Item | Value |
---|---|
geneid | 10541 |
ensemblid | ENSG00000136938.9 |
hgncid | 16677 |
symbol | ANP32B |
name | acidic nuclear phosphoprotein 32 family member B |
refseq_nuc | NM_006401.3 |
refseq_prot | NP_006392.1 |
ensembl_nuc | ENST00000339399.5 |
ensembl_prot | ENSP00000345848.4 |
mane_status | MANE Select |
chr | chr9 |
start | 97983341 |
end | 98015943 |
strand | + |
ver | v1.2 |
region | chr9:97983341-98015943 |
region5000 | chr9:97978341-98020943 |
regionname0 | ANP32B_chr9_97983341_98015943 |
regionname5000 | ANP32B_chr9_97978341_98020943 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 251 | 307 | 85 | 57 | 113 | 14 | 36 | 84 | ANP32B_chr9_97978341_98020943 | ANP32B | MDMKR others(246): Show |
chr9 | 97978341 | 98020943 |
a0002 | 0/0 | 251 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | MDMKR others(246): Show |
chr9 | 97978341 | 98020943 |
a0003 | 0/0 | 251 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | MDMKR others(246): Show |
chr9 | 97978341 | 98020943 |
a0004 | 0/0 | 251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | MDMKR others(246): Show |
chr9 | 97978341 | 98020943 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 753 | 306 | 84 | 57 | 113 | 14 | 36 | ANP32B_chr9_97978341_98020943 | ANP32B | ATGGA others(748): Show |
chr9 | 97978341 | 98020943 | ||
a0001c0003 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | ATGGA others(748): Show |
chr9 | 97978341 | 98020943 | ||
a0002c0002 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | ATGGA others(748): Show |
chr9 | 97978341 | 98020943 | ||
a0003c0005 | 0/0 | 753 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | ATGGA others(748): Show |
chr9 | 97978341 | 98020943 | ||
a0004c0004 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | ATGGA others(748): Show |
chr9 | 97978341 | 98020943 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1483 | 278 | 60 | 54 | 112 | 14 | 36 | ANP32B_chr9_97978341_98020943 | ANP32B | CTTTT others(1478): Show |
chr9 | 97978341 | 98020943 |
a0001c0001t0002 | 0/0 | 1485 | 27 | 24 | 3 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | CTTTT others(1480): Show |
chr9 | 97978341 | 98020943 |
a0001c0001t0003 | 0/0 | 1483 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | CTTTT others(1478): Show |
chr9 | 97978341 | 98020943 |
a0001c0003t0001 | 0/0 | 1483 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | CTTTT others(1478): Show |
chr9 | 97978341 | 98020943 |
a0002c0002t0002 | 0/0 | 1485 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | CTTTT others(1480): Show |
chr9 | 97978341 | 98020943 |
a0003c0005t0001 | 0/0 | 1483 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | CTTTT others(1478): Show |
chr9 | 97978341 | 98020943 |
a0004c0004t0001 | 0/0 | 1483 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | CTTTT others(1478): Show |
chr9 | 97978341 | 98020943 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 17 | 1 | 3 | 9 | 2 | 2 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0002 | 0/0 | 14 | 0 | 2 | 10 | 0 | 2 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0003 | 0/0 | 10 | 2 | 0 | 5 | 1 | 2 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 2 | 4 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0007 | 0/0 | 6 | 5 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0008 | 0/0 | 6 | 1 | 4 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0013 | 1/0 | 4 | 0 | 2 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0017 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0033 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0004 | 0/0 | 8 | 7 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0001c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0003c0005t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
a0004c0004t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0146 | EUR | FIN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | FIN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00642 | hp1 | a0003 | c0005 | t0001 | g0067 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | STU | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | YRI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | LWK | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | LWK | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | ASW | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20129 | hp2 | a0001 | c0003 | t0001 | g0176 | AFR | ASW | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | TSI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | USA | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20300 | hp1 | a0004 | c0004 | t0001 | g0116 | AFR | USA | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | USA | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0041 | AFR | LWK | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0149 | REF | REF | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0013 | REF | REF | ANP32B_chr9_97978341_98020943 | ANP32B | chr9 | 97978341 | 98020943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97998654 | A | C | 1 | a0003 | 1 | HG00642.hp1 | missense_variant | MODERATE | c.303A>C | p.Lys101Asn | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/7 | 518/1483 | 303/756 | 101/251 | chr9 | 97998654 | |||
chr9:98005025 | A | C | 1 | a0004 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.389A>C | p.Asp130Ala | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/7 | 604/1483 | 389/756 | 130/251 | chr9 | 98005025 | |||
chr9:98011368 | C | A | 1 | a0002 | 1 | HG00408.hp2 | missense_variant | MODERATE | c.615C>A | p.Asp205Glu | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/7 | 830/1483 | 615/756 | 205/251 | chr9 | 98011368 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:98011296 | C | T | 1 | a0001c0003 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.543C>T | p.Asp181Asp | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/7 | 758/1483 | 543/756 | 181/251 | chr9 | 98011296 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97983483 | C | T | 1 | a0001c0001t0003 | 1 | NA18944.hp1 | 5_prime_UTR_variant | MODIFIER | c.-73C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/7 | 73 | chr9 | 97983483 | ||||||
chr9:98015502 | T | TA | 2 | a0001c0001t0002 a0002c0002t0002 |
28 | HG00408.hp2 HG01081.hp2 HG01243.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*85dupA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 7/7 | 86 | INFO_REALIGN_3_PRIME | chr9 | 98015502 | |||||
chr9:98015854 | A | AT | 2 | a0001c0001t0002 a0002c0002t0002 |
28 | HG00408.hp2 HG01081.hp2 HG01243.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*431dupT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 7/7 | 432 | INFO_REALIGN_3_PRIME | chr9 | 98015854 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:97983620 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
85 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.54+11A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983620 | |||||||
chr9:97983629 | G | C | 6 | a0001c0001t0001g0042 a0001c0001t0002g0038 a0001c0001t0002g0039 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+20G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983629 | |||||||
chr9:97983688 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.54+79G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983688 | |||||||
chr9:97983732 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA18945.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.54+123C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983732 | |||||||
chr9:97983742 | A | AGGCG | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0002g0036 |
4 | HG02723.hp1 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+142_54+145dupGG others(2): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97983742 | ||||||
chr9:97983759 | G | C | 1 | a0001c0001t0001g0045 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.54+150G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983759 | |||||||
chr9:97983803 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.54+194C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983803 | |||||||
chr9:97983809 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0046 |
3 | HG01106.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.54+200G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983809 | |||||||
chr9:97983824 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.54+215G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983824 | |||||||
chr9:97983903 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.54+294G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983903 | |||||||
chr9:97983904 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.54+295C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983904 | |||||||
chr9:97983941 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.54+332T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97983941 | |||||||
chr9:97984006 | G | A | 4 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG01884.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.54+397G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984006 | |||||||
chr9:97984080 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.54+471C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984080 | |||||||
chr9:97984094 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
196 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.54+485T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984094 | |||||||
chr9:97984194 | G | A | 1 | a0001c0001t0001g0017 | 3 | HG00642.hp2 HG01255.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.54+585G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984194 | |||||||
chr9:97984200 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.54+591C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984200 | |||||||
chr9:97984264 | G | C | 1 | a0001c0001t0001g0054 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.54+655G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984264 | |||||||
chr9:97984287 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.54+678C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984287 | |||||||
chr9:97984391 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.54+782C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984391 | |||||||
chr9:97984521 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.54+912G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984521 | |||||||
chr9:97984573 | G | GCA | 52 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
83 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.54+965_54+966dupCA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97984573 | ||||||
chr9:97984695 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.54+1086C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984695 | |||||||
chr9:97984701 | C | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(29): Show |
59 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.54+1092C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984701 | |||||||
chr9:97984719 | C | G | 1 | a0001c0001t0001g0191 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.54+1110C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984719 | |||||||
chr9:97984794 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.54+1185C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984794 | |||||||
chr9:97984899 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+1290G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984899 | |||||||
chr9:97984951 | G | T | 1 | a0001c0001t0001g0011 | 4 | HG01167.hp1 HG01169.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+1342G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984951 | |||||||
chr9:97984958 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.54+1349G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984958 | |||||||
chr9:97984970 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.54+1361C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97984970 | |||||||
chr9:97985055 | C | A | 1 | a0002c0002t0002g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.54+1446C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985055 | |||||||
chr9:97985066 | G | GC | 25 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(22): Show |
33 | HG00639.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.54+1467dupC | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97985066 | ||||||
chr9:97985084 | ACCGGCGC others(3): Show |
A | 1 | a0001c0001t0001g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.54+1478_54+1487del others(10): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97985084 | ||||||
chr9:97985088 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.54+1479G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985088 | |||||||
chr9:97985094 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.54+1485G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985094 | |||||||
chr9:97985173 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.54+1564C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985173 | |||||||
chr9:97985228 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0002g0038 a0001c0001t0002g0039 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+1619A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985228 | |||||||
chr9:97985277 | C | T | 1 | a0001c0001t0002g0068 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.54+1668C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985277 | |||||||
chr9:97985324 | C | CG | 5 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0037 others(2): Show |
7 | HG02056.hp1 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.54+1719dupG | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97985324 | ||||||
chr9:97985325 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.54+1716G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985325 | |||||||
chr9:97985329 | C | G | 52 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
83 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.54+1720C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985329 | |||||||
chr9:97985601 | C | G | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.54+1992C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985601 | |||||||
chr9:97985602 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.54+1993G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985602 | |||||||
chr9:97985618 | C | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0162 |
3 | HG01109.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.54+2009C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985618 | |||||||
chr9:97985633 | A | G | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.54+2024A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985633 | |||||||
chr9:97985662 | T | C | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.54+2053T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985662 | |||||||
chr9:97985815 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.54+2206T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985815 | |||||||
chr9:97985818 | T | G | 1 | a0001c0001t0001g0159 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.54+2209T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985818 | |||||||
chr9:97985829 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54+2220T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97985829 | |||||||
chr9:97985831 | C | CT | 9 | a0001c0001t0001g0042 a0001c0001t0001g0152 a0001c0001t0001g0153 others(6): Show |
9 | HG01257.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.54+2232dupT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97985831 | ||||||
chr9:97985900 | C | CA | 3 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0152 |
5 | NA18941.hp2 NA18945.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+2292dupA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97985900 | ||||||
chr9:97986036 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0162 |
3 | HG01109.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.54+2427G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986036 | |||||||
chr9:97986106 | C | A | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.54+2497C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986106 | |||||||
chr9:97986108 | A | AC | 34 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(31): Show |
65 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.54+2501dupC | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97986108 | ||||||
chr9:97986108 | A | ACC | 6 | a0001c0001t0001g0022 a0001c0001t0001g0049 a0001c0001t0001g0077 others(3): Show |
7 | HG01952.hp2 HG02258.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+2500_54+2501dup others(2): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97986108 | ||||||
chr9:97986111 | G | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.54+2502G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986111 | |||||||
chr9:97986155 | C | T | 1 | a0001c0001t0001g0103 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.54+2546C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986155 | |||||||
chr9:97986162 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.54+2553G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986162 | |||||||
chr9:97986168 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.54+2559C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986168 | |||||||
chr9:97986238 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.54+2629C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986238 | |||||||
chr9:97986274 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.54+2665A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986274 | |||||||
chr9:97986314 | T | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(188): Show |
302 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(299): Show |
intron_variant | MODIFIER | c.54+2705T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986314 | |||||||
chr9:97986472 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.54+2863C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986472 | |||||||
chr9:97986789 | A | T | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
7 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+3180A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97986789 | |||||||
chr9:97987216 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.54+3607G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97987216 | |||||||
chr9:97987252 | AAG | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.54+3645_54+3646del others(2): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97987252 | ||||||
chr9:97987325 | G | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | NA18945.hp1 NA18994.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.54+3716G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97987325 | |||||||
chr9:97987430 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | HG01257.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.54+3821G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97987430 | |||||||
chr9:97987732 | C | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0101 a0001c0001t0001g0146 others(1): Show |
5 | HG00323.hp1 HG01074.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.54+4123C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97987732 | |||||||
chr9:97987815 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.54+4206T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97987815 | |||||||
chr9:97987963 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.54+4354A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97987963 | |||||||
chr9:97987968 | T | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
7 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.54+4359T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97987968 | |||||||
chr9:97988028 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.54+4419C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988028 | |||||||
chr9:97988051 | A | T | 5 | a0001c0001t0001g0022 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
6 | HG02258.hp1 HG02723.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.54+4442A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988051 | |||||||
chr9:97988232 | C | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.54+4623C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988232 | |||||||
chr9:97988298 | A | G | 1 | a0001c0001t0001g0187 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.54+4689A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988298 | |||||||
chr9:97988315 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.54+4706C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988315 | |||||||
chr9:97988341 | G | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.54+4732G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988341 | |||||||
chr9:97988435 | C | A | 8 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(5): Show |
15 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+4826C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988435 | |||||||
chr9:97988458 | C | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(5): Show |
15 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.54+4849C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988458 | |||||||
chr9:97988460 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.54+4851C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988460 | |||||||
chr9:97988691 | C | G | 1 | a0001c0001t0001g0030 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.54+5082C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988691 | |||||||
chr9:97988712 | G | A | 1 | a0003c0005t0001g0067 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.54+5103G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97988712 | |||||||
chr9:97989169 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.55-5462G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989169 | |||||||
chr9:97989287 | T | A | 1 | a0001c0001t0001g0109 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.55-5344T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989287 | |||||||
chr9:97989346 | T | C | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.55-5285T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989346 | |||||||
chr9:97989369 | G | C | 6 | a0001c0001t0001g0042 a0001c0001t0002g0038 a0001c0001t0002g0039 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.55-5262G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989369 | |||||||
chr9:97989480 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.55-5151A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989480 | |||||||
chr9:97989522 | C | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0075 a0001c0001t0001g0076 |
5 | NA18960.hp1 NA18961.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.55-5109C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989522 | |||||||
chr9:97989665 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.55-4966G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989665 | |||||||
chr9:97989849 | A | G | 8 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(5): Show |
15 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-4782A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97989849 | |||||||
chr9:97990020 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.55-4611A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990020 | |||||||
chr9:97990083 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.55-4548A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990083 | |||||||
chr9:97990151 | C | T | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.55-4480C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990151 | |||||||
chr9:97990210 | G | A | 8 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(5): Show |
15 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-4421G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990210 | |||||||
chr9:97990611 | C | A | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0043 |
3 | HG02559.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.55-4020C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990611 | |||||||
chr9:97990638 | G | A | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG02630.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.55-3993G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990638 | |||||||
chr9:97990785 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.55-3846A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990785 | |||||||
chr9:97990809 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.55-3822T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990809 | |||||||
chr9:97990814 | C | CT | 15 | a0001c0001t0001g0053 a0001c0001t0001g0107 a0001c0001t0001g0139 others(12): Show |
17 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.55-3794dupT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97990814 | ||||||
chr9:97990814 | C | CTT | 8 | a0001c0001t0001g0005 a0001c0001t0001g0049 a0001c0001t0001g0055 others(5): Show |
14 | HG00741.hp2 HG01952.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.55-3795_55-3794dup others(2): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97990814 | ||||||
chr9:97990814 | CT | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(36): Show |
68 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.55-3794delT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97990814 | ||||||
chr9:97990814 | CTT | C | 48 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(45): Show |
77 | HG00323.hp2 HG00738.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.55-3795_55-3794del others(2): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97990814 | ||||||
chr9:97990814 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0164 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.55-3804_55-3794del others(11): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97990814 | ||||||
chr9:97990841 | A | G | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(48): Show |
82 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.55-3790A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990841 | |||||||
chr9:97990866 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA19011.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.55-3765C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990866 | |||||||
chr9:97990906 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.55-3725C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990906 | |||||||
chr9:97990944 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.55-3687C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990944 | |||||||
chr9:97990981 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.55-3650G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97990981 | |||||||
chr9:97991112 | C | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0064 a0001c0001t0002g0065 others(5): Show |
15 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.55-3519C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991112 | |||||||
chr9:97991126 | C | CT | 55 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
86 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.55-3492dupT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97991126 | ||||||
chr9:97991262 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0043 |
3 | HG02559.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.55-3369T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991262 | |||||||
chr9:97991330 | C | G | 1 | a0001c0001t0001g0053 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.55-3301C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991330 | |||||||
chr9:97991396 | C | G | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.55-3235C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991396 | |||||||
chr9:97991448 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.55-3183T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991448 | |||||||
chr9:97991545 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.55-3086A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991545 | |||||||
chr9:97991844 | T | C | 2 | a0001c0001t0002g0094 a0001c0001t0002g0095 |
2 | HG02280.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.55-2787T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991844 | |||||||
chr9:97991866 | C | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.55-2765C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991866 | |||||||
chr9:97991923 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.55-2708A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991923 | |||||||
chr9:97991939 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.55-2692A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991939 | |||||||
chr9:97991961 | A | G | 1 | a0003c0005t0001g0067 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.55-2670A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97991961 | |||||||
chr9:97992183 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.55-2448A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97992183 | |||||||
chr9:97992381 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.55-2250C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97992381 | |||||||
chr9:97992421 | C | T | 15 | a0001c0001t0001g0042 a0001c0001t0002g0004 a0001c0001t0002g0038 others(12): Show |
22 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.55-2210C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97992421 | |||||||
chr9:97992433 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.55-2198T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97992433 | |||||||
chr9:97992673 | T | G | 3 | a0001c0001t0002g0044 a0001c0001t0002g0047 a0001c0001t0002g0070 |
3 | HG01243.hp1 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.55-1958T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97992673 | |||||||
chr9:97992805 | G | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.55-1826G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97992805 | |||||||
chr9:97993629 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02055.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.55-1002A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97993629 | |||||||
chr9:97993704 | C | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.55-927C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97993704 | |||||||
chr9:97993728 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.55-903C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97993728 | |||||||
chr9:97993803 | T | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.55-828T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97993803 | |||||||
chr9:97993847 | G | A | 1 | a0004c0004t0001g0116 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.55-784G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97993847 | |||||||
chr9:97993889 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.55-742T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97993889 | |||||||
chr9:97993947 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.55-684T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97993947 | |||||||
chr9:97994268 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.55-363T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97994268 | |||||||
chr9:97994498 | G | C | 4 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0167 others(1): Show |
4 | HG02451.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.55-133G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | chr9 | 97994498 | |||||||
chr9:97994609 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(95): Show |
167 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(164): Show |
intron_variant | MODIFIER | c.55-16dupT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr9 | 97994609 | ||||||
chr9:97995061 | A | G | 41 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(38): Show |
73 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.204+281A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995061 | |||||||
chr9:97995073 | G | C | 1 | a0001c0001t0002g0043 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.204+293G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995073 | |||||||
chr9:97995260 | T | G | 1 | a0001c0001t0001g0082 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.204+480T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995260 | |||||||
chr9:97995324 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.204+544G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995324 | |||||||
chr9:97995485 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.204+705A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995485 | |||||||
chr9:97995620 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.204+840G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995620 | |||||||
chr9:97995804 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.204+1024T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995804 | |||||||
chr9:97995888 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.204+1108T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995888 | |||||||
chr9:97995930 | T | TA | 7 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0170 others(4): Show |
7 | HG01243.hp1 HG01256.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.204+1171dupA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 97995930 | ||||||
chr9:97995930 | TA | T | 17 | a0001c0001t0001g0042 a0001c0001t0001g0087 a0001c0001t0001g0134 others(14): Show |
26 | HG00408.hp2 HG01081.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.204+1171delA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 97995930 | ||||||
chr9:97995930 | TAAAAA | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+1167_204+1171d others(7): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr9 | 97995930 | ||||||
chr9:97995931 | A | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0163 |
2 | HG03471.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.204+1151A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97995931 | |||||||
chr9:97996121 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.204+1341T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996121 | |||||||
chr9:97996141 | A | G | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0043 |
3 | HG02559.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.204+1361A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996141 | |||||||
chr9:97996464 | T | C | 1 | a0001c0001t0001g0193 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.204+1684T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996464 | |||||||
chr9:97996480 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.204+1700T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996480 | |||||||
chr9:97996535 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.204+1755G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996535 | |||||||
chr9:97996553 | A | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.204+1773A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996553 | |||||||
chr9:97996751 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0002g0044 |
3 | HG01256.hp1 HG02257.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.205-1805G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996751 | |||||||
chr9:97996852 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.205-1704G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996852 | |||||||
chr9:97996880 | G | T | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.205-1676G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996880 | |||||||
chr9:97996945 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0002g0044 |
2 | HG02257.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.205-1611G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97996945 | |||||||
chr9:97997108 | A | G | 1 | a0001c0001t0001g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.205-1448A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997108 | |||||||
chr9:97997195 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.205-1361C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997195 | |||||||
chr9:97997206 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.205-1350A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997206 | |||||||
chr9:97997232 | C | G | 1 | a0001c0001t0001g0024 | 2 | NA18953.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.205-1324C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997232 | |||||||
chr9:97997425 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.205-1131A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997425 | |||||||
chr9:97997662 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.205-894T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997662 | |||||||
chr9:97997663 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.205-893G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997663 | |||||||
chr9:97997821 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
195 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.205-735T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997821 | |||||||
chr9:97997829 | A | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.205-727A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997829 | |||||||
chr9:97997831 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.205-725G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997831 | |||||||
chr9:97997831 | G | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(48): Show |
82 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.205-725G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97997831 | |||||||
chr9:97998440 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.205-116G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 2/6 | chr9 | 97998440 | |||||||
chr9:97998776 | AGAAAGTG others(323): Show |
A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(116): Show |
197 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(194): Show |
intron_variant | MODIFIER | c.327+116_327+445del | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998776 | ||||||
chr9:97998788 | C | CT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(20): Show |
30 | HG00597.hp1 HG01123.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.327+147dupT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97998788 | C | CTT | 12 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0021 others(9): Show |
14 | HG00642.hp2 HG01255.hp2 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+146_327+147dup others(2): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97998788 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0114 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.327+134_327+147dup others(14): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97998788 | CT | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0027 others(9): Show |
17 | HG00408.hp1 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+147delT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97998788 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0140 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.327+136_327+147del others(12): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97998788 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0120 |
2 | NA18990.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.327+130_327+147del others(18): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97998788 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0013 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+129_327+147del others(19): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97998788 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0013 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.327+128_327+147del others(20): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 97998788 | ||||||
chr9:97999243 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.327+565G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 97999243 | |||||||
chr9:97999291 | G | C | 8 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0064 others(5): Show |
17 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.327+613G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 97999291 | |||||||
chr9:97999477 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.327+799G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 97999477 | |||||||
chr9:97999547 | G | A | 3 | a0001c0001t0002g0044 a0001c0001t0002g0047 a0001c0001t0002g0070 |
3 | HG01243.hp1 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.327+869G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 97999547 | |||||||
chr9:97999933 | C | T | 1 | a0002c0002t0002g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.327+1255C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 97999933 | |||||||
chr9:98000213 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.327+1535A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98000213 | |||||||
chr9:98000243 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.327+1565T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98000243 | |||||||
chr9:98000363 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+1685A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98000363 | |||||||
chr9:98000373 | C | A | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.327+1695C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98000373 | |||||||
chr9:98000622 | G | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+1944G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98000622 | |||||||
chr9:98000917 | A | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.327+2239A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98000917 | |||||||
chr9:98000921 | C | CA | 13 | a0001c0001t0001g0051 a0001c0001t0001g0056 a0001c0001t0001g0071 others(10): Show |
13 | HG02056.hp2 HG02074.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.327+2262dupA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 98000921 | ||||||
chr9:98000921 | CA | C | 7 | a0001c0001t0001g0057 a0001c0001t0002g0038 a0001c0001t0002g0039 others(4): Show |
7 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+2262delA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 98000921 | ||||||
chr9:98000992 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0074 |
2 | NA19000.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.327+2314C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98000992 | |||||||
chr9:98001076 | C | T | 23 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(20): Show |
44 | HG00741.hp1 HG01192.hp2 HG01256.hp1 others(41): Show |
intron_variant | MODIFIER | c.327+2398C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98001076 | |||||||
chr9:98001173 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(48): Show |
82 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.327+2495C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98001173 | |||||||
chr9:98001174 | CT | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(48): Show |
82 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(79): Show |
intron_variant | MODIFIER | c.327+2505delT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 98001174 | ||||||
chr9:98001192 | A | AT | 10 | a0001c0001t0001g0034 a0001c0001t0001g0061 a0001c0001t0001g0077 others(7): Show |
11 | HG01109.hp2 HG02572.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.327+2532dupT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 98001192 | ||||||
chr9:98001608 | C | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(46): Show |
80 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(77): Show |
intron_variant | MODIFIER | c.327+2930C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98001608 | |||||||
chr9:98002017 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0002g0041 |
2 | NA19011.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.328-2947C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98002017 | |||||||
chr9:98002236 | T | C | 3 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0043 |
3 | HG02559.hp1 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.328-2728T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98002236 | |||||||
chr9:98002247 | A | G | 1 | a0001c0001t0001g0037 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.328-2717A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98002247 | |||||||
chr9:98002745 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.328-2219C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98002745 | |||||||
chr9:98002855 | A | G | 1 | a0001c0001t0001g0015 | 3 | NA18942.hp2 NA18986.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.328-2109A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98002855 | |||||||
chr9:98002929 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.328-2035G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98002929 | |||||||
chr9:98002983 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.328-1981A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98002983 | |||||||
chr9:98003262 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG02258.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.328-1702A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003262 | |||||||
chr9:98003373 | C | G | 1 | a0001c0001t0001g0034 | 2 | HG02572.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.328-1591C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003373 | |||||||
chr9:98003384 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.328-1580T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003384 | |||||||
chr9:98003468 | AAT | A | 4 | a0001c0001t0001g0015 a0001c0001t0001g0072 a0001c0001t0001g0081 others(1): Show |
6 | HG00597.hp2 HG00621.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-1494_328-1493d others(4): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr9 | 98003468 | ||||||
chr9:98003521 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.328-1443T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003521 | |||||||
chr9:98003559 | C | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02451.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.328-1405C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003559 | |||||||
chr9:98003803 | C | T | 9 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0064 others(6): Show |
18 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.328-1161C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003803 | |||||||
chr9:98003814 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.328-1150C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003814 | |||||||
chr9:98003997 | T | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0087 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.328-967T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98003997 | |||||||
chr9:98004159 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG01496.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.328-805A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004159 | |||||||
chr9:98004252 | T | A | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-712T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004252 | |||||||
chr9:98004266 | A | C | 6 | a0001c0001t0001g0042 a0001c0001t0002g0038 a0001c0001t0002g0039 others(3): Show |
6 | HG01891.hp2 HG02559.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-698A>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004266 | |||||||
chr9:98004513 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0026 a0001c0001t0001g0096 others(12): Show |
22 | HG01069.hp1 HG01099.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.328-451C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004513 | |||||||
chr9:98004560 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
156 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.328-404C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004560 | |||||||
chr9:98004607 | A | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.328-357A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004607 | |||||||
chr9:98004768 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.328-196G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004768 | |||||||
chr9:98004890 | A | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.328-74A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004890 | |||||||
chr9:98004952 | C | A | 1 | a0001c0001t0001g0111 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.328-12C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 3/6 | chr9 | 98004952 | |||||||
chr9:98005191 | C | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+38C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005191 | |||||||
chr9:98005203 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.517+50C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005203 | |||||||
chr9:98005228 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0133 a0001c0001t0002g0038 others(4): Show |
7 | HG01891.hp2 HG02559.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.517+75C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005228 | |||||||
chr9:98005229 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.517+76G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005229 | |||||||
chr9:98005248 | C | T | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
195 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.517+95C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005248 | |||||||
chr9:98005384 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0002g0044 |
2 | HG02257.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.517+231G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005384 | |||||||
chr9:98005422 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.517+269C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005422 | |||||||
chr9:98005494 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.517+341G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005494 | |||||||
chr9:98005578 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(90): Show |
156 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.517+425G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005578 | |||||||
chr9:98005588 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.517+435G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005588 | |||||||
chr9:98005608 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.517+455C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005608 | |||||||
chr9:98005869 | T | C | 3 | a0001c0001t0002g0044 a0001c0001t0002g0047 a0001c0001t0002g0070 |
3 | HG01243.hp1 HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.517+716T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98005869 | |||||||
chr9:98006009 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
195 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(192): Show |
intron_variant | MODIFIER | c.517+856A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006009 | |||||||
chr9:98006093 | G | GGAGCTGA others(13): Show |
38 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0018 others(35): Show |
58 | HG00408.hp1 HG00544.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.517+962_517+981dup others(20): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 98006093 | ||||||
chr9:98006139 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.517+986G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006139 | |||||||
chr9:98006210 | T | G | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517+1057T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006210 | |||||||
chr9:98006227 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.517+1074A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006227 | |||||||
chr9:98006239 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.517+1086G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006239 | |||||||
chr9:98006260 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.517+1107A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006260 | |||||||
chr9:98006346 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.517+1193T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006346 | |||||||
chr9:98006385 | T | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0140 |
3 | HG01071.hp2 HG02735.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.517+1232T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006385 | |||||||
chr9:98006464 | A | ACT | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(176): Show |
284 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(281): Show |
intron_variant | MODIFIER | c.517+1312_517+1313d others(4): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 98006464 | ||||||
chr9:98006478 | G | A | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.517+1325G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006478 | |||||||
chr9:98006508 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517+1355G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006508 | |||||||
chr9:98006597 | A | G | 1 | a0001c0001t0001g0010 | 5 | HG02132.hp2 NA18951.hp1 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.517+1444A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006597 | |||||||
chr9:98006621 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0074 |
2 | NA19000.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.517+1468C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006621 | |||||||
chr9:98006758 | C | T | 8 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0064 others(5): Show |
17 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.517+1605C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006758 | |||||||
chr9:98006907 | G | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.517+1754G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006907 | |||||||
chr9:98006994 | C | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(112): Show |
193 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(190): Show |
intron_variant | MODIFIER | c.517+1841C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98006994 | |||||||
chr9:98007605 | A | C | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.517+2452A>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98007605 | |||||||
chr9:98007916 | A | G | 1 | a0001c0001t0001g0137 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.517+2763A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98007916 | |||||||
chr9:98008063 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.517+2910C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98008063 | |||||||
chr9:98008128 | C | A | 1 | a0001c0001t0002g0047 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517+2975C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98008128 | |||||||
chr9:98008208 | C | T | 1 | a0001c0001t0002g0014 | 3 | HG02109.hp1 HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.517+3055C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98008208 | |||||||
chr9:98008272 | C | T | 1 | a0001c0001t0002g0014 | 3 | HG02109.hp1 HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.518-2999C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98008272 | |||||||
chr9:98009145 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.518-2126G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009145 | |||||||
chr9:98009158 | A | G | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(50): Show |
84 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.518-2113A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009158 | |||||||
chr9:98009472 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.518-1799G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009472 | |||||||
chr9:98009634 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.518-1637G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009634 | |||||||
chr9:98009661 | A | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.518-1610A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009661 | |||||||
chr9:98009664 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.518-1607T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009664 | |||||||
chr9:98009672 | G | T | 1 | a0001c0001t0001g0099 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.518-1599G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009672 | |||||||
chr9:98009766 | A | G | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.518-1505A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009766 | |||||||
chr9:98009838 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.518-1433G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98009838 | |||||||
chr9:98010095 | A | AGG | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.518-1175_518-1174d others(4): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 98010095 | ||||||
chr9:98010162 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.518-1109G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010162 | |||||||
chr9:98010213 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.518-1058G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010213 | |||||||
chr9:98010262 | GT | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(100): Show |
172 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(169): Show |
intron_variant | MODIFIER | c.518-996delT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 98010262 | ||||||
chr9:98010264 | T | G | 6 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(3): Show |
12 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(9): Show |
intron_variant | MODIFIER | c.518-1007T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010264 | |||||||
chr9:98010265 | T | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(36): Show |
71 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.518-1006T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010265 | |||||||
chr9:98010272 | T | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0139 |
2 | HG00544.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.518-999T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010272 | |||||||
chr9:98010275 | T | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0191 a0001c0001t0001g0193 others(1): Show |
4 | HG02257.hp2 HG02738.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-996T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010275 | |||||||
chr9:98010276 | G | T | 4 | a0001c0001t0001g0074 a0001c0001t0001g0191 a0001c0001t0001g0193 others(1): Show |
4 | HG02257.hp2 HG02738.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.518-995G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010276 | |||||||
chr9:98010278 | T | G | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.518-993T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010278 | |||||||
chr9:98010280 | T | G | 1 | a0001c0001t0002g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.518-991T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010280 | |||||||
chr9:98010281 | T | G | 1 | a0001c0001t0002g0094 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.518-990T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010281 | |||||||
chr9:98010284 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.518-987T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010284 | |||||||
chr9:98010288 | T | A | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.518-983T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010288 | |||||||
chr9:98010506 | G | A | 16 | a0001c0001t0001g0042 a0001c0001t0002g0004 a0001c0001t0002g0014 others(13): Show |
25 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.518-765G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010506 | |||||||
chr9:98010703 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.518-568C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010703 | |||||||
chr9:98010840 | AT | A | 105 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(102): Show |
177 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(174): Show |
intron_variant | MODIFIER | c.518-418delT | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 98010840 | ||||||
chr9:98010840 | ATT | A | 9 | a0001c0001t0001g0042 a0001c0001t0001g0061 a0001c0001t0001g0091 others(6): Show |
9 | HG00639.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-419_518-418del others(2): Show |
ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr9 | 98010840 | ||||||
chr9:98010904 | G | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0162 |
3 | HG01109.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.518-367G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98010904 | |||||||
chr9:98011084 | C | A | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.518-187C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98011084 | |||||||
chr9:98011125 | T | C | 1 | a0001c0001t0001g0027 | 2 | NA18943.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.518-146T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98011125 | |||||||
chr9:98011205 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.518-66C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98011205 | |||||||
chr9:98011219 | C | A | 1 | a0001c0001t0001g0021 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.518-52C>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 4/6 | chr9 | 98011219 | |||||||
chr9:98011432 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.636+43C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011432 | |||||||
chr9:98011446 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.636+57G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011446 | |||||||
chr9:98011457 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.636+68A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011457 | |||||||
chr9:98011571 | G | A | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.636+182G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011571 | |||||||
chr9:98011637 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.636+248G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011637 | |||||||
chr9:98011796 | G | C | 9 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0064 others(6): Show |
18 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.636+407G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011796 | |||||||
chr9:98011852 | A | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.636+463A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011852 | |||||||
chr9:98011978 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.637-443T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98011978 | |||||||
chr9:98012072 | G | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.637-349G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98012072 | |||||||
chr9:98012209 | T | TA | 9 | a0001c0001t0002g0004 a0001c0001t0002g0014 a0001c0001t0002g0064 others(6): Show |
18 | HG00408.hp2 HG01081.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.637-204dupA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr9 | 98012209 | ||||||
chr9:98012217 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.637-204A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98012217 | |||||||
chr9:98012364 | A | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(115): Show |
196 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.637-57A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 5/6 | chr9 | 98012364 | |||||||
chr9:98012570 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.688+98C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012570 | |||||||
chr9:98012608 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0121 a0001c0001t0001g0134 |
6 | HG00558.hp2 HG02074.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.688+136T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012608 | |||||||
chr9:98012720 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.688+248C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012720 | |||||||
chr9:98012816 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.688+344C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012816 | |||||||
chr9:98012846 | T | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.688+374T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012846 | |||||||
chr9:98012912 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.688+440A>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012912 | |||||||
chr9:98012965 | C | G | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.688+493C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012965 | |||||||
chr9:98012977 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.688+505G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98012977 | |||||||
chr9:98013062 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0002g0040 |
2 | HG01891.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.688+590C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013062 | |||||||
chr9:98013110 | A | T | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.688+638A>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013110 | |||||||
chr9:98013224 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.688+752T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013224 | |||||||
chr9:98013268 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG02486.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.688+796C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013268 | |||||||
chr9:98013308 | T | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0070 |
2 | HG01243.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.688+836T>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013308 | |||||||
chr9:98013315 | C | T | 40 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
72 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.688+843C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013315 | |||||||
chr9:98013664 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.688+1192C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013664 | |||||||
chr9:98013704 | G | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0030 others(10): Show |
21 | HG00738.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.688+1232G>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013704 | |||||||
chr9:98013841 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
11 | HG00741.hp2 HG02015.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.688+1369G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013841 | |||||||
chr9:98013842 | C | G | 1 | a0001c0001t0002g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.688+1370C>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013842 | |||||||
chr9:98013889 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.688+1417G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013889 | |||||||
chr9:98013928 | G | A | 1 | a0001c0001t0001g0023 | 2 | NA18991.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.689-1436G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98013928 | |||||||
chr9:98014216 | G | T | 1 | a0001c0001t0002g0069 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.689-1148G>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014216 | |||||||
chr9:98014300 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.689-1064C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014300 | |||||||
chr9:98014382 | T | A | 1 | a0003c0005t0001g0067 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.689-982T>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014382 | |||||||
chr9:98014407 | C | CA | 6 | a0001c0001t0001g0106 a0001c0001t0001g0167 a0001c0001t0001g0180 others(3): Show |
6 | HG01243.hp1 HG02922.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.689-946dupA | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr9 | 98014407 | ||||||
chr9:98014607 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0104 a0001c0001t0001g0152 others(1): Show |
6 | NA18941.hp2 NA18944.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.689-757T>C | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014607 | |||||||
chr9:98014778 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.689-586G>A | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014778 | |||||||
chr9:98014835 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.689-529C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014835 | |||||||
chr9:98014845 | C | T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0082 a0001c0001t0001g0086 |
3 | HG01261.hp1 HG02300.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.689-519C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014845 | |||||||
chr9:98014863 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.689-501A>G | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98014863 | |||||||
chr9:98015019 | C | T | 1 | a0002c0002t0002g0059 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.689-345C>T | ANP32B | ENSG00000136938.9 | transcript | ENST00000339399.5 | protein_coding | 6/6 | chr9 | 98015019 |