| geneid | 307 |
|---|---|
| ensemblid | ENSG00000196975.16 |
| hgncid | 542 |
| symbol | ANXA4 |
| name | annexin A4 |
| refseq_nuc | NM_001153.5 |
| refseq_prot | NP_001144.1 |
| ensembl_nuc | ENST00000394295.6 |
| ensembl_prot | ENSP00000377833.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 69742134 |
| end | 69827112 |
| strand | + |
| ver | v1.2 |
| region | chr2:69742134-69827112 |
| region5000 | chr2:69737134-69832112 |
| regionname0 | ANXA4_chr2_69742134_69827112 |
| regionname5000 | ANXA4_chr2_69737134_69832112 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 321 | 217 | 38 | 30 | 111 | 10 | 26 | 81 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0002 | 0/0 | 321 | 75 | 25 | 15 | 29 | 2 | 4 | 26 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0003 | 0/0 | 321 | 49 | 12 | 21 | 16 | 0 | 0 | 13 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0004 | 0/0 | 321 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0005 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 966 | 216 | 37 | 30 | 111 | 10 | 26 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| c0002 | 0/0 | 966 | 75 | 25 | 15 | 29 | 2 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| c0003 | 0/0 | 966 | 49 | 12 | 21 | 16 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| c0004 | 0/0 | 966 | 4 | 4 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| c0005 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| c0006 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/0 | 1686 | 80 | 3 | 14 | 47 | 6 | 9 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0002 | 0/0 | 1686 | 74 | 23 | 17 | 29 | 1 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0003 | 0/1 | 1687 | 56 | 1 | 7 | 37 | 3 | 7 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0004 | 0/0 | 1684 | 48 | 12 | 21 | 15 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0005 | 0/0 | 1687 | 33 | 9 | 0 | 20 | 0 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0006 | 0/0 | 1685 | 19 | 18 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0007 | 0/0 | 1686 | 16 | 7 | 2 | 1 | 1 | 5 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0008 | 0/0 | 1686 | 4 | 0 | 1 | 3 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0009 | 0/0 | 1686 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0010 | 0/0 | 1681 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0011 | 0/0 | 1685 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0012 | 0/0 | 1687 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0013 | 0/0 | 1681 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0014 | 0/0 | 1687 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0015 | 0/0 | 1685 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0016 | 0/0 | 1684 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0017 | 0/0 | 1687 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0018 | 0/0 | 1686 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0019 | 0/0 | 1686 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0020 | 0/0 | 1687 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| t0021 | 0/0 | 1685 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 966 | 216 | 37 | 30 | 111 | 10 | 26 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0006 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0002c0002 | 0/0 | 966 | 75 | 25 | 15 | 29 | 2 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0003c0003 | 0/0 | 966 | 49 | 12 | 21 | 16 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0004c0004 | 0/0 | 966 | 4 | 4 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0005c0005 | 0/0 | 966 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2651 | 79 | 3 | 14 | 47 | 5 | 9 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0002 | 0/0 | 2651 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0003 | 0/1 | 2652 | 56 | 1 | 7 | 37 | 3 | 7 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0004 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0005 | 0/0 | 2652 | 31 | 7 | 0 | 20 | 0 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0006 | 0/0 | 2650 | 18 | 17 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0007 | 0/0 | 2651 | 13 | 4 | 2 | 1 | 1 | 5 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0008 | 0/0 | 2651 | 4 | 0 | 1 | 3 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0009 | 0/0 | 2651 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0011 | 0/0 | 2650 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0012 | 0/0 | 2652 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0014 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0015 | 0/0 | 2650 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0017 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0018 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0019 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0020 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0001t0021 | 0/0 | 2650 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0001c0006t0006 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0002c0002t0001 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0002c0002t0002 | 0/0 | 2651 | 70 | 21 | 15 | 29 | 1 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0002c0002t0004 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0002c0002t0010 | 0/0 | 2646 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0002c0002t0013 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0003c0003t0002 | 0/0 | 2651 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0003c0003t0004 | 0/0 | 2649 | 46 | 10 | 21 | 15 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0003c0003t0016 | 0/0 | 2649 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0004c0004t0005 | 0/0 | 2652 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0004c0004t0007 | 0/0 | 2651 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| a0005c0005t0007 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | copy fasta | chr2 | 69737134 | 69832112 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0226 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0186 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0009g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0011g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0012g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0014g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0015g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0017g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0018g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0020g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0021g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0006t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0010g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0016g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0005c0005t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0311 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0166 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0268 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00323 | hp1 | a0001 | c0001 | t0019 | g0263 | EUR | FIN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0298 | EUR | FIN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00408 | hp2 | a0003 | c0003 | t0004 | g0192 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00423 | hp1 | a0003 | c0003 | t0004 | g0082 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0182 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00642 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0216 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00735 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0053 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00738 | hp2 | a0003 | c0003 | t0004 | g0002 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0230 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0052 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0041 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01099 | hp2 | a0003 | c0003 | t0004 | g0061 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01106 | hp2 | a0003 | c0003 | t0004 | g0002 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0313 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01167 | hp1 | a0001 | c0001 | t0021 | g0128 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0300 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0308 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01169 | hp2 | a0001 | c0001 | t0015 | g0285 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01175 | hp1 | a0003 | c0003 | t0004 | g0033 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01192 | hp1 | a0003 | c0003 | t0004 | g0106 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0187 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0016 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0091 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01256 | hp2 | a0003 | c0003 | t0004 | g0189 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01257 | hp1 | a0003 | c0003 | t0004 | g0066 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0078 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01258 | hp1 | a0003 | c0003 | t0004 | g0063 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01261 | hp1 | a0003 | c0003 | t0004 | g0059 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01346 | hp1 | a0003 | c0003 | t0004 | g0058 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0269 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01358 | hp1 | a0003 | c0003 | t0004 | g0068 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01361 | hp1 | a0003 | c0003 | t0004 | g0036 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0208 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0136 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0039 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0122 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0173 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0021 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0302 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01891 | hp1 | a0003 | c0003 | t0004 | g0109 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0303 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01928 | hp1 | a0003 | c0003 | t0004 | g0046 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0138 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01952 | hp2 | a0003 | c0003 | t0004 | g0035 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01975 | hp2 | a0003 | c0003 | t0004 | g0060 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01978 | hp1 | a0003 | c0003 | t0004 | g0133 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01981 | hp2 | a0003 | c0003 | t0004 | g0067 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02004 | hp1 | a0003 | c0003 | t0004 | g0034 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0172 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02015 | hp2 | a0001 | c0001 | t0014 | g0155 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02027 | hp2 | a0001 | c0001 | t0020 | g0202 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02135 | hp1 | a0003 | c0003 | t0004 | g0096 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02135 | hp2 | a0001 | c0001 | t0017 | g0337 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0113 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0235 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0336 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0320 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0010 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0321 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0256 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02280 | hp1 | a0003 | c0003 | t0004 | g0317 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0212 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02300 | hp1 | a0003 | c0003 | t0004 | g0065 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0229 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0005 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0197 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0306 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0130 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0341 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02630 | hp1 | a0003 | c0003 | t0004 | g0301 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02630 | hp2 | a0005 | c0005 | t0007 | g0006 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0307 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0223 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0310 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02717 | hp1 | a0003 | c0003 | t0004 | g0247 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02717 | hp2 | a0003 | c0003 | t0002 | g0110 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02809 | hp1 | a0004 | c0004 | t0005 | g0206 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02818 | hp1 | a0002 | c0002 | t0010 | g0018 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0305 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0108 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0090 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02896 | hp1 | a0004 | c0004 | t0005 | g0203 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0126 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02897 | hp1 | a0004 | c0004 | t0007 | g0204 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02965 | hp2 | a0003 | c0003 | t0004 | g0014 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0011 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02970 | hp2 | a0001 | c0006 | t0006 | g0007 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02976 | hp1 | a0003 | c0003 | t0004 | g0013 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0116 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0275 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0102 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0309 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0198 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03098 | hp2 | a0002 | c0002 | t0010 | g0220 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0196 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03195 | hp1 | a0002 | c0002 | t0013 | g0129 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0115 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0312 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03225 | hp1 | a0003 | c0003 | t0002 | g0104 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03225 | hp2 | a0003 | c0003 | t0004 | g0111 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0207 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0105 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0195 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0340 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0315 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0221 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0107 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0199 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0282 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0112 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0333 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0276 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0134 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0316 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0117 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0044 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0314 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | CHB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0023 | EAS | CHB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0114 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0103 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18954 | hp1 | a0003 | c0003 | t0004 | g0094 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0169 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0119 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18966 | hp1 | a0003 | c0003 | t0004 | g0181 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0084 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0323 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18974 | hp2 | a0003 | c0003 | t0004 | g0025 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0334 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18980 | hp1 | a0003 | c0003 | t0004 | g0331 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18990 | hp1 | a0003 | c0003 | t0004 | g0097 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0160 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19000 | hp2 | a0001 | c0001 | t0008 | g0144 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19005 | hp2 | a0003 | c0003 | t0004 | g0095 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19011 | hp2 | a0003 | c0003 | t0004 | g0156 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0019 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0222 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0319 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19043 | hp2 | a0004 | c0004 | t0007 | g0205 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19056 | hp2 | a0003 | c0003 | t0004 | g0214 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0153 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0151 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19068 | hp2 | a0003 | c0003 | t0004 | g0074 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19072 | hp2 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19074 | hp1 | a0003 | c0003 | t0004 | g0123 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0225 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0158 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19080 | hp2 | a0003 | c0003 | t0004 | g0093 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19082 | hp1 | a0003 | c0003 | t0016 | g0325 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0101 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19091 | hp1 | a0003 | c0003 | t0004 | g0062 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0290 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19240 | hp1 | a0003 | c0003 | t0004 | g0339 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0342 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0219 | AFR | ASW | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ASW | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0286 | EUR | TSI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0246 | EUR | TSI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | GIH | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20905 | hp2 | a0001 | c0001 | t0012 | g0183 | SAS | GIH | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02486 | hp1 | a0003 | c0003 | t0004 | g0069 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0127 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0304 | AFR | USA | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0077 | AFR | USA | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0200 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0186 | REF | REF | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0226 | REF | REF | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69804538
|
G | C | 1 | a0004 | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.103G>C | p.Asp35His | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/13 | 191/2651 | 103/966 | 35/321 | chr2 | 69804538 | ||
| chr2:69806439
|
G | A | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.247G>A | p.Val83Met | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/13 | 335/2651 | 247/966 | 83/321 | chr2 | 69806439 | ||
| chr2:69806452
|
C | T | 1 | a0002 | 75 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(72): Show |
missense_variant | MODERATE | c.260C>T | p.Thr87Met | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/13 | 348/2651 | 260/966 | 87/321 | chr2 | 69806452 | ||
| chr2:69810607
|
C | G | 2 | a0003a0005 | 50 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(47): Show |
missense_variant | MODERATE | c.411C>G | p.Ser137Arg | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/13 | 499/2651 | 411/966 | 137/321 | chr2 | 69810607 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69818633
|
T | C | 1 | a0001c0006 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.663T>C | p.Asp221Asp | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/13 | 751/2651 | 663/966 | 221/321 | chr2 | 69818633 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69742148
|
C | G | 1 | a0001c0001t0021 | 1 | HG01167.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/13 | 39418 | chr2 | 69742148 | |||||
| chr2:69781553
|
T | C | 1 | a0001c0001t0012 | 1 | NA20905.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-13T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/13 | chr2 | 69781553 | ||||||
| chr2:69825831
|
C | G | 1 | a0001c0001t0020 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 316 | chr2 | 69825831 | |||||
| chr2:69826001
|
A | G | 1 | a0001c0001t0011 | 2 | HG02280.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*486A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 486 | chr2 | 69826001 | |||||
| chr2:69826036
|
A | G | 1 | a0001c0001t0019 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 521 | chr2 | 69826036 | |||||
| chr2:69826290
|
G | A | 1 | a0002c0002t0013 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*775G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 775 | chr2 | 69826290 | |||||
| chr2:69826408
|
T | C | 1 | a0001c0001t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*893T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 893 | chr2 | 69826408 | |||||
| chr2:69826487
|
A | T | 5 | a0001c0001t0003a0001c0001t0008a0001c0001t0012others(2): Show | 63 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*972A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 972 | chr2 | 69826487 | |||||
| chr2:69826507
|
G | A | 1 | a0001c0001t0009 | 2 | HG01069.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*992G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 992 | chr2 | 69826507 | |||||
| chr2:69826536
|
A | G | 25 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(22): Show | 262 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(259): Show |
3_prime_UTR_variant | MODIFIER | c.*1021A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1021 | chr2 | 69826536 | |||||
| chr2:69826628
|
T | C | 1 | a0003c0003t0016 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1113 | chr2 | 69826628 | |||||
| chr2:69826684
|
T | C | 5 | a0001c0001t0002a0002c0002t0002a0002c0002t0010others(2): Show | 77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1169T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1169 | chr2 | 69826684 | |||||
| chr2:69826780
|
T | TA | 8 | a0001c0001t0003a0001c0001t0005a0001c0001t0012others(5): Show | 94 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*1284dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1285 | INFO_REALIGN_3_PRIME | chr2 | 69826780 | ||||
| chr2:69826780
|
TA | T | 5 | a0001c0001t0004a0001c0001t0015a0002c0002t0004others(2): Show | 50 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1284delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1284 | INFO_REALIGN_3_PRIME | chr2 | 69826780 | ||||
| chr2:69826923
|
CAAGAT | C | 2 | a0002c0002t0010a0002c0002t0013 | 3 | HG02818.hp1 HG03098.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1413_*1417delTAAG others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1413 | INFO_REALIGN_3_PRIME | chr2 | 69826923 | ||||
| chr2:69826931
|
GA | G | 9 | a0001c0001t0004a0001c0001t0006a0001c0001t0011others(6): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1426delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1426 | INFO_REALIGN_3_PRIME | chr2 | 69826931 | ||||
| chr2:69827104
|
A | G | 1 | a0001c0001t0017 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1589 | chr2 | 69827104 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69742247
|
C | T | 1 | a0001c0001t0006g0342 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+72C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742247 | ||||||
| chr2:69742434
|
G | A | 13 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+259G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742434 | ||||||
| chr2:69742447
|
G | A | 2 | a0002c0002t0002g0005a0005c0005t0007g0006 | 2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-47+272G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742447 | ||||||
| chr2:69742447
|
G | C | 1 | a0001c0001t0003g0017 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-47+272G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742447 | ||||||
| chr2:69742540
|
T | G | 13 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+365T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742540 | ||||||
| chr2:69742686
|
T | C | 1 | a0002c0002t0010g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-47+511T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742686 | ||||||
| chr2:69742786
|
C | A | 225 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(222): Show | 229 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-47+611C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742786 | ||||||
| chr2:69742877
|
A | C | 1 | a0001c0001t0006g0342 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+702A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742877 | ||||||
| chr2:69742988
|
C | T | 267 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(264): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-47+813C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742988 | ||||||
| chr2:69743004
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+829C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743004 | ||||||
| chr2:69743111
|
T | G | 3 | a0001c0001t0006g0020a0001c0001t0018g0019a0002c0002t0002g0021 | 3 | HG01884.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-47+936T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743111 | ||||||
| chr2:69743178
|
G | C | 83 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(80): Show | 86 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-47+1003G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743178 | ||||||
| chr2:69743270
|
C | T | 13 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+1095C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743270 | ||||||
| chr2:69743360
|
GGCGTGTG others(18): Show |
G | 6 | a0001c0001t0006g0221a0001c0001t0007g0219a0002c0002t0002g0222others(3): Show | 6 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+1186_-47+1210d others(27): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743360 | ||||||
| chr2:69743432
|
G | T | 5 | a0001c0001t0006g0015a0001c0001t0006g0016a0001c0001t0006g0342others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1257G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743432 | ||||||
| chr2:69743517
|
G | A | 17 | a0001c0001t0001g0224a0001c0001t0006g0103a0001c0001t0006g0105others(14): Show | 17 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+1342G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743517 | ||||||
| chr2:69743606
|
G | A | 1 | a0002c0002t0002g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-47+1431G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743606 | ||||||
| chr2:69743687
|
T | A | 2 | a0001c0001t0006g0015a0001c0001t0006g0016 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-47+1512T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743687 | ||||||
| chr2:69743746
|
G | A | 1 | a0002c0002t0002g0022 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-47+1571G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743746 | ||||||
| chr2:69744099
|
C | A | 1 | a0001c0001t0007g0225 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+1924C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744099 | ||||||
| chr2:69744100
|
A | C | 1 | a0001c0001t0007g0225 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+1925A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744100 | ||||||
| chr2:69744102
|
G | A | 1 | a0001c0001t0007g0225 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+1927G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744102 | ||||||
| chr2:69744137
|
G | T | 8 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(5): Show | 8 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+1962G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744137 | ||||||
| chr2:69744185
|
G | A | 212 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-47+2010G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744185 | ||||||
| chr2:69744213
|
G | A | 1 | a0001c0001t0005g0023 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-47+2038G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744213 | ||||||
| chr2:69744282
|
G | A | 10 | a0001c0001t0006g0302a0001c0001t0006g0304a0001c0001t0006g0306others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+2107G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744282 | ||||||
| chr2:69744297
|
G | A | 225 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(222): Show | 229 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-47+2122G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744297 | ||||||
| chr2:69744325
|
A | C | 1 | a0002c0002t0002g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-47+2150A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744325 | ||||||
| chr2:69744332
|
A | T | 13 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+2157A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744332 | ||||||
| chr2:69744455
|
T | A | 1 | a0001c0001t0007g0225 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+2280T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744455 | ||||||
| chr2:69744511
|
T | A | 1 | a0002c0002t0002g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-47+2336T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744511 | ||||||
| chr2:69744744
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-47+2569C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744744 | ||||||
| chr2:69744745
|
GAAAGCTT others(2): Show |
G | 6 | a0001c0001t0006g0221a0001c0001t0007g0219a0002c0002t0002g0222others(3): Show | 6 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+2572_-47+2580d others(11): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69744745 | |||||
| chr2:69744852
|
C | T | 7 | a0001c0001t0001g0213a0001c0001t0003g0217a0001c0001t0005g0211others(4): Show | 7 | HG00673.hp1 HG02132.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+2677C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744852 | ||||||
| chr2:69744912
|
A | G | 1 | a0001c0001t0001g0299 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-47+2737A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744912 | ||||||
| chr2:69744971
|
T | C | 13 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(10): Show | 13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+2796T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744971 | ||||||
| chr2:69745206
|
C | A | 17 | a0001c0001t0001g0224a0001c0001t0006g0103a0001c0001t0006g0105others(14): Show | 17 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+3031C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745206 | ||||||
| chr2:69745276
|
A | G | 1 | a0002c0002t0002g0101 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-47+3101A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745276 | ||||||
| chr2:69745285
|
G | A | 1 | a0001c0001t0006g0342 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+3110G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745285 | ||||||
| chr2:69745572
|
T | C | 225 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(222): Show | 229 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-47+3397T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745572 | ||||||
| chr2:69745633
|
C | T | 2 | a0001c0001t0003g0209a0001c0001t0003g0210 | 2 | NA18987.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-47+3458C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745633 | ||||||
| chr2:69745773
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47+3598C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745773 | ||||||
| chr2:69745821
|
AC | A | 6 | a0001c0001t0007g0207a0002c0002t0002g0208a0004c0004t0005g0203others(3): Show | 6 | HG01433.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+3647delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745821 | ||||||
| chr2:69746070
|
C | T | 1 | a0001c0001t0020g0202 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-47+3895C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746070 | ||||||
| chr2:69746261
|
C | T | 8 | a0001c0001t0001g0213a0001c0001t0003g0217a0001c0001t0005g0211others(5): Show | 8 | HG00673.hp1 HG02132.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+4086C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746261 | ||||||
| chr2:69746605
|
G | A | 212 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-47+4430G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746605 | ||||||
| chr2:69746619
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+4444C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746619 | ||||||
| chr2:69746782
|
G | C | 1 | a0002c0002t0004g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47+4607G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746782 | ||||||
| chr2:69746827
|
GA | G | 334 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(331): Show | 338 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.-47+4664delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69746827 | |||||
| chr2:69746944
|
G | A | 5 | a0001c0001t0005g0310a0001c0001t0006g0342a0001c0001t0007g0311others(2): Show | 5 | HG00099.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+4769G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746944 | ||||||
| chr2:69746946
|
C | A | 17 | a0001c0001t0001g0224a0001c0001t0006g0103a0001c0001t0006g0105others(14): Show | 17 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+4771C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746946 | ||||||
| chr2:69747229
|
G | A | 2 | a0001c0001t0003g0227a0001c0001t0003g0228 | 2 | HG02129.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-47+5054G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747229 | ||||||
| chr2:69747273
|
G | A | 1 | a0001c0001t0003g0229 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-47+5098G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747273 | ||||||
| chr2:69747293
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-47+5118C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747293 | ||||||
| chr2:69747396
|
A | G | 1 | a0001c0001t0001g0100 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-47+5221A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747396 | ||||||
| chr2:69747396
|
A | T | 1 | a0001c0001t0003g0228 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-47+5221A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747396 | ||||||
| chr2:69747587
|
C | T | 3 | a0002c0002t0002g0340a0002c0002t0002g0341a0003c0003t0004g0339 | 3 | HG02622.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+5412C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747587 | ||||||
| chr2:69747588
|
G | A | 4 | a0001c0001t0005g0310a0001c0001t0007g0311a0002c0002t0002g0005others(1): Show | 4 | HG00099.hp1 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+5413G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747588 | ||||||
| chr2:69747689
|
C | T | 17 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0326others(14): Show | 17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+5514C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747689 | ||||||
| chr2:69747741
|
C | A | 229 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47+5566C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747741 | ||||||
| chr2:69747805
|
C | T | 1 | a0001c0001t0005g0201 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-47+5630C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747805 | ||||||
| chr2:69747821
|
G | T | 17 | a0001c0001t0006g0103a0001c0001t0006g0105a0001c0001t0006g0114others(14): Show | 17 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+5646G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747821 | ||||||
| chr2:69747868
|
C | T | 229 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47+5693C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747868 | ||||||
| chr2:69747957
|
G | A | 1 | a0003c0003t0004g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-47+5782G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747957 | ||||||
| chr2:69748146
|
C | T | 10 | a0001c0001t0006g0302a0001c0001t0006g0304a0001c0001t0006g0306others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+5971C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748146 | ||||||
| chr2:69748166
|
G | C | 11 | a0001c0001t0005g0310a0001c0001t0006g0008a0001c0001t0006g0009others(8): Show | 11 | HG00099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+5991G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748166 | ||||||
| chr2:69748210
|
C | G | 4 | a0001c0001t0005g0310a0001c0001t0007g0311a0002c0002t0002g0005others(1): Show | 4 | HG00099.hp1 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+6035C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748210 | ||||||
| chr2:69748377
|
C | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG01358.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-47+6202C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748377 | ||||||
| chr2:69748390
|
G | GA | 9 | a0001c0001t0005g0310a0001c0001t0006g0008a0001c0001t0006g0009others(6): Show | 9 | HG00099.hp1 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+6226dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69748390 | |||||
| chr2:69748422
|
C | T | 2 | a0002c0002t0002g0222a0002c0002t0002g0223 | 2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-47+6247C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748422 | ||||||
| chr2:69748491
|
T | C | 11 | a0001c0001t0005g0310a0001c0001t0006g0008a0001c0001t0006g0009others(8): Show | 11 | HG00099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+6316T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748491 | ||||||
| chr2:69748550
|
C | T | 11 | a0001c0001t0005g0310a0001c0001t0006g0008a0001c0001t0006g0009others(8): Show | 11 | HG00099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+6375C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748550 | ||||||
| chr2:69748687
|
G | A | 200 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(197): Show | 204 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-47+6512G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748687 | ||||||
| chr2:69748710
|
C | CT | 107 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(104): Show | 110 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-47+6552dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69748710 | |||||
| chr2:69748710
|
CT | C | 17 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(14): Show | 17 | HG00099.hp1 HG00544.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+6552delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69748710 | |||||
| chr2:69748796
|
G | T | 18 | a0001c0001t0001g0224a0001c0001t0006g0103a0001c0001t0006g0105others(15): Show | 18 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+6621G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748796 | ||||||
| chr2:69748893
|
TG | T | 12 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0326others(9): Show | 12 | HG03704.hp1 NA18961.hp2 NA18965.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+6719delG | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748893 | ||||||
| chr2:69748894
|
G | T | 5 | a0001c0001t0001g0335a0001c0001t0003g0338a0001c0001t0005g0334others(2): Show | 5 | HG02135.hp2 HG02155.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+6719G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748894 | ||||||
| chr2:69748905
|
G | A | 6 | a0001c0001t0001g0194a0001c0001t0001g0213a0001c0001t0003g0217others(3): Show | 6 | HG00673.hp1 HG02132.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+6730G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748905 | ||||||
| chr2:69749013
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-47+6838T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749013 | ||||||
| chr2:69749020
|
T | A | 2 | a0001c0001t0009g0230a0001c0001t0009g0235 | 2 | HG01069.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-47+6845T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749020 | ||||||
| chr2:69749044
|
A | G | 262 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(259): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.-47+6869A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749044 | ||||||
| chr2:69749074
|
A | G | 5 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+6899A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749074 | ||||||
| chr2:69749167
|
A | G | 1 | a0002c0002t0002g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-47+6992A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749167 | ||||||
| chr2:69749192
|
G | A | 5 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(2): Show | 5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+7017G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749192 | ||||||
| chr2:69749252
|
G | T | 198 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(195): Show | 202 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-47+7077G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749252 | ||||||
| chr2:69749292
|
C | T | 80 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(77): Show | 81 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-47+7117C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749292 | ||||||
| chr2:69749351
|
T | C | 1 | a0001c0001t0001g0236 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-47+7176T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749351 | ||||||
| chr2:69749415
|
G | T | 2 | a0001c0001t0006g0015a0001c0001t0006g0016 | 2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-47+7240G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749415 | ||||||
| chr2:69749460
|
T | C | 82 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(79): Show | 85 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-47+7285T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749460 | ||||||
| chr2:69749487
|
A | G | 4 | a0001c0001t0004g0131a0001c0001t0011g0130a0002c0002t0002g0132others(1): Show | 4 | HG01243.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+7312A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749487 | ||||||
| chr2:69749529
|
T | C | 4 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(1): Show | 4 | HG01106.hp1 HG01517.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+7354T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749529 | ||||||
| chr2:69749717
|
A | T | 10 | a0001c0001t0006g0302a0001c0001t0006g0304a0001c0001t0006g0306others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+7542A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749717 | ||||||
| chr2:69749763
|
T | TA | 14 | a0001c0001t0005g0310a0001c0001t0006g0008a0001c0001t0006g0009others(11): Show | 14 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47+7601dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69749763 | |||||
| chr2:69749789
|
G | A | 9 | a0001c0001t0005g0310a0001c0001t0006g0008a0001c0001t0006g0009others(6): Show | 9 | HG00099.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+7614G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749789 | ||||||
| chr2:69749922
|
C | CAA | 86 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(83): Show | 87 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-47+7758_-47+7759d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69749922 | |||||
| chr2:69750119
|
A | T | 84 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(81): Show | 85 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-47+7944A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750119 | ||||||
| chr2:69750212
|
A | AT | 256 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(253): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.-47+8040dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69750212 | |||||
| chr2:69750236
|
C | T | 1 | a0001c0001t0021g0128 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-47+8061C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750236 | ||||||
| chr2:69750297
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47+8122A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750297 | ||||||
| chr2:69750406
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+8231G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750406 | ||||||
| chr2:69750565
|
G | A | 112 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(109): Show | 115 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-47+8390G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750565 | ||||||
| chr2:69750631
|
T | G | 5 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(2): Show | 5 | NA18963.hp1 NA18971.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+8456T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750631 | ||||||
| chr2:69750956
|
CCT | C | 18 | a0001c0001t0001g0293a0001c0001t0006g0105a0001c0001t0006g0114others(15): Show | 18 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+8788_-47+8789d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69750956 | |||||
| chr2:69751011
|
C | T | 18 | a0001c0001t0001g0293a0001c0001t0006g0105a0001c0001t0006g0114others(15): Show | 18 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+8836C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751011 | ||||||
| chr2:69751158
|
T | G | 250 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(247): Show | 254 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.-47+8983T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751158 | ||||||
| chr2:69751189
|
ACT | A | 110 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(107): Show | 111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-47+9017_-47+9018d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751189 | |||||
| chr2:69751251
|
C | T | 3 | a0001c0001t0006g0114a0002c0002t0002g0115a0002c0002t0002g0116 | 3 | HG02976.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-47+9076C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751251 | ||||||
| chr2:69751362
|
G | T | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-47+9187G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751362 | ||||||
| chr2:69751461
|
T | C | 1 | a0001c0001t0007g0311 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47+9286T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751461 | ||||||
| chr2:69751507
|
C | CA | 99 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(96): Show | 102 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-47+9353dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | |||||
| chr2:69751507
|
C | CAA | 12 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0005g0027others(9): Show | 12 | HG00438.hp1 HG00735.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+9352_-47+9353d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | |||||
| chr2:69751507
|
CA | C | 106 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(103): Show | 107 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.-47+9353delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | |||||
| chr2:69751507
|
CAA | C | 42 | a0001c0001t0001g0293a0001c0001t0003g0017a0001c0001t0003g0190others(39): Show | 42 | HG00099.hp1 HG00741.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-47+9352_-47+9353d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | |||||
| chr2:69751703
|
A | C | 9 | a0001c0001t0006g0302a0001c0001t0006g0304a0001c0001t0006g0306others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+9528A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751703 | ||||||
| chr2:69751813
|
G | A | 110 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(107): Show | 111 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.-47+9638G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751813 | ||||||
| chr2:69752158
|
C | A | 112 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(109): Show | 115 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-47+9983C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752158 | ||||||
| chr2:69752263
|
A | T | 86 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(83): Show | 87 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.-47+10088A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752263 | ||||||
| chr2:69752509
|
G | A | 2 | a0001c0001t0018g0019a0002c0002t0002g0021 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-47+10334G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752509 | ||||||
| chr2:69752581
|
G | A | 3 | a0002c0002t0002g0340a0002c0002t0002g0341a0003c0003t0004g0339 | 3 | HG02622.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+10406G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752581 | ||||||
| chr2:69752682
|
T | C | 9 | a0001c0001t0006g0302a0001c0001t0006g0304a0001c0001t0006g0306others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+10507T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752682 | ||||||
| chr2:69752735
|
A | G | 2 | a0002c0002t0002g0312a0002c0002t0002g0313 | 2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-47+10560A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752735 | ||||||
| chr2:69752745
|
A | C | 3 | a0001c0001t0006g0321a0002c0002t0002g0319a0002c0002t0002g0320 | 3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+10570A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752745 | ||||||
| chr2:69752779
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-47+10604T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752779 | ||||||
| chr2:69752833
|
T | G | 1 | a0001c0001t0003g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47+10658T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752833 | ||||||
| chr2:69752854
|
G | C | 112 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(109): Show | 115 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-47+10679G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752854 | ||||||
| chr2:69753031
|
A | G | 6 | a0001c0001t0006g0012a0001c0001t0007g0200a0001c0001t0007g0207others(3): Show | 6 | HG01433.hp1 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+10856A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753031 | ||||||
| chr2:69753042
|
T | G | 212 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-47+10867T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753042 | ||||||
| chr2:69753061
|
C | T | 212 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-47+10886C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753061 | ||||||
| chr2:69753062
|
C | T | 1 | a0001c0001t0020g0202 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-47+10887C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753062 | ||||||
| chr2:69753072
|
A | G | 34 | a0001c0001t0001g0293a0001c0001t0006g0015a0001c0001t0006g0016others(31): Show | 34 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-47+10897A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753072 | ||||||
| chr2:69753143
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-47+10968C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753143 | ||||||
| chr2:69753164
|
C | G | 1 | a0001c0001t0003g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-47+10989C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753164 | ||||||
| chr2:69753205
|
T | C | 5 | a0001c0001t0006g0221a0002c0002t0002g0222a0002c0002t0002g0223others(2): Show | 5 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11030T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753205 | ||||||
| chr2:69753284
|
A | C | 1 | a0002c0002t0002g0101 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-47+11109A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753284 | ||||||
| chr2:69753287
|
C | G | 100 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(97): Show | 101 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-47+11112C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753287 | ||||||
| chr2:69753294
|
C | G | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+11119C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753294 | ||||||
| chr2:69753295
|
A | G | 241 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(238): Show | 245 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(242): Show |
intron_variant | MODIFIER | c.-47+11120A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753295 | ||||||
| chr2:69753377
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0030 | 2 | NA18963.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-47+11202G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753377 | ||||||
| chr2:69753384
|
C | T | 7 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(4): Show | 7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+11209C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753384 | ||||||
| chr2:69753412
|
C | T | 3 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0006t0006g0007 | 3 | HG02559.hp1 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-47+11237C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753412 | ||||||
| chr2:69753474
|
T | C | 4 | a0002c0002t0002g0037a0002c0002t0002g0038a0002c0002t0002g0039others(1): Show | 4 | HG01074.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+11299T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753474 | ||||||
| chr2:69753636
|
G | A | 5 | a0001c0001t0006g0015a0001c0001t0006g0016a0002c0002t0002g0340others(2): Show | 5 | HG01243.hp1 HG02622.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11461G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753636 | ||||||
| chr2:69753657
|
T | C | 1 | a0002c0002t0002g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-47+11482T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753657 | ||||||
| chr2:69753677
|
G | T | 3 | a0001c0001t0006g0321a0002c0002t0002g0319a0002c0002t0002g0320 | 3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+11502G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753677 | ||||||
| chr2:69753754
|
G | GCTA | 19 | a0001c0001t0001g0293a0001c0001t0006g0105a0001c0001t0006g0114others(16): Show | 19 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-47+11580_-47+1158 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69753754 | |||||
| chr2:69753778
|
C | T | 212 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-47+11603C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753778 | ||||||
| chr2:69753894
|
A | G | 100 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(97): Show | 101 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-47+11719A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753894 | ||||||
| chr2:69753934
|
G | C | 5 | a0001c0001t0006g0221a0002c0002t0002g0222a0002c0002t0002g0223others(2): Show | 5 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11759G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753934 | ||||||
| chr2:69753970
|
T | C | 17 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0326others(14): Show | 17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+11795T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753970 | ||||||
| chr2:69753981
|
C | G | 1 | a0002c0002t0002g0021 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+11806C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753981 | ||||||
| chr2:69753983
|
G | A | 2 | a0001c0001t0001g0191a0001c0001t0003g0246 | 2 | HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-47+11808G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753983 | ||||||
| chr2:69754163
|
G | A | 212 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(209): Show | 216 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(213): Show |
intron_variant | MODIFIER | c.-47+11988G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754163 | ||||||
| chr2:69754376
|
C | A | 2 | a0002c0002t0002g0312a0002c0002t0002g0313 | 2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-47+12201C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754376 | ||||||
| chr2:69754426
|
T | G | 17 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0326others(14): Show | 17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+12251T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754426 | ||||||
| chr2:69754434
|
TTTATTTT others(23): Show |
T | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+12263_-47+1229 others(34): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69754434 | |||||
| chr2:69754653
|
A | G | 3 | a0001c0001t0006g0321a0002c0002t0002g0319a0002c0002t0002g0320 | 3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+12478A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754653 | ||||||
| chr2:69754760
|
G | T | 3 | a0001c0001t0006g0342a0002c0002t0002g0312a0002c0002t0002g0313 | 3 | HG01109.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+12585G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754760 | ||||||
| chr2:69754777
|
T | A | 5 | a0001c0001t0006g0012a0001c0001t0007g0207a0002c0002t0002g0208others(2): Show | 5 | HG01433.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+12602T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754777 | ||||||
| chr2:69754796
|
T | C | 3 | a0001c0001t0006g0342a0002c0002t0002g0312a0002c0002t0002g0313 | 3 | HG01109.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+12621T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754796 | ||||||
| chr2:69754959
|
G | A | 99 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0139others(96): Show | 100 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-47+12784G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754959 | ||||||
| chr2:69755001
|
T | G | 6 | a0001c0001t0001g0224a0001c0001t0006g0015a0001c0001t0006g0016others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+12826T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755001 | ||||||
| chr2:69755021
|
T | G | 17 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0326others(14): Show | 17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+12846T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755021 | ||||||
| chr2:69755110
|
T | A | 1 | a0001c0001t0021g0128 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-47+12935T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755110 | ||||||
| chr2:69755216
|
C | T | 2 | a0001c0001t0018g0019a0002c0002t0002g0021 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-47+13041C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755216 | ||||||
| chr2:69755223
|
G | A | 2 | a0001c0001t0003g0118a0001c0001t0003g0138 | 2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-47+13048G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755223 | ||||||
| chr2:69755378
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-47+13203G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755378 | ||||||
| chr2:69755389
|
G | A | 1 | a0001c0001t0007g0200 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-47+13214G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755389 | ||||||
| chr2:69755472
|
A | C | 3 | a0003c0003t0004g0093a0003c0003t0004g0094a0003c0003t0004g0095 | 3 | NA18954.hp1 NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-47+13297A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755472 | ||||||
| chr2:69755577
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0283 | 2 | HG01109.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-47+13402C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755577 | ||||||
| chr2:69755618
|
T | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0139 | 2 | HG03654.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-47+13443T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755618 | ||||||
| chr2:69755640
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13465A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755640 | ||||||
| chr2:69755646
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13471T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755646 | ||||||
| chr2:69755655
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13480T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755655 | ||||||
| chr2:69755679
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13504A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755679 | ||||||
| chr2:69755682
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13507C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755682 | ||||||
| chr2:69755693
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13518T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755693 | ||||||
| chr2:69755695
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13520T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755695 | ||||||
| chr2:69755696
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13521T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755696 | ||||||
| chr2:69755697
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13522C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755697 | ||||||
| chr2:69755699
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13524T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755699 | ||||||
| chr2:69755700
|
C | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13525C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755700 | ||||||
| chr2:69755702
|
A | C | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13527A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755702 | ||||||
| chr2:69755706
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13531C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755706 | ||||||
| chr2:69755707
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13532C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755707 | ||||||
| chr2:69755708
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13533C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755708 | ||||||
| chr2:69755709
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13534A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755709 | ||||||
| chr2:69755710
|
G | T | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13535G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755710 | ||||||
| chr2:69755712
|
G | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13537G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755712 | ||||||
| chr2:69755801
|
C | T | 5 | a0001c0001t0005g0310a0001c0001t0006g0321a0001c0001t0007g0311others(2): Show | 5 | HG00099.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+13626C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755801 | ||||||
| chr2:69756265
|
C | A | 2 | a0001c0001t0005g0140a0001c0001t0005g0141 | 2 | HG00408.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-47+14090C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756265 | ||||||
| chr2:69756274
|
G | A | 5 | a0001c0001t0005g0310a0001c0001t0006g0321a0001c0001t0007g0311others(2): Show | 5 | HG00099.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+14099G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756274 | ||||||
| chr2:69756531
|
G | C | 233 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(230): Show | 237 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.-47+14356G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756531 | ||||||
| chr2:69756575
|
A | G | 1 | a0001c0001t0007g0282 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47+14400A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756575 | ||||||
| chr2:69756709
|
C | G | 2 | a0001c0001t0006g0010a0002c0002t0002g0011 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-47+14534C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756709 | ||||||
| chr2:69756711
|
A | G | 2 | a0001c0001t0006g0008a0001c0001t0006g0009 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-47+14536A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756711 | ||||||
| chr2:69756927
|
A | AATT | 3 | a0001c0001t0001g0031a0001c0001t0020g0202a0001c0001t0021g0128 | 3 | HG00735.hp1 HG01167.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-47+14759_-47+1476 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69756927 | |||||
| chr2:69756933
|
TA | T | 17 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(14): Show | 17 | HG01106.hp1 HG01109.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+14759delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756933 | ||||||
| chr2:69756934
|
A | ATT | 111 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(108): Show | 114 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.-47+14770_-47+1477 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69756934 | |||||
| chr2:69756934
|
A | ATTT | 118 | a0001c0001t0001g0092a0001c0001t0001g0124a0001c0001t0001g0125others(115): Show | 119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-47+14769_-47+1477 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69756934 | |||||
| chr2:69756934
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0006g0103 | 2 | HG01109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-47+14759A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756934 | ||||||
| chr2:69756978
|
C | T | 1 | a0001c0001t0006g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-47+14803C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756978 | ||||||
| chr2:69757073
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+14898C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757073 | ||||||
| chr2:69757176
|
G | A | 2 | a0001c0001t0001g0322a0001c0001t0001g0324 | 2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-47+15001G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757176 | ||||||
| chr2:69757213
|
G | C | 200 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(197): Show | 204 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.-47+15038G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757213 | ||||||
| chr2:69757222
|
C | G | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47+15047C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757222 | ||||||
| chr2:69757238
|
T | TTATATAT others(7): Show |
1 | a0003c0003t0004g0339 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-47+15079_-47+1509 others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757238 | |||||
| chr2:69757238
|
T | TTTTTTAT others(23): Show |
1 | a0001c0001t0005g0310 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-47+15064_-47+1506 others(34): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757238 | |||||
| chr2:69757240
|
A | T | 8 | a0001c0001t0006g0114a0001c0001t0006g0321a0001c0001t0006g0342others(5): Show | 8 | HG00099.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+15065A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757240 | ||||||
| chr2:69757256
|
ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0030a0002c0002t0002g0040 | 2 | HG02258.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-47+15083_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | |||||
| chr2:69757256
|
ATATATAT others(5): Show |
A | 72 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0032others(69): Show | 75 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.-47+15083_-47+1509 others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | |||||
| chr2:69757256
|
ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0045 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47+15083_-47+1509 others(17): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | |||||
| chr2:69757256
|
ATATATAT others(11): Show |
A | 1 | a0001c0001t0021g0128 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-47+15083_-47+1510 others(22): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | |||||
| chr2:69757258
|
ATATATAT others(3): Show |
A | 3 | a0001c0001t0005g0029a0001c0001t0007g0044a0004c0004t0005g0203 | 3 | HG02896.hp1 HG04204.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1509 others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | |||||
| chr2:69757258
|
ATATATAT others(4): Show |
A | 2 | a0002c0002t0002g0042a0002c0002t0002g0043 | 2 | NA18982.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | |||||
| chr2:69757258
|
ATATATAT others(5): Show |
A | 3 | a0002c0002t0002g0041a0003c0003t0004g0093a0003c0003t0004g0094 | 3 | HG01074.hp2 NA18954.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1509 others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | |||||
| chr2:69757258
|
ATATATAT others(10): Show |
A | 2 | a0002c0002t0002g0005a0005c0005t0007g0006 | 2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1510 others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | |||||
| chr2:69757260
|
ATATATAT others(1): Show |
A | 6 | a0001c0001t0003g0186a0001c0001t0003g0188a0001c0001t0018g0019others(3): Show | 6 | HG01192.hp2 HG01256.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+15087_-47+1509 others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | |||||
| chr2:69757260
|
ATATATAT others(4): Show |
A | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+15087_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | |||||
| chr2:69757260
|
ATATATAT others(8): Show |
A | 9 | a0001c0001t0006g0302a0001c0001t0006g0304a0001c0001t0006g0306others(6): Show | 9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15087_-47+1510 others(19): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | |||||
| chr2:69757260
|
ATATATAT others(9): Show |
A | 4 | a0001c0001t0004g0131a0001c0001t0011g0130a0002c0002t0002g0208others(1): Show | 4 | HG01433.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15087_-47+1510 others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | |||||
| chr2:69757260
|
ATATATAT others(13): Show |
A | 9 | a0001c0001t0005g0211a0001c0001t0005g0318a0001c0001t0006g0008others(6): Show | 9 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15087_-47+1510 others(24): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | |||||
| chr2:69757261
|
TATA | T | 3 | a0001c0001t0006g0321a0002c0002t0002g0319a0002c0002t0002g0320 | 3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+15087_-47+1508 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757261 | ||||||
| chr2:69757262
|
ATATATTT others(1): Show |
A | 56 | a0001c0001t0001g0092a0001c0001t0001g0124a0001c0001t0001g0125others(53): Show | 57 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-47+15089_-47+1509 others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | |||||
| chr2:69757262
|
ATATATTT others(7): Show |
A | 1 | a0001c0001t0005g0199 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-47+15089_-47+1510 others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | |||||
| chr2:69757262
|
ATATATTT others(8): Show |
A | 3 | a0001c0001t0006g0010a0001c0001t0007g0200a0002c0002t0002g0011 | 3 | HG02257.hp2 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+15089_-47+1510 others(19): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | |||||
| chr2:69757262
|
ATATATTT others(9): Show |
A | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-47+15089_-47+1510 others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | |||||
| chr2:69757262
|
ATATATTT others(10): Show |
A | 4 | a0001c0001t0006g0016a0001c0001t0007g0207a0003c0003t0004g0013others(1): Show | 4 | HG01243.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15089_-47+1510 others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | |||||
| chr2:69757264
|
A | AT | 4 | a0001c0001t0001g0284a0001c0001t0001g0294a0001c0001t0001g0299others(1): Show | 4 | HG00741.hp2 HG03654.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15090dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | |||||
| chr2:69757264
|
A | T | 3 | a0001c0001t0001g0277a0001c0001t0001g0278a0001c0001t0001g0297 | 3 | HG00597.hp2 HG02486.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-47+15089A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757264 | ||||||
| chr2:69757264
|
ATATTTT | A | 10 | a0001c0001t0001g0241a0001c0001t0003g0091a0001c0001t0003g0135others(7): Show | 10 | HG01255.hp2 HG01496.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1509 others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | |||||
| chr2:69757264
|
ATATTTTT | A | 9 | a0001c0001t0003g0120a0001c0001t0003g0152a0001c0001t0003g0209others(6): Show | 9 | HG00673.hp1 NA18939.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1509 others(11): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | |||||
| chr2:69757264
|
ATATTTTT others(1): Show |
A | 16 | a0001c0001t0001g0139a0001c0001t0001g0322a0001c0001t0001g0324others(13): Show | 16 | HG00423.hp2 HG03654.hp2 NA18940.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1509 others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | |||||
| chr2:69757264
|
ATATTTTT others(7): Show |
A | 4 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(1): Show | 4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1510 others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | |||||
| chr2:69757264
|
ATATTTTT others(8): Show |
A | 1 | a0001c0001t0006g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-47+15091_-47+1510 others(19): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | |||||
| chr2:69757264
|
ATATTTTT others(10): Show |
A | 1 | a0001c0001t0006g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-47+15091_-47+1510 others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | |||||
| chr2:69757265
|
TA | T | 5 | a0001c0001t0001g0233a0001c0001t0001g0244a0001c0001t0001g0254others(2): Show | 5 | HG01070.hp2 HG01515.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+15091delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757265 | ||||||
| chr2:69757266
|
A | ATATATAT others(24): Show |
1 | a0001c0001t0007g0311 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47+15092_-47+1509 others(35): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757266 | |||||
| chr2:69757266
|
A | T | 50 | a0001c0001t0001g0191a0001c0001t0001g0238a0001c0001t0001g0239others(47): Show | 50 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47+15091A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757266 | ||||||
| chr2:69757266
|
ATTTTTT | A | 10 | a0001c0001t0001g0293a0001c0001t0003g0142a0001c0001t0006g0105others(7): Show | 10 | HG01192.hp1 HG02559.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+15109_-47+1511 others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757266 | |||||
| chr2:69757266
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+15104_-47+1511 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757266 | |||||
| chr2:69757267
|
T | TATATATA others(4): Show |
2 | a0002c0002t0002g0340a0002c0002t0002g0341 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-47+15092_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757267 | ||||||
| chr2:69757268
|
T | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0248a0003c0003t0004g0339 | 3 | HG01109.hp2 HG02132.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+15093T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757268 | ||||||
| chr2:69757269
|
T | A | 3 | a0002c0002t0002g0340a0002c0002t0002g0341a0003c0003t0004g0109 | 3 | HG01891.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-47+15094T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757269 | ||||||
| chr2:69757270
|
T | A | 3 | a0001c0001t0001g0224a0003c0003t0002g0110a0003c0003t0004g0339 | 3 | HG01109.hp2 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+15095T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757270 | ||||||
| chr2:69757271
|
T | A | 4 | a0002c0002t0002g0340a0002c0002t0002g0341a0003c0003t0004g0109others(1): Show | 4 | HG01891.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+15096T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757271 | ||||||
| chr2:69757272
|
T | A | 4 | a0001c0001t0001g0224a0001c0001t0006g0342a0002c0002t0002g0112others(1): Show | 4 | HG01109.hp2 HG02717.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15097T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757272 | ||||||
| chr2:69757273
|
T | A | 2 | a0003c0003t0004g0109a0003c0003t0004g0111 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-47+15098T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757273 | ||||||
| chr2:69757274
|
T | A | 13 | a0001c0001t0001g0224a0001c0001t0001g0293a0001c0001t0006g0105others(10): Show | 13 | HG01109.hp2 HG01192.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-47+15099T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757274 | ||||||
| chr2:69757276
|
T | A | 2 | a0001c0001t0001g0224a0001c0001t0006g0342 | 2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+15101T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757276 | ||||||
| chr2:69757278
|
T | A | 1 | a0001c0001t0006g0342 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+15103T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757278 | ||||||
| chr2:69757279
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+15104T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757279 | ||||||
| chr2:69757281
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+15106T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757281 | ||||||
| chr2:69757363
|
C | T | 1 | a0002c0002t0002g0341 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-47+15188C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757363 | ||||||
| chr2:69757366
|
G | A | 2 | a0001c0001t0003g0157a0001c0001t0003g0158 | 2 | HG00544.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-47+15191G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757366 | ||||||
| chr2:69757440
|
G | GT | 35 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0003g0098others(32): Show | 35 | HG00609.hp2 HG00735.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.-47+15279dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757440 | |||||
| chr2:69757440
|
G | T | 17 | a0001c0001t0001g0293a0001c0001t0006g0105a0001c0001t0006g0114others(14): Show | 17 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+15265G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757440 | ||||||
| chr2:69757447
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+15272T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757447 | ||||||
| chr2:69757508
|
C | T | 14 | a0001c0001t0001g0031a0001c0001t0005g0195a0001c0001t0005g0196others(11): Show | 14 | HG00735.hp1 HG01243.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47+15333C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757508 | ||||||
| chr2:69757570
|
G | A | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+15395G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757570 | ||||||
| chr2:69757624
|
G | A | 1 | a0002c0002t0002g0256 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-47+15449G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757624 | ||||||
| chr2:69757681
|
G | A | 9 | a0001c0001t0005g0211a0001c0001t0005g0318a0001c0001t0006g0008others(6): Show | 9 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15506G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757681 | ||||||
| chr2:69757746
|
C | T | 2 | a0001c0001t0005g0316a0001c0001t0007g0315 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-47+15571C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757746 | ||||||
| chr2:69757958
|
CA | C | 163 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0092others(160): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.-47+15804delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757958 | |||||
| chr2:69757958
|
CAA | C | 97 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(94): Show | 100 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-47+15803_-47+1580 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757958 | |||||
| chr2:69757979
|
A | T | 1 | a0001c0001t0005g0198 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+15804A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757979 | ||||||
| chr2:69758298
|
C | G | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-47+16123C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758298 | ||||||
| chr2:69758303
|
G | A | 222 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(219): Show | 226 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-47+16128G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758303 | ||||||
| chr2:69758357
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47+16182C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758357 | ||||||
| chr2:69758398
|
G | A | 1 | a0003c0003t0002g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-47+16223G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758398 | ||||||
| chr2:69758512
|
C | T | 82 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(79): Show | 85 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.-47+16337C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758512 | ||||||
| chr2:69758526
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+16351A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758526 | ||||||
| chr2:69758606
|
A | G | 1 | a0001c0001t0005g0029 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-47+16431A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758606 | ||||||
| chr2:69758710
|
A | G | 10 | a0001c0001t0005g0211a0001c0001t0005g0318a0001c0001t0006g0008others(7): Show | 10 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+16535A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758710 | ||||||
| chr2:69758737
|
C | T | 10 | a0001c0001t0005g0211a0001c0001t0005g0318a0001c0001t0006g0008others(7): Show | 10 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+16562C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758737 | ||||||
| chr2:69758814
|
G | T | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+16639G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758814 | ||||||
| chr2:69758868
|
C | T | 1 | a0001c0001t0005g0216 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-47+16693C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758868 | ||||||
| chr2:69758887
|
C | T | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+16712C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758887 | ||||||
| chr2:69758905
|
C | G | 230 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(227): Show | 234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-47+16730C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758905 | ||||||
| chr2:69758964
|
T | G | 18 | a0001c0001t0001g0293a0001c0001t0006g0105a0001c0001t0006g0114others(15): Show | 18 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+16789T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758964 | ||||||
| chr2:69759004
|
C | T | 231 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(228): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-47+16829C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759004 | ||||||
| chr2:69759060
|
C | T | 2 | a0002c0002t0002g0005a0005c0005t0007g0006 | 2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-47+16885C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759060 | ||||||
| chr2:69759067
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+16892C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759067 | ||||||
| chr2:69759080
|
G | A | 1 | a0003c0003t0004g0046 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-47+16905G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759080 | ||||||
| chr2:69759124
|
T | C | 230 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(227): Show | 234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-47+16949T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759124 | ||||||
| chr2:69759129
|
CA | C | 20 | a0001c0001t0001g0224a0001c0001t0001g0293a0001c0001t0005g0027others(17): Show | 20 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-47+16973delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69759129 | |||||
| chr2:69759129
|
CAAA | C | 221 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(218): Show | 225 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-47+16971_-47+1697 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69759129 | |||||
| chr2:69759129
|
CAAAA | C | 7 | a0001c0001t0003g0188a0001c0001t0006g0012a0001c0001t0006g0015others(4): Show | 7 | HG01243.hp1 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+16970_-47+1697 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69759129 | |||||
| chr2:69759131
|
A | C | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+16956A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759131 | ||||||
| chr2:69759151
|
T | C | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-47+16976T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759151 | ||||||
| chr2:69759315
|
C | G | 1 | a0001c0001t0001g0286 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-47+17140C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759315 | ||||||
| chr2:69759344
|
A | G | 1 | a0001c0001t0012g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-47+17169A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759344 | ||||||
| chr2:69759439
|
G | A | 5 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(2): Show | 5 | NA18747.hp1 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+17264G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759439 | ||||||
| chr2:69759539
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+17364C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759539 | ||||||
| chr2:69759618
|
A | G | 2 | a0001c0001t0003g0227a0001c0001t0003g0228 | 2 | HG02129.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-47+17443A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759618 | ||||||
| chr2:69759665
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+17490G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759665 | ||||||
| chr2:69759679
|
G | C | 14 | a0001c0001t0001g0031a0001c0001t0005g0195a0001c0001t0005g0196others(11): Show | 14 | HG00735.hp1 HG01243.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47+17504G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759679 | ||||||
| chr2:69759856
|
G | A | 1 | a0001c0001t0003g0164 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-47+17681G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759856 | ||||||
| chr2:69759869
|
A | G | 232 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(229): Show | 236 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.-47+17694A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759869 | ||||||
| chr2:69759960
|
G | A | 1 | a0001c0001t0006g0342 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+17785G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759960 | ||||||
| chr2:69760056
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0277 | 2 | HG00597.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-47+17881T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760056 | ||||||
| chr2:69760074
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-47+17899C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760074 | ||||||
| chr2:69760128
|
G | A | 1 | a0001c0001t0006g0302 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-47+17953G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760128 | ||||||
| chr2:69760247
|
T | C | 5 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(2): Show | 5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+18072T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760247 | ||||||
| chr2:69760252
|
A | G | 231 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(228): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-47+18077A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760252 | ||||||
| chr2:69760575
|
T | C | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+18400T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760575 | ||||||
| chr2:69760608
|
G | A | 8 | a0001c0001t0006g0126a0003c0003t0002g0104a0003c0003t0004g0189others(5): Show | 8 | HG01256.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+18433G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760608 | ||||||
| chr2:69760680
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+18505G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760680 | ||||||
| chr2:69760991
|
G | A | 1 | a0001c0001t0006g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-47+18816G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760991 | ||||||
| chr2:69760998
|
T | TTAAA | 231 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(228): Show | 235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-47+18825_-47+1882 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69760998 | |||||
| chr2:69761000
|
A | AAATT | 8 | a0001c0001t0005g0318a0001c0001t0006g0008a0001c0001t0006g0009others(5): Show | 8 | HG01109.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+18848_-47+1885 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761000 | |||||
| chr2:69761004
|
T | A | 230 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(227): Show | 234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-47+18829T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761004 | ||||||
| chr2:69761008
|
T | A | 125 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(122): Show | 128 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(125): Show |
intron_variant | MODIFIER | c.-47+18833T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761008 | ||||||
| chr2:69761012
|
T | A | 18 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0326others(15): Show | 18 | HG02155.hp1 HG02451.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47+18837T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761012 | ||||||
| chr2:69761016
|
T | A | 11 | a0001c0001t0001g0322a0001c0001t0001g0324a0001c0001t0001g0326others(8): Show | 11 | NA18961.hp2 NA18965.hp1 NA18966.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+18841T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761016 | ||||||
| chr2:69761101
|
A | C | 1 | a0001c0001t0001g0294 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-47+18926A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761101 | ||||||
| chr2:69761220
|
G | A | 2 | a0001c0001t0006g0010a0002c0002t0002g0011 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-47+19045G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761220 | ||||||
| chr2:69761519
|
T | TAAGTA | 268 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(265): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-47+19346_-47+1934 others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761519 | |||||
| chr2:69761541
|
A | G | 5 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(2): Show | 5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+19366A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761541 | ||||||
| chr2:69761572
|
G | A | 3 | a0001c0001t0003g0234a0001c0001t0003g0291a0001c0001t0003g0292 | 3 | NA18943.hp2 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-47+19397G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761572 | ||||||
| chr2:69761585
|
T | C | 259 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(256): Show | 263 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.-47+19410T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761585 | ||||||
| chr2:69761715
|
G | C | 1 | a0001c0001t0005g0215 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-47+19540G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761715 | ||||||
| chr2:69761738
|
T | C | 1 | a0001c0001t0006g0126 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-47+19563T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761738 | ||||||
| chr2:69761746
|
C | T | 11 | a0001c0001t0004g0131a0001c0001t0006g0304a0001c0001t0006g0306others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+19571C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761746 | ||||||
| chr2:69761749
|
C | T | 6 | a0001c0001t0003g0120a0001c0001t0003g0152a0001c0001t0003g0209others(3): Show | 6 | NA18939.hp1 NA18969.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+19574C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761749 | ||||||
| chr2:69761776
|
T | TA | 14 | a0001c0001t0001g0236a0001c0001t0005g0211a0001c0001t0005g0318others(11): Show | 14 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47+19620dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | |||||
| chr2:69761776
|
T | TAA | 15 | a0001c0001t0001g0293a0001c0001t0006g0105a0001c0001t0006g0114others(12): Show | 15 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+19619_-47+1962 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | |||||
| chr2:69761776
|
TA | T | 214 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(211): Show | 218 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.-47+19620delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | |||||
| chr2:69761776
|
TAA | T | 9 | a0001c0001t0001g0031a0001c0001t0001g0289a0001c0001t0001g0324others(6): Show | 9 | HG00735.hp1 HG01496.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+19619_-47+1962 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | |||||
| chr2:69761854
|
A | T | 1 | a0003c0003t0004g0082 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-46-19666A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761854 | ||||||
| chr2:69761927
|
A | G | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-19593A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761927 | ||||||
| chr2:69761946
|
T | C | 1 | a0001c0001t0006g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-46-19574T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761946 | ||||||
| chr2:69762156
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-19364T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762156 | ||||||
| chr2:69762195
|
A | G | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-19325A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762195 | ||||||
| chr2:69762264
|
G | A | 2 | a0001c0001t0004g0131a0001c0001t0011g0130 | 2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-46-19256G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762264 | ||||||
| chr2:69762288
|
G | A | 2 | a0001c0001t0003g0145a0001c0001t0008g0144 | 2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-46-19232G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762288 | ||||||
| chr2:69762306
|
A | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | NA18957.hp1 NA19056.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-19214A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762306 | ||||||
| chr2:69762325
|
G | A | 2 | a0001c0001t0005g0310a0001c0001t0007g0311 | 2 | HG00099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-46-19195G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762325 | ||||||
| chr2:69762389
|
GA | G | 27 | a0001c0001t0001g0293a0001c0001t0005g0211a0001c0001t0005g0318others(24): Show | 27 | HG01109.hp1 HG01192.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46-19116delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69762389 | |||||
| chr2:69762390
|
A | G | 1 | a0003c0003t0004g0339 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-46-19130A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762390 | ||||||
| chr2:69762446
|
T | G | 2 | a0002c0002t0002g0115a0002c0002t0002g0116 | 2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-46-19074T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762446 | ||||||
| chr2:69762484
|
G | A | 1 | a0001c0001t0003g0165 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-46-19036G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762484 | ||||||
| chr2:69762645
|
G | A | 5 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(2): Show | 5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-18875G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762645 | ||||||
| chr2:69762663
|
T | C | 4 | a0001c0001t0001g0045a0001c0001t0001g0080a0001c0001t0001g0081others(1): Show | 4 | NA18957.hp1 NA19056.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-18857T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762663 | ||||||
| chr2:69762669
|
C | G | 119 | a0001c0001t0001g0031a0001c0001t0001g0092a0001c0001t0001g0124others(116): Show | 120 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-46-18851C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762669 | ||||||
| chr2:69762697
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-46-18823C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762697 | ||||||
| chr2:69762777
|
G | A | 1 | a0001c0001t0007g0311 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-46-18743G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762777 | ||||||
| chr2:69762855
|
ACACT | A | 3 | a0001c0001t0005g0310a0001c0001t0007g0311a0001c0001t0009g0235 | 3 | HG00099.hp1 HG02145.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-46-18657_-46-1865 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69762855 | |||||
| chr2:69762863
|
T | TCA | 247 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(244): Show | 251 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.-46-18651_-46-1865 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69762863 | |||||
| chr2:69763158
|
T | G | 134 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0092others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.-46-18362T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763158 | ||||||
| chr2:69763172
|
A | G | 3 | a0002c0002t0002g0132a0003c0003t0004g0189a0003c0003t0004g0247 | 3 | HG01243.hp2 HG01256.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-46-18348A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763172 | ||||||
| chr2:69763277
|
C | T | 3 | a0001c0001t0004g0131a0001c0001t0011g0130a0002c0002t0013g0129 | 3 | HG02451.hp2 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-46-18243C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763277 | ||||||
| chr2:69763295
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-18225C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763295 | ||||||
| chr2:69763309
|
G | A | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-46-18211G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763309 | ||||||
| chr2:69763310
|
T | G | 1 | a0001c0001t0005g0027 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-46-18210T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763310 | ||||||
| chr2:69763449
|
GT | G | 3 | a0001c0001t0006g0012a0003c0003t0004g0013a0003c0003t0004g0014 | 3 | HG02965.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-18069delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69763449 | |||||
| chr2:69763496
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0272 | 2 | HG01109.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-46-18024A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763496 | ||||||
| chr2:69763662
|
C | CT | 17 | a0001c0001t0001g0032a0001c0001t0001g0213a0001c0001t0001g0224others(14): Show | 17 | HG01109.hp2 HG02523.hp2 HG04115.hp1 others(14): Show |
intron_variant | MODIFIER | c.-46-17840dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69763662 | |||||
| chr2:69763662
|
C | CTT | 17 | a0001c0001t0002g0271a0001c0001t0003g0234a0001c0001t0003g0291others(14): Show | 17 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-17841_-46-1784 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69763662 | |||||
| chr2:69763736
|
C | G | 85 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(82): Show | 87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-46-17784C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763736 | ||||||
| chr2:69763820
|
G | A | 15 | a0001c0001t0002g0271a0001c0001t0005g0023a0001c0001t0005g0140others(12): Show | 15 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.-46-17700G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763820 | ||||||
| chr2:69763951
|
G | A | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-17569G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763951 | ||||||
| chr2:69763999
|
A | G | 1 | a0001c0001t0011g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-46-17521A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763999 | ||||||
| chr2:69764128
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0007g0305 | 2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-17392A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764128 | ||||||
| chr2:69764364
|
T | C | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-17156T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764364 | ||||||
| chr2:69764397
|
TTAAA | T | 4 | a0003c0003t0004g0074a0003c0003t0004g0093a0003c0003t0004g0094others(1): Show | 4 | NA18954.hp1 NA19005.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-17119_-46-1711 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69764397 | |||||
| chr2:69764470
|
T | A | 1 | a0001c0001t0003g0146 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-46-17050T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764470 | ||||||
| chr2:69764573
|
C | A | 2 | a0002c0002t0002g0222a0002c0002t0002g0223 | 2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-46-16947C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764573 | ||||||
| chr2:69764644
|
T | G | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-16876T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764644 | ||||||
| chr2:69764696
|
C | T | 98 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(95): Show | 99 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.-46-16824C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764696 | ||||||
| chr2:69764825
|
T | C | 6 | a0001c0001t0007g0300a0001c0001t0007g0308a0001c0001t0021g0128others(3): Show | 6 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46-16695T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764825 | ||||||
| chr2:69764941
|
T | A | 1 | a0001c0001t0003g0338 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-46-16579T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764941 | ||||||
| chr2:69764953
|
T | A | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-16567T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764953 | ||||||
| chr2:69764964
|
ACTTAG | A | 85 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(82): Show | 86 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.-46-16550_-46-1654 others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69764964 | |||||
| chr2:69765075
|
T | TAC | 21 | a0001c0001t0001g0244a0001c0001t0001g0260a0001c0001t0001g0261others(18): Show | 21 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.-46-16422_-46-1642 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69765075 | |||||
| chr2:69765075
|
T | TACAC | 4 | a0001c0001t0001g0224a0001c0001t0006g0321a0001c0001t0007g0305others(1): Show | 4 | HG01109.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-16424_-46-1642 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69765075 | |||||
| chr2:69765075
|
TAC | T | 93 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(90): Show | 94 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-46-16422_-46-1642 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69765075 | |||||
| chr2:69765220
|
G | A | 1 | a0001c0001t0014g0155 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-46-16300G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765220 | ||||||
| chr2:69765302
|
A | G | 11 | a0002c0002t0002g0099a0002c0002t0002g0112a0002c0002t0002g0117others(8): Show | 11 | HG03688.hp1 HG04115.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.-46-16218A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765302 | ||||||
| chr2:69765310
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-46-16210T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765310 | ||||||
| chr2:69765379
|
A | G | 5 | a0001c0001t0011g0212a0002c0002t0002g0089a0002c0002t0002g0090others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-16141A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765379 | ||||||
| chr2:69765414
|
A | G | 100 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(97): Show | 101 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-46-16106A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765414 | ||||||
| chr2:69765474
|
C | T | 1 | a0001c0001t0006g0010 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-46-16046C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765474 | ||||||
| chr2:69765620
|
T | C | 93 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(90): Show | 94 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-46-15900T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765620 | ||||||
| chr2:69765635
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15885C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765635 | ||||||
| chr2:69765657
|
A | G | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-15863A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765657 | ||||||
| chr2:69765763
|
C | T | 33 | a0001c0001t0001g0031a0001c0001t0001g0139a0001c0001t0002g0271others(30): Show | 33 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-46-15757C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765763 | ||||||
| chr2:69765858
|
C | G | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-15662C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765858 | ||||||
| chr2:69765985
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15535C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765985 | ||||||
| chr2:69766052
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15468A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766052 | ||||||
| chr2:69766123
|
A | G | 2 | a0002c0002t0002g0222a0002c0002t0002g0223 | 2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-46-15397A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766123 | ||||||
| chr2:69766140
|
A | G | 5 | a0001c0001t0011g0212a0002c0002t0002g0089a0002c0002t0002g0090others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-15380A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766140 | ||||||
| chr2:69766446
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15074C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766446 | ||||||
| chr2:69766514
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030 | 3 | NA18963.hp1 NA18986.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-46-15006G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766514 | ||||||
| chr2:69766850
|
T | A | 5 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(2): Show | 5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-14670T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766850 | ||||||
| chr2:69766942
|
C | G | 2 | a0001c0001t0001g0224a0001c0001t0007g0305 | 2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-14578C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766942 | ||||||
| chr2:69767050
|
T | C | 3 | a0001c0001t0001g0139a0001c0001t0005g0314a0001c0001t0007g0044 | 3 | HG03654.hp2 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-46-14470T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767050 | ||||||
| chr2:69767142
|
T | C | 3 | a0001c0001t0005g0334a0001c0001t0005g0336a0001c0001t0017g0337 | 3 | HG02135.hp2 HG02155.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-46-14378T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767142 | ||||||
| chr2:69767347
|
C | G | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-14173C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767347 | ||||||
| chr2:69767386
|
A | G | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-14134A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767386 | ||||||
| chr2:69767411
|
T | G | 31 | a0001c0001t0001g0031a0001c0001t0001g0139a0001c0001t0002g0271others(28): Show | 31 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-46-14109T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767411 | ||||||
| chr2:69767616
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-46-13904G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767616 | ||||||
| chr2:69767659
|
G | C | 42 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(39): Show | 44 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-46-13861G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767659 | ||||||
| chr2:69767835
|
T | C | 2 | a0001c0001t0007g0275a0001c0001t0007g0276 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-46-13685T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767835 | ||||||
| chr2:69767905
|
C | T | 1 | a0001c0001t0001g0326 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-46-13615C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767905 | ||||||
| chr2:69767912
|
G | A | 341 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(338): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.-46-13608G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767912 | ||||||
| chr2:69767929
|
A | G | 2 | a0001c0001t0001g0322a0001c0001t0001g0324 | 2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-46-13591A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767929 | ||||||
| chr2:69768328
|
C | T | 3 | a0002c0002t0002g0303a0002c0002t0002g0312a0002c0002t0002g0313 | 3 | HG01109.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-46-13192C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768328 | ||||||
| chr2:69768380
|
C | T | 5 | a0001c0001t0011g0212a0002c0002t0002g0089a0002c0002t0002g0090others(2): Show | 5 | HG02280.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-13140C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768380 | ||||||
| chr2:69768412
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-46-13108G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768412 | ||||||
| chr2:69768434
|
C | T | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-13086C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768434 | ||||||
| chr2:69768435
|
G | T | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-13085G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768435 | ||||||
| chr2:69768447
|
C | T | 3 | a0001c0001t0004g0131a0001c0001t0006g0020a0001c0001t0006g0221 | 3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-13073C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768447 | ||||||
| chr2:69768448
|
A | G | 271 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0047others(268): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.-46-13072A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768448 | ||||||
| chr2:69768474
|
T | C | 145 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0049others(142): Show | 148 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.-46-13046T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768474 | ||||||
| chr2:69768722
|
CT | C | 13 | a0001c0001t0005g0027a0001c0001t0005g0029a0001c0001t0005g0211others(10): Show | 13 | HG02135.hp2 HG02155.hp1 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.-46-12796delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69768722 | |||||
| chr2:69768962
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0007g0305 | 2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-12558C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768962 | ||||||
| chr2:69769022
|
A | G | 93 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(90): Show | 94 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-46-12498A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769022 | ||||||
| chr2:69769148
|
C | T | 7 | a0001c0001t0006g0010a0001c0001t0006g0114a0001c0001t0006g0302others(4): Show | 7 | HG01167.hp1 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-12372C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769148 | ||||||
| chr2:69769181
|
C | T | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-12339C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769181 | ||||||
| chr2:69769237
|
C | T | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-12283C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769237 | ||||||
| chr2:69769250
|
G | A | 93 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(90): Show | 94 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-46-12270G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769250 | ||||||
| chr2:69769266
|
ATCAT | A | 91 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(88): Show | 92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-46-12252_-46-1224 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69769266 | |||||
| chr2:69769284
|
A | C | 1 | a0001c0001t0005g0149 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-46-12236A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769284 | ||||||
| chr2:69769652
|
T | G | 1 | a0001c0001t0006g0342 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-46-11868T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769652 | ||||||
| chr2:69769725
|
G | A | 33 | a0001c0001t0006g0012a0001c0001t0006g0342a0002c0002t0002g0064others(30): Show | 35 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-46-11795G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769725 | ||||||
| chr2:69769785
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-46-11735C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769785 | ||||||
| chr2:69769810
|
G | A | 66 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(63): Show | 67 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-46-11710G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769810 | ||||||
| chr2:69769874
|
G | C | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-11646G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769874 | ||||||
| chr2:69769979
|
T | G | 2 | a0001c0001t0001g0224a0001c0001t0007g0305 | 2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-11541T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769979 | ||||||
| chr2:69769981
|
A | T | 1 | a0001c0001t0005g0149 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-46-11539A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769981 | ||||||
| chr2:69770054
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-11466G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770054 | ||||||
| chr2:69770210
|
C | T | 2 | a0001c0001t0005g0195a0001c0001t0005g0198 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-46-11310C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770210 | ||||||
| chr2:69770234
|
A | C | 3 | a0001c0001t0004g0131a0001c0001t0006g0020a0001c0001t0006g0221 | 3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-11286A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770234 | ||||||
| chr2:69770305
|
A | G | 4 | a0003c0003t0004g0074a0003c0003t0004g0093a0003c0003t0004g0094others(1): Show | 4 | NA18954.hp1 NA19005.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-11215A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770305 | ||||||
| chr2:69770491
|
C | A | 15 | a0001c0001t0001g0031a0001c0001t0006g0008a0001c0001t0006g0009others(12): Show | 15 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-46-11029C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770491 | ||||||
| chr2:69770644
|
A | G | 1 | a0001c0001t0001g0332 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-46-10876A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770644 | ||||||
| chr2:69770659
|
ACTCT | A | 5 | a0003c0003t0002g0110a0003c0003t0004g0109a0003c0003t0004g0111others(2): Show | 5 | HG01891.hp1 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-10855_-46-1085 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770659 | |||||
| chr2:69770736
|
AACACACA others(9): Show |
A | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-46-10760_-46-1074 others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770736 | |||||
| chr2:69770745
|
G | A | 2 | a0001c0001t0018g0019a0002c0002t0002g0021 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-10775G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770745 | ||||||
| chr2:69770761
|
G | A | 1 | a0002c0002t0002g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-46-10759G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770761 | ||||||
| chr2:69770828
|
A | G | 2 | a0001c0001t0003g0004a0001c0001t0003g0193 | 3 | HG03017.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-46-10692A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770828 | ||||||
| chr2:69770863
|
A | G | 189 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0047others(186): Show | 192 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(189): Show |
intron_variant | MODIFIER | c.-46-10657A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770863 | ||||||
| chr2:69770865
|
G | A | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-10655G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770865 | ||||||
| chr2:69770930
|
T | A | 1 | a0001c0001t0003g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-46-10590T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770930 | ||||||
| chr2:69770930
|
T | TAA | 9 | a0001c0001t0003g0079a0001c0001t0003g0091a0001c0001t0003g0118others(6): Show | 9 | HG01255.hp2 HG01975.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-10577_-46-1057 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770930 | |||||
| chr2:69770930
|
T | TAAA | 74 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(71): Show | 75 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-46-10578_-46-1057 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770930 | |||||
| chr2:69771094
|
C | CA | 49 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0070others(46): Show | 51 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-46-10412dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69771094 | |||||
| chr2:69771105
|
A | G | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-10415A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771105 | ||||||
| chr2:69771109
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0011g0130a0002c0002t0013g0129 | 3 | HG01109.hp2 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-46-10411G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771109 | ||||||
| chr2:69771109
|
G | GA | 16 | a0001c0001t0001g0262a0001c0001t0005g0198a0001c0001t0006g0008others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.-46-10395dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69771109 | |||||
| chr2:69771109
|
GA | G | 115 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0139others(112): Show | 116 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-46-10395delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69771109 | |||||
| chr2:69771110
|
A | G | 4 | a0001c0001t0005g0334a0001c0001t0005g0336a0001c0001t0011g0130others(1): Show | 4 | HG02155.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-10410A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771110 | ||||||
| chr2:69771159
|
A | G | 1 | a0001c0001t0007g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-46-10361A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771159 | ||||||
| chr2:69771208
|
T | C | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-10312T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771208 | ||||||
| chr2:69771231
|
A | G | 1 | a0002c0002t0010g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-46-10289A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771231 | ||||||
| chr2:69771305
|
C | A | 16 | a0001c0001t0001g0124a0001c0001t0001g0231a0001c0001t0001g0232others(13): Show | 16 | HG00544.hp2 HG00597.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-10215C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771305 | ||||||
| chr2:69771556
|
G | T | 19 | a0001c0001t0001g0031a0001c0001t0001g0224a0001c0001t0006g0008others(16): Show | 19 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-46-9964G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771556 | ||||||
| chr2:69771651
|
C | G | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-9869C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771651 | ||||||
| chr2:69772001
|
G | A | 1 | a0001c0001t0014g0155 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-46-9519G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772001 | ||||||
| chr2:69772121
|
G | A | 1 | a0001c0001t0007g0275 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-46-9399G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772121 | ||||||
| chr2:69772218
|
G | T | 1 | a0001c0001t0012g0183 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-46-9302G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772218 | ||||||
| chr2:69772304
|
A | G | 51 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0207others(48): Show | 53 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-46-9216A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772304 | ||||||
| chr2:69772328
|
A | C | 1 | a0001c0001t0001g0100 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-46-9192A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772328 | ||||||
| chr2:69772366
|
T | A | 17 | a0001c0001t0001g0031a0001c0001t0006g0008a0001c0001t0006g0009others(14): Show | 17 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-46-9154T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772366 | ||||||
| chr2:69772369
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-46-9151C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772369 | ||||||
| chr2:69772441
|
A | G | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-46-9079A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772441 | ||||||
| chr2:69772490
|
G | A | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-9030G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772490 | ||||||
| chr2:69772501
|
CCTTAGCA others(14): Show |
C | 181 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0125others(178): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-46-9016_-46-8996d others(23): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69772501 | |||||
| chr2:69772525
|
G | A | 181 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0125others(178): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-46-8995G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772525 | ||||||
| chr2:69772526
|
T | C | 181 | a0001c0001t0001g0031a0001c0001t0001g0049a0001c0001t0001g0125others(178): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-46-8994T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772526 | ||||||
| chr2:69772542
|
G | A | 5 | a0001c0001t0002g0171a0001c0001t0003g0091a0001c0001t0003g0170others(2): Show | 5 | HG01255.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-8978G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772542 | ||||||
| chr2:69772542
|
G | T | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-8978G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772542 | ||||||
| chr2:69772585
|
C | T | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-8935C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772585 | ||||||
| chr2:69772595
|
T | C | 100 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(97): Show | 101 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-46-8925T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772595 | ||||||
| chr2:69772596
|
T | A | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-8924T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772596 | ||||||
| chr2:69772617
|
G | C | 1 | a0002c0002t0002g0073 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-46-8903G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772617 | ||||||
| chr2:69772632
|
G | A | 1 | a0001c0001t0001g0326 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-46-8888G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772632 | ||||||
| chr2:69772699
|
G | A | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-8821G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772699 | ||||||
| chr2:69772804
|
G | A | 1 | a0001c0001t0003g0159 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-46-8716G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772804 | ||||||
| chr2:69772922
|
C | T | 2 | a0001c0001t0003g0162a0001c0001t0003g0163 | 2 | NA18747.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-46-8598C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772922 | ||||||
| chr2:69772965
|
C | G | 2 | a0001c0001t0005g0318a0003c0003t0004g0317 | 2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-46-8555C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772965 | ||||||
| chr2:69773020
|
AAAAG | A | 48 | a0001c0001t0006g0103a0001c0001t0006g0342a0001c0001t0007g0219others(45): Show | 50 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.-46-8480_-46-8477d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773020 | |||||
| chr2:69773077
|
A | G | 14 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-8443A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773077 | ||||||
| chr2:69773293
|
C | G | 1 | a0001c0001t0007g0276 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-46-8227C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773293 | ||||||
| chr2:69773519
|
A | T | 1 | a0001c0001t0003g0186 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-46-8001A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773519 | ||||||
| chr2:69773614
|
T | C | 3 | a0001c0001t0007g0207a0001c0001t0007g0300a0001c0001t0007g0308 | 3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-7906T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773614 | ||||||
| chr2:69773621
|
C | CT | 30 | a0001c0001t0001g0032a0001c0001t0001g0070a0001c0001t0001g0072others(27): Show | 30 | HG01175.hp2 HG01257.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.-46-7875dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | |||||
| chr2:69773621
|
C | CTT | 6 | a0002c0002t0002g0022a0002c0002t0002g0026a0002c0002t0002g0087others(3): Show | 6 | HG00438.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-7876_-46-7875d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | |||||
| chr2:69773621
|
CT | C | 119 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0139others(116): Show | 120 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.-46-7875delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | |||||
| chr2:69773621
|
CTT | C | 35 | a0001c0001t0003g0158a0001c0001t0006g0012a0001c0001t0006g0304others(32): Show | 35 | HG00423.hp1 HG01256.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.-46-7876_-46-7875d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | |||||
| chr2:69773621
|
CTTT | C | 10 | a0003c0003t0004g0002a0003c0003t0004g0003a0003c0003t0004g0025others(7): Show | 12 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46-7877_-46-7875d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | |||||
| chr2:69773646
|
G | T | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-7874G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773646 | ||||||
| chr2:69773681
|
G | T | 1 | a0001c0001t0001g0049 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-46-7839G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773681 | ||||||
| chr2:69773866
|
G | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-7654G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773866 | ||||||
| chr2:69773881
|
C | T | 1 | a0002c0002t0002g0005 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-46-7639C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773881 | ||||||
| chr2:69773974
|
A | G | 34 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0011g0130others(31): Show | 36 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-46-7546A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773974 | ||||||
| chr2:69774042
|
C | T | 1 | a0001c0001t0005g0029 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-46-7478C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774042 | ||||||
| chr2:69774043
|
G | A | 1 | a0003c0003t0004g0189 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-46-7477G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774043 | ||||||
| chr2:69774112
|
C | G | 19 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0071others(16): Show | 19 | HG02040.hp1 HG02135.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.-46-7408C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774112 | ||||||
| chr2:69774139
|
A | G | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-7381A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774139 | ||||||
| chr2:69774155
|
C | T | 1 | a0003c0003t0016g0325 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-46-7365C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774155 | ||||||
| chr2:69774157
|
T | TCTGTGCC others(3): Show |
1 | a0003c0003t0016g0325 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-46-7363_-46-7362i others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774157 | ||||||
| chr2:69774310
|
G | T | 3 | a0001c0001t0004g0131a0001c0001t0006g0020a0001c0001t0006g0221 | 3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-7210G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774310 | ||||||
| chr2:69774327
|
G | C | 39 | a0001c0001t0006g0012a0001c0001t0006g0342a0002c0002t0002g0064others(36): Show | 41 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-46-7193G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774327 | ||||||
| chr2:69774327
|
GC | G | 61 | a0001c0001t0001g0024a0001c0001t0001g0072a0001c0001t0001g0139others(58): Show | 61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-46-7180delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69774327 | |||||
| chr2:69774327
|
GCC | G | 100 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0070others(97): Show | 101 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-46-7181_-46-7180d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69774327 | |||||
| chr2:69774337
|
C | CT | 6 | a0003c0003t0004g0025a0003c0003t0004g0033a0003c0003t0004g0035others(3): Show | 6 | HG01175.hp1 HG01256.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-7183_-46-7182i others(3): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774337 | ||||||
| chr2:69774337
|
C | T | 34 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(31): Show | 36 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-46-7183C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774337 | ||||||
| chr2:69774338
|
C | G | 1 | a0001c0001t0005g0182 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-46-7182C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774338 | ||||||
| chr2:69774338
|
C | T | 40 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(37): Show | 42 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-46-7182C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774338 | ||||||
| chr2:69774339
|
C | T | 50 | a0001c0001t0005g0211a0001c0001t0006g0012a0001c0001t0006g0342others(47): Show | 52 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-46-7181C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774339 | ||||||
| chr2:69774340
|
C | CT | 24 | a0001c0001t0001g0092a0001c0001t0001g0237a0001c0001t0001g0250others(21): Show | 24 | HG00099.hp1 HG00099.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.-46-7165dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69774340 | |||||
| chr2:69774340
|
C | T | 294 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(291): Show | 298 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(295): Show |
intron_variant | MODIFIER | c.-46-7180C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774340 | ||||||
| chr2:69774354
|
T | C | 1 | a0002c0002t0002g0077 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-46-7166T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774354 | ||||||
| chr2:69774368
|
C | T | 66 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(63): Show | 67 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-46-7152C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774368 | ||||||
| chr2:69774399
|
C | T | 1 | a0001c0001t0005g0314 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-46-7121C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774399 | ||||||
| chr2:69774425
|
G | A | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-7095G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774425 | ||||||
| chr2:69775122
|
A | G | 1 | a0002c0002t0002g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-46-6398A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775122 | ||||||
| chr2:69775248
|
C | T | 1 | a0001c0001t0007g0200 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-46-6272C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775248 | ||||||
| chr2:69775343
|
C | T | 101 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(98): Show | 102 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.-46-6177C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775343 | ||||||
| chr2:69775601
|
G | A | 2 | a0001c0001t0006g0103a0001c0001t0007g0305 | 2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-46-5919G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775601 | ||||||
| chr2:69775878
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-46-5642A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775878 | ||||||
| chr2:69775920
|
G | T | 2 | a0002c0002t0002g0319a0002c0002t0002g0320 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-46-5600G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775920 | ||||||
| chr2:69775939
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-46-5581C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775939 | ||||||
| chr2:69775960
|
AT | A | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-5556delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775960 | |||||
| chr2:69775961
|
T | TTTA | 5 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0015others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-5557_-46-5556i others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTATTTA | 13 | a0001c0001t0006g0105a0001c0001t0006g0114a0001c0001t0006g0126others(10): Show | 13 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-46-5557_-46-5556i others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTATTTA others(4): Show |
3 | a0001c0001t0001g0224a0001c0001t0006g0010a0001c0001t0006g0307 | 3 | HG01109.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-46-5557_-46-5556i others(13): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTTA | 3 | a0001c0001t0001g0278a0002c0002t0002g0303a0003c0003t0004g0058 | 3 | HG01346.hp1 HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-46-5532_-46-5529d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTTATTT others(1): Show |
7 | a0001c0001t0007g0219a0003c0003t0002g0110a0003c0003t0004g0069others(4): Show | 7 | HG01891.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-5536_-46-5529d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTTATTT others(9): Show |
1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-5544_-46-5529d others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTTATTT others(13): Show |
29 | a0002c0002t0002g0064a0003c0003t0004g0002a0003c0003t0004g0003others(26): Show | 31 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-46-5548_-46-5529d others(22): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTTATTT others(17): Show |
2 | a0001c0001t0006g0342a0002c0002t0013g0129 | 2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-46-5552_-46-5529d others(26): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775961
|
T | TTTTATTT others(21): Show |
1 | a0001c0001t0006g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-46-5556_-46-5529d others(30): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | |||||
| chr2:69775991
|
T | TTATTTAT others(14): Show |
1 | a0003c0003t0004g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-5529_-46-5528i others(23): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775991 | ||||||
| chr2:69775992
|
G | A | 1 | a0003c0003t0004g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-5528G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775992 | ||||||
| chr2:69776032
|
G | A | 144 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(141): Show | 147 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-46-5488G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776032 | ||||||
| chr2:69776066
|
G | A | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-46-5454G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776066 | ||||||
| chr2:69776068
|
G | C | 1 | a0001c0001t0003g0186 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-46-5452G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776068 | ||||||
| chr2:69776070
|
G | T | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-5450G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776070 | ||||||
| chr2:69776164
|
T | G | 1 | a0001c0001t0021g0128 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-46-5356T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776164 | ||||||
| chr2:69776212
|
G | A | 3 | a0001c0001t0004g0131a0001c0001t0006g0020a0001c0001t0006g0221 | 3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-5308G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776212 | ||||||
| chr2:69776220
|
C | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-5300C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776220 | ||||||
| chr2:69776433
|
A | T | 2 | a0001c0001t0018g0019a0002c0002t0002g0021 | 2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-5087A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776433 | ||||||
| chr2:69776530
|
T | C | 3 | a0001c0001t0004g0131a0001c0001t0006g0020a0001c0001t0006g0221 | 3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-4990T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776530 | ||||||
| chr2:69776560
|
GT | G | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-4958delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69776560 | |||||
| chr2:69776706
|
C | A | 3 | a0002c0002t0002g0037a0002c0002t0002g0038a0002c0002t0002g0040 | 3 | HG01074.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-46-4814C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776706 | ||||||
| chr2:69776892
|
A | G | 154 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(151): Show | 157 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-46-4628A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776892 | ||||||
| chr2:69777050
|
A | G | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-4470A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777050 | ||||||
| chr2:69777094
|
A | T | 1 | a0001c0001t0003g0190 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-46-4426A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777094 | ||||||
| chr2:69777133
|
G | A | 2 | a0001c0001t0011g0130a0001c0001t0011g0212 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-46-4387G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777133 | ||||||
| chr2:69777146
|
G | T | 154 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(151): Show | 157 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-46-4374G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777146 | ||||||
| chr2:69777149
|
C | T | 14 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-4371C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777149 | ||||||
| chr2:69777158
|
A | C | 2 | a0002c0002t0002g0309a0002c0002t0004g0102 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-46-4362A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777158 | ||||||
| chr2:69777170
|
T | C | 154 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(151): Show | 157 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-46-4350T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777170 | ||||||
| chr2:69777196
|
C | A | 181 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0139others(178): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.-46-4324C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777196 | ||||||
| chr2:69777236
|
T | C | 154 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(151): Show | 157 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.-46-4284T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777236 | ||||||
| chr2:69777269
|
A | G | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-46-4251A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777269 | ||||||
| chr2:69777351
|
C | G | 5 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0015others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-4169C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777351 | ||||||
| chr2:69777400
|
G | C | 1 | a0001c0001t0003g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-46-4120G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777400 | ||||||
| chr2:69777457
|
C | T | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-4063C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777457 | ||||||
| chr2:69777636
|
C | T | 1 | a0002c0002t0002g0005 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-46-3884C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777636 | ||||||
| chr2:69777650
|
C | T | 9 | a0002c0002t0002g0099a0002c0002t0002g0154a0002c0002t0002g0167others(6): Show | 9 | NA18939.hp2 NA18954.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-3870C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777650 | ||||||
| chr2:69777756
|
G | A | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-3764G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777756 | ||||||
| chr2:69777818
|
C | A | 1 | a0001c0001t0001g0264 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-46-3702C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777818 | ||||||
| chr2:69777974
|
A | G | 1 | a0001c0001t0007g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-46-3546A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777974 | ||||||
| chr2:69777988
|
C | G | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-3532C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777988 | ||||||
| chr2:69778041
|
T | G | 66 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(63): Show | 67 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.-46-3479T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778041 | ||||||
| chr2:69778057
|
A | G | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-3463A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778057 | ||||||
| chr2:69778074
|
T | G | 3 | a0002c0002t0002g0303a0002c0002t0002g0312a0002c0002t0002g0313 | 3 | HG01109.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-46-3446T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778074 | ||||||
| chr2:69778269
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-46-3251G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778269 | ||||||
| chr2:69778337
|
G | T | 3 | a0001c0001t0001g0243a0001c0001t0001g0266a0001c0001t0001g0298 | 3 | HG00323.hp2 HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-46-3183G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778337 | ||||||
| chr2:69778412
|
T | C | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-3108T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778412 | ||||||
| chr2:69778563
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-46-2957G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778563 | ||||||
| chr2:69778584
|
T | C | 2 | a0001c0001t0003g0118a0001c0001t0003g0138 | 2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-46-2936T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778584 | ||||||
| chr2:69778623
|
A | C | 103 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(100): Show | 104 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.-46-2897A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778623 | ||||||
| chr2:69778668
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-2852G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778668 | ||||||
| chr2:69778698
|
C | T | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-2822C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778698 | ||||||
| chr2:69778707
|
G | A | 151 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(148): Show | 154 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-46-2813G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778707 | ||||||
| chr2:69778730
|
G | A | 1 | a0001c0001t0003g0146 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-46-2790G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778730 | ||||||
| chr2:69778757
|
G | A | 151 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(148): Show | 154 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-46-2763G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778757 | ||||||
| chr2:69778775
|
C | CA | 22 | a0001c0001t0001g0032a0001c0001t0001g0249a0001c0001t0001g0251others(19): Show | 22 | HG00323.hp1 HG01099.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-46-2717dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778775
|
CA | C | 16 | a0001c0001t0001g0024a0001c0001t0001g0233a0001c0001t0001g0240others(13): Show | 16 | HG01361.hp1 HG01515.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-2717delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778775
|
CAA | C | 7 | a0001c0001t0001g0324a0001c0001t0005g0323a0001c0001t0006g0321others(4): Show | 7 | HG02027.hp2 HG02258.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-2718_-46-2717d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778775
|
CAAA | C | 90 | a0001c0001t0001g0049a0001c0001t0001g0139a0001c0001t0001g0224others(87): Show | 91 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-46-2719_-46-2717d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778775
|
CAAAA | C | 13 | a0001c0001t0001g0125a0001c0001t0003g0185a0001c0001t0006g0008others(10): Show | 13 | HG00558.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-46-2720_-46-2717d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778775
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0003g0179a0001c0001t0003g0234a0001c0001t0003g0291others(1): Show | 4 | HG00597.hp1 NA18943.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-2726_-46-2717d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778775
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0007g0207a0001c0001t0007g0300a0001c0001t0007g0308 | 3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-2727_-46-2717d others(13): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778775
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-46-2728_-46-2717d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | |||||
| chr2:69778806
|
G | A | 1 | a0001c0001t0002g0271 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-46-2714G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778806 | ||||||
| chr2:69778917
|
G | A | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-2603G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778917 | ||||||
| chr2:69779068
|
G | A | 6 | a0001c0001t0003g0152a0001c0001t0003g0209a0001c0001t0003g0210others(3): Show | 6 | NA18939.hp1 NA18987.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-2452G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779068 | ||||||
| chr2:69779107
|
C | CA | 26 | a0001c0001t0001g0030a0001c0001t0001g0045a0001c0001t0001g0070others(23): Show | 26 | HG00323.hp2 HG00673.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46-2387dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | |||||
| chr2:69779107
|
CA | C | 25 | a0001c0001t0001g0139a0001c0001t0001g0236a0001c0001t0001g0254others(22): Show | 25 | HG01070.hp2 HG01261.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-46-2387delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | |||||
| chr2:69779107
|
CAA | C | 52 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0003g0170others(49): Show | 54 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-46-2388_-46-2387d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | |||||
| chr2:69779107
|
CAAA | C | 83 | a0001c0001t0001g0125a0001c0001t0002g0171a0001c0001t0003g0004others(80): Show | 84 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-46-2389_-46-2387d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | |||||
| chr2:69779123
|
A | G | 5 | a0001c0001t0006g0321a0003c0003t0002g0104a0003c0003t0004g0013others(2): Show | 5 | HG02258.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-2397A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779123 | ||||||
| chr2:69779157
|
C | CT | 6 | a0001c0001t0001g0224a0001c0001t0006g0008a0001c0001t0006g0009others(3): Show | 6 | HG01109.hp2 HG01243.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46-2353dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779157 | |||||
| chr2:69779167
|
T | A | 2 | a0001c0001t0001g0274a0005c0005t0007g0006 | 2 | HG02630.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-46-2353T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779167 | ||||||
| chr2:69779231
|
A | T | 151 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(148): Show | 154 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-46-2289A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779231 | ||||||
| chr2:69779677
|
CAAAA | C | 3 | a0001c0001t0007g0207a0001c0001t0007g0300a0001c0001t0007g0308 | 3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-1840_-46-1837d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779677 | |||||
| chr2:69779736
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0262 | 2 | HG02040.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-46-1784C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779736 | ||||||
| chr2:69779866
|
C | T | 50 | a0001c0001t0006g0012a0001c0001t0006g0321a0001c0001t0006g0342others(47): Show | 52 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-46-1654C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779866 | ||||||
| chr2:69779891
|
T | C | 14 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-1629T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779891 | ||||||
| chr2:69779922
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-1598T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779922 | ||||||
| chr2:69779927
|
C | G | 14 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-1593C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779927 | ||||||
| chr2:69779983
|
C | T | 151 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(148): Show | 154 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-46-1537C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779983 | ||||||
| chr2:69780002
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-46-1518T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780002 | ||||||
| chr2:69780128
|
TG | T | 41 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(38): Show | 43 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-46-1388delG | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69780128 | |||||
| chr2:69780225
|
C | T | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.-46-1295C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780225 | ||||||
| chr2:69780263
|
T | C | 46 | a0001c0001t0006g0012a0001c0001t0006g0321a0001c0001t0006g0342others(43): Show | 48 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.-46-1257T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780263 | ||||||
| chr2:69780266
|
C | T | 1 | a0001c0001t0003g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-46-1254C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780266 | ||||||
| chr2:69780338
|
G | A | 1 | a0002c0002t0002g0187 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-46-1182G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780338 | ||||||
| chr2:69780364
|
T | G | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-1156T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780364 | ||||||
| chr2:69780384
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-1136T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780384 | ||||||
| chr2:69780407
|
G | C | 1 | a0001c0001t0003g0190 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-46-1113G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780407 | ||||||
| chr2:69780424
|
G | C | 5 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0015others(2): Show | 5 | HG01243.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-1096G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780424 | ||||||
| chr2:69780455
|
T | C | 147 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(144): Show | 150 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(147): Show |
intron_variant | MODIFIER | c.-46-1065T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780455 | ||||||
| chr2:69780563
|
A | G | 2 | a0001c0001t0006g0020a0001c0001t0006g0221 | 2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-957A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780563 | ||||||
| chr2:69780612
|
C | T | 41 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(38): Show | 43 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-46-908C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780612 | ||||||
| chr2:69780656
|
C | T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-46-864C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780656 | ||||||
| chr2:69780708
|
C | T | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-812C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780708 | ||||||
| chr2:69781307
|
A | C | 1 | a0003c0003t0004g0025 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-213A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781307 | ||||||
| chr2:69781354
|
A | G | 5 | a0001c0001t0003g0152a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | NA18939.hp1 NA18987.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-166A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781354 | ||||||
| chr2:69781360
|
C | G | 17 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(14): Show | 17 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-160C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781360 | ||||||
| chr2:69781429
|
C | T | 41 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(38): Show | 43 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-46-91C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781429 | ||||||
| chr2:69781475
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0289 | 2 | NA18950.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-46-45G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781475 | ||||||
| chr2:69781903
|
G | T | 104 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(101): Show | 105 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(102): Show |
intron_variant | MODIFIER | c.9+329G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69781903 | ||||||
| chr2:69781926
|
C | A | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9+352C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69781926 | ||||||
| chr2:69782050
|
T | C | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+476T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782050 | ||||||
| chr2:69782337
|
C | A | 1 | a0001c0001t0001g0194 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.9+763C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782337 | ||||||
| chr2:69782356
|
A | T | 1 | a0001c0001t0006g0015 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.9+782A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782356 | ||||||
| chr2:69782508
|
A | T | 180 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0139others(177): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.9+934A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782508 | ||||||
| chr2:69782509
|
A | T | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.9+935A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782509 | ||||||
| chr2:69782702
|
T | G | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.9+1128T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782702 | ||||||
| chr2:69782740
|
C | T | 1 | a0002c0002t0002g0303 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9+1166C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782740 | ||||||
| chr2:69782819
|
C | T | 106 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(103): Show | 107 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.9+1245C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782819 | ||||||
| chr2:69782890
|
T | TA | 180 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0139others(177): Show | 183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.9+1316_9+1317insA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782890 | ||||||
| chr2:69782935
|
G | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.9+1361G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782935 | ||||||
| chr2:69783110
|
T | C | 1 | a0001c0001t0006g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.9+1536T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783110 | ||||||
| chr2:69783215
|
A | G | 1 | a0001c0001t0007g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9+1641A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783215 | ||||||
| chr2:69783219
|
T | C | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.9+1645T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783219 | ||||||
| chr2:69783260
|
C | A | 1 | a0002c0002t0002g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.9+1686C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783260 | ||||||
| chr2:69783304
|
G | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.9+1730G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783304 | ||||||
| chr2:69783321
|
T | C | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9+1747T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783321 | ||||||
| chr2:69783494
|
C | T | 74 | a0001c0001t0001g0139a0001c0001t0002g0271a0001c0001t0003g0152others(71): Show | 76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.9+1920C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783494 | ||||||
| chr2:69783984
|
G | T | 2 | a0002c0002t0002g0309a0002c0002t0004g0102 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.9+2410G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783984 | ||||||
| chr2:69784184
|
T | C | 179 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0139others(176): Show | 182 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.9+2610T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784184 | ||||||
| chr2:69784208
|
T | C | 5 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(2): Show | 5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+2634T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784208 | ||||||
| chr2:69784290
|
TA | T | 29 | a0001c0001t0001g0139a0001c0001t0002g0271a0001c0001t0003g0152others(26): Show | 29 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.9+2719delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69784290 | |||||
| chr2:69784294
|
C | T | 4 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0188others(1): Show | 4 | NA18945.hp1 NA18998.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.9+2720C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784294 | ||||||
| chr2:69784314
|
C | A | 2 | a0001c0001t0006g0321a0003c0003t0002g0104 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9+2740C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784314 | ||||||
| chr2:69784377
|
G | A | 21 | a0001c0001t0002g0271a0001c0001t0003g0152a0001c0001t0003g0209others(18): Show | 21 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.9+2803G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784377 | ||||||
| chr2:69784566
|
G | A | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.9+2992G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784566 | ||||||
| chr2:69784653
|
G | T | 20 | a0001c0001t0002g0271a0001c0001t0003g0152a0001c0001t0003g0209others(17): Show | 20 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.9+3079G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784653 | ||||||
| chr2:69784707
|
G | A | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3133G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784707 | ||||||
| chr2:69784726
|
A | G | 1 | a0002c0002t0002g0052 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.9+3152A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784726 | ||||||
| chr2:69784744
|
G | C | 1 | a0001c0001t0003g0121 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.9+3170G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784744 | ||||||
| chr2:69784744
|
G | T | 73 | a0001c0001t0001g0139a0001c0001t0002g0271a0001c0001t0003g0152others(70): Show | 75 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.9+3170G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784744 | ||||||
| chr2:69784820
|
G | C | 82 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(79): Show | 83 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.10-3234G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784820 | ||||||
| chr2:69784838
|
C | A | 3 | a0001c0001t0007g0207a0001c0001t0007g0300a0001c0001t0007g0308 | 3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.10-3216C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784838 | ||||||
| chr2:69784864
|
G | C | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-3190G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784864 | ||||||
| chr2:69784913
|
G | A | 2 | a0001c0001t0007g0207a0003c0003t0004g0069 | 2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.10-3141G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784913 | ||||||
| chr2:69785047
|
G | A | 1 | a0001c0001t0007g0225 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.10-3007G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785047 | ||||||
| chr2:69785119
|
A | T | 100 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(97): Show | 101 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.10-2935A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785119 | ||||||
| chr2:69785197
|
C | T | 1 | a0001c0001t0003g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.10-2857C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785197 | ||||||
| chr2:69785217
|
A | T | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.10-2837A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785217 | ||||||
| chr2:69785297
|
G | A | 1 | a0001c0001t0003g0145 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.10-2757G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785297 | ||||||
| chr2:69785551
|
T | TTGATGAT others(2): Show |
30 | a0001c0001t0003g0004a0001c0001t0003g0137a0001c0001t0003g0142others(27): Show | 31 | HG00642.hp1 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.10-2482_10-2474dup others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | |||||
| chr2:69785551
|
T | TTGATGAT others(5): Show |
85 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(82): Show | 85 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.10-2485_10-2474dup others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | |||||
| chr2:69785551
|
T | TTGATGAT others(8): Show |
30 | a0001c0001t0003g0122a0001c0001t0003g0173a0001c0001t0006g0012others(27): Show | 32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.10-2488_10-2474dup others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | |||||
| chr2:69785551
|
T | TTGATGAT others(11): Show |
26 | a0001c0001t0001g0139a0001c0001t0002g0271a0001c0001t0003g0152others(23): Show | 26 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.10-2491_10-2474dup others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | |||||
| chr2:69785551
|
T | TTGATGAT others(14): Show |
3 | a0001c0001t0005g0150a0001c0001t0011g0130a0001c0001t0011g0212 | 3 | HG00423.hp2 HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.10-2494_10-2474dup others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | |||||
| chr2:69785634
|
A | C | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.10-2420A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785634 | ||||||
| chr2:69785801
|
C | A | 81 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0002g0171others(78): Show | 82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.10-2253C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785801 | ||||||
| chr2:69786041
|
T | C | 3 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0304 | 3 | HG02559.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.10-2013T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786041 | ||||||
| chr2:69786045
|
G | A | 2 | a0002c0002t0002g0022a0002c0002t0002g0134 | 2 | HG00438.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.10-2009G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786045 | ||||||
| chr2:69786059
|
C | A | 80 | a0001c0001t0001g0139a0001c0001t0002g0271a0001c0001t0003g0152others(77): Show | 82 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.10-1995C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786059 | ||||||
| chr2:69786145
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.10-1909C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786145 | ||||||
| chr2:69786538
|
T | C | 1 | a0002c0002t0002g0005 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10-1516T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786538 | ||||||
| chr2:69786543
|
A | G | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-1511A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786543 | ||||||
| chr2:69786601
|
A | G | 81 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-1453A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786601 | ||||||
| chr2:69786744
|
C | T | 2 | a0001c0001t0011g0130a0001c0001t0011g0212 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.10-1310C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786744 | ||||||
| chr2:69786761
|
G | A | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-1293G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786761 | ||||||
| chr2:69786861
|
A | G | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-1193A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786861 | ||||||
| chr2:69787001
|
T | C | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-1053T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787001 | ||||||
| chr2:69787031
|
T | C | 2 | a0002c0002t0002g0112a0002c0002t0002g0117 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.10-1023T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787031 | ||||||
| chr2:69787120
|
A | G | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-934A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787120 | ||||||
| chr2:69787168
|
T | C | 1 | a0001c0001t0003g0165 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.10-886T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787168 | ||||||
| chr2:69787169
|
A | G | 1 | a0002c0002t0002g0056 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.10-885A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787169 | ||||||
| chr2:69787195
|
G | A | 1 | a0001c0001t0003g0017 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10-859G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787195 | ||||||
| chr2:69787356
|
ATC | A | 177 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(174): Show | 179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.10-688_10-687delCT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69787356 | |||||
| chr2:69787429
|
G | C | 97 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(94): Show | 98 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.10-625G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787429 | ||||||
| chr2:69787578
|
G | A | 76 | a0001c0001t0001g0049a0001c0001t0002g0171a0001c0001t0003g0004others(73): Show | 77 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.10-476G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787578 | ||||||
| chr2:69787597
|
C | G | 3 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0304 | 3 | HG02559.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.10-457C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787597 | ||||||
| chr2:69787824
|
A | G | 2 | a0001c0001t0003g0145a0001c0001t0008g0144 | 2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.10-230A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787824 | ||||||
| chr2:69787854
|
T | C | 81 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-200T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787854 | ||||||
| chr2:69787888
|
C | T | 1 | a0001c0001t0007g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.10-166C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787888 | ||||||
| chr2:69787894
|
C | T | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-160C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787894 | ||||||
| chr2:69787976
|
A | G | 11 | a0002c0002t0001g0268a0002c0002t0002g0037a0002c0002t0002g0038others(8): Show | 11 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.10-78A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787976 | ||||||
| chr2:69787981
|
T | A | 1 | a0001c0001t0001g0262 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.10-73T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787981 | ||||||
| chr2:69788049
|
C | T | 95 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(92): Show | 96 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(93): Show |
splice_region_variant&intron_variant | LOW | c.10-5C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69788049 | ||||||
| chr2:69788311
|
G | A | 1 | a0001c0001t0007g0044 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.97+170G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788311 | ||||||
| chr2:69788359
|
A | G | 178 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(175): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.97+218A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788359 | ||||||
| chr2:69788497
|
G | A | 97 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(94): Show | 98 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.97+356G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788497 | ||||||
| chr2:69788565
|
C | T | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+424C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788565 | ||||||
| chr2:69788649
|
A | G | 81 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+508A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788649 | ||||||
| chr2:69788653
|
C | T | 43 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(40): Show | 45 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.97+512C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788653 | ||||||
| chr2:69788699
|
G | A | 81 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+558G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788699 | ||||||
| chr2:69788707
|
G | A | 95 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(92): Show | 96 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.97+566G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788707 | ||||||
| chr2:69788755
|
G | A | 1 | a0001c0001t0008g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.97+614G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788755 | ||||||
| chr2:69788810
|
G | C | 2 | a0001c0001t0005g0316a0001c0001t0007g0315 | 2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.97+669G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788810 | ||||||
| chr2:69788837
|
C | CA | 8 | a0001c0001t0006g0103a0003c0003t0004g0013a0003c0003t0004g0014others(5): Show | 8 | HG01891.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+713dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69788837 | |||||
| chr2:69788837
|
CA | C | 174 | a0001c0001t0001g0049a0001c0001t0001g0125a0001c0001t0001g0224others(171): Show | 176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.97+713delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69788837 | |||||
| chr2:69788896
|
G | A | 43 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(40): Show | 45 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.97+755G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788896 | ||||||
| chr2:69788921
|
C | T | 95 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(92): Show | 96 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.97+780C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788921 | ||||||
| chr2:69789067
|
C | T | 1 | a0003c0003t0004g0123 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.97+926C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789067 | ||||||
| chr2:69789339
|
G | C | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+1198G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789339 | ||||||
| chr2:69789341
|
G | T | 1 | a0001c0001t0007g0225 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.97+1200G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789341 | ||||||
| chr2:69789392
|
G | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.97+1251G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789392 | ||||||
| chr2:69789587
|
C | T | 1 | a0001c0001t0006g0321 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.97+1446C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789587 | ||||||
| chr2:69789779
|
A | T | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+1638A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789779 | ||||||
| chr2:69789809
|
C | T | 1 | a0001c0001t0003g0229 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.97+1668C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789809 | ||||||
| chr2:69789838
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.97+1697G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789838 | ||||||
| chr2:69789890
|
A | G | 178 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(175): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.97+1749A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789890 | ||||||
| chr2:69789925
|
G | A | 20 | a0001c0001t0002g0271a0001c0001t0003g0152a0001c0001t0003g0209others(17): Show | 20 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+1784G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789925 | ||||||
| chr2:69789971
|
G | T | 97 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(94): Show | 98 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.97+1830G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789971 | ||||||
| chr2:69789972
|
G | A | 2 | a0001c0001t0001g0100a0001c0001t0001g0289 | 2 | NA18950.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.97+1831G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789972 | ||||||
| chr2:69790106
|
T | G | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.97+1965T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790106 | ||||||
| chr2:69790106
|
TTTGAACT others(5): Show |
T | 1 | a0001c0001t0001g0032 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.97+1966_97+1977del others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790106 | ||||||
| chr2:69790211
|
A | C | 1 | a0001c0001t0007g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.97+2070A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790211 | ||||||
| chr2:69790260
|
A | G | 81 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+2119A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790260 | ||||||
| chr2:69790262
|
A | T | 2 | a0002c0002t0002g0222a0002c0002t0002g0223 | 2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.97+2121A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790262 | ||||||
| chr2:69790289
|
G | A | 1 | a0001c0001t0006g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97+2148G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790289 | ||||||
| chr2:69790303
|
A | G | 76 | a0001c0001t0001g0049a0001c0001t0002g0171a0001c0001t0003g0004others(73): Show | 77 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.97+2162A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790303 | ||||||
| chr2:69790389
|
G | A | 1 | a0002c0002t0002g0078 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.97+2248G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790389 | ||||||
| chr2:69790531
|
C | T | 97 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(94): Show | 98 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.97+2390C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790531 | ||||||
| chr2:69790662
|
C | T | 1 | a0002c0002t0002g0087 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.97+2521C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790662 | ||||||
| chr2:69790785
|
T | C | 1 | a0002c0002t0002g0037 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.97+2644T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790785 | ||||||
| chr2:69790809
|
T | C | 1 | a0001c0001t0006g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97+2668T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790809 | ||||||
| chr2:69790907
|
G | C | 1 | a0001c0001t0006g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97+2766G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790907 | ||||||
| chr2:69790910
|
C | T | 1 | a0002c0002t0002g0166 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.97+2769C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790910 | ||||||
| chr2:69791140
|
A | C | 81 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+2999A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791140 | ||||||
| chr2:69791180
|
T | A | 1 | a0001c0001t0001g0030 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.97+3039T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791180 | ||||||
| chr2:69791261
|
A | G | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3120A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791261 | ||||||
| chr2:69791262
|
G | A | 1 | a0002c0002t0010g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97+3121G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791262 | ||||||
| chr2:69791275
|
G | A | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+3134G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791275 | ||||||
| chr2:69791330
|
T | C | 229 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(226): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.97+3189T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791330 | ||||||
| chr2:69791364
|
A | G | 237 | a0001c0001t0001g0049a0001c0001t0001g0139a0001c0001t0001g0224others(234): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.97+3223A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791364 | ||||||
| chr2:69791505
|
G | A | 3 | a0002c0002t0002g0037a0002c0002t0002g0038a0002c0002t0002g0040 | 3 | HG01074.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.97+3364G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791505 | ||||||
| chr2:69791711
|
T | C | 3 | a0002c0002t0002g0011a0002c0002t0002g0115a0002c0002t0002g0116 | 3 | HG02970.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.97+3570T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791711 | ||||||
| chr2:69791995
|
G | A | 229 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(226): Show | 233 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.97+3854G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791995 | ||||||
| chr2:69792035
|
A | G | 1 | a0001c0001t0005g0316 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.97+3894A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792035 | ||||||
| chr2:69792237
|
G | T | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+4096G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792237 | ||||||
| chr2:69792585
|
GT | G | 153 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(150): Show | 156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.97+4453delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69792585 | |||||
| chr2:69792609
|
G | GT | 12 | a0001c0001t0001g0032a0002c0002t0002g0099a0002c0002t0002g0112others(9): Show | 12 | HG03688.hp1 HG04115.hp2 NA18939.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4477dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69792609 | |||||
| chr2:69792619
|
A | T | 74 | a0001c0001t0001g0049a0001c0001t0002g0171a0001c0001t0003g0004others(71): Show | 75 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.97+4478A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792619 | ||||||
| chr2:69792620
|
C | A | 74 | a0001c0001t0001g0049a0001c0001t0002g0171a0001c0001t0003g0004others(71): Show | 75 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.97+4479C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792620 | ||||||
| chr2:69792735
|
T | C | 3 | a0003c0003t0002g0110a0003c0003t0004g0109a0003c0003t0004g0111 | 3 | HG01891.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.97+4594T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792735 | ||||||
| chr2:69792736
|
C | G | 154 | a0001c0001t0001g0049a0001c0001t0001g0224a0001c0001t0002g0171others(151): Show | 157 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.97+4595C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792736 | ||||||
| chr2:69792752
|
T | C | 1 | a0003c0003t0002g0110 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.97+4611T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792752 | ||||||
| chr2:69792999
|
A | G | 4 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(1): Show | 4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+4858A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792999 | ||||||
| chr2:69793020
|
A | G | 1 | a0003c0003t0004g0095 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.97+4879A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793020 | ||||||
| chr2:69793041
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.97+4900C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793041 | ||||||
| chr2:69793044
|
G | C | 1 | a0001c0001t0005g0151 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.97+4903G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793044 | ||||||
| chr2:69793064
|
C | T | 46 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(43): Show | 48 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.97+4923C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793064 | ||||||
| chr2:69793069
|
T | C | 44 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.97+4928T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793069 | ||||||
| chr2:69793078
|
C | T | 44 | a0001c0001t0006g0012a0001c0001t0006g0342a0001c0001t0007g0219others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.97+4937C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793078 | ||||||
| chr2:69793080
|
C | T | 1 | a0001c0001t0005g0150 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.97+4939C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793080 | ||||||
| chr2:69793122
|
C | T | 2 | a0002c0002t0002g0319a0002c0002t0002g0320 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.97+4981C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793122 | ||||||
| chr2:69793156
|
A | G | 1 | a0002c0002t0002g0112 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.97+5015A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793156 | ||||||
| chr2:69793201
|
A | G | 152 | a0001c0001t0001g0049a0001c0001t0002g0171a0001c0001t0003g0004others(149): Show | 155 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.97+5060A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793201 | ||||||
| chr2:69793229
|
C | T | 1 | a0001c0001t0003g0137 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.97+5088C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793229 | ||||||
| chr2:69793250
|
C | CAAAAAAA | 13 | a0001c0001t0003g0135a0001c0001t0003g0234a0001c0001t0005g0027others(10): Show | 13 | HG01167.hp1 HG02486.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.97+5115_97+5121dup others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | |||||
| chr2:69793250
|
C | CAAAAAAA others(1): Show |
132 | a0001c0001t0001g0049a0001c0001t0002g0171a0001c0001t0003g0004others(129): Show | 135 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.97+5114_97+5121dup others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | |||||
| chr2:69793250
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0003g0176a0001c0001t0005g0334a0001c0001t0005g0336others(6): Show | 9 | HG01891.hp1 HG02155.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+5113_97+5121dup others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | |||||
| chr2:69793250
|
C | CAAAAAAA others(3): Show |
3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97+5112_97+5121dup others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | |||||
| chr2:69793262
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97+5121A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793262 | ||||||
| chr2:69793357
|
A | G | 13 | a0001c0001t0004g0131a0001c0001t0006g0010a0001c0001t0006g0016others(10): Show | 13 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+5216A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793357 | ||||||
| chr2:69793400
|
T | C | 2 | a0001c0001t0011g0130a0001c0001t0011g0212 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.97+5259T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793400 | ||||||
| chr2:69793539
|
A | G | 2 | a0001c0001t0003g0174a0001c0001t0008g0119 | 2 | NA18957.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.97+5398A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793539 | ||||||
| chr2:69793552
|
A | G | 4 | a0001c0001t0007g0305a0003c0003t0004g0013a0003c0003t0004g0014others(1): Show | 4 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+5411A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793552 | ||||||
| chr2:69793593
|
T | C | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+5452T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793593 | ||||||
| chr2:69793596
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.97+5455G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793596 | ||||||
| chr2:69793637
|
G | T | 5 | a0001c0001t0006g0126a0002c0002t0002g0021a0002c0002t0002g0303others(2): Show | 5 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+5496G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793637 | ||||||
| chr2:69793638
|
C | T | 156 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(153): Show | 159 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.97+5497C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793638 | ||||||
| chr2:69793645
|
G | C | 57 | a0001c0001t0005g0318a0001c0001t0006g0012a0001c0001t0006g0342others(54): Show | 59 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.97+5504G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793645 | ||||||
| chr2:69793708
|
A | G | 13 | a0001c0001t0005g0318a0001c0001t0007g0207a0001c0001t0007g0300others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+5567A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793708 | ||||||
| chr2:69793760
|
C | T | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.97+5619C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793760 | ||||||
| chr2:69793794
|
G | A | 2 | a0001c0001t0003g0180a0001c0001t0012g0183 | 2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.97+5653G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793794 | ||||||
| chr2:69793833
|
TA | T | 13 | a0001c0001t0005g0318a0001c0001t0007g0207a0001c0001t0007g0300others(10): Show | 13 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+5703delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793833 | |||||
| chr2:69793870
|
A | AC | 256 | a0001c0001t0001g0047a0001c0001t0001g0139a0001c0001t0002g0171others(253): Show | 260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.97+5729_97+5730ins others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793870 | ||||||
| chr2:69793893
|
A | G | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+5752A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793893 | ||||||
| chr2:69794157
|
G | T | 1 | a0001c0001t0005g0318 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.97+6016G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794157 | ||||||
| chr2:69794493
|
GTATGTTA others(8): Show |
G | 45 | a0001c0001t0003g0079a0001c0001t0003g0148a0001c0001t0003g0157others(42): Show | 45 | HG00544.hp1 HG00741.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.97+6381_97+6395del others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794493 | |||||
| chr2:69794493
|
GTATGTTA others(23): Show |
G | 1 | a0001c0001t0006g0304 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97+6366_97+6395del others(30): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794493 | |||||
| chr2:69794493
|
GTATGTTA others(28): Show |
G | 2 | a0001c0001t0006g0008a0001c0001t0006g0009 | 2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.97+6366_97+6400del others(35): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794493 | |||||
| chr2:69794497
|
GTTATGTT others(3): Show |
G | 25 | a0001c0001t0003g0122a0001c0001t0003g0135a0001c0001t0003g0138others(22): Show | 25 | HG00673.hp2 HG01243.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.97+6366_97+6375del others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794497 | |||||
| chr2:69794497
|
GTTATGTT others(18): Show |
G | 3 | a0001c0001t0003g0179a0001c0001t0003g0245a0001c0001t0011g0212 | 3 | HG00597.hp1 HG02280.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.97+6366_97+6390del others(25): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794497 | |||||
| chr2:69794502
|
GTTATA | G | 17 | a0001c0001t0002g0171a0001c0001t0003g0017a0001c0001t0003g0091others(14): Show | 17 | HG00438.hp2 HG00642.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.97+6366_97+6370del others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794502 | |||||
| chr2:69794502
|
GTTATATT others(13): Show |
G | 14 | a0001c0001t0003g0004a0001c0001t0003g0145a0001c0001t0003g0159others(11): Show | 15 | HG02135.hp2 HG02300.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.97+6366_97+6385del others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794502 | |||||
| chr2:69794507
|
A | G | 7 | a0001c0001t0003g0098a0001c0001t0003g0120a0001c0001t0003g0162others(4): Show | 7 | HG00609.hp2 HG02155.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+6366A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794507 | ||||||
| chr2:69794507
|
ATTATGTT others(13): Show |
A | 2 | a0001c0001t0006g0012a0003c0003t0004g0247 | 2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.97+6381_97+6400del others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794507 | |||||
| chr2:69794512
|
GTTATGTT others(3): Show |
G | 15 | a0001c0001t0001g0286a0001c0001t0007g0219a0003c0003t0002g0104others(12): Show | 16 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+6381_97+6390del others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794512 | |||||
| chr2:69794517
|
GTTATA | G | 23 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(20): Show | 24 | HG00738.hp2 HG01106.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.97+6381_97+6385del others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794517 | |||||
| chr2:69794522
|
A | ATTATG | 54 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0071others(51): Show | 54 | HG00099.hp2 HG00597.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.97+6431_97+6435dup others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794522
|
A | ATTATGTT others(3): Show |
57 | a0001c0001t0001g0028a0001c0001t0001g0030a0001c0001t0001g0031others(54): Show | 57 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.97+6426_97+6435dup others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794522
|
A | ATTATGTT others(8): Show |
25 | a0001c0001t0001g0050a0001c0001t0001g0070a0001c0001t0001g0072others(22): Show | 25 | HG00544.hp2 HG01070.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.97+6421_97+6435dup others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794522
|
A | ATTATGTT others(13): Show |
3 | a0001c0001t0001g0326a0001c0001t0005g0149a0001c0001t0007g0200 | 3 | NA19005.hp1 NA19072.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.97+6416_97+6435dup others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794522
|
A | ATTATGTT others(18): Show |
1 | a0001c0001t0001g0295 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97+6411_97+6435dup others(25): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794522
|
A | G | 84 | a0001c0001t0002g0171a0001c0001t0003g0017a0001c0001t0003g0079others(81): Show | 84 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.97+6381A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794522 | ||||||
| chr2:69794522
|
ATTATG | A | 15 | a0001c0001t0005g0023a0002c0002t0002g0001a0002c0002t0002g0021others(12): Show | 16 | HG00438.hp1 HG00609.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+6431_97+6435del others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794522
|
ATTATGTT others(8): Show |
A | 1 | a0002c0002t0002g0051 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97+6421_97+6435del others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794522
|
ATTATGTT others(18): Show |
A | 11 | a0002c0002t0001g0268a0002c0002t0002g0037a0002c0002t0002g0038others(8): Show | 11 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+6411_97+6435del others(25): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | |||||
| chr2:69794601
|
C | T | 5 | a0001c0001t0007g0305a0003c0003t0002g0104a0003c0003t0004g0013others(2): Show | 5 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+6460C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794601 | ||||||
| chr2:69794656
|
G | T | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+6515G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794656 | ||||||
| chr2:69794705
|
G | A | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+6564G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794705 | ||||||
| chr2:69794831
|
A | G | 5 | a0001c0001t0007g0305a0003c0003t0002g0104a0003c0003t0004g0013others(2): Show | 5 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+6690A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794831 | ||||||
| chr2:69794835
|
G | A | 1 | a0001c0001t0007g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97+6694G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794835 | ||||||
| chr2:69794945
|
C | T | 78 | a0001c0001t0004g0131a0001c0001t0005g0318a0001c0001t0006g0008others(75): Show | 80 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.97+6804C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794945 | ||||||
| chr2:69795119
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.97+6978G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795119 | ||||||
| chr2:69795314
|
T | C | 120 | a0001c0001t0002g0171a0001c0001t0006g0012a0001c0001t0006g0114others(117): Show | 123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.97+7173T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795314 | ||||||
| chr2:69795348
|
G | C | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+7207G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795348 | ||||||
| chr2:69795525
|
A | G | 11 | a0001c0001t0006g0010a0001c0001t0006g0016a0001c0001t0006g0105others(8): Show | 11 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+7384A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795525 | ||||||
| chr2:69795654
|
G | A | 5 | a0001c0001t0007g0305a0003c0003t0002g0104a0003c0003t0004g0013others(2): Show | 5 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+7513G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795654 | ||||||
| chr2:69795684
|
C | T | 1 | a0001c0001t0006g0307 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97+7543C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795684 | ||||||
| chr2:69795772
|
C | G | 1 | a0005c0005t0007g0006 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97+7631C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795772 | ||||||
| chr2:69795774
|
T | C | 43 | a0001c0001t0007g0219a0002c0002t0013g0129a0003c0003t0002g0110others(40): Show | 45 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.97+7633T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795774 | ||||||
| chr2:69795786
|
T | C | 1 | a0001c0001t0005g0316 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.97+7645T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795786 | ||||||
| chr2:69796081
|
G | C | 4 | a0001c0001t0006g0321a0002c0002t0002g0021a0002c0002t0002g0312others(1): Show | 4 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+7940G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796081 | ||||||
| chr2:69796111
|
A | G | 1 | a0001c0001t0008g0119 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.97+7970A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796111 | ||||||
| chr2:69796337
|
T | C | 89 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(86): Show | 90 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.97+8196T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796337 | ||||||
| chr2:69796346
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.98-8187G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796346 | ||||||
| chr2:69796364
|
T | A | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-8169T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796364 | ||||||
| chr2:69796411
|
A | G | 1 | a0002c0002t0010g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.98-8122A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796411 | ||||||
| chr2:69796534
|
A | G | 1 | a0003c0003t0004g0301 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98-7999A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796534 | ||||||
| chr2:69796923
|
G | A | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-7610G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796923 | ||||||
| chr2:69796924
|
C | T | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.98-7609C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796924 | ||||||
| chr2:69797001
|
TA | T | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-7530delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69797001 | |||||
| chr2:69797015
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.98-7518A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797015 | ||||||
| chr2:69797128
|
C | T | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-7405C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797128 | ||||||
| chr2:69797159
|
C | T | 1 | a0001c0001t0003g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.98-7374C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797159 | ||||||
| chr2:69797282
|
T | G | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-7251T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797282 | ||||||
| chr2:69797490
|
G | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-7043G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797490 | ||||||
| chr2:69797533
|
A | G | 153 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(150): Show | 156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.98-7000A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797533 | ||||||
| chr2:69797626
|
C | T | 1 | a0001c0001t0001g0031 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.98-6907C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797626 | ||||||
| chr2:69797691
|
G | T | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-6842G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797691 | ||||||
| chr2:69797966
|
T | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-6567T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797966 | ||||||
| chr2:69798007
|
T | C | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-6526T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798007 | ||||||
| chr2:69798033
|
C | A | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-6500C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798033 | ||||||
| chr2:69798086
|
G | A | 1 | a0001c0001t0020g0202 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.98-6447G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798086 | ||||||
| chr2:69798093
|
C | A | 1 | a0001c0001t0001g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.98-6440C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798093 | ||||||
| chr2:69798141
|
G | T | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-6392G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798141 | ||||||
| chr2:69798189
|
A | T | 1 | a0002c0002t0002g0021 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98-6344A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798189 | ||||||
| chr2:69798325
|
A | G | 153 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(150): Show | 156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.98-6208A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798325 | ||||||
| chr2:69798457
|
G | T | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-6076G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798457 | ||||||
| chr2:69798495
|
AG | A | 4 | a0004c0004t0005g0203a0004c0004t0005g0206a0004c0004t0007g0204others(1): Show | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-6035delG | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69798495 | |||||
| chr2:69798576
|
G | T | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-5957G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798576 | ||||||
| chr2:69798605
|
C | T | 79 | a0002c0002t0001g0268a0002c0002t0002g0001a0002c0002t0002g0005others(76): Show | 80 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.98-5928C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798605 | ||||||
| chr2:69798606
|
G | A | 1 | a0001c0001t0003g0185 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.98-5927G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798606 | ||||||
| chr2:69798677
|
G | C | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-5856G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798677 | ||||||
| chr2:69798856
|
G | A | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-5677G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798856 | ||||||
| chr2:69799184
|
CTG | C | 44 | a0001c0001t0007g0219a0003c0003t0002g0104a0003c0003t0002g0110others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-5345_98-5344del others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69799184 | |||||
| chr2:69799224
|
T | C | 1 | a0001c0001t0007g0200 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-5309T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799224 | ||||||
| chr2:69799350
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.98-5183G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799350 | ||||||
| chr2:69799555
|
G | A | 3 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0304 | 3 | HG02559.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-4978G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799555 | ||||||
| chr2:69799676
|
G | A | 44 | a0001c0001t0007g0219a0003c0003t0002g0104a0003c0003t0002g0110others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4857G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799676 | ||||||
| chr2:69799857
|
T | G | 1 | a0001c0001t0006g0012 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.98-4676T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799857 | ||||||
| chr2:69800061
|
CTATT | C | 44 | a0001c0001t0007g0219a0003c0003t0002g0104a0003c0003t0002g0110others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4471_98-4468del others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800061 | ||||||
| chr2:69800067
|
A | C | 44 | a0001c0001t0007g0219a0003c0003t0002g0104a0003c0003t0002g0110others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4466A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800067 | ||||||
| chr2:69800068
|
G | T | 44 | a0001c0001t0007g0219a0003c0003t0002g0104a0003c0003t0002g0110others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4465G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800068 | ||||||
| chr2:69800089
|
A | G | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-4444A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800089 | ||||||
| chr2:69800297
|
G | A | 7 | a0002c0002t0002g0108a0002c0002t0002g0113a0002c0002t0002g0127others(4): Show | 7 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-4236G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800297 | ||||||
| chr2:69800297
|
G | GGTAT | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-4234_98-4233ins others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69800297 | |||||
| chr2:69800319
|
A | C | 1 | a0002c0002t0001g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98-4214A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800319 | ||||||
| chr2:69800354
|
A | G | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-4179A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800354 | ||||||
| chr2:69800664
|
A | G | 24 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(21): Show | 24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.98-3869A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800664 | ||||||
| chr2:69800670
|
T | C | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-3863T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800670 | ||||||
| chr2:69800777
|
G | C | 9 | a0001c0001t0001g0244a0001c0001t0001g0255a0001c0001t0001g0257others(6): Show | 9 | HG00597.hp2 HG02523.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-3756G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800777 | ||||||
| chr2:69800787
|
C | T | 11 | a0001c0001t0003g0148a0002c0002t0001g0268a0002c0002t0002g0037others(8): Show | 11 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-3746C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800787 | ||||||
| chr2:69800864
|
A | G | 1 | a0002c0002t0001g0268 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98-3669A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800864 | ||||||
| chr2:69800963
|
G | T | 1 | a0002c0002t0002g0053 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.98-3570G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800963 | ||||||
| chr2:69801119
|
C | T | 24 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(21): Show | 24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.98-3414C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801119 | ||||||
| chr2:69801321
|
A | G | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.98-3212A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801321 | ||||||
| chr2:69801403
|
G | GT | 127 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(124): Show | 130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-3120dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69801403 | |||||
| chr2:69801450
|
T | A | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.98-3083T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801450 | ||||||
| chr2:69801498
|
G | A | 1 | a0003c0003t0004g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.98-3035G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801498 | ||||||
| chr2:69801726
|
A | C | 15 | a0001c0001t0006g0010a0001c0001t0006g0012a0001c0001t0006g0016others(12): Show | 15 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.98-2807A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801726 | ||||||
| chr2:69801751
|
C | T | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-2782C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801751 | ||||||
| chr2:69801772
|
A | G | 153 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(150): Show | 156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.98-2761A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801772 | ||||||
| chr2:69801844
|
A | G | 82 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(79): Show | 83 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.98-2689A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801844 | ||||||
| chr2:69801943
|
C | T | 1 | a0002c0002t0010g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.98-2590C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801943 | ||||||
| chr2:69801994
|
C | A | 1 | a0002c0002t0002g0041 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.98-2539C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801994 | ||||||
| chr2:69802178
|
A | G | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-2355A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802178 | ||||||
| chr2:69802495
|
A | G | 226 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(223): Show | 230 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.98-2038A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802495 | ||||||
| chr2:69802571
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0262 | 2 | HG02040.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.98-1962C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802571 | ||||||
| chr2:69802680
|
C | T | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-1853C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802680 | ||||||
| chr2:69802709
|
C | CA | 16 | a0001c0001t0001g0032a0001c0001t0001g0270a0001c0001t0006g0008others(13): Show | 16 | HG02280.hp2 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-1807dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | |||||
| chr2:69802709
|
C | CAA | 65 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0011others(62): Show | 66 | HG00438.hp1 HG00609.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.98-1808_98-1807dup others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | |||||
| chr2:69802709
|
CA | C | 7 | a0001c0001t0001g0100a0001c0001t0001g0261a0001c0001t0001g0272others(4): Show | 7 | HG01070.hp1 HG01167.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-1807delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | |||||
| chr2:69802709
|
CAA | C | 126 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(123): Show | 129 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.98-1808_98-1807del others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | |||||
| chr2:69802830
|
T | C | 226 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(223): Show | 230 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.98-1703T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802830 | ||||||
| chr2:69802841
|
C | T | 2 | a0001c0001t0003g0174a0001c0001t0008g0119 | 2 | NA18957.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.98-1692C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802841 | ||||||
| chr2:69802977
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.98-1556G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802977 | ||||||
| chr2:69803070
|
A | G | 226 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(223): Show | 230 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.98-1463A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803070 | ||||||
| chr2:69803137
|
G | A | 25 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.98-1396G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803137 | ||||||
| chr2:69803230
|
A | G | 1 | a0003c0003t0004g0331 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.98-1303A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803230 | ||||||
| chr2:69803321
|
G | A | 2 | a0003c0003t0004g0109a0003c0003t0004g0111 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.98-1212G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803321 | ||||||
| chr2:69803337
|
C | G | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-1196C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803337 | ||||||
| chr2:69803402
|
C | T | 6 | a0001c0001t0005g0323a0001c0001t0005g0327a0001c0001t0005g0328others(3): Show | 6 | NA18961.hp2 NA18965.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-1131C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803402 | ||||||
| chr2:69803695
|
C | T | 226 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(223): Show | 230 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(227): Show |
intron_variant | MODIFIER | c.98-838C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803695 | ||||||
| chr2:69803717
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.98-816A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803717 | ||||||
| chr2:69803773
|
A | G | 128 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(125): Show | 131 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.98-760A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803773 | ||||||
| chr2:69803855
|
T | A | 1 | a0001c0001t0001g0261 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.98-678T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803855 | ||||||
| chr2:69803864
|
G | A | 25 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.98-669G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803864 | ||||||
| chr2:69803878
|
A | G | 291 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(288): Show | 295 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.98-655A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803878 | ||||||
| chr2:69803904
|
G | A | 1 | a0001c0001t0003g0246 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-629G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803904 | ||||||
| chr2:69803921
|
T | A | 1 | a0001c0001t0003g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.98-612T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803921 | ||||||
| chr2:69804093
|
G | A | 2 | a0001c0001t0006g0010a0001c0001t0006g0321 | 2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.98-440G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804093 | ||||||
| chr2:69804137
|
C | CA | 65 | a0001c0001t0001g0261a0001c0001t0001g0272a0001c0001t0007g0225others(62): Show | 66 | HG00438.hp1 HG00609.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.98-374dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | |||||
| chr2:69804137
|
CA | C | 7 | a0001c0001t0001g0028a0001c0001t0001g0147a0001c0001t0001g0241others(4): Show | 7 | HG03834.hp2 HG03927.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-374delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | |||||
| chr2:69804137
|
CAA | C | 78 | a0001c0001t0002g0171a0001c0001t0003g0004a0001c0001t0003g0017others(75): Show | 79 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.98-375_98-374delAA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | |||||
| chr2:69804137
|
CAAA | C | 6 | a0001c0001t0003g0121a0001c0001t0003g0185a0001c0001t0003g0242others(3): Show | 6 | HG02922.hp2 HG03209.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-376_98-374delAA others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | |||||
| chr2:69804137
|
CAAAA | C | 44 | a0001c0001t0007g0219a0001c0001t0007g0305a0003c0003t0002g0104others(41): Show | 46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-377_98-374delAA others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | |||||
| chr2:69804159
|
A | AAAAC | 10 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(7): Show | 10 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-374_98-373insAA others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804159 | ||||||
| chr2:69804159
|
A | AAAC | 13 | a0001c0001t0006g0010a0001c0001t0006g0012a0001c0001t0006g0020others(10): Show | 13 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-374_98-373insAA others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804159 | ||||||
| chr2:69804159
|
A | C | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-374A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804159 | ||||||
| chr2:69804257
|
G | A | 2 | a0003c0003t0004g0063a0003c0003t0004g0066 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.98-276G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804257 | ||||||
| chr2:69804637
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.192+10A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69804637 | ||||||
| chr2:69804665
|
C | G | 250 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(247): Show | 254 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.192+38C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69804665 | ||||||
| chr2:69804809
|
A | G | 250 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(247): Show | 254 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.192+182A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69804809 | ||||||
| chr2:69805013
|
C | T | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+386C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805013 | ||||||
| chr2:69805046
|
C | CA | 50 | a0001c0001t0001g0072a0001c0001t0001g0233a0001c0001t0001g0267others(47): Show | 52 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.192+445dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | |||||
| chr2:69805046
|
C | CAA | 15 | a0001c0001t0003g0079a0001c0001t0003g0157a0001c0001t0003g0158others(12): Show | 15 | HG00544.hp1 HG01074.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+444_192+445dup others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | |||||
| chr2:69805046
|
C | CAAA | 146 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(143): Show | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.192+443_192+445dup others(3): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | |||||
| chr2:69805046
|
C | CAAAA | 23 | a0001c0001t0003g0120a0001c0001t0003g0143a0001c0001t0003g0148others(20): Show | 23 | HG00673.hp2 HG01433.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+442_192+445dup others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | |||||
| chr2:69805046
|
CAAAAAAA | C | 9 | a0001c0001t0006g0016a0001c0001t0006g0105a0001c0001t0006g0114others(6): Show | 9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+439_192+445del others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | |||||
| chr2:69805049
|
A | G | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+422A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805049 | ||||||
| chr2:69805128
|
TCTGACCC others(10): Show |
T | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+502_192+518del others(17): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805128 | ||||||
| chr2:69805146
|
G | A | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+519G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805146 | ||||||
| chr2:69805184
|
C | T | 99 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(96): Show | 100 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.192+557C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805184 | ||||||
| chr2:69805353
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.192+726T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805353 | ||||||
| chr2:69805420
|
A | G | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+793A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805420 | ||||||
| chr2:69805475
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.192+848G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805475 | ||||||
| chr2:69805478
|
C | T | 2 | a0001c0001t0011g0130a0001c0001t0011g0212 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.192+851C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805478 | ||||||
| chr2:69805480
|
C | G | 2 | a0001c0001t0011g0130a0001c0001t0011g0212 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.192+853C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805480 | ||||||
| chr2:69805481
|
C | T | 2 | a0001c0001t0011g0130a0001c0001t0011g0212 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.192+854C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805481 | ||||||
| chr2:69805503
|
G | A | 25 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.192+876G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805503 | ||||||
| chr2:69805521
|
G | A | 25 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(22): Show | 25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.193-864G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805521 | ||||||
| chr2:69805528
|
T | C | 2 | a0001c0001t0004g0131a0001c0001t0006g0103 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-857T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805528 | ||||||
| chr2:69805570
|
C | T | 99 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(96): Show | 100 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.193-815C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805570 | ||||||
| chr2:69805579
|
C | G | 1 | a0001c0001t0003g0174 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.193-806C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805579 | ||||||
| chr2:69805604
|
T | TA | 71 | a0001c0001t0003g0148a0001c0001t0004g0131a0001c0001t0006g0008others(68): Show | 73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.193-765dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805604 | |||||
| chr2:69805621
|
G | A | 1 | a0002c0002t0002g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.193-764G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805621 | ||||||
| chr2:69805622
|
A | G | 1 | a0002c0002t0002g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.193-763A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805622 | ||||||
| chr2:69805709
|
A | G | 1 | a0001c0001t0003g0210 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.193-676A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805709 | ||||||
| chr2:69805735
|
A | G | 100 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(97): Show | 101 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.193-650A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805735 | ||||||
| chr2:69805909
|
C | T | 1 | a0002c0002t0010g0220 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.193-476C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805909 | ||||||
| chr2:69806517
|
G | A | 100 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.306+19G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806517 | ||||||
| chr2:69806579
|
G | C | 151 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(148): Show | 154 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.306+81G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806579 | ||||||
| chr2:69806663
|
A | T | 100 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(97): Show | 101 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.306+165A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806663 | ||||||
| chr2:69806870
|
T | A | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.306+372T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806870 | ||||||
| chr2:69806877
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.306+379A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806877 | ||||||
| chr2:69806948
|
A | T | 1 | a0002c0002t0002g0218 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.306+450A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806948 | ||||||
| chr2:69807251
|
T | C | 1 | a0001c0001t0003g0146 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.307-655T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807251 | ||||||
| chr2:69807311
|
T | C | 5 | a0001c0001t0003g0152a0001c0001t0003g0209a0001c0001t0003g0210others(2): Show | 5 | NA18939.hp1 NA18987.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-595T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807311 | ||||||
| chr2:69807333
|
G | C | 99 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(96): Show | 100 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.307-573G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807333 | ||||||
| chr2:69807358
|
C | T | 2 | a0001c0001t0006g0020a0001c0001t0006g0221 | 2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.307-548C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807358 | ||||||
| chr2:69807661
|
A | G | 247 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(244): Show | 251 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(248): Show |
intron_variant | MODIFIER | c.307-245A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807661 | ||||||
| chr2:69807818
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.307-88A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807818 | ||||||
| chr2:69807882
|
C | T | 2 | a0002c0002t0002g0222a0002c0002t0002g0223 | 2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.307-24C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807882 | ||||||
| chr2:69808020
|
T | C | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+24T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808020 | ||||||
| chr2:69808042
|
A | G | 2 | a0001c0001t0004g0131a0001c0001t0006g0103 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.397+46A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808042 | ||||||
| chr2:69808061
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.397+65G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808061 | ||||||
| chr2:69808153
|
C | G | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.397+157C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808153 | ||||||
| chr2:69808350
|
C | G | 76 | a0001c0001t0001g0045a0001c0001t0001g0081a0001c0001t0001g0125others(73): Show | 77 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.397+354C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808350 | ||||||
| chr2:69808406
|
G | A | 3 | a0002c0002t0002g0037a0002c0002t0002g0038a0002c0002t0002g0040 | 3 | HG01074.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.397+410G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808406 | ||||||
| chr2:69808486
|
C | T | 1 | a0002c0002t0002g0269 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.397+490C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808486 | ||||||
| chr2:69808670
|
C | CT | 9 | a0003c0003t0002g0104a0003c0003t0002g0110a0003c0003t0004g0069others(6): Show | 9 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+683dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 69808670 | |||||
| chr2:69808912
|
T | C | 11 | a0001c0001t0005g0027a0001c0001t0005g0029a0001c0001t0005g0323others(8): Show | 11 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+916T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808912 | ||||||
| chr2:69809081
|
T | G | 4 | a0002c0002t0002g0089a0002c0002t0002g0090a0002c0002t0002g0340others(1): Show | 4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1085T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809081 | ||||||
| chr2:69809156
|
T | C | 24 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(21): Show | 24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.397+1160T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809156 | ||||||
| chr2:69809311
|
A | G | 1 | a0001c0001t0018g0019 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.398-1283A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809311 | ||||||
| chr2:69809418
|
G | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.398-1176G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809418 | ||||||
| chr2:69809579
|
A | G | 246 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(243): Show | 250 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.398-1015A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809579 | ||||||
| chr2:69809906
|
C | T | 24 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(21): Show | 24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.398-688C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809906 | ||||||
| chr2:69809992
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.398-602C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809992 | ||||||
| chr2:69810002
|
G | C | 2 | a0001c0001t0005g0318a0001c0001t0007g0207 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.398-592G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810002 | ||||||
| chr2:69810065
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.398-529C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810065 | ||||||
| chr2:69810359
|
G | T | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.398-235G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810359 | ||||||
| chr2:69810534
|
G | A | 1 | a0003c0003t0004g0061 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.398-60G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810534 | ||||||
| chr2:69810708
|
T | G | 1 | a0002c0002t0002g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.477+35T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69810708 | ||||||
| chr2:69811046
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.477+373G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811046 | ||||||
| chr2:69811066
|
A | G | 49 | a0001c0001t0017g0337a0003c0003t0002g0104a0003c0003t0002g0110others(46): Show | 51 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.477+393A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811066 | ||||||
| chr2:69811100
|
C | G | 248 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(245): Show | 252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.477+427C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811100 | ||||||
| chr2:69811179
|
A | C | 24 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(21): Show | 24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.477+506A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811179 | ||||||
| chr2:69811256
|
G | A | 8 | a0001c0001t0001g0047a0001c0001t0001g0070a0001c0001t0001g0071others(5): Show | 8 | HG02040.hp1 NA18950.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.477+583G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811256 | ||||||
| chr2:69811275
|
G | A | 1 | a0001c0001t0011g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.477+602G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811275 | ||||||
| chr2:69811660
|
A | C | 221 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(218): Show | 225 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.477+987A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811660 | ||||||
| chr2:69811733
|
A | T | 5 | a0001c0001t0003g0091a0001c0001t0003g0118a0001c0001t0003g0138others(2): Show | 5 | HG01255.hp2 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-920A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811733 | ||||||
| chr2:69811794
|
C | T | 3 | a0001c0001t0007g0300a0001c0001t0007g0308a0005c0005t0007g0006 | 3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.478-859C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811794 | ||||||
| chr2:69812092
|
C | T | 249 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(246): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.478-561C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812092 | ||||||
| chr2:69812094
|
A | T | 7 | a0003c0003t0002g0104a0003c0003t0004g0069a0003c0003t0004g0107others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-559A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812094 | ||||||
| chr2:69812121
|
CT | C | 74 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(71): Show | 75 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.478-514delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 69812121 | |||||
| chr2:69812131
|
T | G | 98 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(95): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.478-522T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812131 | ||||||
| chr2:69812223
|
G | C | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.478-430G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812223 | ||||||
| chr2:69812272
|
G | A | 4 | a0004c0004t0005g0203a0004c0004t0005g0206a0004c0004t0007g0204others(1): Show | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-381G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812272 | ||||||
| chr2:69812277
|
C | A | 14 | a0001c0001t0006g0010a0001c0001t0006g0016a0001c0001t0006g0020others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-376C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812277 | ||||||
| chr2:69812277
|
C | G | 1 | a0002c0002t0002g0076 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.478-376C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812277 | ||||||
| chr2:69812496
|
G | A | 1 | a0001c0001t0001g0100 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.478-157G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812496 | ||||||
| chr2:69812496
|
G | C | 1 | a0005c0005t0007g0006 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.478-157G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812496 | ||||||
| chr2:69812545
|
A | C | 249 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(246): Show | 253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.478-108A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812545 | ||||||
| chr2:69812643
|
T | C | 1 | a0001c0001t0017g0337 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.478-10T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812643 | ||||||
| chr2:69812902
|
T | A | 1 | a0002c0002t0002g0187 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.534+193T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69812902 | ||||||
| chr2:69813012
|
C | T | 71 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(68): Show | 73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.534+303C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813012 | ||||||
| chr2:69813015
|
T | C | 103 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(100): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.534+306T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813015 | ||||||
| chr2:69813162
|
A | G | 2 | a0003c0003t0004g0109a0003c0003t0004g0111 | 2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.534+453A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813162 | ||||||
| chr2:69813191
|
C | T | 71 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(68): Show | 73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.534+482C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813191 | ||||||
| chr2:69813249
|
AT | A | 74 | a0001c0001t0001g0147a0001c0001t0001g0233a0001c0001t0001g0297others(71): Show | 76 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.534+556delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813249 | |||||
| chr2:69813410
|
G | A | 180 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(177): Show | 182 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.534+701G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813410 | ||||||
| chr2:69813508
|
C | G | 2 | a0001c0001t0006g0012a0001c0001t0006g0342 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.534+799C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813508 | ||||||
| chr2:69813662
|
A | G | 1 | a0002c0002t0013g0129 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.534+953A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813662 | ||||||
| chr2:69813738
|
TTCTC | T | 13 | a0001c0001t0001g0092a0001c0001t0001g0237a0001c0001t0001g0238others(10): Show | 13 | HG00099.hp2 HG01070.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.534+1047_534+1050d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813738 | |||||
| chr2:69813754
|
CTCTCT | C | 93 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(90): Show | 94 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.534+1047_534+1051d others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813754 | |||||
| chr2:69813757
|
TC | T | 8 | a0001c0001t0006g0126a0002c0002t0002g0078a0002c0002t0002g0115others(5): Show | 8 | HG01257.hp1 HG01257.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+1049delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813757 | ||||||
| chr2:69813758
|
C | T | 138 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0004g0131others(135): Show | 141 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.534+1049C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813758 | ||||||
| chr2:69813758
|
CT | C | 7 | a0001c0001t0001g0024a0001c0001t0001g0233a0001c0001t0001g0279others(4): Show | 7 | HG01515.hp1 HG03017.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+1068delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813758 | |||||
| chr2:69813872
|
C | T | 76 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(73): Show | 77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.534+1163C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813872 | ||||||
| chr2:69813901
|
G | A | 179 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(176): Show | 181 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.534+1192G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813901 | ||||||
| chr2:69814049
|
C | T | 76 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(73): Show | 77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.534+1340C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814049 | ||||||
| chr2:69814145
|
C | CA | 7 | a0002c0002t0002g0218a0003c0003t0004g0069a0003c0003t0004g0107others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+1445dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814145 | |||||
| chr2:69814308
|
G | A | 146 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0004g0131others(143): Show | 149 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.534+1599G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814308 | ||||||
| chr2:69814342
|
C | CT | 52 | a0001c0001t0001g0070a0001c0001t0001g0139a0001c0001t0001g0147others(49): Show | 54 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.534+1654dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | |||||
| chr2:69814342
|
C | CTT | 71 | a0001c0001t0003g0079a0001c0001t0003g0152a0001c0001t0003g0160others(68): Show | 71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.534+1653_534+1654d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | |||||
| chr2:69814342
|
C | CTTT | 120 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(117): Show | 122 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.534+1652_534+1654d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | |||||
| chr2:69814342
|
C | CTTTT | 6 | a0001c0001t0003g0118a0001c0001t0003g0138a0001c0001t0018g0019others(3): Show | 6 | HG01928.hp2 HG01975.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+1651_534+1654d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | |||||
| chr2:69814342
|
CT | C | 9 | a0001c0001t0001g0288a0001c0001t0001g0297a0001c0001t0001g0322others(6): Show | 9 | HG01069.hp2 HG01169.hp2 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1654delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | |||||
| chr2:69814370
|
G | A | 1 | a0003c0003t0004g0069 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.534+1661G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814370 | ||||||
| chr2:69814415
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0072 | 2 | HG02040.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.535-1686G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814415 | ||||||
| chr2:69814597
|
C | T | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1504C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814597 | ||||||
| chr2:69814637
|
C | T | 1 | a0001c0006t0006g0007 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.535-1464C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814637 | ||||||
| chr2:69814652
|
A | T | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1449A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814652 | ||||||
| chr2:69814697
|
A | G | 3 | a0002c0002t0002g0319a0002c0002t0002g0320a0003c0003t0002g0110 | 3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.535-1404A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814697 | ||||||
| chr2:69814726
|
C | A | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1375C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814726 | ||||||
| chr2:69814733
|
G | C | 2 | a0001c0001t0006g0012a0001c0001t0006g0342 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.535-1368G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814733 | ||||||
| chr2:69814743
|
G | GGT | 14 | a0001c0001t0001g0028a0001c0001t0001g0262a0001c0001t0001g0277others(11): Show | 14 | HG00323.hp1 HG00597.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-1308_535-1307d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | |||||
| chr2:69814743
|
G | GGTGT | 9 | a0001c0001t0001g0030a0001c0001t0001g0049a0001c0001t0001g0236others(6): Show | 9 | HG01070.hp2 HG01361.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.535-1310_535-1307d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | |||||
| chr2:69814743
|
G | T | 2 | a0001c0001t0001g0298a0001c0001t0007g0315 | 2 | HG00323.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.535-1358G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814743 | ||||||
| chr2:69814743
|
GGT | G | 19 | a0001c0001t0001g0050a0001c0001t0001g0191a0001c0001t0001g0194others(16): Show | 19 | HG01175.hp2 HG01255.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.535-1308_535-1307d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | |||||
| chr2:69814743
|
GGTGT | G | 18 | a0001c0001t0001g0024a0001c0001t0001g0031a0001c0001t0001g0047others(15): Show | 18 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.535-1310_535-1307d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | |||||
| chr2:69814743
|
GGTGTGT | G | 14 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0092others(11): Show | 14 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-1312_535-1307d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | |||||
| chr2:69814745
|
T | G | 2 | a0001c0001t0005g0323a0001c0006t0006g0007 | 2 | HG02970.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.535-1356T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814745 | ||||||
| chr2:69814746
|
G | A | 1 | a0001c0001t0005g0318 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.535-1355G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814746 | ||||||
| chr2:69814777
|
TGTGTGTG others(17): Show |
T | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.535-1322_535-1299d others(26): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814777 | |||||
| chr2:69814781
|
TGTGTGTG others(7): Show |
T | 2 | a0001c0001t0003g0145a0001c0001t0008g0144 | 2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.535-1318_535-1305d others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814781 | |||||
| chr2:69814782
|
GTGTGTGT others(11): Show |
G | 6 | a0001c0001t0006g0008a0001c0001t0006g0009a0003c0003t0004g0109others(3): Show | 6 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-1318_535-1301d others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814782 | ||||||
| chr2:69814783
|
TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0188 | 3 | NA18945.hp1 NA18998.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.535-1316_535-1305d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814783 | |||||
| chr2:69814783
|
TGTGTGTG others(7): Show |
T | 2 | a0002c0002t0002g0340a0002c0002t0002g0341 | 2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.535-1316_535-1303d others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814783 | |||||
| chr2:69814784
|
GTGTGTGT others(9): Show |
G | 15 | a0001c0001t0006g0010a0001c0001t0006g0012a0001c0001t0006g0016others(12): Show | 15 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-1316_535-1301d others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814784 | ||||||
| chr2:69814785
|
TGTGTGTG others(3): Show |
T | 25 | a0001c0001t0003g0004a0001c0001t0003g0091a0001c0001t0003g0098others(22): Show | 26 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.535-1314_535-1305d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814785 | |||||
| chr2:69814785
|
TGTGTGTG others(5): Show |
T | 2 | a0002c0002t0002g0089a0003c0003t0002g0104 | 2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.535-1314_535-1303d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814785 | |||||
| chr2:69814786
|
GTGTGTGT others(7): Show |
G | 4 | a0001c0001t0006g0020a0001c0001t0006g0221a0001c0001t0006g0304others(1): Show | 4 | HG02922.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1314_535-1301d others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814786 | ||||||
| chr2:69814787
|
TGTGTGTG others(1): Show |
T | 29 | a0001c0001t0003g0017a0001c0001t0003g0137a0001c0001t0003g0142others(26): Show | 29 | HG00642.hp1 HG00741.hp1 HG02129.hp2 others(26): Show |
intron_variant | MODIFIER | c.535-1312_535-1305d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814787 | |||||
| chr2:69814787
|
TGTGTGTG others(3): Show |
T | 18 | a0002c0002t0002g0011a0002c0002t0002g0051a0002c0002t0002g0052others(15): Show | 18 | HG01070.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.535-1312_535-1303d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814787 | |||||
| chr2:69814788
|
GTGTGTGA others(5): Show |
G | 13 | a0001c0001t0011g0130a0003c0003t0004g0035a0003c0003t0004g0036others(10): Show | 13 | HG00423.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.535-1312_535-1301d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814788 | ||||||
| chr2:69814789
|
TGTGTGA | T | 11 | a0001c0001t0003g0079a0001c0001t0003g0120a0001c0001t0003g0122others(8): Show | 11 | HG00673.hp2 HG01496.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.535-1310_535-1305d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814789 | |||||
| chr2:69814789
|
TGTGTGAG others(1): Show |
T | 15 | a0002c0002t0002g0048a0002c0002t0002g0083a0002c0002t0002g0084others(12): Show | 15 | HG02257.hp1 HG02559.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-1310_535-1303d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814789 | |||||
| chr2:69814790
|
GTGTGAGA others(3): Show |
G | 16 | a0003c0003t0004g0002a0003c0003t0004g0003a0003c0003t0004g0025others(13): Show | 18 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.535-1310_535-1301d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814790 | ||||||
| chr2:69814791
|
TGTGA | T | 16 | a0001c0001t0003g0159a0001c0001t0003g0175a0001c0001t0005g0023others(13): Show | 16 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.535-1308_535-1305d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814791 | |||||
| chr2:69814791
|
TGTGAGA | T | 26 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0022others(23): Show | 26 | HG00438.hp1 HG01074.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.535-1308_535-1303d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814791 | |||||
| chr2:69814791
|
TGTGAGAG others(3): Show |
T | 1 | a0001c0001t0006g0103 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.535-1308_535-1299d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814791 | |||||
| chr2:69814792
|
GTGAGAGA others(1): Show |
G | 4 | a0001c0001t0006g0015a0003c0003t0004g0033a0003c0003t0004g0094others(1): Show | 4 | HG01175.hp1 NA18954.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1308_535-1301d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814792 | ||||||
| chr2:69814793
|
T | A | 2 | a0001c0001t0001g0024a0002c0002t0001g0268 | 2 | HG00140.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.535-1308T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814793 | ||||||
| chr2:69814793
|
TGA | T | 7 | a0001c0001t0005g0211a0001c0001t0005g0290a0001c0001t0007g0300others(4): Show | 7 | HG00140.hp1 HG00738.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.535-1303_535-1302d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814793 | |||||
| chr2:69814793
|
TGAGA | T | 9 | a0002c0002t0002g0001a0002c0002t0002g0005a0002c0002t0002g0021others(6): Show | 10 | HG00609.hp1 HG01069.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-1305_535-1302d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814793 | |||||
| chr2:69814794
|
GAGAGAA | G | 6 | a0001c0001t0011g0212a0003c0003t0004g0061a0003c0003t0004g0106others(3): Show | 6 | HG01099.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-1301_535-1296d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814794 | |||||
| chr2:69814795
|
A | T | 17 | a0001c0001t0003g0135a0001c0001t0003g0157a0001c0001t0003g0234others(14): Show | 17 | HG00544.hp1 HG01192.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.535-1306A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814795 | ||||||
| chr2:69814797
|
A | T | 4 | a0002c0002t0002g0053a0002c0002t0002g0073a0002c0002t0002g0166others(1): Show | 4 | HG00140.hp1 HG00738.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1304A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814797 | ||||||
| chr2:69814802
|
G | A | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1299G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814802 | ||||||
| chr2:69814847
|
A | G | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1254A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814847 | ||||||
| chr2:69815086
|
C | G | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1015C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815086 | ||||||
| chr2:69815193
|
C | T | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-908C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815193 | ||||||
| chr2:69815200
|
A | G | 76 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(73): Show | 77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.535-901A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815200 | ||||||
| chr2:69815213
|
T | G | 1 | a0001c0001t0001g0293 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.535-888T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815213 | ||||||
| chr2:69815286
|
A | G | 1 | a0002c0002t0002g0132 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.535-815A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815286 | ||||||
| chr2:69815344
|
G | A | 3 | a0001c0001t0003g0234a0001c0001t0003g0291a0001c0001t0003g0292 | 3 | NA18943.hp2 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.535-757G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815344 | ||||||
| chr2:69815461
|
A | G | 14 | a0001c0001t0006g0010a0001c0001t0006g0016a0001c0001t0006g0020others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-640A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815461 | ||||||
| chr2:69815481
|
A | G | 1 | a0001c0001t0003g0190 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.535-620A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815481 | ||||||
| chr2:69815639
|
G | A | 45 | a0003c0003t0004g0002a0003c0003t0004g0003a0003c0003t0004g0013others(42): Show | 47 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.535-462G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815639 | ||||||
| chr2:69815647
|
G | A | 1 | a0001c0001t0001g0092 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.535-454G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815647 | ||||||
| chr2:69815688
|
C | T | 74 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(71): Show | 76 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.535-413C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815688 | ||||||
| chr2:69815702
|
C | T | 2 | a0001c0001t0004g0131a0001c0001t0006g0103 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.535-399C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815702 | ||||||
| chr2:69815783
|
C | A | 76 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(73): Show | 77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.535-318C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815783 | ||||||
| chr2:69815865
|
T | A | 1 | a0001c0001t0006g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.535-236T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815865 | ||||||
| chr2:69815908
|
G | A | 3 | a0003c0003t0004g0013a0003c0003t0004g0014a0003c0003t0004g0339 | 3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.535-193G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815908 | ||||||
| chr2:69816013
|
G | A | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-88G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69816013 | ||||||
| chr2:69816083
|
T | C | 24 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(21): Show | 24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.535-18T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69816083 | ||||||
| chr2:69816255
|
C | T | 71 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(68): Show | 73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+61C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816255 | ||||||
| chr2:69816388
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.628+194T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816388 | ||||||
| chr2:69816466
|
C | A | 76 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(73): Show | 77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.628+272C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816466 | ||||||
| chr2:69816551
|
G | T | 2 | a0001c0001t0001g0295a0001c0001t0001g0296 | 2 | HG01358.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.628+357G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816551 | ||||||
| chr2:69816643
|
A | T | 76 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(73): Show | 77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.628+449A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816643 | ||||||
| chr2:69816795
|
A | T | 71 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(68): Show | 73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+601A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816795 | ||||||
| chr2:69816820
|
C | T | 2 | a0003c0003t0004g0059a0003c0003t0004g0061 | 2 | HG01099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.628+626C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816820 | ||||||
| chr2:69816883
|
C | T | 1 | a0001c0001t0001g0332 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.628+689C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816883 | ||||||
| chr2:69817027
|
C | G | 98 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(95): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.628+833C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817027 | ||||||
| chr2:69817076
|
C | A | 71 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(68): Show | 73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+882C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817076 | ||||||
| chr2:69817234
|
G | A | 71 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(68): Show | 73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+1040G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817234 | ||||||
| chr2:69817246
|
CTGTT | C | 103 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(100): Show | 104 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.628+1056_628+1059d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 69817246 | |||||
| chr2:69817368
|
G | A | 1 | a0003c0003t0002g0104 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.628+1174G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817368 | ||||||
| chr2:69817418
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.629-1181C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817418 | ||||||
| chr2:69817478
|
G | T | 1 | a0001c0001t0003g0091 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.629-1121G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817478 | ||||||
| chr2:69817576
|
A | C | 3 | a0001c0001t0007g0300a0001c0001t0007g0308a0005c0005t0007g0006 | 3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.629-1023A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817576 | ||||||
| chr2:69817793
|
G | T | 3 | a0003c0003t0004g0109a0003c0003t0004g0111a0003c0003t0004g0301 | 3 | HG01891.hp1 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.629-806G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817793 | ||||||
| chr2:69817881
|
T | A | 46 | a0001c0001t0017g0337a0003c0003t0004g0002a0003c0003t0004g0003others(43): Show | 48 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.629-718T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817881 | ||||||
| chr2:69817931
|
G | A | 79 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0007g0300others(76): Show | 80 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.629-668G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817931 | ||||||
| chr2:69817948
|
A | G | 6 | a0001c0001t0003g0160a0001c0001t0003g0161a0001c0001t0003g0162others(3): Show | 6 | NA18747.hp1 NA18945.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-651A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817948 | ||||||
| chr2:69818013
|
A | G | 14 | a0001c0001t0006g0010a0001c0001t0006g0016a0001c0001t0006g0020others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-586A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818013 | ||||||
| chr2:69818014
|
A | C | 14 | a0001c0001t0006g0010a0001c0001t0006g0016a0001c0001t0006g0020others(11): Show | 14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-585A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818014 | ||||||
| chr2:69818118
|
A | AAACAAC | 68 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(65): Show | 70 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.629-475_629-470dup others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 69818118 | |||||
| chr2:69818118
|
A | C | 1 | a0003c0003t0004g0106 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.629-481A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818118 | ||||||
| chr2:69818134
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.629-465A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818134 | ||||||
| chr2:69818353
|
G | T | 2 | a0001c0001t0001g0286a0001c0001t0015g0285 | 2 | HG01169.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.629-246G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818353 | ||||||
| chr2:69818371
|
G | C | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.629-228G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818371 | ||||||
| chr2:69818390
|
A | C | 2 | a0001c0001t0004g0131a0001c0001t0006g0103 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.629-209A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818390 | ||||||
| chr2:69818544
|
T | G | 1 | a0002c0002t0002g0026 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.629-55T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818544 | ||||||
| chr2:69818770
|
A | T | 1 | a0002c0002t0002g0001 | 2 | HG00609.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.724+76A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818770 | ||||||
| chr2:69818771
|
T | C | 2 | a0001c0001t0001g0288a0001c0001t0003g0338 | 2 | HG03239.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.724+77T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818771 | ||||||
| chr2:69818829
|
A | T | 1 | a0003c0003t0004g0061 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.724+135A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818829 | ||||||
| chr2:69818905
|
C | G | 2 | a0001c0001t0003g0121a0001c0001t0003g0177 | 2 | NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.724+211C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818905 | ||||||
| chr2:69818933
|
A | G | 3 | a0001c0001t0001g0233a0001c0001t0001g0267a0001c0001t0001g0278 | 3 | HG01175.hp2 HG01515.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.724+239A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818933 | ||||||
| chr2:69818938
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.724+244G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818938 | ||||||
| chr2:69819028
|
T | C | 1 | a0001c0001t0003g0165 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.725-252T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819028 | ||||||
| chr2:69819080
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.725-200T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819080 | ||||||
| chr2:69819123
|
G | C | 98 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(95): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.725-157G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819123 | ||||||
| chr2:69819130
|
G | A | 62 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(59): Show | 63 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.725-150G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819130 | ||||||
| chr2:69819728
|
T | A | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.783+390T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819728 | ||||||
| chr2:69819729
|
C | G | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.783+391C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819729 | ||||||
| chr2:69819801
|
C | T | 2 | a0001c0001t0004g0131a0001c0001t0006g0103 | 2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.783+463C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819801 | ||||||
| chr2:69819805
|
C | T | 1 | a0002c0002t0002g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.783+467C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819805 | ||||||
| chr2:69819832
|
C | A | 80 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0007g0300others(77): Show | 81 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.783+494C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819832 | ||||||
| chr2:69819898
|
G | A | 4 | a0001c0001t0006g0010a0001c0001t0006g0016a0001c0001t0006g0321others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+560G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819898 | ||||||
| chr2:69819932
|
G | C | 70 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(67): Show | 72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.783+594G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819932 | ||||||
| chr2:69820074
|
GA | G | 68 | a0001c0001t0002g0171a0001c0001t0002g0271a0002c0002t0002g0001others(65): Show | 69 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.784-612delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 69820074 | |||||
| chr2:69820236
|
G | GT | 98 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(95): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.784-450dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 69820236 | |||||
| chr2:69820236
|
GT | G | 78 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0007g0300others(75): Show | 79 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.784-450delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 69820236 | |||||
| chr2:69820238
|
T | G | 3 | a0002c0002t0002g0319a0002c0002t0002g0320a0003c0003t0002g0110 | 3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.784-461T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820238 | ||||||
| chr2:69820483
|
G | A | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.784-216G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820483 | ||||||
| chr2:69820512
|
G | A | 79 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0007g0300others(76): Show | 80 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.784-187G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820512 | ||||||
| chr2:69820581
|
T | C | 2 | a0002c0002t0002g0112a0002c0002t0002g0117 | 2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.784-118T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820581 | ||||||
| chr2:69821097
|
G | A | 4 | a0001c0001t0005g0195a0001c0001t0005g0196a0001c0001t0005g0197others(1): Show | 4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+276G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821097 | ||||||
| chr2:69821124
|
C | A | 1 | a0001c0001t0006g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.906+303C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821124 | ||||||
| chr2:69821309
|
T | A | 2 | a0003c0003t0004g0097a0003c0003t0004g0181 | 2 | NA18966.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.906+488T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821309 | ||||||
| chr2:69821402
|
C | T | 100 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(97): Show | 101 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.906+581C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821402 | ||||||
| chr2:69821477
|
AT | A | 16 | a0001c0001t0006g0010a0001c0001t0006g0012a0001c0001t0006g0016others(13): Show | 16 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.906+667delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69821477 | |||||
| chr2:69821636
|
G | T | 4 | a0001c0001t0006g0010a0001c0001t0006g0016a0001c0001t0006g0321others(1): Show | 4 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+815G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821636 | ||||||
| chr2:69821644
|
G | A | 1 | a0001c0001t0005g0333 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.906+823G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821644 | ||||||
| chr2:69822045
|
T | A | 8 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+1224T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822045 | ||||||
| chr2:69822090
|
G | A | 80 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0007g0300others(77): Show | 81 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.906+1269G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822090 | ||||||
| chr2:69822110
|
C | G | 24 | a0001c0001t0004g0131a0001c0001t0006g0008a0001c0001t0006g0009others(21): Show | 24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.906+1289C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822110 | ||||||
| chr2:69822151
|
G | A | 7 | a0001c0001t0003g0079a0001c0001t0003g0120a0001c0001t0003g0143others(4): Show | 7 | HG00544.hp1 HG02523.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+1330G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822151 | ||||||
| chr2:69822225
|
G | A | 2 | a0001c0001t0006g0012a0001c0001t0006g0342 | 2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.906+1404G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822225 | ||||||
| chr2:69822362
|
A | G | 1 | a0002c0002t0002g0319 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.906+1541A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822362 | ||||||
| chr2:69822384
|
T | C | 3 | a0001c0001t0007g0300a0001c0001t0007g0308a0005c0005t0007g0006 | 3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.906+1563T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822384 | ||||||
| chr2:69822583
|
C | T | 98 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(95): Show | 99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.906+1762C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822583 | ||||||
| chr2:69822644
|
C | T | 1 | a0001c0001t0001g0072 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.906+1823C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822644 | ||||||
| chr2:69822844
|
A | C | 2 | a0001c0001t0011g0130a0001c0001t0011g0212 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.906+2023A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822844 | ||||||
| chr2:69823366
|
A | T | 2 | a0001c0001t0007g0300a0001c0001t0007g0308 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.907-2090A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823366 | ||||||
| chr2:69823509
|
T | C | 99 | a0001c0001t0003g0004a0001c0001t0003g0017a0001c0001t0003g0079others(96): Show | 100 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.907-1947T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823509 | ||||||
| chr2:69823593
|
G | A | 250 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(247): Show | 254 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(251): Show |
intron_variant | MODIFIER | c.907-1863G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823593 | ||||||
| chr2:69823626
|
C | G | 2 | a0001c0001t0005g0318a0001c0001t0007g0207 | 2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-1830C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823626 | ||||||
| chr2:69823636
|
T | C | 1 | a0003c0003t0004g0096 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.907-1820T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823636 | ||||||
| chr2:69824011
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.907-1445C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824011 | ||||||
| chr2:69824054
|
G | T | 3 | a0001c0001t0007g0300a0001c0001t0007g0308a0005c0005t0007g0006 | 3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.907-1402G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824054 | ||||||
| chr2:69824177
|
C | T | 2 | a0001c0001t0006g0020a0001c0001t0006g0221 | 2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.907-1279C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824177 | ||||||
| chr2:69824251
|
C | G | 3 | a0001c0001t0007g0300a0001c0001t0007g0308a0005c0005t0007g0006 | 3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.907-1205C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824251 | ||||||
| chr2:69824435
|
G | A | 3 | a0001c0001t0007g0300a0001c0001t0007g0308a0005c0005t0007g0006 | 3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.907-1021G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824435 | ||||||
| chr2:69824456
|
T | C | 1 | a0001c0001t0005g0334 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.907-1000T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824456 | ||||||
| chr2:69824490
|
G | A | 42 | a0003c0003t0004g0002a0003c0003t0004g0003a0003c0003t0004g0025others(39): Show | 44 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.907-966G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824490 | ||||||
| chr2:69824504
|
G | GA | 102 | a0001c0001t0001g0045a0001c0001t0003g0004a0001c0001t0003g0017others(99): Show | 103 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.907-935dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69824504 | |||||
| chr2:69824510
|
A | G | 1 | a0001c0001t0007g0305 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.907-946A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824510 | ||||||
| chr2:69824970
|
C | T | 1 | a0002c0002t0002g0041 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.907-486C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824970 | ||||||
| chr2:69824992
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.907-464G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824992 | ||||||
| chr2:69825066
|
C | CA | 55 | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0001g0072others(52): Show | 55 | HG01106.hp1 HG01109.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.907-366dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825066 | |||||
| chr2:69825066
|
CA | C | 13 | a0001c0001t0006g0008a0001c0001t0006g0009a0001c0001t0006g0010others(10): Show | 13 | HG01175.hp1 HG01261.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-366delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825066 | |||||
| chr2:69825066
|
CAA | C | 57 | a0001c0001t0004g0131a0001c0001t0006g0012a0001c0001t0006g0015others(54): Show | 59 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.907-367_907-366del others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825066 | |||||
| chr2:69825090
|
AC | A | 13 | a0001c0001t0003g0121a0001c0001t0003g0178a0001c0001t0003g0234others(10): Show | 13 | HG00673.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-364delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825090 | |||||
| chr2:69825091
|
C | A | 167 | a0001c0001t0002g0171a0001c0001t0002g0271a0001c0001t0003g0004others(164): Show | 169 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.907-365C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69825091 |