Item | Value |
---|---|
geneid | 54766 |
ensemblid | ENSG00000137707.14 |
hgncid | 13862 |
symbol | BTG4 |
name | BTG anti-proliferation factor 4 |
refseq_nuc | NM_001367975.1 |
refseq_prot | NP_001354904.1 |
ensembl_nuc | ENST00000692032.1 |
ensembl_prot | ENSP00000509850.1 |
mane_status | MANE Select |
chr | chr11 |
start | 111494815 |
end | 111512386 |
strand | - |
ver | v1.2 |
region | chr11:111494815-111512386 |
region5000 | chr11:111489815-111517386 |
regionname0 | BTG4_chr11_111494815_111512386 |
regionname5000 | BTG4_chr11_111489815_111517386 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 229 | 350 | 95 | 67 | 144 | 10 | 32 | 122 | BTG4_chr11_111489815_111517386 | BTG4 | MRDEI others(224): Show |
chr11 | 111489815 | 111517386 |
a0002 | 0/0 | 228 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | MRDEI others(223): Show |
chr11 | 111489815 | 111517386 |
a0003 | 0/0 | 229 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | MRDEI others(224): Show |
chr11 | 111489815 | 111517386 |
a0004 | 0/0 | 229 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | MRDEI others(224): Show |
chr11 | 111489815 | 111517386 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 687 | 339 | 89 | 63 | 144 | 10 | 32 | BTG4_chr11_111489815_111517386 | BTG4 | ATGAG others(682): Show |
chr11 | 111489815 | 111517386 | ||
a0001c0002 | 1/0 | 687 | 11 | 6 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | ATGAG others(682): Show |
chr11 | 111489815 | 111517386 | ||
a0002c0003 | 0/0 | 687 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | ATGAG others(682): Show |
chr11 | 111489815 | 111517386 | ||
a0003c0004 | 0/0 | 687 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | ATGAG others(682): Show |
chr11 | 111489815 | 111517386 | ||
a0004c0005 | 0/0 | 687 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | ATGAG others(682): Show |
chr11 | 111489815 | 111517386 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1242 | 307 | 61 | 60 | 144 | 10 | 31 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0001c0001t0002 | 0/0 | 1242 | 10 | 9 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0001c0001t0003 | 0/0 | 1242 | 9 | 6 | 2 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0001c0001t0004 | 0/0 | 1242 | 8 | 8 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0001c0001t0005 | 0/0 | 1242 | 5 | 5 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0001c0002t0001 | 1/0 | 1242 | 11 | 6 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0002c0003t0001 | 0/0 | 1242 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0003c0004t0001 | 0/0 | 1242 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
a0004c0005t0001 | 0/0 | 1242 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | GAGGA others(1237): Show |
chr11 | 111489815 | 111517386 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 84 | 5 | 15 | 52 | 2 | 10 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0002 | 0/0 | 59 | 4 | 13 | 33 | 2 | 7 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0003 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0012 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0002g0007 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0002g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0013 | 0/0 | 4 | 2 | 1 | 0 | 0 | 1 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0002t0001g0004 | 0/0 | 8 | 4 | 4 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0002t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0001c0002t0001g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0002c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0003c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
a0004c0005t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0105 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01099 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02293 | hp1 | a0003 | c0004 | t0001 | g0064 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02630 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02895 | hp2 | a0004 | c0005 | t0001 | g0090 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03486 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18970 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18990 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | YRI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0041 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | USA | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0071 | REF | REF | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0089 | REF | REF | BTG4_chr11_111489815_111517386 | BTG4 | chr11 | 111489815 | 111517386 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111495140 | G | A | 1 | a0002 | 2 | NA18970.hp1 NA18990.hp1 |
stop_gained | HIGH | c.685C>T | p.Arg229* | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 917/1242 | 685/690 | 229/229 | chr11 | 111495140 | |||
chr11:111495179 | T | C | 1 | a0004 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.646A>G | p.Met216Val | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 878/1242 | 646/690 | 216/229 | chr11 | 111495179 | |||
chr11:111498719 | C | T | 1 | a0003 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.58G>A | p.Asp20Asn | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/5 | 290/1242 | 58/690 | 20/229 | chr11 | 111498719 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111497322 | G | T | 4 | a0001c0001 a0002c0003 a0003c0004 others(1): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
synonymous_variant | LOW | c.399C>A | p.Ala133Ala | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/5 | 631/1242 | 399/690 | 133/229 | chr11 | 111497322 | |||
chr11:111498684 | T | C | 1 | a0004c0005 | 1 | HG02895.hp2 | synonymous_variant | LOW | c.93A>G | p.Ala31Ala | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/5 | 325/1242 | 93/690 | 31/229 | chr11 | 111498684 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111494934 | C | T | 1 | a0001c0001t0003 | 9 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*201G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 201 | chr11 | 111494934 | ||||||
chr11:111495134 | G | A | 1 | a0001c0001t0005 | 5 | HG02630.hp2 HG02717.hp1 HG02922.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 5/5 | 1 | chr11 | 111495134 | ||||||
chr11:111512223 | G | A | 1 | a0001c0001t0002 | 10 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-69C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/5 | 13447 | chr11 | 111512223 | ||||||
chr11:111512347 | C | T | 1 | a0001c0001t0004 | 8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-193G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/5 | 13571 | chr11 | 111512347 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:111495707 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.511-393A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495707 | |||||||
chr11:111495735 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(28): Show |
111 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.511-421A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495735 | |||||||
chr11:111495737 | G | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.511-423C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495737 | |||||||
chr11:111495833 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.511-519C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495833 | |||||||
chr11:111495986 | G | C | 1 | a0001c0001t0003g0052 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.511-672C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111495986 | |||||||
chr11:111496067 | A | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(27): Show |
110 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.511-753T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496067 | |||||||
chr11:111496119 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(37): Show |
125 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.511-805C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496119 | |||||||
chr11:111496299 | T | C | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.510+912A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496299 | |||||||
chr11:111496331 | T | G | 1 | a0001c0001t0001g0027 | 2 | HG02922.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510+880A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496331 | |||||||
chr11:111496358 | T | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(37): Show |
125 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.510+853A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496358 | |||||||
chr11:111496466 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.510+745T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496466 | |||||||
chr11:111496477 | A | G | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+734T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496477 | |||||||
chr11:111496504 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.510+707C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496504 | |||||||
chr11:111496758 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.510+453A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496758 | |||||||
chr11:111496892 | G | GA | 10 | a0001c0001t0001g0037 a0001c0001t0001g0055 a0001c0001t0001g0069 others(7): Show |
21 | HG00738.hp1 HG01099.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.510+318dupT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496892 | |||||||
chr11:111496892 | G | GAAA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0026 others(4): Show |
19 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+316_510+318dup others(3): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111496892 | |||||||
chr11:111497164 | G | T | 4 | a0001c0001t0003g0056 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.510+47C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 4/4 | chr11 | 111497164 | |||||||
chr11:111497444 | G | A | 3 | a0001c0001t0001g0103 a0001c0001t0003g0013 a0001c0001t0003g0052 |
6 | HG00733.hp1 HG01099.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-35C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497444 | |||||||
chr11:111497522 | A | G | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.312-113T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497522 | |||||||
chr11:111497555 | T | A | 1 | a0001c0001t0004g0045 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.312-146A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497555 | |||||||
chr11:111497571 | A | T | 1 | a0001c0001t0001g0065 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.312-162T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497571 | |||||||
chr11:111497819 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.311+179T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497819 | |||||||
chr11:111497866 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0030 |
5 | HG00733.hp2 HG02148.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+132T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497866 | |||||||
chr11:111497966 | TCA | T | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.311+30_311+31delTG | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 3/4 | chr11 | 111497966 | |||||||
chr11:111498368 | A | G | 4 | a0001c0001t0004g0008 a0001c0001t0004g0043 a0001c0001t0004g0044 others(1): Show |
8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.174-233T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498368 | |||||||
chr11:111498407 | G | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.173+197C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498407 | |||||||
chr11:111498469 | C | T | 1 | a0001c0001t0001g0029 | 2 | NA18952.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.173+135G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498469 | |||||||
chr11:111498570 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.173+34C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 2/4 | chr11 | 111498570 | |||||||
chr11:111499026 | G | GA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
12 | HG01928.hp1 HG01928.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-26-225dupT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499026 | |||||||
chr11:111499027 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0062 |
8 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-225T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499027 | |||||||
chr11:111499034 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-232T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499034 | |||||||
chr11:111499630 | T | C | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-828A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499630 | |||||||
chr11:111499690 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(36): Show |
126 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.-26-888G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499690 | |||||||
chr11:111499702 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-26-900C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499702 | |||||||
chr11:111499812 | C | A | 1 | a0001c0001t0001g0015 | 4 | HG02965.hp1 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-1010G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499812 | |||||||
chr11:111499867 | C | T | 1 | a0001c0001t0003g0085 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-26-1065G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499867 | |||||||
chr11:111499870 | G | A | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-1068C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499870 | |||||||
chr11:111499877 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-26-1075G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499877 | |||||||
chr11:111499970 | C | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(26): Show |
104 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-26-1168G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111499970 | |||||||
chr11:111500141 | C | CA | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0051 others(2): Show |
7 | HG02055.hp1 HG02280.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-26-1340dupT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500141 | |||||||
chr11:111500147 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-26-1345T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500147 | |||||||
chr11:111500147 | AT | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0003g0086 |
3 | NA19011.hp2 NA19043.hp2 NA19059.hp2 |
intron_variant | MODIFIER | c.-26-1346delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500147 | |||||||
chr11:111500148 | T | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(99): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.-26-1346A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500148 | |||||||
chr11:111500179 | T | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-1377A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500179 | |||||||
chr11:111500434 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-1632C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500434 | |||||||
chr11:111500543 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-26-1741G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500543 | |||||||
chr11:111500679 | C | CT | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(48): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-26-1878dupA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500679 | |||||||
chr11:111500679 | C | CTT | 6 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0026 others(3): Show |
18 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-26-1879_-26-1878d others(4): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500679 | |||||||
chr11:111500679 | CT | C | 12 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0001g0055 others(9): Show |
23 | HG00733.hp1 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-26-1878delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500679 | |||||||
chr11:111500752 | TCCCTC | T | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-1955_-26-1951d others(7): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500752 | |||||||
chr11:111500780 | A | G | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-1978T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500780 | |||||||
chr11:111500948 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-26-2146C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111500948 | |||||||
chr11:111501068 | AG | A | 3 | a0001c0001t0001g0023 a0001c0001t0001g0099 a0001c0001t0001g0109 |
5 | HG01255.hp1 HG01884.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-2267delC | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501068 | |||||||
chr11:111501092 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0114 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-26-2290C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501092 | |||||||
chr11:111501136 | C | A | 1 | a0001c0001t0001g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-26-2334G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501136 | |||||||
chr11:111501256 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-26-2454G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501256 | |||||||
chr11:111501340 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0005g0081 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-26-2538G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501340 | |||||||
chr11:111501381 | A | T | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-2579T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501381 | |||||||
chr11:111501519 | AATAG | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0018 |
10 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-26-2721_-26-2718d others(6): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501519 | |||||||
chr11:111501520 | A | C | 4 | a0001c0001t0003g0056 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-2718T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501520 | |||||||
chr11:111501580 | A | C | 1 | a0001c0001t0001g0040 | 2 | HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-26-2778T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501580 | |||||||
chr11:111501713 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-26-2911A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501713 | |||||||
chr11:111501774 | C | T | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-2972G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111501774 | |||||||
chr11:111502074 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(25): Show |
103 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.-26-3272G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502074 | |||||||
chr11:111502077 | T | C | 1 | a0001c0001t0001g0072 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-26-3275A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502077 | |||||||
chr11:111502088 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-26-3286C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502088 | |||||||
chr11:111502120 | C | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-3318G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502120 | |||||||
chr11:111502138 | AT | A | 6 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0073 others(3): Show |
11 | HG02109.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-3337delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502138 | |||||||
chr11:111502150 | TC | T | 4 | a0001c0001t0004g0008 a0001c0001t0004g0043 a0001c0001t0004g0044 others(1): Show |
8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-3349delG | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502150 | |||||||
chr11:111502195 | C | T | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-3393G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502195 | |||||||
chr11:111502301 | G | A | 1 | a0001c0001t0001g0016 | 4 | NA18942.hp1 NA18957.hp2 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-3499C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502301 | |||||||
chr11:111502323 | T | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-3521A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502323 | |||||||
chr11:111502329 | T | C | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-3527A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502329 | |||||||
chr11:111502348 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-26-3546C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502348 | |||||||
chr11:111502378 | A | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(32): Show |
115 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(112): Show |
intron_variant | MODIFIER | c.-26-3576T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502378 | |||||||
chr11:111502396 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0113 |
7 | NA18963.hp2 NA18968.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-3594T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502396 | |||||||
chr11:111502420 | C | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0079 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-26-3618G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502420 | |||||||
chr11:111502487 | G | A | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-3685C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502487 | |||||||
chr11:111502527 | T | G | 4 | a0001c0001t0003g0056 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-3725A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502527 | |||||||
chr11:111502637 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0114 |
2 | HG01891.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-26-3835G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111502637 | |||||||
chr11:111503111 | C | T | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-4309G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503111 | |||||||
chr11:111503214 | C | A | 4 | a0001c0001t0004g0008 a0001c0001t0004g0043 a0001c0001t0004g0044 others(1): Show |
8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-4412G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503214 | |||||||
chr11:111503379 | C | T | 1 | a0001c0001t0003g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-26-4577G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503379 | |||||||
chr11:111503381 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-26-4579C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503381 | |||||||
chr11:111503439 | A | G | 1 | a0001c0001t0001g0020 | 3 | HG01256.hp1 HG01258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-26-4637T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503439 | |||||||
chr11:111503466 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0079 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-26-4664A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503466 | |||||||
chr11:111503580 | TC | T | 1 | a0001c0001t0001g0010 | 5 | HG01257.hp2 HG01258.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-4779delG | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503580 | |||||||
chr11:111503609 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0015 others(36): Show |
126 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(123): Show |
intron_variant | MODIFIER | c.-26-4807G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503609 | |||||||
chr11:111503664 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-26-4862T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503664 | |||||||
chr11:111503710 | T | G | 4 | a0001c0001t0004g0008 a0001c0001t0004g0043 a0001c0001t0004g0044 others(1): Show |
8 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-26-4908A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503710 | |||||||
chr11:111503711 | T | C | 6 | a0001c0001t0003g0013 a0001c0001t0003g0052 a0001c0001t0003g0056 others(3): Show |
9 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-26-4909A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503711 | |||||||
chr11:111503770 | A | G | 4 | a0001c0001t0003g0056 a0001c0001t0003g0085 a0001c0001t0003g0086 others(1): Show |
4 | HG02145.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-26-4968T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503770 | |||||||
chr11:111503792 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-4990C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503792 | |||||||
chr11:111503861 | G | A | 1 | a0001c0001t0003g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-26-5059C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503861 | |||||||
chr11:111503876 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-5074G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503876 | |||||||
chr11:111503905 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-26-5103C>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503905 | |||||||
chr11:111503911 | T | A | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5109A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111503911 | |||||||
chr11:111504059 | C | A | 1 | a0001c0001t0001g0107 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-26-5257G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504059 | |||||||
chr11:111504105 | C | A | 1 | a0004c0005t0001g0090 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-26-5303G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504105 | |||||||
chr11:111504383 | G | T | 1 | a0001c0001t0005g0034 | 2 | NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-26-5581C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504383 | |||||||
chr11:111504412 | A | G | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5610T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504412 | |||||||
chr11:111504575 | C | A | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5773G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504575 | |||||||
chr11:111504724 | A | C | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-5922T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504724 | |||||||
chr11:111504806 | G | A | 1 | a0001c0001t0003g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-26-6004C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504806 | |||||||
chr11:111504845 | T | G | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-26-6043A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111504845 | |||||||
chr11:111505062 | A | C | 2 | a0001c0001t0001g0080 a0001c0001t0005g0081 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-26-6260T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505062 | |||||||
chr11:111505382 | C | G | 1 | a0001c0001t0001g0019 | 3 | HG00733.hp2 HG02148.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.-26-6580G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505382 | |||||||
chr11:111505393 | A | T | 1 | a0001c0001t0001g0061 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-26-6591T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505393 | |||||||
chr11:111505540 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG01934.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-27+6641G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505540 | |||||||
chr11:111505617 | CGAAG | C | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+6560_-27+6563d others(6): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505617 | |||||||
chr11:111505618 | G | A | 2 | a0001c0001t0001g0080 a0001c0001t0005g0081 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-27+6563C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505618 | |||||||
chr11:111505623 | T | A | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+6558A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505623 | |||||||
chr11:111505740 | T | A | 1 | a0001c0001t0001g0024 | 3 | HG01109.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-27+6441A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505740 | |||||||
chr11:111505828 | T | A | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6353A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505828 | |||||||
chr11:111505829 | T | C | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6352A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505829 | |||||||
chr11:111505830 | T | A | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6351A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505830 | |||||||
chr11:111505831 | C | T | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6350G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505831 | |||||||
chr11:111505832 | T | A | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6349A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505832 | |||||||
chr11:111505835 | G | A | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6346C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505835 | |||||||
chr11:111505838 | G | T | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6343C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505838 | |||||||
chr11:111505840 | A | T | 1 | a0001c0001t0004g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-27+6341T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505840 | |||||||
chr11:111505953 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0076 |
4 | NA18955.hp1 NA18991.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+6228A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111505953 | |||||||
chr11:111506066 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0005g0081 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-27+6115G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506066 | |||||||
chr11:111506101 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-27+6080G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506101 | |||||||
chr11:111506163 | A | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(48): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-27+6018T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506163 | |||||||
chr11:111506210 | A | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27+5971T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506210 | |||||||
chr11:111506264 | T | C | 7 | a0001c0001t0001g0037 a0001c0001t0001g0108 a0001c0001t0003g0056 others(4): Show |
8 | HG02145.hp1 HG02895.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-27+5917A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506264 | |||||||
chr11:111506287 | T | C | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+5894A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506287 | |||||||
chr11:111506510 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-27+5671T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506510 | |||||||
chr11:111506585 | A | T | 1 | a0001c0001t0001g0014 | 4 | HG00099.hp2 HG00741.hp1 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+5596T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506585 | |||||||
chr11:111506769 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0079 |
2 | HG02055.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.-27+5412T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506769 | |||||||
chr11:111506921 | C | CTATAGA | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+5254_-27+5259d others(8): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111506921 | |||||||
chr11:111507033 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(48): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.-27+5148C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507033 | |||||||
chr11:111507226 | C | T | 1 | a0001c0001t0001g0046 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+4955G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507226 | |||||||
chr11:111507363 | T | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27+4818A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507363 | |||||||
chr11:111507562 | T | C | 1 | a0001c0002t0001g0036 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-27+4619A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507562 | |||||||
chr11:111507671 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-27+4510A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507671 | |||||||
chr11:111507793 | C | G | 1 | a0001c0001t0001g0058 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-27+4388G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507793 | |||||||
chr11:111507979 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-27+4202T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111507979 | |||||||
chr11:111508032 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+4149T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508032 | |||||||
chr11:111508097 | G | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0054 |
6 | HG00438.hp2 HG02165.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.-27+4084C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508097 | |||||||
chr11:111508202 | T | G | 1 | a0001c0001t0001g0078 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-27+3979A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508202 | |||||||
chr11:111508311 | C | T | 8 | a0001c0001t0001g0037 a0001c0001t0003g0013 a0001c0001t0003g0052 others(5): Show |
12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+3870G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508311 | |||||||
chr11:111508329 | C | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(26): Show |
104 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.-27+3852G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508329 | |||||||
chr11:111508346 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-27+3835A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508346 | |||||||
chr11:111508366 | C | CT | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.-27+3814dupA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508366 | |||||||
chr11:111508747 | A | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0018 |
10 | HG01243.hp1 HG02109.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-27+3434T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508747 | |||||||
chr11:111508753 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-27+3428T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508753 | |||||||
chr11:111508841 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-27+3340A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508841 | |||||||
chr11:111508926 | T | A | 1 | a0001c0001t0001g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-27+3255A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111508926 | |||||||
chr11:111509108 | A | G | 8 | a0001c0001t0001g0037 a0001c0001t0003g0013 a0001c0001t0003g0052 others(5): Show |
12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+3073T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509108 | |||||||
chr11:111509134 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0027 |
10 | HG01952.hp1 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.-27+3047T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509134 | |||||||
chr11:111509178 | G | A | 9 | a0001c0001t0001g0037 a0001c0001t0001g0084 a0001c0001t0003g0013 others(6): Show |
13 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-27+3003C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509178 | |||||||
chr11:111509179 | C | A | 8 | a0001c0001t0001g0037 a0001c0001t0003g0013 a0001c0001t0003g0052 others(5): Show |
12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+3002G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509179 | |||||||
chr11:111509191 | T | A | 8 | a0001c0001t0001g0037 a0001c0001t0003g0013 a0001c0001t0003g0052 others(5): Show |
12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2990A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509191 | |||||||
chr11:111509192 | T | G | 8 | a0001c0001t0001g0037 a0001c0001t0003g0013 a0001c0001t0003g0052 others(5): Show |
12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2989A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509192 | |||||||
chr11:111509193 | T | A | 8 | a0001c0001t0001g0037 a0001c0001t0003g0013 a0001c0001t0003g0052 others(5): Show |
12 | HG00733.hp1 HG01099.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2988A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509193 | |||||||
chr11:111509254 | C | G | 1 | a0001c0001t0001g0026 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-27+2927G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509254 | |||||||
chr11:111509273 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-27+2908C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509273 | |||||||
chr11:111509305 | T | C | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-27+2876A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509305 | |||||||
chr11:111509700 | AAAAAAC | A | 5 | a0001c0001t0001g0110 a0001c0001t0004g0008 a0001c0001t0004g0043 others(2): Show |
9 | HG00639.hp2 HG01884.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-27+2475_-27+2480d others(8): Show |
BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509700 | |||||||
chr11:111509821 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2360T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509821 | |||||||
chr11:111509823 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2358G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509823 | |||||||
chr11:111509827 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2354C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509827 | |||||||
chr11:111509831 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2350C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509831 | |||||||
chr11:111509832 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2349T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509832 | |||||||
chr11:111509832 | A | T | 2 | a0001c0001t0001g0055 a0001c0001t0003g0056 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-27+2349T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509832 | |||||||
chr11:111509833 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2348A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509833 | |||||||
chr11:111509836 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2345A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509836 | |||||||
chr11:111509840 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2341A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509840 | |||||||
chr11:111509844 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2337A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509844 | |||||||
chr11:111509846 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2335A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509846 | |||||||
chr11:111509848 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2333A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509848 | |||||||
chr11:111509855 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2326C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509855 | |||||||
chr11:111509856 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2325C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509856 | |||||||
chr11:111509863 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2318A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509863 | |||||||
chr11:111509867 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2314A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509867 | |||||||
chr11:111509871 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2310G>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509871 | |||||||
chr11:111509872 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2309A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509872 | |||||||
chr11:111509873 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2308G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509873 | |||||||
chr11:111509874 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2307G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509874 | |||||||
chr11:111509874 | CA | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(103): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-27+2306delT | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509874 | |||||||
chr11:111509876 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2305T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509876 | |||||||
chr11:111509879 | G | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2302C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509879 | |||||||
chr11:111509880 | T | G | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2301A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509880 | |||||||
chr11:111509882 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2299A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509882 | |||||||
chr11:111509883 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2298G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509883 | |||||||
chr11:111509885 | A | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2296T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509885 | |||||||
chr11:111509890 | T | C | 1 | a0004c0005t0001g0090 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+2291A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509890 | |||||||
chr11:111509891 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2290A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509891 | |||||||
chr11:111509897 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2284G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509897 | |||||||
chr11:111509904 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2277G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509904 | |||||||
chr11:111509911 | C | CT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(3): Show |
7 | HG00609.hp1 HG02976.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+2269dupA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509911 | |||||||
chr11:111509911 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-27+2270G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509911 | |||||||
chr11:111509911 | CT | C | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0021 others(2): Show |
12 | HG00140.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+2269delA | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509911 | |||||||
chr11:111509975 | G | A | 1 | a0004c0005t0001g0090 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-27+2206C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111509975 | |||||||
chr11:111510004 | C | T | 1 | a0001c0001t0001g0039 | 2 | HG01891.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-27+2177G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510004 | |||||||
chr11:111510057 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-27+2124C>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510057 | |||||||
chr11:111510064 | A | G | 2 | a0001c0001t0003g0013 a0001c0001t0003g0052 |
5 | HG00733.hp1 HG01099.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-27+2117T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510064 | |||||||
chr11:111510205 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-27+1976G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510205 | |||||||
chr11:111510206 | G | A | 1 | a0001c0001t0001g0025 | 3 | NA18946.hp1 NA19072.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-27+1975C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510206 | |||||||
chr11:111510237 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-27+1944G>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510237 | |||||||
chr11:111510449 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0046 |
3 | NA18957.hp1 NA18971.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-27+1732A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510449 | |||||||
chr11:111510568 | G | A | 2 | a0001c0001t0001g0037 a0004c0005t0001g0090 |
3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-27+1613C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510568 | |||||||
chr11:111510760 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-27+1421C>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111510760 | |||||||
chr11:111511093 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-27+1088A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511093 | |||||||
chr11:111511278 | T | A | 1 | a0001c0001t0001g0093 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-27+903A>T | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511278 | |||||||
chr11:111511328 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-27+853G>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511328 | |||||||
chr11:111511455 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-27+726A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511455 | |||||||
chr11:111511520 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-27+661A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511520 | |||||||
chr11:111511668 | A | C | 1 | a0002c0003t0001g0038 | 2 | NA18970.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-27+513T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511668 | |||||||
chr11:111511789 | A | G | 1 | a0001c0001t0001g0048 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-27+392T>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511789 | |||||||
chr11:111511840 | T | C | 31 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0015 others(28): Show |
111 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.-27+341A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511840 | |||||||
chr11:111511851 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-27+330A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511851 | |||||||
chr11:111511895 | T | G | 1 | a0001c0001t0001g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-27+286A>C | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511895 | |||||||
chr11:111511900 | A | T | 1 | a0001c0001t0001g0047 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-27+281T>A | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511900 | |||||||
chr11:111511901 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0113 |
5 | NA18963.hp2 NA18968.hp2 NA19080.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+280A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511901 | |||||||
chr11:111511914 | A | C | 1 | a0001c0001t0001g0046 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-27+267T>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511914 | |||||||
chr11:111511930 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-27+251A>G | BTG4 | ENSG00000137707.14 | transcript | ENST00000692032.1 | protein_coding | 1/4 | chr11 | 111511930 |