393685 | C | T | 3 | a0001c0002t0027g0213 a0001c0002t0027g0214 a0001c0002t0074g0212 |
3 | HG02922.hp2 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1675+10063C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393685 | |||||||
chr12:53393787 | G | A | 2 | a0001c0001t0025g0187 a0001c0001t0025g0286 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1675+10165G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53393787 | |||||||
chr12:53393993 | T | TC | 7 | a0001c0001t0025g0187 a0001c0001t0025g0286 a0001c0001t0067g0291 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+10372dupC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53393993 | ||||||
chr12:53394082 | A | G | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10460A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394082 | |||||||
chr12:53394169 | T | C | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1675+10547T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394169 | |||||||
chr12:53394218 | G | GA | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10605dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394218 | ||||||
chr12:53394385 | T | G | 1 | a0001c0002t0002g0254 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1675+10763T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394385 | |||||||
chr12:53394409 | C | CT | 21 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0058 others(18): Show |
22 | HG00738.hp2 HG01243.hp2 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.1675+10808dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394409 | ||||||
chr12:53394409 | CT | C | 39 | a0001c0001t0001g0173 a0001c0001t0005g0016 a0001c0001t0005g0186 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1675+10808delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394409 | ||||||
chr12:53394409 | CTTTTTT | C | 94 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(91): Show |
97 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1675+10803_1675+10 others(12): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394409 | ||||||
chr12:53394458 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1675+10836T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394458 | |||||||
chr12:53394486 | GC | G | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10867delC | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394486 | ||||||
chr12:53394489 | C | T | 1 | a0001c0001t0014g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1675+10867C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394489 | |||||||
chr12:53394502 | G | A | 38 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0181 others(35): Show |
39 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1675+10880G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394502 | |||||||
chr12:53394551 | G | A | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1675+10929G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394551 | |||||||
chr12:53394583 | C | CT | 63 | a0001c0001t0019g0191 a0001c0001t0032g0264 a0001c0001t0038g0271 others(60): Show |
64 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.1675+10973dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394583 | ||||||
chr12:53394583 | C | CTT | 35 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0175 others(32): Show |
37 | HG00280.hp2 HG00323.hp1 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1675+10972_1675+10 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394583 | ||||||
chr12:53394607 | C | CT | 50 | a0001c0001t0001g0024 a0001c0001t0001g0058 a0001c0001t0001g0065 others(47): Show |
50 | HG00609.hp2 HG00741.hp2 HG01099.hp1 others(47): Show |
intron_variant | MODIFIER | c.1675+11010dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | ||||||
chr12:53394607 | C | CTT | 8 | a0001c0001t0003g0092 a0001c0001t0005g0272 a0001c0001t0005g0273 others(5): Show |
8 | HG01109.hp1 HG02055.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1675+11009_1675+11 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | ||||||
chr12:53394607 | CT | C | 7 | a0001c0001t0001g0127 a0001c0001t0003g0021 a0001c0001t0007g0020 others(4): Show |
7 | HG00323.hp2 HG00733.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1675+11010delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | ||||||
chr12:53394607 | CTT | C | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1675+11009_1675+11 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | ||||||
chr12:53394607 | CTTT | C | 9 | a0001c0002t0002g0198 a0001c0002t0002g0230 a0001c0002t0006g0226 others(6): Show |
9 | HG00597.hp1 HG00733.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1675+11008_1675+11 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | ||||||
chr12:53394607 | CTTTT | C | 78 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(75): Show |
81 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.1675+11007_1675+11 others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53394607 | ||||||
chr12:53394637 | C | T | 8 | a0001c0001t0003g0004 a0001c0001t0003g0143 a0001c0001t0013g0004 others(5): Show |
8 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1675+11015C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394637 | |||||||
chr12:53394796 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1675+11174A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394796 | |||||||
chr12:53394856 | C | T | 20 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(17): Show |
20 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1675+11234C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394856 | |||||||
chr12:53394957 | C | T | 1 | a0001c0001t0062g0091 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1675+11335C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394957 | |||||||
chr12:53394957 | CT | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0102 |
3 | HG00738.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1675+11336delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53394957 | |||||||
chr12:53395170 | G | A | 1 | a0001c0001t0010g0278 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1676-11415G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395170 | |||||||
chr12:53395273 | G | T | 1 | a0001c0001t0010g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1676-11312G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395273 | |||||||
chr12:53395645 | C | CTAGCTTC others(4): Show |
1 | a0001c0001t0056g0098 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1676-10939_1676-10 others(17): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53395645 | ||||||
chr12:53395689 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1676-10896C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395689 | |||||||
chr12:53395811 | CA | C | 10 | a0001c0001t0001g0090 a0001c0001t0005g0281 a0001c0001t0030g0285 others(7): Show |
10 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1676-10758delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53395811 | ||||||
chr12:53395811 | CAA | C | 90 | a0001c0001t0004g0096 a0001c0001t0019g0191 a0001c0002t0002g0003 others(87): Show |
93 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1676-10759_1676-10 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53395811 | ||||||
chr12:53395838 | G | A | 4 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0085g0042 others(1): Show |
4 | HG01167.hp2 HG01169.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676-10747G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395838 | |||||||
chr12:53395979 | G | A | 41 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0181 others(38): Show |
42 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1676-10606G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53395979 | |||||||
chr12:53396036 | C | T | 1 | a0006c0007t0002g0253 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1676-10549C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396036 | |||||||
chr12:53396205 | C | T | 2 | a0001c0002t0031g0223 a0001c0002t0031g0224 |
2 | HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1676-10380C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396205 | |||||||
chr12:53396274 | C | CA | 14 | a0001c0001t0001g0097 a0001c0001t0001g0136 a0001c0001t0003g0068 others(11): Show |
14 | HG00609.hp1 HG00609.hp2 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1676-10297dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53396274 | ||||||
chr12:53396289 | G | A | 24 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-10296G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396289 | |||||||
chr12:53396298 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1676-10287G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396298 | |||||||
chr12:53396378 | G | C | 4 | a0001c0003t0016g0287 a0001c0003t0016g0289 a0001c0003t0016g0290 others(1): Show |
4 | HG02486.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1676-10207G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396378 | |||||||
chr12:53396512 | T | G | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-10073T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396512 | |||||||
chr12:53396568 | AAAAACAA others(3): Show |
A | 1 | a0001c0001t0003g0143 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1676-10002_1676-99 others(15): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53396568 | ||||||
chr12:53396666 | T | C | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-9919T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396666 | |||||||
chr12:53396907 | G | T | 1 | a0001c0001t0065g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1676-9678G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396907 | |||||||
chr12:53396980 | A | T | 1 | a0001c0002t0002g0215 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1676-9605A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53396980 | |||||||
chr12:53397201 | A | G | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-9384A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397201 | |||||||
chr12:53397387 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0008t0001g0073 |
4 | HG00140.hp2 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676-9198G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397387 | |||||||
chr12:53397464 | A | AT | 8 | a0001c0001t0001g0057 a0001c0001t0001g0131 a0001c0001t0001g0169 others(5): Show |
8 | HG01981.hp1 HG02647.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-9103dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397464 | ||||||
chr12:53397464 | AT | A | 41 | a0001c0001t0003g0130 a0001c0001t0003g0176 a0001c0001t0005g0016 others(38): Show |
41 | HG00597.hp1 HG01109.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1676-9103delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397464 | ||||||
chr12:53397464 | ATT | A | 90 | a0001c0001t0032g0268 a0001c0002t0002g0003 a0001c0002t0002g0013 others(87): Show |
93 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1676-9104_1676-910 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397464 | ||||||
chr12:53397579 | CTTTTTTT others(5): Show |
C | 95 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(92): Show |
98 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1676-8996_1676-898 others(16): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397579 | ||||||
chr12:53397579 | CTTTTTTT others(6): Show |
C | 1 | a0002c0004t0076g0257 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1676-8996_1676-898 others(17): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53397579 | ||||||
chr12:53397624 | C | T | 20 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(17): Show |
20 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1676-8961C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397624 | |||||||
chr12:53397826 | T | G | 1 | a0001c0002t0041g0236 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1676-8759T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397826 | |||||||
chr12:53397846 | G | A | 103 | a0001c0001t0004g0096 a0001c0001t0012g0078 a0001c0001t0012g0151 others(100): Show |
106 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.1676-8739G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397846 | |||||||
chr12:53397923 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1676-8662A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397923 | |||||||
chr12:53397975 | T | C | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-8610T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53397975 | |||||||
chr12:53398075 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1676-8510T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398075 | |||||||
chr12:53398129 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1676-8456C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398129 | |||||||
chr12:53398183 | T | C | 2 | a0001c0001t0004g0094 a0001c0010t0060g0079 |
2 | NA19068.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1676-8402T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398183 | |||||||
chr12:53398204 | T | G | 24 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-8381T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398204 | |||||||
chr12:53398224 | T | G | 2 | a0001c0001t0003g0105 a0001c0001t0066g0155 |
2 | HG01256.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1676-8361T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398224 | |||||||
chr12:53398363 | A | G | 1 | a0001c0001t0082g0126 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1676-8222A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398363 | |||||||
chr12:53398371 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0047 a0001c0001t0001g0102 |
3 | HG00738.hp2 HG01975.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1676-8214C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398371 | |||||||
chr12:53398376 | G | A | 12 | a0001c0001t0003g0010 a0001c0001t0004g0010 a0001c0001t0004g0080 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1676-8209G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398376 | |||||||
chr12:53398480 | A | G | 24 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-8105A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398480 | |||||||
chr12:53398548 | G | T | 2 | a0001c0002t0027g0213 a0001c0002t0027g0214 |
2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1676-8037G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398548 | |||||||
chr12:53398585 | T | C | 7 | a0001c0001t0025g0187 a0001c0001t0025g0286 a0001c0001t0067g0291 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1676-8000T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398585 | |||||||
chr12:53398851 | T | C | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-7734T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53398851 | |||||||
chr12:53399103 | T | G | 1 | a0001c0002t0087g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1676-7482T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399103 | |||||||
chr12:53399130 | T | G | 97 | a0001c0001t0001g0081 a0001c0002t0002g0003 a0001c0002t0002g0013 others(94): Show |
100 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.1676-7455T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399130 | |||||||
chr12:53399273 | C | T | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-7312C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399273 | |||||||
chr12:53399336 | G | GT | 93 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(90): Show |
96 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1676-7244dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399336 | ||||||
chr12:53399342 | GT | G | 41 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(38): Show |
41 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(38): Show |
intron_variant | MODIFIER | c.1676-7234delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399342 | ||||||
chr12:53399343 | T | TTTTTG | 93 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(90): Show |
96 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.1676-7238_1676-723 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399343 | ||||||
chr12:53399372 | C | T | 1 | a0001c0006t0043g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1676-7213C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399372 | |||||||
chr12:53399425 | G | A | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-7160G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399425 | |||||||
chr12:53399480 | C | T | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-7105C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399480 | |||||||
chr12:53399530 | C | A | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-7055C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399530 | |||||||
chr12:53399642 | AT | A | 95 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(92): Show |
98 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.1676-6932delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53399642 | ||||||
chr12:53399697 | C | T | 1 | a0001c0002t0088g0043 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1676-6888C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399697 | |||||||
chr12:53399820 | G | A | 3 | a0001c0001t0010g0017 a0001c0001t0010g0266 a0001c0001t0010g0267 |
3 | HG03209.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1676-6765G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399820 | |||||||
chr12:53399821 | G | A | 2 | a0001c0002t0033g0045 a0001c0002t0033g0046 |
2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1676-6764G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399821 | |||||||
chr12:53399851 | G | T | 1 | a0001c0001t0058g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1676-6734G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399851 | |||||||
chr12:53399863 | T | A | 1 | a0001c0001t0011g0109 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1676-6722T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399863 | |||||||
chr12:53399869 | C | G | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-6716C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399869 | |||||||
chr12:53399877 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1676-6708C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53399877 | |||||||
chr12:53400230 | C | T | 3 | a0001c0001t0032g0264 a0001c0001t0038g0271 a0001c0001t0086g0263 |
3 | HG02559.hp1 HG03130.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1676-6355C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400230 | |||||||
chr12:53400263 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1676-6322C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400263 | |||||||
chr12:53400333 | C | A | 1 | a0001c0002t0002g0258 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1676-6252C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400333 | |||||||
chr12:53400385 | A | AT | 7 | a0001c0001t0025g0187 a0001c0001t0025g0286 a0001c0001t0067g0291 others(4): Show |
7 | HG02486.hp1 HG02572.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1676-6199dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400385 | ||||||
chr12:53400405 | A | G | 1 | a0002c0004t0076g0257 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1676-6180A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400405 | |||||||
chr12:53400431 | T | G | 1 | a0001c0001t0036g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1676-6154T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400431 | |||||||
chr12:53400452 | A | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0052 a0001c0001t0007g0051 |
3 | NA18949.hp1 NA19002.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1676-6133A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400452 | |||||||
chr12:53400456 | A | G | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-6129A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400456 | |||||||
chr12:53400499 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1676-6086G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400499 | |||||||
chr12:53400504 | T | G | 41 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0181 others(38): Show |
42 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1676-6081T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400504 | |||||||
chr12:53400692 | G | A | 9 | a0001c0002t0002g0240 a0001c0002t0002g0241 a0001c0002t0002g0242 others(6): Show |
9 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-5893G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400692 | |||||||
chr12:53400700 | T | C | 1 | a0001c0001t0065g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1676-5885T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400700 | |||||||
chr12:53400755 | AT | A | 182 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(179): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.1676-5806delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | ||||||
chr12:53400755 | ATT | A | 7 | a0001c0001t0001g0081 a0001c0001t0001g0173 a0001c0001t0003g0120 others(4): Show |
7 | HG01070.hp1 HG02896.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1676-5807_1676-580 others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | ||||||
chr12:53400755 | ATTT | A | 11 | a0001c0002t0002g0221 a0001c0002t0002g0240 a0001c0002t0002g0252 others(8): Show |
11 | HG01167.hp2 HG01169.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1676-5808_1676-580 others(7): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | ||||||
chr12:53400755 | ATTTT | A | 83 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(80): Show |
86 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1676-5809_1676-580 others(8): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53400755 | ||||||
chr12:53400800 | C | T | 1 | a0001c0001t0014g0086 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1676-5785C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400800 | |||||||
chr12:53400874 | G | A | 1 | a0001c0002t0002g0239 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1676-5711G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53400874 | |||||||
chr12:53401003 | C | T | 89 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(86): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1676-5582C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401003 | |||||||
chr12:53401221 | C | T | 1 | a0001c0006t0043g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1676-5364C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401221 | |||||||
chr12:53401254 | C | T | 1 | a0001c0001t0005g0186 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1676-5331C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401254 | |||||||
chr12:53401307 | C | T | 7 | a0001c0002t0002g0202 a0001c0002t0002g0205 a0001c0002t0002g0206 others(4): Show |
7 | HG00609.hp1 HG00673.hp1 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-5278C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401307 | |||||||
chr12:53401457 | G | GA | 15 | a0001c0001t0001g0102 a0001c0001t0001g0135 a0001c0001t0003g0129 others(12): Show |
15 | HG00738.hp2 HG01099.hp2 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1676-5108dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53401457 | ||||||
chr12:53401457 | GA | G | 94 | a0001c0001t0001g0085 a0001c0001t0001g0097 a0001c0001t0004g0174 others(91): Show |
97 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.1676-5108delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53401457 | ||||||
chr12:53401459 | A | G | 9 | a0001c0001t0003g0004 a0001c0001t0003g0143 a0001c0001t0013g0004 others(6): Show |
9 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-5126A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401459 | |||||||
chr12:53401518 | A | G | 2 | a0001c0001t0011g0109 a0001c0001t0011g0115 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1676-5067A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401518 | |||||||
chr12:53401524 | C | CT | 5 | a0001c0002t0006g0243 a0001c0002t0006g0244 a0001c0002t0006g0245 others(2): Show |
5 | HG00280.hp2 HG00733.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1676-5060dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53401524 | ||||||
chr12:53401581 | C | A | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(16): Show |
20 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1676-5004C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401581 | |||||||
chr12:53401838 | T | C | 1 | a0001c0001t0073g0019 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1676-4747T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401838 | |||||||
chr12:53401961 | A | G | 24 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-4624A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53401961 | |||||||
chr12:53402159 | A | G | 1 | a0001c0001t0078g0262 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1676-4426A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402159 | |||||||
chr12:53402168 | A | G | 9 | a0001c0001t0003g0105 a0001c0001t0003g0121 a0001c0001t0003g0176 others(6): Show |
9 | HG00733.hp1 HG01192.hp2 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.1676-4417A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402168 | |||||||
chr12:53402220 | C | CT | 8 | a0001c0001t0001g0173 a0001c0001t0014g0086 a0001c0001t0015g0101 others(5): Show |
8 | HG01433.hp1 HG02145.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-4345dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53402220 | ||||||
chr12:53402220 | CT | C | 88 | a0001c0001t0001g0081 a0001c0001t0001g0150 a0001c0001t0003g0105 others(85): Show |
91 | HG00280.hp2 HG00323.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.1676-4345delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53402220 | ||||||
chr12:53402262 | C | T | 1 | a0001c0001t0004g0123 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1676-4323C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402262 | |||||||
chr12:53402375 | C | T | 1 | a0001c0002t0002g0227 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1676-4210C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402375 | |||||||
chr12:53402778 | A | C | 39 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1676-3807A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402778 | |||||||
chr12:53402960 | T | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1676-3625T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402960 | |||||||
chr12:53402968 | C | CA | 6 | a0001c0001t0001g0008 a0001c0001t0059g0170 a0001c0002t0002g0250 others(3): Show |
7 | HG01169.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-3616dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53402968 | ||||||
chr12:53402969 | AG | A | 3 | a0001c0001t0001g0033 a0001c0002t0018g0203 a0004c0009t0083g0163 |
3 | NA18951.hp1 NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1676-3615delG | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402969 | |||||||
chr12:53402970 | G | A | 227 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
238 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.1676-3615G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402970 | |||||||
chr12:53402973 | A | G | 1 | a0001c0001t0065g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1676-3612A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53402973 | |||||||
chr12:53403214 | G | A | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-3371G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403214 | |||||||
chr12:53403452 | A | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0023 others(16): Show |
20 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.1676-3133A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403452 | |||||||
chr12:53403519 | A | AT | 12 | a0001c0001t0003g0122 a0001c0001t0008g0064 a0001c0002t0002g0175 others(9): Show |
12 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.1676-3051dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53403519 | ||||||
chr12:53403519 | AT | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
148 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(145): Show |
intron_variant | MODIFIER | c.1676-3051delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53403519 | ||||||
chr12:53403800 | G | C | 1 | a0001c0001t0067g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1676-2785G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403800 | |||||||
chr12:53403932 | G | A | 1 | a0002c0004t0002g0247 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1676-2653G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403932 | |||||||
chr12:53403933 | A | G | 1 | a0002c0004t0002g0247 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1676-2652A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53403933 | |||||||
chr12:53404172 | AAAAAAAA others(15): Show |
A | 1 | a0002c0004t0002g0247 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1676-2412_1676-239 others(26): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404172 | |||||||
chr12:53404194 | C | A | 1 | a0001c0001t0004g0132 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1676-2391C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404194 | |||||||
chr12:53404328 | G | A | 1 | a0001c0001t0071g0183 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1676-2257G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404328 | |||||||
chr12:53404484 | A | G | 1 | a0001c0001t0014g0093 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1676-2101A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404484 | |||||||
chr12:53404542 | C | CA | 90 | a0001c0001t0004g0107 a0001c0001t0020g0292 a0001c0001t0092g0036 others(87): Show |
93 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1676-2027dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53404542 | ||||||
chr12:53404566 | A | G | 5 | a0001c0001t0032g0264 a0001c0001t0032g0268 a0001c0001t0037g0269 others(2): Show |
5 | HG01099.hp1 HG02559.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1676-2019A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404566 | |||||||
chr12:53404613 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1676-1972A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404613 | |||||||
chr12:53404763 | G | A | 9 | a0001c0001t0003g0004 a0001c0001t0003g0143 a0001c0001t0013g0004 others(6): Show |
9 | HG00280.hp1 HG00639.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-1822G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404763 | |||||||
chr12:53404848 | T | C | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1676-1737T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404848 | |||||||
chr12:53404973 | A | G | 1 | a0001c0002t0002g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1676-1612A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404973 | |||||||
chr12:53404984 | C | T | 39 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0181 others(36): Show |
40 | HG00597.hp1 HG00609.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.1676-1601C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404984 | |||||||
chr12:53404996 | G | C | 2 | a0001c0001t0011g0109 a0001c0001t0011g0115 |
2 | HG02451.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1676-1589G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53404996 | |||||||
chr12:53405024 | T | C | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1676-1561T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405024 | |||||||
chr12:53405265 | A | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1320A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405265 | |||||||
chr12:53405267 | A | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1318A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405267 | |||||||
chr12:53405274 | T | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1311T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405274 | |||||||
chr12:53405275 | A | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1310A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405275 | |||||||
chr12:53405277 | A | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1308A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405277 | |||||||
chr12:53405278 | T | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1307T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405278 | |||||||
chr12:53405280 | G | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1305G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405280 | |||||||
chr12:53405281 | G | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1304G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405281 | |||||||
chr12:53405283 | A | T | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1302A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405283 | |||||||
chr12:53405287 | C | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1298C>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405287 | |||||||
chr12:53405288 | T | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1297T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405288 | |||||||
chr12:53405289 | G | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1296G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405289 | |||||||
chr12:53405291 | T | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1294T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405291 | |||||||
chr12:53405292 | T | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1293T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405292 | |||||||
chr12:53405293 | C | T | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1292C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405293 | |||||||
chr12:53405294 | A | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1291A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405294 | |||||||
chr12:53405296 | A | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1289A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405296 | |||||||
chr12:53405297 | T | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1288T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405297 | |||||||
chr12:53405298 | T | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1287T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405298 | |||||||
chr12:53405301 | A | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1284A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405301 | |||||||
chr12:53405302 | T | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1283T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405302 | |||||||
chr12:53405304 | T | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1281T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405304 | |||||||
chr12:53405307 | A | T | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1278A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405307 | |||||||
chr12:53405308 | T | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1277T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405308 | |||||||
chr12:53405309 | T | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1276T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405309 | |||||||
chr12:53405311 | A | T | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1274A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405311 | |||||||
chr12:53405312 | A | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1273A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405312 | |||||||
chr12:53405314 | T | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1271T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405314 | |||||||
chr12:53405325 | T | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1260T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405325 | |||||||
chr12:53405326 | G | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1259G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405326 | |||||||
chr12:53405331 | T | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1254T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405331 | |||||||
chr12:53405335 | A | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1250A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405335 | |||||||
chr12:53405344 | T | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1241T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405344 | |||||||
chr12:53405345 | T | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1240T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405345 | |||||||
chr12:53405346 | A | G | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1239A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405346 | |||||||
chr12:53405359 | T | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1226T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405359 | |||||||
chr12:53405363 | G | C | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1222G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405363 | |||||||
chr12:53405367 | G | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1218G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405367 | |||||||
chr12:53405371 | A | T | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1214A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405371 | |||||||
chr12:53405373 | G | A | 3 | a0001c0001t0032g0268 a0001c0001t0037g0269 a0001c0002t0044g0218 |
3 | HG01099.hp1 HG02647.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1676-1212G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405373 | |||||||
chr12:53405374 | T | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1211T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405374 | |||||||
chr12:53405375 | C | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1210C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405375 | |||||||
chr12:53405377 | C | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1208C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405377 | |||||||
chr12:53405378 | T | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1207T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405378 | |||||||
chr12:53405396 | G | A | 1 | a0001c0002t0044g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1676-1189G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405396 | |||||||
chr12:53405428 | G | A | 6 | a0001c0001t0003g0005 a0001c0001t0003g0068 a0001c0001t0008g0157 others(3): Show |
6 | HG00099.hp2 HG01175.hp1 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1676-1157G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405428 | |||||||
chr12:53405567 | G | C | 2 | a0001c0001t0025g0187 a0001c0001t0025g0286 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1676-1018G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405567 | |||||||
chr12:53405600 | A | G | 1 | a0001c0001t0007g0295 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1676-985A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405600 | |||||||
chr12:53405660 | T | G | 2 | a0001c0001t0025g0187 a0001c0001t0025g0286 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1676-925T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405660 | |||||||
chr12:53405697 | A | AGGAAGGA others(1): Show |
37 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(34): Show |
37 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1676-876_1676-869d others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53405697 | ||||||
chr12:53405832 | A | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(6): Show |
9 | HG00738.hp1 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1676-753A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405832 | |||||||
chr12:53405926 | A | G | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-659A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405926 | |||||||
chr12:53405930 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(227): Show |
241 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.1676-655G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405930 | |||||||
chr12:53405963 | T | A | 1 | a0001c0001t0066g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1676-622T>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53405963 | |||||||
chr12:53405999 | T | TA | 229 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(226): Show |
240 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.1676-577dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53405999 | ||||||
chr12:53406065 | C | CT | 48 | a0001c0001t0001g0137 a0001c0001t0001g0152 a0001c0001t0001g0188 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1676-496dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53406065 | ||||||
chr12:53406065 | CT | C | 8 | a0001c0001t0001g0035 a0001c0001t0003g0069 a0001c0001t0003g0180 others(5): Show |
8 | HG00140.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1676-496delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | INFO_REALIGN_3_PRIME | chr12 | 53406065 | ||||||
chr12:53406070 | T | C | 39 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1676-515T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406070 | |||||||
chr12:53406111 | A | G | 135 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(132): Show |
138 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.1676-474A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406111 | |||||||
chr12:53406141 | G | C | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-444G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406141 | |||||||
chr12:53406258 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1676-327G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406258 | |||||||
chr12:53406348 | C | T | 24 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.1676-237C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406348 | |||||||
chr12:53406364 | C | T | 13 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0061 others(10): Show |
13 | HG00140.hp1 HG00738.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1676-221C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406364 | |||||||
chr12:53406436 | G | A | 1 | a0001c0001t0025g0286 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1676-149G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406436 | |||||||
chr12:53406539 | T | C | 2 | a0001c0001t0071g0183 a0001c0001t0072g0184 |
2 | HG02818.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1676-46T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 3/5 | chr12 | 53406539 | |||||||
chr12:53406785 | T | C | 1 | a0001c0001t0066g0155 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1844+32T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53406785 | |||||||
chr12:53406828 | AT | A | 134 | a0001c0001t0001g0053 a0001c0001t0003g0105 a0001c0001t0005g0016 others(131): Show |
137 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.1844+89delT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53406828 | ||||||
chr12:53406848 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1844+95C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53406848 | |||||||
chr12:53407074 | T | G | 1 | a0001c0001t0036g0167 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1844+321T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407074 | |||||||
chr12:53407075 | C | T | 1 | a0001c0001t0058g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1844+322C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407075 | |||||||
chr12:53407318 | GA | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
81 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.1844+578delA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53407318 | ||||||
chr12:53407330 | A | T | 1 | a0001c0006t0043g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1844+577A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407330 | |||||||
chr12:53407331 | A | T | 131 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(128): Show |
134 | HG00280.hp2 HG00597.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.1844+578A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407331 | |||||||
chr12:53407357 | A | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
250 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1844+604A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407357 | |||||||
chr12:53407358 | G | T | 239 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
250 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1844+605G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407358 | |||||||
chr12:53407387 | G | A | 1 | a0001c0001t0042g0265 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1844+634G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407387 | |||||||
chr12:53407506 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1844+753A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407506 | |||||||
chr12:53407620 | G | A | 1 | a0001c0002t0002g0202 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1844+867G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407620 | |||||||
chr12:53407625 | A | G | 1 | a0001c0001t0013g0144 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1844+872A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407625 | |||||||
chr12:53407629 | AATTT | A | 89 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(86): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1844+889_1844+892d others(6): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53407629 | ||||||
chr12:53407677 | C | A | 89 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(86): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1844+924C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407677 | |||||||
chr12:53407785 | C | T | 1 | a0001c0001t0064g0166 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1844+1032C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407785 | |||||||
chr12:53407786 | G | A | 4 | a0001c0001t0010g0017 a0001c0001t0010g0266 a0001c0001t0010g0267 others(1): Show |
4 | HG02145.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1844+1033G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407786 | |||||||
chr12:53407838 | G | A | 39 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.1844+1085G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407838 | |||||||
chr12:53407914 | G | T | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1844+1161G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407914 | |||||||
chr12:53407938 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1844+1185C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407938 | |||||||
chr12:53407960 | T | G | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1844+1207T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407960 | |||||||
chr12:53407969 | G | A | 1 | a0001c0001t0004g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1844+1216G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53407969 | |||||||
chr12:53408185 | G | A | 3 | a0001c0001t0004g0082 a0001c0001t0012g0133 a0001c0001t0056g0098 |
3 | HG01934.hp2 NA18970.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1845-1177G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408185 | |||||||
chr12:53408245 | C | CA | 7 | a0001c0002t0023g0040 a0001c0002t0023g0041 a0001c0002t0033g0045 others(4): Show |
7 | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.1845-1103dupA | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53408245 | ||||||
chr12:53408245 | C | CAAAAA | 78 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(75): Show |
81 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1845-1107_1845-110 others(9): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53408245 | ||||||
chr12:53408245 | C | CAAAAAA | 10 | a0001c0002t0002g0201 a0001c0002t0002g0205 a0001c0002t0002g0209 others(7): Show |
10 | HG02145.hp2 HG02970.hp1 NA18972.hp1 others(7): Show |
intron_variant | MODIFIER | c.1845-1108_1845-110 others(10): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53408245 | ||||||
chr12:53408266 | C | T | 1 | a0002c0004t0076g0257 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1845-1096C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408266 | |||||||
chr12:53408306 | G | A | 1 | a0001c0006t0043g0270 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1845-1056G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408306 | |||||||
chr12:53408341 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1845-1021A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408341 | |||||||
chr12:53408364 | G | C | 1 | a0001c0001t0079g0284 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1845-998G>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408364 | |||||||
chr12:53408375 | T | G | 1 | a0001c0001t0004g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1845-987T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408375 | |||||||
chr12:53408403 | A | T | 1 | a0001c0002t0002g0194 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1845-959A>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408403 | |||||||
chr12:53408511 | C | T | 3 | a0001c0001t0010g0017 a0001c0001t0010g0266 a0001c0001t0010g0267 |
3 | HG03209.hp1 HG03471.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1845-851C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408511 | |||||||
chr12:53408575 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1845-787C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408575 | |||||||
chr12:53408672 | C | T | 1 | a0001c0001t0004g0138 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1845-690C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408672 | |||||||
chr12:53408872 | C | T | 1 | a0001c0001t0065g0128 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1845-490C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408872 | |||||||
chr12:53408916 | A | G | 1 | a0001c0001t0037g0269 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1845-446A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53408916 | |||||||
chr12:53409006 | C | A | 1 | a0001c0001t0067g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1845-356C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409006 | |||||||
chr12:53409035 | G | A | 1 | a0001c0002t0002g0216 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1845-327G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409035 | |||||||
chr12:53409060 | A | G | 1 | a0001c0001t0008g0064 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1845-302A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409060 | |||||||
chr12:53409218 | C | CTG | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.1845-143_1845-142i others(4): Show |
SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chr12 | 53409218 | ||||||
chr12:53409249 | A | C | 1 | a0001c0001t0001g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1845-113A>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409249 | |||||||
chr12:53409295 | G | T | 2 | a0001c0001t0025g0187 a0001c0001t0025g0286 |
2 | HG02572.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1845-67G>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 4/5 | chr12 | 53409295 | |||||||
chr12:53409768 | T | G | 39 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(36): Show |
39 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.2044+207T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53409768 | |||||||
chr12:53409849 | T | C | 89 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(86): Show |
92 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.2044+288T>C | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53409849 | |||||||
chr12:53410328 | A | G | 4 | a0001c0001t0010g0017 a0001c0001t0010g0266 a0001c0001t0010g0267 others(1): Show |
4 | HG02145.hp1 HG03209.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2045-599A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410328 | |||||||
chr12:53410482 | A | G | 1 | a0001c0001t0015g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2045-445A>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410482 | |||||||
chr12:53410516 | G | GT | 6 | a0001c0001t0001g0024 a0001c0001t0003g0125 a0001c0001t0004g0106 others(3): Show |
6 | HG00609.hp2 HG01099.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2045-401dupT | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | INFO_REALIGN_3_PRIME | chr12 | 53410516 | ||||||
chr12:53410523 | T | G | 96 | a0001c0002t0002g0003 a0001c0002t0002g0013 a0001c0002t0002g0014 others(93): Show |
99 | HG00280.hp2 HG00323.hp1 HG00597.hp1 others(96): Show |
intron_variant | MODIFIER | c.2045-404T>G | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410523 | |||||||
chr12:53410580 | C | T | 38 | a0001c0001t0005g0016 a0001c0001t0005g0272 a0001c0001t0005g0273 others(35): Show |
38 | HG01099.hp1 HG01109.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.2045-347C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410580 | |||||||
chr12:53410602 | C | A | 2 | a0001c0002t0002g0209 a0001c0002t0077g0210 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2045-325C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410602 | |||||||
chr12:53410666 | C | A | 1 | a0001c0001t0007g0295 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2045-261C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410666 | |||||||
chr12:53410706 | C | T | 24 | a0001c0001t0005g0016 a0001c0001t0005g0186 a0001c0001t0005g0272 others(21): Show |
24 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2045-221C>T | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410706 | |||||||
chr12:53410752 | C | A | 1 | a0001c0001t0014g0086 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.2045-175C>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410752 | |||||||
chr12:53410785 | G | A | 1 | a0001c0001t0004g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2045-142G>A | SP1 | ENSG00000185591.10 | transcript | ENST00000327443.9 | protein_coding | 5/5 | chr12 | 53410785 |