Item | Value |
---|---|
geneid | 23787 |
ensemblid | ENSG00000137409.21 |
hgncid | 17586 |
symbol | MTCH1 |
name | mitochondrial carrier 1 |
refseq_nuc | NM_001271641.2 |
refseq_prot | NP_001258570.1 |
ensembl_nuc | ENST00000373627.10 |
ensembl_prot | ENSP00000362730.5 |
mane_status | MANE Select |
chr | chr6 |
start | 36968141 |
end | 36986196 |
strand | - |
ver | v1.2 |
region | chr6:36968141-36986196 |
region5000 | chr6:36963141-36991196 |
regionname0 | MTCH1_chr6_36968141_36986196 |
regionname5000 | MTCH1_chr6_36963141_36991196 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 389 | 394 | 94 | 71 | 175 | 13 | 39 | 133 | MTCH1_chr6_36963141_36991196 | MTCH1 | MGASD others(384): Show |
chr6 | 36963141 | 36991196 |
a0002 | 0/0 | 91 | 16 | 1 | 0 | 13 | 0 | 2 | 11 | MTCH1_chr6_36963141_36991196 | MTCH1 | MGASD others(86): Show |
chr6 | 36963141 | 36991196 |
a0003 | 0/0 | 389 | 3 | 0 | 1 | 0 | 1 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | MGASD others(384): Show |
chr6 | 36963141 | 36991196 |
a0004 | 0/0 | 389 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | MGASD others(384): Show |
chr6 | 36963141 | 36991196 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1167 | 329 | 77 | 68 | 140 | 10 | 32 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0001c0002 | 0/0 | 1167 | 30 | 14 | 3 | 5 | 3 | 5 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0001c0003 | 0/0 | 1167 | 29 | 0 | 0 | 27 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0001c0005 | 0/0 | 1167 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0001c0006 | 0/0 | 1167 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0001c0009 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0002c0004 | 0/0 | 1166 | 14 | 1 | 0 | 13 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1161): Show |
chr6 | 36963141 | 36991196 | ||
a0002c0008 | 0/0 | 1166 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1161): Show |
chr6 | 36963141 | 36991196 | ||
a0003c0007 | 0/0 | 1167 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0003c0011 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 | ||
a0004c0010 | 0/0 | 1167 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | ATGGG others(1162): Show |
chr6 | 36963141 | 36991196 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1955 | 301 | 63 | 59 | 139 | 8 | 31 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0001t0002 | 0/0 | 1955 | 17 | 13 | 4 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0001t0004 | 0/1 | 1955 | 6 | 0 | 3 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0001t0005 | 0/0 | 1955 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0001t0006 | 0/0 | 1955 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0001t0007 | 0/0 | 1955 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0001t0008 | 0/0 | 1955 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0001t0009 | 0/0 | 1955 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0002t0001 | 0/0 | 1955 | 18 | 8 | 1 | 5 | 0 | 4 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0002t0002 | 0/0 | 1955 | 4 | 4 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0002t0003 | 0/0 | 1955 | 8 | 2 | 2 | 0 | 3 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0003t0001 | 0/0 | 1955 | 29 | 0 | 0 | 27 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0005t0002 | 0/0 | 1955 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0006t0001 | 0/0 | 1955 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0001c0009t0001 | 0/0 | 1955 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0002c0004t0001 | 0/0 | 1954 | 14 | 1 | 0 | 13 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1949): Show |
chr6 | 36963141 | 36991196 |
a0002c0008t0001 | 0/0 | 1954 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1949): Show |
chr6 | 36963141 | 36991196 |
a0003c0007t0001 | 0/0 | 1955 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0003c0011t0001 | 0/0 | 1955 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
a0004c0010t0002 | 0/0 | 1955 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | GAGTG others(1950): Show |
chr6 | 36963141 | 36991196 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 37 | 1 | 2 | 32 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0002 | 1/0 | 21 | 0 | 5 | 8 | 0 | 7 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0003 | 0/0 | 17 | 3 | 0 | 14 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0004 | 0/0 | 15 | 1 | 1 | 11 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0005 | 0/0 | 15 | 1 | 11 | 0 | 0 | 3 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0008 | 0/0 | 10 | 0 | 3 | 2 | 0 | 5 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0009 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0010 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0011 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0013 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0015 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0016 | 0/0 | 6 | 0 | 4 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0018 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0020 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0022 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0023 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0025 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0027 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0031 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0032 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0034 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0035 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0036 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0012 | 0/0 | 7 | 5 | 2 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0004g0014 | 0/1 | 6 | 0 | 3 | 0 | 2 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0008g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0001t0009g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0019 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0002g0037 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0003g0017 | 0/0 | 5 | 0 | 1 | 0 | 3 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0002t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0006 | 0/0 | 13 | 0 | 0 | 12 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0021 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0024 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0033 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0005t0002g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0005t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0006t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0001c0009t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0002c0004t0001g0007 | 0/0 | 12 | 0 | 0 | 12 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0002c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0002c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0002c0008t0001g0057 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0003c0007t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0003c0007t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0003c0011t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
a0004c0010t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0014 | EUR | GBR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | FIN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00423 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00438 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0110 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00597 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00597 | hp2 | a0001 | c0009 | t0001 | g0058 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00609 | hp1 | a0001 | c0006 | t0001 | g0038 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00733 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0014 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0062 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01168 | hp2 | a0001 | c0001 | t0009 | g0159 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01261 | hp1 | a0001 | c0002 | t0003 | g0079 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0017 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0050 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01515 | hp2 | a0001 | c0002 | t0003 | g0017 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01517 | hp2 | a0001 | c0002 | t0003 | g0017 | EUR | IBS | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0140 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01943 | hp2 | a0001 | c0002 | t0001 | g0019 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0113 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0033 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02155 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02258 | hp2 | a0001 | c0005 | t0002 | g0039 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02280 | hp1 | a0004 | c0010 | t0002 | g0153 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02572 | hp1 | a0001 | c0005 | t0002 | g0059 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02683 | hp2 | a0001 | c0003 | t0001 | g0006 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0019 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02723 | hp2 | a0001 | c0005 | t0002 | g0039 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02886 | hp2 | a0001 | c0002 | t0003 | g0081 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0151 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0091 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0040 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0088 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0109 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0017 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0100 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0144 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03710 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04115 | hp1 | a0002 | c0008 | t0001 | g0057 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0051 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18747 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | CHB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18939 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18941 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18942 | hp2 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18946 | hp2 | a0002 | c0004 | t0001 | g0158 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18947 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18953 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18954 | hp1 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18960 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18963 | hp1 | a0001 | c0006 | t0001 | g0038 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18964 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18979 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18983 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18985 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18997 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19001 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19054 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19066 | hp2 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19076 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19081 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19082 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19083 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19085 | hp1 | a0001 | c0003 | t0001 | g0024 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19088 | hp1 | a0002 | c0004 | t0001 | g0007 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19090 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19091 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ASW | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20752 | hp2 | a0001 | c0002 | t0003 | g0017 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20805 | hp1 | a0003 | c0007 | t0001 | g0154 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | TSI | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20905 | hp1 | a0003 | c0011 | t0001 | g0156 | SAS | GIH | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20905 | hp2 | a0002 | c0008 | t0001 | g0057 | SAS | GIH | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01123 | hp1 | a0003 | c0007 | t0001 | g0155 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | USA | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA21309 | hp1 | a0002 | c0004 | t0001 | g0157 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
NA21309 | hp2 | a0001 | c0002 | t0003 | g0086 | AFR | LWK | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0014 | REF | REF | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | MTCH1_chr6_36963141_36991196 | MTCH1 | chr6 | 36963141 | 36991196 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36986004 | G | A | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.170C>T | p.Ala57Val | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 193/1955 | 170/1170 | 57/389 | chr6 | 36986004 | |||
chr6:36986127 | G | A | 1 | a0003 | 2 | HG01123.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.47C>T | p.Ala16Val | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 70/1955 | 47/1170 | 16/389 | chr6 | 36986127 | |||
chr6:36986128 | C | A | 1 | a0003 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.46G>T | p.Ala16Ser | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 69/1955 | 46/1170 | 16/389 | chr6 | 36986128 | |||
chr6:36986143 | AG | A | 1 | a0002 | 16 | HG00597.hp1 HG04115.hp1 NA18747.hp2 others(13): Show |
frameshift_variant | HIGH | c.30delC | p.Trp11fs | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 53/1955 | 30/1170 | 10/389 | chr6 | 36986143 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36968921 | T | C | 1 | a0001c0002 | 30 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(27): Show |
synonymous_variant | LOW | c.1152A>G | p.Ser384Ser | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 1175/1955 | 1152/1170 | 384/389 | chr6 | 36968921 | |||
chr6:36970656 | G | A | 3 | a0001c0003 a0001c0009 a0002c0008 |
32 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(29): Show |
synonymous_variant | LOW | c.945C>T | p.Phe315Phe | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 9/12 | 968/1955 | 945/1170 | 315/389 | chr6 | 36970656 | |||
chr6:36986087 | G | T | 1 | a0001c0005 | 3 | HG02258.hp2 HG02572.hp1 HG02723.hp2 |
synonymous_variant | LOW | c.87C>A | p.Arg29Arg | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 110/1955 | 87/1170 | 29/389 | chr6 | 36986087 | |||
chr6:36986162 | C | T | 2 | a0001c0006 a0001c0009 |
3 | HG00597.hp2 HG00609.hp1 NA18963.hp1 |
synonymous_variant | LOW | c.12G>A | p.Ser4Ser | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 35/1955 | 12/1170 | 4/389 | chr6 | 36986162 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36968435 | C | T | 1 | a0001c0001t0007 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 468 | chr6 | 36968435 | ||||||
chr6:36968676 | C | T | 1 | a0001c0001t0008 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*227G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 227 | chr6 | 36968676 | ||||||
chr6:36968707 | C | T | 1 | a0001c0002t0003 | 8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*196G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 196 | chr6 | 36968707 | ||||||
chr6:36968740 | A | C | 1 | a0001c0001t0006 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 163 | chr6 | 36968740 | ||||||
chr6:36968803 | C | T | 1 | a0001c0001t0005 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*100G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 100 | chr6 | 36968803 | ||||||
chr6:36968830 | T | C | 5 | a0001c0001t0002 a0001c0001t0008 a0001c0002t0002 others(2): Show |
26 | HG00733.hp2 HG00741.hp2 HG01243.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*73A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 73 | chr6 | 36968830 | ||||||
chr6:36968864 | G | A | 1 | a0001c0001t0004 | 5 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*39C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 12/12 | 39 | chr6 | 36968864 | ||||||
chr6:36986189 | G | C | 1 | a0001c0001t0009 | 1 | HG01168.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/12 | 16 | chr6 | 36986189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:36968995 | A | G | 41 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(38): Show |
93 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.1099-21T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36968995 | |||||||
chr6:36969089 | G | A | 2 | a0001c0001t0002g0067 a0001c0001t0002g0083 |
2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1099-115C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969089 | |||||||
chr6:36969181 | T | C | 1 | a0002c0004t0001g0158 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1099-207A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969181 | |||||||
chr6:36969282 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0139 |
6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1099-308C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969282 | |||||||
chr6:36969310 | T | G | 4 | a0001c0002t0003g0017 a0001c0002t0003g0079 a0001c0002t0003g0081 others(1): Show |
8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1099-336A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969310 | |||||||
chr6:36969320 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1099-346A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969320 | |||||||
chr6:36969352 | T | C | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1099-378A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969352 | |||||||
chr6:36969480 | C | A | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1099-506G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969480 | |||||||
chr6:36969505 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0093 |
2 | HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1099-531G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969505 | |||||||
chr6:36969506 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1099-532C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969506 | |||||||
chr6:36969585 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1098+454T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969585 | |||||||
chr6:36969658 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1098+381G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969658 | |||||||
chr6:36969864 | C | T | 4 | a0001c0002t0003g0017 a0001c0002t0003g0079 a0001c0002t0003g0081 others(1): Show |
8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+175G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969864 | |||||||
chr6:36969871 | T | C | 1 | a0001c0001t0001g0015 | 6 | HG00639.hp1 HG01070.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1098+168A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969871 | |||||||
chr6:36969899 | T | C | 2 | a0001c0001t0002g0067 a0001c0001t0002g0083 |
2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1098+140A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969899 | |||||||
chr6:36969906 | C | G | 4 | a0001c0002t0003g0017 a0001c0002t0003g0079 a0001c0002t0003g0081 others(1): Show |
8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098+133G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969906 | |||||||
chr6:36969993 | T | C | 2 | a0001c0002t0002g0037 a0001c0002t0002g0140 |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1098+46A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36969993 | |||||||
chr6:36970021 | C | T | 1 | a0001c0001t0001g0030 | 3 | HG02809.hp2 HG03471.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1098+18G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36970021 | |||||||
chr6:36970022 | G | A | 12 | a0001c0002t0001g0019 a0001c0002t0001g0040 a0001c0002t0001g0051 others(9): Show |
18 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.1098+17C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 11/11 | chr6 | 36970022 | |||||||
chr6:36970168 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1023-54C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970168 | |||||||
chr6:36970248 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1023-134C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970248 | |||||||
chr6:36970272 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1022+134T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970272 | |||||||
chr6:36970375 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0028 |
8 | NA18957.hp1 NA18983.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.1022+31A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 10/11 | chr6 | 36970375 | |||||||
chr6:36970731 | C | T | 1 | a0001c0002t0001g0144 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.907-37G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970731 | |||||||
chr6:36970853 | G | C | 1 | a0001c0003t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.907-159C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970853 | |||||||
chr6:36970975 | C | G | 1 | a0001c0001t0001g0035 | 3 | HG02258.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.907-281G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970975 | |||||||
chr6:36970991 | C | G | 1 | a0001c0001t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.907-297G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36970991 | |||||||
chr6:36971102 | C | T | 1 | a0003c0007t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.907-408G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971102 | |||||||
chr6:36971123 | T | G | 8 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0076 others(5): Show |
12 | HG01069.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.907-429A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971123 | |||||||
chr6:36971192 | C | G | 4 | a0001c0002t0003g0017 a0001c0002t0003g0079 a0001c0002t0003g0081 others(1): Show |
8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.907-498G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971192 | |||||||
chr6:36971275 | G | T | 1 | a0001c0001t0001g0073 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.907-581C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971275 | |||||||
chr6:36971430 | C | T | 2 | a0001c0001t0002g0063 a0001c0002t0001g0151 |
2 | HG02630.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.907-736G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971430 | |||||||
chr6:36971437 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(41): Show |
144 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.907-743G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971437 | |||||||
chr6:36971466 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.907-772T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971466 | |||||||
chr6:36971503 | C | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(20): Show |
55 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.907-809G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971503 | |||||||
chr6:36971506 | G | A | 2 | a0001c0002t0003g0079 a0001c0002t0003g0081 |
2 | HG01261.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.907-812C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971506 | |||||||
chr6:36971587 | C | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0009 others(28): Show |
103 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.907-893G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971587 | |||||||
chr6:36971587 | C | T | 45 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(42): Show |
91 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(88): Show |
intron_variant | MODIFIER | c.907-893G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971587 | |||||||
chr6:36971606 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.907-912G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971606 | |||||||
chr6:36971752 | C | G | 42 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(39): Show |
88 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.906+900G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971752 | |||||||
chr6:36971947 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.906+705A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36971947 | |||||||
chr6:36972041 | G | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0030 others(9): Show |
27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.906+611C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972041 | |||||||
chr6:36972361 | C | T | 1 | a0001c0001t0004g0014 | 5 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+291G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972361 | |||||||
chr6:36972425 | C | CT | 47 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(44): Show |
93 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.906+226_906+227ins others(1): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972425 | |||||||
chr6:36972430 | A | G | 2 | a0001c0001t0002g0060 a0001c0001t0002g0064 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.906+222T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972430 | |||||||
chr6:36972483 | C | T | 1 | a0001c0002t0003g0017 | 5 | HG01433.hp2 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+169G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972483 | |||||||
chr6:36972484 | G | A | 1 | a0001c0002t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.906+168C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972484 | |||||||
chr6:36972497 | G | A | 41 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(38): Show |
82 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.906+155C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972497 | |||||||
chr6:36972567 | G | C | 47 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(44): Show |
93 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(90): Show |
intron_variant | MODIFIER | c.906+85C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972567 | |||||||
chr6:36972619 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.906+33G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 8/11 | chr6 | 36972619 | |||||||
chr6:36972959 | C | T | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-163G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36972959 | |||||||
chr6:36972973 | C | G | 1 | a0001c0009t0001g0058 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.762-177G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36972973 | |||||||
chr6:36972995 | T | A | 2 | a0001c0002t0002g0037 a0001c0002t0002g0140 |
4 | HG01884.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.762-199A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36972995 | |||||||
chr6:36973001 | G | C | 1 | a0001c0001t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.762-205C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973001 | |||||||
chr6:36973009 | G | T | 1 | a0001c0001t0001g0128 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.762-213C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973009 | |||||||
chr6:36973029 | T | C | 82 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(79): Show |
162 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(159): Show |
intron_variant | MODIFIER | c.762-233A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973029 | |||||||
chr6:36973302 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.762-506G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973302 | |||||||
chr6:36973319 | A | C | 1 | a0001c0001t0002g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.762-523T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973319 | |||||||
chr6:36973335 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.762-539C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973335 | |||||||
chr6:36973360 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.762-564T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973360 | |||||||
chr6:36973486 | T | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0139 |
6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.762-690A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973486 | |||||||
chr6:36973486 | T | TA | 11 | a0001c0002t0001g0019 a0001c0002t0001g0040 a0001c0002t0001g0051 others(8): Show |
17 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.762-691dupT | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973486 | |||||||
chr6:36973660 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.762-864A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973660 | |||||||
chr6:36973791 | G | T | 1 | a0001c0001t0001g0027 | 3 | HG02735.hp1 HG03490.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.762-995C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973791 | |||||||
chr6:36973836 | G | C | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-1040C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973836 | |||||||
chr6:36973847 | C | T | 1 | a0001c0001t0001g0055 | 2 | NA18990.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.762-1051G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36973847 | |||||||
chr6:36974040 | C | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(21): Show |
56 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.762-1244G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974040 | |||||||
chr6:36974086 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.762-1290G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974086 | |||||||
chr6:36974156 | A | G | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.762-1360T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974156 | |||||||
chr6:36974168 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.762-1372G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974168 | |||||||
chr6:36974275 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0119 |
3 | HG02486.hp2 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.761+1383T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974275 | |||||||
chr6:36974325 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.761+1333G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974325 | |||||||
chr6:36974342 | A | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0093 |
3 | HG02630.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.761+1316T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974342 | |||||||
chr6:36974456 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+1202A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974456 | |||||||
chr6:36974489 | T | A | 37 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(34): Show |
74 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.761+1169A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974489 | |||||||
chr6:36974498 | C | G | 37 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(34): Show |
74 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.761+1160G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974498 | |||||||
chr6:36974534 | C | T | 1 | a0001c0001t0001g0036 | 3 | NA18946.hp1 NA18989.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.761+1124G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974534 | |||||||
chr6:36974641 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+1017C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974641 | |||||||
chr6:36974688 | A | G | 2 | a0001c0005t0002g0039 a0001c0005t0002g0059 |
3 | HG02258.hp2 HG02572.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.761+970T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974688 | |||||||
chr6:36974696 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.761+962A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974696 | |||||||
chr6:36974705 | A | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+953T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974705 | |||||||
chr6:36974706 | T | C | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.761+952A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974706 | |||||||
chr6:36974707 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0149 others(2): Show |
9 | HG01069.hp2 HG01496.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.761+951T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974707 | |||||||
chr6:36974887 | T | TGTATGTC others(10): Show |
1 | a0001c0001t0001g0095 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.761+770_761+771ins others(17): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974887 | |||||||
chr6:36974888 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.761+770T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974888 | |||||||
chr6:36974970 | C | T | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+688G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36974970 | |||||||
chr6:36975101 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0041 |
10 | NA18964.hp2 NA18981.hp1 NA18994.hp2 others(7): Show |
intron_variant | MODIFIER | c.761+557A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975101 | |||||||
chr6:36975152 | A | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+506T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975152 | |||||||
chr6:36975157 | C | A | 1 | a0001c0001t0001g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.761+501G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975157 | |||||||
chr6:36975203 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.761+455A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975203 | |||||||
chr6:36975240 | A | G | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0030 others(9): Show |
27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.761+418T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975240 | |||||||
chr6:36975348 | C | G | 1 | a0001c0001t0002g0082 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.761+310G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975348 | |||||||
chr6:36975563 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.761+95C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 7/11 | chr6 | 36975563 | |||||||
chr6:36975737 | G | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-20C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975737 | |||||||
chr6:36975746 | G | A | 1 | a0001c0001t0001g0050 | 2 | HG01192.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.702-29C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975746 | |||||||
chr6:36975755 | G | A | 4 | a0001c0002t0003g0017 a0001c0002t0003g0079 a0001c0002t0003g0081 others(1): Show |
8 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.702-38C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975755 | |||||||
chr6:36975778 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0030 others(9): Show |
27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.702-61A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975778 | |||||||
chr6:36975797 | A | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-80T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975797 | |||||||
chr6:36975799 | C | T | 5 | a0001c0001t0001g0010 a0001c0002t0003g0017 a0001c0002t0003g0079 others(2): Show |
15 | HG01257.hp1 HG01258.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.702-82G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975799 | |||||||
chr6:36975829 | A | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-112T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975829 | |||||||
chr6:36975915 | T | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-198A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36975915 | |||||||
chr6:36976011 | A | G | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-294T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976011 | |||||||
chr6:36976035 | G | A | 5 | a0001c0002t0001g0040 a0001c0002t0001g0065 a0001c0002t0001g0091 others(2): Show |
6 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.702-318C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976035 | |||||||
chr6:36976052 | C | A | 1 | a0001c0001t0001g0074 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.702-335G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976052 | |||||||
chr6:36976135 | G | A | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-418C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976135 | |||||||
chr6:36976147 | G | C | 43 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(40): Show |
85 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(82): Show |
intron_variant | MODIFIER | c.702-430C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976147 | |||||||
chr6:36976180 | AC | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0149 others(2): Show |
9 | HG01069.hp2 HG01496.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.702-464delG | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976180 | |||||||
chr6:36976365 | C | A | 1 | a0001c0001t0008g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.702-648G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976365 | |||||||
chr6:36976462 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0093 |
3 | HG02630.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.701+737A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976462 | |||||||
chr6:36976703 | T | C | 29 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0053 others(26): Show |
52 | HG01069.hp2 HG01257.hp1 HG01258.hp2 others(49): Show |
intron_variant | MODIFIER | c.701+496A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976703 | |||||||
chr6:36976719 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(106): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.701+480T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976719 | |||||||
chr6:36976778 | C | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0018 others(21): Show |
56 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.701+421G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976778 | |||||||
chr6:36976825 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.701+374G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976825 | |||||||
chr6:36976852 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.701+347G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36976852 | |||||||
chr6:36977115 | G | A | 2 | a0001c0002t0003g0079 a0001c0002t0003g0081 |
2 | HG01261.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.701+84C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36977115 | |||||||
chr6:36977126 | T | C | 19 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0076 others(16): Show |
29 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.701+73A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 6/11 | chr6 | 36977126 | |||||||
chr6:36977257 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18979.hp2 | splice_region_variant&intron_variant | LOW | c.650-7T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977257 | |||||||
chr6:36977286 | G | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0023 others(18): Show |
47 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.650-36C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977286 | |||||||
chr6:36977360 | C | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.650-110G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977360 | |||||||
chr6:36977402 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0005g0105 |
5 | HG00438.hp2 HG02083.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-152G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977402 | |||||||
chr6:36977506 | C | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0023 others(18): Show |
47 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.649+128G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977506 | |||||||
chr6:36977583 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.649+51G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977583 | |||||||
chr6:36977617 | G | A | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.649+17C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977617 | |||||||
chr6:36977622 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.649+12C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 5/11 | chr6 | 36977622 | |||||||
chr6:36977761 | T | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0119 a0001c0002t0003g0017 others(3): Show |
11 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.592-70A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977761 | |||||||
chr6:36977804 | T | A | 1 | a0001c0001t0001g0152 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.592-113A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977804 | |||||||
chr6:36977872 | C | T | 1 | a0001c0002t0001g0040 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.592-181G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977872 | |||||||
chr6:36977970 | A | G | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.591+108T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977970 | |||||||
chr6:36977978 | A | G | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.591+100T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36977978 | |||||||
chr6:36978005 | C | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.591+73G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 4/11 | chr6 | 36978005 | |||||||
chr6:36978162 | C | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
splice_region_variant&intron_variant | LOW | c.514-7G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978162 | |||||||
chr6:36978162 | CAG | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0145 |
7 | HG00735.hp1 HG01358.hp2 HG01433.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.514-9_514-8delCT | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978162 | |||||||
chr6:36978169 | G | A | 1 | a0001c0001t0001g0054 | 2 | HG01106.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.514-14C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978169 | |||||||
chr6:36978213 | G | A | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.514-58C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978213 | |||||||
chr6:36978310 | G | A | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.514-155C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 3/11 | chr6 | 36978310 | |||||||
chr6:36978665 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.407-54A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978665 | |||||||
chr6:36978682 | C | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0066 others(5): Show |
16 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.407-71G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978682 | |||||||
chr6:36978694 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.407-83G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978694 | |||||||
chr6:36978735 | G | A | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.407-124C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978735 | |||||||
chr6:36978829 | G | A | 1 | a0002c0004t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.407-218C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978829 | |||||||
chr6:36978872 | C | T | 5 | a0001c0002t0001g0040 a0001c0002t0001g0065 a0001c0002t0001g0091 others(2): Show |
6 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-261G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978872 | |||||||
chr6:36978873 | TCC | T | 5 | a0001c0002t0001g0040 a0001c0002t0001g0065 a0001c0002t0001g0091 others(2): Show |
6 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.407-264_407-263del others(2): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978873 | |||||||
chr6:36978875 | C | CT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(12): Show |
21 | HG02257.hp1 HG02523.hp2 HG02723.hp1 others(18): Show |
intron_variant | MODIFIER | c.407-265dupA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | |||||||
chr6:36978875 | C | CTTT | 6 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0149 others(3): Show |
9 | HG01069.hp2 HG01496.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.407-267_407-265dup others(3): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | |||||||
chr6:36978875 | C | CTTTT | 10 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0076 others(7): Show |
15 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.407-268_407-265dup others(4): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | |||||||
chr6:36978875 | CT | C | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(40): Show |
87 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(84): Show |
intron_variant | MODIFIER | c.407-265delA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | |||||||
chr6:36978875 | CTT | C | 7 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0068 others(4): Show |
10 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.407-266_407-265del others(2): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | |||||||
chr6:36978875 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.407-274_407-265del others(10): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | |||||||
chr6:36978875 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0060 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.407-276_407-265del others(12): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36978875 | |||||||
chr6:36979041 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.407-430C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979041 | |||||||
chr6:36979128 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0028 |
8 | NA18957.hp1 NA18983.hp2 NA18985.hp2 others(5): Show |
intron_variant | MODIFIER | c.407-517G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979128 | |||||||
chr6:36979170 | A | G | 1 | a0001c0001t0002g0067 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.407-559T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979170 | |||||||
chr6:36979172 | C | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0023 others(15): Show |
42 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.407-561G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979172 | |||||||
chr6:36979192 | A | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.407-581T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979192 | |||||||
chr6:36979194 | A | T | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG01069.hp2 HG01496.hp1 HG01943.hp2 others(32): Show |
intron_variant | MODIFIER | c.407-583T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979194 | |||||||
chr6:36979355 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.407-744C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979355 | |||||||
chr6:36979482 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.407-871G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979482 | |||||||
chr6:36979502 | G | A | 1 | a0001c0002t0001g0040 | 2 | HG02615.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.407-891C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979502 | |||||||
chr6:36979530 | T | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0076 others(5): Show |
12 | HG01069.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.407-919A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979530 | |||||||
chr6:36979610 | T | C | 8 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0076 others(5): Show |
12 | HG01069.hp2 HG01496.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.407-999A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979610 | |||||||
chr6:36979741 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.407-1130C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979741 | |||||||
chr6:36979923 | C | G | 3 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0093 |
3 | HG02630.hp1 HG02976.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.407-1312G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979923 | |||||||
chr6:36979973 | T | C | 12 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0030 others(9): Show |
27 | HG01243.hp2 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.407-1362A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36979973 | |||||||
chr6:36980259 | A | T | 18 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0023 others(15): Show |
42 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.406+1329T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980259 | |||||||
chr6:36980306 | T | C | 3 | a0001c0003t0001g0021 a0001c0003t0001g0033 a0001c0003t0001g0137 |
9 | HG02015.hp2 HG02129.hp2 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.406+1282A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980306 | |||||||
chr6:36980348 | A | T | 6 | a0001c0001t0001g0068 a0001c0001t0002g0060 a0001c0001t0002g0064 others(3): Show |
8 | HG01884.hp2 HG01891.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.406+1240T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980348 | |||||||
chr6:36980386 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.406+1202C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980386 | |||||||
chr6:36980439 | T | C | 6 | a0001c0001t0001g0053 a0001c0001t0001g0119 a0001c0002t0003g0017 others(3): Show |
11 | HG01261.hp1 HG01433.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.406+1149A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980439 | |||||||
chr6:36980470 | C | T | 20 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0023 others(17): Show |
46 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.406+1118G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980470 | |||||||
chr6:36980532 | G | C | 11 | a0001c0002t0001g0019 a0001c0002t0001g0040 a0001c0002t0001g0051 others(8): Show |
17 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.406+1056C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980532 | |||||||
chr6:36980583 | C | T | 4 | a0001c0002t0001g0040 a0001c0002t0001g0065 a0001c0002t0001g0091 others(1): Show |
5 | HG02109.hp2 HG02615.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.406+1005G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980583 | |||||||
chr6:36980588 | A | G | 1 | a0001c0002t0001g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.406+1000T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980588 | |||||||
chr6:36980752 | A | G | 22 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
35 | HG00741.hp2 HG01069.hp2 HG01496.hp1 others(32): Show |
intron_variant | MODIFIER | c.406+836T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36980752 | |||||||
chr6:36981029 | A | G | 71 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(68): Show |
145 | HG00099.hp1 HG00639.hp1 HG00735.hp1 others(142): Show |
intron_variant | MODIFIER | c.406+559T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981029 | |||||||
chr6:36981060 | C | G | 1 | a0001c0005t0002g0059 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.406+528G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981060 | |||||||
chr6:36981318 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0139 |
6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+270A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981318 | |||||||
chr6:36981341 | G | T | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.406+247C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981341 | |||||||
chr6:36981419 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.406+169G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981419 | |||||||
chr6:36981502 | A | G | 3 | a0001c0001t0001g0035 a0001c0001t0001g0043 a0001c0001t0001g0139 |
6 | HG02109.hp1 HG02258.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.406+86T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981502 | |||||||
chr6:36981508 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.406+80G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981508 | |||||||
chr6:36981536 | TG | T | 5 | a0001c0002t0001g0019 a0001c0002t0001g0051 a0001c0002t0001g0090 others(2): Show |
10 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.406+51delC | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 2/11 | chr6 | 36981536 | |||||||
chr6:36981751 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0008 others(102): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.322-79G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981751 | |||||||
chr6:36981760 | C | T | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-88G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981760 | |||||||
chr6:36981764 | A | G | 1 | a0001c0001t0001g0069 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.322-92T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981764 | |||||||
chr6:36981822 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.322-150G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981822 | |||||||
chr6:36981859 | C | T | 8 | a0001c0001t0001g0066 a0001c0001t0001g0093 a0001c0001t0001g0114 others(5): Show |
15 | HG00733.hp2 HG01243.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.322-187G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36981859 | |||||||
chr6:36982032 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-360G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982032 | |||||||
chr6:36982033 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-361A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982033 | |||||||
chr6:36982034 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-362G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982034 | |||||||
chr6:36982036 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-364A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982036 | |||||||
chr6:36982037 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-365G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982037 | |||||||
chr6:36982038 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-366A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982038 | |||||||
chr6:36982039 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-367G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982039 | |||||||
chr6:36982040 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-368G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982040 | |||||||
chr6:36982042 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-370C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982042 | |||||||
chr6:36982044 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-372A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982044 | |||||||
chr6:36982045 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-373C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982045 | |||||||
chr6:36982052 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-380A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982052 | |||||||
chr6:36982053 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-381A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982053 | |||||||
chr6:36982054 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-382G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982054 | |||||||
chr6:36982056 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-384A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982056 | |||||||
chr6:36982057 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-385A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982057 | |||||||
chr6:36982059 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-387G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982059 | |||||||
chr6:36982063 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-391G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982063 | |||||||
chr6:36982064 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-392A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982064 | |||||||
chr6:36982065 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-393G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982065 | |||||||
chr6:36982068 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-396A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982068 | |||||||
chr6:36982070 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-398G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982070 | |||||||
chr6:36982072 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-400T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982072 | |||||||
chr6:36982073 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-401T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982073 | |||||||
chr6:36982074 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-402T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982074 | |||||||
chr6:36982076 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-404C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982076 | |||||||
chr6:36982078 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-406C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982078 | |||||||
chr6:36982079 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-407C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982079 | |||||||
chr6:36982084 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-412T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982084 | |||||||
chr6:36982085 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-413T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982085 | |||||||
chr6:36982088 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-416T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982088 | |||||||
chr6:36982089 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-417T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982089 | |||||||
chr6:36982093 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-421G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982093 | |||||||
chr6:36982104 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-432T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982104 | |||||||
chr6:36982106 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-434G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982106 | |||||||
chr6:36982107 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-435G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982107 | |||||||
chr6:36982109 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-437G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982109 | |||||||
chr6:36982111 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-439C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982111 | |||||||
chr6:36982114 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-442T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982114 | |||||||
chr6:36982116 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-444C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982116 | |||||||
chr6:36982117 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-445A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982117 | |||||||
chr6:36982118 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-446G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982118 | |||||||
chr6:36982120 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-448C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982120 | |||||||
chr6:36982122 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-450G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982122 | |||||||
chr6:36982125 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-453A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982125 | |||||||
chr6:36982126 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-454T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982126 | |||||||
chr6:36982128 | G | T | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-456C>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982128 | |||||||
chr6:36982129 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-457A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982129 | |||||||
chr6:36982130 | C | G | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-458G>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982130 | |||||||
chr6:36982131 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.322-459T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982131 | |||||||
chr6:36982132 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-460A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982132 | |||||||
chr6:36982133 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-461G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982133 | |||||||
chr6:36982139 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.322-467G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982139 | |||||||
chr6:36982231 | CT | C | 31 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(28): Show |
85 | HG00642.hp1 HG00735.hp1 HG00735.hp2 others(82): Show |
intron_variant | MODIFIER | c.322-560delA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982231 | |||||||
chr6:36982285 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.322-613T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982285 | |||||||
chr6:36982384 | A | AT | 6 | a0001c0001t0001g0080 a0001c0002t0001g0019 a0001c0002t0001g0090 others(3): Show |
10 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-713dupA | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982384 | |||||||
chr6:36982384 | A | T | 8 | a0001c0001t0001g0052 a0001c0001t0001g0093 a0001c0001t0001g0094 others(5): Show |
17 | HG00733.hp2 HG01243.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.322-712T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982384 | |||||||
chr6:36982387 | T | TA | 2 | a0001c0002t0001g0051 a0001c0002t0001g0091 |
3 | HG02970.hp2 HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.322-716_322-715ins others(1): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982387 | |||||||
chr6:36982388 | T | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(30): Show |
80 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.322-716A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982388 | |||||||
chr6:36982391 | T | A | 1 | a0001c0002t0001g0091 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.322-719A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982391 | |||||||
chr6:36982439 | C | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0076 others(5): Show |
11 | HG01255.hp2 HG01261.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.322-767G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982439 | |||||||
chr6:36982548 | C | T | 1 | a0001c0001t0001g0119 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.322-876G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982548 | |||||||
chr6:36982636 | G | A | 11 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0027 others(8): Show |
43 | HG00642.hp1 HG00735.hp2 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.322-964C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982636 | |||||||
chr6:36982709 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.322-1037G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982709 | |||||||
chr6:36982710 | G | A | 2 | a0001c0001t0001g0152 a0001c0002t0001g0151 |
2 | HG02922.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.322-1038C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982710 | |||||||
chr6:36982733 | T | C | 4 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0002g0012 others(1): Show |
10 | HG00733.hp2 HG01243.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-1061A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982733 | |||||||
chr6:36982838 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0025 others(9): Show |
31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.322-1166A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982838 | |||||||
chr6:36982843 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.322-1171G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36982843 | |||||||
chr6:36983003 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0149 a0003c0011t0001g0156 |
6 | HG01069.hp2 HG01496.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-1331C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983003 | |||||||
chr6:36983010 | G | A | 1 | a0001c0001t0002g0064 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.322-1338C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983010 | |||||||
chr6:36983113 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.322-1441A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983113 | |||||||
chr6:36983157 | T | C | 1 | a0001c0001t0001g0034 | 3 | HG03130.hp2 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.322-1485A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983157 | |||||||
chr6:36983208 | A | G | 1 | a0002c0004t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.322-1536T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983208 | |||||||
chr6:36983229 | C | T | 1 | a0001c0002t0001g0090 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.322-1557G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983229 | |||||||
chr6:36983285 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0025 others(9): Show |
31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.322-1613C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983285 | |||||||
chr6:36983356 | T | C | 1 | a0001c0003t0001g0117 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.322-1684A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983356 | |||||||
chr6:36983389 | T | C | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.322-1717A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983389 | |||||||
chr6:36983434 | T | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0025 others(10): Show |
32 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.322-1762A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983434 | |||||||
chr6:36983578 | G | A | 1 | a0001c0001t0008g0088 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.322-1906C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983578 | |||||||
chr6:36983610 | A | G | 2 | a0001c0001t0001g0068 a0001c0001t0002g0067 |
2 | HG01891.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.322-1938T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983610 | |||||||
chr6:36983696 | C | T | 5 | a0001c0002t0001g0019 a0001c0002t0001g0051 a0001c0002t0001g0090 others(2): Show |
10 | HG01943.hp2 HG02015.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-2024G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983696 | |||||||
chr6:36983720 | T | C | 1 | a0001c0002t0001g0051 | 2 | HG03710.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.322-2048A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983720 | |||||||
chr6:36983749 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.322-2077C>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983749 | |||||||
chr6:36983931 | A | T | 12 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0025 others(9): Show |
31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.321+1922T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36983931 | |||||||
chr6:36984056 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0025 others(9): Show |
31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.321+1797T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984056 | |||||||
chr6:36984060 | A | C | 1 | a0001c0001t0001g0047 | 2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.321+1793T>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984060 | |||||||
chr6:36984089 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0026 others(10): Show |
34 | HG00673.hp1 HG00738.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.321+1764G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984089 | |||||||
chr6:36984133 | T | G | 1 | a0001c0002t0001g0118 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.321+1720A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984133 | |||||||
chr6:36984177 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.321+1676G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984177 | |||||||
chr6:36984206 | G | GTCCCACC others(3): Show |
91 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(88): Show |
252 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.321+1646_321+1647i others(12): Show |
MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984206 | |||||||
chr6:36984216 | C | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0025 others(9): Show |
31 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.321+1637G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984216 | |||||||
chr6:36984450 | G | A | 34 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(31): Show |
105 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.321+1403C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984450 | |||||||
chr6:36984518 | G | A | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.321+1335C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984518 | |||||||
chr6:36984566 | A | G | 1 | a0001c0001t0004g0014 | 5 | HG00099.hp2 HG00280.hp1 HG00733.hp1 others(2): Show |
intron_variant | MODIFIER | c.321+1287T>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984566 | |||||||
chr6:36984592 | T | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0136 a0001c0001t0001g0138 others(1): Show |
8 | HG00673.hp2 HG02004.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.321+1261A>C | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984592 | |||||||
chr6:36984643 | C | T | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+1210G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984643 | |||||||
chr6:36984693 | C | T | 3 | a0001c0001t0001g0066 a0001c0002t0001g0040 a0001c0002t0001g0065 |
4 | HG02615.hp2 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+1160G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984693 | |||||||
chr6:36984754 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.321+1099G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36984754 | |||||||
chr6:36985026 | T | C | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.321+827A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985026 | |||||||
chr6:36985255 | C | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0150 a0001c0002t0002g0037 |
6 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+598G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985255 | |||||||
chr6:36985260 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0139 a0001c0002t0002g0140 |
5 | HG01884.hp2 HG02258.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+593C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985260 | |||||||
chr6:36985363 | T | C | 1 | a0001c0001t0002g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.321+490A>G | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985363 | |||||||
chr6:36985454 | C | T | 1 | a0001c0002t0001g0142 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.321+399G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985454 | |||||||
chr6:36985491 | A | T | 7 | a0001c0001t0001g0023 a0001c0001t0001g0061 a0001c0001t0002g0060 others(4): Show |
14 | HG00099.hp1 HG00738.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.321+362T>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985491 | |||||||
chr6:36985566 | C | A | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+287G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985566 | |||||||
chr6:36985615 | G | A | 13 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0025 others(10): Show |
32 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.321+238C>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985615 | |||||||
chr6:36985651 | T | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0150 a0001c0002t0002g0037 |
6 | HG02615.hp1 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+202A>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985651 | |||||||
chr6:36985685 | C | A | 2 | a0001c0001t0001g0152 a0001c0002t0001g0151 |
2 | HG02922.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.321+168G>T | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985685 | |||||||
chr6:36985807 | C | T | 1 | a0001c0001t0001g0010 | 7 | HG01257.hp1 HG01258.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+46G>A | MTCH1 | ENSG00000137409.21 | transcript | ENST00000373627.10 | protein_coding | 1/11 | chr6 | 36985807 |