Item | Value |
---|---|
geneid | 26526 |
ensemblid | ENSG00000130167.14 |
hgncid | 30725 |
symbol | TSPAN16 |
name | tetraspanin 16 |
refseq_nuc | NM_001282509.2 |
refseq_prot | NP_001269438.1 |
ensembl_nuc | ENST00000590327.6 |
ensembl_prot | ENSP00000467341.1 |
mane_status | MANE Select |
chr | chr19 |
start | 11296160 |
end | 11315967 |
strand | + |
ver | v1.2 |
region | chr19:11296160-11315967 |
region5000 | chr19:11291160-11320967 |
regionname0 | TSPAN16_chr19_11296160_11315967 |
regionname5000 | TSPAN16_chr19_11291160_11320967 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 244 | 360 | 76 | 66 | 168 | 18 | 30 | 127 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | MAEIH others(239): Show |
chr19 | 11291160 | 11320967 |
a0002 | 0/0 | 244 | 17 | 16 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | MAEIH others(239): Show |
chr19 | 11291160 | 11320967 |
a0003 | 0/0 | 244 | 3 | 1 | 1 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | MAEIH others(239): Show |
chr19 | 11291160 | 11320967 |
a0004 | 0/0 | 244 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | MAEIH others(239): Show |
chr19 | 11291160 | 11320967 |
a0005 | 0/0 | 244 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | MAEIH others(239): Show |
chr19 | 11291160 | 11320967 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 732 | 357 | 74 | 66 | 168 | 17 | 30 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 | ||
a0001c0006 | 0/0 | 732 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 | ||
a0001c0007 | 0/0 | 732 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 | ||
a0001c0008 | 0/0 | 732 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 | ||
a0002c0002 | 0/0 | 732 | 17 | 16 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 | ||
a0003c0003 | 0/0 | 732 | 3 | 1 | 1 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 | ||
a0004c0005 | 0/0 | 732 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 | ||
a0005c0004 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | ATGGC others(727): Show |
chr19 | 11291160 | 11320967 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 1002 | 121 | 32 | 23 | 50 | 6 | 10 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGGA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0001t0002 | 0/0 | 1002 | 110 | 10 | 20 | 70 | 4 | 6 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0001t0003 | 1/0 | 1002 | 82 | 2 | 21 | 43 | 6 | 9 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0001t0004 | 0/0 | 1002 | 20 | 19 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0001t0005 | 0/1 | 1002 | 23 | 11 | 2 | 3 | 1 | 5 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0001t0007 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGGA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0006t0003 | 0/0 | 1002 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0007t0001 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGGA others(997): Show |
chr19 | 11291160 | 11320967 |
a0001c0008t0004 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0002c0002t0001 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGGA others(997): Show |
chr19 | 11291160 | 11320967 |
a0002c0002t0004 | 0/0 | 1002 | 16 | 15 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0003c0003t0002 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0003c0003t0006 | 0/0 | 1002 | 2 | 0 | 1 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0004c0005t0004 | 0/0 | 1002 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
a0005c0004t0002 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | AGGCA others(997): Show |
chr19 | 11291160 | 11320967 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 24 | 7 | 3 | 13 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0004 | 0/0 | 16 | 0 | 5 | 11 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0005 | 0/0 | 15 | 2 | 4 | 5 | 1 | 3 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 3 | 0 | 3 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0018 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0041 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0002 | 0/0 | 30 | 2 | 7 | 15 | 3 | 3 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0006 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0001 | 1/0 | 32 | 1 | 12 | 8 | 5 | 5 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0009 | 0/0 | 6 | 0 | 2 | 0 | 1 | 3 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0006t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0007t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0001c0008t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0017 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0002c0002t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0003c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0003c0003t0006g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0003c0003t0006g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0004c0005t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
a0005c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | GBR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00140 | hp1 | a0001 | c0006 | t0003 | g0097 | EUR | GBR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0118 | EUR | GBR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0157 | EUR | FIN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | FIN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00408 | hp1 | a0003 | c0003 | t0006 | g0052 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0092 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | CHS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01109 | hp1 | a0002 | c0002 | t0004 | g0017 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0121 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0106 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0120 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01346 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | IBS | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01978 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0064 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0004 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02155 | hp1 | a0001 | c0001 | t0005 | g0038 | EAS | CDX | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CDX | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0094 | AMR | PEL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0019 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0072 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02615 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02630 | hp2 | a0002 | c0002 | t0004 | g0023 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02647 | hp2 | a0002 | c0002 | t0004 | g0125 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02723 | hp1 | a0002 | c0002 | t0004 | g0035 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02738 | hp2 | a0001 | c0001 | t0005 | g0179 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02809 | hp2 | a0002 | c0002 | t0004 | g0023 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02818 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02895 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0132 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0129 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02922 | hp2 | a0001 | c0008 | t0004 | g0050 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02965 | hp2 | a0002 | c0002 | t0004 | g0034 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0038 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03041 | hp1 | a0002 | c0002 | t0004 | g0130 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0049 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03098 | hp2 | a0002 | c0002 | t0004 | g0017 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03139 | hp2 | a0002 | c0002 | t0004 | g0023 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03225 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03486 | hp2 | a0001 | c0007 | t0001 | g0124 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | STU | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | BEB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03942 | hp2 | a0001 | c0001 | t0003 | g0102 | SAS | BEB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0076 | SAS | STU | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG04228 | hp1 | a0001 | c0001 | t0005 | g0009 | SAS | STU | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18522 | hp1 | a0002 | c0002 | t0004 | g0036 | AFR | YRI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | YRI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18906 | hp1 | a0002 | c0002 | t0004 | g0036 | AFR | YRI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18986 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18987 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | LWK | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19043 | hp1 | a0002 | c0002 | t0004 | g0017 | AFR | LWK | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19057 | hp2 | a0005 | c0004 | t0002 | g0103 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19240 | hp1 | a0002 | c0002 | t0004 | g0034 | AFR | YRI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA19240 | hp2 | a0002 | c0002 | t0004 | g0126 | AFR | YRI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20129 | hp1 | a0003 | c0003 | t0002 | g0046 | AFR | ASW | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0127 | AFR | ASW | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0009 | EUR | TSI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | GIH | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG01123 | hp2 | a0003 | c0003 | t0006 | g0051 | AMR | CLM | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02559 | hp1 | a0004 | c0005 | t0004 | g0045 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | MSL | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | USA | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20300 | hp1 | a0002 | c0002 | t0004 | g0035 | AFR | USA | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | USA | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | LWK | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0140 | REF | REF | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0001 | REF | REF | TSPAN16_chr19_11291160_11320967 | TSPAN16 | chr19 | 11291160 | 11320967 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:11298163 | G | C | 1 | a0005 | 1 | NA19057.hp2 | missense_variant | MODERATE | c.91G>C | p.Gly31Arg | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/7 | 229/1002 | 91/735 | 31/244 | chr19 | 11298163 | |||
chr19:11298229 | T | G | 1 | a0002 | 17 | HG01109.hp1 HG02280.hp1 HG02630.hp2 others(14): Show |
missense_variant | MODERATE | c.157T>G | p.Tyr53Asp | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/7 | 295/1002 | 157/735 | 53/244 | chr19 | 11298229 | |||
chr19:11298236 | T | C | 1 | a0003 | 3 | HG00408.hp1 HG01123.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.164T>C | p.Leu55Pro | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/7 | 302/1002 | 164/735 | 55/244 | chr19 | 11298236 | |||
chr19:11306725 | G | A | 1 | a0004 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.572G>A | p.Arg191His | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/7 | 710/1002 | 572/735 | 191/244 | chr19 | 11306725 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:11296360 | C | T | 1 | a0001c0008 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.63C>T | p.Phe21Phe | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/7 | 201/1002 | 63/735 | 21/244 | chr19 | 11296360 | |||
chr19:11312141 | C | A | 1 | a0001c0006 | 1 | HG00140.hp1 | splice_region_variant&synonymous_variant | LOW | c.606C>A | p.Gly202Gly | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/7 | 744/1002 | 606/735 | 202/244 | chr19 | 11312141 | |||
chr19:11315835 | C | A | 1 | a0001c0007 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.732C>A | p.Gly244Gly | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 7/7 | 870/1002 | 732/735 | 244/244 | chr19 | 11315835 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:11296163 | C | G | 4 | a0001c0001t0001 a0001c0001t0007 a0001c0007t0001 others(1): Show |
124 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(121): Show |
5_prime_UTR_variant | MODIFIER | c.-135C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/7 | 135 | chr19 | 11296163 | ||||||
chr19:11296170 | G | C | 1 | a0001c0001t0007 | 1 | HG02083.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/7 | 128 | chr19 | 11296170 | ||||||
chr19:11296276 | A | G | 9 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(6): Show |
184 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(181): Show |
5_prime_UTR_variant | MODIFIER | c.-22A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/7 | 22 | chr19 | 11296276 | ||||||
chr19:11296287 | G | A | 1 | a0003c0003t0006 | 2 | HG00408.hp1 HG01123.hp2 |
5_prime_UTR_variant | MODIFIER | c.-11G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/7 | 11 | chr19 | 11296287 | ||||||
chr19:11315963 | C | A | 11 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(8): Show |
274 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
3_prime_UTR_variant | MODIFIER | c.*125C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 7/7 | 125 | chr19 | 11315963 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:11296443 | A | C | 3 | a0001c0001t0002g0011 a0001c0001t0002g0180 a0001c0001t0002g0181 |
8 | NA18612.hp1 NA18950.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+77A>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296443 | |||||||
chr19:11296582 | T | G | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+216T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296582 | |||||||
chr19:11296612 | G | A | 1 | a0003c0003t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.69+246G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296612 | |||||||
chr19:11296639 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.69+273C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296639 | |||||||
chr19:11296761 | G | C | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+395G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296761 | |||||||
chr19:11296764 | G | T | 82 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(79): Show |
173 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.69+398G>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296764 | |||||||
chr19:11296767 | G | A | 5 | a0001c0001t0004g0012 a0001c0001t0004g0047 a0001c0001t0004g0048 others(2): Show |
9 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+401G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296767 | |||||||
chr19:11296898 | G | A | 1 | a0001c0007t0001g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.69+532G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11296898 | |||||||
chr19:11297028 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.69+662G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297028 | |||||||
chr19:11297065 | C | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
174 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.69+699C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297065 | |||||||
chr19:11297079 | A | G | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.69+713A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297079 | |||||||
chr19:11297259 | C | T | 3 | a0001c0001t0004g0019 a0001c0001t0005g0179 a0004c0005t0004g0045 |
5 | HG02451.hp1 HG02559.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-883C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297259 | |||||||
chr19:11297482 | A | ATTATT | 14 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 others(11): Show |
20 | HG00408.hp1 HG00544.hp1 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.70-632_70-628dupAT others(3): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 11297482 | ||||||
chr19:11297482 | A | ATTATTTT others(3): Show |
56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
132 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(129): Show |
intron_variant | MODIFIER | c.70-637_70-628dupAT others(8): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 11297482 | ||||||
chr19:11297482 | A | ATTATTTT others(8): Show |
15 | a0001c0001t0001g0037 a0001c0001t0001g0135 a0001c0001t0001g0136 others(12): Show |
24 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.70-642_70-628dupAT others(13): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 11297482 | ||||||
chr19:11297482 | A | ATTATTTT others(13): Show |
4 | a0001c0001t0004g0127 a0001c0001t0005g0128 a0001c0001t0005g0129 others(1): Show |
6 | HG02630.hp2 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.70-647_70-628dupAT others(18): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 11297482 | ||||||
chr19:11297482 | A | ATTATTTT others(18): Show |
4 | a0001c0001t0004g0033 a0002c0002t0004g0017 a0002c0002t0004g0125 others(1): Show |
8 | HG01109.hp1 HG02647.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.70-652_70-628dupAT others(23): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 11297482 | ||||||
chr19:11297543 | C | T | 2 | a0001c0001t0003g0120 a0001c0001t0003g0121 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.70-599C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297543 | |||||||
chr19:11297599 | C | T | 54 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(51): Show |
123 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.70-543C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297599 | |||||||
chr19:11297954 | A | AT | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(67): Show |
153 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(150): Show |
intron_variant | MODIFIER | c.70-178dupT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 11297954 | ||||||
chr19:11297954 | A | ATT | 8 | a0001c0001t0001g0138 a0001c0001t0004g0033 a0001c0001t0004g0133 others(5): Show |
14 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.70-179_70-178dupTT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | 11297954 | ||||||
chr19:11297958 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.70-184T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297958 | |||||||
chr19:11297990 | C | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0119 |
3 | HG03453.hp2 HG03579.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.70-152C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 1/6 | chr19 | 11297990 | |||||||
chr19:11298363 | C | T | 7 | a0001c0001t0004g0033 a0001c0001t0004g0133 a0001c0001t0005g0008 others(4): Show |
13 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.267+24C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298363 | |||||||
chr19:11298385 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.267+46C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298385 | |||||||
chr19:11298435 | ATT | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
170 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(167): Show |
intron_variant | MODIFIER | c.267+109_267+110del others(2): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 11298435 | ||||||
chr19:11298469 | C | G | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.267+130C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298469 | |||||||
chr19:11298520 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.267+181T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298520 | |||||||
chr19:11298683 | C | T | 1 | a0001c0001t0002g0032 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.268-189C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298683 | |||||||
chr19:11298733 | G | A | 1 | a0001c0001t0004g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.268-139G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298733 | |||||||
chr19:11298769 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.268-103G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298769 | |||||||
chr19:11298800 | T | A | 8 | a0001c0001t0004g0012 a0001c0001t0004g0026 a0001c0001t0004g0047 others(5): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.268-72T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298800 | |||||||
chr19:11298818 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.268-54G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | chr19 | 11298818 | |||||||
chr19:11298821 | GGGA | G | 4 | a0002c0002t0004g0017 a0002c0002t0004g0023 a0002c0002t0004g0125 others(1): Show |
9 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.268-45_268-43delAG others(1): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | 11298821 | ||||||
chr19:11299008 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
190 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.342+62A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299008 | |||||||
chr19:11299040 | G | A | 1 | a0002c0002t0004g0034 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.342+94G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299040 | |||||||
chr19:11299146 | T | C | 7 | a0001c0001t0004g0033 a0001c0001t0004g0133 a0001c0001t0005g0008 others(4): Show |
13 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.342+200T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299146 | |||||||
chr19:11299152 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0144 |
7 | HG00099.hp1 HG00639.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.342+206G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299152 | |||||||
chr19:11299204 | C | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0118 |
2 | HG00140.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.342+258C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299204 | |||||||
chr19:11299267 | G | A | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+321G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299267 | |||||||
chr19:11299277 | TA | T | 8 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0002g0113 others(5): Show |
8 | HG01257.hp1 HG02895.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.342+345delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 11299277 | ||||||
chr19:11299314 | G | A | 3 | a0001c0001t0001g0039 a0001c0001t0004g0033 a0001c0001t0005g0128 |
5 | HG02976.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.342+368G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299314 | |||||||
chr19:11299338 | A | T | 1 | a0001c0001t0002g0181 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.342+392A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299338 | |||||||
chr19:11299341 | G | A | 2 | a0001c0001t0003g0065 a0001c0001t0003g0066 |
2 | HG00099.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.342+395G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299341 | |||||||
chr19:11299392 | G | A | 5 | a0001c0001t0004g0133 a0001c0001t0005g0008 a0001c0001t0005g0129 others(2): Show |
10 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.342+446G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299392 | |||||||
chr19:11299465 | C | T | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.342+519C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299465 | |||||||
chr19:11299772 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.342+826C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299772 | |||||||
chr19:11299937 | A | G | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.342+991A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299937 | |||||||
chr19:11299952 | G | C | 1 | a0001c0001t0004g0047 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.342+1006G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11299952 | |||||||
chr19:11299985 | GA | G | 68 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(65): Show |
148 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.342+1054delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 11299985 | ||||||
chr19:11299985 | GAA | G | 7 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0004g0133 others(4): Show |
12 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.342+1053_342+1054d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | 11299985 | ||||||
chr19:11300077 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.343-1124G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300077 | |||||||
chr19:11300094 | T | C | 1 | a0001c0001t0003g0027 | 2 | HG00673.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.343-1107T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300094 | |||||||
chr19:11300103 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.343-1098T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300103 | |||||||
chr19:11300153 | T | G | 8 | a0001c0001t0004g0012 a0001c0001t0004g0026 a0001c0001t0004g0047 others(5): Show |
13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.343-1048T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300153 | |||||||
chr19:11300169 | T | C | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.343-1032T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300169 | |||||||
chr19:11300257 | G | A | 80 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(77): Show |
171 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(168): Show |
intron_variant | MODIFIER | c.343-944G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300257 | |||||||
chr19:11300623 | C | G | 1 | a0001c0001t0001g0044 | 2 | HG02080.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.343-578C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300623 | |||||||
chr19:11300786 | A | G | 7 | a0001c0001t0004g0139 a0001c0001t0005g0009 a0001c0001t0005g0038 others(4): Show |
13 | HG01346.hp2 HG01978.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-415A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300786 | |||||||
chr19:11300857 | C | T | 1 | a0001c0001t0001g0043 | 2 | NA18953.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.343-344C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300857 | |||||||
chr19:11300976 | C | T | 7 | a0001c0001t0004g0139 a0001c0001t0005g0009 a0001c0001t0005g0038 others(4): Show |
13 | HG01346.hp2 HG01978.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.343-225C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11300976 | |||||||
chr19:11301068 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
172 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.343-133G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11301068 | |||||||
chr19:11301078 | T | C | 15 | a0001c0001t0003g0007 a0001c0001t0003g0014 a0001c0001t0003g0020 others(12): Show |
29 | HG00423.hp1 HG00544.hp1 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.343-123T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11301078 | |||||||
chr19:11301098 | C | T | 4 | a0001c0001t0004g0012 a0001c0001t0004g0048 a0001c0001t0004g0049 others(1): Show |
8 | HG02451.hp2 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.343-103C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11301098 | |||||||
chr19:11301106 | G | T | 1 | a0001c0001t0004g0019 | 3 | HG02451.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.343-95G>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11301106 | |||||||
chr19:11301138 | C | G | 3 | a0001c0001t0002g0022 a0001c0001t0002g0109 a0001c0001t0002g0110 |
5 | NA18971.hp1 NA18986.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.343-63C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11301138 | |||||||
chr19:11301192 | C | A | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
188 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.343-9C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 3/6 | chr19 | 11301192 | |||||||
chr19:11301361 | C | T | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+53C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301361 | |||||||
chr19:11301365 | C | T | 2 | a0001c0001t0002g0016 a0001c0001t0002g0108 |
5 | HG02056.hp2 NA18943.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+57C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301365 | |||||||
chr19:11301455 | C | G | 1 | a0001c0001t0004g0019 | 3 | HG02451.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.450+147C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301455 | |||||||
chr19:11301468 | C | T | 1 | a0001c0007t0001g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.450+160C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301468 | |||||||
chr19:11301469 | G | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
172 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.450+161G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301469 | |||||||
chr19:11301558 | C | T | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450+250C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301558 | |||||||
chr19:11301627 | G | C | 1 | a0001c0001t0002g0071 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.450+319G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301627 | |||||||
chr19:11301638 | T | TA | 11 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
17 | HG01346.hp2 HG01978.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.450+346dupA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11301638 | ||||||
chr19:11301638 | TA | T | 7 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0176 others(4): Show |
8 | HG00673.hp2 HG01257.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.450+346delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11301638 | ||||||
chr19:11301692 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0149 |
5 | HG00738.hp2 HG01074.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.450+384T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301692 | |||||||
chr19:11301820 | C | T | 11 | a0001c0001t0004g0012 a0001c0001t0004g0026 a0001c0001t0004g0047 others(8): Show |
16 | HG00408.hp1 HG01123.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.450+512C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301820 | |||||||
chr19:11301828 | A | AT | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(68): Show |
154 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(151): Show |
intron_variant | MODIFIER | c.450+533dupT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11301828 | ||||||
chr19:11301828 | A | ATT | 10 | a0001c0001t0004g0127 a0002c0002t0001g0131 a0002c0002t0004g0017 others(7): Show |
18 | HG01109.hp1 HG02280.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+532_450+533dup others(2): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11301828 | ||||||
chr19:11301885 | G | A | 2 | a0001c0001t0002g0122 a0001c0001t0002g0123 |
2 | HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.450+577G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301885 | |||||||
chr19:11301970 | CCCA | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
168 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.450+670_450+672del others(3): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11301970 | ||||||
chr19:11301987 | C | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(76): Show |
168 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(165): Show |
intron_variant | MODIFIER | c.450+679C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11301987 | |||||||
chr19:11302094 | G | C | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+786G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302094 | |||||||
chr19:11302097 | T | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
172 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(169): Show |
intron_variant | MODIFIER | c.450+789T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302097 | |||||||
chr19:11302105 | T | C | 95 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(92): Show |
192 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.450+797T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302105 | |||||||
chr19:11302134 | A | G | 1 | a0001c0008t0004g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.450+826A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302134 | |||||||
chr19:11302156 | G | A | 1 | a0001c0001t0002g0073 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.450+848G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302156 | |||||||
chr19:11302171 | C | A | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450+863C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302171 | |||||||
chr19:11302443 | C | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.450+1135C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302443 | |||||||
chr19:11302528 | C | CA | 11 | a0001c0001t0002g0015 a0001c0001t0002g0071 a0001c0001t0002g0074 others(8): Show |
15 | HG00408.hp1 HG00558.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.450+1243dupA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302528 | ||||||
chr19:11302528 | C | CAA | 7 | a0001c0001t0004g0012 a0001c0001t0004g0047 a0001c0001t0004g0048 others(4): Show |
11 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+1242_450+1243d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302528 | ||||||
chr19:11302528 | CA | C | 26 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0151 others(23): Show |
45 | HG01109.hp1 HG01346.hp2 HG01978.hp1 others(42): Show |
intron_variant | MODIFIER | c.450+1243delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302528 | ||||||
chr19:11302528 | CAA | C | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(43): Show |
115 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.450+1242_450+1243d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302528 | ||||||
chr19:11302528 | CAAA | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0138 a0001c0001t0001g0168 others(5): Show |
10 | HG00735.hp1 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.450+1241_450+1243d others(5): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302528 | ||||||
chr19:11302632 | T | C | 8 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0004g0127 others(5): Show |
13 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+1324T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302632 | |||||||
chr19:11302637 | A | G | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1329A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302637 | |||||||
chr19:11302642 | C | CATATATA others(19): Show |
3 | a0001c0001t0002g0022 a0001c0001t0002g0109 a0001c0001t0002g0110 |
5 | NA18971.hp1 NA18986.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.450+1350_450+1375d others(28): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302642 | ||||||
chr19:11302652 | TACACATA others(21): Show |
T | 1 | a0001c0001t0005g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.450+1350_450+1377d others(30): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302652 | ||||||
chr19:11302652 | TACACATA others(23): Show |
T | 3 | a0001c0001t0004g0033 a0002c0002t0001g0131 a0002c0002t0004g0130 |
4 | HG02280.hp1 HG03041.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1350_450+1379d others(32): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302652 | ||||||
chr19:11302652 | TACACATA others(25): Show |
T | 6 | a0001c0001t0004g0127 a0001c0001t0004g0133 a0001c0001t0005g0008 others(3): Show |
11 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.450+1350_450+1381d others(34): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302652 | ||||||
chr19:11302660 | C | CAT | 6 | a0001c0001t0002g0119 a0001c0001t0003g0007 a0001c0001t0003g0025 others(3): Show |
9 | HG00544.hp1 HG02523.hp2 HG03942.hp2 others(6): Show |
intron_variant | MODIFIER | c.450+1370_450+1371d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302660 | ||||||
chr19:11302660 | C | CATATATA others(6): Show |
1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450+1362_450+1363i others(15): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302660 | ||||||
chr19:11302660 | C | CATATATA others(16): Show |
1 | a0001c0001t0004g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.450+1362_450+1363i others(25): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302660 | ||||||
chr19:11302660 | C | CATATATA others(18): Show |
1 | a0001c0001t0004g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.450+1362_450+1363i others(27): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302660 | ||||||
chr19:11302660 | C | CATATATA others(22): Show |
1 | a0001c0001t0004g0019 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.450+1362_450+1363i others(31): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302660 | ||||||
chr19:11302660 | CAT | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0013 a0001c0001t0002g0117 others(7): Show |
15 | HG00140.hp2 HG00280.hp2 HG00673.hp2 others(12): Show |
intron_variant | MODIFIER | c.450+1370_450+1371d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302660 | ||||||
chr19:11302665 | A | ATATATAT others(3): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0147 others(5): Show |
11 | HG02083.hp2 HG02145.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.450+1364_450+1365i others(12): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302665 | ||||||
chr19:11302667 | A | ATATATGT others(1): Show |
47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
111 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.450+1364_450+1365i others(10): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302667 | ||||||
chr19:11302669 | A | ATATATG | 5 | a0002c0002t0004g0017 a0002c0002t0004g0023 a0002c0002t0004g0035 others(2): Show |
9 | HG02630.hp2 HG02809.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.450+1366_450+1367i others(8): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302669 | ||||||
chr19:11302669 | A | ATATG | 3 | a0002c0002t0004g0017 a0002c0002t0004g0023 a0002c0002t0004g0035 |
3 | HG01109.hp1 HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.450+1364_450+1365i others(6): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302669 | ||||||
chr19:11302672 | T | C | 2 | a0001c0001t0004g0026 a0001c0001t0004g0064 |
2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.450+1364T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302672 | |||||||
chr19:11302674 | T | C | 8 | a0001c0001t0004g0012 a0001c0001t0004g0026 a0001c0001t0004g0047 others(5): Show |
13 | HG00408.hp1 HG01891.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.450+1366T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302674 | |||||||
chr19:11302676 | T | C | 10 | a0001c0001t0004g0012 a0001c0001t0004g0026 a0001c0001t0004g0047 others(7): Show |
15 | HG00408.hp1 HG01123.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.450+1368T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302676 | |||||||
chr19:11302678 | T | C | 22 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0013 others(19): Show |
32 | HG00408.hp1 HG00438.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.450+1370T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302678 | |||||||
chr19:11302678 | T | TAC | 10 | a0001c0001t0002g0002 a0001c0001t0002g0011 a0001c0001t0002g0015 others(7): Show |
14 | HG01109.hp2 HG01346.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.450+1398_450+1399d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302678 | ||||||
chr19:11302678 | T | TATAC | 2 | a0001c0001t0003g0020 a0001c0001t0005g0009 |
3 | HG02738.hp1 HG04228.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.450+1371_450+1372i others(6): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302678 | ||||||
chr19:11302678 | T | TATACACA others(25): Show |
1 | a0001c0001t0003g0072 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.450+1371_450+1372i others(34): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302678 | ||||||
chr19:11302680 | C | T | 65 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(62): Show |
145 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.450+1372C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302680 | |||||||
chr19:11302682 | C | T | 60 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(57): Show |
128 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.450+1374C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302682 | |||||||
chr19:11302684 | C | T | 32 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(29): Show |
64 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.450+1376C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302684 | |||||||
chr19:11302686 | C | T | 8 | a0001c0001t0004g0019 a0002c0002t0004g0017 a0002c0002t0004g0023 others(5): Show |
18 | HG01109.hp1 HG02451.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.450+1378C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302686 | |||||||
chr19:11302688 | C | T | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1380C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302688 | |||||||
chr19:11302690 | C | T | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450+1382C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302690 | |||||||
chr19:11302692 | C | T | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.450+1384C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302692 | |||||||
chr19:11302778 | A | G | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
188 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.450+1470A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302778 | |||||||
chr19:11302879 | TGGCTAAT others(1799): Show |
T | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+1584_451-1907d others(2): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302879 | ||||||
chr19:11302885 | A | AT | 13 | a0001c0001t0001g0037 a0001c0001t0001g0135 a0001c0001t0001g0138 others(10): Show |
14 | HG00408.hp1 HG00597.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.450+1594dupT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11302885 | ||||||
chr19:11302961 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.450+1653C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302961 | |||||||
chr19:11302998 | C | T | 1 | a0003c0003t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.450+1690C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11302998 | |||||||
chr19:11303044 | G | A | 4 | a0001c0001t0004g0133 a0001c0001t0005g0008 a0001c0001t0005g0132 others(1): Show |
9 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.450+1736G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303044 | |||||||
chr19:11303094 | C | G | 1 | a0001c0001t0004g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.450+1786C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303094 | |||||||
chr19:11303148 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0151 |
3 | HG01934.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.450+1840G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303148 | |||||||
chr19:11303156 | T | C | 11 | a0001c0001t0004g0033 a0001c0001t0004g0127 a0002c0002t0001g0131 others(8): Show |
20 | HG01109.hp1 HG02280.hp1 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.450+1848T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303156 | |||||||
chr19:11303158 | G | C | 1 | a0001c0001t0004g0026 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.450+1850G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303158 | |||||||
chr19:11303170 | AAAG | A | 10 | a0001c0001t0004g0127 a0002c0002t0004g0017 a0002c0002t0004g0023 others(7): Show |
18 | HG00408.hp1 HG01109.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.450+1866_450+1868d others(5): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11303170 | ||||||
chr19:11303206 | G | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(88): Show |
186 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.450+1898G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303206 | |||||||
chr19:11303266 | T | C | 8 | a0001c0001t0004g0127 a0002c0002t0004g0017 a0002c0002t0004g0023 others(5): Show |
16 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(13): Show |
intron_variant | MODIFIER | c.450+1958T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303266 | |||||||
chr19:11303373 | G | C | 7 | a0001c0001t0004g0139 a0001c0001t0005g0009 a0001c0001t0005g0038 others(4): Show |
13 | HG01346.hp2 HG01978.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.450+2065G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303373 | |||||||
chr19:11303376 | G | A | 2 | a0001c0001t0002g0113 a0003c0003t0002g0046 |
2 | NA19001.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.450+2068G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303376 | |||||||
chr19:11303399 | T | A | 5 | a0001c0001t0002g0113 a0001c0001t0003g0007 a0001c0001t0003g0025 others(2): Show |
8 | HG00544.hp1 HG02523.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.450+2091T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303399 | |||||||
chr19:11303460 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
125 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.450+2152T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303460 | |||||||
chr19:11303469 | T | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
125 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.450+2161T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303469 | |||||||
chr19:11303528 | G | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
125 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.450+2220G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303528 | |||||||
chr19:11303529 | T | C | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
125 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.450+2221T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303529 | |||||||
chr19:11303556 | AAAAT | A | 3 | a0001c0001t0003g0001 a0001c0001t0003g0078 a0001c0001t0003g0084 |
4 | HG00438.hp2 HG01081.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.450+2265_450+2268d others(6): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11303556 | ||||||
chr19:11303572 | T | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0010 |
3 | HG01515.hp1 HG01517.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.450+2264T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303572 | |||||||
chr19:11303573 | A | T | 2 | a0001c0001t0002g0002 a0001c0001t0003g0001 |
2 | HG02129.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.450+2265A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303573 | |||||||
chr19:11303574 | AATT | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(4): Show |
7 | HG01515.hp1 HG02280.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.450+2268_450+2270d others(5): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11303574 | ||||||
chr19:11303575 | AT | A | 6 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(3): Show |
6 | HG02080.hp1 HG02647.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.450+2269delT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11303575 | ||||||
chr19:11303575 | ATT | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(42): Show |
99 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.450+2268_450+2269d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303575 | |||||||
chr19:11303576 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.450+2268T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303576 | |||||||
chr19:11303576 | TTA | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(7): Show |
12 | HG00621.hp2 HG01106.hp1 HG01261.hp2 others(9): Show |
intron_variant | MODIFIER | c.450+2269_450+2270d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303576 | |||||||
chr19:11303577 | T | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0044 others(4): Show |
7 | HG02080.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.450+2269T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303577 | |||||||
chr19:11303577 | T | TA | 29 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0015 others(26): Show |
57 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.450+2289dupA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11303577 | ||||||
chr19:11303577 | TA | T | 15 | a0001c0001t0004g0053 a0001c0001t0004g0139 a0001c0001t0005g0009 others(12): Show |
27 | HG01109.hp1 HG01891.hp2 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.450+2289delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11303577 | ||||||
chr19:11303578 | A | T | 1 | a0001c0001t0003g0001 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.450+2270A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303578 | |||||||
chr19:11303583 | A | T | 1 | a0001c0001t0001g0003 | 2 | HG03225.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.450+2275A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303583 | |||||||
chr19:11303585 | A | C | 2 | a0001c0001t0001g0003 a0001c0001t0002g0067 |
4 | NA18990.hp1 NA18991.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.450+2277A>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303585 | |||||||
chr19:11303587 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.450+2279A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303587 | |||||||
chr19:11303590 | A | C | 5 | a0001c0001t0004g0012 a0001c0001t0004g0047 a0001c0001t0004g0048 others(2): Show |
9 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.450+2282A>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303590 | |||||||
chr19:11303594 | A | C | 1 | a0001c0001t0002g0032 | 2 | HG03453.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.450+2286A>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303594 | |||||||
chr19:11303675 | C | A | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(78): Show |
170 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(167): Show |
intron_variant | MODIFIER | c.450+2367C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303675 | |||||||
chr19:11303764 | T | C | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.450+2456T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303764 | |||||||
chr19:11303935 | T | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(90): Show |
188 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.450+2627T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11303935 | |||||||
chr19:11304030 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.451-2574C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304030 | |||||||
chr19:11304071 | C | T | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.451-2533C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304071 | |||||||
chr19:11304141 | C | T | 1 | a0001c0001t0002g0013 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.451-2463C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304141 | |||||||
chr19:11304357 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.451-2247C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304357 | |||||||
chr19:11304370 | C | T | 1 | a0001c0001t0005g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.451-2234C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304370 | |||||||
chr19:11304517 | A | T | 1 | a0001c0001t0001g0003 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.451-2087A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304517 | |||||||
chr19:11304603 | C | A | 5 | a0001c0001t0004g0133 a0001c0001t0005g0008 a0001c0001t0005g0129 others(2): Show |
10 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.451-2001C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304603 | |||||||
chr19:11304716 | G | A | 1 | a0001c0001t0002g0079 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.451-1888G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304716 | |||||||
chr19:11304726 | A | G | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1878A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304726 | |||||||
chr19:11304743 | CT | C | 1 | a0001c0001t0004g0019 | 3 | HG02451.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.451-1859delT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11304743 | ||||||
chr19:11304759 | C | A | 1 | a0001c0001t0003g0080 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.451-1845C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304759 | |||||||
chr19:11304760 | G | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.451-1844G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304760 | |||||||
chr19:11304804 | G | C | 1 | a0001c0001t0001g0153 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.451-1800G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304804 | |||||||
chr19:11304815 | T | C | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1789T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304815 | |||||||
chr19:11304870 | C | T | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1734C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11304870 | |||||||
chr19:11305209 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.451-1395A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305209 | |||||||
chr19:11305296 | G | A | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1308G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305296 | |||||||
chr19:11305430 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.451-1174C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305430 | |||||||
chr19:11305487 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.451-1117G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305487 | |||||||
chr19:11305516 | A | G | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-1088A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305516 | |||||||
chr19:11305538 | T | TAATAAA | 1 | a0001c0001t0004g0019 | 3 | HG02451.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.451-1034_451-1029d others(8): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11305538 | ||||||
chr19:11305538 | TAATAAA | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0018 a0001c0001t0001g0042 others(21): Show |
50 | HG00738.hp2 HG01074.hp2 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.451-1034_451-1029d others(8): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11305538 | ||||||
chr19:11305538 | TAATAAAA others(5): Show |
T | 1 | a0001c0001t0004g0139 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.451-1040_451-1029d others(14): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr19 | 11305538 | ||||||
chr19:11305621 | C | A | 1 | a0001c0001t0005g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.451-983C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305621 | |||||||
chr19:11305623 | T | C | 1 | a0001c0001t0003g0081 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.451-981T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305623 | |||||||
chr19:11305637 | T | C | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-967T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305637 | |||||||
chr19:11305780 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.451-824C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305780 | |||||||
chr19:11305901 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.451-703G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305901 | |||||||
chr19:11305947 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.451-657G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305947 | |||||||
chr19:11305955 | T | G | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-649T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305955 | |||||||
chr19:11305989 | C | T | 1 | a0002c0002t0004g0034 | 2 | HG02965.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.451-615C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305989 | |||||||
chr19:11305995 | C | T | 1 | a0001c0001t0005g0143 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.451-609C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11305995 | |||||||
chr19:11306524 | C | T | 56 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
125 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.451-80C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11306524 | |||||||
chr19:11306541 | G | A | 2 | a0001c0001t0004g0019 a0004c0005t0004g0045 |
4 | HG02451.hp1 HG02559.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.451-63G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11306541 | |||||||
chr19:11306600 | A | G | 1 | a0001c0001t0005g0128 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.451-4A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 4/6 | chr19 | 11306600 | |||||||
chr19:11306884 | C | T | 4 | a0001c0001t0003g0020 a0001c0001t0003g0027 a0001c0001t0003g0028 others(1): Show |
9 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(6): Show |
intron_variant | MODIFIER | c.603+128C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11306884 | |||||||
chr19:11306885 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0004g0019 |
4 | HG02451.hp1 HG02886.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+129G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11306885 | |||||||
chr19:11306939 | C | A | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.603+183C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11306939 | |||||||
chr19:11306940 | C | A | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.603+184C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11306940 | |||||||
chr19:11306949 | G | A | 7 | a0001c0007t0001g0124 a0002c0002t0004g0017 a0002c0002t0004g0023 others(4): Show |
14 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.603+193G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11306949 | |||||||
chr19:11307122 | T | G | 58 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(55): Show |
127 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.603+366T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307122 | |||||||
chr19:11307126 | G | T | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.603+370G>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307126 | |||||||
chr19:11307281 | G | C | 8 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(5): Show |
14 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.603+525G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307281 | |||||||
chr19:11307307 | A | G | 1 | a0005c0004t0002g0103 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.603+551A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307307 | |||||||
chr19:11307328 | C | A | 1 | a0001c0001t0003g0068 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.603+572C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307328 | |||||||
chr19:11307371 | C | T | 1 | a0001c0001t0003g0077 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.603+615C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307371 | |||||||
chr19:11307662 | A | C | 1 | a0001c0001t0001g0166 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.603+906A>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307662 | |||||||
chr19:11307846 | G | C | 11 | a0001c0001t0004g0033 a0001c0001t0004g0127 a0001c0007t0001g0124 others(8): Show |
20 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.603+1090G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11307846 | |||||||
chr19:11308024 | G | A | 1 | a0002c0002t0004g0036 | 2 | NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.603+1268G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308024 | |||||||
chr19:11308061 | T | C | 1 | a0001c0001t0003g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.603+1305T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308061 | |||||||
chr19:11308109 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.603+1353C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308109 | |||||||
chr19:11308290 | C | CACA | 92 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(89): Show |
184 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.603+1545_603+1547d others(5): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11308290 | ||||||
chr19:11308291 | A | ACAG | 5 | a0001c0001t0004g0133 a0002c0002t0004g0017 a0002c0002t0004g0023 others(2): Show |
10 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.603+1537_603+1538i others(5): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11308291 | ||||||
chr19:11308309 | G | GT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(82): Show |
176 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.603+1560dupT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11308309 | ||||||
chr19:11308367 | C | T | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.603+1611C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308367 | |||||||
chr19:11308376 | G | A | 1 | a0003c0003t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.603+1620G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308376 | |||||||
chr19:11308473 | A | AT | 11 | a0001c0001t0001g0148 a0001c0001t0001g0153 a0001c0001t0001g0164 others(8): Show |
11 | HG01243.hp1 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.603+1732dupT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11308473 | ||||||
chr19:11308616 | T | A | 9 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(6): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.603+1860T>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308616 | |||||||
chr19:11308616 | T | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(85): Show |
179 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.603+1860T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308616 | |||||||
chr19:11308663 | C | T | 3 | a0001c0001t0005g0008 a0001c0001t0005g0132 a0001c0001t0005g0134 |
8 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.603+1907C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308663 | |||||||
chr19:11308716 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.603+1960G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308716 | |||||||
chr19:11308752 | C | T | 3 | a0001c0001t0005g0008 a0001c0001t0005g0132 a0001c0001t0005g0134 |
8 | HG02257.hp2 HG02559.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.603+1996C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308752 | |||||||
chr19:11308839 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.603+2083C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11308839 | |||||||
chr19:11309090 | TC | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0024 others(19): Show |
43 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.603+2337delC | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11309090 | ||||||
chr19:11309168 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.603+2412C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309168 | |||||||
chr19:11309169 | G | A | 12 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0016 others(9): Show |
28 | HG02040.hp1 HG02056.hp2 NA18612.hp1 others(25): Show |
intron_variant | MODIFIER | c.603+2413G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309169 | |||||||
chr19:11309217 | C | CA | 6 | a0001c0001t0001g0136 a0001c0001t0001g0165 a0001c0001t0002g0180 others(3): Show |
6 | HG01081.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+2475dupA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11309217 | ||||||
chr19:11309217 | CA | C | 14 | a0001c0001t0004g0139 a0001c0001t0005g0008 a0001c0001t0005g0009 others(11): Show |
25 | HG00408.hp1 HG01123.hp2 HG01346.hp2 others(22): Show |
intron_variant | MODIFIER | c.603+2475delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11309217 | ||||||
chr19:11309229 | A | G | 2 | a0001c0001t0002g0058 a0001c0001t0002g0062 |
2 | NA19056.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.603+2473A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309229 | |||||||
chr19:11309250 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.603+2494G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309250 | |||||||
chr19:11309324 | C | T | 83 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(80): Show |
174 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.603+2568C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309324 | |||||||
chr19:11309484 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.604-2655G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309484 | |||||||
chr19:11309618 | G | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0011 others(63): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.604-2521G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309618 | |||||||
chr19:11309640 | C | T | 1 | a0001c0001t0004g0019 | 3 | HG02451.hp1 HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.604-2499C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11309640 | |||||||
chr19:11310091 | G | A | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.604-2048G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310091 | |||||||
chr19:11310138 | G | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.604-2001G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310138 | |||||||
chr19:11310210 | G | C | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.604-1929G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310210 | |||||||
chr19:11310297 | G | A | 1 | a0001c0001t0002g0085 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.604-1842G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310297 | |||||||
chr19:11310318 | G | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.604-1821G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310318 | |||||||
chr19:11310372 | G | A | 1 | a0001c0001t0004g0127 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.604-1767G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310372 | |||||||
chr19:11310456 | G | A | 9 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(6): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.604-1683G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310456 | |||||||
chr19:11310510 | C | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.604-1629C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310510 | |||||||
chr19:11310511 | G | A | 2 | a0001c0001t0002g0083 a0001c0001t0002g0116 |
2 | NA18957.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.604-1628G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310511 | |||||||
chr19:11310515 | CA | C | 68 | a0001c0001t0001g0161 a0001c0001t0001g0168 a0001c0001t0002g0002 others(65): Show |
137 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.604-1606delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11310515 | ||||||
chr19:11310515 | CAA | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(59): Show |
138 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.604-1607_604-1606d others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11310515 | ||||||
chr19:11310561 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.604-1578C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310561 | |||||||
chr19:11310563 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.604-1576T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310563 | |||||||
chr19:11310576 | G | A | 1 | a0001c0001t0003g0092 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.604-1563G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310576 | |||||||
chr19:11310587 | G | A | 3 | a0001c0001t0001g0155 a0001c0001t0002g0108 a0002c0002t0004g0126 |
3 | HG02015.hp1 NA18943.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.604-1552G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310587 | |||||||
chr19:11310653 | G | A | 1 | a0003c0003t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604-1486G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310653 | |||||||
chr19:11310679 | G | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.604-1460G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310679 | |||||||
chr19:11310857 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.604-1282G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310857 | |||||||
chr19:11310880 | CTGGA | C | 139 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
287 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.604-1254_604-1251d others(6): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr19 | 11310880 | ||||||
chr19:11310911 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.604-1228C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11310911 | |||||||
chr19:11311033 | C | T | 5 | a0001c0001t0004g0012 a0001c0001t0004g0047 a0001c0001t0004g0048 others(2): Show |
9 | HG02451.hp2 HG02572.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.604-1106C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11311033 | |||||||
chr19:11311113 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0174 |
2 | NA18948.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.604-1026G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11311113 | |||||||
chr19:11311224 | T | G | 2 | a0001c0001t0003g0020 a0001c0001t0003g0029 |
5 | HG02132.hp2 HG02155.hp2 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.604-915T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11311224 | |||||||
chr19:11311350 | G | C | 1 | a0003c0003t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.604-789G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11311350 | |||||||
chr19:11311428 | C | A | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.604-711C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11311428 | |||||||
chr19:11312008 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.604-131C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11312008 | |||||||
chr19:11312101 | T | C | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.604-38T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 5/6 | chr19 | 11312101 | |||||||
chr19:11312322 | TA | T | 77 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0159 others(74): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.687+117delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11312322 | ||||||
chr19:11312426 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.687+204A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11312426 | |||||||
chr19:11312540 | T | C | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.687+318T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11312540 | |||||||
chr19:11312611 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.687+389G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11312611 | |||||||
chr19:11312752 | G | A | 2 | a0001c0001t0003g0075 a0001c0001t0003g0096 |
2 | NA18977.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.687+530G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11312752 | |||||||
chr19:11313001 | G | C | 142 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(139): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.687+779G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313001 | |||||||
chr19:11313025 | G | C | 1 | a0001c0001t0001g0156 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.687+803G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313025 | |||||||
chr19:11313027 | C | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.687+805C>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313027 | |||||||
chr19:11313324 | G | A | 1 | a0001c0001t0003g0069 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.687+1102G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313324 | |||||||
chr19:11313352 | A | G | 1 | a0001c0001t0001g0042 | 2 | NA18947.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.687+1130A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313352 | |||||||
chr19:11313372 | C | T | 1 | a0001c0001t0002g0091 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.687+1150C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313372 | |||||||
chr19:11313373 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.687+1151G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313373 | |||||||
chr19:11313441 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.687+1219C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313441 | |||||||
chr19:11313476 | G | A | 8 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(5): Show |
14 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.687+1254G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313476 | |||||||
chr19:11313526 | C | CA | 6 | a0001c0001t0002g0122 a0001c0001t0003g0031 a0001c0001t0003g0054 others(3): Show |
7 | HG00408.hp2 HG02717.hp2 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.687+1320dupA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11313526 | ||||||
chr19:11313526 | CA | C | 62 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0018 others(59): Show |
125 | HG00408.hp1 HG00621.hp2 HG00735.hp1 others(122): Show |
intron_variant | MODIFIER | c.687+1320delA | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11313526 | ||||||
chr19:11313541 | A | T | 1 | a0001c0001t0001g0169 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.687+1319A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313541 | |||||||
chr19:11313542 | AT | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0024 others(17): Show |
42 | HG00099.hp1 HG00323.hp1 HG00544.hp2 others(39): Show |
intron_variant | MODIFIER | c.687+1322delT | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11313542 | ||||||
chr19:11313665 | CATTA | C | 8 | a0001c0001t0004g0133 a0001c0007t0001g0124 a0002c0002t0004g0017 others(5): Show |
15 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.687+1448_687+1451d others(6): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11313665 | ||||||
chr19:11313735 | G | A | 1 | a0003c0003t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.687+1513G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313735 | |||||||
chr19:11313905 | G | A | 11 | a0001c0001t0004g0033 a0001c0001t0004g0133 a0001c0007t0001g0124 others(8): Show |
20 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.687+1683G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11313905 | |||||||
chr19:11314204 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.688-1587G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11314204 | |||||||
chr19:11314407 | T | G | 8 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(5): Show |
14 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.688-1384T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11314407 | |||||||
chr19:11314421 | T | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(133): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.688-1370T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11314421 | |||||||
chr19:11314524 | T | G | 55 | a0001c0001t0002g0002 a0001c0001t0002g0006 a0001c0001t0002g0011 others(52): Show |
116 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.688-1267T>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11314524 | |||||||
chr19:11314739 | AGGCTCTA others(5): Show |
A | 2 | a0001c0001t0005g0141 a0001c0001t0005g0142 |
2 | NA19000.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.688-1048_688-1037d others(14): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11314739 | ||||||
chr19:11314835 | C | T | 9 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(6): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.688-956C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11314835 | |||||||
chr19:11314944 | G | C | 9 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(6): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.688-847G>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11314944 | |||||||
chr19:11315060 | A | T | 1 | a0004c0005t0004g0045 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.688-731A>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315060 | |||||||
chr19:11315074 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.688-717A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315074 | |||||||
chr19:11315109 | G | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.688-682G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315109 | |||||||
chr19:11315163 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.688-628G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315163 | |||||||
chr19:11315170 | A | G | 8 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(5): Show |
14 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.688-621A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315170 | |||||||
chr19:11315234 | TCAA | T | 5 | a0001c0001t0002g0030 a0001c0001t0002g0061 a0001c0001t0002g0071 others(2): Show |
6 | HG00735.hp2 HG01943.hp1 HG02004.hp1 others(3): Show |
intron_variant | MODIFIER | c.688-556_688-554del others(3): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315234 | |||||||
chr19:11315235 | C | CAAT | 54 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0010 others(51): Show |
110 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.688-518_688-516dup others(3): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315235 | ||||||
chr19:11315235 | C | CAATAAT | 30 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0018 others(27): Show |
46 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.688-521_688-516dup others(6): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315235 | ||||||
chr19:11315235 | C | CAATAATA others(2): Show |
10 | a0001c0001t0001g0024 a0001c0001t0001g0163 a0001c0001t0001g0164 others(7): Show |
10 | HG02083.hp2 HG02257.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.688-524_688-516dup others(9): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315235 | ||||||
chr19:11315235 | C | CAATAATA others(5): Show |
2 | a0001c0001t0001g0169 a0001c0001t0005g0038 |
2 | HG02155.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.688-527_688-516dup others(12): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315235 | ||||||
chr19:11315235 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0106 |
4 | HG00639.hp1 HG01168.hp2 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.688-556C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315235 | |||||||
chr19:11315235 | CAAT | C | 10 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(7): Show |
16 | HG01175.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.688-518_688-516del others(3): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315235 | ||||||
chr19:11315235 | CAATAATA others(8): Show |
C | 5 | a0001c0001t0004g0133 a0002c0002t0004g0017 a0002c0002t0004g0023 others(2): Show |
10 | HG01109.hp1 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.688-530_688-516del others(15): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315235 | ||||||
chr19:11315235 | CAATAATA others(11): Show |
C | 1 | a0001c0001t0003g0001 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.688-533_688-516del others(18): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315235 | ||||||
chr19:11315256 | TAATAATA | T | 9 | a0001c0001t0002g0032 a0001c0001t0004g0012 a0001c0001t0004g0026 others(6): Show |
15 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.688-533_688-527del others(7): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315256 | ||||||
chr19:11315286 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.688-505G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315286 | |||||||
chr19:11315417 | C | T | 1 | a0003c0003t0002g0046 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.688-374C>T | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315417 | |||||||
chr19:11315506 | A | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(135): Show |
285 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.688-285A>G | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315506 | |||||||
chr19:11315535 | G | A | 2 | a0003c0003t0006g0051 a0003c0003t0006g0052 |
2 | HG00408.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.688-256G>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315535 | |||||||
chr19:11315557 | A | AAAAT | 54 | a0001c0001t0001g0157 a0001c0001t0002g0002 a0001c0001t0002g0006 others(51): Show |
114 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.688-210_688-207dup others(4): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315557 | ||||||
chr19:11315557 | A | AAAATAAA others(1): Show |
5 | a0001c0001t0002g0021 a0001c0001t0002g0058 a0001c0001t0002g0062 others(2): Show |
8 | HG00597.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.688-214_688-207dup others(8): Show |
TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr19 | 11315557 | ||||||
chr19:11315724 | C | A | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.688-67C>A | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315724 | |||||||
chr19:11315778 | T | C | 1 | a0001c0001t0005g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.688-13T>C | TSPAN16 | ENSG00000130167.14 | transcript | ENST00000590327.6 | protein_coding | 6/6 | chr19 | 11315778 |