Item | Value |
---|---|
geneid | 5676 |
ensemblid | ENSG00000221878.13 |
hgncid | 9524 |
symbol | PSG7 |
name | pregnancy specific beta-1-glycoprotein 7 |
refseq_nuc | NM_002783.3 |
refseq_prot | NP_002774.2 |
ensembl_nuc | ENST00000406070.7 |
ensembl_prot | ENSP00000421986.1 |
mane_status | MANE Select |
chr | chr19 |
start | 42924132 |
end | 42937207 |
strand | - |
ver | v1.2 |
region | chr19:42924132-42937207 |
region5000 | chr19:42919132-42942207 |
regionname0 | PSG7_chr19_42924132_42937207 |
regionname5000 | PSG7_chr19_42919132_42942207 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 97 | 374 | 75 | 65 | 184 | 11 | 38 | 148 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(92): Show |
chr19 | 42919132 | 42942207 |
a0002 | 0/0 | 419 | 31 | 8 | 12 | 2 | 3 | 6 | 2 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(414): Show |
chr19 | 42919132 | 42942207 |
a0003 | 0/0 | 419 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(414): Show |
chr19 | 42919132 | 42942207 |
a0004 | 1/0 | 419 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(414): Show |
chr19 | 42919132 | 42942207 |
a0005 | 0/0 | 97 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(92): Show |
chr19 | 42919132 | 42942207 |
a0006 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(414): Show |
chr19 | 42919132 | 42942207 |
a0007 | 0/0 | 419 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(414): Show |
chr19 | 42919132 | 42942207 |
a0008 | 0/0 | 97 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(92): Show |
chr19 | 42919132 | 42942207 |
a0009 | 0/0 | 33 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MFFYL others(28): Show |
chr19 | 42919132 | 42942207 |
a0010 | 0/0 | 97 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | MGPLS others(92): Show |
chr19 | 42919132 | 42942207 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0000 | 0/0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 | |||
a0001c0001 | 0/1 | 1257 | 223 | 31 | 50 | 114 | 8 | 19 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0002 | 0/0 | 1257 | 108 | 23 | 13 | 54 | 3 | 15 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0004 | 0/0 | 1257 | 9 | 0 | 0 | 9 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0005 | 0/0 | 1257 | 6 | 1 | 0 | 1 | 0 | 4 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0006 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0007 | 0/0 | 1257 | 4 | 0 | 0 | 4 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0009 | 0/0 | 1257 | 3 | 2 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0010 | 0/0 | 1257 | 3 | 3 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0011 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0012 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0013 | 0/0 | 1257 | 2 | 1 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0014 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0020 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0021 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0022 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0023 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0001c0024 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0002c0003 | 0/0 | 1257 | 29 | 6 | 12 | 2 | 3 | 6 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0002c0015 | 0/0 | 1257 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0003c0008 | 0/0 | 1257 | 4 | 4 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0004c0019 | 1/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0005c0018 | 0/0 | 1257 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0006c0026 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0007c0025 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0008c0017 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 | ||
a0009c0028 | 0/0 | 1193 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | CATCA others(1188): Show |
chr19 | 42919132 | 42942207 | ||
a0010c0027 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | ATGGG others(1252): Show |
chr19 | 42919132 | 42942207 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0000t0000 | 0/0 | 0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 | |
a0001c0001t0001 | 0/1 | 2067 | 214 | 30 | 48 | 109 | 8 | 18 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0001t0002 | 0/0 | 2067 | 3 | 0 | 0 | 3 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0001t0006 | 0/0 | 2067 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0001t0007 | 0/0 | 2067 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0001t0008 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0001t0009 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0001t0011 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0001t0012 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0002t0002 | 0/0 | 2067 | 107 | 23 | 13 | 54 | 3 | 14 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0002t0010 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0004t0002 | 0/0 | 2067 | 9 | 0 | 0 | 9 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0005t0002 | 0/0 | 2067 | 6 | 1 | 0 | 1 | 0 | 4 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0006t0001 | 0/0 | 2067 | 4 | 4 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0007t0002 | 0/0 | 2067 | 4 | 0 | 0 | 4 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0009t0002 | 0/0 | 2067 | 3 | 2 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0010t0002 | 0/0 | 2067 | 3 | 3 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0011t0002 | 0/0 | 2067 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0012t0001 | 0/0 | 2067 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0013t0001 | 0/0 | 2067 | 2 | 1 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0014t0002 | 0/0 | 2067 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0020t0002 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0021t0002 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0022t0001 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0023t0001 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0001c0024t0001 | 0/0 | 2067 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0002c0003t0003 | 0/0 | 2067 | 29 | 6 | 12 | 2 | 3 | 6 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0002c0015t0004 | 0/0 | 2067 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0003c0008t0002 | 0/0 | 2067 | 4 | 4 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0004c0019t0001 | 1/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0005c0018t0001 | 0/0 | 2067 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0006c0026t0002 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0007c0025t0002 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0008c0017t0002 | 0/0 | 2067 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
a0009c0028t0013 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | CATCA others(1867): Show |
chr19 | 42919132 | 42942207 |
a0010c0027t0002 | 0/0 | 2067 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | AGAAG others(2062): Show |
chr19 | 42919132 | 42942207 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0000t0000g0000 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0001 | 0/0 | 37 | 5 | 8 | 18 | 1 | 5 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0005 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0006 | 0/0 | 9 | 2 | 3 | 1 | 3 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0007 | 0/0 | 8 | 0 | 1 | 4 | 1 | 2 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 1 | 0 | 5 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0013 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0014 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0015 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0027 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0028 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0029 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0053 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0055 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0060 | 0/1 | 2 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0007g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0008g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0011g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0001t0012g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0002 | 0/0 | 21 | 0 | 8 | 12 | 1 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0003 | 0/0 | 12 | 0 | 1 | 6 | 1 | 4 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0004 | 0/0 | 10 | 9 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0021 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0002t0010g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0004t0002g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0004t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0004t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0004t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0004t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0005t0002g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0005t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0005t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0005t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0005t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0006t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0006t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0007t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0009t0002g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0009t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0010t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0011t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0011t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0012t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0013t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0013t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0014t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0014t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0020t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0021t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0022t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0023t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0001c0024t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0010 | 0/0 | 5 | 0 | 1 | 1 | 2 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0024 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0033 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0003t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0002c0015t0004g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0003c0008t0002g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0003c0008t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0003c0008t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0004c0019t0001g0123 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0005c0018t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0006c0026t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0007c0025t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0008c0017t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0009c0028t0013g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
a0010c0027t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | GBR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00140 | hp1 | a0002 | c0003 | t0003 | g0033 | EUR | GBR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00140 | hp2 | a0001 | c0002 | t0002 | g0003 | EUR | GBR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00544 | hp1 | a0001 | c0001 | t0008 | g0164 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0096 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00639 | hp2 | a0002 | c0003 | t0003 | g0080 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00642 | hp1 | a0002 | c0003 | t0003 | g0070 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00673 | hp2 | a0001 | c0004 | t0002 | g0040 | EAS | CHS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00738 | hp1 | a0001 | c0009 | t0002 | g0030 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01070 | hp2 | a0002 | c0003 | t0003 | g0034 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01071 | hp1 | a0002 | c0003 | t0003 | g0034 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01099 | hp1 | a0001 | c0013 | t0001 | g0177 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01106 | hp1 | a0001 | c0001 | t0007 | g0115 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0205 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01168 | hp1 | a0002 | c0003 | t0003 | g0072 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01243 | hp2 | a0002 | c0003 | t0003 | g0032 | AMR | PUR | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0090 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01256 | hp2 | a0001 | c0002 | t0002 | g0021 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01433 | hp1 | a0002 | c0003 | t0003 | g0071 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01515 | hp1 | a0002 | c0003 | t0003 | g0010 | EUR | IBS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01517 | hp2 | a0002 | c0003 | t0003 | g0010 | EUR | IBS | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01884 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01891 | hp1 | a0001 | c0009 | t0002 | g0063 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01928 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01978 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01978 | hp2 | a0002 | c0003 | t0003 | g0068 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01981 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01981 | hp2 | a0005 | c0018 | t0001 | g0153 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01993 | hp1 | a0002 | c0003 | t0003 | g0069 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02015 | hp1 | a0001 | c0004 | t0002 | g0038 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02055 | hp2 | a0001 | c0011 | t0002 | g0091 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02056 | hp2 | a0001 | c0005 | t0002 | g0094 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02071 | hp1 | a0001 | c0004 | t0002 | g0118 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02148 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02155 | hp1 | a0001 | c0004 | t0002 | g0040 | EAS | CDX | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02155 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CDX | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02165 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CDX | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02273 | hp1 | a0002 | c0003 | t0003 | g0067 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02280 | hp1 | a0001 | c0010 | t0002 | g0020 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02451 | hp2 | a0003 | c0008 | t0002 | g0137 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02572 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02602 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02630 | hp2 | a0001 | c0006 | t0001 | g0026 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02647 | hp1 | a0001 | c0014 | t0002 | g0065 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0103 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02717 | hp1 | a0001 | c0012 | t0001 | g0036 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02723 | hp2 | a0001 | c0000 | t0000 | g0000 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02735 | hp2 | a0002 | c0003 | t0003 | g0066 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0121 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02818 | hp2 | a0001 | c0009 | t0002 | g0030 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02886 | hp1 | a0001 | c0011 | t0002 | g0139 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02886 | hp2 | a0001 | c0006 | t0001 | g0204 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02896 | hp1 | a0002 | c0015 | t0004 | g0051 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02896 | hp2 | a0003 | c0008 | t0002 | g0052 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02897 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02897 | hp2 | a0002 | c0015 | t0004 | g0051 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02922 | hp2 | a0001 | c0002 | t0002 | g0077 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02970 | hp1 | a0001 | c0014 | t0002 | g0064 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02970 | hp2 | a0002 | c0003 | t0003 | g0031 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02976 | hp2 | a0001 | c0002 | t0002 | g0104 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03017 | hp2 | a0002 | c0003 | t0003 | g0024 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03041 | hp1 | a0001 | c0010 | t0002 | g0020 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03041 | hp2 | a0002 | c0003 | t0003 | g0117 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03098 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03130 | hp1 | a0001 | c0021 | t0002 | g0120 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03130 | hp2 | a0001 | c0001 | t0009 | g0165 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03139 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03225 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03239 | hp2 | a0002 | c0003 | t0003 | g0033 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03453 | hp2 | a0002 | c0003 | t0003 | g0032 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03486 | hp1 | a0001 | c0005 | t0002 | g0113 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03490 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03491 | hp2 | a0002 | c0003 | t0003 | g0024 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03492 | hp2 | a0002 | c0003 | t0003 | g0024 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03516 | hp1 | a0003 | c0008 | t0002 | g0052 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03516 | hp2 | a0001 | c0002 | t0002 | g0105 | AFR | ESN | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03540 | hp1 | a0001 | c0002 | t0002 | g0023 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03669 | hp2 | a0001 | c0005 | t0002 | g0042 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03704 | hp1 | a0001 | c0001 | t0012 | g0214 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03710 | hp1 | a0008 | c0017 | t0002 | g0081 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0045 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03831 | hp2 | a0009 | c0028 | t0013 | g0219 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03834 | hp1 | a0001 | c0002 | t0002 | g0082 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0045 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03927 | hp1 | a0001 | c0002 | t0002 | g0109 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03927 | hp2 | a0001 | c0005 | t0002 | g0042 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03942 | hp1 | a0002 | c0003 | t0003 | g0010 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03942 | hp2 | a0001 | c0005 | t0002 | g0119 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04115 | hp1 | a0001 | c0005 | t0002 | g0095 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0003 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0035 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04204 | hp1 | a0001 | c0002 | t0010 | g0074 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04204 | hp2 | a0001 | c0002 | t0002 | g0122 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0083 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG04228 | hp2 | a0001 | c0002 | t0002 | g0035 | SAS | STU | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18522 | hp1 | a0002 | c0003 | t0003 | g0108 | AFR | YRI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | YRI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18747 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18906 | hp1 | a0001 | c0012 | t0001 | g0036 | AFR | YRI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18906 | hp2 | a0001 | c0010 | t0002 | g0020 | AFR | YRI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18940 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18941 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18946 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18948 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18961 | hp1 | a0001 | c0024 | t0001 | g0184 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18962 | hp2 | a0001 | c0001 | t0011 | g0213 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18964 | hp1 | a0001 | c0022 | t0001 | g0175 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18966 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18973 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18981 | hp1 | a0001 | c0004 | t0002 | g0039 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18981 | hp2 | a0001 | c0007 | t0002 | g0016 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18983 | hp1 | a0001 | c0004 | t0002 | g0041 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18986 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18990 | hp1 | a0001 | c0004 | t0002 | g0039 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18990 | hp2 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18991 | hp2 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18997 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18999 | hp2 | a0002 | c0003 | t0003 | g0073 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19000 | hp2 | a0001 | c0004 | t0002 | g0038 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19001 | hp1 | a0001 | c0007 | t0002 | g0016 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19011 | hp2 | a0002 | c0003 | t0003 | g0010 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19012 | hp1 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19012 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0093 | AFR | LWK | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19030 | hp2 | a0001 | c0006 | t0001 | g0026 | AFR | LWK | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19043 | hp1 | a0001 | c0006 | t0001 | g0026 | AFR | LWK | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19054 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0012 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19062 | hp1 | a0001 | c0002 | t0002 | g0098 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19065 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19066 | hp2 | a0001 | c0007 | t0002 | g0016 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19070 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19074 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19076 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19078 | hp1 | a0001 | c0004 | t0002 | g0041 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19079 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19083 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19084 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19088 | hp1 | a0001 | c0007 | t0002 | g0016 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19090 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19091 | hp1 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0022 | AFR | YRI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA19240 | hp2 | a0010 | c0027 | t0002 | g0138 | AFR | YRI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20129 | hp2 | a0003 | c0008 | t0002 | g0136 | AFR | ASW | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | TSI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0075 | EUR | TSI | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0021 | SAS | GIH | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | GIH | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01123 | hp1 | a0002 | c0003 | t0003 | g0107 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG01123 | hp2 | a0002 | c0003 | t0003 | g0010 | AMR | CLM | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02109 | hp1 | a0006 | c0026 | t0002 | g0134 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02486 | hp2 | a0001 | c0020 | t0002 | g0078 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02559 | hp1 | a0007 | c0025 | t0002 | g0135 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG02559 | hp2 | a0002 | c0003 | t0003 | g0079 | AFR | ACB | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0092 | AFR | MSL | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | USA | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
HG06807 | hp2 | a0001 | c0013 | t0001 | g0168 | AFR | USA | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20300 | hp1 | a0002 | c0003 | t0003 | g0031 | AFR | USA | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | USA | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA21309 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | LWK | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
NA21309 | hp2 | a0001 | c0023 | t0001 | g0116 | AFR | LWK | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0060 | REF | REF | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
homoSapiens | grch38p0 | a0004 | c0019 | t0001 | g0123 | REF | REF | PSG7_chr19_42919132_42942207 | PSG7 | chr19 | 42919132 | 42942207 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42924810 | A | G | 1 | a0001 | 1 | HG01167.hp2 | stop_lost | HIGH | c.1258T>C | p.Ter420Argext*? | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 1389/2067 | 1258/1260 | 420/419 | chr19 | 42924810 | |||
chr19:42925830 | C | G | 1 | a0001 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.1186G>C | p.Val396Leu | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/6 | 1317/2067 | 1186/1260 | 396/419 | chr19 | 42925830 | |||
chr19:42925892 | G | T | 1 | a0001 | 1 | NA18961.hp1 | stop_gained | HIGH | c.1124C>A | p.Ser375* | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/6 | 1255/2067 | 1124/1260 | 375/419 | chr19 | 42925892 | |||
chr19:42925908 | C | T | 1 | a0001 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1108G>A | p.Gly370Arg | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/6 | 1239/2067 | 1108/1260 | 370/419 | chr19 | 42925908 | |||
chr19:42925974 | G | C | 1 | a0001 | 3 | HG02280.hp1 HG03041.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.1042C>G | p.Gln348Glu | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/6 | 1173/2067 | 1042/1260 | 348/419 | chr19 | 42925974 | |||
chr19:42926016 | G | A | 1 | a0001 | 2 | HG02055.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.1000C>T | p.Leu334Phe | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/6 | 1131/2067 | 1000/1260 | 334/419 | chr19 | 42926016 | |||
chr19:42926486 | C | T | 2 | a0006 a0007 |
2 | HG02109.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.940G>A | p.Asp314Asn | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 1071/2067 | 940/1260 | 314/419 | chr19 | 42926486 | |||
chr19:42926560 | C | G | 1 | a0001 | 1 | NA18964.hp1 | missense_variant | MODERATE | c.866G>C | p.Arg289Pro | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 997/2067 | 866/1260 | 289/419 | chr19 | 42926560 | |||
chr19:42926620 | T | C | 1 | a0001 | 6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
missense_variant | MODERATE | c.806A>G | p.Tyr269Cys | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 937/2067 | 806/1260 | 269/419 | chr19 | 42926620 | |||
chr19:42926651 | T | C | 1 | a0006 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.775A>G | p.Thr259Ala | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 906/2067 | 775/1260 | 259/419 | chr19 | 42926651 | |||
chr19:42926674 | G | T | 1 | a0001 | 2 | HG02717.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.752C>A | p.Pro251His | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 883/2067 | 752/1260 | 251/419 | chr19 | 42926674 | |||
chr19:42926692 | G | A | 1 | a0001 | 2 | HG02055.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.734C>T | p.Thr245Ile | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 865/2067 | 734/1260 | 245/419 | chr19 | 42926692 | |||
chr19:42926716 | G | A | 1 | a0001 | 1 | HG03130.hp1 | missense_variant&splice_region_variant | MODERATE | c.710C>T | p.Pro237Leu | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 841/2067 | 710/1260 | 237/419 | chr19 | 42926716 | |||
chr19:42929535 | C | A | 1 | a0001 | 9 | HG00673.hp2 HG02015.hp1 HG02071.hp1 others(6): Show |
missense_variant | MODERATE | c.616G>T | p.Gly206Cys | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/6 | 747/2067 | 616/1260 | 206/419 | chr19 | 42929535 | |||
chr19:42929584 | C | A | 1 | a0001 | 7 | HG02056.hp2 HG03130.hp1 HG03486.hp1 others(4): Show |
missense_variant | MODERATE | c.567G>T | p.Met189Ile | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/6 | 698/2067 | 567/1260 | 189/419 | chr19 | 42929584 | |||
chr19:42935425 | G | A | 1 | a0001 | 2 | HG02647.hp1 HG02970.hp1 |
missense_variant | MODERATE | c.409C>T | p.Arg137Cys | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 540/2067 | 409/1260 | 137/419 | chr19 | 42935425 | |||
chr19:42935476 | A | G | 3 | a0003 a0006 a0007 |
6 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
missense_variant | MODERATE | c.358T>C | p.Tyr120His | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 489/2067 | 358/1260 | 120/419 | chr19 | 42935476 | |||
chr19:42935542 | G | A | 4 | a0001 a0005 a0008 others(1): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(372): Show |
stop_gained | HIGH | c.292C>T | p.Arg98* | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 423/2067 | 292/1260 | 98/419 | chr19 | 42935542 | |||
chr19:42935587 | T | C | 6 | a0002 a0003 a0006 others(3): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
missense_variant | MODERATE | c.247A>G | p.Ile83Val | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 378/2067 | 247/1260 | 83/419 | chr19 | 42935587 | |||
chr19:42935599 | C | T | 1 | a0005 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.235G>A | p.Val79Ile | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 366/2067 | 235/1260 | 79/419 | chr19 | 42935599 | |||
chr19:42935767 | A | G | 1 | a0008 | 1 | HG03710.hp1 | missense_variant&splice_region_variant | MODERATE | c.67T>C | p.Ser23Pro | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 198/2067 | 67/1260 | 23/419 | chr19 | 42935767 | |||
chr19:42935895 | CACACACA others(1510): Show |
C | 1 | a0009 | 1 | HG03831.hp2 | exon_loss_variant&splice_region_variant | HIGH | c.-336_65-127del | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/6 | chr19 | 42935895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42925810 | G | A | 4 | a0003c0008 a0006c0026 a0007c0025 others(1): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.1206C>T | p.Gly402Gly | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/6 | 1337/2067 | 1206/1260 | 402/419 | chr19 | 42925810 | |||
chr19:42926529 | A | G | 1 | a0001c0006 | 4 | HG02630.hp2 HG02886.hp2 NA19030.hp2 others(1): Show |
synonymous_variant | LOW | c.897T>C | p.Ser299Ser | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 1028/2067 | 897/1260 | 299/419 | chr19 | 42926529 | |||
chr19:42926544 | G | T | 1 | a0001c0013 | 2 | HG01099.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.882C>A | p.Ile294Ile | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 1013/2067 | 882/1260 | 294/419 | chr19 | 42926544 | |||
chr19:42926625 | C | T | 2 | a0001c0009 a0001c0010 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
synonymous_variant | LOW | c.801G>A | p.Glu267Glu | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/6 | 932/2067 | 801/1260 | 267/419 | chr19 | 42926625 | |||
chr19:42929653 | A | G | 18 | a0001c0002 a0001c0004 a0001c0005 others(15): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
synonymous_variant | LOW | c.498T>C | p.Ile166Ile | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/6 | 629/2067 | 498/1260 | 166/419 | chr19 | 42929653 | |||
chr19:42935579 | G | A | 1 | a0001c0007 | 4 | NA18981.hp2 NA19001.hp1 NA19066.hp2 others(1): Show |
synonymous_variant | LOW | c.255C>T | p.Asp85Asp | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 386/2067 | 255/1260 | 85/419 | chr19 | 42935579 | |||
chr19:42935657 | G | A | 1 | a0002c0015 | 2 | HG02896.hp1 HG02897.hp2 |
synonymous_variant | LOW | c.177C>T | p.Pro59Pro | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 308/2067 | 177/1260 | 59/419 | chr19 | 42935657 | |||
chr19:42935696 | G | A | 2 | a0002c0003 a0009c0028 |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
synonymous_variant | LOW | c.138C>T | p.Ser46Ser | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/6 | 269/2067 | 138/1260 | 46/419 | chr19 | 42935696 | |||
chr19:42937017 | G | A | 1 | a0001c0001 | 3 | NA18945.hp1 NA18972.hp1 NA19005.hp2 |
synonymous_variant | LOW | c.60C>T | p.Leu20Leu | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/6 | 191/2067 | 60/1260 | 20/419 | chr19 | 42937017 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42924226 | C | T | 1 | a0001c0001t0008 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*582G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 582 | chr19 | 42924226 | ||||||
chr19:42924246 | G | C | 3 | a0002c0003t0003 a0002c0015t0004 a0009c0028t0013 |
32 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*562C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 562 | chr19 | 42924246 | ||||||
chr19:42924256 | A | C | 1 | a0001c0002t0010 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*552T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 552 | chr19 | 42924256 | ||||||
chr19:42924360 | G | A | 1 | a0002c0015t0004 | 2 | HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*448C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 448 | chr19 | 42924360 | ||||||
chr19:42924434 | C | A | 1 | a0001c0001t0009 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*374G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 374 | chr19 | 42924434 | ||||||
chr19:42924573 | G | A | 20 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0010 others(17): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*235C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 235 | chr19 | 42924573 | ||||||
chr19:42924574 | C | T | 1 | a0001c0001t0007 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*234G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 234 | chr19 | 42924574 | ||||||
chr19:42924639 | T | C | 1 | a0001c0001t0011 | 1 | NA18962.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 169 | chr19 | 42924639 | ||||||
chr19:42924687 | G | A | 1 | a0001c0001t0012 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*121C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 6/6 | 121 | chr19 | 42924687 | ||||||
chr19:42937087 | C | T | 1 | a0001c0001t0001 | 1 | NA19068.hp2 | 5_prime_UTR_variant | MODIFIER | c.-11G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/6 | 11 | chr19 | 42937087 | ||||||
chr19:42937120 | G | A | 2 | a0001c0001t0001 a0001c0001t0009 |
8 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-44C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/6 | 44 | chr19 | 42937120 | ||||||
chr19:42937126 | A | G | 4 | a0003c0008t0002 a0006c0026t0002 a0007c0025t0002 others(1): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-50T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/6 | 50 | chr19 | 42937126 | ||||||
chr19:42937161 | C | T | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0002t0002 others(8): Show |
130 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(127): Show |
5_prime_UTR_variant | MODIFIER | c.-85G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/6 | 85 | chr19 | 42937161 | ||||||
chr19:42937176 | A | T | 1 | a0001c0002t0002 | 1 | NA19012.hp1 | 5_prime_UTR_variant | MODIFIER | c.-100T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/6 | 100 | chr19 | 42937176 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42924829 | A | AG | 31 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(28): Show |
47 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
splice_region_variant&intron_variant | LOW | c.1244-6dupC | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42924829 | |||||||
chr19:42924890 | G | A | 1 | a0001c0002t0002g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1244-66C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42924890 | |||||||
chr19:42924893 | T | A | 1 | a0001c0002t0002g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1244-69A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42924893 | |||||||
chr19:42924925 | C | T | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1244-101G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42924925 | |||||||
chr19:42924991 | T | A | 59 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(56): Show |
133 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1244-167A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42924991 | |||||||
chr19:42925040 | C | T | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1244-216G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925040 | |||||||
chr19:42925183 | A | G | 1 | a0001c0011t0002g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1244-359T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925183 | |||||||
chr19:42925184 | G | T | 1 | a0001c0011t0002g0139 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1244-360C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925184 | |||||||
chr19:42925235 | T | C | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1244-411A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925235 | |||||||
chr19:42925241 | G | C | 1 | a0001c0001t0001g0047 | 2 | HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1244-417C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925241 | |||||||
chr19:42925362 | A | G | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1243+411T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925362 | |||||||
chr19:42925380 | T | G | 1 | a0001c0001t0001g0146 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1243+393A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925380 | |||||||
chr19:42925426 | T | C | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1243+347A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925426 | |||||||
chr19:42925546 | A | G | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1243+227T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925546 | |||||||
chr19:42925644 | G | A | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.1243+129C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925644 | |||||||
chr19:42925755 | A | G | 2 | a0001c0004t0002g0039 a0001c0004t0002g0041 |
4 | NA18981.hp1 NA18983.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1243+18T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 5/5 | chr19 | 42925755 | |||||||
chr19:42926066 | G | A | 2 | a0001c0002t0002g0082 a0001c0002t0002g0109 |
2 | HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.989-39C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926066 | |||||||
chr19:42926079 | G | C | 1 | a0001c0001t0001g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.989-52C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926079 | |||||||
chr19:42926080 | C | T | 1 | a0001c0004t0002g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.989-53G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926080 | |||||||
chr19:42926293 | G | A | 93 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(90): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.988+145C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926293 | |||||||
chr19:42926311 | G | A | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.988+127C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926311 | |||||||
chr19:42926319 | A | C | 1 | a0001c0010t0002g0020 | 3 | HG02280.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.988+119T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926319 | |||||||
chr19:42926335 | A | T | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.988+103T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926335 | |||||||
chr19:42926346 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0183 |
2 | HG01943.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.988+92C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926346 | |||||||
chr19:42926429 | G | C | 1 | a0001c0001t0001g0166 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.988+9C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 4/5 | chr19 | 42926429 | |||||||
chr19:42926774 | C | T | 1 | a0001c0002t0010g0074 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.710-58G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926774 | |||||||
chr19:42926783 | A | T | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.710-67T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926783 | |||||||
chr19:42926785 | T | C | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.710-69A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926785 | |||||||
chr19:42926793 | G | A | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.710-77C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926793 | |||||||
chr19:42926813 | C | T | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-97G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926813 | |||||||
chr19:42926815 | T | G | 1 | a0001c0023t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.710-99A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926815 | |||||||
chr19:42926888 | C | T | 15 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0033 others(12): Show |
23 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.710-172G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926888 | |||||||
chr19:42926889 | T | G | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.710-173A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926889 | |||||||
chr19:42926954 | C | T | 93 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(90): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.710-238G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926954 | |||||||
chr19:42926990 | C | T | 1 | a0001c0004t0002g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.710-274G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926990 | |||||||
chr19:42926991 | G | A | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-275C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42926991 | |||||||
chr19:42927011 | C | T | 55 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(52): Show |
125 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.710-295G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927011 | |||||||
chr19:42927070 | G | T | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.710-354C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927070 | |||||||
chr19:42927088 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.710-372A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927088 | |||||||
chr19:42927138 | C | A | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.710-422G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927138 | |||||||
chr19:42927189 | C | T | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.710-473G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927189 | |||||||
chr19:42927203 | G | T | 93 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(90): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.710-487C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927203 | |||||||
chr19:42927255 | T | G | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.710-539A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927255 | |||||||
chr19:42927298 | T | A | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.710-582A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927298 | |||||||
chr19:42927300 | A | C | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.710-584T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927300 | |||||||
chr19:42927301 | A | G | 1 | a0001c0005t0002g0095 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.710-585T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927301 | |||||||
chr19:42927388 | A | C | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.710-672T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927388 | |||||||
chr19:42927407 | A | G | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.710-691T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927407 | |||||||
chr19:42927422 | T | C | 93 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(90): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.710-706A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927422 | |||||||
chr19:42927492 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0106 a0001c0012t0001g0036 |
5 | HG02055.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.710-776C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927492 | |||||||
chr19:42927547 | C | G | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-831G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927547 | |||||||
chr19:42927551 | T | A | 17 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(14): Show |
27 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.710-835A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927551 | |||||||
chr19:42927553 | G | C | 1 | a0001c0020t0002g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.710-837C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927553 | |||||||
chr19:42927558 | T | G | 7 | a0001c0001t0001g0190 a0003c0008t0002g0052 a0003c0008t0002g0136 others(4): Show |
8 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.710-842A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927558 | |||||||
chr19:42927575 | G | A | 2 | a0001c0001t0001g0180 a0001c0022t0001g0175 |
2 | NA18954.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.710-859C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927575 | |||||||
chr19:42927673 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.710-957G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927673 | |||||||
chr19:42927748 | G | T | 2 | a0003c0008t0002g0052 a0003c0008t0002g0137 |
3 | HG02451.hp2 HG02896.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.710-1032C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927748 | |||||||
chr19:42927772 | G | A | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.710-1056C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927772 | |||||||
chr19:42927804 | T | C | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.710-1088A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927804 | |||||||
chr19:42927843 | A | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.710-1127T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927843 | |||||||
chr19:42927865 | A | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(210): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.710-1149T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42927865 | |||||||
chr19:42928000 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.710-1284G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928000 | |||||||
chr19:42928040 | T | A | 1 | a0007c0025t0002g0135 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.710-1324A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928040 | |||||||
chr19:42928075 | C | CT | 4 | a0003c0008t0002g0052 a0003c0008t0002g0137 a0006c0026t0002g0134 others(1): Show |
5 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.710-1360dupA | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928075 | |||||||
chr19:42928086 | C | G | 2 | a0001c0009t0002g0030 a0001c0009t0002g0063 |
3 | HG00738.hp1 HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.709+1356G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928086 | |||||||
chr19:42928186 | A | G | 3 | a0002c0003t0003g0107 a0002c0003t0003g0108 a0002c0003t0003g0117 |
3 | HG01123.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.709+1256T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928186 | |||||||
chr19:42928206 | G | C | 1 | a0001c0013t0001g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.709+1236C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928206 | |||||||
chr19:42928350 | T | A | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+1092A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928350 | |||||||
chr19:42928371 | C | T | 7 | a0002c0015t0004g0051 a0003c0008t0002g0052 a0003c0008t0002g0136 others(4): Show |
9 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.709+1071G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928371 | |||||||
chr19:42928380 | T | G | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.709+1062A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928380 | |||||||
chr19:42928398 | A | C | 4 | a0001c0001t0001g0126 a0001c0002t0002g0105 a0001c0014t0002g0064 others(1): Show |
4 | HG02647.hp1 HG02970.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.709+1044T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928398 | |||||||
chr19:42928399 | T | G | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.709+1043A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928399 | |||||||
chr19:42928445 | A | G | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.709+997T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928445 | |||||||
chr19:42928452 | A | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.709+990T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928452 | |||||||
chr19:42928604 | C | A | 17 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(14): Show |
27 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.709+838G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928604 | |||||||
chr19:42928608 | A | C | 55 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(52): Show |
125 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.709+834T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928608 | |||||||
chr19:42928622 | A | G | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.709+820T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928622 | |||||||
chr19:42928667 | A | C | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.709+775T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928667 | |||||||
chr19:42928713 | G | A | 5 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(2): Show |
6 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+729C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928713 | |||||||
chr19:42928729 | T | C | 1 | a0001c0002t0002g0102 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.709+713A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928729 | |||||||
chr19:42928736 | C | T | 1 | a0001c0010t0002g0020 | 3 | HG02280.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.709+706G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928736 | |||||||
chr19:42928748 | C | A | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.709+694G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928748 | |||||||
chr19:42928760 | A | G | 10 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0150 others(7): Show |
13 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.709+682T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928760 | |||||||
chr19:42928775 | G | A | 2 | a0001c0013t0001g0168 a0001c0013t0001g0177 |
2 | HG01099.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.709+667C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928775 | |||||||
chr19:42928794 | C | T | 1 | a0001c0002t0002g0098 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.709+648G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928794 | |||||||
chr19:42928815 | G | T | 1 | a0001c0001t0001g0050 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.709+627C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928815 | |||||||
chr19:42928837 | G | A | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.709+605C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928837 | |||||||
chr19:42928904 | A | G | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.709+538T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42928904 | |||||||
chr19:42929030 | G | A | 1 | a0001c0001t0001g0176 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.709+412C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929030 | |||||||
chr19:42929131 | T | C | 1 | a0003c0008t0002g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.709+311A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929131 | |||||||
chr19:42929137 | C | T | 1 | a0003c0008t0002g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.709+305G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929137 | |||||||
chr19:42929162 | C | A | 1 | a0001c0002t0002g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.709+280G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929162 | |||||||
chr19:42929188 | T | C | 1 | a0002c0003t0003g0031 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.709+254A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929188 | |||||||
chr19:42929219 | C | A | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.709+223G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929219 | |||||||
chr19:42929283 | G | A | 1 | a0001c0020t0002g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.709+159C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929283 | |||||||
chr19:42929333 | A | C | 5 | a0001c0004t0002g0038 a0001c0004t0002g0039 a0001c0004t0002g0040 others(2): Show |
9 | HG00673.hp2 HG02015.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.709+109T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929333 | |||||||
chr19:42929369 | C | T | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.709+73G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929369 | |||||||
chr19:42929381 | G | A | 1 | a0001c0002t0002g0102 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.709+61C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929381 | |||||||
chr19:42929388 | G | A | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.709+54C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929388 | |||||||
chr19:42929418 | A | C | 85 | a0001c0001t0001g0114 a0001c0001t0002g0044 a0001c0001t0002g0097 others(82): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.709+24T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929418 | |||||||
chr19:42929441 | C | T | 1 | a0001c0002t0002g0099 | 1 | NA18951.hp1 | splice_donor_variant&intron_variant | HIGH | c.709+1G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 3/5 | chr19 | 42929441 | |||||||
chr19:42929727 | G | A | 2 | a0001c0002t0002g0088 a0001c0002t0002g0112 |
2 | NA18953.hp2 NA19077.hp2 |
splice_region_variant&intron_variant | LOW | c.431-7C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42929727 | |||||||
chr19:42929766 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0125 a0001c0001t0001g0181 others(1): Show |
13 | HG02015.hp2 HG02080.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.431-46G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42929766 | |||||||
chr19:42929805 | A | C | 1 | a0010c0027t0002g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.431-85T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42929805 | |||||||
chr19:42929889 | A | T | 1 | a0002c0003t0003g0067 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.431-169T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42929889 | |||||||
chr19:42929938 | G | A | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-218C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42929938 | |||||||
chr19:42929996 | T | C | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.431-276A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42929996 | |||||||
chr19:42930126 | T | A | 1 | a0001c0001t0001g0169 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.431-406A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930126 | |||||||
chr19:42930127 | T | G | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-407A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930127 | |||||||
chr19:42930173 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.431-453G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930173 | |||||||
chr19:42930234 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.431-514C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930234 | |||||||
chr19:42930284 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0006g0205 |
3 | HG00735.hp1 HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.431-564G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930284 | |||||||
chr19:42930289 | A | G | 9 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0028 others(6): Show |
25 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(22): Show |
intron_variant | MODIFIER | c.431-569T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930289 | |||||||
chr19:42930321 | G | T | 1 | a0001c0001t0001g0199 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.431-601C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930321 | |||||||
chr19:42930415 | T | G | 1 | a0001c0002t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.431-695A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930415 | |||||||
chr19:42930421 | G | C | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.431-701C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930421 | |||||||
chr19:42930427 | C | A | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.431-707G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930427 | |||||||
chr19:42930495 | A | T | 5 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(2): Show |
6 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-775T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930495 | |||||||
chr19:42930603 | T | C | 1 | a0002c0003t0003g0031 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.431-883A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930603 | |||||||
chr19:42930673 | C | T | 4 | a0001c0001t0001g0124 a0001c0002t0002g0011 a0001c0002t0002g0037 others(1): Show |
9 | HG01358.hp1 HG02129.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.431-953G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930673 | |||||||
chr19:42930707 | C | G | 85 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0027 others(82): Show |
170 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.431-987G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930707 | |||||||
chr19:42930717 | G | T | 1 | a0001c0002t0002g0086 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.431-997C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930717 | |||||||
chr19:42930816 | A | C | 1 | a0001c0022t0001g0175 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.431-1096T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930816 | |||||||
chr19:42930853 | C | T | 1 | a0010c0027t0002g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.431-1133G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930853 | |||||||
chr19:42930998 | G | A | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.431-1278C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42930998 | |||||||
chr19:42931000 | C | G | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.431-1280G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931000 | |||||||
chr19:42931121 | T | A | 1 | a0001c0001t0001g0014 | 5 | HG01069.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.431-1401A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931121 | |||||||
chr19:42931205 | T | A | 29 | a0001c0002t0002g0104 a0001c0002t0002g0105 a0002c0003t0003g0010 others(26): Show |
41 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.431-1485A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931205 | |||||||
chr19:42931243 | C | G | 2 | a0001c0002t0002g0086 a0001c0002t0002g0087 |
2 | NA18948.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.431-1523G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931243 | |||||||
chr19:42931248 | G | T | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-1528C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931248 | |||||||
chr19:42931274 | G | A | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.431-1554C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931274 | |||||||
chr19:42931334 | T | C | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.431-1614A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931334 | |||||||
chr19:42931349 | G | GA | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.431-1630dupT | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931349 | |||||||
chr19:42931361 | C | G | 1 | a0001c0012t0001g0036 | 2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.431-1641G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931361 | |||||||
chr19:42931381 | G | A | 1 | a0001c0002t0002g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431-1661C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931381 | |||||||
chr19:42931384 | A | G | 1 | a0001c0002t0002g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431-1664T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931384 | |||||||
chr19:42931392 | A | C | 1 | a0001c0002t0002g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431-1672T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931392 | |||||||
chr19:42931422 | A | G | 1 | a0001c0002t0002g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431-1702T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931422 | |||||||
chr19:42931426 | G | A | 1 | a0001c0002t0002g0089 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.431-1706C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931426 | |||||||
chr19:42931454 | A | T | 106 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0061 others(103): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.431-1734T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931454 | |||||||
chr19:42931612 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.431-1892A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931612 | |||||||
chr19:42931641 | G | A | 1 | a0001c0002t0002g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.431-1921C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931641 | |||||||
chr19:42931641 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.431-1921C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931641 | |||||||
chr19:42931657 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.431-1937C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931657 | |||||||
chr19:42931710 | G | T | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-1990C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931710 | |||||||
chr19:42931754 | G | A | 1 | a0002c0003t0003g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.431-2034C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931754 | |||||||
chr19:42931796 | T | G | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.431-2076A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931796 | |||||||
chr19:42931814 | C | T | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.431-2094G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931814 | |||||||
chr19:42931830 | T | A | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-2110A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931830 | |||||||
chr19:42931836 | A | G | 19 | a0001c0014t0002g0064 a0001c0014t0002g0065 a0002c0003t0003g0010 others(16): Show |
29 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.431-2116T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931836 | |||||||
chr19:42931890 | T | A | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.431-2170A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931890 | |||||||
chr19:42931890 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.431-2170A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931890 | |||||||
chr19:42931894 | T | TC | 3 | a0001c0001t0001g0025 a0001c0001t0001g0050 a0001c0001t0001g0143 |
6 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.431-2175dupG | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931894 | |||||||
chr19:42931894 | TC | T | 29 | a0001c0002t0002g0104 a0001c0002t0002g0105 a0002c0003t0003g0010 others(26): Show |
41 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.431-2175delG | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931894 | |||||||
chr19:42931898 | C | T | 13 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0061 others(10): Show |
18 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.431-2178G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931898 | |||||||
chr19:42931972 | A | C | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.431-2252T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931972 | |||||||
chr19:42931981 | T | C | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-2261A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931981 | |||||||
chr19:42931992 | A | G | 3 | a0002c0003t0003g0107 a0002c0003t0003g0108 a0002c0003t0003g0117 |
3 | HG01123.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.431-2272T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42931992 | |||||||
chr19:42932014 | C | G | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.431-2294G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932014 | |||||||
chr19:42932043 | A | T | 2 | a0001c0009t0002g0030 a0001c0009t0002g0063 |
3 | HG00738.hp1 HG01891.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.431-2323T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932043 | |||||||
chr19:42932050 | G | A | 1 | a0001c0001t0001g0215 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.431-2330C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932050 | |||||||
chr19:42932100 | T | C | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-2380A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932100 | |||||||
chr19:42932118 | G | A | 12 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0012 others(9): Show |
22 | HG00423.hp2 HG00544.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.431-2398C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932118 | |||||||
chr19:42932137 | C | T | 184 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.431-2417G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932137 | |||||||
chr19:42932141 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.431-2421T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932141 | |||||||
chr19:42932149 | G | A | 211 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.431-2429C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932149 | |||||||
chr19:42932150 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(207): Show |
401 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(398): Show |
intron_variant | MODIFIER | c.431-2430T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932150 | |||||||
chr19:42932215 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02071.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.431-2495C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932215 | |||||||
chr19:42932216 | G | A | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-2496C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932216 | |||||||
chr19:42932264 | T | A | 1 | a0001c0002t0002g0100 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.431-2544A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932264 | |||||||
chr19:42932270 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.431-2550C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932270 | |||||||
chr19:42932310 | G | A | 1 | a0001c0002t0002g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.431-2590C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932310 | |||||||
chr19:42932336 | C | T | 3 | a0001c0001t0001g0141 a0001c0001t0001g0160 a0001c0001t0006g0205 |
3 | HG00735.hp1 HG01167.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.431-2616G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932336 | |||||||
chr19:42932370 | A | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.431-2650T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932370 | |||||||
chr19:42932478 | A | G | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.431-2758T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932478 | |||||||
chr19:42932537 | T | G | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.431-2817A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932537 | |||||||
chr19:42932545 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0216 |
2 | HG01361.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.431-2825A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932545 | |||||||
chr19:42932580 | C | G | 2 | a0001c0011t0002g0091 a0001c0011t0002g0139 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.430+2824G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932580 | |||||||
chr19:42932591 | A | C | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.430+2813T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932591 | |||||||
chr19:42932682 | T | C | 1 | a0010c0027t0002g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.430+2722A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932682 | |||||||
chr19:42932777 | G | A | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.430+2627C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932777 | |||||||
chr19:42932982 | C | T | 1 | a0001c0001t0001g0019 | 4 | NA18959.hp2 NA18979.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2422G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42932982 | |||||||
chr19:42933128 | G | A | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+2276C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933128 | |||||||
chr19:42933136 | G | A | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+2268C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933136 | |||||||
chr19:42933160 | C | G | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+2244G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933160 | |||||||
chr19:42933265 | C | CTATATAT others(11): Show |
1 | a0002c0003t0003g0066 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.430+2138_430+2139i others(20): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933265 | |||||||
chr19:42933265 | CAATATAT others(11): Show |
C | 1 | a0002c0003t0003g0032 | 2 | HG01243.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.430+2121_430+2138d others(20): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933265 | |||||||
chr19:42933266 | A | AATATAT | 3 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0151 |
3 | HG02080.hp1 HG02280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.430+2132_430+2137d others(8): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | AATATATA others(3): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
12 | HG01069.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.430+2128_430+2137d others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | AATATATA others(5): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0049 a0001c0002t0002g0022 others(1): Show |
4 | NA18971.hp2 NA19084.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2126_430+2137d others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | AATATATA others(7): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0178 a0001c0001t0001g0179 others(2): Show |
5 | HG00438.hp1 HG01109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2124_430+2137d others(16): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0025 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.430+2122_430+2137d others(18): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | AATATATA others(11): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0130 others(2): Show |
6 | HG02293.hp1 HG03139.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+2120_430+2137d others(20): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0208 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.430+2118_430+2137d others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | AATATATA others(15): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0216 a0002c0003t0003g0107 |
3 | HG00738.hp2 HG01123.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.430+2116_430+2137d others(24): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | A | T | 16 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(13): Show |
25 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.430+2138T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | AAT | A | 3 | a0001c0001t0001g0014 a0001c0002t0002g0104 a0001c0005t0002g0094 |
3 | HG02056.hp2 HG02148.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.430+2136_430+2137d others(4): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | AATAT | A | 3 | a0001c0001t0001g0200 a0001c0001t0001g0210 a0001c0002t0002g0085 |
3 | HG01978.hp1 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.430+2134_430+2137d others(6): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | AATATATA others(1): Show |
A | 3 | a0001c0002t0002g0011 a0001c0014t0002g0064 a0001c0014t0002g0065 |
3 | HG02647.hp1 HG02970.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.430+2130_430+2137d others(10): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933266 | AATATATA others(3): Show |
A | 2 | a0001c0002t0002g0105 a0001c0009t0002g0030 |
3 | HG00738.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+2128_430+2137d others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933266 | |||||||
chr19:42933283 | ATATATAT others(22): Show |
A | 1 | a0001c0001t0001g0001 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.430+2092_430+2120d others(31): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933283 | |||||||
chr19:42933289 | A | T | 1 | a0001c0005t0002g0094 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.430+2115T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933289 | |||||||
chr19:42933290 | TATATATA others(10): Show |
T | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.430+2097_430+2113d others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933290 | |||||||
chr19:42933291 | A | T | 1 | a0001c0005t0002g0094 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.430+2113T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933291 | |||||||
chr19:42933293 | A | T | 4 | a0001c0002t0002g0110 a0001c0005t0002g0094 a0001c0009t0002g0063 others(1): Show |
4 | HG01891.hp1 HG02056.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2111T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933293 | |||||||
chr19:42933295 | A | T | 6 | a0001c0002t0002g0110 a0001c0005t0002g0094 a0001c0009t0002g0063 others(3): Show |
6 | HG01891.hp1 HG02056.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+2109T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933295 | |||||||
chr19:42933297 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0002g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.430+2106_430+2107i others(13): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933297 | |||||||
chr19:42933297 | A | ATTTTTTT others(5): Show |
1 | a0001c0002t0002g0096 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.430+2106_430+2107i others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933297 | |||||||
chr19:42933297 | A | T | 14 | a0001c0002t0002g0043 a0001c0002t0002g0085 a0001c0002t0002g0098 others(11): Show |
17 | HG01891.hp1 HG01978.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.430+2107T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933297 | |||||||
chr19:42933299 | A | ATTTTTTT others(3): Show |
1 | a0001c0002t0002g0004 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.430+2104_430+2105i others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933299 | |||||||
chr19:42933299 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0002g0004 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.430+2104_430+2105i others(13): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933299 | |||||||
chr19:42933299 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0002g0044 a0001c0002t0002g0012 |
3 | NA18983.hp2 NA18990.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.430+2104_430+2105i others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933299 | |||||||
chr19:42933299 | A | T | 23 | a0001c0001t0002g0097 a0001c0002t0002g0011 a0001c0002t0002g0012 others(20): Show |
26 | HG00423.hp2 HG00544.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.430+2105T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933299 | |||||||
chr19:42933301 | A | T | 28 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0004 others(25): Show |
38 | HG00423.hp2 HG00544.hp2 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.430+2103T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933301 | |||||||
chr19:42933303 | A | ATTT | 2 | a0001c0001t0001g0001 a0001c0002t0002g0003 |
3 | HG01515.hp2 NA18943.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.430+2100_430+2101i others(5): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933303 | |||||||
chr19:42933303 | A | ATTTTTTT others(3): Show |
1 | a0001c0002t0002g0004 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.430+2100_430+2101i others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933303 | |||||||
chr19:42933303 | A | T | 33 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0001t0012g0214 others(30): Show |
47 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.430+2101T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933303 | |||||||
chr19:42933305 | A | ATTTTTTT others(4): Show |
1 | a0001c0002t0002g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.430+2098_430+2099i others(13): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933305 | |||||||
chr19:42933305 | A | ATTTTTTT others(5): Show |
1 | a0001c0002t0002g0004 | 2 | HG01261.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.430+2098_430+2099i others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933305 | |||||||
chr19:42933305 | A | ATTTTTTT others(9): Show |
1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+2098_430+2099i others(18): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933305 | |||||||
chr19:42933305 | A | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0002g0044 others(38): Show |
58 | HG00423.hp2 HG00544.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.430+2099T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933305 | |||||||
chr19:42933307 | A | ATATATAT others(2): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0206 others(3): Show |
9 | HG00544.hp1 HG01261.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(11): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0126 others(6): Show |
11 | HG01943.hp2 HG02165.hp1 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(13): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0053 a0001c0001t0001g0114 |
4 | HG01255.hp1 HG01361.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(15): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(8): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0019 |
2 | NA19054.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(17): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0048 a0001c0001t0001g0215 others(1): Show |
4 | HG00099.hp2 NA19011.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0007 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(21): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0014 a0001c0001t0011g0213 a0001c0004t0002g0039 |
3 | HG02293.hp2 NA18962.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 |
3 | HG00597.hp1 HG01175.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0015 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(40): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(24): Show |
1 | a0001c0002t0002g0035 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(33): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(24): Show |
1 | a0001c0002t0002g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(33): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0008 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(27): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(28): Show |
1 | a0001c0002t0002g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(37): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0001 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0217 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(26): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(22): Show |
1 | a0001c0002t0002g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(31): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0008 a0001c0001t0001g0029 |
2 | HG04184.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0007 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(24): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0166 |
2 | HG00423.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0006 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(26): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0008 a0001c0002t0002g0003 |
2 | HG02735.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(20): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(12): Show |
1 | a0001c0002t0002g0003 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(21): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0133 |
2 | NA18995.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0028 a0001c0002t0002g0112 |
2 | HG02738.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(24): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0212 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(10): Show |
2 | a0001c0002t0002g0011 a0002c0003t0003g0067 |
2 | HG02273.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(13): Show |
2 | a0001c0002t0002g0002 a0001c0002t0002g0088 |
2 | NA18953.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(14): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0012t0001g0036 |
3 | HG01074.hp2 HG01517.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
2 | a0001c0002t0002g0003 a0001c0002t0002g0009 |
4 | HG02155.hp2 NA19003.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(17): Show |
1 | a0001c0002t0002g0009 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(26): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(18): Show |
1 | a0001c0002t0002g0003 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(27): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(23): Show |
1 | a0001c0001t0001g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(32): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(7): Show |
4 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0140 others(1): Show |
4 | HG00558.hp1 HG01109.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(16): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0005 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(17): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(9): Show |
1 | a0001c0004t0002g0118 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(18): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0202 a0001c0002t0002g0011 |
2 | HG03540.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0156 a0001c0002t0002g0003 |
3 | HG00323.hp1 HG00323.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(20): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(12): Show |
2 | a0001c0002t0002g0003 a0001c0002t0002g0011 |
2 | HG01243.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(21): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(13): Show |
2 | a0001c0002t0002g0002 a0001c0002t0002g0089 |
2 | HG02129.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0006 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(15): Show |
1 | a0001c0002t0002g0002 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(24): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
1 | a0001c0002t0002g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0002t0002g0086 |
3 | HG02129.hp2 NA18948.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(6): Show |
5 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(2): Show |
5 | HG02683.hp1 HG04184.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(15): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(7): Show |
3 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0143 |
3 | HG00642.hp2 HG01106.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(16): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0048 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(17): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0015 a0001c0002t0002g0002 a0001c0002t0002g0003 others(1): Show |
4 | HG00140.hp2 HG01192.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(18): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(10): Show |
1 | a0005c0018t0001g0153 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0006 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(20): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(12): Show |
2 | a0001c0002t0002g0009 a0001c0002t0002g0021 |
2 | HG01256.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(21): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(13): Show |
2 | a0001c0002t0002g0002 a0001c0002t0002g0021 |
2 | HG02300.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(15): Show |
2 | a0001c0005t0002g0095 a0001c0005t0002g0119 |
2 | HG03942.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(24): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
1 | a0001c0005t0002g0042 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(17): Show |
1 | a0001c0002t0002g0002 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(26): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(18): Show |
1 | a0001c0002t0002g0002 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(27): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(19): Show |
2 | a0001c0002t0002g0002 a0001c0007t0002g0016 |
4 | NA18966.hp1 NA18981.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(28): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(30): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0013 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0004t0002g0040 |
4 | HG00673.hp2 HG01433.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(13): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0008c0017t0002g0081 |
4 | HG03492.hp1 HG03669.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0001 a0001c0002t0002g0011 a0001c0006t0001g0204 |
3 | HG01358.hp2 HG02886.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(15): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0006 a0001c0001t0001g0028 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(16): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(9): Show |
1 | a0001c0012t0001g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(18): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(12): Show |
1 | a0001c0002t0002g0003 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(21): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(13): Show |
1 | a0001c0002t0002g0002 | 2 | HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(14): Show |
1 | a0001c0002t0002g0002 | 3 | HG01928.hp2 HG01981.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(16): Show |
2 | a0001c0002t0002g0002 a0001c0002t0002g0111 |
2 | HG00438.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0001 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0001 a0001c0002t0002g0037 |
4 | HG00735.hp2 HG02004.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+2096_430+2097i others(13): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(5): Show |
1 | a0001c0002t0002g0082 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(6): Show |
1 | a0001c0002t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(15): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(9): Show |
1 | a0003c0008t0002g0052 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(18): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(11): Show |
1 | a0001c0002t0002g0002 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(20): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(13): Show |
2 | a0001c0002t0002g0002 a0001c0005t0002g0113 |
2 | HG03486.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(14): Show |
1 | a0001c0002t0002g0002 | 2 | NA18955.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATAT others(15): Show |
2 | a0001c0002t0002g0002 a0001c0007t0002g0016 |
3 | HG02148.hp2 NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(24): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATTT others(3): Show |
1 | a0001c0002t0002g0003 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATTT others(5): Show |
1 | a0001c0001t0001g0006 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(14): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATTT others(8): Show |
1 | a0001c0002t0002g0002 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(17): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATATTT others(13): Show |
1 | a0001c0001t0001g0047 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.430+2096_430+2097i others(22): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATTTTT others(6): Show |
1 | a0001c0002t0002g0035 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(15): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATTTTT others(9): Show |
1 | a0003c0008t0002g0052 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.430+2096_430+2097i others(18): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATATTTTT others(10): Show |
3 | a0001c0002t0002g0012 a0001c0002t0002g0084 a0001c0005t0002g0042 |
3 | HG03927.hp2 NA18970.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.430+2096_430+2097i others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | ATTTTTTT others(3): Show |
1 | a0001c0002t0002g0004 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.430+2087_430+2096d others(12): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933307 | A | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(44): Show |
75 | HG00423.hp2 HG00544.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.430+2097T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933307 | |||||||
chr19:42933308 | T | TA | 5 | a0001c0001t0001g0061 a0001c0001t0001g0132 a0001c0001t0001g0150 others(2): Show |
6 | HG00639.hp2 HG02258.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(3): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATA | 4 | a0001c0001t0001g0076 a0001c0001t0001g0129 a0001c0001t0001g0194 others(1): Show |
4 | HG02109.hp2 NA18967.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(7): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA | 6 | a0001c0001t0001g0189 a0001c0001t0001g0193 a0001c0001t0001g0196 others(3): Show |
6 | HG01099.hp1 HG01975.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(9): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(2): Show |
4 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0002c0003t0003g0033 others(1): Show |
6 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(11): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(4): Show |
9 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0060 others(6): Show |
11 | HG01192.hp1 HG01433.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(13): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(6): Show |
9 | a0001c0001t0001g0056 a0001c0001t0001g0144 a0001c0001t0001g0188 others(6): Show |
11 | HG01978.hp2 HG02083.hp1 HG02132.hp2 others(8): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(15): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(8): Show |
8 | a0001c0001t0001g0055 a0001c0001t0001g0058 a0001c0001t0001g0146 others(5): Show |
10 | HG02135.hp1 HG02486.hp1 NA18953.hp1 others(7): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(17): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(10): Show |
5 | a0001c0001t0001g0054 a0001c0001t0001g0154 a0001c0001t0001g0155 others(2): Show |
6 | HG00597.hp2 HG02071.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(19): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(12): Show |
7 | a0001c0001t0001g0124 a0001c0001t0001g0148 a0001c0001t0001g0185 others(4): Show |
7 | HG01168.hp1 HG01358.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(21): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(14): Show |
3 | a0001c0001t0001g0172 a0001c0001t0001g0183 a0002c0003t0003g0070 |
3 | HG00642.hp1 NA19004.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.430+2095_430+2096i others(23): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(16): Show |
5 | a0001c0001t0001g0158 a0001c0001t0001g0180 a0001c0001t0001g0201 others(2): Show |
5 | HG01993.hp1 HG03041.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+2095_430+2096i others(25): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(18): Show |
1 | a0002c0003t0003g0079 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.430+2095_430+2096i others(27): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933308 | T | TATATATA others(26): Show |
1 | a0001c0001t0001g0157 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.430+2095_430+2096i others(35): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933308 | |||||||
chr19:42933309 | T | A | 10 | a0001c0001t0001g0130 a0001c0001t0001g0151 a0001c0001t0001g0178 others(7): Show |
14 | HG00438.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.430+2095A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933309 | |||||||
chr19:42933310 | T | A | 41 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(38): Show |
44 | HG00597.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.430+2094A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933310 | |||||||
chr19:42933311 | T | A | 3 | a0001c0001t0001g0208 a0001c0002t0002g0023 a0001c0020t0002g0078 |
5 | HG02486.hp2 HG02602.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+2093A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933311 | |||||||
chr19:42933312 | T | A | 27 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0076 others(24): Show |
28 | HG00597.hp2 HG01168.hp1 HG02071.hp2 others(25): Show |
intron_variant | MODIFIER | c.430+2092A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933312 | |||||||
chr19:42933313 | T | A | 1 | a0001c0020t0002g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430+2091A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933313 | |||||||
chr19:42933314 | T | A | 8 | a0001c0001t0001g0060 a0001c0001t0001g0132 a0001c0001t0001g0191 others(5): Show |
8 | HG03831.hp2 NA18967.hp1 NA19003.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+2090A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933314 | |||||||
chr19:42933315 | T | A | 1 | a0001c0020t0002g0078 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.430+2089A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933315 | |||||||
chr19:42933316 | T | A | 2 | a0001c0001t0001g0132 a0001c0001t0001g0195 |
2 | NA19003.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.430+2088A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933316 | |||||||
chr19:42933369 | A | T | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+2035T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933369 | |||||||
chr19:42933491 | T | A | 1 | a0001c0002t0002g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.430+1913A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933491 | |||||||
chr19:42933523 | G | A | 1 | a0001c0002t0002g0102 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.430+1881C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933523 | |||||||
chr19:42933599 | A | T | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+1805T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933599 | |||||||
chr19:42933616 | T | C | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+1788A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933616 | |||||||
chr19:42933631 | C | G | 4 | a0001c0001t0001g0159 a0001c0014t0002g0064 a0001c0014t0002g0065 others(1): Show |
5 | HG02647.hp1 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.430+1773G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933631 | |||||||
chr19:42933643 | C | A | 3 | a0002c0003t0003g0107 a0002c0003t0003g0108 a0002c0003t0003g0117 |
3 | HG01123.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.430+1761G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933643 | |||||||
chr19:42933643 | C | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+1761G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933643 | |||||||
chr19:42933644 | A | G | 4 | a0002c0003t0003g0107 a0002c0003t0003g0108 a0002c0003t0003g0117 others(1): Show |
5 | HG01123.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+1760T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933644 | |||||||
chr19:42933649 | A | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+1755T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933649 | |||||||
chr19:42933684 | G | C | 26 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(23): Show |
37 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.430+1720C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933684 | |||||||
chr19:42933760 | C | A | 1 | a0001c0001t0001g0196 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430+1644G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933760 | |||||||
chr19:42933761 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430+1643A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933761 | |||||||
chr19:42933832 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.430+1572T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933832 | |||||||
chr19:42933892 | G | T | 5 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(2): Show |
6 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+1512C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933892 | |||||||
chr19:42933901 | T | G | 1 | a0010c0027t0002g0138 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.430+1503A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933901 | |||||||
chr19:42933925 | C | T | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1479G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933925 | |||||||
chr19:42933961 | G | T | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+1443C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933961 | |||||||
chr19:42933980 | C | T | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.430+1424G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42933980 | |||||||
chr19:42934028 | T | C | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.430+1376A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934028 | |||||||
chr19:42934083 | C | T | 1 | a0001c0006t0001g0204 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.430+1321G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934083 | |||||||
chr19:42934147 | A | C | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.430+1257T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934147 | |||||||
chr19:42934149 | C | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+1255G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934149 | |||||||
chr19:42934207 | C | T | 1 | a0001c0002t0002g0075 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.430+1197G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934207 | |||||||
chr19:42934219 | T | C | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.430+1185A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934219 | |||||||
chr19:42934262 | A | T | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.430+1142T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934262 | |||||||
chr19:42934270 | C | G | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430+1134G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934270 | |||||||
chr19:42934273 | A | C | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+1131T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934273 | |||||||
chr19:42934280 | G | A | 1 | a0001c0002t0002g0084 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.430+1124C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934280 | |||||||
chr19:42934285 | C | T | 2 | a0001c0002t0002g0037 a0001c0004t0002g0038 |
4 | HG02015.hp1 NA18946.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.430+1119G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934285 | |||||||
chr19:42934291 | C | G | 1 | a0003c0008t0002g0136 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.430+1113G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934291 | |||||||
chr19:42934346 | G | C | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.430+1058C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934346 | |||||||
chr19:42934355 | G | C | 26 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(23): Show |
37 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.430+1049C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934355 | |||||||
chr19:42934452 | T | C | 1 | a0001c0002t0002g0103 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.430+952A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934452 | |||||||
chr19:42934460 | T | C | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.430+944A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934460 | |||||||
chr19:42934486 | A | C | 4 | a0001c0005t0002g0042 a0001c0005t0002g0094 a0001c0005t0002g0095 others(1): Show |
5 | HG02056.hp2 HG03669.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.430+918T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934486 | |||||||
chr19:42934543 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.430+861G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934543 | |||||||
chr19:42934598 | T | C | 103 | a0001c0001t0001g0027 a0001c0001t0001g0047 a0001c0001t0001g0061 others(100): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.430+806A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934598 | |||||||
chr19:42934652 | A | C | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.430+752T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934652 | |||||||
chr19:42934752 | G | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0197 |
2 | HG02083.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.430+652C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934752 | |||||||
chr19:42934753 | C | T | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.430+651G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934753 | |||||||
chr19:42934770 | C | G | 1 | a0001c0002t0002g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.430+634G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934770 | |||||||
chr19:42934772 | G | A | 1 | a0001c0002t0002g0090 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.430+632C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934772 | |||||||
chr19:42934865 | G | T | 114 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(111): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.430+539C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934865 | |||||||
chr19:42934866 | C | T | 114 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0027 others(111): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.430+538G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934866 | |||||||
chr19:42934903 | A | C | 1 | a0001c0002t0002g0093 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.430+501T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934903 | |||||||
chr19:42934929 | G | A | 20 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(17): Show |
30 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.430+475C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934929 | |||||||
chr19:42934951 | T | C | 10 | a0001c0001t0001g0027 a0001c0001t0001g0061 a0001c0001t0001g0150 others(7): Show |
13 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.430+453A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934951 | |||||||
chr19:42934961 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.430+443G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934961 | |||||||
chr19:42934984 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02717.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.430+420A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42934984 | |||||||
chr19:42935017 | G | T | 15 | a0001c0002t0002g0003 a0001c0002t0002g0035 a0001c0002t0002g0037 others(12): Show |
35 | HG00140.hp2 HG00673.hp2 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.430+387C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935017 | |||||||
chr19:42935024 | C | T | 1 | a0002c0003t0003g0031 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.430+380G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935024 | |||||||
chr19:42935037 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.430+367C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935037 | |||||||
chr19:42935086 | T | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0106 a0001c0001t0001g0133 |
4 | HG02055.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.430+318A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935086 | |||||||
chr19:42935086 | T | C | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+318A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935086 | |||||||
chr19:42935123 | G | A | 52 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(49): Show |
122 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.430+281C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935123 | |||||||
chr19:42935124 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0217 |
2 | HG03225.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.430+280G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935124 | |||||||
chr19:42935139 | T | C | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.430+265A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935139 | |||||||
chr19:42935194 | A | G | 2 | a0006c0026t0002g0134 a0007c0025t0002g0135 |
2 | HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.430+210T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935194 | |||||||
chr19:42935244 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.430+160A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935244 | |||||||
chr19:42935269 | A | C | 1 | a0001c0014t0002g0064 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430+135T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935269 | |||||||
chr19:42935276 | C | T | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+128G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935276 | |||||||
chr19:42935287 | G | A | 2 | a0001c0002t0002g0045 a0001c0002t0002g0122 |
3 | HG03831.hp1 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.430+117C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935287 | |||||||
chr19:42935309 | G | T | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG02071.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.430+95C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935309 | |||||||
chr19:42935317 | G | A | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.430+87C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935317 | |||||||
chr19:42935320 | C | G | 29 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0009 others(26): Show |
79 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.430+84G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935320 | |||||||
chr19:42935338 | T | C | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.430+66A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935338 | |||||||
chr19:42935368 | C | T | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.430+36G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935368 | |||||||
chr19:42935376 | C | A | 59 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(56): Show |
133 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.430+28G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 2/5 | chr19 | 42935376 | |||||||
chr19:42935812 | G | A | 6 | a0003c0008t0002g0052 a0003c0008t0002g0136 a0003c0008t0002g0137 others(3): Show |
7 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.65-43C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935812 | |||||||
chr19:42935818 | T | G | 27 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(24): Show |
39 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.65-49A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935818 | |||||||
chr19:42935851 | C | G | 55 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(52): Show |
125 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.65-82G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935851 | |||||||
chr19:42935873 | G | GAC | 15 | a0001c0001t0001g0053 a0001c0001t0001g0140 a0001c0001t0001g0141 others(12): Show |
16 | HG00558.hp1 HG00558.hp2 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.65-106_65-105dupGT | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | G | GACAC | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.65-108_65-105dupGT others(2): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | G | GACACAC | 11 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0203 others(8): Show |
15 | HG01167.hp2 HG01168.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.65-110_65-105dupGT others(4): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | G | GACACACA others(1): Show |
8 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0212 others(5): Show |
15 | HG00099.hp1 HG01074.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.65-112_65-105dupGT others(6): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | G | GACACACA others(3): Show |
1 | a0001c0001t0001g0218 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.65-114_65-105dupGT others(8): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | GAC | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0048 others(10): Show |
26 | HG00099.hp2 HG00438.hp2 HG00733.hp2 others(23): Show |
intron_variant | MODIFIER | c.65-106_65-105delGT | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | GACAC | G | 45 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0106 others(42): Show |
107 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.65-108_65-105delGT others(2): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | GACACAC | G | 13 | a0001c0001t0001g0076 a0001c0002t0002g0021 a0001c0002t0002g0022 others(10): Show |
23 | HG00639.hp2 HG01256.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.65-110_65-105delGT others(4): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | GACACACA others(1): Show |
G | 14 | a0001c0002t0002g0009 a0002c0003t0003g0010 a0002c0003t0003g0031 others(11): Show |
26 | HG00140.hp1 HG00642.hp1 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.65-112_65-105delGT others(6): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | GACACACA others(3): Show |
G | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.65-114_65-105delGT others(8): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935873 | GACACACA others(11): Show |
G | 3 | a0001c0009t0002g0030 a0001c0009t0002g0063 a0001c0010t0002g0020 |
6 | HG00738.hp1 HG01891.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.65-122_65-105delGT others(16): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935873 | |||||||
chr19:42935905 | CACACACA others(3): Show |
C | 1 | a0001c0001t0001g0007 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.65-146_65-137delTT others(8): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935905 | |||||||
chr19:42935914 | A | ACACAC | 3 | a0001c0001t0001g0049 a0001c0001t0001g0125 a0001c0001t0001g0131 |
3 | HG00738.hp2 NA18993.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.65-146_65-145insGT others(3): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935914 | |||||||
chr19:42935915 | A | C | 8 | a0001c0001t0001g0124 a0002c0015t0004g0051 a0003c0008t0002g0052 others(5): Show |
10 | HG01358.hp1 HG02109.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.65-146T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935915 | |||||||
chr19:42935917 | C | A | 2 | a0001c0002t0002g0121 a0010c0027t0002g0138 |
2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.65-148G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935917 | |||||||
chr19:42935917 | C | CACACACA others(1): Show |
4 | a0003c0008t0002g0136 a0003c0008t0002g0137 a0006c0026t0002g0134 others(1): Show |
4 | HG02109.hp1 HG02451.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.65-149_65-148insTT others(6): Show |
PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935917 | |||||||
chr19:42935943 | A | G | 1 | a0001c0002t0002g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.65-174T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42935943 | |||||||
chr19:42936104 | C | T | 1 | a0001c0002t0002g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65-335G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936104 | |||||||
chr19:42936108 | G | A | 1 | a0002c0003t0003g0070 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.65-339C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936108 | |||||||
chr19:42936181 | G | C | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.65-412C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936181 | |||||||
chr19:42936188 | C | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.65-419G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936188 | |||||||
chr19:42936258 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.65-489C>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936258 | |||||||
chr19:42936265 | C | T | 1 | a0001c0002t0002g0011 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.65-496G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936265 | |||||||
chr19:42936347 | T | C | 1 | a0001c0002t0002g0092 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.65-578A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936347 | |||||||
chr19:42936355 | G | C | 2 | a0001c0002t0002g0104 a0001c0002t0002g0105 |
2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.65-586C>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936355 | |||||||
chr19:42936422 | T | C | 1 | a0001c0001t0001g0019 | 2 | NA18959.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.64+591A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936422 | |||||||
chr19:42936433 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.64+580A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936433 | |||||||
chr19:42936451 | C | T | 2 | a0001c0011t0002g0091 a0001c0011t0002g0139 |
2 | HG02055.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.64+562G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936451 | |||||||
chr19:42936458 | T | G | 2 | a0001c0014t0002g0064 a0001c0014t0002g0065 |
2 | HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.64+555A>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936458 | |||||||
chr19:42936471 | T | A | 26 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(23): Show |
38 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.64+542A>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936471 | |||||||
chr19:42936473 | C | T | 1 | a0001c0002t0002g0004 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.64+540G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936473 | |||||||
chr19:42936545 | C | G | 1 | a0002c0003t0003g0031 | 2 | HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.64+468G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936545 | |||||||
chr19:42936552 | C | T | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+461G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936552 | |||||||
chr19:42936581 | C | T | 25 | a0002c0003t0003g0010 a0002c0003t0003g0024 a0002c0003t0003g0031 others(22): Show |
36 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.64+432G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936581 | |||||||
chr19:42936616 | C | A | 1 | a0001c0002t0002g0003 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.64+397G>T | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936616 | |||||||
chr19:42936637 | T | C | 1 | a0001c0002t0002g0002 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.64+376A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936637 | |||||||
chr19:42936670 | C | T | 4 | a0001c0002t0002g0022 a0001c0002t0002g0023 a0001c0002t0002g0077 others(1): Show |
8 | HG02451.hp1 HG02486.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.64+343G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936670 | |||||||
chr19:42936689 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.64+324G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936689 | |||||||
chr19:42936708 | T | C | 92 | a0001c0001t0002g0044 a0001c0001t0002g0097 a0001c0002t0002g0002 others(89): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.64+305A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936708 | |||||||
chr19:42936748 | T | C | 92 | a0001c0001t0001g0187 a0001c0001t0002g0044 a0001c0001t0002g0097 others(89): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.64+265A>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936748 | |||||||
chr19:42936755 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.64+258G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936755 | |||||||
chr19:42936777 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.64+236T>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936777 | |||||||
chr19:42936787 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64+226T>G | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936787 | |||||||
chr19:42936789 | A | T | 1 | a0001c0002t0002g0003 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.64+224T>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936789 | |||||||
chr19:42936842 | C | T | 3 | a0001c0001t0001g0152 a0001c0001t0001g0199 a0001c0001t0001g0200 |
3 | HG02717.hp2 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.64+171G>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936842 | |||||||
chr19:42936866 | C | G | 1 | a0002c0015t0004g0051 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.64+147G>C | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936866 | |||||||
chr19:42936953 | G | T | 1 | a0001c0001t0001g0013 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.64+60C>A | PSG7 | ENSG00000221878.13 | transcript | ENST00000406070.7 | protein_coding | 1/5 | chr19 | 42936953 |