Item | Value |
---|---|
geneid | 28969 |
ensemblid | ENSG00000136261.16 |
hgncid | 18808 |
symbol | BZW2 |
name | basic leucine zipper and W2 domains 2 |
refseq_nuc | NM_014038.3 |
refseq_prot | NP_054757.1 |
ensembl_nuc | ENST00000258761.8 |
ensembl_prot | ENSP00000258761.3 |
mane_status | MANE Select |
chr | chr7 |
start | 16646181 |
end | 16706517 |
strand | + |
ver | v1.2 |
region | chr7:16646181-16706517 |
region5000 | chr7:16641181-16711517 |
regionname0 | BZW2_chr7_16646181_16706517 |
regionname5000 | BZW2_chr7_16641181_16711517 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1257 | 407 | 91 | 72 | 179 | 18 | 45 | BZW2_chr7_16641181_16711517 | BZW2 | ATGAA others(1252): Show |
chr7 | 16641181 | 16711517 | ||
a0001c0002 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ATGAA others(1252): Show |
chr7 | 16641181 | 16711517 | ||
a0001c0003 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ATGAA others(1252): Show |
chr7 | 16641181 | 16711517 | ||
a0001c0004 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ATGAA others(1252): Show |
chr7 | 16641181 | 16711517 | ||
a0001c0005 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | ATGAA others(1252): Show |
chr7 | 16641181 | 16711517 | ||
a0001c0006 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ATGAA others(1252): Show |
chr7 | 16641181 | 16711517 | ||
a0001c0007 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ATGAA others(1252): Show |
chr7 | 16641181 | 16711517 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 1804 | 203 | 23 | 33 | 115 | 8 | 23 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0002 | 0/1 | 1804 | 176 | 45 | 35 | 63 | 10 | 22 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0003 | 0/0 | 1807 | 10 | 7 | 3 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1802): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0004 | 0/0 | 1804 | 6 | 6 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0005 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0006 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0007 | 0/0 | 1804 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0008 | 0/0 | 1804 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0009 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0010 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0001t0011 | 0/0 | 1804 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | AGTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0002t0002 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0002t0003 | 0/0 | 1807 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1802): Show |
chr7 | 16641181 | 16711517 |
a0001c0003t0002 | 0/0 | 1804 | 3 | 3 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0004t0002 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0005t0001 | 0/0 | 1804 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0006t0002 | 0/0 | 1804 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
a0001c0007t0002 | 0/0 | 1804 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | ACTCC others(1799): Show |
chr7 | 16641181 | 16711517 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0395 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0001g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0040 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0355 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0382 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0396 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0002g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0006g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0007g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0008g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0009g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0010g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0001t0011g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0003t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0003t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0003t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0004t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0006t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
a0001c0007t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0355 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0396 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0232 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0371 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0382 | EUR | FIN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0392 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0394 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0369 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0380 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0351 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0317 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0340 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0286 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0275 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0357 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0367 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0373 | AMR | PUR | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0370 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0391 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0087 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0379 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0304 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0376 | EUR | IBS | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0323 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0356 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0307 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0363 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02055 | hp1 | a0001 | c0007 | t0002 | g0336 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0365 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0311 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0386 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0378 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0388 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0348 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0338 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0341 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0152 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0313 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0301 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0337 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0364 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0112 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0387 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0306 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0010 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0374 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0095 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0324 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03130 | hp2 | a0001 | c0002 | t0002 | g0293 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0290 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03209 | hp2 | a0001 | c0003 | t0002 | g0295 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0400 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03225 | hp2 | a0001 | c0001 | t0010 | g0399 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0298 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0360 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0366 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0361 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ESN | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | GWD | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0305 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0362 | SAS | PJL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0383 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04204 | hp2 | a0001 | c0005 | t0001 | g0028 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18522 | hp2 | a0001 | c0002 | t0002 | g0322 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | CHB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18906 | hp1 | a0001 | c0002 | t0003 | g0281 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0381 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18943 | hp2 | a0001 | c0001 | t0011 | g0312 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18951 | hp1 | a0001 | c0006 | t0002 | g0057 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0384 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0393 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0372 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0389 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0401 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0349 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0377 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0390 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0352 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0397 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19030 | hp2 | a0001 | c0004 | t0002 | g0299 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19043 | hp1 | a0001 | c0001 | t0006 | g0067 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0385 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0359 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0375 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0314 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | YRI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0094 | AFR | ASW | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0368 | AFR | ASW | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0224 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0350 | EUR | TSI | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | GIH | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0068 | SAS | GIH | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0398 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0327 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ACB | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
HG06807 | hp2 | a0001 | c0003 | t0002 | g0321 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | USA | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0320 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0040 | REF | REF | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0395 | REF | REF | BZW2_chr7_16641181_16711517 | BZW2 | chr7 | 16641181 | 16711517 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16674434 | C | G | 1 | a0001c0007 | 1 | HG02055.hp1 | synonymous_variant | LOW | c.81C>G | p.Pro27Pro | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/12 | 196/1804 | 81/1260 | 27/419 | chr7 | 16674434 | |||
chr7:16689843 | A | G | 1 | a0001c0006 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.588A>G | p.Ala196Ala | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/12 | 703/1804 | 588/1260 | 196/419 | chr7 | 16689843 | |||
chr7:16694842 | T | C | 2 | a0001c0003 a0001c0004 |
4 | HG02622.hp2 HG03209.hp2 HG06807.hp2 others(1): Show |
synonymous_variant | LOW | c.660T>C | p.Phe220Phe | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/12 | 775/1804 | 660/1260 | 220/419 | chr7 | 16694842 | |||
chr7:16694995 | G | A | 1 | a0001c0005 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.813G>A | p.Pro271Pro | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/12 | 928/1804 | 813/1260 | 271/419 | chr7 | 16694995 | |||
chr7:16706070 | G | A | 2 | a0001c0002 a0001c0004 |
5 | HG01884.hp2 HG03130.hp2 NA18522.hp2 others(2): Show |
synonymous_variant | LOW | c.1242G>A | p.Ser414Ser | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 1357/1804 | 1242/1260 | 414/419 | chr7 | 16706070 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16646182 | C | G | 1 | a0001c0001t0011 | 1 | NA18943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-114C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19262 | chr7 | 16646182 | ||||||
chr7:16646202 | A | ACTG | 2 | a0001c0001t0003 a0001c0002t0003 |
11 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-74_-72dupTGC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19219 | INFO_REALIGN_3_PRIME | chr7 | 16646202 | |||||
chr7:16646210 | T | C | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0008 |
9 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-86T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19234 | chr7 | 16646210 | ||||||
chr7:16646245 | C | T | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0006 others(8): Show |
196 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(193): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/12 | 19199 | chr7 | 16646245 | ||||||
chr7:16706091 | G | T | 3 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 |
7 | HG01081.hp2 HG02451.hp2 HG02896.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 3 | chr7 | 16706091 | ||||||
chr7:16706182 | C | T | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*94C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 94 | chr7 | 16706182 | ||||||
chr7:16706311 | A | G | 1 | a0001c0001t0010 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*223A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 12/12 | 223 | chr7 | 16706311 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:16646335 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-8+47G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646335 | |||||||
chr7:16646369 | G | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
25 | HG01069.hp2 HG01257.hp2 HG01433.hp2 others(22): Show |
intron_variant | MODIFIER | c.-8+81G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646369 | |||||||
chr7:16646438 | C | T | 1 | a0001c0001t0001g0401 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8+150C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646438 | |||||||
chr7:16646502 | C | A | 1 | a0001c0001t0002g0039 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-8+214C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646502 | |||||||
chr7:16646554 | G | A | 51 | a0001c0001t0002g0004 a0001c0001t0002g0039 a0001c0001t0002g0041 others(48): Show |
52 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.-8+266G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646554 | |||||||
chr7:16646584 | C | T | 1 | a0001c0001t0001g0401 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8+296C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646584 | |||||||
chr7:16646635 | G | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0091 |
2 | NA18949.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-8+347G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646635 | |||||||
chr7:16646673 | G | T | 2 | a0001c0001t0002g0400 a0001c0001t0010g0399 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-8+385G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646673 | |||||||
chr7:16646847 | C | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0398 |
3 | HG01123.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-8+559C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646847 | |||||||
chr7:16646876 | T | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(265): Show |
273 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-8+588T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16646876 | |||||||
chr7:16647041 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8+753A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647041 | |||||||
chr7:16647048 | C | G | 15 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(12): Show |
15 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-8+760C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647048 | |||||||
chr7:16647200 | G | A | 1 | a0001c0001t0002g0286 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-8+912G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647200 | |||||||
chr7:16647315 | G | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(283): Show |
303 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.-8+1027G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647315 | |||||||
chr7:16647544 | A | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(284): Show |
304 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(301): Show |
intron_variant | MODIFIER | c.-8+1256A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647544 | |||||||
chr7:16647629 | G | C | 1 | a0001c0001t0001g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+1341G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647629 | |||||||
chr7:16647747 | G | A | 1 | a0001c0001t0007g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+1459G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647747 | |||||||
chr7:16647833 | A | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG01069.hp2 HG01257.hp2 HG01433.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8+1545A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647833 | |||||||
chr7:16647917 | C | T | 23 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0070 others(20): Show |
23 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.-8+1629C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647917 | |||||||
chr7:16647917 | CACTGGGG others(4): Show |
C | 12 | a0001c0001t0001g0007 a0001c0001t0002g0001 a0001c0001t0002g0002 others(9): Show |
19 | HG00423.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+1630_-8+1640del others(11): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647917 | |||||||
chr7:16647929 | C | G | 12 | a0001c0001t0001g0007 a0001c0001t0002g0001 a0001c0001t0002g0002 others(9): Show |
19 | HG00423.hp1 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+1641C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647929 | |||||||
chr7:16647952 | A | G | 2 | a0001c0001t0002g0386 a0001c0001t0002g0387 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-8+1664A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16647952 | |||||||
chr7:16648494 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-8+2206A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648494 | |||||||
chr7:16648521 | C | A | 17 | a0001c0001t0002g0015 a0001c0001t0002g0287 a0001c0001t0002g0288 others(14): Show |
17 | HG02559.hp2 HG02622.hp1 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+2233C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648521 | |||||||
chr7:16648601 | T | G | 1 | a0001c0001t0001g0163 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-8+2313T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648601 | |||||||
chr7:16648641 | T | G | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-8+2353T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648641 | |||||||
chr7:16648685 | C | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-8+2397C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16648685 | |||||||
chr7:16649162 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-8+2874G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649162 | |||||||
chr7:16649176 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-8+2888T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649176 | |||||||
chr7:16649204 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-8+2916A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649204 | |||||||
chr7:16649486 | T | C | 1 | a0001c0001t0001g0401 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-8+3198T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649486 | |||||||
chr7:16649578 | C | T | 1 | a0001c0001t0002g0385 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-8+3290C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649578 | |||||||
chr7:16649962 | A | G | 1 | a0001c0001t0002g0089 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-8+3674A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649962 | |||||||
chr7:16649963 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+3675T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16649963 | |||||||
chr7:16650002 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-8+3714C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650002 | |||||||
chr7:16650032 | T | G | 10 | a0001c0001t0002g0286 a0001c0001t0002g0302 a0001c0001t0002g0303 others(7): Show |
10 | HG01167.hp1 HG01516.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8+3744T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650032 | |||||||
chr7:16650043 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-8+3755T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650043 | |||||||
chr7:16650183 | T | G | 2 | a0001c0001t0002g0400 a0001c0001t0010g0399 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-8+3895T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650183 | |||||||
chr7:16650327 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0098 |
3 | HG00609.hp1 NA18968.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.-8+4039G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650327 | |||||||
chr7:16650474 | G | T | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+4186G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650474 | |||||||
chr7:16650554 | T | G | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+4266T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650554 | |||||||
chr7:16650591 | C | G | 277 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(274): Show |
294 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.-8+4303C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650591 | |||||||
chr7:16650656 | T | A | 13 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+4368T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650656 | |||||||
chr7:16650732 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0002g0088 |
2 | HG01175.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.-8+4444C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650732 | |||||||
chr7:16650822 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-8+4534C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650822 | |||||||
chr7:16650907 | G | A | 1 | a0001c0001t0002g0311 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-8+4619G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650907 | |||||||
chr7:16650980 | C | A | 6 | a0001c0001t0001g0273 a0001c0001t0003g0270 a0001c0001t0003g0271 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+4692C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16650980 | |||||||
chr7:16651091 | A | G | 1 | a0001c0001t0002g0300 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-8+4803A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651091 | |||||||
chr7:16651179 | T | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(55): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8+4891T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651179 | |||||||
chr7:16651398 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0002g0149 a0001c0001t0002g0150 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+5110T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651398 | |||||||
chr7:16651619 | A | C | 52 | a0001c0001t0001g0148 a0001c0001t0002g0004 a0001c0001t0002g0039 others(49): Show |
53 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-8+5331A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651619 | |||||||
chr7:16651696 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-8+5408G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651696 | |||||||
chr7:16651781 | C | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG02572.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-8+5493C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651781 | |||||||
chr7:16651886 | C | T | 73 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(70): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.-8+5598C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651886 | |||||||
chr7:16651887 | G | A | 13 | a0001c0001t0002g0015 a0001c0001t0002g0287 a0001c0001t0002g0288 others(10): Show |
13 | HG02559.hp2 HG02622.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.-8+5599G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16651887 | |||||||
chr7:16652306 | G | A | 6 | a0001c0001t0004g0008 a0001c0001t0004g0314 a0001c0001t0004g0315 others(3): Show |
7 | HG01081.hp2 HG01891.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+6018G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652306 | |||||||
chr7:16652359 | C | CTTGTTCT others(6): Show |
1 | a0001c0001t0002g0012 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-8+6076_-8+6088dup others(13): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16652359 | ||||||
chr7:16652457 | T | C | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-8+6169T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652457 | |||||||
chr7:16652505 | TTC | T | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG00738.hp2 HG02258.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-8+6221_-8+6222del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16652505 | ||||||
chr7:16652538 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-8+6250C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652538 | |||||||
chr7:16652539 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG00597.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.-8+6251G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652539 | |||||||
chr7:16652631 | T | A | 1 | a0001c0001t0007g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+6343T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652631 | |||||||
chr7:16652649 | C | T | 1 | a0001c0001t0002g0384 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-8+6361C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652649 | |||||||
chr7:16652772 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-8+6484G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652772 | |||||||
chr7:16652800 | C | T | 128 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(125): Show |
141 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-8+6512C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652800 | |||||||
chr7:16652986 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-8+6698C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16652986 | |||||||
chr7:16653001 | A | G | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(55): Show |
60 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.-8+6713A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653001 | |||||||
chr7:16653034 | TTG | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(208): Show |
226 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.-8+6768_-8+6769del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16653034 | ||||||
chr7:16653429 | T | A | 1 | a0001c0001t0002g0290 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8+7141T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653429 | |||||||
chr7:16653497 | G | C | 183 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0037 others(180): Show |
197 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.-8+7209G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653497 | |||||||
chr7:16653507 | A | G | 286 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(283): Show |
303 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(300): Show |
intron_variant | MODIFIER | c.-8+7219A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653507 | |||||||
chr7:16653763 | T | C | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0278 others(3): Show |
6 | HG01074.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+7475T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653763 | |||||||
chr7:16653797 | C | G | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0278 others(3): Show |
6 | HG01074.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+7509C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653797 | |||||||
chr7:16653891 | T | G | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0269 |
3 | HG02165.hp2 HG03195.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-8+7603T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16653891 | |||||||
chr7:16654078 | C | A | 6 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
6 | HG02004.hp1 HG02109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+7790C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654078 | |||||||
chr7:16654083 | CA | C | 77 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0105 others(74): Show |
77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.-8+7823delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | ||||||
chr7:16654083 | CAAAA | C | 35 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0022 others(32): Show |
35 | HG01106.hp1 HG01167.hp1 HG01952.hp2 others(32): Show |
intron_variant | MODIFIER | c.-8+7820_-8+7823del others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | ||||||
chr7:16654083 | CAAAAA | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0016 others(159): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.-8+7819_-8+7823del others(5): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | ||||||
chr7:16654083 | CAAAAAA | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(68): Show |
74 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.-8+7818_-8+7823del others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654083 | ||||||
chr7:16654341 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0002g0149 a0001c0001t0002g0150 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+8053T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654341 | |||||||
chr7:16654352 | T | C | 1 | a0001c0001t0002g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-8+8064T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654352 | |||||||
chr7:16654435 | T | C | 1 | a0001c0001t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-8+8147T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654435 | |||||||
chr7:16654473 | A | G | 55 | a0001c0001t0001g0016 a0001c0001t0002g0004 a0001c0001t0002g0039 others(52): Show |
56 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-8+8185A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654473 | |||||||
chr7:16654509 | A | AC | 54 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0033 others(51): Show |
55 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.-8+8233dupC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654509 | ||||||
chr7:16654509 | AC | A | 73 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(70): Show |
74 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-8+8233delC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654509 | ||||||
chr7:16654509 | ACC | A | 112 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(109): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-8+8232_-8+8233del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654509 | ||||||
chr7:16654520 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0401 |
2 | HG02523.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.-8+8232C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654520 | |||||||
chr7:16654521 | C | A | 9 | a0001c0001t0001g0240 a0001c0001t0002g0052 a0001c0001t0002g0053 others(6): Show |
9 | HG01515.hp2 HG02717.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.-8+8233C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654521 | |||||||
chr7:16654521 | C | CA | 6 | a0001c0001t0001g0101 a0001c0001t0001g0183 a0001c0001t0001g0189 others(3): Show |
6 | HG00609.hp2 HG00735.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8+8242dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654521 | ||||||
chr7:16654522 | A | C | 6 | a0001c0001t0001g0199 a0001c0001t0001g0224 a0001c0001t0003g0278 others(3): Show |
6 | HG02896.hp1 HG02897.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.-8+8234A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654522 | |||||||
chr7:16654557 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-8+8269C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654557 | |||||||
chr7:16654594 | G | A | 1 | a0001c0001t0002g0342 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-8+8306G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654594 | |||||||
chr7:16654680 | G | A | 1 | a0001c0001t0002g0054 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-8+8392G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654680 | |||||||
chr7:16654704 | G | GT | 25 | a0001c0001t0001g0092 a0001c0001t0001g0126 a0001c0001t0001g0147 others(22): Show |
25 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8+8430dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654704 | ||||||
chr7:16654704 | GT | G | 117 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0102 others(114): Show |
117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.-8+8430delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16654704 | ||||||
chr7:16654745 | C | G | 1 | a0001c0005t0001g0028 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-8+8457C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654745 | |||||||
chr7:16654801 | A | G | 2 | a0001c0001t0002g0392 a0001c0001t0002g0393 |
2 | HG00423.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.-8+8513A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654801 | |||||||
chr7:16654864 | G | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(49): Show |
54 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-8+8576G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654864 | |||||||
chr7:16654868 | A | G | 1 | a0001c0001t0002g0375 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-8+8580A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16654868 | |||||||
chr7:16655160 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18986.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-8+8872A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655160 | |||||||
chr7:16655197 | A | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0276 others(16): Show |
19 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.-8+8909A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655197 | |||||||
chr7:16655242 | A | T | 17 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0273 others(14): Show |
17 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-8+8954A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655242 | |||||||
chr7:16655416 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-8+9128A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655416 | |||||||
chr7:16655542 | C | T | 1 | a0001c0001t0007g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+9254C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655542 | |||||||
chr7:16655594 | A | G | 13 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-8+9306A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655594 | |||||||
chr7:16655686 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-8+9398C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655686 | |||||||
chr7:16655694 | C | T | 2 | a0001c0001t0002g0386 a0001c0001t0002g0387 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-8+9406C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655694 | |||||||
chr7:16655788 | G | A | 3 | a0001c0001t0002g0337 a0001c0001t0002g0338 a0001c0007t0002g0336 |
3 | HG02055.hp1 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-8+9500G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655788 | |||||||
chr7:16655790 | G | A | 1 | a0001c0001t0007g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-8+9502G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655790 | |||||||
chr7:16655832 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-8+9544T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655832 | |||||||
chr7:16655861 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(76): Show |
81 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.-8+9573G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16655861 | |||||||
chr7:16655994 | CA | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(18): Show |
22 | HG01069.hp2 HG01257.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-9434delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16655994 | ||||||
chr7:16656063 | G | A | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(53): Show |
58 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-7-9374G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656063 | |||||||
chr7:16656081 | A | ATG | 20 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(17): Show |
21 | HG01069.hp2 HG01257.hp2 HG01516.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7-9342_-7-9341dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656081 | ||||||
chr7:16656133 | A | T | 1 | a0001c0001t0001g0256 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-7-9304A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656133 | |||||||
chr7:16656137 | C | CTATATAT others(7): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-9299_-7-9286dup others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | ||||||
chr7:16656137 | C | CTATATAT others(13): Show |
3 | a0001c0001t0003g0270 a0001c0001t0003g0271 a0001c0001t0003g0272 |
3 | HG01255.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(20): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | ||||||
chr7:16656137 | C | CTATATAT others(15): Show |
6 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
6 | HG01074.hp2 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(22): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | ||||||
chr7:16656137 | C | CTATATAT others(19): Show |
1 | a0001c0002t0003g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(26): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | ||||||
chr7:16656137 | C | CTATATAT others(21): Show |
2 | a0001c0001t0003g0274 a0001c0001t0003g0275 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(28): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | ||||||
chr7:16656137 | C | CTATATAT others(23): Show |
1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(30): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656137 | ||||||
chr7:16656143 | A | G | 14 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0036 others(11): Show |
14 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-9294A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656143 | |||||||
chr7:16656150 | T | TATAC | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(53): Show |
58 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | ||||||
chr7:16656150 | T | TATATATA others(13): Show |
1 | a0001c0001t0001g0157 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(20): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | ||||||
chr7:16656150 | T | TATATATA others(17): Show |
2 | a0001c0001t0007g0093 a0001c0001t0009g0112 |
2 | HG02717.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(24): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | ||||||
chr7:16656150 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(26): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | ||||||
chr7:16656150 | T | TATATATA others(23): Show |
1 | a0001c0001t0005g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(30): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | ||||||
chr7:16656150 | T | TATATATA others(25): Show |
2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02004.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(32): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | ||||||
chr7:16656150 | T | TATATATA others(29): Show |
1 | a0001c0001t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-7-9286_-7-9285ins others(36): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656150 | ||||||
chr7:16656190 | ATG | A | 13 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-9243_-7-9242del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656190 | ||||||
chr7:16656267 | A | G | 13 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-9170A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656267 | |||||||
chr7:16656317 | A | C | 1 | a0001c0001t0002g0064 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-7-9120A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656317 | |||||||
chr7:16656506 | G | A | 2 | a0001c0001t0003g0274 a0001c0001t0003g0275 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-7-8931G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656506 | |||||||
chr7:16656544 | A | AGC | 8 | a0001c0001t0002g0011 a0001c0001t0002g0035 a0001c0001t0002g0036 others(5): Show |
9 | HG01109.hp1 HG02895.hp1 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-8882_-7-8881dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656544 | ||||||
chr7:16656544 | AGC | A | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG02129.hp2 NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.-7-8882_-7-8881del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656544 | ||||||
chr7:16656548 | C | T | 1 | a0001c0001t0002g0373 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-7-8889C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656548 | |||||||
chr7:16656551 | GCGCGCA | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0198 a0001c0001t0001g0208 |
3 | HG02004.hp2 HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-7-8884_-7-8879del others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656551 | ||||||
chr7:16656552 | C | T | 1 | a0001c0001t0002g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-8885C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656552 | |||||||
chr7:16656553 | G | A | 2 | a0001c0001t0001g0180 a0001c0001t0001g0210 |
2 | HG01978.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.-7-8884G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656553 | |||||||
chr7:16656553 | GCGCACAC others(7): Show |
G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0113 a0001c0001t0001g0115 others(6): Show |
9 | HG00597.hp2 HG00738.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-8882_-7-8869del others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656553 | ||||||
chr7:16656553 | GCGCACAC others(9): Show |
G | 43 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(40): Show |
44 | HG00438.hp1 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-7-8882_-7-8867del others(16): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656553 | ||||||
chr7:16656554 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-7-8883C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656554 | |||||||
chr7:16656555 | G | A | 6 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
6 | HG02895.hp2 HG02897.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-8882G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656555 | |||||||
chr7:16656555 | G | GCA | 19 | a0001c0001t0001g0020 a0001c0001t0001g0165 a0001c0001t0001g0166 others(16): Show |
20 | HG01070.hp2 HG01071.hp2 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-8841_-7-8840dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | G | GCACA | 5 | a0001c0001t0002g0289 a0001c0001t0002g0342 a0001c0001t0002g0345 others(2): Show |
5 | HG00741.hp2 HG02056.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-8843_-7-8840dup others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | G | GCACACA | 5 | a0001c0001t0002g0015 a0001c0001t0002g0291 a0001c0001t0002g0297 others(2): Show |
5 | HG02622.hp1 HG02622.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-8845_-7-8840dup others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | G | GCACACAC others(1): Show |
6 | a0001c0001t0002g0287 a0001c0001t0002g0290 a0001c0001t0002g0292 others(3): Show |
6 | HG02886.hp2 HG02970.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-7-8847_-7-8840dup others(8): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | G | GCACACAC others(3): Show |
3 | a0001c0001t0002g0288 a0001c0003t0002g0295 a0001c0004t0002g0299 |
3 | HG03209.hp2 NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-7-8849_-7-8840dup others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | G | GCACACAC others(5): Show |
2 | a0001c0001t0002g0296 a0001c0001t0002g0298 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-7-8851_-7-8840dup others(12): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | GCA | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0022 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.-7-8841_-7-8840del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | GCACA | G | 40 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0204 others(37): Show |
40 | HG00597.hp1 HG01106.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.-7-8843_-7-8840del others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | GCACACA | G | 8 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0261 others(5): Show |
9 | HG01496.hp2 HG02572.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-8845_-7-8840del others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656555 | GCACACAC others(9): Show |
G | 1 | a0001c0001t0001g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-7-8855_-7-8840del others(16): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16656555 | ||||||
chr7:16656557 | A | G | 13 | a0001c0001t0001g0187 a0001c0001t0001g0244 a0001c0001t0001g0263 others(10): Show |
13 | HG01884.hp2 HG01975.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.-7-8880A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656557 | |||||||
chr7:16656559 | A | G | 17 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0254 others(14): Show |
20 | HG00280.hp2 HG00558.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.-7-8878A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656559 | |||||||
chr7:16656561 | A | G | 14 | a0001c0001t0001g0171 a0001c0001t0001g0198 a0001c0001t0001g0205 others(11): Show |
15 | HG01081.hp2 HG01891.hp1 HG02004.hp2 others(12): Show |
intron_variant | MODIFIER | c.-7-8876A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656561 | |||||||
chr7:16656563 | A | G | 3 | a0001c0001t0002g0332 a0001c0001t0002g0400 a0001c0001t0010g0399 |
3 | HG03139.hp2 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-8874A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656563 | |||||||
chr7:16656922 | A | C | 1 | a0001c0001t0002g0398 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-7-8515A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16656922 | |||||||
chr7:16657222 | A | T | 1 | a0001c0001t0001g0251 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-7-8215A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657222 | |||||||
chr7:16657223 | G | T | 1 | a0001c0001t0001g0251 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-7-8214G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657223 | |||||||
chr7:16657477 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-7-7960A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657477 | |||||||
chr7:16657486 | C | T | 2 | a0001c0001t0003g0279 a0001c0001t0003g0280 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-7-7951C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657486 | |||||||
chr7:16657691 | T | C | 14 | a0001c0001t0001g0209 a0001c0001t0001g0273 a0001c0001t0001g0276 others(11): Show |
14 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-7746T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657691 | |||||||
chr7:16657710 | A | G | 372 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(369): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.-7-7727A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657710 | |||||||
chr7:16657805 | A | C | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0250 |
3 | HG00423.hp2 NA19084.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-7-7632A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657805 | |||||||
chr7:16657811 | C | T | 3 | a0001c0001t0001g0171 a0001c0001t0001g0198 a0001c0001t0001g0208 |
3 | HG02004.hp2 HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.-7-7626C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657811 | |||||||
chr7:16657813 | C | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(65): Show |
70 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-7-7624C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16657813 | |||||||
chr7:16658084 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0002g0319 a0001c0001t0009g0112 |
3 | HG02647.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-7353A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658084 | |||||||
chr7:16658196 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-7-7241G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658196 | |||||||
chr7:16658356 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-7-7081T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658356 | |||||||
chr7:16658409 | C | A | 1 | a0001c0001t0002g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-7-7028C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658409 | |||||||
chr7:16658642 | C | A | 187 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0037 others(184): Show |
201 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.-7-6795C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658642 | |||||||
chr7:16658692 | T | C | 19 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0036 others(16): Show |
19 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.-7-6745T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658692 | |||||||
chr7:16658883 | G | GTA | 4 | a0001c0001t0001g0175 a0001c0001t0001g0401 a0001c0001t0002g0289 others(1): Show |
4 | HG02523.hp2 HG02886.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-7-6538_-7-6537dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16658883 | ||||||
chr7:16658883 | GTA | G | 69 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(66): Show |
71 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-7-6538_-7-6537del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16658883 | ||||||
chr7:16658934 | T | G | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-7-6503T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16658934 | |||||||
chr7:16659026 | C | T | 1 | a0001c0001t0002g0052 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-7-6411C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659026 | |||||||
chr7:16659083 | G | A | 1 | a0001c0001t0002g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-7-6354G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659083 | |||||||
chr7:16659193 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-7-6244T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659193 | |||||||
chr7:16659223 | A | T | 3 | a0001c0001t0002g0302 a0001c0001t0002g0303 a0001c0001t0002g0304 |
3 | HG01516.hp2 HG04115.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-7-6214A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659223 | |||||||
chr7:16659288 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-7-6149G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659288 | |||||||
chr7:16659838 | G | T | 1 | a0001c0001t0001g0264 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-7-5599G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659838 | |||||||
chr7:16659852 | A | AT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0002g0149 others(3): Show |
6 | HG02055.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-5574dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16659852 | ||||||
chr7:16659852 | AT | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(50): Show |
55 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-7-5574delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16659852 | ||||||
chr7:16659857 | T | A | 15 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0276 others(12): Show |
15 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-7-5580T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659857 | |||||||
chr7:16659858 | T | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(71): Show |
75 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.-7-5579T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659858 | |||||||
chr7:16659888 | A | C | 16 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0273 others(13): Show |
16 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-7-5549A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659888 | |||||||
chr7:16659958 | G | A | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0128 |
3 | HG00438.hp1 NA19060.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-7-5479G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659958 | |||||||
chr7:16659972 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-5465G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16659972 | |||||||
chr7:16660006 | C | T | 1 | a0001c0001t0002g0286 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-7-5431C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660006 | |||||||
chr7:16660008 | C | T | 12 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0270 others(9): Show |
12 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-5429C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660008 | |||||||
chr7:16660010 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-7-5427C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660010 | |||||||
chr7:16660036 | C | A | 282 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(279): Show |
299 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(296): Show |
intron_variant | MODIFIER | c.-7-5401C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660036 | |||||||
chr7:16660113 | G | A | 12 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0003g0270 others(9): Show |
12 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7-5324G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660113 | |||||||
chr7:16660130 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-7-5307G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660130 | |||||||
chr7:16660171 | T | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18939.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-7-5266T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660171 | |||||||
chr7:16660229 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-7-5208A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660229 | |||||||
chr7:16660249 | T | C | 69 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(66): Show |
71 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-7-5188T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660249 | |||||||
chr7:16660260 | A | G | 48 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(45): Show |
50 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-7-5177A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660260 | |||||||
chr7:16660352 | A | T | 143 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0037 others(140): Show |
156 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-7-5085A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660352 | |||||||
chr7:16660400 | T | TA | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(123): Show |
129 | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.-7-5020dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16660400 | ||||||
chr7:16660400 | T | TAA | 10 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0030 others(7): Show |
11 | HG01069.hp2 HG01257.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.-7-5021_-7-5020dup others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16660400 | ||||||
chr7:16660400 | TA | T | 8 | a0001c0001t0001g0099 a0001c0001t0001g0248 a0001c0001t0002g0310 others(5): Show |
8 | HG00621.hp1 HG02698.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-5020delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16660400 | ||||||
chr7:16660401 | A | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0249 a0001c0001t0007g0301 |
3 | HG02630.hp1 HG04228.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-7-5036A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660401 | |||||||
chr7:16660430 | C | T | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7-5007C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660430 | |||||||
chr7:16660485 | T | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(69): Show |
74 | HG00544.hp1 HG00544.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-7-4952T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660485 | |||||||
chr7:16660529 | G | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-4908G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660529 | |||||||
chr7:16660543 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-7-4894G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660543 | |||||||
chr7:16660736 | C | T | 3 | a0001c0001t0001g0115 a0001c0001t0002g0319 a0001c0001t0009g0112 |
3 | HG02647.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-4701C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660736 | |||||||
chr7:16660741 | C | G | 9 | a0001c0001t0001g0016 a0001c0001t0002g0149 a0001c0001t0002g0150 others(6): Show |
9 | HG02055.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.-7-4696C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660741 | |||||||
chr7:16660812 | A | G | 14 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0036 others(11): Show |
14 | HG01109.hp1 HG01884.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-7-4625A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660812 | |||||||
chr7:16660822 | A | G | 78 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0037 others(75): Show |
89 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.-7-4615A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660822 | |||||||
chr7:16660870 | G | A | 220 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(217): Show |
233 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.-7-4567G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660870 | |||||||
chr7:16660928 | C | T | 222 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(219): Show |
235 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.-7-4509C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16660928 | |||||||
chr7:16661023 | C | A | 203 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(200): Show |
216 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.-7-4414C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661023 | |||||||
chr7:16661109 | A | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0367 a0001c0001t0002g0368 others(1): Show |
5 | HG01243.hp1 HG02486.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7-4328A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661109 | |||||||
chr7:16661131 | C | T | 1 | a0001c0001t0002g0338 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-7-4306C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661131 | |||||||
chr7:16661132 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.-7-4305G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661132 | |||||||
chr7:16661173 | G | A | 202 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(199): Show |
215 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.-7-4264G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661173 | |||||||
chr7:16661260 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0145 |
2 | NA18962.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-7-4177C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661260 | |||||||
chr7:16661377 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0002g0319 |
2 | HG02647.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-7-4060A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661377 | |||||||
chr7:16661481 | G | A | 5 | a0001c0001t0002g0337 a0001c0001t0002g0338 a0001c0001t0002g0386 others(2): Show |
5 | HG02055.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-3956G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661481 | |||||||
chr7:16661520 | C | A | 2 | a0001c0001t0002g0400 a0001c0001t0010g0399 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-3917C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661520 | |||||||
chr7:16661711 | A | G | 2 | a0001c0001t0002g0335 a0001c0003t0002g0321 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-7-3726A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661711 | |||||||
chr7:16661941 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7-3496T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661941 | |||||||
chr7:16661968 | G | C | 2 | a0001c0001t0002g0400 a0001c0001t0010g0399 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-3469G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16661968 | |||||||
chr7:16662043 | T | C | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7-3394T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662043 | |||||||
chr7:16662091 | T | C | 273 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
288 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.-7-3346T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662091 | |||||||
chr7:16662179 | C | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-7-3258C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662179 | |||||||
chr7:16662364 | T | C | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-7-3073T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662364 | |||||||
chr7:16662482 | G | C | 205 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(202): Show |
218 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.-7-2955G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662482 | |||||||
chr7:16662496 | A | G | 1 | a0001c0001t0002g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-7-2941A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662496 | |||||||
chr7:16662674 | C | T | 67 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(64): Show |
77 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.-7-2763C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662674 | |||||||
chr7:16662719 | T | C | 3 | a0001c0001t0002g0346 a0001c0001t0002g0347 a0001c0001t0002g0381 |
3 | NA18747.hp2 NA18942.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-7-2718T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662719 | |||||||
chr7:16662774 | A | AAAGG | 4 | a0001c0001t0002g0324 a0001c0001t0002g0327 a0001c0002t0002g0322 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-2649_-7-2646dup others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16662774 | ||||||
chr7:16662814 | G | A | 2 | a0001c0001t0002g0348 a0001c0001t0002g0382 |
2 | HG00323.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-7-2623G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662814 | |||||||
chr7:16662840 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-7-2597G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16662840 | |||||||
chr7:16663005 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-2432A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663005 | |||||||
chr7:16663054 | C | T | 1 | a0001c0001t0007g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-7-2383C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663054 | |||||||
chr7:16663136 | C | A | 200 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(197): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.-7-2301C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663136 | |||||||
chr7:16663179 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-7-2258A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663179 | |||||||
chr7:16663190 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-2247T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663190 | |||||||
chr7:16663231 | A | G | 1 | a0001c0001t0002g0347 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-7-2206A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663231 | |||||||
chr7:16663242 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(73): Show |
87 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.-7-2195C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663242 | |||||||
chr7:16663253 | CTG | C | 9 | a0001c0001t0001g0097 a0001c0001t0002g0074 a0001c0001t0002g0075 others(6): Show |
9 | HG00544.hp2 HG00558.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7-2180_-7-2179del others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16663253 | ||||||
chr7:16663298 | G | C | 1 | a0001c0001t0001g0131 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-7-2139G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663298 | |||||||
chr7:16663327 | A | G | 2 | a0001c0001t0002g0400 a0001c0001t0010g0399 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-7-2110A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663327 | |||||||
chr7:16663332 | A | G | 3 | a0001c0001t0001g0115 a0001c0001t0002g0319 a0001c0001t0009g0112 |
3 | HG02647.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-7-2105A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663332 | |||||||
chr7:16663468 | C | T | 200 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(197): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.-7-1969C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663468 | |||||||
chr7:16663477 | T | A | 201 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(198): Show |
214 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-7-1960T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663477 | |||||||
chr7:16663492 | C | A | 200 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(197): Show |
213 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(210): Show |
intron_variant | MODIFIER | c.-7-1945C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663492 | |||||||
chr7:16663493 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-7-1944G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663493 | |||||||
chr7:16663604 | TA | T | 5 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0283 others(2): Show |
5 | HG01109.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7-1825delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16663604 | ||||||
chr7:16663605 | A | T | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-7-1832A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663605 | |||||||
chr7:16663700 | G | A | 201 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(198): Show |
214 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.-7-1737G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663700 | |||||||
chr7:16663748 | A | G | 5 | a0001c0001t0004g0008 a0001c0001t0004g0314 a0001c0001t0004g0315 others(2): Show |
6 | HG01891.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7-1689A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663748 | |||||||
chr7:16663791 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-7-1646C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663791 | |||||||
chr7:16663973 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0092 others(60): Show |
65 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-7-1464G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16663973 | |||||||
chr7:16664042 | A | G | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | HG02135.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.-7-1395A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664042 | |||||||
chr7:16664074 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-1363T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664074 | |||||||
chr7:16664075 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-1362C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664075 | |||||||
chr7:16664076 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-1361T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664076 | |||||||
chr7:16664102 | A | G | 1 | a0001c0001t0002g0071 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-7-1335A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664102 | |||||||
chr7:16664127 | A | G | 99 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0038 others(96): Show |
110 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.-7-1310A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664127 | |||||||
chr7:16664149 | GAAA | G | 51 | a0001c0001t0001g0099 a0001c0001t0001g0101 a0001c0001t0001g0103 others(48): Show |
51 | HG00438.hp2 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.-7-1286_-7-1284del others(3): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16664149 | ||||||
chr7:16664265 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-7-1172C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664265 | |||||||
chr7:16664296 | A | G | 3 | a0001c0001t0002g0296 a0001c0001t0004g0315 a0001c0001t0004g0318 |
3 | HG01891.hp1 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-7-1141A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664296 | |||||||
chr7:16664566 | C | A | 34 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(31): Show |
35 | HG00544.hp2 HG00741.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-7-871C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664566 | |||||||
chr7:16664587 | A | G | 174 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(171): Show |
177 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.-7-850A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664587 | |||||||
chr7:16664590 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0002g0055 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-7-847T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664590 | |||||||
chr7:16664594 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0004g0318 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-7-843G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664594 | |||||||
chr7:16664627 | C | T | 168 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(165): Show |
170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.-7-810C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664627 | |||||||
chr7:16664640 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-797T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664640 | |||||||
chr7:16664709 | A | G | 1 | a0001c0001t0002g0345 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-7-728A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664709 | |||||||
chr7:16664788 | A | C | 1 | a0001c0001t0001g0122 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-7-649A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664788 | |||||||
chr7:16664797 | C | G | 1 | a0001c0001t0002g0349 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-7-640C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664797 | |||||||
chr7:16664852 | T | TTATAGTA others(2): Show |
65 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0154 others(62): Show |
65 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.-7-582_-7-574dupTA others(7): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 16664852 | ||||||
chr7:16664966 | A | G | 76 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0154 others(73): Show |
76 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(73): Show |
intron_variant | MODIFIER | c.-7-471A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16664966 | |||||||
chr7:16665067 | T | C | 1 | a0001c0001t0001g0264 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-7-370T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665067 | |||||||
chr7:16665071 | T | A | 1 | a0001c0001t0002g0393 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-7-366T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665071 | |||||||
chr7:16665071 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(314): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.-7-366T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665071 | |||||||
chr7:16665290 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0003g0193 |
2 | HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-7-147C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665290 | |||||||
chr7:16665298 | T | C | 80 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(77): Show |
81 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(78): Show |
intron_variant | MODIFIER | c.-7-139T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665298 | |||||||
chr7:16665353 | A | C | 1 | a0001c0001t0002g0298 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-7-84A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 1/11 | chr7 | 16665353 | |||||||
chr7:16665507 | T | TTG | 17 | a0001c0001t0002g0034 a0001c0001t0002g0074 a0001c0001t0002g0090 others(14): Show |
18 | HG00544.hp2 HG01255.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.58+28_58+29dupGT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | ||||||
chr7:16665507 | T | TTGTG | 11 | a0001c0001t0001g0029 a0001c0001t0001g0161 a0001c0001t0001g0168 others(8): Show |
11 | HG01074.hp2 HG01433.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+26_58+29dupGTGT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | ||||||
chr7:16665507 | T | TTGTGTGT others(1): Show |
3 | a0001c0001t0001g0154 a0001c0001t0002g0015 a0001c0001t0004g0318 |
3 | HG02109.hp1 HG02622.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.58+22_58+29dupGTGT others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | ||||||
chr7:16665507 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58+20_58+29dupGTGT others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16665507 | ||||||
chr7:16665638 | G | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0098 others(40): Show |
45 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.58+137G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16665638 | |||||||
chr7:16665725 | A | G | 9 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0001g0161 others(6): Show |
9 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+224A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16665725 | |||||||
chr7:16665859 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.58+358A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16665859 | |||||||
chr7:16666128 | A | T | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG03688.hp2 HG03704.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.58+627A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666128 | |||||||
chr7:16666159 | A | G | 5 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0001g0161 others(2): Show |
5 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+658A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666159 | |||||||
chr7:16666261 | C | T | 1 | a0001c0001t0002g0048 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58+760C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666261 | |||||||
chr7:16666286 | G | A | 6 | a0001c0001t0002g0290 a0001c0001t0002g0300 a0001c0001t0002g0319 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+785G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666286 | |||||||
chr7:16666303 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58+802C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666303 | |||||||
chr7:16666310 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0002g0149 a0001c0001t0002g0150 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+809C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666310 | |||||||
chr7:16666386 | G | T | 6 | a0001c0001t0002g0290 a0001c0001t0002g0300 a0001c0001t0002g0319 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.58+885G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666386 | |||||||
chr7:16666389 | T | TTTTA | 9 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0123 others(6): Show |
9 | HG02055.hp2 HG02258.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.58+917_58+920dupTT others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | ||||||
chr7:16666389 | T | TTTTATTT others(1): Show |
50 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0022 others(47): Show |
52 | HG00140.hp1 HG01081.hp2 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.58+913_58+920dupTT others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | ||||||
chr7:16666389 | T | TTTTATTT others(5): Show |
34 | a0001c0001t0001g0029 a0001c0001t0001g0115 a0001c0001t0001g0121 others(31): Show |
34 | HG00597.hp1 HG00738.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.58+909_58+920dupTT others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | ||||||
chr7:16666389 | T | TTTTATTT others(9): Show |
59 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0032 others(56): Show |
60 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.58+905_58+920dupTT others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | ||||||
chr7:16666389 | T | TTTTATTT others(13): Show |
11 | a0001c0001t0001g0026 a0001c0001t0001g0174 a0001c0001t0001g0196 others(8): Show |
11 | HG00621.hp1 HG01884.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.58+901_58+920dupTT others(18): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | ||||||
chr7:16666389 | TTTTATTT others(1): Show |
T | 8 | a0001c0001t0001g0177 a0001c0001t0002g0340 a0001c0001t0002g0348 others(5): Show |
8 | HG00323.hp2 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+913_58+920delTT others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666389 | ||||||
chr7:16666419 | T | TTATTTAT others(5): Show |
1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.58+920_58+921insTT others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666419 | ||||||
chr7:16666419 | T | TTATTTAT others(9): Show |
5 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(2): Show |
5 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+920_58+921insTT others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666419 | ||||||
chr7:16666419 | T | TTATTTAT others(13): Show |
1 | a0001c0001t0003g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.58+920_58+921insTT others(18): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16666419 | ||||||
chr7:16666426 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0002g0034 a0001c0001t0003g0193 |
3 | HG02723.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.58+925C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666426 | |||||||
chr7:16666443 | G | T | 20 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0273 others(17): Show |
20 | HG01106.hp2 HG01516.hp2 HG01952.hp2 others(17): Show |
intron_variant | MODIFIER | c.58+942G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666443 | |||||||
chr7:16666463 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0002g0343 a0001c0001t0002g0344 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+962C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666463 | |||||||
chr7:16666505 | C | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(184): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.58+1004C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666505 | |||||||
chr7:16666541 | T | G | 2 | a0001c0001t0002g0335 a0001c0004t0002g0299 |
2 | NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.58+1040T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666541 | |||||||
chr7:16666600 | A | C | 1 | a0001c0002t0002g0293 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.58+1099A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666600 | |||||||
chr7:16666704 | C | G | 5 | a0001c0001t0001g0016 a0001c0001t0002g0149 a0001c0001t0002g0150 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.58+1203C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666704 | |||||||
chr7:16666807 | T | A | 1 | a0001c0001t0002g0347 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.58+1306T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666807 | |||||||
chr7:16666924 | T | G | 26 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0162 others(23): Show |
27 | HG01106.hp2 HG01243.hp1 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.58+1423T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16666924 | |||||||
chr7:16667055 | A | G | 194 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(191): Show |
198 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.58+1554A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667055 | |||||||
chr7:16667071 | T | A | 1 | a0001c0001t0002g0368 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.58+1570T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667071 | |||||||
chr7:16667075 | T | G | 398 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(395): Show |
415 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(412): Show |
intron_variant | MODIFIER | c.58+1574T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667075 | |||||||
chr7:16667132 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0002g0367 |
2 | HG01243.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.58+1631A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667132 | |||||||
chr7:16667188 | A | T | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(1): Show |
4 | HG03688.hp1 HG03704.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1687A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667188 | |||||||
chr7:16667211 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.58+1710A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667211 | |||||||
chr7:16667230 | G | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0370 a0001c0001t0002g0371 |
4 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1729G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667230 | |||||||
chr7:16667239 | C | A | 26 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0162 others(23): Show |
27 | HG01106.hp2 HG01243.hp1 HG01516.hp2 others(24): Show |
intron_variant | MODIFIER | c.58+1738C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667239 | |||||||
chr7:16667243 | T | C | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.58+1742T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667243 | |||||||
chr7:16667246 | A | G | 1 | a0001c0001t0002g0308 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.58+1745A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667246 | |||||||
chr7:16667279 | CA | C | 10 | a0001c0001t0001g0154 a0001c0001t0001g0186 a0001c0001t0002g0015 others(7): Show |
10 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.58+1791delA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16667279 | ||||||
chr7:16667287 | A | C | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58+1786A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667287 | |||||||
chr7:16667291 | A | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.58+1790A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667291 | |||||||
chr7:16667292 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.58+1791A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667292 | |||||||
chr7:16667293 | C | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0169 a0001c0001t0002g0034 others(1): Show |
4 | HG02647.hp2 HG02723.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+1792C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667293 | |||||||
chr7:16667293 | C | CA | 7 | a0001c0001t0001g0025 a0001c0001t0001g0168 a0001c0001t0001g0177 others(4): Show |
7 | HG02622.hp2 HG02738.hp2 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+1803dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16667293 | ||||||
chr7:16667304 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.58+1803A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667304 | |||||||
chr7:16667719 | T | A | 2 | a0001c0001t0002g0056 a0001c0001t0002g0065 |
2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.58+2218T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667719 | |||||||
chr7:16667784 | T | C | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.58+2283T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667784 | |||||||
chr7:16667803 | C | T | 8 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(5): Show |
8 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.58+2302C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667803 | |||||||
chr7:16667833 | T | G | 1 | a0001c0001t0002g0343 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.58+2332T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667833 | |||||||
chr7:16667879 | C | T | 1 | a0001c0001t0010g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.58+2378C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667879 | |||||||
chr7:16667894 | C | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0027 |
2 | HG03688.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.58+2393C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16667894 | |||||||
chr7:16668007 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+2506G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668007 | |||||||
chr7:16668031 | C | G | 3 | a0001c0001t0002g0341 a0001c0001t0002g0363 a0001c0001t0002g0391 |
3 | HG01361.hp2 HG01981.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.58+2530C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668031 | |||||||
chr7:16668122 | T | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(97): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.58+2621T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668122 | |||||||
chr7:16668188 | G | T | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(4): Show |
7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+2687G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668188 | |||||||
chr7:16668236 | A | G | 43 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0155 others(40): Show |
44 | HG01081.hp2 HG01109.hp1 HG01123.hp1 others(41): Show |
intron_variant | MODIFIER | c.58+2735A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668236 | |||||||
chr7:16668403 | G | T | 75 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0029 others(72): Show |
77 | HG01074.hp2 HG01081.hp2 HG01106.hp2 others(74): Show |
intron_variant | MODIFIER | c.58+2902G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668403 | |||||||
chr7:16668437 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58+2936T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668437 | |||||||
chr7:16668528 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.58+3027T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668528 | |||||||
chr7:16668687 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0002g0343 a0001c0001t0002g0344 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+3186C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668687 | |||||||
chr7:16668795 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.58+3294C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668795 | |||||||
chr7:16668813 | T | C | 1 | a0001c0001t0002g0386 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.58+3312T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668813 | |||||||
chr7:16668838 | C | G | 1 | a0001c0001t0002g0329 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.58+3337C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668838 | |||||||
chr7:16668983 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.58+3482A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16668983 | |||||||
chr7:16669043 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.58+3542G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669043 | |||||||
chr7:16669075 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.58+3574G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669075 | |||||||
chr7:16669079 | G | T | 5 | a0001c0001t0001g0097 a0001c0001t0002g0074 a0001c0001t0002g0077 others(2): Show |
5 | HG00544.hp2 NA18945.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.58+3578G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669079 | |||||||
chr7:16669084 | T | C | 1 | a0001c0001t0001g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.58+3583T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669084 | |||||||
chr7:16669114 | T | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0154 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3613T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669114 | |||||||
chr7:16669137 | T | C | 7 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0041 others(4): Show |
9 | HG02132.hp2 NA18941.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.58+3636T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669137 | |||||||
chr7:16669186 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.58+3685C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669186 | |||||||
chr7:16669194 | C | T | 1 | a0001c0001t0002g0304 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.58+3693C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669194 | |||||||
chr7:16669286 | C | G | 1 | a0001c0001t0002g0385 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.58+3785C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669286 | |||||||
chr7:16669341 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0055 |
2 | HG03710.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.58+3840C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669341 | |||||||
chr7:16669364 | G | A | 1 | a0001c0001t0002g0319 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.58+3863G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669364 | |||||||
chr7:16669492 | A | G | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(4): Show |
7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+3991A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669492 | |||||||
chr7:16669520 | A | G | 4 | a0001c0001t0001g0021 a0001c0001t0002g0343 a0001c0001t0002g0344 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.58+4019A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669520 | |||||||
chr7:16669621 | TC | T | 97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(94): Show |
99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.58+4122delC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16669621 | ||||||
chr7:16669649 | A | G | 10 | a0001c0001t0002g0082 a0001c0001t0002g0302 a0001c0001t0002g0303 others(7): Show |
10 | HG01106.hp2 HG01516.hp2 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.58+4148A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669649 | |||||||
chr7:16669819 | A | G | 1 | a0001c0001t0010g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.58+4318A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16669819 | |||||||
chr7:16670083 | T | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(184): Show |
191 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.59-4329T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670083 | |||||||
chr7:16670099 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.59-4313G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670099 | |||||||
chr7:16670104 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.59-4308G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670104 | |||||||
chr7:16670154 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.59-4258A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670154 | |||||||
chr7:16670175 | G | T | 1 | a0001c0001t0001g0246 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.59-4237G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670175 | |||||||
chr7:16670430 | T | C | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(4): Show |
7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3982T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670430 | |||||||
chr7:16670482 | T | C | 3 | a0001c0001t0001g0169 a0001c0001t0002g0034 a0001c0001t0003g0193 |
3 | HG02723.hp1 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.59-3930T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670482 | |||||||
chr7:16670528 | A | G | 34 | a0001c0001t0001g0029 a0001c0001t0001g0215 a0001c0001t0001g0283 others(31): Show |
35 | HG01081.hp2 HG01109.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.59-3884A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670528 | |||||||
chr7:16670677 | T | G | 1 | a0001c0004t0002g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-3735T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670677 | |||||||
chr7:16670678 | A | T | 1 | a0001c0004t0002g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-3734A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670678 | |||||||
chr7:16670797 | G | A | 4 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(1): Show |
4 | HG03688.hp1 HG03704.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-3615G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670797 | |||||||
chr7:16670908 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.59-3504C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670908 | |||||||
chr7:16670940 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0065 |
2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.59-3472C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670940 | |||||||
chr7:16670941 | A | G | 102 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(99): Show |
104 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.59-3471A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16670941 | |||||||
chr7:16671254 | A | G | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(4): Show |
7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-3158A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671254 | |||||||
chr7:16671295 | C | G | 5 | a0001c0001t0001g0176 a0001c0001t0001g0183 a0001c0001t0001g0184 others(2): Show |
5 | HG00735.hp1 HG01981.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.59-3117C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671295 | |||||||
chr7:16671444 | C | T | 17 | a0001c0001t0002g0010 a0001c0001t0002g0053 a0001c0001t0002g0055 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.59-2968C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671444 | |||||||
chr7:16671445 | G | A | 6 | a0001c0001t0002g0290 a0001c0001t0002g0300 a0001c0001t0002g0319 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.59-2967G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671445 | |||||||
chr7:16671503 | A | G | 1 | a0001c0001t0004g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.59-2909A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671503 | |||||||
chr7:16671534 | C | G | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(4): Show |
7 | HG01074.hp2 HG01891.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.59-2878C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671534 | |||||||
chr7:16671593 | G | A | 1 | a0001c0001t0002g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.59-2819G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671593 | |||||||
chr7:16671679 | C | T | 1 | a0001c0001t0002g0303 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.59-2733C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671679 | |||||||
chr7:16671813 | C | A | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(96): Show |
101 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(98): Show |
intron_variant | MODIFIER | c.59-2599C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671813 | |||||||
chr7:16671814 | C | T | 12 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0001g0168 others(9): Show |
12 | HG01884.hp2 HG02109.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.59-2598C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671814 | |||||||
chr7:16671895 | C | A | 48 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0115 others(45): Show |
49 | HG01074.hp2 HG01106.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.59-2517C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16671895 | |||||||
chr7:16671930 | C | CA | 25 | a0001c0001t0001g0025 a0001c0001t0001g0096 a0001c0001t0001g0100 others(22): Show |
27 | HG00438.hp2 HG00558.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.59-2465dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | ||||||
chr7:16671930 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0002g0289 a0001c0005t0001g0028 |
2 | HG02886.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.59-2474_59-2465dup others(10): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | ||||||
chr7:16671930 | C | CAAAAAAA others(4): Show |
29 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0024 others(26): Show |
29 | HG01106.hp2 HG01516.hp2 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.59-2475_59-2465dup others(11): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | ||||||
chr7:16671930 | C | CAAAAAAA others(5): Show |
97 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(94): Show |
100 | HG00280.hp1 HG00621.hp1 HG00735.hp1 others(97): Show |
intron_variant | MODIFIER | c.59-2476_59-2465dup others(12): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | ||||||
chr7:16671930 | C | CAAAAAAA others(6): Show |
42 | a0001c0001t0001g0022 a0001c0001t0001g0124 a0001c0001t0001g0130 others(39): Show |
42 | HG00099.hp1 HG00140.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.59-2477_59-2465dup others(13): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | ||||||
chr7:16671930 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0017 a0001c0001t0002g0296 a0001c0001t0002g0332 |
3 | HG02559.hp2 HG02818.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.59-2478_59-2465dup others(14): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | ||||||
chr7:16671930 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0373 a0001c0001t0002g0387 |
2 | HG01243.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.59-2479_59-2465dup others(15): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16671930 | ||||||
chr7:16672208 | A | G | 47 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0115 others(44): Show |
48 | HG01074.hp2 HG01106.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.59-2204A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672208 | |||||||
chr7:16672237 | A | G | 2 | a0001c0001t0001g0115 a0001c0001t0004g0318 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.59-2175A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672237 | |||||||
chr7:16672268 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0215 a0001c0001t0002g0014 others(1): Show |
5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-2144C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672268 | |||||||
chr7:16672389 | G | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(180): Show |
186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.59-2023G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672389 | |||||||
chr7:16672586 | G | T | 1 | a0001c0001t0002g0368 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.59-1826G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672586 | |||||||
chr7:16672605 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.59-1807C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672605 | |||||||
chr7:16672708 | A | G | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(3): Show |
6 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1704A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672708 | |||||||
chr7:16672850 | C | A | 1 | a0001c0004t0002g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-1562C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672850 | |||||||
chr7:16672856 | ACTTCTGC others(107): Show |
A | 1 | a0001c0004t0002g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.59-1555_59-1442del | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672856 | |||||||
chr7:16672896 | A | C | 1 | a0001c0001t0002g0055 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.59-1516A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672896 | |||||||
chr7:16672952 | C | CT | 31 | a0001c0001t0001g0027 a0001c0001t0001g0283 a0001c0001t0002g0287 others(28): Show |
31 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.59-1449dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16672952 | ||||||
chr7:16672999 | G | C | 1 | a0001c0001t0001g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.59-1413G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16672999 | |||||||
chr7:16673076 | G | A | 9 | a0001c0001t0002g0082 a0001c0001t0002g0302 a0001c0001t0002g0303 others(6): Show |
9 | HG01106.hp2 HG01516.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-1336G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673076 | |||||||
chr7:16673082 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.59-1330A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673082 | |||||||
chr7:16673099 | A | G | 1 | a0001c0001t0002g0004 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.59-1313A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673099 | |||||||
chr7:16673105 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0161 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.59-1307C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673105 | |||||||
chr7:16673150 | G | C | 1 | a0001c0001t0002g0394 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.59-1262G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673150 | |||||||
chr7:16673182 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.59-1230G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673182 | |||||||
chr7:16673188 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.59-1224C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673188 | |||||||
chr7:16673193 | G | A | 1 | a0001c0001t0002g0075 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.59-1219G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673193 | |||||||
chr7:16673202 | T | C | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(3): Show |
6 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.59-1210T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673202 | |||||||
chr7:16673235 | C | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0020 others(95): Show |
100 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.59-1177C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673235 | |||||||
chr7:16673236 | A | G | 25 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(22): Show |
25 | HG00140.hp2 HG00323.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.59-1176A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673236 | |||||||
chr7:16673254 | T | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0115 a0001c0001t0001g0154 others(6): Show |
9 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.59-1158T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673254 | |||||||
chr7:16673331 | T | A | 1 | a0001c0001t0001g0228 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.59-1081T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673331 | |||||||
chr7:16673338 | A | G | 1 | a0001c0001t0002g0373 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.59-1074A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673338 | |||||||
chr7:16673346 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0243 |
2 | NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.59-1066C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673346 | |||||||
chr7:16673619 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.59-793C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673619 | |||||||
chr7:16673674 | C | A | 1 | a0001c0001t0005g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.59-738C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673674 | |||||||
chr7:16673687 | G | T | 1 | a0001c0001t0001g0123 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.59-725G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673687 | |||||||
chr7:16673721 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.59-691A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673721 | |||||||
chr7:16673961 | AC | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0020 others(97): Show |
102 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.59-450delC | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673961 | |||||||
chr7:16673963 | T | C | 11 | a0001c0001t0001g0155 a0001c0001t0001g0159 a0001c0001t0001g0160 others(8): Show |
11 | HG02004.hp1 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.59-449T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16673963 | |||||||
chr7:16674132 | T | C | 45 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0024 others(42): Show |
46 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.59-280T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674132 | |||||||
chr7:16674143 | A | C | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.59-269A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674143 | |||||||
chr7:16674196 | G | A | 4 | a0001c0001t0001g0021 a0001c0001t0002g0343 a0001c0001t0002g0344 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.59-216G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674196 | |||||||
chr7:16674203 | A | G | 1 | a0001c0001t0002g0388 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.59-209A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674203 | |||||||
chr7:16674308 | A | AT | 193 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(190): Show |
197 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.59-95dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 16674308 | ||||||
chr7:16674361 | C | T | 1 | a0001c0001t0011g0312 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.59-51C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 2/11 | chr7 | 16674361 | |||||||
chr7:16674672 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.235+84A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674672 | |||||||
chr7:16674775 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0261 |
2 | HG01169.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.235+187T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674775 | |||||||
chr7:16674852 | G | A | 14 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0332 others(11): Show |
14 | HG01074.hp2 HG01243.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.235+264G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674852 | |||||||
chr7:16674967 | T | A | 13 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0332 others(10): Show |
13 | HG01074.hp2 HG01243.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+379T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16674967 | |||||||
chr7:16675029 | AT | A | 22 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0124 others(19): Show |
23 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(20): Show |
intron_variant | MODIFIER | c.235+445delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16675029 | ||||||
chr7:16675112 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.235+524A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675112 | |||||||
chr7:16675168 | T | C | 4 | a0001c0001t0001g0029 a0001c0001t0001g0215 a0001c0001t0002g0014 others(1): Show |
5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.235+580T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675168 | |||||||
chr7:16675349 | A | G | 141 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(138): Show |
144 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.235+761A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675349 | |||||||
chr7:16675352 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(3): Show |
7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+764C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675352 | |||||||
chr7:16675353 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.235+765G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675353 | |||||||
chr7:16675419 | C | T | 2 | a0001c0001t0002g0346 a0001c0001t0002g0381 |
2 | NA18942.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.235+831C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675419 | |||||||
chr7:16675491 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.235+903G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675491 | |||||||
chr7:16675579 | G | T | 11 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(8): Show |
11 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.235+991G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675579 | |||||||
chr7:16675736 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.235+1148C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675736 | |||||||
chr7:16675737 | A | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(125): Show |
131 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.235+1149A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675737 | |||||||
chr7:16675832 | C | T | 6 | a0001c0001t0001g0156 a0001c0001t0002g0035 a0001c0001t0002g0036 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.235+1244C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675832 | |||||||
chr7:16675854 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG01261.hp1 HG01361.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.235+1266C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675854 | |||||||
chr7:16675885 | G | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0096 others(64): Show |
68 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.235+1297G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675885 | |||||||
chr7:16675885 | G | T | 2 | a0001c0001t0002g0343 a0001c0001t0002g0344 |
2 | HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.235+1297G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675885 | |||||||
chr7:16675895 | C | T | 1 | a0001c0001t0002g0012 | 2 | HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.235+1307C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675895 | |||||||
chr7:16675945 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0006g0152 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.235+1357G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675945 | |||||||
chr7:16675978 | T | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(132): Show |
137 | HG00140.hp1 HG00597.hp1 HG00621.hp1 others(134): Show |
intron_variant | MODIFIER | c.235+1390T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16675978 | |||||||
chr7:16676035 | C | T | 1 | a0001c0001t0003g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.235+1447C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676035 | |||||||
chr7:16676067 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.235+1479C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676067 | |||||||
chr7:16676284 | C | T | 7 | a0001c0001t0002g0326 a0001c0001t0002g0330 a0001c0001t0002g0331 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.235+1696C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676284 | |||||||
chr7:16676293 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0065 |
2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.235+1705A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676293 | |||||||
chr7:16676411 | A | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(125): Show |
131 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.235+1823A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676411 | |||||||
chr7:16676503 | A | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(125): Show |
131 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(128): Show |
intron_variant | MODIFIER | c.235+1915A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676503 | |||||||
chr7:16676520 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.235+1932A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676520 | |||||||
chr7:16676527 | A | G | 127 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(124): Show |
129 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.235+1939A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676527 | |||||||
chr7:16676580 | T | C | 10 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(7): Show |
10 | HG01074.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+1992T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676580 | |||||||
chr7:16676586 | ATG | A | 125 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(122): Show |
127 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.235+2000_235+2001d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16676586 | ||||||
chr7:16676642 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(137): Show |
142 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(139): Show |
intron_variant | MODIFIER | c.235+2054G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16676642 | |||||||
chr7:16677051 | C | CT | 13 | a0001c0001t0001g0106 a0001c0001t0001g0126 a0001c0001t0001g0161 others(10): Show |
13 | HG01109.hp2 HG01243.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.235+2480dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16677051 | ||||||
chr7:16677051 | C | CTT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(103): Show |
108 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(105): Show |
intron_variant | MODIFIER | c.235+2479_235+2480d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16677051 | ||||||
chr7:16677051 | CTTTTTTT | C | 6 | a0001c0001t0002g0326 a0001c0001t0002g0330 a0001c0001t0002g0331 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.235+2474_235+2480d others(9): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16677051 | ||||||
chr7:16677153 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(111): Show |
116 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.235+2565A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677153 | |||||||
chr7:16677219 | T | C | 13 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(10): Show |
13 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+2631T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677219 | |||||||
chr7:16677346 | C | G | 7 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(4): Show |
7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+2758C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677346 | |||||||
chr7:16677398 | C | A | 13 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(10): Show |
13 | HG01884.hp2 HG02109.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.235+2810C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677398 | |||||||
chr7:16677444 | A | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(73): Show |
78 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.235+2856A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677444 | |||||||
chr7:16677450 | G | A | 7 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(4): Show |
7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.235+2862G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677450 | |||||||
chr7:16677477 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(100): Show |
104 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.235+2889G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677477 | |||||||
chr7:16677510 | G | A | 1 | a0001c0001t0010g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.235+2922G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677510 | |||||||
chr7:16677528 | G | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(122): Show |
127 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(124): Show |
intron_variant | MODIFIER | c.235+2940G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677528 | |||||||
chr7:16677569 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.235+2981G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677569 | |||||||
chr7:16677640 | C | T | 1 | a0001c0003t0002g0321 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.235+3052C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677640 | |||||||
chr7:16677641 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(117): Show |
122 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.235+3053G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677641 | |||||||
chr7:16677781 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.235+3193A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677781 | |||||||
chr7:16677798 | G | C | 120 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(117): Show |
122 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.235+3210G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677798 | |||||||
chr7:16677800 | G | A | 120 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(117): Show |
122 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.235+3212G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677800 | |||||||
chr7:16677821 | A | C | 2 | a0001c0001t0001g0169 a0001c0001t0002g0034 |
2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.235+3233A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677821 | |||||||
chr7:16677901 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.235+3313A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677901 | |||||||
chr7:16677918 | A | G | 7 | a0001c0001t0002g0009 a0001c0001t0002g0011 a0001c0001t0002g0041 others(4): Show |
9 | HG02132.hp2 NA18941.hp2 NA18962.hp2 others(6): Show |
intron_variant | MODIFIER | c.235+3330A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677918 | |||||||
chr7:16677945 | A | T | 1 | a0001c0001t0001g0249 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.236-3356A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677945 | |||||||
chr7:16677988 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(116): Show |
121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3313G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16677988 | |||||||
chr7:16678055 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(116): Show |
121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3246C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678055 | |||||||
chr7:16678087 | C | CT | 26 | a0001c0001t0001g0016 a0001c0001t0001g0097 a0001c0001t0001g0126 others(23): Show |
26 | HG00544.hp2 HG00597.hp2 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.236-3189dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | ||||||
chr7:16678087 | C | CTT | 87 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(84): Show |
88 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.236-3190_236-3189d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | ||||||
chr7:16678087 | C | CTTT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0170 a0001c0001t0001g0175 others(6): Show |
9 | HG00735.hp1 HG02523.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-3191_236-3189d others(5): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | ||||||
chr7:16678087 | CT | C | 15 | a0001c0001t0001g0107 a0001c0001t0001g0116 a0001c0001t0001g0159 others(12): Show |
16 | HG00323.hp1 HG01081.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.236-3189delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | ||||||
chr7:16678087 | CTTTTTT | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(3): Show |
7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-3194_236-3189d others(8): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 16678087 | ||||||
chr7:16678112 | T | A | 2 | a0001c0001t0002g0343 a0001c0001t0002g0344 |
2 | HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.236-3189T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678112 | |||||||
chr7:16678117 | C | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(115): Show |
120 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.236-3184C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678117 | |||||||
chr7:16678122 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-3179G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678122 | |||||||
chr7:16678155 | C | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(4): Show |
7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-3146C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678155 | |||||||
chr7:16678165 | A | G | 119 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(116): Show |
121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-3136A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678165 | |||||||
chr7:16678210 | G | C | 3 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0001t0002g0387 |
3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.236-3091G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678210 | |||||||
chr7:16678241 | G | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(115): Show |
120 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(117): Show |
intron_variant | MODIFIER | c.236-3060G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678241 | |||||||
chr7:16678336 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(116): Show |
121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-2965C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678336 | |||||||
chr7:16678350 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.236-2951G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678350 | |||||||
chr7:16678360 | T | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(116): Show |
121 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.236-2941T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678360 | |||||||
chr7:16678362 | G | A | 2 | a0001c0001t0001g0119 a0001c0001t0001g0132 |
2 | NA18952.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.236-2939G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678362 | |||||||
chr7:16678363 | C | T | 1 | a0001c0001t0002g0292 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.236-2938C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678363 | |||||||
chr7:16678598 | C | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(4): Show |
7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-2703C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678598 | |||||||
chr7:16678652 | C | T | 1 | a0001c0001t0002g0397 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.236-2649C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678652 | |||||||
chr7:16678765 | C | T | 6 | a0001c0001t0001g0239 a0001c0001t0002g0072 a0001c0001t0002g0342 others(3): Show |
6 | HG02056.hp2 NA18950.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.236-2536C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678765 | |||||||
chr7:16678795 | G | A | 111 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(108): Show |
113 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(110): Show |
intron_variant | MODIFIER | c.236-2506G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678795 | |||||||
chr7:16678819 | C | T | 7 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(4): Show |
7 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.236-2482C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678819 | |||||||
chr7:16678830 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.236-2471A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678830 | |||||||
chr7:16678840 | G | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0267 a0001c0001t0002g0296 |
3 | HG00738.hp2 HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.236-2461G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678840 | |||||||
chr7:16678959 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(101): Show |
105 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.236-2342G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16678959 | |||||||
chr7:16679025 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-2276G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679025 | |||||||
chr7:16679029 | G | A | 1 | a0001c0001t0002g0367 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.236-2272G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679029 | |||||||
chr7:16679071 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.236-2230T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679071 | |||||||
chr7:16679201 | T | C | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(20): Show |
24 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.236-2100T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679201 | |||||||
chr7:16679211 | G | A | 1 | a0001c0001t0002g0341 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.236-2090G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679211 | |||||||
chr7:16679222 | A | G | 15 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(12): Show |
15 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.236-2079A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679222 | |||||||
chr7:16679343 | C | T | 1 | a0001c0001t0002g0326 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.236-1958C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679343 | |||||||
chr7:16679364 | C | T | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(5): Show |
9 | HG02257.hp1 HG02559.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.236-1937C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679364 | |||||||
chr7:16679448 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(99): Show |
103 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.236-1853T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679448 | |||||||
chr7:16679492 | T | C | 1 | a0001c0001t0002g0335 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.236-1809T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679492 | |||||||
chr7:16679523 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(130): Show |
136 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(133): Show |
intron_variant | MODIFIER | c.236-1778T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679523 | |||||||
chr7:16679675 | T | A | 105 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(102): Show |
106 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(103): Show |
intron_variant | MODIFIER | c.236-1626T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679675 | |||||||
chr7:16679744 | C | A | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.236-1557C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679744 | |||||||
chr7:16679785 | A | G | 1 | a0001c0001t0001g0118 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.236-1516A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679785 | |||||||
chr7:16679855 | G | A | 2 | a0001c0001t0001g0168 a0001c0001t0002g0296 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.236-1446G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679855 | |||||||
chr7:16679961 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(3): Show |
7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.236-1340G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16679961 | |||||||
chr7:16680061 | C | A | 5 | a0001c0001t0001g0016 a0001c0001t0002g0149 a0001c0001t0002g0150 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-1240C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680061 | |||||||
chr7:16680101 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.236-1200C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680101 | |||||||
chr7:16680114 | G | A | 118 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(115): Show |
119 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(116): Show |
intron_variant | MODIFIER | c.236-1187G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680114 | |||||||
chr7:16680132 | G | T | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.236-1169G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680132 | |||||||
chr7:16680139 | C | A | 1 | a0001c0001t0001g0268 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.236-1162C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680139 | |||||||
chr7:16680159 | G | A | 14 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(11): Show |
14 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.236-1142G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680159 | |||||||
chr7:16680241 | C | A | 1 | a0001c0001t0001g0172 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.236-1060C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680241 | |||||||
chr7:16680292 | T | C | 146 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(143): Show |
149 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.236-1009T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680292 | |||||||
chr7:16680303 | T | C | 6 | a0001c0001t0001g0156 a0001c0001t0002g0035 a0001c0001t0002g0036 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-998T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680303 | |||||||
chr7:16680363 | T | C | 1 | a0001c0001t0002g0352 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.236-938T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680363 | |||||||
chr7:16680402 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0142 |
2 | NA18963.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.236-899C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680402 | |||||||
chr7:16680450 | A | G | 1 | a0001c0001t0002g0352 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.236-851A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680450 | |||||||
chr7:16680455 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0002g0296 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.236-846A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680455 | |||||||
chr7:16680501 | A | G | 1 | a0001c0001t0002g0070 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.236-800A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680501 | |||||||
chr7:16680591 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.236-710G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680591 | |||||||
chr7:16680648 | T | C | 5 | a0001c0001t0001g0200 a0001c0001t0001g0217 a0001c0001t0001g0218 others(2): Show |
5 | HG02129.hp1 NA18940.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-653T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680648 | |||||||
chr7:16680719 | A | G | 5 | a0001c0001t0001g0016 a0001c0001t0002g0149 a0001c0001t0002g0150 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-582A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680719 | |||||||
chr7:16680748 | G | A | 2 | a0001c0001t0002g0307 a0001c0001t0002g0310 |
2 | HG01952.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.236-553G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680748 | |||||||
chr7:16680968 | G | A | 28 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(25): Show |
30 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.236-333G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680968 | |||||||
chr7:16680975 | A | G | 10 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(7): Show |
10 | HG01074.hp2 HG02615.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.236-326A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16680975 | |||||||
chr7:16681028 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | NA18940.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.236-273G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16681028 | |||||||
chr7:16681086 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0006g0152 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.236-215G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16681086 | |||||||
chr7:16681227 | A | T | 1 | a0001c0001t0007g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.236-74A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 3/11 | chr7 | 16681227 | |||||||
chr7:16681674 | A | C | 1 | a0001c0001t0002g0309 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.339+270A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681674 | |||||||
chr7:16681677 | C | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(3): Show |
7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.339+273C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681677 | |||||||
chr7:16681715 | C | A | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.339+311C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681715 | |||||||
chr7:16681757 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(176): Show |
183 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.339+353A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681757 | |||||||
chr7:16681876 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0273 others(9): Show |
12 | HG01255.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.339+472C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16681876 | |||||||
chr7:16682104 | G | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0096 others(65): Show |
69 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.340-676G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682104 | |||||||
chr7:16682156 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(101): Show |
105 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.340-624A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682156 | |||||||
chr7:16682172 | A | G | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0002g0334 others(3): Show |
6 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-608A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682172 | |||||||
chr7:16682345 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.340-435A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682345 | |||||||
chr7:16682348 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.340-432A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682348 | |||||||
chr7:16682398 | A | T | 6 | a0001c0001t0001g0156 a0001c0001t0002g0035 a0001c0001t0002g0036 others(3): Show |
6 | HG02280.hp2 HG02559.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.340-382A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682398 | |||||||
chr7:16682435 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(160): Show |
166 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.340-345G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682435 | |||||||
chr7:16682438 | G | A | 357 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(354): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(371): Show |
intron_variant | MODIFIER | c.340-342G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682438 | |||||||
chr7:16682473 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.340-307G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682473 | |||||||
chr7:16682473 | G | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.340-307G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682473 | |||||||
chr7:16682476 | A | G | 3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0002g0081 |
3 | HG00738.hp2 HG01175.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.340-304A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682476 | |||||||
chr7:16682551 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.340-229A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682551 | |||||||
chr7:16682631 | A | T | 39 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(36): Show |
41 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.340-149A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682631 | |||||||
chr7:16682721 | A | G | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.340-59A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682721 | |||||||
chr7:16682728 | A | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(161): Show |
167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.340-52A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682728 | |||||||
chr7:16682745 | G | A | 41 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(38): Show |
43 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.340-35G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | chr7 | 16682745 | |||||||
chr7:16682767 | G | GT | 44 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(41): Show |
46 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(43): Show |
splice_acceptor_variant&intron_variant | HIGH | c.340-3dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr7 | 16682767 | ||||||
chr7:16682869 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.405+24A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682869 | |||||||
chr7:16682925 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.405+80C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682925 | |||||||
chr7:16682938 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.405+93C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682938 | |||||||
chr7:16682963 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.405+118C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16682963 | |||||||
chr7:16683050 | C | G | 1 | a0001c0001t0002g0043 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.405+205C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683050 | |||||||
chr7:16683063 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.405+218G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683063 | |||||||
chr7:16683167 | G | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.405+322G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683167 | |||||||
chr7:16683175 | A | G | 41 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(38): Show |
43 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.405+330A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683175 | |||||||
chr7:16683266 | T | G | 10 | a0001c0001t0001g0283 a0001c0001t0002g0324 a0001c0001t0002g0328 others(7): Show |
10 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.405+421T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683266 | |||||||
chr7:16683333 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(107): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.405+488A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683333 | |||||||
chr7:16683377 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.405+532A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683377 | |||||||
chr7:16683497 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(257): Show |
265 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.405+652G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683497 | |||||||
chr7:16683503 | T | C | 164 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(161): Show |
167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.405+658T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683503 | |||||||
chr7:16683542 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.405+697G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683542 | |||||||
chr7:16683580 | G | A | 3 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0003g0193 |
3 | HG02723.hp1 NA18906.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.405+735G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683580 | |||||||
chr7:16683592 | A | G | 5 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(2): Show |
5 | HG01981.hp2 HG02300.hp1 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.405+747A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683592 | |||||||
chr7:16683688 | C | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0079 |
2 | NA18945.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.405+843C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683688 | |||||||
chr7:16683698 | C | T | 10 | a0001c0001t0001g0018 a0001c0001t0001g0273 a0001c0001t0002g0329 others(7): Show |
10 | HG01255.hp1 HG02572.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.405+853C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683698 | |||||||
chr7:16683715 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.405+870G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683715 | |||||||
chr7:16683858 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.405+1013C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683858 | |||||||
chr7:16683908 | T | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(107): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.405+1063T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683908 | |||||||
chr7:16683967 | A | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.405+1122A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16683967 | |||||||
chr7:16684033 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(161): Show |
167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.405+1188G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684033 | |||||||
chr7:16684084 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.405+1239A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684084 | |||||||
chr7:16684109 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(107): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.405+1264A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684109 | |||||||
chr7:16684148 | T | A | 154 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(151): Show |
157 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(154): Show |
intron_variant | MODIFIER | c.405+1303T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684148 | |||||||
chr7:16684209 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.405+1364C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684209 | |||||||
chr7:16684305 | A | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(105): Show |
109 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.405+1460A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684305 | |||||||
chr7:16684340 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0002g0367 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.405+1495A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684340 | |||||||
chr7:16684361 | C | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0273 others(13): Show |
16 | HG01255.hp1 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.405+1516C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684361 | |||||||
chr7:16684380 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(105): Show |
109 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.406-1525G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684380 | |||||||
chr7:16684460 | GTTA | G | 7 | a0001c0001t0001g0137 a0001c0001t0001g0196 a0001c0001t0001g0203 others(4): Show |
7 | HG00621.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-1439_406-1437d others(5): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16684460 | ||||||
chr7:16684618 | A | G | 1 | a0001c0001t0002g0367 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.406-1287A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684618 | |||||||
chr7:16684774 | G | T | 3 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0001t0002g0387 |
3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.406-1131G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684774 | |||||||
chr7:16684821 | T | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(107): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.406-1084T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684821 | |||||||
chr7:16684902 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(107): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.406-1003A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684902 | |||||||
chr7:16684995 | G | A | 1 | a0001c0001t0002g0015 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.406-910G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16684995 | |||||||
chr7:16685004 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.406-901T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685004 | |||||||
chr7:16685054 | A | G | 110 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(107): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.406-851A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685054 | |||||||
chr7:16685195 | G | C | 109 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(106): Show |
110 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(107): Show |
intron_variant | MODIFIER | c.406-710G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685195 | |||||||
chr7:16685206 | T | C | 1 | a0001c0001t0003g0272 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.406-699T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685206 | |||||||
chr7:16685222 | A | G | 19 | a0001c0001t0001g0162 a0001c0001t0001g0283 a0001c0001t0002g0287 others(16): Show |
19 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.406-683A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685222 | |||||||
chr7:16685367 | A | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(3): Show |
7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.406-538A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685367 | |||||||
chr7:16685401 | G | A | 6 | a0001c0001t0002g0326 a0001c0001t0002g0330 a0001c0001t0002g0331 others(3): Show |
6 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.406-504G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685401 | |||||||
chr7:16685409 | C | T | 2 | a0001c0003t0002g0295 a0001c0003t0002g0313 |
2 | HG02622.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.406-496C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685409 | |||||||
chr7:16685412 | G | GT | 12 | a0001c0001t0001g0176 a0001c0001t0001g0232 a0001c0001t0001g0245 others(9): Show |
13 | HG00280.hp1 HG01074.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.406-481dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16685412 | ||||||
chr7:16685431 | G | T | 1 | a0001c0001t0001g0025 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.406-474G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685431 | |||||||
chr7:16685463 | G | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0124 others(18): Show |
22 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(19): Show |
intron_variant | MODIFIER | c.406-442G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685463 | |||||||
chr7:16685655 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0002g0367 |
2 | HG01243.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.406-250A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685655 | |||||||
chr7:16685761 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.406-144C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685761 | |||||||
chr7:16685842 | T | C | 1 | a0001c0001t0002g0354 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.406-63T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | chr7 | 16685842 | |||||||
chr7:16685876 | C | CT | 122 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0018 others(119): Show |
124 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(121): Show |
intron_variant | MODIFIER | c.406-10dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16685876 | ||||||
chr7:16685876 | CT | C | 17 | a0001c0001t0001g0104 a0001c0001t0001g0133 a0001c0001t0001g0144 others(14): Show |
17 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.406-10delT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 16685876 | ||||||
chr7:16686121 | T | C | 1 | a0001c0001t0002g0352 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.541+81T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686121 | |||||||
chr7:16686130 | T | C | 1 | a0001c0001t0006g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541+90T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686130 | |||||||
chr7:16686228 | G | T | 2 | a0001c0001t0002g0376 a0001c0001t0002g0379 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.541+188G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686228 | |||||||
chr7:16686279 | A | C | 26 | a0001c0001t0001g0157 a0001c0001t0001g0256 a0001c0001t0002g0010 others(23): Show |
27 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(24): Show |
intron_variant | MODIFIER | c.541+239A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686279 | |||||||
chr7:16686394 | T | C | 1 | a0001c0001t0002g0014 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.541+354T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686394 | |||||||
chr7:16686527 | A | C | 38 | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0024 others(35): Show |
40 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(37): Show |
intron_variant | MODIFIER | c.541+487A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686527 | |||||||
chr7:16686529 | T | C | 9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(6): Show |
10 | HG01243.hp1 HG02257.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.541+489T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686529 | |||||||
chr7:16686629 | A | ATT | 3 | a0001c0001t0001g0130 a0001c0001t0001g0175 a0001c0001t0001g0401 |
3 | HG02523.hp2 NA18939.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.541+590_541+591ins others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16686629 | ||||||
chr7:16686712 | T | C | 1 | a0001c0001t0006g0152 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541+672T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686712 | |||||||
chr7:16686718 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.541+678G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686718 | |||||||
chr7:16686738 | C | G | 1 | a0001c0001t0001g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.541+698C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686738 | |||||||
chr7:16686742 | A | T | 19 | a0001c0001t0001g0162 a0001c0001t0001g0283 a0001c0001t0002g0287 others(16): Show |
19 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.541+702A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686742 | |||||||
chr7:16686998 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.541+958C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16686998 | |||||||
chr7:16687006 | CACACAGA others(6): Show |
C | 2 | a0001c0001t0001g0021 a0001c0001t0006g0152 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.541+970_541+982del others(13): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16687006 | ||||||
chr7:16687154 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.541+1114C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687154 | |||||||
chr7:16687226 | A | G | 1 | a0001c0003t0002g0313 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.541+1186A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687226 | |||||||
chr7:16687331 | A | G | 1 | a0001c0001t0008g0317 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.541+1291A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687331 | |||||||
chr7:16687582 | G | A | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.541+1542G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687582 | |||||||
chr7:16687610 | G | T | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.541+1570G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687610 | |||||||
chr7:16687721 | A | G | 6 | a0001c0001t0002g0290 a0001c0001t0002g0300 a0001c0001t0002g0319 others(3): Show |
6 | HG01884.hp2 HG02647.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+1681A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687721 | |||||||
chr7:16687723 | A | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0124 others(26): Show |
30 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(27): Show |
intron_variant | MODIFIER | c.541+1683A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687723 | |||||||
chr7:16687727 | A | G | 1 | a0001c0001t0002g0333 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.541+1687A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687727 | |||||||
chr7:16687778 | C | A | 1 | a0001c0001t0002g0367 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.541+1738C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687778 | |||||||
chr7:16687802 | G | A | 4 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0015 others(1): Show |
4 | HG02109.hp1 HG02622.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+1762G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687802 | |||||||
chr7:16687809 | C | T | 2 | a0001c0001t0001g0021 a0001c0001t0006g0152 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.541+1769C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687809 | |||||||
chr7:16687816 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.541+1776G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687816 | |||||||
chr7:16687860 | A | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(3): Show |
7 | HG02257.hp1 HG03516.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+1820A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687860 | |||||||
chr7:16687884 | C | T | 1 | a0001c0001t0010g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.541+1844C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687884 | |||||||
chr7:16687904 | T | C | 91 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0022 others(88): Show |
93 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.541+1864T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687904 | |||||||
chr7:16687997 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.542-1800G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16687997 | |||||||
chr7:16688031 | G | GT | 6 | a0001c0001t0001g0030 a0001c0001t0001g0138 a0001c0001t0001g0158 others(3): Show |
7 | HG01257.hp2 HG02015.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-1756dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16688031 | ||||||
chr7:16688125 | A | C | 3 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0174 |
3 | HG02129.hp2 NA18963.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.542-1672A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688125 | |||||||
chr7:16688173 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0002g0333 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.542-1624G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688173 | |||||||
chr7:16688286 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0002g0050 |
2 | HG03017.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.542-1511C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688286 | |||||||
chr7:16688426 | A | G | 24 | a0001c0001t0001g0005 a0001c0001t0001g0098 a0001c0001t0001g0110 others(21): Show |
25 | HG00099.hp1 HG00280.hp1 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.542-1371A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688426 | |||||||
chr7:16688553 | G | C | 2 | a0001c0001t0004g0008 a0001c0001t0004g0316 |
3 | HG02257.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.542-1244G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688553 | |||||||
chr7:16688559 | T | G | 4 | a0001c0001t0001g0200 a0001c0001t0001g0217 a0001c0001t0001g0218 others(1): Show |
4 | NA18940.hp2 NA18982.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-1238T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688559 | |||||||
chr7:16688626 | T | A | 1 | a0001c0001t0003g0278 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-1171T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688626 | |||||||
chr7:16688856 | A | AT | 35 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(32): Show |
36 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.542-932dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 16688856 | ||||||
chr7:16688973 | C | A | 21 | a0001c0001t0001g0162 a0001c0001t0001g0283 a0001c0001t0002g0015 others(18): Show |
21 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.542-824C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16688973 | |||||||
chr7:16689127 | G | A | 1 | a0001c0001t0002g0367 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.542-670G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689127 | |||||||
chr7:16689180 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.542-617C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689180 | |||||||
chr7:16689292 | A | G | 1 | a0001c0001t0008g0317 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.542-505A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689292 | |||||||
chr7:16689318 | A | C | 1 | a0001c0001t0001g0244 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.542-479A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689318 | |||||||
chr7:16689380 | A | G | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(10): Show |
14 | HG01109.hp1 HG02257.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.542-417A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689380 | |||||||
chr7:16689470 | G | A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(10): Show |
14 | HG01109.hp1 HG02257.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.542-327G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689470 | |||||||
chr7:16689627 | G | T | 22 | a0001c0001t0001g0162 a0001c0001t0001g0283 a0001c0001t0002g0015 others(19): Show |
22 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.542-170G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689627 | |||||||
chr7:16689636 | A | T | 1 | a0001c0001t0002g0400 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.542-161A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689636 | |||||||
chr7:16689712 | A | C | 2 | a0001c0001t0001g0021 a0001c0001t0006g0152 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.542-85A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689712 | |||||||
chr7:16689747 | A | T | 1 | a0001c0001t0002g0289 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.542-50A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689747 | |||||||
chr7:16689768 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.542-29G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 6/11 | chr7 | 16689768 | |||||||
chr7:16690143 | T | C | 1 | a0001c0006t0002g0057 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.651+237T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690143 | |||||||
chr7:16690195 | A | G | 6 | a0001c0001t0001g0168 a0001c0001t0002g0300 a0001c0001t0002g0337 others(3): Show |
6 | HG01891.hp1 HG02055.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.651+289A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690195 | |||||||
chr7:16690207 | C | CT | 36 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(33): Show |
38 | HG01070.hp2 HG01071.hp2 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.651+314dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16690207 | ||||||
chr7:16690212 | T | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0110 others(49): Show |
54 | HG00099.hp1 HG00280.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.651+306T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690212 | |||||||
chr7:16690272 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.651+366G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690272 | |||||||
chr7:16690384 | T | A | 3 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0001t0002g0387 |
3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.651+478T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690384 | |||||||
chr7:16690722 | C | A | 1 | a0001c0001t0001g0003 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.651+816C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690722 | |||||||
chr7:16690756 | T | C | 1 | a0001c0001t0002g0354 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.651+850T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690756 | |||||||
chr7:16690917 | C | T | 32 | a0001c0001t0001g0005 a0001c0001t0001g0110 a0001c0001t0001g0124 others(29): Show |
33 | HG00099.hp1 HG00280.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.651+1011C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16690917 | |||||||
chr7:16691217 | G | T | 14 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0001g0273 others(11): Show |
14 | HG01074.hp2 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+1311G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691217 | |||||||
chr7:16691219 | T | G | 2 | a0001c0001t0002g0014 a0001c0001t0002g0398 |
3 | HG01123.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.651+1313T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691219 | |||||||
chr7:16691417 | G | T | 109 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0019 others(106): Show |
111 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.651+1511G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691417 | |||||||
chr7:16691553 | G | A | 3 | a0001c0001t0002g0355 a0001c0001t0002g0369 a0001c0001t0002g0380 |
3 | HG00099.hp2 HG00735.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.651+1647G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691553 | |||||||
chr7:16691567 | A | G | 35 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(32): Show |
36 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.651+1661A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691567 | |||||||
chr7:16691588 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.651+1682A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691588 | |||||||
chr7:16691592 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.651+1686A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691592 | |||||||
chr7:16691602 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0002g0077 |
2 | NA18967.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.651+1696G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691602 | |||||||
chr7:16691628 | A | G | 168 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(165): Show |
172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.651+1722A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691628 | |||||||
chr7:16691653 | C | T | 1 | a0001c0001t0009g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.651+1747C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691653 | |||||||
chr7:16691741 | A | G | 2 | a0001c0001t0001g0144 a0001c0001t0001g0249 |
2 | NA18939.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.651+1835A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691741 | |||||||
chr7:16691789 | A | C | 4 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0002g0335 others(1): Show |
4 | HG02109.hp1 HG02647.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+1883A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691789 | |||||||
chr7:16691878 | C | CTG | 11 | a0001c0001t0001g0192 a0001c0001t0001g0250 a0001c0001t0002g0082 others(8): Show |
11 | HG00423.hp2 HG01106.hp2 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.651+1996_651+1997d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16691878 | ||||||
chr7:16691878 | CTG | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(167): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.651+1996_651+1997d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16691878 | ||||||
chr7:16691878 | CTGTG | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0154 a0001c0001t0001g0206 others(4): Show |
7 | HG02109.hp1 HG02647.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.651+1994_651+1997d others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16691878 | ||||||
chr7:16691912 | G | A | 10 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
10 | HG01074.hp2 HG01243.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.651+2006G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691912 | |||||||
chr7:16691928 | A | G | 21 | a0001c0001t0001g0162 a0001c0001t0001g0283 a0001c0001t0002g0015 others(18): Show |
21 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.651+2022A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691928 | |||||||
chr7:16691999 | C | G | 4 | a0001c0001t0001g0246 a0001c0001t0001g0247 a0001c0001t0001g0260 others(1): Show |
4 | HG02071.hp1 HG02071.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.651+2093C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16691999 | |||||||
chr7:16692236 | AACCCTTA others(2): Show |
A | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(10): Show |
14 | HG01109.hp1 HG02257.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.651+2333_651+2341d others(11): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16692236 | ||||||
chr7:16692307 | A | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0019 others(104): Show |
109 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.651+2401A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692307 | |||||||
chr7:16692460 | T | A | 10 | a0001c0001t0001g0273 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
10 | HG01074.hp2 HG01243.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.652-2374T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692460 | |||||||
chr7:16692621 | G | A | 16 | a0001c0001t0001g0283 a0001c0001t0002g0287 a0001c0001t0002g0288 others(13): Show |
16 | HG01081.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.652-2213G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692621 | |||||||
chr7:16692734 | G | A | 11 | a0001c0001t0001g0031 a0001c0001t0001g0037 a0001c0001t0001g0157 others(8): Show |
11 | HG00738.hp1 HG00741.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.652-2100G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692734 | |||||||
chr7:16692758 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.652-2076C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16692758 | |||||||
chr7:16693231 | C | T | 1 | a0001c0001t0002g0371 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.652-1603C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693231 | |||||||
chr7:16693354 | A | G | 1 | a0001c0001t0002g0320 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.652-1480A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693354 | |||||||
chr7:16693394 | A | G | 1 | a0001c0001t0002g0328 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.652-1440A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693394 | |||||||
chr7:16693542 | T | C | 34 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(31): Show |
35 | HG01081.hp2 HG01109.hp1 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.652-1292T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693542 | |||||||
chr7:16693606 | TGCTTTAC others(3): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.652-1226_652-1217d others(12): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 16693606 | ||||||
chr7:16693620 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.652-1214A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693620 | |||||||
chr7:16693639 | T | A | 1 | a0001c0001t0001g0168 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.652-1195T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693639 | |||||||
chr7:16693639 | T | C | 13 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(10): Show |
14 | HG01109.hp1 HG02257.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.652-1195T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693639 | |||||||
chr7:16693885 | A | G | 7 | a0001c0001t0002g0012 a0001c0001t0002g0034 a0001c0001t0002g0290 others(4): Show |
8 | HG01884.hp2 HG02486.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.652-949A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693885 | |||||||
chr7:16693942 | G | C | 1 | a0001c0001t0001g0139 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.652-892G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693942 | |||||||
chr7:16693946 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.652-888C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693946 | |||||||
chr7:16693989 | A | G | 2 | a0001c0001t0002g0015 a0001c0001t0002g0296 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.652-845A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16693989 | |||||||
chr7:16694186 | A | G | 4 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0001c0001t0001g0107 others(1): Show |
4 | NA18943.hp1 NA18983.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-648A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694186 | |||||||
chr7:16694247 | G | A | 3 | a0001c0001t0002g0010 a0001c0001t0002g0370 a0001c0001t0002g0371 |
4 | HG00280.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.652-587G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694247 | |||||||
chr7:16694432 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0199 |
2 | HG01257.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.652-402G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694432 | |||||||
chr7:16694434 | G | T | 1 | a0001c0001t0010g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.652-400G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694434 | |||||||
chr7:16694682 | G | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0023 others(95): Show |
100 | HG00423.hp2 HG00438.hp1 HG00558.hp1 others(97): Show |
intron_variant | MODIFIER | c.652-152G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694682 | |||||||
chr7:16694800 | C | A | 10 | a0001c0001t0001g0019 a0001c0001t0002g0329 a0001c0001t0002g0368 others(7): Show |
10 | HG01255.hp1 HG02622.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.652-34C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 7/11 | chr7 | 16694800 | |||||||
chr7:16695017 | G | A | 6 | a0001c0001t0001g0283 a0001c0001t0002g0328 a0001c0001t0005g0153 others(3): Show |
6 | HG01081.hp2 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+13G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695017 | |||||||
chr7:16695062 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0004g0318 |
2 | HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.822+58G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695062 | |||||||
chr7:16695063 | C | T | 1 | a0001c0001t0002g0368 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.822+59C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695063 | |||||||
chr7:16695112 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.822+108T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695112 | |||||||
chr7:16695120 | G | A | 164 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0019 others(161): Show |
167 | HG00140.hp1 HG00544.hp1 HG00597.hp1 others(164): Show |
intron_variant | MODIFIER | c.822+116G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695120 | |||||||
chr7:16695266 | A | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(156): Show |
162 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.822+262A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695266 | |||||||
chr7:16695282 | A | T | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.822+278A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695282 | |||||||
chr7:16695347 | G | T | 1 | a0001c0004t0002g0299 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.822+343G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695347 | |||||||
chr7:16695514 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.822+510T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695514 | |||||||
chr7:16695536 | A | G | 6 | a0001c0001t0001g0130 a0001c0001t0001g0167 a0001c0001t0001g0175 others(3): Show |
6 | HG02523.hp2 NA18747.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.822+532A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695536 | |||||||
chr7:16695617 | C | CT | 9 | a0001c0001t0001g0185 a0001c0001t0001g0248 a0001c0001t0001g0273 others(6): Show |
9 | HG01074.hp2 HG02615.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.822+621dupT | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 16695617 | ||||||
chr7:16695646 | G | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(229): Show |
238 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(235): Show |
intron_variant | MODIFIER | c.822+642G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695646 | |||||||
chr7:16695697 | A | G | 1 | a0001c0002t0003g0281 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.822+693A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695697 | |||||||
chr7:16695705 | C | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0021 others(49): Show |
53 | HG00140.hp1 HG00597.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.822+701C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695705 | |||||||
chr7:16695713 | C | T | 3 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0001t0002g0387 |
3 | HG01243.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.822+709C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695713 | |||||||
chr7:16695923 | T | G | 347 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(344): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.822+919T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695923 | |||||||
chr7:16695961 | T | C | 320 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(317): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.823-954T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695961 | |||||||
chr7:16695971 | G | A | 1 | a0001c0001t0002g0400 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.823-944G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695971 | |||||||
chr7:16695972 | T | C | 20 | a0001c0001t0001g0016 a0001c0001t0001g0154 a0001c0001t0001g0156 others(17): Show |
21 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.823-943T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16695972 | |||||||
chr7:16696035 | C | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0250 a0001c0001t0002g0073 |
3 | HG00423.hp2 HG02135.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.823-880C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696035 | |||||||
chr7:16696041 | C | T | 4 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0001t0002g0387 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-874C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696041 | |||||||
chr7:16696114 | T | G | 4 | a0001c0001t0001g0169 a0001c0001t0002g0335 a0001c0002t0002g0322 others(1): Show |
4 | HG01884.hp2 NA18522.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.823-801T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696114 | |||||||
chr7:16696135 | G | C | 5 | a0001c0001t0001g0017 a0001c0001t0001g0161 a0001c0001t0001g0168 others(2): Show |
6 | HG02486.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.823-780G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696135 | |||||||
chr7:16696138 | AG | A | 8 | a0001c0001t0001g0234 a0001c0001t0001g0243 a0001c0001t0001g0244 others(5): Show |
8 | NA18945.hp1 NA18956.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.823-774delG | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 16696138 | ||||||
chr7:16696141 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0022 others(115): Show |
123 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.823-774G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696141 | |||||||
chr7:16696157 | C | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0032 others(73): Show |
80 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.823-758C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696157 | |||||||
chr7:16696178 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.823-737G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696178 | |||||||
chr7:16696191 | G | A | 24 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0032 others(21): Show |
24 | HG00099.hp2 HG00558.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.823-724G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696191 | |||||||
chr7:16696192 | A | C | 230 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0017 others(227): Show |
238 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.823-723A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696192 | |||||||
chr7:16696199 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.823-716T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696199 | |||||||
chr7:16696207 | T | C | 6 | a0001c0001t0002g0289 a0001c0001t0002g0324 a0001c0001t0002g0335 others(3): Show |
6 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.823-708T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696207 | |||||||
chr7:16696268 | T | C | 1 | a0001c0001t0001g0263 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.823-647T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696268 | |||||||
chr7:16696388 | A | G | 4 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0001t0002g0387 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-527A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696388 | |||||||
chr7:16696436 | A | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0110 others(50): Show |
55 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(52): Show |
intron_variant | MODIFIER | c.823-479A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696436 | |||||||
chr7:16696542 | T | C | 4 | a0001c0001t0001g0187 a0001c0001t0001g0205 a0001c0001t0001g0254 others(1): Show |
4 | NA18972.hp1 NA18978.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.823-373T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696542 | |||||||
chr7:16696544 | G | GA | 115 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0023 others(112): Show |
117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.823-371_823-370ins others(1): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696544 | |||||||
chr7:16696561 | G | T | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.823-354G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696561 | |||||||
chr7:16696718 | T | TA | 42 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0115 others(39): Show |
43 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.823-192dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 16696718 | ||||||
chr7:16696720 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0017 others(128): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.823-195A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696720 | |||||||
chr7:16696754 | T | C | 1 | a0001c0001t0001g0258 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.823-161T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696754 | |||||||
chr7:16696780 | T | C | 1 | a0001c0001t0001g0252 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.823-135T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696780 | |||||||
chr7:16696853 | G | A | 26 | a0001c0001t0001g0033 a0001c0001t0001g0161 a0001c0001t0001g0168 others(23): Show |
27 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.823-62G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696853 | |||||||
chr7:16696854 | C | G | 182 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(179): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.823-61C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 8/11 | chr7 | 16696854 | |||||||
chr7:16697113 | T | TTTTG | 27 | a0001c0001t0001g0017 a0001c0001t0001g0154 a0001c0001t0001g0156 others(24): Show |
28 | HG01074.hp2 HG01109.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.969+73_969+76dupTT others(2): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr7 | 16697113 | ||||||
chr7:16697265 | T | G | 107 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(104): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.969+204T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697265 | |||||||
chr7:16697288 | G | A | 5 | a0001c0001t0001g0189 a0001c0001t0001g0246 a0001c0001t0001g0247 others(2): Show |
5 | HG00609.hp2 HG02071.hp1 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.969+227G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697288 | |||||||
chr7:16697299 | C | G | 3 | a0001c0001t0002g0331 a0001c0001t0002g0333 a0001c0001t0002g0338 |
3 | HG01109.hp1 HG02258.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.969+238C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697299 | |||||||
chr7:16697361 | A | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0176 a0001c0001t0001g0183 others(16): Show |
19 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+300A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697361 | |||||||
chr7:16697377 | A | T | 19 | a0001c0001t0001g0033 a0001c0001t0001g0176 a0001c0001t0001g0183 others(16): Show |
19 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.969+316A>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697377 | |||||||
chr7:16697487 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.969+426C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697487 | |||||||
chr7:16697710 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.970-338C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697710 | |||||||
chr7:16697995 | G | T | 5 | a0001c0001t0003g0282 a0001c0002t0002g0293 a0001c0002t0002g0322 others(2): Show |
5 | HG01884.hp2 HG02572.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.970-53G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 9/11 | chr7 | 16697995 | |||||||
chr7:16698363 | G | A | 1 | a0001c0001t0010g0399 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1108+177G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698363 | |||||||
chr7:16698374 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1108+188G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698374 | |||||||
chr7:16698381 | T | C | 99 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(96): Show |
102 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.1108+195T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698381 | |||||||
chr7:16698414 | A | G | 8 | a0001c0001t0001g0162 a0001c0001t0002g0319 a0001c0001t0002g0325 others(5): Show |
8 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108+228A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698414 | |||||||
chr7:16698454 | A | G | 44 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0033 others(41): Show |
45 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.1108+268A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698454 | |||||||
chr7:16698460 | A | C | 5 | a0001c0001t0001g0256 a0001c0001t0002g0050 a0001c0001t0002g0355 others(2): Show |
5 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108+274A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698460 | |||||||
chr7:16698670 | A | G | 37 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0033 others(34): Show |
38 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1108+484A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698670 | |||||||
chr7:16698671 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1108+485G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698671 | |||||||
chr7:16698776 | A | G | 1 | a0001c0001t0002g0319 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1108+590A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16698776 | |||||||
chr7:16699292 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1108+1106T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699292 | |||||||
chr7:16699322 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1108+1136A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699322 | |||||||
chr7:16699469 | C | T | 56 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0025 others(53): Show |
64 | HG00544.hp2 HG00597.hp1 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.1108+1283C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699469 | |||||||
chr7:16699538 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1108+1352G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699538 | |||||||
chr7:16699592 | C | T | 1 | a0001c0001t0002g0049 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1108+1406C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699592 | |||||||
chr7:16699696 | A | C | 1 | a0001c0001t0002g0292 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1108+1510A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699696 | |||||||
chr7:16699725 | A | G | 275 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(272): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.1108+1539A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699725 | |||||||
chr7:16699784 | G | A | 5 | a0001c0001t0001g0162 a0001c0001t0002g0319 a0001c0001t0002g0326 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108+1598G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699784 | |||||||
chr7:16699859 | T | C | 1 | a0001c0001t0002g0329 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1108+1673T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699859 | |||||||
chr7:16699946 | A | G | 1 | a0001c0001t0001g0184 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1108+1760A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16699946 | |||||||
chr7:16700078 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1108+1892T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700078 | |||||||
chr7:16700308 | G | A | 5 | a0001c0001t0001g0195 a0001c0001t0002g0001 a0001c0001t0002g0076 others(2): Show |
8 | HG00642.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108+2122G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700308 | |||||||
chr7:16700344 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1108+2158T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700344 | |||||||
chr7:16700422 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0002g0375 |
2 | NA19004.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1108+2236T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700422 | |||||||
chr7:16700476 | G | A | 268 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(265): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.1108+2290G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700476 | |||||||
chr7:16700517 | A | G | 1 | a0001c0001t0002g0394 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1108+2331A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700517 | |||||||
chr7:16700759 | A | G | 13 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0284 others(10): Show |
14 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1108+2573A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700759 | |||||||
chr7:16700824 | G | A | 3 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0007t0002g0336 |
3 | HG01243.hp2 HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1108+2638G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700824 | |||||||
chr7:16700929 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(101): Show |
107 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.1108+2743A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16700929 | |||||||
chr7:16701077 | A | G | 4 | a0001c0001t0001g0164 a0001c0001t0001g0284 a0001c0001t0002g0014 others(1): Show |
5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1108+2891A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701077 | |||||||
chr7:16701526 | A | G | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1109-3021A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701526 | |||||||
chr7:16701530 | C | G | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1109-3017C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701530 | |||||||
chr7:16701655 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(100): Show |
106 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.1109-2892T>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701655 | |||||||
chr7:16701659 | C | CTA | 6 | a0001c0001t0001g0256 a0001c0001t0002g0050 a0001c0001t0002g0355 others(3): Show |
6 | HG00099.hp2 HG00735.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109-2888_1109-288 others(6): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701659 | |||||||
chr7:16701850 | A | C | 1 | a0001c0001t0001g0259 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1109-2697A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16701850 | |||||||
chr7:16702075 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1109-2472C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702075 | |||||||
chr7:16702391 | C | A | 20 | a0001c0001t0001g0017 a0001c0001t0001g0154 a0001c0001t0001g0156 others(17): Show |
20 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1109-2156C>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702391 | |||||||
chr7:16702419 | C | T | 3 | a0001c0001t0002g0332 a0001c0001t0002g0373 a0001c0007t0002g0336 |
3 | HG01243.hp2 HG02055.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1109-2128C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702419 | |||||||
chr7:16702507 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1109-2040G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702507 | |||||||
chr7:16702510 | C | T | 3 | a0001c0001t0002g0320 a0001c0001t0002g0386 a0001c0003t0002g0321 |
3 | HG02145.hp1 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1109-2037C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702510 | |||||||
chr7:16702606 | T | C | 21 | a0001c0001t0001g0017 a0001c0001t0001g0154 a0001c0001t0001g0156 others(18): Show |
21 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.1109-1941T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702606 | |||||||
chr7:16702840 | T | C | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1109-1707T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702840 | |||||||
chr7:16702996 | G | A | 4 | a0001c0001t0002g0332 a0001c0001t0002g0335 a0001c0001t0002g0373 others(1): Show |
4 | HG01243.hp2 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-1551G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16702996 | |||||||
chr7:16703114 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1109-1433C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703114 | |||||||
chr7:16703230 | C | T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0284 a0001c0001t0002g0014 others(1): Show |
5 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1109-1317C>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703230 | |||||||
chr7:16703332 | A | G | 1 | a0001c0001t0007g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1109-1215A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703332 | |||||||
chr7:16703571 | T | C | 1 | a0001c0001t0002g0390 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1109-976T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703571 | |||||||
chr7:16703865 | C | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0165 a0001c0001t0002g0084 others(3): Show |
6 | HG01952.hp2 HG02602.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1109-682C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16703865 | |||||||
chr7:16704090 | T | C | 3 | a0001c0001t0002g0004 a0001c0001t0002g0053 a0001c0001t0002g0357 |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.1109-457T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16704090 | |||||||
chr7:16704413 | G | C | 1 | a0001c0001t0004g0315 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1109-134G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16704413 | |||||||
chr7:16704528 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1109-19C>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 10/11 | chr7 | 16704528 | |||||||
chr7:16704746 | G | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0245 |
2 | HG02040.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1231+77G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704746 | |||||||
chr7:16704791 | G | T | 1 | a0001c0001t0001g0132 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1231+122G>T | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704791 | |||||||
chr7:16704800 | A | C | 1 | a0001c0001t0001g0097 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1231+131A>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704800 | |||||||
chr7:16704884 | T | G | 2 | a0001c0001t0002g0400 a0001c0001t0010g0399 |
2 | HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1231+215T>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16704884 | |||||||
chr7:16705144 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(93): Show |
99 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.1231+475G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705144 | |||||||
chr7:16705236 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1231+567G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705236 | |||||||
chr7:16705258 | G | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0154 a0001c0001t0001g0156 others(17): Show |
20 | HG01074.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1231+589G>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705258 | |||||||
chr7:16705307 | AAG | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0022 others(92): Show |
98 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.1231+640_1231+641d others(4): Show |
BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 16705307 | ||||||
chr7:16705457 | G | A | 1 | a0001c0001t0002g0368 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1232-603G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705457 | |||||||
chr7:16705610 | A | G | 330 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(327): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1232-450A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705610 | |||||||
chr7:16705684 | C | CA | 30 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0021 others(27): Show |
30 | HG00738.hp1 HG01074.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1232-358dupA | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr7 | 16705684 | ||||||
chr7:16705746 | A | G | 1 | a0001c0003t0002g0295 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1232-314A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705746 | |||||||
chr7:16705803 | A | G | 7 | a0001c0001t0001g0162 a0001c0001t0002g0319 a0001c0001t0002g0331 others(4): Show |
7 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1232-257A>G | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705803 | |||||||
chr7:16705939 | G | A | 18 | a0001c0001t0001g0018 a0001c0001t0001g0161 a0001c0001t0001g0176 others(15): Show |
18 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1232-121G>A | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705939 | |||||||
chr7:16705964 | T | C | 204 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0016 others(201): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.1232-96T>C | BZW2 | ENSG00000136261.16 | transcript | ENST00000258761.8 | protein_coding | 11/11 | chr7 | 16705964 |