Item | Value |
---|---|
geneid | 9360 |
ensemblid | ENSG00000138398.17 |
hgncid | 14650 |
symbol | PPIG |
name | peptidylprolyl isomerase G |
refseq_nuc | NM_004792.3 |
refseq_prot | NP_004783.2 |
ensembl_nuc | ENST00000260970.8 |
ensembl_prot | ENSP00000260970.3 |
mane_status | MANE Select |
chr | chr2 |
start | 169584351 |
end | 169641406 |
strand | + |
ver | v1.2 |
region | chr2:169584351-169641406 |
region5000 | chr2:169579351-169646406 |
regionname0 | PPIG_chr2_169584351_169641406 |
regionname5000 | PPIG_chr2_169579351_169646406 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 754 | 161 | 45 | 19 | 78 | 4 | 14 | 60 | PPIG_chr2_169579351_169646406 | PPIG | MGIKV others(749): Show |
chr2 | 169579351 | 169646406 |
a0002 | 1/0 | 754 | 160 | 23 | 30 | 85 | 6 | 15 | 69 | PPIG_chr2_169579351_169646406 | PPIG | MGIKV others(749): Show |
chr2 | 169579351 | 169646406 |
a0003 | 0/0 | 754 | 57 | 24 | 13 | 6 | 4 | 10 | 4 | PPIG_chr2_169579351_169646406 | PPIG | MGIKV others(749): Show |
chr2 | 169579351 | 169646406 |
a0004 | 0/0 | 754 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | MGIKV others(749): Show |
chr2 | 169579351 | 169646406 |
a0005 | 0/0 | 754 | 2 | 0 | 0 | 1 | 0 | 1 | 1 | PPIG_chr2_169579351_169646406 | PPIG | MGIKV others(749): Show |
chr2 | 169579351 | 169646406 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2262 | 156 | 43 | 19 | 75 | 4 | 14 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 | ||
a0001c0005 | 0/0 | 2262 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 | ||
a0001c0007 | 0/0 | 2262 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 | ||
a0002c0002 | 1/0 | 2262 | 151 | 23 | 28 | 78 | 6 | 15 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 | ||
a0002c0004 | 0/0 | 2262 | 9 | 0 | 2 | 7 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 | ||
a0003c0003 | 0/0 | 2262 | 57 | 24 | 13 | 6 | 4 | 10 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 | ||
a0004c0008 | 0/0 | 2262 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 | ||
a0005c0006 | 0/0 | 2262 | 2 | 0 | 0 | 1 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | ATGGG others(2257): Show |
chr2 | 169579351 | 169646406 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6356 | 48 | 0 | 8 | 30 | 3 | 7 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0005 | 0/0 | 6356 | 26 | 0 | 0 | 22 | 1 | 3 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0006 | 0/1 | 6357 | 22 | 1 | 9 | 8 | 0 | 3 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0007 | 0/0 | 6357 | 20 | 20 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0009 | 0/0 | 6356 | 10 | 0 | 0 | 9 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0011 | 0/0 | 6357 | 8 | 8 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0012 | 0/0 | 6357 | 5 | 5 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0013 | 0/0 | 6356 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0015 | 0/0 | 6357 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0017 | 0/0 | 6356 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0019 | 0/0 | 6357 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0021 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0022 | 0/0 | 6356 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0025 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0026 | 0/0 | 6358 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6353): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0027 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0028 | 0/0 | 6357 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0029 | 0/0 | 6357 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0032 | 0/0 | 6356 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0001t0033 | 0/0 | 6356 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0005t0002 | 0/0 | 6356 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0001c0007t0013 | 0/0 | 6356 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6351): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0001 | 1/0 | 6357 | 101 | 16 | 28 | 40 | 4 | 12 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0003 | 0/0 | 6358 | 35 | 6 | 0 | 25 | 1 | 3 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6353): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0010 | 0/0 | 6357 | 8 | 0 | 0 | 8 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0014 | 0/0 | 6357 | 3 | 1 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0020 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0023 | 0/0 | 6357 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0030 | 0/0 | 6358 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6353): Show |
chr2 | 169579351 | 169646406 |
a0002c0002t0034 | 0/0 | 6357 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0002c0004t0003 | 0/0 | 6358 | 9 | 0 | 2 | 7 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6353): Show |
chr2 | 169579351 | 169646406 |
a0003c0003t0004 | 0/0 | 6354 | 36 | 22 | 6 | 1 | 2 | 5 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6349): Show |
chr2 | 169579351 | 169646406 |
a0003c0003t0008 | 0/0 | 6354 | 17 | 2 | 7 | 2 | 2 | 4 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6349): Show |
chr2 | 169579351 | 169646406 |
a0003c0003t0016 | 0/0 | 6354 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6349): Show |
chr2 | 169579351 | 169646406 |
a0003c0003t0024 | 0/0 | 6354 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6349): Show |
chr2 | 169579351 | 169646406 |
a0003c0003t0031 | 0/0 | 6354 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6349): Show |
chr2 | 169579351 | 169646406 |
a0004c0008t0001 | 0/0 | 6357 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6352): Show |
chr2 | 169579351 | 169646406 |
a0005c0006t0018 | 0/0 | 6354 | 2 | 0 | 0 | 1 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | GCGAC others(6349): Show |
chr2 | 169579351 | 169646406 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0341 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0005g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0152 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0006g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0007g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0011g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0011g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0011g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0011g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0012g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0012g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0012g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0012g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0012g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0013g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0013g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0015g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0017g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0019g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0019g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0021g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0022g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0025g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0026g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0027g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0028g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0029g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0032g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0001t0033g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0005t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0005t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0007t0013g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0001c0007t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0001 | 0/0 | 4 | 0 | 1 | 1 | 1 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0119 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0010g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0014g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0014g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0014g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0020g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0023g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0030g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0002t0034g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0002c0004t0003g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0003 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0004g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0008g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0016g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0016g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0024g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0003c0003t0031g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0004c0008t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0004c0008t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0005c0006t0018g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
a0005c0006t0018g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0240 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00140 | hp1 | a0001 | c0001 | t0005 | g0344 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00140 | hp2 | a0003 | c0003 | t0008 | g0321 | EUR | GBR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0276 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00280 | hp2 | a0003 | c0003 | t0004 | g0114 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0083 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00323 | hp2 | a0003 | c0003 | t0004 | g0096 | EUR | FIN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00423 | hp1 | a0002 | c0002 | t0003 | g0182 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00438 | hp1 | a0001 | c0001 | t0019 | g0304 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0338 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00558 | hp2 | a0003 | c0003 | t0031 | g0359 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00609 | hp1 | a0001 | c0001 | t0005 | g0333 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00609 | hp2 | a0002 | c0002 | t0010 | g0265 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00621 | hp1 | a0001 | c0001 | t0019 | g0132 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00621 | hp2 | a0001 | c0001 | t0005 | g0348 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0244 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0222 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00733 | hp1 | a0003 | c0003 | t0004 | g0097 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0135 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00735 | hp1 | a0003 | c0003 | t0008 | g0323 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0224 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01069 | hp1 | a0003 | c0003 | t0008 | g0325 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0133 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0247 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01070 | hp2 | a0001 | c0001 | t0033 | g0141 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01071 | hp1 | a0001 | c0001 | t0029 | g0134 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01071 | hp2 | a0001 | c0001 | t0006 | g0149 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01074 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0136 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01081 | hp1 | a0001 | c0001 | t0006 | g0146 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01099 | hp1 | a0003 | c0003 | t0004 | g0129 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01099 | hp2 | a0001 | c0001 | t0006 | g0154 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01106 | hp1 | a0003 | c0003 | t0008 | g0131 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01109 | hp1 | a0003 | c0003 | t0008 | g0360 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0263 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01168 | hp1 | a0003 | c0003 | t0008 | g0318 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0142 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0316 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01192 | hp2 | a0002 | c0004 | t0003 | g0012 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0231 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01255 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01256 | hp1 | a0003 | c0003 | t0004 | g0010 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01256 | hp2 | a0003 | c0003 | t0008 | g0123 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01258 | hp1 | a0003 | c0003 | t0004 | g0010 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0274 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0277 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01346 | hp1 | a0001 | c0001 | t0006 | g0148 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0234 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01358 | hp2 | a0002 | c0004 | t0003 | g0012 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0178 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01496 | hp1 | a0003 | c0003 | t0004 | g0356 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0278 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0296 | EUR | IBS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0008 | EUR | IBS | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0282 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01884 | hp2 | a0003 | c0003 | t0004 | g0128 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01891 | hp1 | a0001 | c0001 | t0007 | g0176 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01891 | hp2 | a0003 | c0003 | t0004 | g0109 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01978 | hp2 | a0003 | c0003 | t0008 | g0327 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02027 | hp1 | a0003 | c0003 | t0004 | g0099 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0208 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02055 | hp1 | a0003 | c0003 | t0004 | g0098 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02056 | hp1 | a0002 | c0002 | t0003 | g0195 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0140 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0258 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0251 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02080 | hp2 | a0001 | c0001 | t0005 | g0345 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02083 | hp1 | a0001 | c0001 | t0006 | g0155 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02129 | hp1 | a0002 | c0002 | t0003 | g0171 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02132 | hp1 | a0002 | c0002 | t0020 | g0235 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0157 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0343 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02135 | hp2 | a0002 | c0002 | t0030 | g0199 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02145 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0255 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CDX | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | CDX | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0297 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0306 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02258 | hp2 | a0001 | c0007 | t0013 | g0029 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0211 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0250 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02280 | hp1 | a0001 | c0001 | t0028 | g0138 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0016 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0272 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0254 | AMR | PEL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02451 | hp1 | a0003 | c0003 | t0008 | g0320 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02451 | hp2 | a0001 | c0001 | t0015 | g0033 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0145 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02523 | hp2 | a0001 | c0001 | t0009 | g0067 | EAS | KHV | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02572 | hp1 | a0003 | c0003 | t0004 | g0101 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02602 | hp1 | a0003 | c0003 | t0008 | g0326 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02615 | hp1 | a0001 | c0001 | t0007 | g0094 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02615 | hp2 | a0003 | c0003 | t0004 | g0117 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0303 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02630 | hp2 | a0001 | c0001 | t0011 | g0162 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0288 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02647 | hp2 | a0001 | c0001 | t0011 | g0164 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02698 | hp1 | a0001 | c0001 | t0005 | g0349 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02698 | hp2 | a0003 | c0003 | t0024 | g0118 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0031 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0024 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0095 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02735 | hp1 | a0002 | c0002 | t0003 | g0188 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02735 | hp2 | a0001 | c0001 | t0006 | g0147 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02738 | hp1 | a0003 | c0003 | t0008 | g0357 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0216 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02809 | hp2 | a0003 | c0003 | t0004 | g0124 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02886 | hp1 | a0003 | c0003 | t0004 | g0108 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02886 | hp2 | a0001 | c0001 | t0006 | g0151 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02895 | hp1 | a0002 | c0002 | t0003 | g0179 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02895 | hp2 | a0003 | c0003 | t0004 | g0354 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02896 | hp1 | a0003 | c0003 | t0004 | g0100 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0023 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02897 | hp1 | a0002 | c0002 | t0014 | g0183 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02897 | hp2 | a0001 | c0001 | t0007 | g0022 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02922 | hp1 | a0003 | c0003 | t0004 | g0127 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02922 | hp2 | a0003 | c0003 | t0004 | g0105 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02965 | hp1 | a0001 | c0001 | t0015 | g0032 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02965 | hp2 | a0003 | c0003 | t0004 | g0003 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0042 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02970 | hp2 | a0004 | c0008 | t0001 | g0301 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02976 | hp1 | a0003 | c0003 | t0008 | g0328 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0293 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03017 | hp1 | a0001 | c0001 | t0005 | g0341 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03041 | hp1 | a0002 | c0002 | t0003 | g0184 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03098 | hp1 | a0001 | c0001 | t0012 | g0041 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03098 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03130 | hp1 | a0003 | c0003 | t0004 | g0126 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03130 | hp2 | a0004 | c0008 | t0001 | g0300 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03139 | hp1 | a0001 | c0007 | t0013 | g0030 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0092 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03195 | hp1 | a0001 | c0001 | t0012 | g0036 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03195 | hp2 | a0003 | c0003 | t0004 | g0355 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03209 | hp1 | a0002 | c0002 | t0003 | g0309 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03209 | hp2 | a0001 | c0001 | t0025 | g0034 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03225 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03225 | hp2 | a0002 | c0002 | t0003 | g0310 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03239 | hp1 | a0003 | c0003 | t0004 | g0112 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03239 | hp2 | a0002 | c0002 | t0003 | g0185 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0286 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03453 | hp2 | a0003 | c0003 | t0004 | g0107 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03486 | hp1 | a0001 | c0001 | t0011 | g0305 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03486 | hp2 | a0001 | c0001 | t0026 | g0035 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03490 | hp1 | a0003 | c0003 | t0008 | g0319 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03490 | hp2 | a0003 | c0003 | t0004 | g0120 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03491 | hp1 | a0001 | c0001 | t0005 | g0331 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0245 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03492 | hp2 | a0003 | c0003 | t0004 | g0122 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0307 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0242 | AFR | ESN | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03540 | hp1 | a0003 | c0003 | t0004 | g0003 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0284 | AFR | GWD | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03654 | hp1 | a0005 | c0006 | t0018 | g0115 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0275 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0161 | SAS | PJL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0139 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03831 | hp2 | a0003 | c0003 | t0004 | g0121 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0253 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03834 | hp2 | a0002 | c0002 | t0001 | g0221 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0236 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03927 | hp2 | a0001 | c0001 | t0009 | g0069 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0279 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0210 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0317 | SAS | BEB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04199 | hp2 | a0002 | c0002 | t0003 | g0192 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04228 | hp1 | a0003 | c0003 | t0004 | g0116 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG04228 | hp2 | a0002 | c0002 | t0001 | g0243 | SAS | STU | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18522 | hp1 | a0001 | c0001 | t0013 | g0028 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0093 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18612 | hp1 | a0002 | c0002 | t0003 | g0196 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18612 | hp2 | a0001 | c0005 | t0002 | g0080 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0334 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18747 | hp2 | a0002 | c0002 | t0010 | g0239 | EAS | CHB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0173 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0298 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18939 | hp2 | a0002 | c0002 | t0003 | g0206 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0262 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18942 | hp2 | a0001 | c0001 | t0009 | g0077 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18943 | hp2 | a0001 | c0001 | t0022 | g0060 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18945 | hp1 | a0002 | c0002 | t0010 | g0013 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18945 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18946 | hp1 | a0002 | c0004 | t0003 | g0201 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18946 | hp2 | a0001 | c0001 | t0006 | g0143 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18947 | hp1 | a0002 | c0002 | t0034 | g0232 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18948 | hp1 | a0002 | c0002 | t0010 | g0312 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18948 | hp2 | a0002 | c0002 | t0003 | g0186 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18950 | hp1 | a0002 | c0002 | t0001 | g0220 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18950 | hp2 | a0002 | c0002 | t0003 | g0193 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0271 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18951 | hp2 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18952 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18953 | hp1 | a0002 | c0002 | t0010 | g0238 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18953 | hp2 | a0002 | c0002 | t0003 | g0177 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18954 | hp1 | a0002 | c0002 | t0003 | g0189 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18957 | hp2 | a0002 | c0002 | t0010 | g0294 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18960 | hp1 | a0002 | c0002 | t0003 | g0205 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18961 | hp1 | a0002 | c0002 | t0003 | g0190 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18962 | hp2 | a0002 | c0002 | t0003 | g0191 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18965 | hp1 | a0002 | c0004 | t0003 | g0197 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18965 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18966 | hp2 | a0001 | c0001 | t0009 | g0007 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18972 | hp2 | a0002 | c0002 | t0010 | g0209 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0229 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18980 | hp1 | a0002 | c0002 | t0001 | g0280 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0351 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18982 | hp2 | a0002 | c0002 | t0014 | g0207 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18984 | hp1 | a0002 | c0002 | t0003 | g0011 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18985 | hp2 | a0001 | c0001 | t0009 | g0027 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18986 | hp1 | a0002 | c0002 | t0003 | g0204 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18986 | hp2 | a0002 | c0002 | t0003 | g0168 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18990 | hp2 | a0001 | c0001 | t0005 | g0346 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18991 | hp2 | a0001 | c0001 | t0005 | g0347 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0332 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18993 | hp2 | a0002 | c0002 | t0003 | g0200 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0268 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18995 | hp2 | a0001 | c0001 | t0005 | g0335 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18997 | hp1 | a0002 | c0002 | t0001 | g0230 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18997 | hp2 | a0003 | c0003 | t0008 | g0324 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18998 | hp2 | a0003 | c0003 | t0008 | g0358 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18999 | hp2 | a0001 | c0001 | t0021 | g0007 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19000 | hp1 | a0001 | c0005 | t0002 | g0078 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19000 | hp2 | a0002 | c0004 | t0003 | g0198 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0340 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19001 | hp2 | a0001 | c0001 | t0009 | g0052 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19002 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19002 | hp2 | a0002 | c0002 | t0003 | g0170 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19003 | hp1 | a0005 | c0006 | t0018 | g0110 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19003 | hp2 | a0001 | c0001 | t0009 | g0039 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19004 | hp2 | a0002 | c0004 | t0003 | g0202 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19006 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19006 | hp2 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19007 | hp1 | a0002 | c0002 | t0003 | g0169 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19007 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19009 | hp1 | a0001 | c0001 | t0005 | g0342 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19009 | hp2 | a0003 | c0003 | t0016 | g0113 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0267 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19010 | hp2 | a0002 | c0004 | t0003 | g0363 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0241 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0038 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0287 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19043 | hp2 | a0003 | c0003 | t0004 | g0106 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19056 | hp1 | a0002 | c0002 | t0014 | g0167 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19062 | hp1 | a0001 | c0001 | t0005 | g0339 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19062 | hp2 | a0002 | c0004 | t0003 | g0180 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19064 | hp2 | a0002 | c0004 | t0003 | g0362 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0281 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0226 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0350 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19068 | hp1 | a0002 | c0002 | t0010 | g0212 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19070 | hp1 | a0001 | c0001 | t0009 | g0005 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19074 | hp1 | a0003 | c0003 | t0016 | g0111 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19074 | hp2 | a0001 | c0001 | t0005 | g0353 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19075 | hp1 | a0002 | c0002 | t0003 | g0203 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19075 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19077 | hp1 | a0002 | c0002 | t0003 | g0181 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19077 | hp2 | a0001 | c0001 | t0009 | g0059 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0259 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19082 | hp2 | a0001 | c0001 | t0005 | g0361 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19083 | hp1 | a0002 | c0002 | t0003 | g0166 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19083 | hp2 | a0002 | c0002 | t0001 | g0290 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19088 | hp1 | a0001 | c0005 | t0002 | g0079 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19088 | hp2 | a0002 | c0002 | t0003 | g0194 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19091 | hp1 | a0001 | c0001 | t0009 | g0074 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0352 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0283 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA19240 | hp2 | a0003 | c0003 | t0004 | g0130 | AFR | YRI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20129 | hp1 | a0002 | c0002 | t0003 | g0311 | AFR | ASW | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0158 | AFR | ASW | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0001 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20752 | hp2 | a0002 | c0002 | t0003 | g0187 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20805 | hp1 | a0002 | c0002 | t0023 | g0219 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20805 | hp2 | a0003 | c0003 | t0008 | g0329 | EUR | TSI | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20905 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | GIH | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20905 | hp2 | a0003 | c0003 | t0008 | g0322 | SAS | GIH | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02109 | hp1 | a0003 | c0003 | t0004 | g0103 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02109 | hp2 | a0001 | c0001 | t0027 | g0018 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0291 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02486 | hp2 | a0001 | c0001 | t0011 | g0163 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02559 | hp1 | a0003 | c0003 | t0004 | g0125 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0037 | AFR | ACB | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03471 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG03471 | hp2 | a0002 | c0002 | t0003 | g0308 | AFR | MSL | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG06807 | hp1 | a0003 | c0003 | t0004 | g0104 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0299 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18955 | hp1 | a0002 | c0002 | t0003 | g0172 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA18955 | hp2 | a0001 | c0001 | t0017 | g0004 | EAS | JPT | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20300 | hp1 | a0003 | c0003 | t0004 | g0102 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA20300 | hp2 | a0001 | c0001 | t0007 | g0175 | AFR | USA | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0285 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
NA21309 | hp2 | a0001 | c0001 | t0032 | g0137 | AFR | LWK | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0152 | REF | REF | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0119 | REF | REF | PPIG_chr2_169579351_169646406 | PPIG | chr2 | 169579351 | 169646406 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:169604026 | A | C | 1 | a0001 | 8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
splice_region_variant | LOW | c.-16A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 3/14 | chr2 | 169604026 | |||||||
chr2:169636593 | T | A | 3 | a0001 a0003 a0005 |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
missense_variant | MODERATE | c.1335T>A | p.Asp445Glu | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1544/6357 | 1335/2265 | 445/754 | chr2 | 169636593 | |||
chr2:169637057 | G | C | 1 | a0005 | 2 | HG03654.hp1 NA19003.hp1 |
missense_variant | MODERATE | c.1799G>C | p.Arg600Thr | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2008/6357 | 1799/2265 | 600/754 | chr2 | 169637057 | |||
chr2:169637167 | C | G | 1 | a0004 | 2 | HG02970.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1909C>G | p.Gln637Glu | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2118/6357 | 1909/2265 | 637/754 | chr2 | 169637167 | |||
chr2:169637353 | A | G | 2 | a0003 a0005 |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
missense_variant | MODERATE | c.2095A>G | p.Asn699Asp | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2304/6357 | 2095/2265 | 699/754 | chr2 | 169637353 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:169608672 | C | T | 1 | a0001c0005 | 3 | NA18612.hp2 NA19000.hp1 NA19088.hp1 |
splice_region_variant&synonymous_variant | LOW | c.291C>T | p.Asp97Asp | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/14 | 500/6357 | 291/2265 | 97/754 | chr2 | 169608672 | |||
chr2:169636743 | A | G | 1 | a0002c0004 | 9 | HG01192.hp2 HG01358.hp2 NA18946.hp1 others(6): Show |
synonymous_variant | LOW | c.1485A>G | p.Glu495Glu | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1694/6357 | 1485/2265 | 495/754 | chr2 | 169636743 | |||
chr2:169637274 | T | C | 1 | a0001c0007 | 2 | HG02258.hp2 HG03139.hp1 |
synonymous_variant | LOW | c.2016T>C | p.Asn672Asn | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2225/6357 | 2016/2265 | 672/754 | chr2 | 169637274 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:169584385 | G | T | 1 | a0001c0001t0019 | 2 | HG00438.hp1 HG00621.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-175G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/14 | chr2 | 169584385 | |||||||
chr2:169584406 | G | A | 1 | a0002c0002t0020 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-154G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/14 | 19636 | chr2 | 169584406 | ||||||
chr2:169584452 | G | A | 1 | a0001c0001t0021 | 1 | NA18999.hp2 | 5_prime_UTR_variant | MODIFIER | c.-108G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/14 | 19590 | chr2 | 169584452 | ||||||
chr2:169637557 | G | A | 2 | a0001c0001t0009 a0001c0001t0022 |
11 | HG02523.hp2 HG03927.hp2 NA18942.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*34G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 34 | chr2 | 169637557 | ||||||
chr2:169637935 | T | C | 1 | a0002c0002t0023 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 412 | chr2 | 169637935 | ||||||
chr2:169638324 | T | G | 1 | a0003c0003t0024 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*801T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 801 | chr2 | 169638324 | ||||||
chr2:169638341 | T | TA | 14 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0011 others(11): Show |
108 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*830dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 831 | INFO_REALIGN_3_PRIME | chr2 | 169638341 | |||||
chr2:169638747 | A | G | 1 | a0001c0001t0022 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1224A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1224 | chr2 | 169638747 | ||||||
chr2:169638856 | A | G | 1 | a0002c0002t0034 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1333 | chr2 | 169638856 | ||||||
chr2:169639157 | C | A | 4 | a0001c0001t0012 a0001c0001t0015 a0001c0001t0025 others(1): Show |
9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1634C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1634 | chr2 | 169639157 | ||||||
chr2:169639294 | T | C | 1 | a0001c0001t0015 | 2 | HG02451.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1771T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1771 | chr2 | 169639294 | ||||||
chr2:169639299 | T | A | 1 | a0002c0002t0010 | 8 | HG00609.hp2 NA18747.hp2 NA18945.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1776T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1776 | chr2 | 169639299 | ||||||
chr2:169639418 | AT | A | 27 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(24): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
3_prime_UTR_variant | MODIFIER | c.*1903delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1903 | INFO_REALIGN_3_PRIME | chr2 | 169639418 | |||||
chr2:169639505 | C | T | 4 | a0001c0001t0006 a0001c0001t0019 a0001c0001t0029 others(1): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1982C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 1982 | chr2 | 169639505 | ||||||
chr2:169639976 | C | T | 1 | a0005c0006t0018 | 2 | HG03654.hp1 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2453C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2453 | chr2 | 169639976 | ||||||
chr2:169640080 | C | T | 1 | a0001c0001t0025 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2557C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2557 | chr2 | 169640080 | ||||||
chr2:169640102 | G | T | 2 | a0001c0001t0013 a0001c0007t0013 |
4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2579G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2579 | chr2 | 169640102 | ||||||
chr2:169640171 | A | G | 2 | a0001c0001t0028 a0001c0001t0032 |
2 | HG02280.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2648A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 2648 | chr2 | 169640171 | ||||||
chr2:169640535 | G | T | 1 | a0002c0002t0030 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3012G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3012 | chr2 | 169640535 | ||||||
chr2:169640669 | T | C | 1 | a0001c0001t0005 | 26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3146T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3146 | chr2 | 169640669 | ||||||
chr2:169640911 | G | A | 2 | a0003c0003t0008 a0003c0003t0031 |
18 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3388G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3388 | chr2 | 169640911 | ||||||
chr2:169640989 | T | G | 1 | a0003c0003t0031 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3466T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3466 | chr2 | 169640989 | ||||||
chr2:169641024 | A | G | 5 | a0001c0001t0017 a0002c0002t0003 a0002c0002t0014 others(2): Show |
50 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*3501A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3501 | chr2 | 169641024 | ||||||
chr2:169641043 | T | C | 1 | a0003c0003t0016 | 2 | NA19009.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3520T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3520 | chr2 | 169641043 | ||||||
chr2:169641136 | G | A | 1 | a0001c0001t0027 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3613G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3613 | chr2 | 169641136 | ||||||
chr2:169641136 | GCT | G | 6 | a0003c0003t0004 a0003c0003t0008 a0003c0003t0016 others(3): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3618_*3619delCT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3618 | INFO_REALIGN_3_PRIME | chr2 | 169641136 | |||||
chr2:169641254 | A | C | 2 | a0001c0001t0028 a0001c0001t0032 |
2 | HG02280.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3731A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3731 | chr2 | 169641254 | ||||||
chr2:169641254 | A | G | 2 | a0001c0001t0029 a0001c0001t0033 |
2 | HG01070.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3731A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 14/14 | 3731 | chr2 | 169641254 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:169584491 | G | A | 83 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(80): Show |
88 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(85): Show |
splice_donor_variant&intron_variant | HIGH | c.-70+1G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584491 | |||||||
chr2:169584508 | C | G | 2 | a0002c0004t0003g0362 a0002c0004t0003g0363 |
2 | NA19010.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-70+18C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584508 | |||||||
chr2:169584916 | G | A | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+426G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584916 | |||||||
chr2:169584952 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-70+462C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169584952 | |||||||
chr2:169585020 | C | A | 1 | a0001c0001t0005g0091 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-70+530C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585020 | |||||||
chr2:169585050 | T | C | 5 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70+560T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585050 | |||||||
chr2:169585253 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-70+763T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585253 | |||||||
chr2:169585270 | C | CCTTTTTT others(5): Show |
1 | a0001c0001t0009g0027 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-70+780_-70+781ins others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585270 | |||||||
chr2:169585270 | C | CTTTTTTT others(3): Show |
32 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(29): Show |
32 | HG00621.hp1 HG00733.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585270 | C | CTTTTTTT others(4): Show |
160 | a0001c0001t0002g0040 a0001c0001t0007g0173 a0001c0001t0007g0174 others(157): Show |
166 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585270 | C | CTTTTTTT others(5): Show |
74 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(71): Show |
81 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585270 | C | CTTTTTTT others(6): Show |
13 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(10): Show |
13 | HG01433.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585270 | C | CTTTTTTT others(7): Show |
2 | a0001c0001t0007g0024 a0001c0001t0007g0025 |
2 | HG02572.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585270 | C | CTTTTTTT others(8): Show |
2 | a0003c0003t0008g0318 a0003c0003t0008g0319 |
2 | HG01168.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585270 | C | CTTTTTTT others(9): Show |
35 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(32): Show |
35 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(16): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585270 | C | CTTTTTTT others(10): Show |
8 | a0001c0001t0005g0361 a0003c0003t0004g0354 a0003c0003t0004g0355 others(5): Show |
8 | HG00558.hp2 HG01109.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.-70+789_-70+790ins others(17): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169585270 | ||||||
chr2:169585533 | A | G | 7 | a0002c0002t0001g0297 a0002c0002t0001g0298 a0002c0002t0001g0299 others(4): Show |
7 | HG01261.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+1043A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585533 | |||||||
chr2:169585591 | G | C | 2 | a0001c0001t0019g0132 a0001c0001t0019g0304 |
2 | HG00438.hp1 HG00621.hp1 |
intron_variant | MODIFIER | c.-70+1101G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585591 | |||||||
chr2:169585657 | A | G | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+1167A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585657 | |||||||
chr2:169585827 | A | T | 1 | a0001c0001t0006g0161 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-70+1337A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169585827 | |||||||
chr2:169586077 | T | C | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-70+1587T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586077 | |||||||
chr2:169586078 | G | C | 4 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(1): Show |
4 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+1588G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586078 | |||||||
chr2:169586112 | A | G | 1 | a0001c0001t0002g0086 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-70+1622A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586112 | |||||||
chr2:169586130 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-70+1640C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586130 | |||||||
chr2:169586132 | TAAAC | T | 17 | a0003c0003t0008g0131 a0003c0003t0008g0318 a0003c0003t0008g0319 others(14): Show |
17 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-70+1645_-70+1648d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169586132 | ||||||
chr2:169586165 | T | A | 4 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+1675T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586165 | |||||||
chr2:169586200 | C | A | 7 | a0002c0002t0003g0165 a0002c0002t0003g0166 a0002c0002t0003g0168 others(4): Show |
7 | HG02129.hp1 NA18986.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.-70+1710C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586200 | |||||||
chr2:169586230 | A | G | 4 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(1): Show |
4 | NA18981.hp2 NA19066.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+1740A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586230 | |||||||
chr2:169586238 | T | A | 1 | a0002c0002t0003g0172 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-70+1748T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586238 | |||||||
chr2:169586241 | T | C | 27 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(24): Show |
27 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.-70+1751T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586241 | |||||||
chr2:169586249 | T | C | 46 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(43): Show |
48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70+1759T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586249 | |||||||
chr2:169586265 | A | C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+1775A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586265 | |||||||
chr2:169586266 | G | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+1776G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586266 | |||||||
chr2:169586275 | T | TTGTCAGG others(11): Show |
1 | a0002c0002t0003g0177 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-70+1797_-70+1814d others(20): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169586275 | ||||||
chr2:169586503 | A | T | 1 | a0002c0002t0001g0296 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-70+2013A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586503 | |||||||
chr2:169586525 | A | C | 39 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(36): Show |
40 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-70+2035A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586525 | |||||||
chr2:169586555 | G | C | 31 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(28): Show |
32 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.-70+2065G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586555 | |||||||
chr2:169586560 | G | T | 1 | a0001c0001t0005g0349 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-70+2070G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586560 | |||||||
chr2:169586619 | A | C | 1 | a0001c0001t0007g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-70+2129A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586619 | |||||||
chr2:169586738 | C | T | 1 | a0002c0002t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-70+2248C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586738 | |||||||
chr2:169586742 | TTTAG | T | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+2257_-70+2260d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169586742 | ||||||
chr2:169586933 | T | G | 9 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70+2443T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169586933 | |||||||
chr2:169587023 | T | C | 1 | a0002c0002t0001g0178 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-70+2533T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587023 | |||||||
chr2:169587177 | T | C | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0026g0035 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-70+2687T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587177 | |||||||
chr2:169587233 | C | T | 2 | a0001c0001t0007g0022 a0001c0001t0007g0023 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-70+2743C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587233 | |||||||
chr2:169587249 | C | CT | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+2769dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169587249 | ||||||
chr2:169587308 | C | G | 110 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(107): Show |
114 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-70+2818C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587308 | |||||||
chr2:169587435 | T | A | 1 | a0001c0001t0012g0031 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-70+2945T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587435 | |||||||
chr2:169587511 | A | G | 88 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(85): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.-70+3021A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587511 | |||||||
chr2:169587691 | C | G | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+3201C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587691 | |||||||
chr2:169587894 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+3404A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169587894 | |||||||
chr2:169588004 | G | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+3514G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588004 | |||||||
chr2:169588146 | C | CAA | 281 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(278): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.-70+3656_-70+3657i others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588146 | |||||||
chr2:169588234 | C | CGT | 4 | a0001c0001t0002g0008 a0001c0001t0002g0083 a0001c0001t0002g0084 others(1): Show |
5 | HG00323.hp1 HG01123.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+3757_-70+3758d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588234 | ||||||
chr2:169588239 | G | A | 1 | a0001c0001t0005g0330 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-70+3749G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588239 | |||||||
chr2:169588247 | G | A | 154 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(151): Show |
160 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-70+3757G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588247 | |||||||
chr2:169588249 | A | G | 1 | a0003c0003t0008g0329 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-70+3759A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588249 | |||||||
chr2:169588359 | A | T | 1 | a0001c0001t0012g0031 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-70+3869A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588359 | |||||||
chr2:169588478 | A | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+3988A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588478 | |||||||
chr2:169588536 | A | T | 4 | a0002c0002t0003g0204 a0002c0002t0003g0205 a0002c0002t0003g0206 others(1): Show |
4 | NA18939.hp2 NA18960.hp1 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+4046A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588536 | |||||||
chr2:169588546 | G | A | 2 | a0002c0002t0003g0165 a0002c0002t0003g0166 |
2 | NA19006.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-70+4056G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588546 | |||||||
chr2:169588690 | A | G | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-70+4200A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588690 | |||||||
chr2:169588752 | G | A | 46 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(43): Show |
48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70+4262G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588752 | |||||||
chr2:169588803 | A | G | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+4313A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588803 | |||||||
chr2:169588928 | C | A | 1 | a0003c0003t0004g0096 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-70+4438C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169588928 | |||||||
chr2:169588958 | C | CA | 12 | a0001c0001t0002g0043 a0001c0001t0002g0044 a0001c0001t0002g0045 others(9): Show |
12 | HG00733.hp1 HG01255.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.-70+4493dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | ||||||
chr2:169588958 | CA | C | 128 | a0001c0001t0002g0051 a0001c0001t0002g0053 a0001c0001t0002g0054 others(125): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.-70+4493delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | ||||||
chr2:169588958 | CAA | C | 99 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(96): Show |
104 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.-70+4492_-70+4493d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | ||||||
chr2:169588958 | CAAA | C | 46 | a0001c0001t0006g0156 a0002c0002t0001g0292 a0002c0002t0001g0293 others(43): Show |
48 | HG01168.hp2 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.-70+4491_-70+4493d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | ||||||
chr2:169588958 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0007g0176 a0001c0001t0011g0015 a0001c0001t0011g0162 others(4): Show |
8 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-70+4485_-70+4493d others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169588958 | ||||||
chr2:169589104 | T | C | 1 | a0002c0002t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-70+4614T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589104 | |||||||
chr2:169589272 | A | G | 3 | a0001c0001t0002g0002 a0001c0001t0002g0081 a0001c0001t0002g0082 |
5 | NA18947.hp2 NA18964.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+4782A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589272 | |||||||
chr2:169589286 | C | T | 4 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(1): Show |
4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+4796C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589286 | |||||||
chr2:169589370 | T | C | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-70+4880T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589370 | |||||||
chr2:169589409 | G | A | 1 | a0002c0002t0003g0181 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-70+4919G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589409 | |||||||
chr2:169589545 | A | G | 3 | a0001c0005t0002g0078 a0001c0005t0002g0079 a0001c0005t0002g0080 |
3 | NA18612.hp2 NA19000.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-70+5055A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589545 | |||||||
chr2:169589652 | G | GT | 4 | a0001c0001t0006g0161 a0001c0001t0009g0077 a0002c0002t0001g0273 others(1): Show |
4 | HG03669.hp2 HG04184.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+5169dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169589652 | ||||||
chr2:169589660 | G | T | 3 | a0003c0003t0004g0354 a0003c0003t0004g0355 a0003c0003t0004g0356 |
3 | HG01496.hp1 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-70+5170G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589660 | |||||||
chr2:169589667 | G | T | 1 | a0001c0001t0006g0155 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-70+5177G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589667 | |||||||
chr2:169589680 | G | A | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18939.hp1 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+5190G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589680 | |||||||
chr2:169589689 | C | A | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+5199C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589689 | |||||||
chr2:169589811 | A | G | 7 | a0003c0003t0004g0124 a0003c0003t0004g0125 a0003c0003t0004g0126 others(4): Show |
7 | HG01099.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+5321A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589811 | |||||||
chr2:169589861 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+5371A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169589861 | |||||||
chr2:169590085 | G | A | 9 | a0002c0002t0001g0216 a0002c0002t0001g0274 a0002c0002t0001g0275 others(6): Show |
9 | HG00280.hp1 HG01192.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-70+5595G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590085 | |||||||
chr2:169590129 | C | CA | 13 | a0001c0001t0005g0333 a0001c0001t0007g0009 a0001c0001t0007g0092 others(10): Show |
15 | HG00609.hp1 HG02145.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-70+5651dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169590129 | ||||||
chr2:169590129 | C | CAA | 151 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(148): Show |
157 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.-70+5650_-70+5651d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169590129 | ||||||
chr2:169590136 | A | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(79): Show |
87 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.-70+5646A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590136 | |||||||
chr2:169590158 | G | A | 13 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(10): Show |
15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-70+5668G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590158 | |||||||
chr2:169590289 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(67): Show |
75 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-70+5799G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590289 | |||||||
chr2:169590369 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+5879A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590369 | |||||||
chr2:169590388 | G | A | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0026g0035 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-70+5898G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590388 | |||||||
chr2:169590403 | G | A | 1 | a0003c0003t0004g0099 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-70+5913G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590403 | |||||||
chr2:169590534 | C | T | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-70+6044C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590534 | |||||||
chr2:169590784 | C | G | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+6294C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590784 | |||||||
chr2:169590847 | A | T | 6 | a0001c0001t0006g0154 a0001c0001t0007g0158 a0001c0001t0007g0173 others(3): Show |
6 | HG01099.hp2 HG01891.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+6357A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590847 | |||||||
chr2:169590848 | T | A | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+6358T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590848 | |||||||
chr2:169590877 | C | T | 1 | a0002c0002t0001g0270 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-70+6387C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590877 | |||||||
chr2:169590879 | C | T | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+6389C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169590879 | |||||||
chr2:169591026 | C | T | 3 | a0002c0004t0003g0012 a0002c0004t0003g0201 a0002c0004t0003g0202 |
4 | HG01192.hp2 HG01358.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+6536C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591026 | |||||||
chr2:169591035 | T | C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+6545T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591035 | |||||||
chr2:169591065 | G | A | 1 | a0003c0003t0004g0354 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-70+6575G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591065 | |||||||
chr2:169591186 | G | A | 3 | a0002c0002t0003g0179 a0002c0002t0003g0184 a0002c0002t0014g0183 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.-70+6696G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591186 | |||||||
chr2:169591188 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+6698C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591188 | |||||||
chr2:169591224 | T | C | 1 | a0002c0002t0001g0217 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-70+6734T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591224 | |||||||
chr2:169591271 | A | G | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+6781A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591271 | |||||||
chr2:169591341 | A | C | 1 | a0001c0001t0002g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-70+6851A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591341 | |||||||
chr2:169591677 | G | A | 4 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(1): Show |
4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+7187G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591677 | |||||||
chr2:169591754 | A | C | 1 | a0001c0001t0002g0076 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-70+7264A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169591754 | |||||||
chr2:169591781 | A | AT | 280 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(277): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.-70+7302dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591781 | ||||||
chr2:169591781 | A | ATT | 21 | a0001c0001t0006g0136 a0001c0001t0006g0139 a0001c0001t0006g0142 others(18): Show |
21 | HG00438.hp1 HG00621.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.-70+7301_-70+7302d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591781 | ||||||
chr2:169591920 | A | AT | 32 | a0001c0001t0005g0332 a0001c0001t0006g0133 a0001c0001t0006g0136 others(29): Show |
34 | HG00438.hp1 HG01069.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.-70+7455dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | ||||||
chr2:169591920 | A | ATT | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(38): Show |
45 | HG00099.hp1 HG00323.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.-70+7454_-70+7455d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | ||||||
chr2:169591920 | A | ATTT | 27 | a0001c0001t0002g0006 a0001c0001t0002g0026 a0001c0001t0002g0045 others(24): Show |
28 | HG00438.hp2 HG00733.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.-70+7453_-70+7455d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | ||||||
chr2:169591920 | AT | A | 49 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0333 others(46): Show |
52 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-70+7455delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | ||||||
chr2:169591920 | ATT | A | 44 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(41): Show |
45 | HG00609.hp2 HG00673.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.-70+7454_-70+7455d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | ||||||
chr2:169591920 | ATTT | A | 123 | a0001c0001t0012g0031 a0001c0001t0015g0032 a0001c0001t0015g0033 others(120): Show |
128 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.-70+7453_-70+7455d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | ||||||
chr2:169591920 | ATTTTTTT others(2): Show |
A | 21 | a0003c0003t0004g0354 a0003c0003t0004g0355 a0003c0003t0004g0356 others(18): Show |
21 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.-70+7447_-70+7455d others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169591920 | ||||||
chr2:169592007 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7517A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592007 | |||||||
chr2:169592099 | AT | A | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7619delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592099 | ||||||
chr2:169592192 | C | T | 19 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(16): Show |
19 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.-70+7702C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592192 | |||||||
chr2:169592207 | T | C | 1 | a0003c0003t0004g0100 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-70+7717T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592207 | |||||||
chr2:169592267 | T | C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7777T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592267 | |||||||
chr2:169592272 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+7782C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592272 | |||||||
chr2:169592303 | C | CT | 66 | a0001c0001t0007g0019 a0001c0001t0007g0025 a0001c0001t0007g0094 others(63): Show |
69 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(66): Show |
intron_variant | MODIFIER | c.-70+7832dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | ||||||
chr2:169592303 | C | CTT | 132 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(129): Show |
136 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.-70+7831_-70+7832d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | ||||||
chr2:169592303 | C | CTTT | 15 | a0001c0001t0005g0343 a0001c0001t0005g0344 a0001c0001t0005g0348 others(12): Show |
15 | HG00140.hp1 HG00621.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.-70+7830_-70+7832d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | ||||||
chr2:169592303 | CT | C | 57 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(54): Show |
62 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-70+7832delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169592303 | ||||||
chr2:169592306 | T | TC | 5 | a0001c0001t0007g0016 a0001c0001t0007g0020 a0001c0001t0007g0022 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-70+7816_-70+7817i others(3): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592306 | |||||||
chr2:169592402 | T | G | 1 | a0002c0002t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-70+7912T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592402 | |||||||
chr2:169592492 | G | A | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-70+8002G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592492 | |||||||
chr2:169592565 | G | A | 277 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(274): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-70+8075G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592565 | |||||||
chr2:169592755 | C | A | 1 | a0001c0001t0027g0018 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-70+8265C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592755 | |||||||
chr2:169592771 | A | G | 4 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(1): Show |
4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+8281A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169592771 | |||||||
chr2:169593037 | A | G | 99 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(96): Show |
105 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.-70+8547A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593037 | |||||||
chr2:169593050 | C | T | 1 | a0002c0002t0003g0168 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-70+8560C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593050 | |||||||
chr2:169593056 | G | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-70+8566G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593056 | |||||||
chr2:169593126 | G | GTA | 32 | a0001c0001t0002g0085 a0003c0003t0004g0003 a0003c0003t0004g0097 others(29): Show |
34 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.-70+8652_-70+8653d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593126 | ||||||
chr2:169593126 | GTA | G | 66 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(63): Show |
68 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(65): Show |
intron_variant | MODIFIER | c.-70+8652_-70+8653d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593126 | ||||||
chr2:169593128 | A | G | 110 | a0001c0001t0006g0154 a0002c0002t0001g0001 a0002c0002t0001g0013 others(107): Show |
114 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.-70+8638A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593128 | |||||||
chr2:169593130 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-70+8640A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593130 | |||||||
chr2:169593142 | A | ATC | 3 | a0003c0003t0008g0325 a0003c0003t0008g0326 a0003c0003t0008g0360 |
3 | HG01069.hp1 HG01109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.-70+8654_-70+8655d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593142 | ||||||
chr2:169593174 | C | G | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-70+8684C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593174 | |||||||
chr2:169593338 | A | G | 282 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(279): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.-70+8848A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593338 | |||||||
chr2:169593398 | A | G | 5 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(2): Show |
5 | HG01891.hp1 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.-70+8908A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593398 | |||||||
chr2:169593491 | G | C | 1 | a0002c0002t0001g0215 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-70+9001G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593491 | |||||||
chr2:169593511 | C | G | 4 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(1): Show |
4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.-70+9021C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593511 | |||||||
chr2:169593517 | A | T | 3 | a0001c0001t0012g0036 a0001c0001t0012g0037 a0001c0001t0026g0035 |
3 | HG02559.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-70+9027A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593517 | |||||||
chr2:169593650 | C | CTT | 38 | a0001c0001t0002g0076 a0001c0001t0002g0083 a0001c0001t0006g0133 others(35): Show |
39 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.-70+9178_-70+9179d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593650 | ||||||
chr2:169593650 | C | CTTT | 58 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(55): Show |
63 | HG00099.hp1 HG00639.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.-70+9177_-70+9179d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593650 | ||||||
chr2:169593650 | CT | C | 166 | a0001c0001t0005g0334 a0001c0001t0007g0022 a0001c0001t0012g0031 others(163): Show |
172 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(169): Show |
intron_variant | MODIFIER | c.-70+9179delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593650 | ||||||
chr2:169593674 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0217 a0002c0002t0001g0268 |
4 | HG02155.hp2 NA18942.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-70+9184C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593674 | |||||||
chr2:169593720 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-70+9230C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593720 | |||||||
chr2:169593813 | A | AT | 190 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(187): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.-70+9338dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593813 | ||||||
chr2:169593813 | A | ATT | 6 | a0001c0001t0006g0153 a0002c0002t0001g0254 a0002c0002t0001g0255 others(3): Show |
6 | HG01261.hp1 HG02148.hp1 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-70+9337_-70+9338d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169593813 | ||||||
chr2:169593875 | T | C | 9 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-70+9385T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593875 | |||||||
chr2:169593950 | C | T | 9 | a0001c0001t0002g0054 a0002c0004t0003g0012 a0002c0004t0003g0180 others(6): Show |
10 | HG01175.hp2 HG01192.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.-70+9460C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169593950 | |||||||
chr2:169594028 | G | A | 7 | a0002c0002t0001g0297 a0002c0002t0001g0298 a0002c0002t0001g0299 others(4): Show |
7 | HG01261.hp2 HG02257.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70+9538G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594028 | |||||||
chr2:169594074 | T | C | 7 | a0003c0003t0004g0124 a0003c0003t0004g0125 a0003c0003t0004g0126 others(4): Show |
7 | HG01099.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-9568T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594074 | |||||||
chr2:169594099 | C | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-9543C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594099 | |||||||
chr2:169594189 | T | C | 1 | a0002c0002t0003g0185 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-69-9453T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594189 | |||||||
chr2:169594324 | C | CA | 136 | a0001c0001t0002g0008 a0001c0001t0002g0056 a0001c0001t0002g0083 others(133): Show |
141 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.-69-9305dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594324 | ||||||
chr2:169594324 | C | CAA | 127 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0040 others(124): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-69-9306_-69-9305d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594324 | ||||||
chr2:169594324 | C | CAAA | 62 | a0001c0001t0002g0002 a0001c0001t0002g0026 a0001c0001t0002g0043 others(59): Show |
64 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.-69-9307_-69-9305d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594324 | ||||||
chr2:169594359 | T | A | 3 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 |
3 | HG02486.hp2 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-69-9283T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594359 | |||||||
chr2:169594392 | G | C | 2 | a0002c0002t0003g0169 a0002c0002t0003g0170 |
2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-69-9250G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594392 | |||||||
chr2:169594438 | G | A | 1 | a0002c0002t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-69-9204G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594438 | |||||||
chr2:169594502 | C | A | 1 | a0002c0002t0001g0264 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-69-9140C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594502 | |||||||
chr2:169594625 | C | CT | 22 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(19): Show |
23 | HG00280.hp2 HG00735.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.-69-8996dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | ||||||
chr2:169594625 | CT | C | 81 | a0001c0001t0002g0051 a0001c0001t0002g0082 a0001c0001t0005g0091 others(78): Show |
82 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-69-8996delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | ||||||
chr2:169594625 | CTT | C | 72 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(69): Show |
77 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-69-8997_-69-8996d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | ||||||
chr2:169594625 | CTTT | C | 136 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(133): Show |
142 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.-69-8998_-69-8996d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | ||||||
chr2:169594625 | CTTTT | C | 6 | a0002c0002t0001g0233 a0002c0002t0001g0262 a0002c0002t0003g0203 others(3): Show |
6 | HG01074.hp1 HG02897.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-8999_-69-8996d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169594625 | ||||||
chr2:169594631 | T | C | 40 | a0001c0001t0002g0051 a0001c0001t0002g0082 a0001c0001t0006g0135 others(37): Show |
41 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.-69-9011T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594631 | |||||||
chr2:169594632 | T | C | 59 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(56): Show |
64 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-69-9010T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594632 | |||||||
chr2:169594755 | G | C | 1 | a0001c0001t0007g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-69-8887G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594755 | |||||||
chr2:169594762 | T | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-8880T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594762 | |||||||
chr2:169594883 | A | T | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-69-8759A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169594883 | |||||||
chr2:169595022 | G | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0070 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-69-8620G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595022 | |||||||
chr2:169595032 | G | A | 1 | a0001c0001t0005g0330 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-69-8610G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595032 | |||||||
chr2:169595053 | T | C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-8589T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595053 | |||||||
chr2:169595359 | G | A | 329 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-69-8283G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595359 | |||||||
chr2:169595380 | G | A | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-8262G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595380 | |||||||
chr2:169595456 | T | C | 2 | a0002c0002t0001g0299 a0002c0002t0001g0302 |
2 | HG01261.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-69-8186T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595456 | |||||||
chr2:169595516 | A | T | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69-8126A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595516 | |||||||
chr2:169595539 | C | T | 20 | a0002c0002t0001g0014 a0002c0002t0001g0217 a0002c0002t0001g0218 others(17): Show |
21 | HG00673.hp1 HG01081.hp2 HG02080.hp1 others(18): Show |
intron_variant | MODIFIER | c.-69-8103C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595539 | |||||||
chr2:169595632 | G | T | 4 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0029 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-8010G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595632 | |||||||
chr2:169595661 | G | C | 1 | a0002c0002t0010g0294 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-69-7981G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595661 | |||||||
chr2:169595801 | T | C | 28 | a0001c0001t0007g0009 a0001c0001t0007g0016 a0001c0001t0007g0017 others(25): Show |
29 | HG02055.hp2 HG02109.hp2 HG02145.hp1 others(26): Show |
intron_variant | MODIFIER | c.-69-7841T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595801 | |||||||
chr2:169595865 | G | A | 2 | a0002c0002t0003g0186 a0002c0002t0010g0312 |
2 | NA18948.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.-69-7777G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595865 | |||||||
chr2:169595966 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-69-7676G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595966 | |||||||
chr2:169595977 | T | A | 2 | a0002c0002t0001g0248 a0002c0002t0001g0314 |
2 | NA18954.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-69-7665T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595977 | |||||||
chr2:169595996 | G | C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-7646G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169595996 | |||||||
chr2:169596095 | C | T | 2 | a0001c0007t0013g0029 a0001c0007t0013g0030 |
2 | HG02258.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-69-7547C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596095 | |||||||
chr2:169596104 | T | G | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-7538T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596104 | |||||||
chr2:169596253 | C | T | 9 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(6): Show |
10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-7389C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596253 | |||||||
chr2:169596404 | C | T | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-69-7238C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596404 | |||||||
chr2:169596414 | G | A | 4 | a0001c0001t0005g0350 a0001c0001t0005g0351 a0001c0001t0005g0352 others(1): Show |
4 | NA18981.hp2 NA19066.hp2 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-7228G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596414 | |||||||
chr2:169596657 | G | A | 4 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-6985G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596657 | |||||||
chr2:169596677 | G | C | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-69-6965G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596677 | |||||||
chr2:169596715 | T | C | 1 | a0001c0001t0015g0032 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-69-6927T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596715 | |||||||
chr2:169596760 | C | T | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-6882C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596760 | |||||||
chr2:169596802 | C | T | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-6840C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596802 | |||||||
chr2:169596982 | G | A | 1 | a0002c0002t0003g0187 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-69-6660G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169596982 | |||||||
chr2:169597005 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-6637A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597005 | |||||||
chr2:169597035 | TA | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-6606delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597035 | |||||||
chr2:169597159 | T | C | 34 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(31): Show |
36 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-69-6483T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597159 | |||||||
chr2:169597243 | C | T | 2 | a0005c0006t0018g0110 a0005c0006t0018g0115 |
2 | HG03654.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-69-6399C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597243 | |||||||
chr2:169597315 | T | A | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-6327T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597315 | |||||||
chr2:169597388 | G | A | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-6254G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597388 | |||||||
chr2:169597458 | C | T | 2 | a0002c0002t0001g0231 a0002c0002t0001g0247 |
2 | HG01070.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-69-6184C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597458 | |||||||
chr2:169597491 | CCTTTT | C | 5 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(2): Show |
5 | HG01891.hp1 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-6140_-69-6136d others(7): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597491 | ||||||
chr2:169597496 | T | C | 1 | a0001c0001t0002g0073 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-69-6146T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597496 | |||||||
chr2:169597502 | C | CT | 39 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0332 others(36): Show |
40 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.-69-6126dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597502 | ||||||
chr2:169597502 | CT | C | 156 | a0001c0001t0002g0071 a0001c0001t0007g0092 a0001c0001t0009g0039 others(153): Show |
162 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-69-6126delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597502 | ||||||
chr2:169597521 | CAG | C | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-69-6118_-69-6117d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597521 | ||||||
chr2:169597584 | C | T | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-69-6058C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597584 | |||||||
chr2:169597642 | C | T | 3 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0253 |
3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-69-6000C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597642 | |||||||
chr2:169597643 | G | A | 10 | a0002c0002t0001g0160 a0002c0002t0001g0178 a0002c0002t0001g0211 others(7): Show |
10 | HG00642.hp1 HG00735.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.-69-5999G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597643 | |||||||
chr2:169597678 | T | C | 4 | a0002c0002t0001g0277 a0002c0002t0001g0279 a0002c0002t0001g0316 others(1): Show |
4 | HG01192.hp1 HG01261.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-5964T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597678 | |||||||
chr2:169597850 | CCTTG | C | 5 | a0001c0001t0005g0331 a0001c0001t0005g0341 a0001c0001t0005g0346 others(2): Show |
5 | HG00621.hp2 HG03017.hp1 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-69-5787_-69-5784d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597850 | ||||||
chr2:169597855 | C | CTTGCTTG others(1): Show |
3 | a0003c0003t0004g0097 a0003c0003t0004g0100 a0003c0003t0004g0105 |
3 | HG00733.hp1 HG02896.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-69-5784_-69-5783i others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | ||||||
chr2:169597855 | C | CTTGCTTG others(5): Show |
1 | a0003c0003t0004g0101 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-69-5784_-69-5783i others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | ||||||
chr2:169597855 | C | CTTGT | 18 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0007g0158 others(15): Show |
20 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.-69-5751_-69-5748d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | ||||||
chr2:169597855 | CTTGT | C | 116 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(113): Show |
122 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.-69-5751_-69-5748d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | ||||||
chr2:169597855 | CTTGTTTG others(1): Show |
C | 13 | a0001c0001t0002g0040 a0001c0001t0002g0062 a0001c0001t0007g0176 others(10): Show |
14 | HG00639.hp1 HG01106.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-69-5755_-69-5748d others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | ||||||
chr2:169597855 | CTTGTTTG others(5): Show |
C | 6 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(3): Show |
7 | HG00323.hp2 HG02145.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-69-5759_-69-5748d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | ||||||
chr2:169597855 | CTTGTTTG others(9): Show |
C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-5763_-69-5748d others(18): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169597855 | ||||||
chr2:169597912 | T | C | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-5730T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597912 | |||||||
chr2:169597913 | C | T | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-5729C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597913 | |||||||
chr2:169597940 | A | G | 156 | a0001c0001t0002g0064 a0002c0002t0001g0001 a0002c0002t0001g0013 others(153): Show |
162 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-69-5702A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597940 | |||||||
chr2:169597952 | C | T | 1 | a0002c0002t0003g0194 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-69-5690C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169597952 | |||||||
chr2:169598004 | C | CT | 152 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(149): Show |
158 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.-69-5624dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598004 | ||||||
chr2:169598024 | A | T | 79 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-69-5618A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598024 | |||||||
chr2:169598087 | G | A | 2 | a0001c0001t0005g0346 a0001c0001t0005g0361 |
2 | NA18990.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-69-5555G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598087 | |||||||
chr2:169598381 | C | T | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-5261C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598381 | |||||||
chr2:169598384 | G | A | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69-5258G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598384 | |||||||
chr2:169598482 | G | A | 3 | a0001c0001t0011g0015 a0001c0001t0011g0306 a0001c0001t0011g0307 |
4 | HG02258.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-5160G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598482 | |||||||
chr2:169598493 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-69-5149G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598493 | |||||||
chr2:169598541 | G | A | 5 | a0001c0001t0005g0091 a0001c0001t0005g0332 a0001c0001t0005g0337 others(2): Show |
5 | HG02280.hp1 NA18993.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.-69-5101G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598541 | |||||||
chr2:169598542 | C | A | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-5100C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598542 | |||||||
chr2:169598697 | A | C | 5 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-69-4945A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598697 | |||||||
chr2:169598814 | T | C | 154 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(151): Show |
160 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-69-4828T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598814 | |||||||
chr2:169598815 | T | G | 34 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(31): Show |
36 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-69-4827T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598815 | |||||||
chr2:169598836 | T | TATGTATA others(13): Show |
9 | a0001c0001t0002g0006 a0001c0001t0002g0068 a0001c0001t0002g0071 others(6): Show |
11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4806_-69-4805i others(22): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598836 | |||||||
chr2:169598837 | T | A | 9 | a0001c0001t0002g0006 a0001c0001t0002g0068 a0001c0001t0002g0071 others(6): Show |
11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4805T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598837 | |||||||
chr2:169598837 | T | TTATATGT others(17): Show |
1 | a0001c0001t0006g0157 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-69-4799_-69-4776d others(26): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598837 | ||||||
chr2:169598843 | G | GTATATAA others(17): Show |
61 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(58): Show |
62 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.-69-4771_-69-4748d others(26): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598843 | ||||||
chr2:169598843 | G | GTATATAA others(45): Show |
3 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0029g0134 |
3 | HG00733.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-69-4778_-69-4777i others(54): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598843 | ||||||
chr2:169598843 | G | T | 9 | a0001c0001t0002g0006 a0001c0001t0002g0068 a0001c0001t0002g0071 others(6): Show |
11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4799G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598843 | |||||||
chr2:169598869 | A | ATATAAAT others(41): Show |
4 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0029 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-4748_-69-4747i others(50): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598869 | ||||||
chr2:169598869 | A | ATATAAAT others(17): Show |
75 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0008 others(72): Show |
79 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.-69-4750_-69-4749i others(26): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169598869 | ||||||
chr2:169598869 | A | G | 9 | a0001c0001t0002g0006 a0001c0001t0002g0068 a0001c0001t0002g0071 others(6): Show |
11 | NA18941.hp2 NA18945.hp2 NA18955.hp2 others(8): Show |
intron_variant | MODIFIER | c.-69-4773A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598869 | |||||||
chr2:169598871 | A | G | 1 | a0001c0001t0006g0157 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-69-4771A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169598871 | |||||||
chr2:169599354 | A | C | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-69-4288A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599354 | |||||||
chr2:169599419 | T | G | 10 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(7): Show |
10 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-4223T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599419 | |||||||
chr2:169599670 | C | T | 329 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-69-3972C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599670 | |||||||
chr2:169599707 | A | G | 359 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(356): Show |
375 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(372): Show |
intron_variant | MODIFIER | c.-69-3935A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599707 | |||||||
chr2:169599732 | C | A | 1 | a0001c0001t0002g0054 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-69-3910C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599732 | |||||||
chr2:169599812 | G | A | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-3830G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599812 | |||||||
chr2:169599923 | T | A | 1 | a0005c0006t0018g0110 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-69-3719T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599923 | |||||||
chr2:169599957 | A | G | 2 | a0001c0001t0002g0040 a0001c0001t0002g0062 |
2 | HG00639.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-69-3685A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599957 | |||||||
chr2:169599973 | A | G | 3 | a0002c0002t0003g0309 a0002c0002t0003g0310 a0002c0002t0003g0311 |
3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-69-3669A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169599973 | |||||||
chr2:169600006 | G | A | 4 | a0002c0002t0001g0280 a0002c0002t0001g0281 a0002c0002t0001g0290 others(1): Show |
4 | NA18980.hp1 NA19056.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-3636G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600006 | |||||||
chr2:169600078 | A | AT | 6 | a0001c0001t0002g0081 a0001c0001t0028g0138 a0001c0001t0032g0137 others(3): Show |
6 | HG01496.hp1 HG02027.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-69-3548dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600078 | ||||||
chr2:169600078 | AT | A | 157 | a0001c0001t0002g0046 a0001c0001t0002g0072 a0001c0001t0005g0351 others(154): Show |
163 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.-69-3548delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600078 | ||||||
chr2:169600079 | T | A | 1 | a0005c0006t0018g0110 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-69-3563T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600079 | |||||||
chr2:169600405 | A | T | 4 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-3237A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600405 | |||||||
chr2:169600507 | C | T | 1 | a0002c0002t0003g0200 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-69-3135C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600507 | |||||||
chr2:169600620 | G | GTTTTTCA others(4): Show |
1 | a0001c0001t0009g0039 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-69-3021_-69-3020i others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600620 | ||||||
chr2:169600646 | T | C | 4 | a0002c0002t0001g0178 a0002c0002t0001g0222 a0002c0002t0001g0223 others(1): Show |
4 | HG00642.hp1 HG01346.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-2996T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600646 | |||||||
chr2:169600789 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-2853C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600789 | |||||||
chr2:169600865 | T | G | 127 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(124): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-69-2777T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600865 | |||||||
chr2:169600937 | T | TA | 127 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(124): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-69-2704dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169600937 | ||||||
chr2:169600941 | C | T | 127 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(124): Show |
134 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-69-2701C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169600941 | |||||||
chr2:169601078 | G | T | 1 | a0002c0002t0001g0296 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-69-2564G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601078 | |||||||
chr2:169601105 | T | C | 4 | a0002c0002t0001g0226 a0002c0002t0001g0264 a0002c0002t0001g0315 others(1): Show |
4 | HG02132.hp1 NA18943.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-2537T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601105 | |||||||
chr2:169601302 | A | G | 4 | a0001c0001t0012g0031 a0001c0001t0015g0032 a0001c0001t0015g0033 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-2340A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601302 | |||||||
chr2:169601450 | C | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-2192C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601450 | |||||||
chr2:169601484 | A | G | 92 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(89): Show |
98 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.-69-2158A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601484 | |||||||
chr2:169601504 | G | A | 1 | a0001c0001t0005g0349 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-69-2138G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601504 | |||||||
chr2:169601564 | A | G | 18 | a0003c0003t0008g0123 a0003c0003t0008g0131 a0003c0003t0008g0318 others(15): Show |
18 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-69-2078A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601564 | |||||||
chr2:169601820 | T | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-69-1822T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601820 | |||||||
chr2:169601865 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-1777C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601865 | |||||||
chr2:169601906 | C | CA | 154 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(151): Show |
160 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.-69-1724dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169601906 | ||||||
chr2:169601922 | A | T | 1 | a0001c0001t0007g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-69-1720A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601922 | |||||||
chr2:169601966 | T | A | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.-69-1676T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601966 | |||||||
chr2:169601967 | T | C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-1675T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169601967 | |||||||
chr2:169602206 | A | C | 342 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(339): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.-69-1436A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602206 | |||||||
chr2:169602221 | T | TA | 7 | a0002c0002t0003g0165 a0002c0002t0003g0166 a0002c0002t0003g0168 others(4): Show |
7 | HG02129.hp1 NA18986.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-1421_-69-1420i others(3): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602221 | |||||||
chr2:169602222 | C | A | 7 | a0002c0002t0003g0165 a0002c0002t0003g0166 a0002c0002t0003g0168 others(4): Show |
7 | HG02129.hp1 NA18986.hp2 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.-69-1420C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602222 | |||||||
chr2:169602222 | C | CA | 145 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(142): Show |
151 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.-69-1410dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169602222 | ||||||
chr2:169602408 | C | T | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-69-1234C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602408 | |||||||
chr2:169602409 | G | A | 1 | a0003c0003t0004g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-69-1233G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602409 | |||||||
chr2:169602409 | G | C | 1 | a0001c0001t0005g0332 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-69-1233G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602409 | |||||||
chr2:169602461 | A | G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-69-1181A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602461 | |||||||
chr2:169602601 | C | T | 4 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-69-1041C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602601 | |||||||
chr2:169602607 | C | T | 3 | a0002c0002t0001g0228 a0002c0002t0001g0229 a0002c0002t0001g0313 |
3 | NA18977.hp2 NA18985.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.-69-1035C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602607 | |||||||
chr2:169602612 | C | G | 3 | a0002c0002t0001g0014 a0002c0002t0001g0217 a0002c0002t0001g0268 |
4 | HG02155.hp2 NA18942.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.-69-1030C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602612 | |||||||
chr2:169602763 | A | C | 2 | a0001c0001t0011g0015 a0001c0001t0011g0307 |
3 | HG03225.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-69-879A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602763 | |||||||
chr2:169602881 | A | G | 37 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(34): Show |
38 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-69-761A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602881 | |||||||
chr2:169602997 | A | T | 1 | a0001c0001t0005g0334 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-69-645A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169602997 | |||||||
chr2:169603060 | A | G | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.-69-582A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603060 | |||||||
chr2:169603061 | G | C | 1 | a0001c0001t0002g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-69-581G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603061 | |||||||
chr2:169603141 | T | C | 9 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(6): Show |
10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-69-501T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603141 | |||||||
chr2:169603259 | A | T | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-69-383A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603259 | |||||||
chr2:169603483 | CATATACT others(30): Show |
C | 309 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(306): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-69-111_-69-75delT others(36): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | 169603483 | ||||||
chr2:169603581 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-69-61C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 1/13 | chr2 | 169603581 | |||||||
chr2:169603831 | A | G | 1 | a0001c0001t0006g0136 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-17+137A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 2/13 | chr2 | 169603831 | |||||||
chr2:169604307 | A | ATGGC | 8 | a0002c0002t0001g0229 a0002c0002t0001g0313 a0002c0002t0003g0165 others(5): Show |
8 | HG04199.hp2 NA18948.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+48_136+51dupGG others(2): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604307 | ||||||
chr2:169604313 | T | G | 147 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(144): Show |
153 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.136+52T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604313 | |||||||
chr2:169604325 | T | TG | 3 | a0001c0001t0007g0016 a0001c0001t0007g0019 a0001c0001t0007g0020 |
3 | HG02257.hp2 HG02280.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.136+66dupG | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604325 | ||||||
chr2:169604326 | G | GCTT | 53 | a0002c0002t0001g0159 a0002c0002t0001g0208 a0002c0002t0001g0210 others(50): Show |
55 | HG00423.hp1 HG01175.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.136+65_136+66insCT others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604326 | |||||||
chr2:169604327 | G | C | 94 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(91): Show |
98 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.136+66G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604327 | |||||||
chr2:169604327 | G | GGT | 7 | a0001c0001t0007g0017 a0001c0001t0007g0021 a0001c0001t0007g0022 others(4): Show |
7 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.136+66_136+67insGT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604327 | |||||||
chr2:169604327 | G | GT | 28 | a0001c0001t0002g0045 a0001c0001t0002g0053 a0001c0001t0002g0057 others(25): Show |
28 | HG00733.hp1 HG01243.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.136+94dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | ||||||
chr2:169604327 | G | GTT | 7 | a0001c0001t0007g0092 a0001c0001t0007g0093 a0001c0001t0007g0094 others(4): Show |
8 | HG02615.hp1 HG02723.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.136+93_136+94dupTT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | ||||||
chr2:169604327 | G | GTTT | 9 | a0001c0001t0007g0009 a0001c0001t0011g0162 a0001c0001t0011g0163 others(6): Show |
10 | HG02145.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.136+92_136+94dupTT others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | ||||||
chr2:169604327 | GT | G | 9 | a0001c0001t0002g0072 a0001c0001t0002g0083 a0001c0001t0006g0133 others(6): Show |
9 | HG00323.hp1 HG01069.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.136+94delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | ||||||
chr2:169604327 | GTT | G | 17 | a0001c0001t0005g0336 a0001c0001t0005g0347 a0003c0003t0004g0354 others(14): Show |
17 | HG00735.hp1 HG01069.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.136+93_136+94delTT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | ||||||
chr2:169604327 | GTTT | G | 25 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(22): Show |
25 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(22): Show |
intron_variant | MODIFIER | c.136+92_136+94delTT others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | ||||||
chr2:169604327 | GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0007g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.136+84_136+94delTT others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169604327 | ||||||
chr2:169604328 | T | G | 53 | a0002c0002t0001g0159 a0002c0002t0001g0208 a0002c0002t0001g0210 others(50): Show |
55 | HG00423.hp1 HG01175.hp1 HG01192.hp2 others(52): Show |
intron_variant | MODIFIER | c.136+67T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604328 | |||||||
chr2:169604329 | T | TG | 6 | a0002c0002t0001g0289 a0002c0002t0001g0295 a0002c0002t0001g0299 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+68_136+69insG | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604329 | |||||||
chr2:169604329 | T | TGG | 88 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(85): Show |
92 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.136+68_136+69insGG | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604329 | |||||||
chr2:169604330 | T | G | 6 | a0002c0002t0001g0289 a0002c0002t0001g0295 a0002c0002t0001g0299 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.136+69T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604330 | |||||||
chr2:169604390 | A | T | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+129A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604390 | |||||||
chr2:169604391 | G | A | 4 | a0003c0003t0004g0354 a0003c0003t0004g0355 a0003c0003t0004g0356 others(1): Show |
4 | HG00140.hp2 HG01496.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+130G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604391 | |||||||
chr2:169604425 | G | A | 88 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(85): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.136+164G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604425 | |||||||
chr2:169604657 | C | T | 3 | a0001c0001t0006g0139 a0001c0001t0006g0149 a0001c0001t0033g0141 |
3 | HG01070.hp2 HG01071.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.136+396C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604657 | |||||||
chr2:169604747 | G | A | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.136+486G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604747 | |||||||
chr2:169604797 | C | G | 37 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(34): Show |
38 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.136+536C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604797 | |||||||
chr2:169604904 | T | G | 1 | a0003c0003t0008g0321 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.136+643T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169604904 | |||||||
chr2:169605047 | T | C | 9 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.136+786T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605047 | |||||||
chr2:169605163 | A | G | 1 | a0002c0002t0003g0188 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.137-876A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605163 | |||||||
chr2:169605213 | A | G | 2 | a0002c0002t0003g0179 a0002c0002t0014g0183 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.137-826A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605213 | |||||||
chr2:169605226 | C | T | 3 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0253 |
3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.137-813C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605226 | |||||||
chr2:169605308 | G | A | 6 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(3): Show |
7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-731G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605308 | |||||||
chr2:169605481 | C | T | 3 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0030 |
3 | HG03139.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.137-558C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605481 | |||||||
chr2:169605520 | G | GC | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.137-517dupC | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr2 | 169605520 | ||||||
chr2:169605547 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.137-492T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605547 | |||||||
chr2:169605556 | T | A | 3 | a0003c0003t0004g0354 a0003c0003t0004g0355 a0003c0003t0004g0356 |
3 | HG01496.hp1 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.137-483T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605556 | |||||||
chr2:169605566 | C | T | 13 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(10): Show |
15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.137-473C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605566 | |||||||
chr2:169605591 | A | G | 3 | a0002c0002t0003g0309 a0002c0002t0003g0310 a0002c0002t0003g0311 |
3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.137-448A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605591 | |||||||
chr2:169605611 | G | C | 45 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(42): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.137-428G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605611 | |||||||
chr2:169605638 | C | CT | 193 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(190): Show |
200 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.137-401_137-400ins others(1): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605638 | |||||||
chr2:169605639 | G | A | 193 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(190): Show |
200 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.137-400G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605639 | |||||||
chr2:169605639 | G | T | 89 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(86): Show |
95 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.137-400G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605639 | |||||||
chr2:169605732 | C | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.137-307C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605732 | |||||||
chr2:169605820 | C | T | 9 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.137-219C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605820 | |||||||
chr2:169605838 | A | G | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.137-201A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605838 | |||||||
chr2:169605902 | A | T | 10 | a0003c0003t0004g0010 a0003c0003t0004g0099 a0003c0003t0004g0112 others(7): Show |
11 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.137-137A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605902 | |||||||
chr2:169605932 | T | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.137-107T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 4/13 | chr2 | 169605932 | |||||||
chr2:169606321 | C | T | 2 | a0002c0002t0001g0263 a0002c0002t0023g0219 |
2 | HG01109.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.244+175C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606321 | |||||||
chr2:169606578 | C | G | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.244+432C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606578 | |||||||
chr2:169606587 | G | T | 1 | a0003c0003t0004g0105 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.244+441G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606587 | |||||||
chr2:169606591 | C | CAAAAAAA | 12 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(9): Show |
13 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.244+456_244+462dup others(7): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(1): Show |
43 | a0002c0002t0001g0271 a0002c0002t0001g0313 a0002c0002t0003g0011 others(40): Show |
45 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.244+455_244+462dup others(8): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(2): Show |
105 | a0001c0001t0005g0335 a0001c0001t0005g0339 a0001c0001t0005g0340 others(102): Show |
109 | HG00099.hp2 HG00280.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.244+454_244+462dup others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(3): Show |
9 | a0001c0001t0006g0156 a0002c0002t0001g0210 a0002c0002t0001g0227 others(6): Show |
9 | HG00423.hp2 HG01123.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.244+453_244+462dup others(10): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(4): Show |
18 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(15): Show |
18 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.244+452_244+462dup others(11): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(5): Show |
20 | a0001c0001t0005g0342 a0001c0001t0005g0346 a0001c0001t0005g0361 others(17): Show |
21 | HG01081.hp1 HG02258.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.244+451_244+462dup others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0007g0023 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.244+450_244+462dup others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(7): Show |
15 | a0001c0001t0005g0347 a0001c0001t0005g0350 a0001c0001t0005g0351 others(12): Show |
15 | HG02055.hp2 HG02109.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.244+449_244+462dup others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0005g0331 a0001c0001t0007g0021 a0001c0001t0007g0025 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.244+448_244+462dup others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(9): Show |
2 | a0001c0001t0005g0341 a0001c0001t0005g0345 |
2 | HG02080.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.244+447_244+462dup others(16): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0012g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.244+446_244+462dup others(17): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0012g0036 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(18): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0005g0344 a0001c0001t0026g0035 |
2 | HG00140.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.244+462_244+463ins others(19): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0032g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.244+462_244+463ins others(23): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0028g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(24): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0005g0332 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(25): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0005g0334 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(28): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(23): Show |
2 | a0001c0001t0005g0091 a0001c0001t0005g0349 |
2 | HG02698.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.244+462_244+463ins others(30): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(27): Show |
2 | a0001c0001t0005g0330 a0001c0001t0005g0336 |
2 | NA18952.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.244+462_244+463ins others(34): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(28): Show |
1 | a0001c0001t0005g0337 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(35): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(29): Show |
1 | a0001c0001t0005g0338 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(36): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(30): Show |
1 | a0001c0001t0005g0343 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(37): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(38): Show |
1 | a0001c0001t0005g0333 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.244+462_244+463ins others(45): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | C | CAAAAAAA others(39): Show |
1 | a0001c0001t0005g0348 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.244+462_244+463ins others(46): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606591 | CA | C | 80 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(77): Show |
85 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.244+462delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | 169606591 | ||||||
chr2:169606646 | A | G | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.245-458A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606646 | |||||||
chr2:169606873 | T | C | 4 | a0002c0002t0003g0168 a0002c0002t0003g0169 a0002c0002t0003g0170 others(1): Show |
4 | NA18986.hp2 NA19002.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-231T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606873 | |||||||
chr2:169606896 | G | A | 3 | a0003c0003t0004g0112 a0003c0003t0004g0116 a0003c0003t0004g0121 |
3 | HG03239.hp1 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.245-208G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606896 | |||||||
chr2:169606910 | A | G | 4 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0029 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.245-194A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169606910 | |||||||
chr2:169607000 | T | C | 1 | a0001c0001t0007g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.245-104T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169607000 | |||||||
chr2:169607037 | T | C | 83 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(80): Show |
88 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.245-67T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169607037 | |||||||
chr2:169607041 | T | G | 110 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(107): Show |
114 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.245-63T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 5/13 | chr2 | 169607041 | |||||||
chr2:169607169 | A | G | 39 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(36): Show |
40 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.289+21A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607169 | |||||||
chr2:169607320 | T | C | 1 | a0001c0001t0002g0065 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.289+172T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607320 | |||||||
chr2:169607401 | A | G | 1 | a0001c0001t0007g0093 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.289+253A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607401 | |||||||
chr2:169607418 | G | A | 12 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(9): Show |
13 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.289+270G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607418 | |||||||
chr2:169607482 | G | A | 1 | a0002c0002t0001g0313 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.289+334G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607482 | |||||||
chr2:169607486 | A | AT | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+344dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 169607486 | ||||||
chr2:169607512 | A | G | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.289+364A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607512 | |||||||
chr2:169607678 | G | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.289+530G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607678 | |||||||
chr2:169607694 | C | T | 1 | a0002c0002t0001g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.289+546C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607694 | |||||||
chr2:169607706 | T | G | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.289+558T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607706 | |||||||
chr2:169607750 | G | A | 4 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.289+602G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607750 | |||||||
chr2:169607996 | T | C | 1 | a0002c0002t0003g0189 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.290-675T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169607996 | |||||||
chr2:169608113 | A | G | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.290-558A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608113 | |||||||
chr2:169608137 | GATA | G | 3 | a0002c0002t0003g0179 a0002c0002t0003g0184 a0002c0002t0014g0183 |
3 | HG02895.hp1 HG02897.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.290-530_290-528del others(3): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 169608137 | ||||||
chr2:169608218 | C | T | 1 | a0002c0002t0003g0311 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.290-453C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608218 | |||||||
chr2:169608223 | G | A | 34 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(31): Show |
36 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.290-448G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608223 | |||||||
chr2:169608349 | C | T | 13 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(10): Show |
15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.290-322C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608349 | |||||||
chr2:169608401 | A | G | 1 | a0002c0002t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.290-270A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608401 | |||||||
chr2:169608453 | G | A | 1 | a0002c0002t0003g0188 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.290-218G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608453 | |||||||
chr2:169608454 | C | CA | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.290-216dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | 169608454 | ||||||
chr2:169608470 | A | G | 5 | a0002c0002t0001g0277 a0002c0002t0001g0278 a0002c0002t0001g0279 others(2): Show |
5 | HG01192.hp1 HG01261.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.290-201A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608470 | |||||||
chr2:169608597 | A | G | 1 | a0001c0001t0005g0344 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.290-74A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608597 | |||||||
chr2:169608615 | G | A | 46 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(43): Show |
48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.290-56G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608615 | |||||||
chr2:169608636 | T | C | 1 | a0001c0001t0002g0047 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.290-35T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608636 | |||||||
chr2:169608639 | A | G | 1 | a0002c0002t0001g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.290-32A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 6/13 | chr2 | 169608639 | |||||||
chr2:169608843 | G | A | 1 | a0002c0002t0003g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.377+85G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169608843 | |||||||
chr2:169608854 | G | A | 3 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0030 |
3 | HG03139.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.377+96G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169608854 | |||||||
chr2:169608898 | C | T | 1 | a0002c0002t0003g0196 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.377+140C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169608898 | |||||||
chr2:169609013 | G | A | 1 | a0003c0003t0004g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.377+255G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609013 | |||||||
chr2:169609081 | C | CA | 24 | a0001c0001t0002g0040 a0001c0001t0002g0044 a0001c0001t0002g0053 others(21): Show |
24 | HG00438.hp1 HG00639.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.377+342dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169609081 | ||||||
chr2:169609081 | CA | C | 150 | a0001c0001t0006g0156 a0002c0002t0001g0001 a0002c0002t0001g0013 others(147): Show |
156 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.377+342delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169609081 | ||||||
chr2:169609100 | A | G | 1 | a0003c0003t0004g0097 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.377+342A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609100 | |||||||
chr2:169609104 | C | T | 1 | a0003c0003t0008g0131 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.377+346C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609104 | |||||||
chr2:169609177 | G | A | 6 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(3): Show |
7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.377+419G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609177 | |||||||
chr2:169609195 | G | A | 1 | a0001c0001t0005g0333 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.377+437G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609195 | |||||||
chr2:169609223 | G | A | 2 | a0001c0001t0013g0028 a0001c0007t0013g0030 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.377+465G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609223 | |||||||
chr2:169609250 | A | C | 1 | a0002c0002t0001g0314 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.377+492A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609250 | |||||||
chr2:169609266 | T | C | 1 | a0002c0002t0003g0177 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.377+508T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609266 | |||||||
chr2:169609267 | G | T | 109 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(106): Show |
113 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.377+509G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609267 | |||||||
chr2:169609268 | T | G | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.377+510T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609268 | |||||||
chr2:169609277 | T | C | 2 | a0002c0002t0003g0169 a0002c0002t0003g0170 |
2 | NA19002.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.377+519T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609277 | |||||||
chr2:169609446 | CAT | C | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+689_377+690del others(2): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609446 | |||||||
chr2:169609518 | T | C | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.377+760T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609518 | |||||||
chr2:169609520 | C | T | 2 | a0003c0003t0004g0354 a0003c0003t0004g0355 |
2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.377+762C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609520 | |||||||
chr2:169609728 | A | G | 88 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(85): Show |
94 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.377+970A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609728 | |||||||
chr2:169609736 | A | T | 2 | a0002c0002t0001g0231 a0002c0002t0001g0247 |
2 | HG01070.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.377+978A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609736 | |||||||
chr2:169609895 | C | A | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | NA18939.hp1 NA19005.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.377+1137C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609895 | |||||||
chr2:169609923 | T | C | 1 | a0002c0002t0001g0286 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.377+1165T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609923 | |||||||
chr2:169609939 | C | A | 308 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(305): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.377+1181C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169609939 | |||||||
chr2:169610017 | A | T | 39 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(36): Show |
40 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.377+1259A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610017 | |||||||
chr2:169610063 | A | G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.377+1305A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610063 | |||||||
chr2:169610307 | T | G | 1 | a0003c0003t0008g0318 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.377+1549T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610307 | |||||||
chr2:169610479 | A | ATT | 23 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(20): Show |
23 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.377+1730_377+1731d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169610479 | ||||||
chr2:169610512 | T | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.377+1754T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610512 | |||||||
chr2:169610603 | T | C | 43 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(40): Show |
45 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(42): Show |
intron_variant | MODIFIER | c.377+1845T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610603 | |||||||
chr2:169610641 | A | C | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.377+1883A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610641 | |||||||
chr2:169610742 | G | GTA | 4 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0029 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+1987_377+1988d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169610742 | ||||||
chr2:169610787 | C | T | 1 | a0001c0001t0005g0345 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.377+2029C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610787 | |||||||
chr2:169610890 | A | G | 1 | a0002c0004t0003g0180 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.377+2132A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169610890 | |||||||
chr2:169611101 | G | A | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2343G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611101 | |||||||
chr2:169611120 | G | T | 37 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(34): Show |
38 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.377+2362G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611120 | |||||||
chr2:169611145 | G | A | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.377+2387G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611145 | |||||||
chr2:169611181 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2423C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611181 | |||||||
chr2:169611261 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2503A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611261 | |||||||
chr2:169611343 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2585A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611343 | |||||||
chr2:169611443 | TTAA | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.377+2687_377+2689d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169611443 | ||||||
chr2:169611605 | T | C | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.377+2847T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611605 | |||||||
chr2:169611788 | A | G | 1 | a0002c0002t0003g0172 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.378-2676A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611788 | |||||||
chr2:169611883 | A | T | 7 | a0001c0001t0011g0015 a0001c0001t0011g0162 a0001c0001t0011g0163 others(4): Show |
8 | HG02258.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.378-2581A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169611883 | |||||||
chr2:169612005 | T | C | 1 | a0002c0004t0003g0201 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.378-2459T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612005 | |||||||
chr2:169612011 | T | G | 1 | a0002c0002t0001g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.378-2453T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612011 | |||||||
chr2:169612090 | C | T | 9 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.378-2374C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612090 | |||||||
chr2:169612094 | G | A | 6 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(3): Show |
7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-2370G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612094 | |||||||
chr2:169612249 | T | C | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.378-2215T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612249 | |||||||
chr2:169612379 | A | AT | 14 | a0001c0001t0005g0353 a0001c0001t0006g0139 a0001c0001t0006g0154 others(11): Show |
16 | HG00733.hp1 HG01099.hp2 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.378-2063dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | ||||||
chr2:169612379 | AT | A | 115 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(112): Show |
121 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.378-2063delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | ||||||
chr2:169612379 | ATT | A | 16 | a0001c0001t0002g0055 a0001c0001t0002g0070 a0001c0001t0005g0361 others(13): Show |
17 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.378-2064_378-2063d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | ||||||
chr2:169612379 | ATTT | A | 6 | a0002c0002t0001g0244 a0002c0002t0001g0258 a0002c0002t0001g0297 others(3): Show |
6 | HG00639.hp2 HG02074.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.378-2065_378-2063d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | ||||||
chr2:169612379 | ATTTT | A | 146 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(143): Show |
152 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.378-2066_378-2063d others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612379 | ||||||
chr2:169612493 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.378-1971C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612493 | |||||||
chr2:169612601 | C | T | 1 | a0002c0002t0003g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.378-1863C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612601 | |||||||
chr2:169612664 | G | A | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.378-1800G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612664 | |||||||
chr2:169612685 | A | C | 1 | a0003c0003t0004g0130 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.378-1779A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612685 | |||||||
chr2:169612709 | T | TA | 3 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 |
4 | HG02145.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-1754dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169612709 | ||||||
chr2:169612788 | G | C | 3 | a0002c0002t0001g0249 a0002c0002t0001g0250 a0002c0002t0001g0254 |
3 | HG01081.hp2 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.378-1676G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612788 | |||||||
chr2:169612802 | A | G | 2 | a0001c0001t0006g0144 a0001c0001t0006g0150 |
2 | NA18965.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.378-1662A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612802 | |||||||
chr2:169612949 | C | T | 1 | a0003c0003t0008g0328 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.378-1515C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612949 | |||||||
chr2:169612957 | A | G | 1 | a0001c0001t0005g0344 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378-1507A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169612957 | |||||||
chr2:169613015 | A | G | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.378-1449A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613015 | |||||||
chr2:169613329 | A | G | 37 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(34): Show |
38 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.378-1135A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613329 | |||||||
chr2:169613387 | C | T | 1 | a0002c0002t0001g0243 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.378-1077C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613387 | |||||||
chr2:169613398 | T | C | 2 | a0001c0001t0009g0027 a0001c0001t0022g0060 |
2 | NA18943.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.378-1066T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613398 | |||||||
chr2:169613420 | G | GT | 39 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(36): Show |
40 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.378-1038dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr2 | 169613420 | ||||||
chr2:169613550 | T | A | 1 | a0002c0002t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.378-914T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613550 | |||||||
chr2:169613688 | A | G | 1 | a0002c0002t0001g0211 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.378-776A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613688 | |||||||
chr2:169613792 | G | C | 3 | a0001c0001t0005g0331 a0001c0001t0005g0341 a0001c0001t0005g0348 |
3 | HG00621.hp2 HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.378-672G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613792 | |||||||
chr2:169613793 | G | T | 3 | a0001c0001t0005g0331 a0001c0001t0005g0341 a0001c0001t0005g0348 |
3 | HG00621.hp2 HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.378-671G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613793 | |||||||
chr2:169613911 | A | G | 1 | a0001c0001t0006g0145 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.378-553A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613911 | |||||||
chr2:169613993 | C | T | 46 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(43): Show |
48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.378-471C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169613993 | |||||||
chr2:169614022 | A | G | 5 | a0002c0002t0001g0208 a0002c0002t0001g0213 a0002c0002t0001g0237 others(2): Show |
5 | HG00423.hp2 HG02027.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.378-442A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614022 | |||||||
chr2:169614116 | A | G | 1 | a0002c0002t0034g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.378-348A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614116 | |||||||
chr2:169614234 | G | A | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.378-230G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614234 | |||||||
chr2:169614236 | A | G | 3 | a0002c0002t0003g0309 a0002c0002t0003g0310 a0002c0002t0003g0311 |
3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.378-228A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614236 | |||||||
chr2:169614452 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.378-12G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 7/13 | chr2 | 169614452 | |||||||
chr2:169614760 | A | G | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+36A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169614760 | |||||||
chr2:169615036 | G | GT | 16 | a0001c0001t0002g0073 a0001c0001t0002g0082 a0001c0001t0006g0149 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.547+322dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169615036 | ||||||
chr2:169615069 | G | A | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.547+345G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615069 | |||||||
chr2:169615109 | C | T | 1 | a0003c0003t0004g0106 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.547+385C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615109 | |||||||
chr2:169615219 | C | T | 155 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(152): Show |
161 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.547+495C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615219 | |||||||
chr2:169615235 | G | T | 7 | a0001c0001t0005g0330 a0001c0001t0005g0333 a0001c0001t0005g0336 others(4): Show |
7 | HG00609.hp1 NA18952.hp1 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.547+511G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615235 | |||||||
chr2:169615370 | A | G | 282 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(279): Show |
295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.547+646A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615370 | |||||||
chr2:169615531 | G | A | 1 | a0002c0002t0001g0258 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.547+807G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615531 | |||||||
chr2:169615561 | T | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+837T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615561 | |||||||
chr2:169615720 | CA | C | 56 | a0003c0003t0004g0003 a0003c0003t0004g0010 a0003c0003t0004g0096 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.547+997delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615720 | |||||||
chr2:169615784 | C | T | 1 | a0002c0002t0003g0196 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.547+1060C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615784 | |||||||
chr2:169615901 | G | A | 82 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(79): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.547+1177G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615901 | |||||||
chr2:169615926 | C | T | 2 | a0001c0001t0005g0331 a0001c0001t0005g0341 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.547+1202C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169615926 | |||||||
chr2:169616031 | A | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+1307A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616031 | |||||||
chr2:169616363 | A | G | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+1639A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616363 | |||||||
chr2:169616453 | C | T | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+1729C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616453 | |||||||
chr2:169616502 | G | A | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+1778G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616502 | |||||||
chr2:169616545 | C | A | 21 | a0003c0003t0004g0354 a0003c0003t0004g0355 a0003c0003t0004g0356 others(18): Show |
21 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.547+1821C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616545 | |||||||
chr2:169616561 | A | G | 4 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(1): Show |
4 | NA18906.hp1 NA19030.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+1837A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616561 | |||||||
chr2:169616602 | T | C | 12 | a0002c0002t0001g0013 a0002c0002t0001g0280 a0002c0002t0001g0281 others(9): Show |
12 | HG00609.hp2 NA18747.hp2 NA18945.hp1 others(9): Show |
intron_variant | MODIFIER | c.547+1878T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616602 | |||||||
chr2:169616695 | T | G | 56 | a0003c0003t0004g0003 a0003c0003t0004g0010 a0003c0003t0004g0096 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.547+1971T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616695 | |||||||
chr2:169616698 | G | GT | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+1981dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169616698 | ||||||
chr2:169616799 | C | T | 1 | a0001c0001t0005g0344 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.547+2075C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616799 | |||||||
chr2:169616802 | G | A | 10 | a0003c0003t0004g0010 a0003c0003t0004g0099 a0003c0003t0004g0112 others(7): Show |
11 | HG00280.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.547+2078G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169616802 | |||||||
chr2:169617056 | G | A | 1 | a0002c0002t0001g0284 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.547+2332G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617056 | |||||||
chr2:169617293 | T | A | 5 | a0002c0002t0001g0208 a0002c0002t0001g0213 a0002c0002t0001g0237 others(2): Show |
5 | HG00423.hp2 HG02027.hp2 HG02083.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+2569T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617293 | |||||||
chr2:169617309 | G | C | 6 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(3): Show |
7 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+2585G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617309 | |||||||
chr2:169617619 | A | G | 1 | a0003c0003t0008g0328 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.547+2895A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617619 | |||||||
chr2:169617792 | T | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+3068T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617792 | |||||||
chr2:169617948 | G | A | 1 | a0003c0003t0016g0113 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.547+3224G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169617948 | |||||||
chr2:169618001 | GTTC | G | 22 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(19): Show |
22 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.547+3280_547+3282d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169618001 | ||||||
chr2:169618179 | A | C | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.547+3455A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618179 | |||||||
chr2:169618302 | G | A | 1 | a0001c0001t0002g0008 | 2 | HG01123.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.547+3578G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618302 | |||||||
chr2:169618365 | C | T | 1 | a0004c0008t0001g0301 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.547+3641C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618365 | |||||||
chr2:169618380 | G | C | 5 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(2): Show |
6 | HG02145.hp1 HG02615.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+3656G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618380 | |||||||
chr2:169618431 | C | A | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+3707C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618431 | |||||||
chr2:169618552 | G | A | 1 | a0001c0001t0002g0026 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.547+3828G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618552 | |||||||
chr2:169618639 | G | A | 3 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0030 |
3 | HG03139.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.547+3915G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618639 | |||||||
chr2:169618682 | A | G | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+3958A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618682 | |||||||
chr2:169618826 | A | AT | 178 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(175): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.547+4115dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169618826 | ||||||
chr2:169618852 | G | T | 9 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.547+4128G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618852 | |||||||
chr2:169618898 | G | A | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+4174G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169618898 | |||||||
chr2:169619066 | C | T | 1 | a0003c0003t0008g0326 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.547+4342C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619066 | |||||||
chr2:169619156 | A | G | 255 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(252): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.547+4432A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619156 | |||||||
chr2:169619175 | A | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+4451A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619175 | |||||||
chr2:169619237 | G | A | 1 | a0002c0002t0003g0191 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.547+4513G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619237 | |||||||
chr2:169619318 | C | A | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+4594C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619318 | |||||||
chr2:169619357 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.547+4633G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619357 | |||||||
chr2:169619422 | C | T | 1 | a0003c0003t0004g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.547+4698C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619422 | |||||||
chr2:169619443 | T | A | 1 | a0002c0002t0001g0282 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.547+4719T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619443 | |||||||
chr2:169619568 | A | G | 3 | a0001c0001t0005g0091 a0001c0001t0005g0332 a0001c0001t0005g0337 |
3 | NA18993.hp1 NA19007.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.547+4844A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619568 | |||||||
chr2:169619575 | T | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+4851T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619575 | |||||||
chr2:169619628 | C | T | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+4904C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619628 | |||||||
chr2:169619661 | A | G | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.547+4937A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619661 | |||||||
chr2:169619751 | CT | C | 46 | a0001c0001t0002g0070 a0002c0002t0003g0011 a0002c0002t0003g0165 others(43): Show |
48 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(45): Show |
intron_variant | MODIFIER | c.547+5037delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169619751 | ||||||
chr2:169619755 | T | C | 2 | a0003c0003t0008g0320 a0003c0003t0008g0328 |
2 | HG02451.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.547+5031T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619755 | |||||||
chr2:169619983 | G | A | 361 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(358): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.547+5259G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169619983 | |||||||
chr2:169620008 | A | G | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+5284A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620008 | |||||||
chr2:169620018 | A | G | 3 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0001g0253 |
3 | HG03491.hp2 HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.547+5294A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620018 | |||||||
chr2:169620032 | A | G | 1 | a0002c0002t0003g0190 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.547+5308A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620032 | |||||||
chr2:169620152 | T | C | 31 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(28): Show |
33 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.547+5428T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620152 | |||||||
chr2:169620164 | A | G | 79 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(76): Show |
84 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.547+5440A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620164 | |||||||
chr2:169620169 | A | G | 37 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(34): Show |
38 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.547+5445A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620169 | |||||||
chr2:169620319 | G | A | 1 | a0001c0001t0011g0307 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.547+5595G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620319 | |||||||
chr2:169620347 | T | C | 1 | a0002c0002t0010g0238 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.547+5623T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620347 | |||||||
chr2:169620360 | G | A | 1 | a0003c0003t0008g0323 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.547+5636G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620360 | |||||||
chr2:169620391 | C | T | 9 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(6): Show |
10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.547+5667C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620391 | |||||||
chr2:169620523 | A | G | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.547+5799A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620523 | |||||||
chr2:169620665 | G | A | 3 | a0001c0001t0013g0028 a0001c0007t0013g0029 a0001c0007t0013g0030 |
3 | HG02258.hp2 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.547+5941G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620665 | |||||||
chr2:169620680 | T | G | 1 | a0001c0001t0005g0350 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.547+5956T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620680 | |||||||
chr2:169620884 | C | A | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.547+6160C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620884 | |||||||
chr2:169620888 | G | T | 3 | a0003c0003t0008g0324 a0003c0003t0008g0358 a0003c0003t0031g0359 |
3 | HG00558.hp2 NA18997.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.547+6164G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620888 | |||||||
chr2:169620961 | A | G | 1 | a0003c0003t0004g0108 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.547+6237A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169620961 | |||||||
chr2:169621290 | A | T | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.547+6566A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621290 | |||||||
chr2:169621440 | C | T | 1 | a0002c0002t0003g0189 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.547+6716C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621440 | |||||||
chr2:169621544 | G | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+6820G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621544 | |||||||
chr2:169621608 | AC | A | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+6887delC | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169621608 | ||||||
chr2:169621619 | A | G | 9 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(6): Show |
10 | HG02145.hp1 HG02258.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.547+6895A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621619 | |||||||
chr2:169621672 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.547+6948A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621672 | |||||||
chr2:169621734 | A | ATT | 78 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.547+7023_547+7024d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169621734 | ||||||
chr2:169621776 | G | A | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.547+7052G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621776 | |||||||
chr2:169621923 | C | T | 361 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(358): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.547+7199C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621923 | |||||||
chr2:169621942 | A | T | 7 | a0002c0002t0001g0242 a0002c0002t0001g0244 a0002c0002t0001g0258 others(4): Show |
7 | HG00639.hp2 HG01884.hp1 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.547+7218A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621942 | |||||||
chr2:169621942 | AT | A | 206 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(203): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.547+7227delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169621942 | ||||||
chr2:169621943 | T | A | 1 | a0001c0001t0005g0337 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.547+7219T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621943 | |||||||
chr2:169621944 | T | A | 11 | a0001c0001t0005g0091 a0001c0001t0005g0332 a0001c0001t0005g0335 others(8): Show |
11 | HG00558.hp1 HG02080.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.547+7220T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621944 | |||||||
chr2:169621999 | A | C | 31 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(28): Show |
33 | HG00140.hp2 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.547+7275A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169621999 | |||||||
chr2:169622009 | C | G | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+7285C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622009 | |||||||
chr2:169622019 | G | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547+7295G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622019 | |||||||
chr2:169622066 | A | G | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+7342A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622066 | |||||||
chr2:169622088 | A | G | 3 | a0002c0002t0003g0309 a0002c0002t0003g0310 a0002c0002t0003g0311 |
3 | HG03209.hp1 HG03225.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.547+7364A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622088 | |||||||
chr2:169622105 | T | C | 1 | a0001c0005t0002g0078 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.547+7381T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622105 | |||||||
chr2:169622186 | C | T | 78 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.547+7462C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622186 | |||||||
chr2:169622303 | A | G | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.547+7579A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622303 | |||||||
chr2:169622487 | T | C | 1 | a0002c0002t0001g0253 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.547+7763T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622487 | |||||||
chr2:169622534 | A | G | 60 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.547+7810A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622534 | |||||||
chr2:169622794 | C | T | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.548-7980C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622794 | |||||||
chr2:169622858 | A | C | 1 | a0002c0002t0001g0236 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.548-7916A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622858 | |||||||
chr2:169622866 | A | G | 1 | a0002c0002t0001g0295 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.548-7908A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622866 | |||||||
chr2:169622911 | C | T | 3 | a0003c0003t0004g0354 a0003c0003t0004g0355 a0003c0003t0004g0356 |
3 | HG01496.hp1 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.548-7863C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622911 | |||||||
chr2:169622942 | T | A | 1 | a0002c0002t0001g0274 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.548-7832T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169622942 | |||||||
chr2:169623002 | TA | T | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-7771delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623002 | |||||||
chr2:169623015 | G | T | 152 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(149): Show |
159 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.548-7759G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623015 | |||||||
chr2:169623108 | A | C | 1 | a0001c0001t0007g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.548-7666A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623108 | |||||||
chr2:169623152 | T | C | 35 | a0003c0003t0004g0003 a0003c0003t0004g0010 a0003c0003t0004g0096 others(32): Show |
38 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.548-7622T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623152 | |||||||
chr2:169623154 | G | A | 1 | a0001c0001t0006g0135 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.548-7620G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623154 | |||||||
chr2:169623241 | C | A | 1 | a0002c0002t0003g0203 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.548-7533C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623241 | |||||||
chr2:169623429 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(67): Show |
75 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.548-7345G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623429 | |||||||
chr2:169623453 | G | A | 2 | a0002c0002t0003g0165 a0002c0002t0003g0166 |
2 | NA19006.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.548-7321G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623453 | |||||||
chr2:169623513 | C | T | 45 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(42): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.548-7261C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623513 | |||||||
chr2:169623707 | T | C | 5 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 others(2): Show |
5 | HG00099.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-7067T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623707 | |||||||
chr2:169623892 | G | T | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.548-6882G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623892 | |||||||
chr2:169623953 | T | G | 1 | a0001c0001t0012g0031 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.548-6821T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623953 | |||||||
chr2:169623955 | C | T | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.548-6819C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169623955 | |||||||
chr2:169624000 | T | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-6774T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624000 | |||||||
chr2:169624010 | A | T | 1 | a0001c0005t0002g0078 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.548-6764A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624010 | |||||||
chr2:169624157 | A | G | 10 | a0002c0002t0001g0160 a0002c0002t0001g0178 a0002c0002t0001g0211 others(7): Show |
10 | HG00642.hp1 HG00735.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.548-6617A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624157 | |||||||
chr2:169624160 | TCTCGCTA others(5): Show |
T | 2 | a0005c0006t0018g0110 a0005c0006t0018g0115 |
2 | HG03654.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.548-6612_548-6601d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169624160 | ||||||
chr2:169624223 | A | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-6551A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624223 | |||||||
chr2:169624244 | A | G | 255 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(252): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.548-6530A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624244 | |||||||
chr2:169624368 | C | A | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.548-6406C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624368 | |||||||
chr2:169624388 | T | A | 1 | a0003c0003t0004g0098 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.548-6386T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624388 | |||||||
chr2:169624464 | C | T | 361 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(358): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.548-6310C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624464 | |||||||
chr2:169624650 | C | T | 4 | a0002c0002t0001g0280 a0002c0002t0001g0281 a0002c0002t0001g0290 others(1): Show |
4 | NA18980.hp1 NA19056.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-6124C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624650 | |||||||
chr2:169624737 | A | G | 4 | a0002c0002t0001g0249 a0002c0002t0001g0250 a0002c0002t0001g0254 others(1): Show |
4 | HG01081.hp2 HG02273.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-6037A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624737 | |||||||
chr2:169624932 | C | T | 1 | a0002c0002t0001g0302 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.548-5842C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624932 | |||||||
chr2:169624939 | G | A | 3 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 |
4 | HG02145.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-5835G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624939 | |||||||
chr2:169624946 | A | T | 1 | a0002c0002t0001g0244 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.548-5828A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169624946 | |||||||
chr2:169625026 | A | G | 1 | a0001c0001t0011g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.548-5748A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625026 | |||||||
chr2:169625217 | G | A | 71 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(68): Show |
73 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.548-5557G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625217 | |||||||
chr2:169625259 | A | G | 56 | a0003c0003t0004g0003 a0003c0003t0004g0010 a0003c0003t0004g0096 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.548-5515A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625259 | |||||||
chr2:169625565 | G | A | 60 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.548-5209G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625565 | |||||||
chr2:169625586 | A | C | 60 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.548-5188A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625586 | |||||||
chr2:169625726 | C | T | 1 | a0001c0001t0025g0034 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.548-5048C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625726 | |||||||
chr2:169625728 | AT | A | 7 | a0001c0001t0002g0072 a0001c0001t0005g0361 a0002c0002t0001g0277 others(4): Show |
7 | HG01192.hp1 HG01261.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-5035delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169625728 | ||||||
chr2:169625841 | A | G | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.548-4933A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625841 | |||||||
chr2:169625989 | T | C | 14 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(11): Show |
15 | HG01891.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.548-4785T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169625989 | |||||||
chr2:169626047 | G | T | 103 | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(100): Show |
107 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.548-4727G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626047 | |||||||
chr2:169626081 | T | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-4693T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626081 | |||||||
chr2:169626535 | A | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-4239A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626535 | |||||||
chr2:169626581 | G | T | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-4193G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626581 | |||||||
chr2:169626732 | C | T | 1 | a0003c0003t0004g0125 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.548-4042C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626732 | |||||||
chr2:169626956 | T | A | 3 | a0002c0002t0001g0226 a0002c0002t0001g0264 a0002c0002t0001g0315 |
3 | NA18943.hp1 NA19005.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.548-3818T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169626956 | |||||||
chr2:169627047 | T | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-3727T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627047 | |||||||
chr2:169627049 | A | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-3725A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627049 | |||||||
chr2:169627150 | T | G | 13 | a0003c0003t0004g0003 a0003c0003t0004g0097 a0003c0003t0004g0098 others(10): Show |
15 | HG00733.hp1 HG01255.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.548-3624T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627150 | |||||||
chr2:169627239 | C | T | 56 | a0003c0003t0004g0003 a0003c0003t0004g0010 a0003c0003t0004g0096 others(53): Show |
59 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.548-3535C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627239 | |||||||
chr2:169627285 | G | A | 1 | a0001c0001t0013g0038 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.548-3489G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627285 | |||||||
chr2:169627309 | C | T | 2 | a0001c0001t0007g0094 a0001c0001t0007g0095 |
2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.548-3465C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627309 | |||||||
chr2:169627411 | T | C | 1 | a0002c0002t0003g0172 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.548-3363T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627411 | |||||||
chr2:169627470 | T | A | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-3304T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627470 | |||||||
chr2:169627598 | C | T | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-3176C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627598 | |||||||
chr2:169627704 | C | CTTTTT | 70 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(67): Show |
75 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.548-3053_548-3049d others(7): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | ||||||
chr2:169627704 | C | CTTTTTT | 35 | a0001c0001t0002g0054 a0001c0001t0002g0063 a0001c0001t0002g0076 others(32): Show |
38 | HG00323.hp2 HG00438.hp2 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.548-3054_548-3049d others(8): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | ||||||
chr2:169627704 | C | CTTTTTTT | 12 | a0001c0001t0012g0031 a0001c0001t0012g0042 a0001c0001t0015g0033 others(9): Show |
12 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.548-3055_548-3049d others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | ||||||
chr2:169627704 | CT | C | 34 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(31): Show |
34 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.548-3049delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169627704 | ||||||
chr2:169627725 | T | A | 24 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(21): Show |
24 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.548-3049T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627725 | |||||||
chr2:169627725 | T | TTTTTTA | 9 | a0001c0001t0005g0352 a0001c0001t0005g0353 a0001c0001t0007g0092 others(6): Show |
9 | HG02630.hp2 HG02647.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.548-3049_548-3048i others(8): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627725 | |||||||
chr2:169627725 | T | TTTTTTTA | 27 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(24): Show |
28 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.548-3049_548-3048i others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627725 | |||||||
chr2:169627808 | A | G | 4 | a0001c0001t0009g0059 a0001c0001t0009g0067 a0001c0001t0009g0069 others(1): Show |
4 | HG02523.hp2 HG03927.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-2966A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627808 | |||||||
chr2:169627965 | T | A | 1 | a0002c0002t0003g0309 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.548-2809T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169627965 | |||||||
chr2:169628146 | A | G | 255 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(252): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.548-2628A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628146 | |||||||
chr2:169628214 | A | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-2560A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628214 | |||||||
chr2:169628272 | G | A | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-2502G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628272 | |||||||
chr2:169628370 | C | T | 1 | a0002c0002t0001g0211 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.548-2404C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628370 | |||||||
chr2:169628422 | T | A | 1 | a0002c0004t0003g0198 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.548-2352T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628422 | |||||||
chr2:169628534 | A | G | 21 | a0003c0003t0004g0354 a0003c0003t0004g0355 a0003c0003t0004g0356 others(18): Show |
21 | HG00140.hp2 HG00558.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.548-2240A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628534 | |||||||
chr2:169628698 | C | T | 4 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0029 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-2076C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628698 | |||||||
chr2:169628731 | G | A | 1 | a0004c0008t0001g0301 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.548-2043G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628731 | |||||||
chr2:169628808 | T | C | 10 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0019 others(7): Show |
10 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.548-1966T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628808 | |||||||
chr2:169628930 | C | A | 54 | a0003c0003t0004g0003 a0003c0003t0004g0010 a0003c0003t0004g0096 others(51): Show |
57 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.548-1844C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628930 | |||||||
chr2:169628939 | C | CA | 52 | a0001c0001t0005g0338 a0001c0001t0012g0031 a0002c0002t0001g0208 others(49): Show |
52 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.548-1806dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | C | CAA | 8 | a0002c0002t0001g0286 a0002c0002t0001g0297 a0002c0002t0001g0303 others(5): Show |
8 | HG01192.hp1 HG02135.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.548-1807_548-1806d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | C | CAAA | 7 | a0001c0001t0012g0036 a0001c0001t0026g0035 a0002c0002t0001g0266 others(4): Show |
7 | HG00673.hp1 HG02735.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-1808_548-1806d others(5): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0028g0138 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.548-1815_548-1806d others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0007g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.548-1816_548-1806d others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0007g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.548-1817_548-1806d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0007g0025 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.548-1818_548-1806d others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0027g0018 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.548-1823_548-1806d others(20): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | CA | C | 21 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0333 others(18): Show |
21 | HG00140.hp1 HG00609.hp1 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.548-1806delA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | CAAAAAAA others(3): Show |
C | 26 | a0001c0001t0007g0016 a0001c0001t0007g0017 a0001c0001t0007g0020 others(23): Show |
27 | HG00280.hp2 HG01099.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.548-1815_548-1806d others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | CAAAAAAA others(4): Show |
C | 39 | a0001c0001t0002g0044 a0001c0001t0002g0046 a0001c0001t0002g0054 others(36): Show |
41 | HG00140.hp2 HG00323.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.548-1816_548-1806d others(13): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | CAAAAAAA others(5): Show |
C | 93 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(90): Show |
100 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.548-1817_548-1806d others(14): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628939 | CAAAAAAA others(6): Show |
C | 4 | a0001c0001t0011g0162 a0001c0001t0011g0163 a0001c0001t0011g0164 others(1): Show |
4 | HG02486.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-1818_548-1806d others(15): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169628939 | ||||||
chr2:169628966 | A | G | 1 | a0003c0003t0008g0324 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.548-1808A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628966 | |||||||
chr2:169628968 | A | G | 1 | a0002c0002t0001g0261 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.548-1806A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169628968 | |||||||
chr2:169629041 | A | G | 207 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(204): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.548-1733A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629041 | |||||||
chr2:169629237 | A | G | 1 | a0003c0003t0008g0318 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.548-1537A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629237 | |||||||
chr2:169629662 | A | G | 10 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 others(7): Show |
12 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.548-1112A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629662 | |||||||
chr2:169629757 | C | T | 1 | a0001c0001t0007g0176 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.548-1017C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629757 | |||||||
chr2:169629830 | T | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-944T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629830 | |||||||
chr2:169629925 | T | C | 3 | a0002c0002t0001g0284 a0002c0002t0001g0285 a0002c0002t0001g0293 |
3 | HG02976.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.548-849T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629925 | |||||||
chr2:169629935 | T | C | 25 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(22): Show |
25 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.548-839T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169629935 | |||||||
chr2:169630081 | C | G | 2 | a0003c0003t0004g0125 a0003c0003t0004g0130 |
2 | HG02559.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.548-693C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630081 | |||||||
chr2:169630141 | G | GT | 6 | a0002c0002t0001g0013 a0002c0002t0003g0179 a0002c0002t0010g0013 others(3): Show |
6 | HG02895.hp1 HG02897.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-620dupT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169630141 | ||||||
chr2:169630141 | GT | G | 194 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0008 others(191): Show |
202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.548-620delT | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169630141 | ||||||
chr2:169630141 | GTT | G | 6 | a0001c0001t0002g0002 a0001c0001t0002g0068 a0001c0001t0002g0081 others(3): Show |
8 | NA18943.hp2 NA18947.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.548-621_548-620del others(2): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | 169630141 | ||||||
chr2:169630274 | C | G | 78 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.548-500C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630274 | |||||||
chr2:169630497 | A | T | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.548-277A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630497 | |||||||
chr2:169630586 | C | T | 4 | a0001c0001t0013g0028 a0001c0001t0013g0038 a0001c0007t0013g0029 others(1): Show |
4 | HG02258.hp2 HG03139.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-188C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630586 | |||||||
chr2:169630644 | C | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.548-130C>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630644 | |||||||
chr2:169630660 | G | T | 4 | a0001c0001t0006g0147 a0001c0001t0006g0148 a0001c0001t0006g0151 others(1): Show |
4 | HG01099.hp2 HG01346.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-114G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630660 | |||||||
chr2:169630746 | G | A | 1 | a0002c0002t0003g0182 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.548-28G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 9/13 | chr2 | 169630746 | |||||||
chr2:169631089 | G | T | 1 | a0001c0001t0007g0019 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.761+102G>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631089 | |||||||
chr2:169631170 | G | C | 253 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(250): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.761+183G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631170 | |||||||
chr2:169631329 | G | A | 78 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.761+342G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631329 | |||||||
chr2:169631477 | T | C | 5 | a0001c0001t0007g0158 a0001c0001t0007g0173 a0001c0001t0007g0174 others(2): Show |
5 | HG01891.hp1 NA18906.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.762-289T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631477 | |||||||
chr2:169631721 | A | G | 1 | a0003c0003t0008g0357 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.762-45A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 10/13 | chr2 | 169631721 | |||||||
chr2:169631944 | A | G | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.929+11A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169631944 | |||||||
chr2:169632058 | A | C | 3 | a0002c0002t0001g0284 a0002c0002t0001g0285 a0002c0002t0001g0293 |
3 | HG02976.hp2 HG03540.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.929+125A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632058 | |||||||
chr2:169632117 | A | C | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.929+184A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632117 | |||||||
chr2:169632149 | A | G | 6 | a0001c0001t0012g0031 a0001c0001t0012g0041 a0001c0001t0012g0042 others(3): Show |
6 | HG02451.hp2 HG02717.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.929+216A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632149 | |||||||
chr2:169632173 | A | G | 1 | a0002c0002t0003g0189 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.929+240A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632173 | |||||||
chr2:169632182 | G | A | 1 | a0002c0002t0001g0221 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.929+249G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632182 | |||||||
chr2:169632189 | T | C | 60 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.929+256T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632189 | |||||||
chr2:169632209 | C | A | 60 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.929+276C>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632209 | |||||||
chr2:169632230 | A | G | 60 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.929+297A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632230 | |||||||
chr2:169632249 | T | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.929+316T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632249 | |||||||
chr2:169632260 | T | G | 78 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(75): Show |
83 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.929+327T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632260 | |||||||
chr2:169632356 | T | G | 90 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(87): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.929+423T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632356 | |||||||
chr2:169632467 | C | T | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.929+534C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632467 | |||||||
chr2:169632590 | A | T | 4 | a0002c0002t0001g0280 a0002c0002t0001g0281 a0002c0002t0001g0290 others(1): Show |
4 | NA18980.hp1 NA19056.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.930-570A>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632590 | |||||||
chr2:169632677 | G | A | 45 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(42): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.930-483G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632677 | |||||||
chr2:169632701 | C | T | 1 | a0001c0001t0007g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.930-459C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632701 | |||||||
chr2:169632747 | A | AAATAAT | 198 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(195): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.930-398_930-393dup others(6): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 169632747 | ||||||
chr2:169632747 | A | AAATAATA others(2): Show |
10 | a0001c0001t0002g0068 a0001c0001t0007g0009 a0001c0001t0007g0092 others(7): Show |
11 | HG02145.hp1 HG02280.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.930-401_930-393dup others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | 169632747 | ||||||
chr2:169632796 | T | G | 3 | a0001c0001t0007g0009 a0001c0001t0007g0092 a0001c0001t0007g0093 |
4 | HG02145.hp1 HG03098.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.930-364T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632796 | |||||||
chr2:169632864 | G | C | 1 | a0002c0002t0003g0177 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.930-296G>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 11/13 | chr2 | 169632864 | |||||||
chr2:169633315 | T | A | 5 | a0001c0001t0007g0016 a0001c0001t0007g0020 a0001c0001t0007g0022 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1017+68T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633315 | |||||||
chr2:169633460 | A | G | 28 | a0003c0003t0004g0003 a0003c0003t0004g0010 a0003c0003t0004g0096 others(25): Show |
31 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1017+213A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633460 | |||||||
chr2:169633656 | C | T | 2 | a0003c0003t0004g0120 a0003c0003t0004g0122 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1017+409C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633656 | |||||||
chr2:169633663 | T | TA | 39 | a0001c0001t0006g0133 a0001c0001t0006g0135 a0001c0001t0006g0136 others(36): Show |
40 | HG00438.hp1 HG00621.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1017+417dupA | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 169633663 | ||||||
chr2:169633693 | C | T | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1017+446C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633693 | |||||||
chr2:169633830 | C | T | 1 | a0002c0002t0034g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1017+583C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633830 | |||||||
chr2:169633835 | CCT | C | 206 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(203): Show |
216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1017+589_1017+590d others(4): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633835 | |||||||
chr2:169633837 | T | C | 1 | a0002c0002t0001g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1017+590T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633837 | |||||||
chr2:169633900 | G | A | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1017+653G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169633900 | |||||||
chr2:169634143 | C | T | 6 | a0003c0003t0008g0319 a0003c0003t0008g0323 a0003c0003t0008g0325 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1017+896C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634143 | |||||||
chr2:169634159 | C | T | 26 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(23): Show |
26 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.1017+912C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634159 | |||||||
chr2:169634604 | G | A | 8 | a0001c0001t0012g0031 a0001c0001t0012g0036 a0001c0001t0012g0037 others(5): Show |
8 | HG02451.hp2 HG02559.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1017+1357G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634604 | |||||||
chr2:169634643 | T | G | 1 | a0002c0002t0001g0276 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1017+1396T>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634643 | |||||||
chr2:169634739 | TCTGCCTC others(1): Show |
T | 45 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(42): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1352_1018-134 others(12): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634739 | |||||||
chr2:169634748 | T | A | 45 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(42): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1344T>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634748 | |||||||
chr2:169634750 | A | C | 45 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(42): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1342A>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634750 | |||||||
chr2:169634752 | T | C | 45 | a0002c0002t0003g0011 a0002c0002t0003g0165 a0002c0002t0003g0166 others(42): Show |
47 | HG00423.hp1 HG01192.hp2 HG01358.hp2 others(44): Show |
intron_variant | MODIFIER | c.1018-1340T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169634752 | |||||||
chr2:169635006 | A | G | 1 | a0003c0003t0008g0357 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1018-1086A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635006 | |||||||
chr2:169635053 | TAATGA | T | 82 | a0001c0001t0005g0091 a0001c0001t0005g0330 a0001c0001t0005g0331 others(79): Show |
85 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.1018-1035_1018-103 others(9): Show |
PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | 169635053 | ||||||
chr2:169635135 | A | G | 4 | a0002c0002t0001g0249 a0002c0002t0001g0250 a0002c0002t0001g0254 others(1): Show |
4 | HG01081.hp2 HG02273.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018-957A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635135 | |||||||
chr2:169635268 | G | A | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1018-824G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635268 | |||||||
chr2:169635313 | G | A | 60 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(57): Show |
65 | HG00099.hp1 HG00323.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1018-779G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635313 | |||||||
chr2:169635317 | T | C | 1 | a0003c0003t0008g0357 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1018-775T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635317 | |||||||
chr2:169635329 | T | C | 2 | a0001c0001t0028g0138 a0001c0001t0032g0137 |
2 | HG02280.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1018-763T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635329 | |||||||
chr2:169635569 | G | A | 208 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(205): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.1018-523G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635569 | |||||||
chr2:169635745 | G | A | 1 | a0002c0002t0010g0265 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1018-347G>A | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169635745 | |||||||
chr2:169636026 | C | T | 1 | a0003c0003t0004g0355 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1018-66C>T | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169636026 | |||||||
chr2:169636057 | A | G | 209 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(206): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.1018-35A>G | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169636057 | |||||||
chr2:169636074 | T | C | 255 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(252): Show |
267 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1018-18T>C | PPIG | ENSG00000138398.17 | transcript | ENST00000260970.8 | protein_coding | 12/13 | chr2 | 169636074 |