| geneid | 84448 |
|---|---|
| ensemblid | ENSG00000163995.22 |
| hgncid | 19195 |
| symbol | ABLIM2 |
| name | actin binding LIM protein family member 2 |
| refseq_nuc | NM_001130083.2 |
| refseq_prot | NP_001123555.1 |
| ensembl_nuc | ENST00000447017.7 |
| ensembl_prot | ENSP00000393511.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 7965327 |
| end | 8158813 |
| strand | - |
| ver | v1.2 |
| region | chr4:7965327-8158813 |
| region5000 | chr4:7960327-8163813 |
| regionname0 | ABLIM2_chr4_7965327_8158813 |
| regionname5000 | ABLIM2_chr4_7960327_8163813 |
| 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 | 645 | 317 | 89 | 62 | 107 | 13 | 44 | 70 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0002 | 0/0 | 645 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0003 | 0/0 | 645 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0004 | 0/0 | 645 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0005 | 0/0 | 645 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| 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 | 0/1 | 1938 | 199 | 53 | 40 | 76 | 9 | 20 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0002 | 1/0 | 1938 | 81 | 20 | 17 | 25 | 3 | 15 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0003 | 0/0 | 1938 | 27 | 12 | 4 | 4 | 1 | 6 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0004 | 0/0 | 1938 | 8 | 3 | 1 | 2 | 0 | 2 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0005 | 0/0 | 1938 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0006 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0007 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0008 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0009 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| c0010 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| 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 | 0/1 | 1788 | 114 | 7 | 21 | 61 | 6 | 18 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0002 | 0/0 | 1788 | 60 | 29 | 20 | 1 | 4 | 6 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0003 | 0/0 | 1788 | 47 | 5 | 1 | 35 | 0 | 6 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0004 | 0/0 | 1788 | 15 | 7 | 1 | 2 | 0 | 5 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0005 | 0/0 | 1788 | 14 | 4 | 9 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0006 | 0/0 | 1777 | 14 | 5 | 3 | 2 | 2 | 2 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0007 | 0/0 | 1786 | 9 | 9 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0008 | 1/0 | 1788 | 6 | 0 | 2 | 0 | 2 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0009 | 0/0 | 1788 | 5 | 5 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0010 | 0/0 | 1788 | 5 | 5 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0011 | 0/0 | 1788 | 4 | 0 | 0 | 4 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0012 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0013 | 0/0 | 1788 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0014 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0015 | 0/0 | 1788 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0016 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0017 | 0/0 | 1788 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0018 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0019 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0020 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0021 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0022 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0023 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0024 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0025 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0026 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0027 | 0/0 | 1788 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0028 | 0/0 | 1777 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0029 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0030 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0031 | 0/0 | 1788 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0032 | 0/0 | 1788 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0033 | 0/0 | 1777 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| t0034 | 0/0 | 1788 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| 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 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| 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 | 0/1 | 1938 | 199 | 53 | 40 | 76 | 9 | 20 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002 | 1/0 | 1938 | 81 | 20 | 17 | 25 | 3 | 15 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003 | 0/0 | 1938 | 27 | 12 | 4 | 4 | 1 | 6 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0004 | 0/0 | 1938 | 8 | 3 | 1 | 2 | 0 | 2 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0008 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0010 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0002c0005 | 0/0 | 1938 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0003c0007 | 0/0 | 1938 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0004c0009 | 0/0 | 1938 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0005c0006 | 0/0 | 1938 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3725 | 75 | 3 | 15 | 44 | 3 | 9 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0002 | 0/0 | 3725 | 39 | 18 | 13 | 0 | 4 | 4 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0003 | 0/0 | 3725 | 25 | 1 | 0 | 21 | 0 | 3 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0004 | 0/0 | 3725 | 8 | 4 | 0 | 2 | 0 | 2 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0005 | 0/0 | 3725 | 6 | 1 | 4 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0006 | 0/0 | 3714 | 6 | 2 | 0 | 2 | 2 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0007 | 0/0 | 3723 | 5 | 5 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0008 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0009 | 0/0 | 3725 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0010 | 0/0 | 3725 | 5 | 5 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0011 | 0/0 | 3725 | 4 | 0 | 0 | 4 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0012 | 0/0 | 3725 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0013 | 0/0 | 3725 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0014 | 0/0 | 3725 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0015 | 0/0 | 3725 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0016 | 0/0 | 3725 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0017 | 0/0 | 3725 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0018 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0020 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0022 | 0/0 | 3725 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0025 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0026 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0027 | 0/0 | 3725 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0028 | 0/0 | 3714 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0029 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0030 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0032 | 0/0 | 3725 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0001t0034 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0001 | 0/0 | 3725 | 30 | 3 | 5 | 13 | 1 | 8 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0002 | 0/0 | 3725 | 14 | 9 | 4 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0003 | 0/0 | 3725 | 17 | 2 | 1 | 12 | 0 | 2 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0004 | 0/0 | 3725 | 5 | 2 | 1 | 0 | 0 | 2 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0005 | 0/0 | 3725 | 8 | 3 | 5 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0008 | 1/0 | 3725 | 4 | 0 | 1 | 0 | 2 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0019 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0024 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0002t0031 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0001 | 0/0 | 3725 | 6 | 1 | 0 | 4 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0002 | 0/0 | 3725 | 3 | 1 | 1 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0003 | 0/0 | 3725 | 2 | 2 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0004 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0006 | 0/0 | 3714 | 6 | 1 | 3 | 0 | 0 | 2 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0007 | 0/0 | 3723 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0009 | 0/0 | 3725 | 3 | 3 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0021 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0023 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0003t0033 | 0/0 | 3714 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0004t0001 | 0/0 | 3725 | 2 | 0 | 1 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0004t0002 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0004t0003 | 0/0 | 3725 | 3 | 0 | 0 | 2 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0004t0004 | 0/0 | 3725 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0004t0007 | 0/0 | 3723 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0008t0006 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0001c0010t0008 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0002c0005t0002 | 0/0 | 3725 | 2 | 0 | 2 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0003c0007t0001 | 0/0 | 3725 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0004c0009t0002 | 0/0 | 3725 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| a0005c0006t0006 | 0/0 | 3714 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | copy fasta | chr4 | 7960327 | 8163813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0117 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0004g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0005g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0006g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0008g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0009g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0010g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0010g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0010g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0010g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0011g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0011g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0011g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0012g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0012g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0013g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0013g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0014g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0014g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0015g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0015g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0016g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0016g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0017g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0017g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0018g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0020g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0022g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0025g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0026g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0027g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0028g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0029g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0030g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0032g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0001t0034g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0004g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0005g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0008g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0008g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0008g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0008g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0019g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0024g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0002t0031g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0006g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0006g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0006g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0009g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0009g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0021g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0023g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0003t0033g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0004t0007g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0008t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0001c0010t0008g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0002c0005t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0002c0005t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0003c0007t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0004c0009t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| a0005c0006t0006g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0008 | g0035 | EUR | GBR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0147 | EUR | GBR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0152 | EUR | GBR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | FIN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00423 | hp2 | a0001 | c0003 | t0001 | g0214 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00558 | hp1 | a0001 | c0002 | t0003 | g0051 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00597 | hp2 | a0001 | c0001 | t0005 | g0009 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0296 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0116 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0034 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0079 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG00738 | hp2 | a0001 | c0003 | t0006 | g0106 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0072 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01081 | hp1 | a0001 | c0003 | t0006 | g0155 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0312 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0090 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0140 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01167 | hp1 | a0001 | c0002 | t0003 | g0031 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0093 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01168 | hp1 | a0002 | c0005 | t0002 | g0097 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01168 | hp2 | a0001 | c0004 | t0001 | g0069 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01169 | hp1 | a0001 | c0001 | t0013 | g0094 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01169 | hp2 | a0002 | c0005 | t0002 | g0096 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01243 | hp2 | a0001 | c0001 | t0018 | g0001 | AMR | PUR | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01256 | hp1 | a0001 | c0002 | t0005 | g0082 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01256 | hp2 | a0001 | c0001 | t0015 | g0189 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01261 | hp2 | a0001 | c0001 | t0005 | g0294 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0298 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0299 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01361 | hp2 | a0001 | c0003 | t0006 | g0199 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01433 | hp1 | a0001 | c0002 | t0004 | g0007 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01433 | hp2 | a0001 | c0001 | t0015 | g0188 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01496 | hp1 | a0001 | c0001 | t0005 | g0084 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01515 | hp1 | a0001 | c0002 | t0008 | g0114 | EUR | IBS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | IBS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0259 | EUR | IBS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01516 | hp2 | a0001 | c0001 | t0006 | g0178 | EUR | IBS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0092 | EUR | IBS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01517 | hp2 | a0001 | c0001 | t0006 | g0179 | EUR | IBS | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01891 | hp1 | a0001 | c0003 | t0023 | g0039 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01891 | hp2 | a0001 | c0008 | t0006 | g0289 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01928 | hp1 | a0001 | c0002 | t0005 | g0107 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01952 | hp1 | a0001 | c0001 | t0028 | g0062 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01975 | hp1 | a0001 | c0001 | t0005 | g0019 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02004 | hp2 | a0001 | c0002 | t0005 | g0029 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02071 | hp1 | a0001 | c0002 | t0003 | g0226 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02071 | hp2 | a0004 | c0009 | t0002 | g0191 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02129 | hp2 | a0001 | c0001 | t0022 | g0153 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02145 | hp1 | a0005 | c0006 | t0006 | g0205 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02145 | hp2 | a0001 | c0002 | t0005 | g0292 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02148 | hp2 | a0001 | c0002 | t0005 | g0316 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CDX | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CDX | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02257 | hp2 | a0001 | c0004 | t0007 | g0131 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0301 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02280 | hp1 | a0001 | c0002 | t0005 | g0053 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02280 | hp2 | a0001 | c0001 | t0012 | g0253 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02293 | hp1 | a0001 | c0002 | t0008 | g0100 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02293 | hp2 | a0001 | c0001 | t0027 | g0315 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02451 | hp1 | a0001 | c0001 | t0012 | g0008 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02451 | hp2 | a0001 | c0001 | t0034 | g0322 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02572 | hp1 | a0001 | c0002 | t0019 | g0003 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0200 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0210 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02615 | hp2 | a0001 | c0001 | t0017 | g0300 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0234 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0286 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02630 | hp1 | a0001 | c0003 | t0003 | g0030 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0236 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02647 | hp2 | a0001 | c0003 | t0002 | g0025 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02683 | hp1 | a0001 | c0002 | t0024 | g0136 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0251 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02698 | hp1 | a0001 | c0001 | t0025 | g0198 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0138 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0129 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02717 | hp2 | a0001 | c0003 | t0007 | g0217 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02723 | hp1 | a0001 | c0003 | t0003 | g0227 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02723 | hp2 | a0001 | c0001 | t0007 | g0112 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02735 | hp2 | a0001 | c0004 | t0003 | g0016 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0239 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0307 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0127 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0237 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02886 | hp2 | a0001 | c0003 | t0009 | g0211 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0309 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0212 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02897 | hp1 | a0001 | c0002 | t0003 | g0238 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0306 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0064 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02965 | hp1 | a0001 | c0003 | t0009 | g0223 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02965 | hp2 | a0001 | c0001 | t0006 | g0216 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0215 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0204 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0196 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0241 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03098 | hp1 | a0001 | c0004 | t0002 | g0040 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03098 | hp2 | a0001 | c0004 | t0004 | g0126 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0283 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03130 | hp2 | a0001 | c0003 | t0009 | g0221 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0203 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0005 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0224 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0128 | AFR | ESN | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03209 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03225 | hp1 | a0001 | c0001 | t0026 | g0285 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03225 | hp2 | a0001 | c0001 | t0016 | g0233 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0305 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03239 | hp2 | a0001 | c0003 | t0002 | g0081 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0308 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03453 | hp2 | a0001 | c0001 | t0016 | g0111 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03486 | hp1 | a0001 | c0003 | t0007 | g0218 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03486 | hp2 | a0001 | c0003 | t0006 | g0209 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03491 | hp1 | a0001 | c0003 | t0006 | g0143 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03492 | hp1 | a0001 | c0003 | t0006 | g0142 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03540 | hp2 | a0001 | c0001 | t0020 | g0002 | AFR | GWD | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0232 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0088 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0083 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0148 | SAS | PJL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03831 | hp1 | a0001 | c0010 | t0008 | g0252 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03834 | hp1 | a0001 | c0002 | t0004 | g0075 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03927 | hp1 | a0001 | c0002 | t0003 | g0159 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0012 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03942 | hp1 | a0001 | c0004 | t0001 | g0249 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0248 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04115 | hp1 | a0001 | c0003 | t0033 | g0321 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0273 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04184 | hp1 | a0001 | c0002 | t0004 | g0044 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04184 | hp2 | a0001 | c0002 | t0031 | g0319 | SAS | BEB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04199 | hp2 | a0001 | c0003 | t0021 | g0004 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04204 | hp2 | a0001 | c0003 | t0004 | g0036 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | STU | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18522 | hp1 | a0001 | c0003 | t0007 | g0021 | AFR | YRI | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | YRI | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | CHB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | CHB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | CHB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0170 | EAS | CHB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18942 | hp2 | a0001 | c0001 | t0011 | g0193 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18948 | hp1 | a0001 | c0002 | t0003 | g0229 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18948 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0043 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0281 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18962 | hp2 | a0001 | c0002 | t0003 | g0280 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18970 | hp1 | a0001 | c0004 | t0003 | g0257 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18970 | hp2 | a0001 | c0001 | t0011 | g0271 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0049 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18979 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18984 | hp1 | a0001 | c0001 | t0011 | g0154 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18995 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0102 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0258 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18999 | hp1 | a0001 | c0002 | t0003 | g0220 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18999 | hp2 | a0001 | c0003 | t0001 | g0066 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19005 | hp1 | a0001 | c0001 | t0006 | g0272 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0026 | AFR | LWK | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19030 | hp2 | a0001 | c0001 | t0029 | g0022 | AFR | LWK | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19043 | hp1 | a0001 | c0001 | t0014 | g0291 | AFR | LWK | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | LWK | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19056 | hp1 | a0001 | c0002 | t0003 | g0045 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19063 | hp1 | a0001 | c0002 | t0003 | g0245 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19063 | hp2 | a0001 | c0001 | t0011 | g0254 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19067 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19070 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19090 | hp1 | a0001 | c0004 | t0003 | g0065 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19240 | hp1 | a0001 | c0001 | t0010 | g0302 | AFR | YRI | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | YRI | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | ASW | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | ASW | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA20752 | hp1 | a0001 | c0003 | t0001 | g0150 | EUR | TSI | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA20752 | hp2 | a0003 | c0007 | t0001 | g0297 | EUR | TSI | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | GIH | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA20905 | hp2 | a0001 | c0001 | t0030 | g0099 | SAS | GIH | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0145 | AMR | CLM | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02109 | hp1 | a0001 | c0001 | t0010 | g0033 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0194 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02486 | hp1 | a0001 | c0002 | t0002 | g0115 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG02486 | hp2 | a0001 | c0001 | t0009 | g0235 | AFR | ACB | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0038 | AFR | MSL | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0290 | AFR | USA | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | USA | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18955 | hp1 | a0001 | c0001 | t0032 | g0320 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | LWK | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | LWK | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0117 | REF | REF | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0008 | g0068 | REF | REF | ABLIM2_chr4_7960327_8163813 | ABLIM2 | chr4 | 7960327 | 8163813 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:7967088
|
C | T | 1 | a0004 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.1840G>A | p.Glu614Lys | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1964/3725 | 1840/1938 | 614/645 | chr4 | 7967088 | ||
| chr4:8080745
|
T | C | 1 | a0002 | 2 | HG01168.hp1 HG01169.hp2 |
missense_variant | MODERATE | c.512A>G | p.Lys171Arg | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 5/21 | 636/3725 | 512/1938 | 171/645 | chr4 | 8080745 | ||
| chr4:8088205
|
C | T | 1 | a0003 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.418G>A | p.Val140Met | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 4/21 | 542/3725 | 418/1938 | 140/645 | chr4 | 8088205 | ||
| chr4:8097256
|
C | T | 1 | a0005 | 1 | HG02145.hp1 | missense_variant | MODERATE | c.181G>A | p.Gly61Ser | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 3/21 | 305/3725 | 181/1938 | 61/645 | chr4 | 8097256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:8009097
|
T | G | 1 | a0001c0008 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.1429A>C | p.Arg477Arg | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 15/21 | 1553/3725 | 1429/1938 | 477/645 | chr4 | 8009097 | ||
| chr4:8029744
|
A | G | 6 | a0001c0001a0001c0003a0001c0008others(3): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
synonymous_variant | LOW | c.1080T>C | p.Cys360Cys | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 11/21 | 1204/3725 | 1080/1938 | 360/645 | chr4 | 8029744 | ||
| chr4:8106564
|
C | A | 1 | a0001c0010 | 1 | HG03831.hp1 | synonymous_variant | LOW | c.84G>T | p.Gly28Gly | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 2/21 | 208/3725 | 84/1938 | 28/645 | chr4 | 8106564 | ||
| chr4:8106588
|
C | T | 4 | a0001c0003a0001c0004a0003c0007others(1): Show | 37 | HG00423.hp2 HG00738.hp2 HG01081.hp1 others(34): Show |
synonymous_variant | LOW | c.60G>A | p.Thr20Thr | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 2/21 | 184/3725 | 60/1938 | 20/645 | chr4 | 8106588 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:7965364
|
G | A | 1 | a0001c0001t0026 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1626C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1626 | chr4 | 7965364 | |||||
| chr4:7965516
|
G | C | 13 | a0001c0001t0003a0001c0001t0004a0001c0001t0014others(10): Show | 68 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1474C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1474 | chr4 | 7965516 | |||||
| chr4:7965560
|
A | G | 1 | a0001c0001t0025 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1430T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1430 | chr4 | 7965560 | |||||
| chr4:7965662
|
C | T | 1 | a0001c0001t0010 | 5 | HG02109.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1328G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1328 | chr4 | 7965662 | |||||
| chr4:7965742
|
C | T | 1 | a0001c0001t0017 | 2 | HG02615.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1248G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1248 | chr4 | 7965742 | |||||
| chr4:7965772
|
A | G | 1 | a0001c0001t0014 | 2 | HG03471.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1218T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1218 | chr4 | 7965772 | |||||
| chr4:7965779
|
CATCTCCA others(4): Show |
C | 6 | a0001c0001t0006a0001c0001t0028a0001c0003t0006others(3): Show | 16 | HG00738.hp2 HG01081.hp1 HG01361.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1200_*1210delAGGA others(7): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1200 | chr4 | 7965779 | |||||
| chr4:7965812
|
T | A | 1 | a0001c0001t0027 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1178A>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1178 | chr4 | 7965812 | |||||
| chr4:7965877
|
TTA | T | 3 | a0001c0001t0007a0001c0003t0007a0001c0004t0007 | 9 | HG02257.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1111_*1112delTA | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1111 | chr4 | 7965877 | |||||
| chr4:7965955
|
A | C | 1 | a0001c0001t0017 | 2 | HG02615.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1035T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1035 | chr4 | 7965955 | |||||
| chr4:7965956
|
C | T | 12 | a0001c0001t0003a0001c0001t0005a0001c0001t0013others(9): Show | 69 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1034G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1034 | chr4 | 7965956 | |||||
| chr4:7966148
|
G | A | 15 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(12): Show | 75 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*842C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 842 | chr4 | 7966148 | |||||
| chr4:7966205
|
C | T | 1 | a0001c0001t0016 | 2 | HG03225.hp2 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*785G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 785 | chr4 | 7966205 | |||||
| chr4:7966206
|
G | A | 1 | a0001c0003t0023 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 784 | chr4 | 7966206 | |||||
| chr4:7966226
|
G | A | 1 | a0001c0001t0028 | 1 | HG01952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 764 | chr4 | 7966226 | |||||
| chr4:7966242
|
C | T | 1 | a0001c0001t0013 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*748G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 748 | chr4 | 7966242 | |||||
| chr4:7966501
|
C | T | 1 | a0001c0001t0015 | 2 | HG01256.hp2 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*489G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 489 | chr4 | 7966501 | |||||
| chr4:7966514
|
G | A | 14 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(11): Show | 74 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*476C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 476 | chr4 | 7966514 | |||||
| chr4:7966522
|
G | A | 1 | a0001c0002t0024 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*468C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 468 | chr4 | 7966522 | |||||
| chr4:7966553
|
C | T | 15 | a0001c0001t0001a0001c0001t0007a0001c0001t0011others(12): Show | 134 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*437G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 437 | chr4 | 7966553 | |||||
| chr4:7966592
|
A | C | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*398T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 398 | chr4 | 7966592 | |||||
| chr4:7966595
|
A | G | 55 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(52): Show | 316 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*395T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 395 | chr4 | 7966595 | |||||
| chr4:7966776
|
A | G | 1 | a0001c0001t0011 | 4 | NA18942.hp2 NA18970.hp2 NA18984.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*214T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 214 | chr4 | 7966776 | |||||
| chr4:7966831
|
G | A | 1 | a0001c0001t0029 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 159 | chr4 | 7966831 | |||||
| chr4:7966845
|
C | T | 16 | a0001c0001t0003a0001c0001t0005a0001c0001t0009others(13): Show | 77 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*145G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 145 | chr4 | 7966845 | |||||
| chr4:7966923
|
T | C | 1 | a0001c0001t0017 | 2 | HG02615.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*67A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 67 | chr4 | 7966923 | |||||
| chr4:7966989
|
G | A | 1 | a0001c0001t0030 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 21/21 | 1 | chr4 | 7966989 | |||||
| chr4:8158746
|
C | T | 1 | a0001c0003t0021 | 1 | HG04199.hp2 | 5_prime_UTR_variant | MODIFIER | c.-57G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 1/21 | 57 | chr4 | 8158746 | |||||
| chr4:8158760
|
G | C | 1 | a0001c0002t0031 | 1 | HG04184.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 1/21 | 71 | chr4 | 8158760 | |||||
| chr4:8158767
|
C | A | 1 | a0001c0001t0032 | 1 | NA18955.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 1/21 | 78 | chr4 | 8158767 | |||||
| chr4:8158786
|
C | G | 3 | a0001c0001t0018a0001c0001t0020a0001c0002t0019 | 3 | HG01243.hp2 HG02572.hp1 HG03540.hp2 |
5_prime_UTR_variant | MODIFIER | c.-97G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 1/21 | 97 | chr4 | 8158786 | |||||
| chr4:8158804
|
T | G | 1 | a0001c0003t0033 | 1 | HG04115.hp1 | 5_prime_UTR_variant | MODIFIER | c.-115A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 1/21 | 115 | chr4 | 8158804 | |||||
| chr4:8158807
|
C | A | 1 | a0001c0001t0034 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-118G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 1/21 | 118 | chr4 | 8158807 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:7967161
|
T | C | 76 | a0001c0001t0003g0012a0001c0001t0003g0046a0001c0001t0003g0047others(73): Show | 76 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.1825-58A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967161 | ||||||
| chr4:7967209
|
G | C | 100 | a0001c0001t0001g0304a0001c0001t0002g0024a0001c0001t0002g0071others(97): Show | 100 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.1825-106C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967209 | ||||||
| chr4:7967226
|
G | C | 99 | a0001c0001t0002g0024a0001c0001t0002g0071a0001c0001t0002g0110others(96): Show | 99 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.1825-123C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967226 | ||||||
| chr4:7967489
|
C | T | 1 | a0001c0002t0003g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1825-386G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967489 | ||||||
| chr4:7967530
|
C | T | 1 | a0001c0001t0010g0215 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1825-427G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967530 | ||||||
| chr4:7967560
|
C | T | 1 | a0001c0002t0003g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1825-457G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967560 | ||||||
| chr4:7967641
|
G | A | 2 | a0001c0001t0017g0203a0001c0001t0017g0300 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1825-538C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967641 | ||||||
| chr4:7967650
|
C | T | 2 | a0001c0001t0017g0203a0001c0001t0017g0300 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1825-547G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967650 | ||||||
| chr4:7967654
|
T | A | 1 | a0001c0001t0017g0203 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1825-551A>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967654 | ||||||
| chr4:7967734
|
T | C | 39 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0077others(36): Show | 39 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1825-631A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967734 | ||||||
| chr4:7967764
|
A | C | 2 | a0001c0001t0017g0203a0001c0001t0017g0300 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1825-661T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967764 | ||||||
| chr4:7967766
|
C | T | 2 | a0001c0001t0017g0203a0001c0001t0017g0300 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1825-663G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967766 | ||||||
| chr4:7967768
|
T | C | 2 | a0001c0001t0017g0203a0001c0001t0017g0300 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1825-665A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967768 | ||||||
| chr4:7967800
|
G | A | 2 | a0001c0001t0017g0203a0001c0001t0017g0300 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1825-697C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967800 | ||||||
| chr4:7967867
|
G | A | 85 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0011others(82): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1825-764C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967867 | ||||||
| chr4:7967882
|
T | G | 2 | a0001c0001t0017g0203a0001c0001t0017g0300 | 2 | HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1825-779A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7967882 | ||||||
| chr4:7968030
|
G | A | 2 | a0001c0001t0002g0119a0001c0002t0008g0100 | 2 | HG01175.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1825-927C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968030 | ||||||
| chr4:7968167
|
A | G | 5 | a0001c0001t0006g0102a0001c0001t0006g0272a0001c0001t0028g0062others(2): Show | 5 | HG01952.hp1 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825-1064T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968167 | ||||||
| chr4:7968285
|
C | G | 5 | a0001c0001t0010g0005a0001c0001t0010g0033a0001c0001t0010g0127others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1825-1182G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968285 | ||||||
| chr4:7968376
|
C | T | 79 | a0001c0001t0002g0024a0001c0001t0002g0071a0001c0001t0002g0110others(76): Show | 79 | HG00140.hp2 HG00558.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1825-1273G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968376 | ||||||
| chr4:7968470
|
T | C | 10 | a0001c0001t0006g0210a0001c0001t0006g0216a0001c0001t0010g0005others(7): Show | 10 | HG01891.hp2 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825-1367A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968470 | ||||||
| chr4:7968553
|
C | G | 134 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(131): Show | 134 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1825-1450G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968553 | ||||||
| chr4:7968802
|
C | T | 2 | a0001c0001t0002g0024a0001c0003t0002g0025 | 2 | HG02647.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1825-1699G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968802 | ||||||
| chr4:7968862
|
C | T | 39 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0077others(36): Show | 39 | HG00140.hp1 HG00639.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1825-1759G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968862 | ||||||
| chr4:7968863
|
G | A | 2 | a0001c0001t0016g0111a0001c0001t0026g0285 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1825-1760C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968863 | ||||||
| chr4:7968911
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1825-1808G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968911 | ||||||
| chr4:7968986
|
G | A | 1 | a0001c0002t0003g0049 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1825-1883C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7968986 | ||||||
| chr4:7969022
|
C | T | 59 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0042others(56): Show | 59 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.1825-1919G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969022 | ||||||
| chr4:7969061
|
G | A | 1 | a0001c0001t0004g0175 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1825-1958C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969061 | ||||||
| chr4:7969252
|
G | A | 4 | a0001c0001t0016g0111a0001c0001t0017g0203a0001c0001t0017g0300others(1): Show | 4 | HG02615.hp2 HG03139.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825-2149C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969252 | ||||||
| chr4:7969355
|
G | A | 4 | a0001c0001t0010g0005a0001c0001t0010g0033a0001c0001t0010g0127others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-2252C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969355 | ||||||
| chr4:7969573
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1825-2470G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969573 | ||||||
| chr4:7969730
|
G | GACAC | 6 | a0001c0001t0001g0076a0001c0001t0006g0102a0001c0001t0006g0272others(3): Show | 6 | HG01952.hp1 HG02148.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825-2631_1825-262 others(8): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(5): Show |
1 | a0001c0001t0026g0285 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1825-2639_1825-262 others(16): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(7): Show |
7 | a0001c0001t0001g0243a0001c0001t0001g0267a0001c0001t0001g0277others(4): Show | 7 | HG02040.hp1 HG03209.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825-2641_1825-262 others(18): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(9): Show |
6 | a0001c0001t0001g0104a0001c0002t0001g0083a0001c0002t0001g0113others(3): Show | 6 | HG01361.hp1 HG02683.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825-2643_1825-262 others(20): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(11): Show |
10 | a0001c0001t0001g0078a0001c0001t0001g0117a0001c0001t0001g0168others(7): Show | 10 | HG00438.hp1 HG00642.hp1 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825-2645_1825-262 others(22): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(13): Show |
19 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0070others(16): Show | 19 | HG00323.hp2 HG00609.hp2 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1825-2647_1825-262 others(24): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(15): Show |
19 | a0001c0001t0001g0017a0001c0001t0001g0080a0001c0001t0001g0098others(16): Show | 19 | HG00099.hp2 HG00423.hp2 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.1825-2649_1825-262 others(26): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(17): Show |
12 | a0001c0001t0001g0087a0001c0001t0001g0146a0001c0001t0001g0169others(9): Show | 12 | HG00323.hp1 HG00423.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.1825-2651_1825-262 others(28): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(19): Show |
6 | a0001c0001t0001g0073a0001c0001t0001g0192a0001c0001t0001g0247others(3): Show | 6 | HG00544.hp2 HG01975.hp2 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.1825-2653_1825-262 others(30): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(21): Show |
7 | a0001c0001t0001g0061a0001c0001t0001g0095a0001c0001t0001g0173others(4): Show | 7 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(4): Show |
intron_variant | MODIFIER | c.1825-2655_1825-262 others(32): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(23): Show |
2 | a0001c0001t0001g0288a0001c0002t0001g0134 | 2 | HG03579.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1825-2657_1825-262 others(34): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
G | GACACACA others(27): Show |
1 | a0001c0001t0001g0275 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1825-2661_1825-262 others(38): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
GAC | G | 10 | a0001c0001t0002g0206a0001c0001t0004g0148a0001c0001t0005g0294others(7): Show | 10 | HG01261.hp2 HG02486.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.1825-2629_1825-262 others(6): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
GACAC | G | 30 | a0001c0001t0002g0006a0001c0001t0002g0010a0001c0001t0002g0032others(27): Show | 30 | HG00609.hp1 HG01123.hp1 HG01243.hp2 others(27): Show |
intron_variant | MODIFIER | c.1825-2631_1825-262 others(8): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
GACACAC | G | 129 | a0001c0001t0001g0056a0001c0001t0001g0144a0001c0001t0002g0011others(126): Show | 129 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1825-2633_1825-262 others(10): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
GACACACA others(1): Show |
G | 43 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0020others(40): Show | 43 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1825-2635_1825-262 others(12): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969730
|
GACACACA others(3): Show |
G | 6 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0001t0002g0230others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825-2637_1825-262 others(14): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969730 | ||||||
| chr4:7969958
|
G | A | 1 | a0001c0002t0003g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1825-2855C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7969958 | ||||||
| chr4:7970043
|
T | C | 5 | a0001c0001t0009g0212a0001c0001t0009g0235a0001c0003t0009g0211others(2): Show | 5 | HG02486.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1825-2940A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970043 | ||||||
| chr4:7970060
|
C | A | 1 | a0001c0003t0004g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1825-2957G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970060 | ||||||
| chr4:7970092
|
C | A | 1 | a0001c0001t0017g0300 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1825-2989G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970092 | ||||||
| chr4:7970353
|
G | A | 1 | a0001c0003t0004g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1825-3250C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970353 | ||||||
| chr4:7970407
|
G | A | 1 | a0001c0002t0002g0290 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1825-3304C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970407 | ||||||
| chr4:7970509
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1825-3406C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970509 | ||||||
| chr4:7970535
|
G | C | 4 | a0001c0001t0010g0005a0001c0001t0010g0033a0001c0001t0010g0127others(1): Show | 4 | HG02109.hp1 HG02818.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-3432C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970535 | ||||||
| chr4:7970538
|
T | G | 8 | a0001c0001t0006g0102a0001c0001t0006g0272a0001c0001t0016g0111others(5): Show | 8 | HG01952.hp1 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825-3435A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970538 | ||||||
| chr4:7970548
|
C | G | 8 | a0001c0001t0006g0102a0001c0001t0006g0272a0001c0001t0016g0111others(5): Show | 8 | HG01952.hp1 HG03139.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825-3445G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970548 | ||||||
| chr4:7970611
|
C | G | 6 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0001t0002g0230others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1825-3508G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970611 | ||||||
| chr4:7970642
|
G | T | 44 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0027others(41): Show | 44 | HG00438.hp2 HG00621.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1825-3539C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970642 | ||||||
| chr4:7970684
|
G | C | 11 | a0001c0001t0001g0061a0001c0001t0001g0073a0001c0001t0001g0104others(8): Show | 11 | HG00544.hp2 HG01069.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1825-3581C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970684 | ||||||
| chr4:7970903
|
G | A | 4 | a0001c0002t0002g0079a0001c0002t0002g0115a0001c0002t0002g0194others(1): Show | 4 | HG00738.hp1 HG01099.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-3800C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970903 | ||||||
| chr4:7970904
|
G | A | 8 | a0001c0001t0002g0110a0001c0001t0002g0152a0001c0001t0002g0246others(5): Show | 8 | HG00140.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825-3801C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970904 | ||||||
| chr4:7970938
|
C | T | 1 | a0001c0001t0010g0215 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1825-3835G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970938 | ||||||
| chr4:7970972
|
G | A | 3 | a0001c0001t0009g0212a0001c0001t0009g0235a0001c0003t0009g0211 | 3 | HG02486.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1825-3869C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7970972 | ||||||
| chr4:7971028
|
G | T | 1 | a0001c0001t0004g0163 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1825-3925C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971028 | ||||||
| chr4:7971298
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1825-4195G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971298 | ||||||
| chr4:7971336
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1825-4233A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971336 | ||||||
| chr4:7971337
|
C | T | 1 | a0001c0001t0002g0206 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1825-4234G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971337 | ||||||
| chr4:7971352
|
C | T | 1 | a0001c0002t0004g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1825-4249G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971352 | ||||||
| chr4:7971415
|
A | G | 259 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(256): Show | 259 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1825-4312T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971415 | ||||||
| chr4:7971505
|
T | C | 1 | a0001c0001t0006g0102 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1825-4402A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971505 | ||||||
| chr4:7971595
|
C | T | 1 | a0001c0001t0014g0291 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1825-4492G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971595 | ||||||
| chr4:7971678
|
C | T | 1 | a0001c0002t0003g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1825-4575G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971678 | ||||||
| chr4:7971833
|
C | G | 3 | a0001c0001t0026g0285a0001c0003t0001g0241a0001c0003t0007g0217 | 3 | HG02717.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1825-4730G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971833 | ||||||
| chr4:7971852
|
T | C | 5 | a0001c0001t0002g0032a0001c0001t0002g0237a0001c0001t0010g0215others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825-4749A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971852 | ||||||
| chr4:7971969
|
T | C | 256 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(253): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1825-4866A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7971969 | ||||||
| chr4:7972135
|
G | C | 1 | a0001c0002t0002g0160 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1825-5032C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972135 | ||||||
| chr4:7972145
|
C | T | 5 | a0001c0001t0002g0032a0001c0001t0002g0237a0001c0001t0010g0215others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1825-5042G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972145 | ||||||
| chr4:7972227
|
G | C | 1 | a0001c0002t0001g0088 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1825-5124C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972227 | ||||||
| chr4:7972263
|
C | T | 105 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0020others(102): Show | 105 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1825-5160G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972263 | ||||||
| chr4:7972321
|
T | C | 200 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0020others(197): Show | 200 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.1825-5218A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972321 | ||||||
| chr4:7972322
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1825-5219C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972322 | ||||||
| chr4:7972344
|
C | T | 42 | a0001c0001t0001g0311a0001c0001t0002g0006a0001c0001t0002g0119others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1825-5241G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972344 | ||||||
| chr4:7972414
|
C | T | 1 | a0001c0002t0003g0226 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1825-5311G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972414 | ||||||
| chr4:7972495
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1825-5392C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972495 | ||||||
| chr4:7972824
|
A | G | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1825-5721T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972824 | ||||||
| chr4:7972879
|
C | T | 3 | a0001c0001t0009g0212a0001c0001t0009g0235a0001c0003t0009g0211 | 3 | HG02486.hp2 HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1825-5776G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972879 | ||||||
| chr4:7972954
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0304 | 2 | HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1825-5851C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7972954 | ||||||
| chr4:7973024
|
AGAC | A | 5 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1825-5924_1825-592 others(7): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973024 | ||||||
| chr4:7973043
|
C | G | 2 | a0001c0001t0007g0132a0001c0003t0007g0218 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1825-5940G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973043 | ||||||
| chr4:7973055
|
G | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0192 | 2 | HG02056.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1825-5952C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973055 | ||||||
| chr4:7973075
|
C | CTCTGTGT others(21): Show |
2 | a0001c0001t0003g0166a0001c0002t0003g0245 | 2 | NA18971.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1825-5973_1825-597 others(32): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTG | 8 | a0001c0001t0001g0078a0001c0001t0001g0117a0001c0001t0001g0158others(5): Show | 8 | HG00621.hp2 HG00642.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1825-5974_1825-597 others(6): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTG | 15 | a0001c0001t0001g0260a0001c0001t0002g0237a0001c0001t0003g0201others(12): Show | 15 | HG00609.hp1 HG02083.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1825-5976_1825-597 others(8): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTG | 76 | a0001c0001t0001g0017a0001c0001t0001g0027a0001c0001t0001g0028others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1825-5978_1825-597 others(10): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(1): Show |
30 | a0001c0001t0001g0013a0001c0001t0001g0020a0001c0001t0001g0042others(27): Show | 30 | HG00438.hp2 HG00738.hp2 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1825-5980_1825-597 others(12): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(3): Show |
15 | a0001c0001t0002g0137a0001c0001t0002g0147a0001c0001t0002g0263others(12): Show | 15 | HG00140.hp1 HG01081.hp1 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.1825-5982_1825-597 others(14): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(5): Show |
11 | a0001c0001t0001g0261a0001c0001t0002g0006a0001c0001t0002g0119others(8): Show | 11 | HG00544.hp2 HG00639.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.1825-5984_1825-597 others(16): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0012g0253a0001c0001t0014g0038a0004c0009t0002g0191 | 3 | HG02071.hp2 HG02280.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1825-5988_1825-597 others(20): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(11): Show |
4 | a0001c0001t0001g0267a0001c0001t0007g0132a0001c0003t0007g0218others(1): Show | 4 | HG02257.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825-5990_1825-597 others(22): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(13): Show |
2 | a0001c0001t0004g0148a0001c0003t0002g0081 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1825-5992_1825-597 others(24): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(15): Show |
3 | a0001c0001t0001g0278a0001c0001t0010g0127a0001c0002t0004g0075 | 3 | HG02818.hp2 HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1825-5994_1825-597 others(26): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(17): Show |
4 | a0001c0001t0001g0085a0001c0001t0002g0141a0001c0001t0010g0005others(1): Show | 4 | HG00323.hp2 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1825-5996_1825-597 others(28): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(19): Show |
7 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0130others(4): Show | 7 | HG01515.hp2 HG01517.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1825-5998_1825-597 others(30): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(21): Show |
3 | a0001c0001t0002g0230a0001c0001t0002g0283a0001c0002t0031g0319 | 3 | HG02976.hp2 HG03130.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1825-6000_1825-597 others(32): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(23): Show |
3 | a0001c0001t0015g0189a0001c0002t0008g0035a0001c0003t0001g0241 | 3 | HG00099.hp1 HG01256.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1825-6002_1825-597 others(34): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(25): Show |
10 | a0001c0001t0001g0279a0001c0001t0001g0311a0001c0001t0003g0190others(7): Show | 10 | HG01069.hp2 HG02451.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.1825-6004_1825-597 others(36): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(27): Show |
5 | a0001c0001t0003g0255a0001c0001t0003g0268a0001c0001t0004g0163others(2): Show | 5 | HG00408.hp2 HG00609.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1825-6006_1825-597 others(38): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973075
|
C | CTGTGTGT others(29): Show |
2 | a0001c0001t0002g0310a0001c0002t0001g0182 | 2 | HG01261.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1825-6008_1825-597 others(40): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973075 | ||||||
| chr4:7973078
|
T | TGTGTGA | 4 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(1): Show | 4 | HG02572.hp2 HG02630.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1825-5976_1825-597 others(10): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973078 | ||||||
| chr4:7973198
|
G | C | 19 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(16): Show | 19 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.1825-6095C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973198 | ||||||
| chr4:7973278
|
A | G | 3 | a0001c0001t0026g0285a0001c0003t0001g0241a0001c0003t0007g0217 | 3 | HG02717.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1825-6175T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973278 | ||||||
| chr4:7973326
|
C | T | 106 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0020others(103): Show | 106 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1825-6223G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973326 | ||||||
| chr4:7973329
|
C | A | 5 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(2): Show | 5 | HG02572.hp2 HG02630.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1825-6226G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973329 | ||||||
| chr4:7973332
|
C | G | 1 | a0001c0001t0001g0304 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1825-6229G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973332 | ||||||
| chr4:7973374
|
G | GCTC | 8 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-6272_1825-627 others(7): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973374 | ||||||
| chr4:7973377
|
T | G | 8 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-6274A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973377 | ||||||
| chr4:7973512
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1825-6409T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973512 | ||||||
| chr4:7973676
|
C | T | 2 | a0001c0002t0002g0306a0001c0002t0002g0309 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1825-6573G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973676 | ||||||
| chr4:7973835
|
C | T | 1 | a0001c0001t0001g0042 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1825-6732G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973835 | ||||||
| chr4:7973852
|
G | C | 57 | a0001c0001t0001g0098a0001c0001t0001g0311a0001c0001t0002g0006others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1825-6749C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973852 | ||||||
| chr4:7973879
|
T | TA | 3 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0002t0002g0129 | 3 | HG01109.hp2 HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1825-6777dupT | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973879 | ||||||
| chr4:7973952
|
G | T | 1 | a0001c0001t0008g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1825-6849C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7973952 | ||||||
| chr4:7974003
|
A | G | 8 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-6900T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974003 | ||||||
| chr4:7974382
|
CCCATCCA others(5): Show |
C | 3 | a0001c0001t0001g0288a0001c0001t0008g0116a0001c0010t0008g0252 | 3 | HG00639.hp2 HG03579.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1825-7291_1825-728 others(16): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974382 | ||||||
| chr4:7974396
|
C | T | 2 | a0001c0001t0008g0116a0001c0010t0008g0252 | 2 | HG00639.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1825-7293G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974396 | ||||||
| chr4:7974404
|
CATCCATC others(5): Show |
C | 1 | a0001c0002t0003g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1825-7313_1825-730 others(16): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974404 | ||||||
| chr4:7974406
|
T | C | 2 | a0001c0001t0008g0116a0001c0010t0008g0252 | 2 | HG00639.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1825-7303A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974406 | ||||||
| chr4:7974406
|
T | TCCATCTA others(9): Show |
82 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.1825-7304_1825-730 others(20): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974406 | ||||||
| chr4:7974594
|
A | C | 321 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(318): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.1825-7491T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974594 | ||||||
| chr4:7974598
|
TA | T | 313 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1825-7496delT | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974598 | ||||||
| chr4:7974598
|
TACCATC | T | 8 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-7501_1825-749 others(10): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974598 | ||||||
| chr4:7974605
|
CA | C | 313 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(310): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.1825-7503delT | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974605 | ||||||
| chr4:7974606
|
A | C | 8 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-7503T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974606 | ||||||
| chr4:7974670
|
C | CACCA | 8 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1825-7568_1825-756 others(8): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974670 | ||||||
| chr4:7974811
|
C | T | 5 | a0001c0001t0003g0046a0001c0001t0003g0047a0001c0001t0003g0048others(2): Show | 5 | HG02129.hp2 NA18947.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1825-7708G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7974811 | ||||||
| chr4:7975171
|
C | T | 192 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0020others(189): Show | 192 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.1825-8068G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975171 | ||||||
| chr4:7975268
|
G | C | 14 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0001t0002g0283others(11): Show | 14 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1824+7996C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975268 | ||||||
| chr4:7975338
|
C | T | 5 | a0001c0001t0002g0246a0001c0001t0002g0312a0001c0001t0002g0313others(2): Show | 5 | HG01069.hp1 HG01071.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824+7926G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975338 | ||||||
| chr4:7975411
|
T | C | 1 | a0001c0002t0003g0051 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1824+7853A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975411 | ||||||
| chr4:7975473
|
C | T | 1 | a0004c0009t0002g0191 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1824+7791G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975473 | ||||||
| chr4:7975529
|
C | A | 1 | a0001c0002t0002g0129 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1824+7735G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975529 | ||||||
| chr4:7975767
|
C | T | 15 | a0001c0001t0001g0061a0001c0001t0001g0076a0001c0001t0001g0104others(12): Show | 15 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.1824+7497G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975767 | ||||||
| chr4:7975863
|
C | T | 7 | a0001c0001t0005g0072a0001c0001t0005g0084a0001c0002t0005g0029others(4): Show | 7 | HG01071.hp2 HG01109.hp1 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.1824+7401G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975863 | ||||||
| chr4:7975884
|
A | T | 105 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(102): Show | 105 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1824+7380T>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975884 | ||||||
| chr4:7975907
|
G | A | 1 | a0001c0002t0001g0088 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1824+7357C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975907 | ||||||
| chr4:7975985
|
C | G | 1 | a0001c0001t0026g0285 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1824+7279G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7975985 | ||||||
| chr4:7976091
|
T | C | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1824+7173A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976091 | ||||||
| chr4:7976140
|
T | C | 2 | a0001c0001t0002g0067a0001c0002t0002g0129 | 2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1824+7124A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976140 | ||||||
| chr4:7976171
|
T | G | 1 | a0001c0001t0012g0253 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1824+7093A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976171 | ||||||
| chr4:7976216
|
C | T | 36 | a0001c0001t0001g0311a0001c0001t0002g0006a0001c0001t0002g0119others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1824+7048G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976216 | ||||||
| chr4:7976528
|
G | A | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+6736C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976528 | ||||||
| chr4:7976528
|
G | C | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1824+6736C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976528 | ||||||
| chr4:7976661
|
C | CAACACAT others(23): Show |
1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1824+6573_1824+660 others(34): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976661 | ||||||
| chr4:7976662
|
AACACATG others(23): Show |
A | 4 | a0001c0001t0012g0008a0001c0001t0012g0253a0001c0001t0014g0038others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824+6572_1824+660 others(34): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976662 | ||||||
| chr4:7976734
|
T | C | 5 | a0001c0001t0002g0240a0001c0001t0007g0232a0001c0001t0007g0236others(2): Show | 5 | HG01891.hp2 HG02572.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1824+6530A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976734 | ||||||
| chr4:7976792
|
T | C | 17 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0001t0002g0240others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.1824+6472A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976792 | ||||||
| chr4:7976858
|
C | T | 1 | a0001c0002t0003g0200 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1824+6406G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976858 | ||||||
| chr4:7976870
|
CATAA | C | 3 | a0001c0002t0002g0079a0001c0002t0002g0194a0001c0003t0002g0090 | 3 | HG00738.hp1 HG01099.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1824+6390_1824+639 others(8): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976870 | ||||||
| chr4:7976887
|
G | A | 4 | a0001c0001t0001g0288a0001c0001t0007g0132a0001c0003t0007g0218others(1): Show | 4 | HG02257.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824+6377C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976887 | ||||||
| chr4:7976905
|
G | GTA | 180 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(177): Show | 180 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1824+6357_1824+635 others(6): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976905 | ||||||
| chr4:7976907
|
A | ATG | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+6356_1824+635 others(6): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976907 | ||||||
| chr4:7976913
|
A | C | 196 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1824+6351T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976913 | ||||||
| chr4:7976916
|
C | T | 196 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1824+6348G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976916 | ||||||
| chr4:7976963
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1824+6301C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7976963 | ||||||
| chr4:7977008
|
T | C | 196 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1824+6256A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977008 | ||||||
| chr4:7977085
|
TG | T | 5 | a0001c0001t0002g0283a0001c0001t0010g0005a0001c0001t0010g0033others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824+6178delC | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977085 | ||||||
| chr4:7977265
|
A | C | 3 | a0001c0001t0026g0285a0001c0003t0001g0241a0001c0003t0007g0217 | 3 | HG02717.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1824+5999T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977265 | ||||||
| chr4:7977293
|
C | A | 1 | a0001c0002t0003g0200 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1824+5971G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977293 | ||||||
| chr4:7977501
|
G | C | 85 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0267others(82): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1824+5763C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977501 | ||||||
| chr4:7977527
|
T | C | 92 | a0001c0001t0001g0085a0001c0001t0001g0098a0001c0001t0001g0267others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.1824+5737A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977527 | ||||||
| chr4:7977609
|
G | A | 4 | a0001c0001t0001g0085a0001c0001t0002g0091a0001c0001t0002g0092others(1): Show | 4 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824+5655C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977609 | ||||||
| chr4:7977787
|
T | C | 107 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(104): Show | 107 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1824+5477A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977787 | ||||||
| chr4:7977790
|
C | CAATA | 47 | a0001c0001t0001g0078a0001c0001t0001g0109a0001c0001t0001g0118others(44): Show | 47 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.1824+5470_1824+547 others(8): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977790
|
C | CAATAAAT others(1): Show |
38 | a0001c0001t0001g0098a0001c0001t0002g0032a0001c0001t0002g0067others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.1824+5466_1824+547 others(12): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977790
|
C | CAATAAAT others(5): Show |
19 | a0001c0001t0001g0085a0001c0001t0001g0267a0001c0001t0002g0091others(16): Show | 19 | HG00323.hp2 HG01515.hp2 HG01517.hp1 others(16): Show |
intron_variant | MODIFIER | c.1824+5462_1824+547 others(16): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977790
|
C | CAATAAAT others(9): Show |
3 | a0001c0001t0001g0278a0001c0001t0001g0279a0001c0001t0004g0163 | 3 | HG00408.hp2 HG01069.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1824+5458_1824+547 others(20): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977790
|
C | CAATAAAT others(9): Show |
13 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0225others(10): Show | 13 | HG01167.hp1 HG01243.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1824+5473_1824+547 others(20): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977790
|
C | CAATAAAT others(13): Show |
76 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0028others(73): Show | 76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.1824+5473_1824+547 others(24): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977790
|
C | CAATAAAT others(17): Show |
13 | a0001c0001t0001g0014a0001c0001t0001g0017a0001c0001t0002g0011others(10): Show | 13 | HG01433.hp1 HG02165.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.1824+5473_1824+547 others(28): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977790
|
CAATA | C | 3 | a0001c0001t0026g0285a0001c0003t0001g0241a0001c0003t0007g0217 | 3 | HG02717.hp2 HG03041.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1824+5470_1824+547 others(8): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977790 | ||||||
| chr4:7977794
|
A | AAATAAAT others(5): Show |
5 | a0001c0001t0001g0168a0001c0001t0005g0019a0001c0001t0012g0008others(2): Show | 5 | HG01975.hp1 HG02015.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824+5469_1824+547 others(16): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7977794 | ||||||
| chr4:7978080
|
A | C | 3 | a0001c0001t0002g0024a0001c0002t0001g0287a0001c0003t0002g0025 | 3 | HG02647.hp2 HG03041.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1824+5184T>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978080 | ||||||
| chr4:7978082
|
G | A | 1 | a0001c0001t0025g0198 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1824+5182C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978082 | ||||||
| chr4:7978089
|
T | A | 5 | a0001c0001t0002g0032a0001c0001t0002g0237a0001c0001t0010g0215others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824+5175A>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978089 | ||||||
| chr4:7978176
|
C | T | 1 | a0001c0003t0021g0004 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1824+5088G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978176 | ||||||
| chr4:7978177
|
A | G | 106 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(103): Show | 106 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1824+5087T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978177 | ||||||
| chr4:7978182
|
C | G | 1 | a0001c0001t0001g0146 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1824+5082G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978182 | ||||||
| chr4:7978202
|
T | C | 195 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(192): Show | 195 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.1824+5062A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978202 | ||||||
| chr4:7978259
|
A | G | 1 | a0001c0001t0008g0116 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1824+5005T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978259 | ||||||
| chr4:7978309
|
G | C | 4 | a0001c0001t0014g0291a0001c0001t0026g0285a0001c0003t0001g0241others(1): Show | 4 | HG02717.hp2 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824+4955C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978309 | ||||||
| chr4:7978474
|
T | C | 196 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(193): Show | 196 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.1824+4790A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978474 | ||||||
| chr4:7978492
|
T | C | 144 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(141): Show | 144 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1824+4772A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978492 | ||||||
| chr4:7978508
|
T | C | 144 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(141): Show | 144 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.1824+4756A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978508 | ||||||
| chr4:7978509
|
G | C | 2 | a0001c0001t0007g0112a0001c0001t0016g0111 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1824+4755C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978509 | ||||||
| chr4:7978528
|
G | T | 4 | a0001c0001t0002g0010a0001c0001t0012g0008a0001c0001t0014g0038others(1): Show | 4 | HG02451.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824+4736C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978528 | ||||||
| chr4:7978532
|
C | T | 4 | a0001c0001t0002g0010a0001c0001t0012g0008a0001c0001t0014g0038others(1): Show | 4 | HG02451.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1824+4732G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978532 | ||||||
| chr4:7978571
|
C | A | 102 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(99): Show | 102 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1824+4693G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978571 | ||||||
| chr4:7978661
|
C | A | 1 | a0001c0001t0002g0263 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1824+4603G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978661 | ||||||
| chr4:7978724
|
A | AC | 45 | a0001c0001t0001g0098a0001c0001t0001g0311a0001c0001t0002g0006others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1824+4539dupG | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978724 | ||||||
| chr4:7978910
|
G | A | 15 | a0001c0001t0001g0098a0001c0001t0002g0119a0001c0001t0002g0133others(12): Show | 15 | HG00140.hp1 HG00738.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.1824+4354C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978910 | ||||||
| chr4:7978912
|
C | T | 1 | a0001c0001t0010g0215 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1824+4352G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978912 | ||||||
| chr4:7978925
|
C | T | 64 | a0001c0001t0001g0288a0001c0001t0001g0311a0001c0001t0002g0006others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1824+4339G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978925 | ||||||
| chr4:7978926
|
G | C | 1 | a0001c0001t0001g0293 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1824+4338C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978926 | ||||||
| chr4:7978998
|
A | G | 203 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(200): Show | 203 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.1824+4266T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7978998 | ||||||
| chr4:7979010
|
G | A | 42 | a0001c0001t0001g0098a0001c0001t0001g0311a0001c0001t0002g0006others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1824+4254C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7979010 | ||||||
| chr4:7979019
|
C | T | 21 | a0001c0001t0001g0288a0001c0001t0002g0067a0001c0001t0002g0213others(18): Show | 21 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1824+4245G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7979019 | ||||||
| chr4:7979023
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1824+4241C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7979023 | ||||||
| chr4:7979104
|
G | A | 3 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0314 | 3 | HG01069.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1824+4160C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7979104 | ||||||
| chr4:7979511
|
T | C | 198 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(195): Show | 198 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.1824+3753A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7979511 | ||||||
| chr4:7979620
|
T | A | 5 | a0001c0001t0002g0032a0001c0001t0002g0237a0001c0001t0010g0215others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824+3644A>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7979620 | ||||||
| chr4:7979624
|
T | C | 1 | a0001c0001t0022g0153 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1824+3640A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7979624 | ||||||
| chr4:7980146
|
C | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1824+3118G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980146 | ||||||
| chr4:7980148
|
C | A | 66 | a0001c0001t0001g0267a0001c0001t0001g0288a0001c0001t0001g0311others(63): Show | 66 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1824+3116G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980148 | ||||||
| chr4:7980214
|
C | A | 1 | a0001c0001t0001g0267 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1824+3050G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980214 | ||||||
| chr4:7980338
|
T | C | 5 | a0001c0001t0002g0032a0001c0001t0002g0237a0001c0001t0010g0215others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824+2926A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980338 | ||||||
| chr4:7980385
|
T | C | 104 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1824+2879A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980385 | ||||||
| chr4:7980409
|
G | A | 2 | a0001c0001t0032g0320a0001c0002t0001g0060 | 2 | HG02040.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1824+2855C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980409 | ||||||
| chr4:7980530
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1824+2734G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980530 | ||||||
| chr4:7980642
|
G | T | 1 | a0001c0003t0006g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1824+2622C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980642 | ||||||
| chr4:7980668
|
T | C | 2 | a0001c0001t0002g0230a0001c0002t0002g0290 | 2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1824+2596A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980668 | ||||||
| chr4:7980698
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1824+2566C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980698 | ||||||
| chr4:7980718
|
G | GA | 21 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(18): Show | 21 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1824+2545dupT | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980718 | ||||||
| chr4:7980777
|
T | C | 104 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1824+2487A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980777 | ||||||
| chr4:7980859
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1824+2405G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980859 | ||||||
| chr4:7980941
|
A | ATCTTTT | 39 | a0001c0001t0001g0311a0001c0001t0002g0006a0001c0001t0002g0119others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1824+2322_1824+232 others(10): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATCTTTTT | 21 | a0001c0001t0002g0032a0001c0001t0002g0137a0001c0001t0002g0230others(18): Show | 21 | HG00408.hp2 HG01106.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.1824+2322_1824+232 others(11): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATCTTTTT others(1): Show |
6 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(3): Show | 6 | HG00323.hp2 HG01069.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.1824+2322_1824+232 others(12): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATCTTTTT others(6): Show |
1 | a0001c0001t0006g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1824+2322_1824+232 others(17): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATCTTTTT others(15): Show |
2 | a0001c0001t0002g0010a0001c0001t0017g0203 | 2 | HG03139.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1824+2322_1824+232 others(26): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATCTTTTT others(16): Show |
2 | a0001c0001t0012g0008a0001c0001t0014g0038 | 2 | HG02451.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1824+2322_1824+232 others(27): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1824+2309_1824+232 others(18): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(8): Show |
1 | a0001c0001t0005g0019 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1824+2308_1824+232 others(19): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0265a0001c0001t0003g0046 | 2 | NA18962.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.1824+2307_1824+232 others(20): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(10): Show |
60 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0020others(57): Show | 60 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(57): Show |
intron_variant | MODIFIER | c.1824+2306_1824+232 others(21): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(11): Show |
50 | a0001c0001t0001g0017a0001c0001t0001g0061a0001c0001t0001g0135others(47): Show | 50 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1824+2305_1824+232 others(22): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(12): Show |
25 | a0001c0001t0001g0042a0001c0001t0001g0078a0001c0001t0001g0117others(22): Show | 25 | HG00544.hp1 HG00544.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.1824+2304_1824+232 others(23): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(13): Show |
10 | a0001c0001t0001g0274a0001c0001t0002g0152a0001c0001t0002g0246others(7): Show | 10 | HG00140.hp2 HG01099.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.1824+2303_1824+232 others(24): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980941
|
A | ATTTTTTT others(15): Show |
3 | a0001c0002t0001g0120a0001c0002t0001g0145a0001c0004t0003g0065 | 3 | HG01123.hp2 NA19090.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.1824+2322_1824+232 others(26): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980941 | ||||||
| chr4:7980942
|
T | TC | 6 | a0001c0001t0001g0288a0001c0001t0002g0283a0001c0001t0010g0005others(3): Show | 6 | HG02109.hp1 HG02818.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1824+2321_1824+232 others(5): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980942 | ||||||
| chr4:7980991
|
C | T | 5 | a0001c0001t0002g0283a0001c0001t0010g0005a0001c0001t0010g0033others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1824+2273G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7980991 | ||||||
| chr4:7981006
|
C | G | 8 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0001t0006g0210others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1824+2258G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981006 | ||||||
| chr4:7981045
|
G | A | 103 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(100): Show | 103 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1824+2219C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981045 | ||||||
| chr4:7981234
|
C | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1824+2030G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981234 | ||||||
| chr4:7981263
|
C | A | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1824+2001G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981263 | ||||||
| chr4:7981269
|
T | C | 3 | a0001c0001t0003g0012a0001c0001t0030g0099a0001c0002t0001g0174 | 3 | HG03704.hp2 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1824+1995A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981269 | ||||||
| chr4:7981390
|
G | C | 62 | a0001c0001t0001g0288a0001c0001t0001g0311a0001c0001t0002g0006others(59): Show | 62 | HG00099.hp1 HG00609.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1824+1874C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981390 | ||||||
| chr4:7981582
|
G | C | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1824+1682C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981582 | ||||||
| chr4:7981610
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1824+1654C>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981610 | ||||||
| chr4:7981818
|
C | T | 104 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(101): Show | 104 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1824+1446G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981818 | ||||||
| chr4:7981906
|
TG | T | 21 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(18): Show | 21 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(18): Show |
intron_variant | MODIFIER | c.1824+1357delC | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7981906 | ||||||
| chr4:7982071
|
TGCCCCTC others(51): Show |
T | 1 | a0001c0001t0001g0228 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1824+1135_1824+119 others(62): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982071 | ||||||
| chr4:7982097
|
GAGACTGA others(51): Show |
G | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+1109_1824+116 others(62): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982097 | ||||||
| chr4:7982110
|
T | C | 5 | a0001c0001t0007g0132a0001c0001t0008g0116a0001c0003t0007g0218others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1824+1154A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982110 | ||||||
| chr4:7982121
|
T | G | 5 | a0001c0001t0007g0132a0001c0001t0008g0116a0001c0003t0007g0218others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1824+1143A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982121 | ||||||
| chr4:7982130
|
G | A | 8 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0001t0006g0210others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1824+1134C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982130 | ||||||
| chr4:7982144
|
CTCCCCAG others(51): Show |
C | 2 | a0001c0001t0002g0149a0001c0003t0002g0081 | 2 | HG01943.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1824+1062_1824+111 others(62): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982144 | ||||||
| chr4:7982189
|
C | T | 1 | a0001c0001t0003g0244 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1824+1075G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982189 | ||||||
| chr4:7982202
|
T | C | 318 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1824+1062A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982202 | ||||||
| chr4:7982222
|
C | T | 103 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(100): Show | 103 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1824+1042G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982222 | ||||||
| chr4:7982230
|
TG | T | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+1033delC | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982230 | ||||||
| chr4:7982309
|
A | T | 1 | a0001c0001t0004g0208 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1824+955T>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982309 | ||||||
| chr4:7982313
|
T | G | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+951A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982313 | ||||||
| chr4:7982383
|
G | A | 5 | a0001c0001t0007g0132a0001c0001t0008g0116a0001c0003t0007g0218others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1824+881C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982383 | ||||||
| chr4:7982417
|
C | G | 3 | a0001c0002t0001g0034a0001c0002t0001g0259a0001c0004t0001g0069 | 3 | HG00642.hp2 HG01168.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1824+847G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982417 | ||||||
| chr4:7982441
|
C | G | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+823G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982441 | ||||||
| chr4:7982491
|
C | T | 103 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(100): Show | 103 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1824+773G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982491 | ||||||
| chr4:7982554
|
T | A | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+710A>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982554 | ||||||
| chr4:7982666
|
C | G | 1 | a0001c0001t0012g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1824+598G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982666 | ||||||
| chr4:7982701
|
C | CATT | 51 | a0001c0001t0001g0098a0001c0001t0001g0311a0001c0001t0002g0006others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1824+560_1824+562d others(5): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982701 | ||||||
| chr4:7982779
|
C | T | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+485G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982779 | ||||||
| chr4:7982796
|
C | T | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+468G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982796 | ||||||
| chr4:7982826
|
C | T | 6 | a0001c0001t0002g0067a0001c0001t0002g0213a0001c0001t0004g0224others(3): Show | 6 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1824+438G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982826 | ||||||
| chr4:7982850
|
C | T | 6 | a0001c0001t0026g0285a0001c0003t0001g0241a0001c0003t0006g0209others(3): Show | 6 | HG02145.hp1 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1824+414G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982850 | ||||||
| chr4:7982983
|
G | A | 1 | a0001c0001t0004g0204 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1824+281C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7982983 | ||||||
| chr4:7983009
|
T | C | 16 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(13): Show | 16 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.1824+255A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7983009 | ||||||
| chr4:7983191
|
C | T | 17 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(14): Show | 17 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.1824+73G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7983191 | ||||||
| chr4:7983222
|
G | T | 1 | a0001c0008t0006g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1824+42C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7983222 | ||||||
| chr4:7983243
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1824+21G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 20/20 | chr4 | 7983243 | ||||||
| chr4:7983354
|
G | A | 6 | a0001c0001t0026g0285a0001c0003t0001g0241a0001c0003t0006g0209others(3): Show | 6 | HG02145.hp1 HG02717.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1744-10C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 19/20 | chr4 | 7983354 | ||||||
| chr4:7983363
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1744-19T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 19/20 | chr4 | 7983363 | ||||||
| chr4:7983398
|
C | T | 1 | a0001c0001t0005g0019 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1744-54G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 19/20 | chr4 | 7983398 | ||||||
| chr4:7983476
|
A | G | 1 | a0001c0001t0003g0089 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1743+71T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 19/20 | chr4 | 7983476 | ||||||
| chr4:7983559
|
A | AAG | 4 | a0001c0001t0002g0010a0001c0001t0012g0008a0001c0001t0014g0038others(1): Show | 4 | HG02451.hp1 HG03139.hp1 HG03209.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1736-7_1736-6dupCT | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983559 | ||||||
| chr4:7983665
|
C | G | 122 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(119): Show | 122 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1736-111G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983665 | ||||||
| chr4:7983744
|
T | TCC | 7 | a0001c0001t0005g0294a0001c0001t0026g0285a0001c0003t0001g0241others(4): Show | 7 | HG01261.hp2 HG02145.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1736-192_1736-191d others(4): Show |
ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983744 | ||||||
| chr4:7983751
|
G | A | 2 | a0001c0001t0003g0176a0001c0002t0003g0049 | 2 | NA18612.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1736-197C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983751 | ||||||
| chr4:7983868
|
T | C | 1 | a0001c0001t0017g0300 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1736-314A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983868 | ||||||
| chr4:7983897
|
C | T | 15 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1736-343G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983897 | ||||||
| chr4:7983921
|
G | A | 15 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1736-367C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983921 | ||||||
| chr4:7983977
|
C | T | 5 | a0001c0001t0007g0132a0001c0001t0008g0116a0001c0003t0007g0218others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1736-423G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983977 | ||||||
| chr4:7983998
|
C | T | 15 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1736-444G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7983998 | ||||||
| chr4:7984026
|
C | G | 1 | a0001c0002t0001g0305 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1736-472G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984026 | ||||||
| chr4:7984030
|
C | A | 5 | a0001c0001t0007g0132a0001c0001t0008g0116a0001c0003t0007g0218others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1736-476G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984030 | ||||||
| chr4:7984033
|
CT | C | 8 | a0001c0001t0001g0267a0001c0001t0002g0067a0001c0001t0002g0213others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1736-480delA | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984033 | ||||||
| chr4:7984047
|
C | A | 5 | a0001c0001t0007g0132a0001c0001t0008g0116a0001c0003t0007g0218others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1736-493G>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984047 | ||||||
| chr4:7984103
|
C | T | 15 | a0001c0001t0001g0085a0001c0001t0001g0278a0001c0001t0001g0279others(12): Show | 15 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1736-549G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984103 | ||||||
| chr4:7984200
|
A | G | 50 | a0001c0001t0001g0085a0001c0001t0001g0267a0001c0001t0001g0278others(47): Show | 50 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.1735+639T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984200 | ||||||
| chr4:7984250
|
T | C | 135 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(132): Show | 135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1735+589A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984250 | ||||||
| chr4:7984344
|
G | A | 39 | a0001c0001t0001g0098a0001c0001t0001g0311a0001c0001t0002g0006others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1735+495C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984344 | ||||||
| chr4:7984370
|
C | T | 1 | a0001c0002t0004g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1735+469G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984370 | ||||||
| chr4:7984391
|
C | T | 5 | a0001c0001t0002g0283a0001c0001t0010g0005a0001c0001t0010g0033others(2): Show | 5 | HG02109.hp1 HG02818.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735+448G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984391 | ||||||
| chr4:7984399
|
C | G | 49 | a0001c0001t0001g0085a0001c0001t0001g0267a0001c0001t0001g0278others(46): Show | 49 | HG00323.hp2 HG00408.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.1735+440G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984399 | ||||||
| chr4:7984468
|
G | A | 1 | a0001c0002t0001g0083 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1735+371C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984468 | ||||||
| chr4:7984472
|
C | T | 14 | a0001c0001t0001g0288a0001c0001t0002g0010a0001c0001t0002g0231others(11): Show | 14 | HG02109.hp1 HG02451.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1735+367G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984472 | ||||||
| chr4:7984519
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1735+320G>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984519 | ||||||
| chr4:7984580
|
T | G | 1 | a0001c0001t0004g0163 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1735+259A>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984580 | ||||||
| chr4:7984630
|
A | G | 14 | a0001c0001t0001g0288a0001c0001t0002g0010a0001c0001t0002g0231others(11): Show | 14 | HG02109.hp1 HG02451.hp1 HG02723.hp2 others(11): Show |
intron_variant | MODIFIER | c.1735+209T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 18/20 | chr4 | 7984630 | ||||||
| chr4:7984932
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0003g0244 | 2 | NA18954.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1681-39C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7984932 | ||||||
| chr4:7985048
|
G | T | 5 | a0001c0001t0007g0132a0001c0001t0008g0116a0001c0003t0007g0218others(2): Show | 5 | HG00639.hp2 HG02257.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1681-155C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985048 | ||||||
| chr4:7985067
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1681-174C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985067 | ||||||
| chr4:7985094
|
C | T | 108 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(105): Show | 108 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1681-201G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985094 | ||||||
| chr4:7985096
|
T | C | 92 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(89): Show | 92 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1681-203A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985096 | ||||||
| chr4:7985098
|
G | A | 1 | a0001c0001t0010g0215 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1681-205C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985098 | ||||||
| chr4:7985133
|
T | C | 182 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(179): Show | 182 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.1681-240A>G | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985133 | ||||||
| chr4:7985182
|
A | G | 314 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.1681-289T>C | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985182 | ||||||
| chr4:7985209
|
G | A | 5 | a0001c0001t0001g0303a0001c0001t0002g0177a0001c0002t0001g0145others(2): Show | 5 | HG01123.hp2 HG01358.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.1681-316C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985209 | ||||||
| chr4:7985270
|
C | T | 4 | a0001c0001t0002g0032a0001c0001t0002g0237a0001c0001t0010g0215others(1): Show | 4 | HG02647.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1681-377G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985270 | ||||||
| chr4:7985302
|
C | T | 3 | a0001c0002t0002g0306a0001c0002t0002g0309a0001c0002t0003g0026 | 3 | HG02895.hp1 HG02897.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1681-409G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985302 | ||||||
| chr4:7985327
|
G | A | 1 | a0001c0002t0001g0105 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1681-434C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985327 | ||||||
| chr4:7985337
|
T | A | 84 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(81): Show | 84 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1681-444A>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985337 | ||||||
| chr4:7985429
|
G | T | 2 | a0001c0002t0002g0306a0001c0002t0002g0309 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1681-536C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985429 | ||||||
| chr4:7985659
|
C | T | 1 | a0001c0002t0001g0134 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1681-766G>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985659 | ||||||
| chr4:7985732
|
G | T | 2 | a0001c0002t0002g0306a0001c0002t0002g0309 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1681-839C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985732 | ||||||
| chr4:7985830
|
G | A | 85 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(82): Show | 85 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1681-937C>T | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985830 | ||||||
| chr4:7985830
|
G | T | 6 | a0001c0001t0001g0288a0001c0001t0002g0283a0001c0001t0010g0005others(3): Show | 6 | HG02109.hp1 HG02818.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1681-937C>A | ABLIM2 | ENSG00000163995.22 | transcript | ENST00000447017.7 | protein_coding | 17/20 | chr4 | 7985830 | ||||||
| chr4:7985913
|
T | C | 8 | a0001c0001t0001g0267a0001c0001t0002g0067a0001c0001t0002g0213others(5): Show | 8 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(5): Show |