Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 196528 |
|---|---|
| ensemblid | ENSG00000189079.18 |
| hgncid | 18037 |
| symbol | ARID2 |
| name | AT-rich interaction domain 2 |
| refseq_nuc | NM_152641.4 |
| refseq_prot | NP_689854.2 |
| ensembl_nuc | ENST00000334344.11 |
| ensembl_prot | ENSP00000335044.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 45729706 |
| end | 45908037 |
| strand | + |
| ver | v1.2 |
| region | chr12:45729706-45908037 |
| region5000 | chr12:45724706-45913037 |
| regionname0 | ARID2_chr12_45729706_45908037 |
| regionname5000 | ARID2_chr12_45724706_45913037 |
| 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 | 1835 | 285 | 67 | 63 | 103 | 12 | 38 | 74 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0002 | 0/0 | 1835 | 13 | 0 | 0 | 13 | 0 | 0 | 9 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0003 | 0/0 | 1835 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0004 | 0/0 | 1835 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0005 | 0/0 | 1835 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0006 | 0/0 | 1835 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0007 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0008 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0009 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0010 | 0/0 | 1835 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0011 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0012 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0013 | 0/0 | 1835 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0014 | 0/0 | 1835 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 5508 | 258 | 41 | 62 | 103 | 12 | 38 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0002 | 0/0 | 5508 | 20 | 19 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0003 | 0/0 | 5508 | 12 | 0 | 0 | 12 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0004 | 0/0 | 5508 | 5 | 5 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0005 | 0/0 | 5508 | 3 | 0 | 0 | 3 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0006 | 0/0 | 5508 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0007 | 0/0 | 5508 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0008 | 0/0 | 5508 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0009 | 0/0 | 5508 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0010 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0011 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0012 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0013 | 0/0 | 5508 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0014 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0015 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0016 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0017 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0018 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0019 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| c0020 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 3091 | 253 | 29 | 59 | 123 | 12 | 28 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0002 | 0/0 | 3092 | 21 | 20 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0003 | 0/0 | 3091 | 6 | 0 | 0 | 0 | 0 | 6 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0004 | 0/0 | 3092 | 5 | 5 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0005 | 0/0 | 3091 | 4 | 4 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0006 | 0/0 | 3092 | 4 | 4 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0007 | 0/0 | 3091 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0008 | 0/0 | 3091 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0009 | 0/0 | 3091 | 3 | 1 | 2 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0010 | 0/0 | 3091 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0011 | 0/0 | 3091 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0012 | 0/0 | 3091 | 2 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0013 | 0/0 | 3091 | 2 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0014 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0015 | 0/0 | 3091 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0016 | 0/0 | 3091 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0017 | 0/0 | 3091 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0018 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0019 | 0/0 | 3079 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0020 | 0/0 | 3092 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| t0021 | 0/0 | 3092 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 5508 | 258 | 41 | 62 | 103 | 12 | 38 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0002 | 0/0 | 5508 | 20 | 19 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0006 | 0/0 | 5508 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0009 | 0/0 | 5508 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0011 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0016 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0002c0003 | 0/0 | 5508 | 12 | 0 | 0 | 12 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0002c0020 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0003c0004 | 0/0 | 5508 | 5 | 5 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0004c0005 | 0/0 | 5508 | 3 | 0 | 0 | 3 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0005c0008 | 0/0 | 5508 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0006c0007 | 0/0 | 5508 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0007c0017 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0008c0015 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0009c0014 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0010c0013 | 0/0 | 5508 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0011c0010 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0012c0012 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0013c0018 | 0/0 | 5508 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0014c0019 | 0/0 | 5508 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 8598 | 226 | 26 | 58 | 100 | 12 | 28 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0003 | 0/0 | 8598 | 6 | 0 | 0 | 0 | 0 | 6 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0004 | 0/0 | 8599 | 5 | 5 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0005 | 0/0 | 8598 | 4 | 4 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0007 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0009 | 0/0 | 8598 | 3 | 1 | 2 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0010 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0012 | 0/0 | 8598 | 2 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0013 | 0/0 | 8598 | 2 | 0 | 1 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0014 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0015 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0016 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0017 | 0/0 | 8598 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0001t0020 | 0/0 | 8599 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0002t0002 | 0/0 | 8599 | 20 | 19 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0006t0008 | 0/0 | 8598 | 3 | 3 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0009t0011 | 0/0 | 8598 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0011t0019 | 0/0 | 8586 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0001c0016t0001 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0002c0003t0001 | 0/0 | 8598 | 12 | 0 | 0 | 12 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0002c0020t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0003c0004t0006 | 0/0 | 8599 | 4 | 4 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0003c0004t0018 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0004c0005t0001 | 0/0 | 8598 | 3 | 0 | 0 | 3 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0005c0008t0001 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0006c0007t0001 | 0/0 | 8598 | 2 | 0 | 0 | 2 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0007c0017t0001 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0008c0015t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0009c0014t0021 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0010c0013t0001 | 0/0 | 8598 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0011c0010t0002 | 0/0 | 8599 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0012c0012t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0013c0018t0001 | 0/0 | 8598 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| a0014c0019t0001 | 0/0 | 8598 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | copy fasta | chr12 | 45724706 | 45913037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0005g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0009g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0009g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0010g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0010g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0012g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0012g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0013g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0013g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0014g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0015g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0017g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0001t0020g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0002t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0006t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0006t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0006t0008g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0009t0011g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0009t0011g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0011t0019g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0001c0016t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0002c0020t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0003c0004t0018g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0004c0005t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0004c0005t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0004c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0005c0008t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0005c0008t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0006c0007t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0006c0007t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0007c0017t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0008c0015t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0009c0014t0021g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0010c0013t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0011c0010t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0012c0012t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0013c0018t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| a0014c0019t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0050 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0276 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | FIN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | FIN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00408 | hp2 | a0001 | c0001 | t0010 | g0191 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00597 | hp1 | a0014 | c0019 | t0001 | g0079 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00597 | hp2 | a0002 | c0003 | t0001 | g0307 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00673 | hp2 | a0002 | c0003 | t0001 | g0254 | EAS | CHS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00741 | hp1 | a0001 | c0001 | t0013 | g0265 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01167 | hp1 | a0001 | c0001 | t0009 | g0112 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01169 | hp2 | a0001 | c0001 | t0009 | g0211 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0226 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01358 | hp1 | a0001 | c0001 | t0012 | g0182 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01433 | hp1 | a0010 | c0013 | t0001 | g0263 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0038 | EUR | IBS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01884 | hp1 | a0001 | c0011 | t0019 | g0272 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0305 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0286 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02135 | hp1 | a0005 | c0008 | t0001 | g0043 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02165 | hp1 | a0002 | c0020 | t0001 | g0251 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CDX | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0223 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02280 | hp1 | a0007 | c0017 | t0001 | g0008 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0221 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02451 | hp1 | a0003 | c0004 | t0018 | g0205 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02451 | hp2 | a0001 | c0002 | t0002 | g0215 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02622 | hp2 | a0001 | c0006 | t0008 | g0114 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0237 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0260 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02647 | hp2 | a0003 | c0004 | t0006 | g0107 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02698 | hp2 | a0001 | c0001 | t0012 | g0183 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02717 | hp1 | a0001 | c0009 | t0011 | g0207 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02738 | hp1 | a0001 | c0001 | t0020 | g0030 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02809 | hp1 | a0001 | c0016 | t0001 | g0302 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02886 | hp1 | a0003 | c0004 | t0006 | g0105 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0217 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02895 | hp2 | a0001 | c0006 | t0008 | g0113 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0259 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0228 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02965 | hp1 | a0003 | c0004 | t0006 | g0106 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0214 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03098 | hp2 | a0003 | c0004 | t0006 | g0108 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03130 | hp1 | a0011 | c0010 | t0002 | g0206 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0288 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0269 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0219 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03209 | hp1 | a0001 | c0001 | t0016 | g0313 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0227 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0261 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0212 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0184 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0229 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03516 | hp1 | a0001 | c0009 | t0011 | g0209 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | GWD | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03654 | hp2 | a0001 | c0001 | t0013 | g0266 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03942 | hp1 | a0001 | c0001 | t0017 | g0131 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0283 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0280 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18747 | hp1 | a0004 | c0005 | t0001 | g0111 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0225 | AFR | YRI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0258 | AFR | YRI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18940 | hp2 | a0012 | c0012 | t0001 | g0127 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18945 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18956 | hp2 | a0004 | c0005 | t0001 | g0147 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18957 | hp2 | a0006 | c0007 | t0001 | g0010 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18962 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18986 | hp2 | a0006 | c0007 | t0001 | g0012 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19001 | hp2 | a0005 | c0008 | t0001 | g0080 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19003 | hp2 | a0001 | c0001 | t0015 | g0149 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19011 | hp2 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19030 | hp1 | a0001 | c0006 | t0008 | g0115 | AFR | LWK | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | LWK | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19060 | hp2 | a0002 | c0003 | t0001 | g0210 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19062 | hp2 | a0002 | c0003 | t0001 | g0253 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19065 | hp1 | a0001 | c0001 | t0010 | g0109 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19070 | hp1 | a0002 | c0003 | t0001 | g0186 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0250 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19077 | hp1 | a0004 | c0005 | t0001 | g0169 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19078 | hp1 | a0008 | c0015 | t0001 | g0294 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19088 | hp2 | a0002 | c0003 | t0001 | g0262 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0308 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0268 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0281 | SAS | GIH | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | GIH | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0218 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0220 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02559 | hp1 | a0009 | c0014 | t0021 | g0213 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0287 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0216 | AFR | MSL | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20300 | hp1 | a0013 | c0018 | t0001 | g0230 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | USA | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0137 | REF | REF | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0039 | REF | REF | ARID2_chr12_45724706_45913037 | ARID2 | chr12 | 45724706 | 45913037 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45836741
|
A | G | 1 | a0014 | 1 | HG00597.hp1 | missense_variant&splice_region_variant | MODERATE | c.773A>G | p.Glu258Gly | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 8/21 | 904/8598 | 773/5508 | 258/1835 | chr12 | 45836741 | ||
| chr12:45839421
|
C | T | 1 | a0013 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1423C>T | p.His475Tyr | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/21 | 1554/8598 | 1423/5508 | 475/1835 | chr12 | 45839421 | ||
| chr12:45849582
|
C | T | 1 | a0007 | 1 | HG02280.hp1 | missense_variant&splice_region_variant | MODERATE | c.1718C>T | p.Thr573Met | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 14/21 | 1849/8598 | 1718/5508 | 573/1835 | chr12 | 45849582 | ||
| chr12:45849623
|
A | G | 1 | a0005 | 2 | HG02135.hp1 NA19001.hp2 |
missense_variant | MODERATE | c.1759A>G | p.Ser587Gly | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 14/21 | 1890/8598 | 1759/5508 | 587/1835 | chr12 | 45849623 | ||
| chr12:45850152
|
G | A | 1 | a0006 | 2 | NA18957.hp2 NA18986.hp2 |
missense_variant | MODERATE | c.2029G>A | p.Val677Met | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2160/8598 | 2029/5508 | 677/1835 | chr12 | 45850152 | ||
| chr12:45850551
|
G | C | 1 | a0004 | 3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
missense_variant | MODERATE | c.2428G>C | p.Ala810Pro | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2559/8598 | 2428/5508 | 810/1835 | chr12 | 45850551 | ||
| chr12:45850887
|
A | G | 1 | a0003 | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.2764A>G | p.Thr922Ala | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2895/8598 | 2764/5508 | 922/1835 | chr12 | 45850887 | ||
| chr12:45850929
|
G | T | 1 | a0008 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.2806G>T | p.Gly936Cys | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2937/8598 | 2806/5508 | 936/1835 | chr12 | 45850929 | ||
| chr12:45851868
|
G | A | 1 | a0012 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.3745G>A | p.Glu1249Lys | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 3876/8598 | 3745/5508 | 1249/1835 | chr12 | 45851868 | ||
| chr12:45852423
|
G | T | 1 | a0002 | 13 | HG00597.hp2 HG00673.hp2 HG02155.hp1 others(10): Show |
missense_variant | MODERATE | c.4300G>T | p.Ala1434Ser | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4431/8598 | 4300/5508 | 1434/1835 | chr12 | 45852423 | ||
| chr12:45852465
|
C | T | 1 | a0009 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4342C>T | p.Leu1448Phe | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4473/8598 | 4342/5508 | 1448/1835 | chr12 | 45852465 | ||
| chr12:45852615
|
G | A | 1 | a0011 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.4492G>A | p.Ala1498Thr | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4623/8598 | 4492/5508 | 1498/1835 | chr12 | 45852615 | ||
| chr12:45852847
|
A | G | 1 | a0010 | 1 | HG01433.hp1 | missense_variant | MODERATE | c.4724A>G | p.Gln1575Arg | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4855/8598 | 4724/5508 | 1575/1835 | chr12 | 45852847 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45730131
|
C | T | 1 | a0002c0020 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.180C>T | p.Phe60Phe | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/21 | 311/8598 | 180/5508 | 60/1835 | chr12 | 45730131 | ||
| chr12:45811472
|
A | C | 1 | a0001c0009 | 2 | HG02717.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.339A>C | p.Val113Val | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/21 | 470/8598 | 339/5508 | 113/1835 | chr12 | 45811472 | ||
| chr12:45850634
|
A | T | 1 | a0001c0016 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2511A>T | p.Ser837Ser | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 2642/8598 | 2511/5508 | 837/1835 | chr12 | 45850634 | ||
| chr12:45851294
|
G | A | 3 | a0001c0002a0001c0006a0011c0010 | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
synonymous_variant | LOW | c.3171G>A | p.Ser1057Ser | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 3302/8598 | 3171/5508 | 1057/1835 | chr12 | 45851294 | ||
| chr12:45851486
|
G | A | 1 | a0001c0011 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.3363G>A | p.Leu1121Leu | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 3494/8598 | 3363/5508 | 1121/1835 | chr12 | 45851486 | ||
| chr12:45852311
|
A | G | 1 | a0001c0006 | 3 | HG02622.hp2 HG02895.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.4188A>G | p.Gln1396Gln | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/21 | 4319/8598 | 4188/5508 | 1396/1835 | chr12 | 45852311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45729822
|
T | A | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 1/21 | 15 | chr12 | 45729822 | |||||
| chr12:45729823
|
C | G | 1 | a0001c0001t0003 | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-14C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 1/21 | chr12 | 45729823 | ||||||
| chr12:45905383
|
G | A | 1 | a0001c0001t0007 | 3 | HG02630.hp1 HG03195.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*305G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 305 | chr12 | 45905383 | |||||
| chr12:45905466
|
T | C | 1 | a0001c0001t0015 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*388T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 388 | chr12 | 45905466 | |||||
| chr12:45905513
|
G | A | 1 | a0001c0001t0010 | 2 | HG00408.hp2 NA19065.hp1 |
3_prime_UTR_variant | MODIFIER | c.*435G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 435 | chr12 | 45905513 | |||||
| chr12:45905933
|
CTTTTTTC others(5): Show |
C | 1 | a0001c0011t0019 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*874_*885delCTTTTT others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 874 | INFO_REALIGN_3_PRIME | chr12 | 45905933 | ||||
| chr12:45905940
|
C | CT | 4 | a0001c0001t0020a0001c0002t0002a0009c0014t0021others(1): Show | 23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*873dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 874 | INFO_REALIGN_3_PRIME | chr12 | 45905940 | ||||
| chr12:45905952
|
C | CT | 3 | a0001c0001t0004a0003c0004t0006a0003c0004t0018 | 10 | HG02451.hp1 HG02615.hp1 HG02647.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*885dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 886 | INFO_REALIGN_3_PRIME | chr12 | 45905952 | ||||
| chr12:45905952
|
C | T | 2 | a0001c0001t0009a0009c0014t0021 | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*874C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 874 | chr12 | 45905952 | |||||
| chr12:45906057
|
T | A | 1 | a0001c0009t0011 | 2 | HG02717.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*979T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 979 | chr12 | 45906057 | |||||
| chr12:45906102
|
G | A | 2 | a0003c0004t0006a0003c0004t0018 | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1024G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1024 | chr12 | 45906102 | |||||
| chr12:45906317
|
C | T | 1 | a0001c0001t0013 | 2 | HG00741.hp1 HG03654.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1239C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1239 | chr12 | 45906317 | |||||
| chr12:45906324
|
A | T | 2 | a0001c0001t0005a0001c0001t0014 | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1246A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1246 | chr12 | 45906324 | |||||
| chr12:45906855
|
T | G | 2 | a0003c0004t0006a0003c0004t0018 | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1777T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 1777 | chr12 | 45906855 | |||||
| chr12:45907096
|
T | C | 1 | a0003c0004t0018 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2018T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2018 | chr12 | 45907096 | |||||
| chr12:45907285
|
T | C | 1 | a0001c0001t0016 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2207T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2207 | chr12 | 45907285 | |||||
| chr12:45907298
|
G | A | 4 | a0001c0001t0004a0001c0002t0002a0001c0006t0008others(1): Show | 29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2220G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2220 | chr12 | 45907298 | |||||
| chr12:45907420
|
T | C | 1 | a0001c0001t0017 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2342T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2342 | chr12 | 45907420 | |||||
| chr12:45907877
|
C | T | 1 | a0001c0001t0012 | 2 | HG01358.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2799C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 21/21 | 2799 | chr12 | 45907877 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:45730556
|
A | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.186+419A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730556 | ||||||
| chr12:45730612
|
G | T | 1 | a0001c0001t0001g0315 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.186+475G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730612 | ||||||
| chr12:45730630
|
A | G | 214 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0116others(211): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.186+493A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730630 | ||||||
| chr12:45730818
|
G | GC | 29 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(26): Show | 29 | HG00438.hp1 HG00597.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.187-389dupC | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 45730818 | |||||
| chr12:45730824
|
C | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-393C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45730824 | ||||||
| chr12:45730873
|
C | CT | 12 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0096others(9): Show | 12 | HG00438.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.187-322dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 45730873 | |||||
| chr12:45730873
|
CT | C | 111 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(108): Show | 112 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.187-322delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr12 | 45730873 | |||||
| chr12:45731076
|
T | A | 1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.187-141T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45731076 | ||||||
| chr12:45731077
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.187-140A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 2/20 | chr12 | 45731077 | ||||||
| chr12:45731346
|
G | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+32G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731346 | ||||||
| chr12:45731465
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+151G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731465 | ||||||
| chr12:45731809
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.284+495A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731809 | ||||||
| chr12:45731859
|
T | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+545T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45731859 | ||||||
| chr12:45732070
|
C | A | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.284+756C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732070 | ||||||
| chr12:45732071
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.284+757G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732071 | ||||||
| chr12:45732071
|
G | GT | 11 | a0001c0001t0001g0092a0001c0001t0001g0203a0001c0001t0001g0204others(8): Show | 11 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(8): Show |
intron_variant | MODIFIER | c.284+768dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45732071 | |||||
| chr12:45732239
|
G | T | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+925G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732239 | ||||||
| chr12:45732383
|
C | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+1069C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732383 | ||||||
| chr12:45732734
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.284+1420A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732734 | ||||||
| chr12:45732794
|
A | C | 1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.284+1480A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45732794 | ||||||
| chr12:45733320
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.284+2006G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733320 | ||||||
| chr12:45733462
|
C | T | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+2148C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733462 | ||||||
| chr12:45733816
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+2502G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733816 | ||||||
| chr12:45733877
|
C | T | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.284+2563C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733877 | ||||||
| chr12:45733927
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.284+2613T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45733927 | ||||||
| chr12:45734016
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+2702A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734016 | ||||||
| chr12:45734131
|
G | A | 1 | a0001c0001t0010g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.284+2817G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734131 | ||||||
| chr12:45734310
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.284+2996A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734310 | ||||||
| chr12:45734340
|
G | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+3026G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734340 | ||||||
| chr12:45734350
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+3036C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734350 | ||||||
| chr12:45734384
|
A | T | 3 | a0001c0001t0001g0271a0001c0001t0001g0292a0001c0011t0019g0272 | 3 | HG01884.hp1 HG02257.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.284+3070A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734384 | ||||||
| chr12:45734593
|
T | C | 1 | a0004c0005t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.284+3279T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45734593 | ||||||
| chr12:45735038
|
A | G | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+3724A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735038 | ||||||
| chr12:45735400
|
T | C | 3 | a0001c0001t0001g0208a0001c0009t0011g0207a0001c0009t0011g0209 | 3 | HG02717.hp1 HG03516.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.284+4086T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735400 | ||||||
| chr12:45735417
|
TCGTGTGT others(1): Show |
T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+4104_284+4111d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735417 | ||||||
| chr12:45735418
|
C | CGT | 82 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0082others(79): Show | 82 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.284+4145_284+4146d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
C | CGTGT | 54 | a0001c0001t0001g0001a0001c0001t0001g0089a0001c0001t0001g0090others(51): Show | 55 | HG00438.hp1 HG00639.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.284+4143_284+4146d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
C | CGTGTGT | 16 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0188others(13): Show | 16 | HG00408.hp2 HG01358.hp1 HG02148.hp1 others(13): Show |
intron_variant | MODIFIER | c.284+4141_284+4146d others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
C | CGTGTGTG others(1): Show |
9 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0270others(6): Show | 9 | HG02615.hp1 HG02647.hp1 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+4139_284+4146d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
CGT | C | 50 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0015others(47): Show | 50 | HG00140.hp2 HG00408.hp1 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.284+4145_284+4146d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
CGTGT | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0013a0006c0007t0001g0010others(1): Show | 4 | NA18612.hp2 NA18957.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+4143_284+4146d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
CGTGTGT | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(4): Show | 7 | HG00544.hp1 HG02132.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+4141_284+4146d others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+4139_284+4146d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
CGTGTGTG others(3): Show |
C | 1 | a0002c0003t0001g0210 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.284+4137_284+4146d others(12): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735418
|
CGTGTGTG others(17): Show |
C | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.284+4123_284+4146d others(26): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45735418 | |||||
| chr12:45735487
|
T | C | 1 | a0001c0001t0001g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.284+4173T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735487 | ||||||
| chr12:45735524
|
G | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+4210G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735524 | ||||||
| chr12:45735677
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.284+4363C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735677 | ||||||
| chr12:45735771
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.284+4457C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45735771 | ||||||
| chr12:45736123
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284+4809C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736123 | ||||||
| chr12:45736172
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.284+4858A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736172 | ||||||
| chr12:45736214
|
A | G | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+4900A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736214 | ||||||
| chr12:45736351
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+5037C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736351 | ||||||
| chr12:45736356
|
G | GA | 6 | a0001c0001t0001g0001a0001c0001t0001g0130a0003c0004t0006g0105others(3): Show | 7 | HG02293.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.284+5057dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45736356 | |||||
| chr12:45736572
|
A | G | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+5258A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736572 | ||||||
| chr12:45736602
|
G | A | 4 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(1): Show | 4 | HG00408.hp1 HG00544.hp1 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+5288G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736602 | ||||||
| chr12:45736843
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+5529G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45736843 | ||||||
| chr12:45737094
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0309 | 2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.284+5780A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737094 | ||||||
| chr12:45737251
|
C | T | 14 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.284+5937C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737251 | ||||||
| chr12:45737357
|
C | T | 1 | a0002c0003t0001g0262 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.284+6043C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737357 | ||||||
| chr12:45737633
|
A | G | 1 | a0001c0001t0001g0201 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.284+6319A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737633 | ||||||
| chr12:45737851
|
A | C | 2 | a0001c0006t0008g0114a0001c0006t0008g0115 | 2 | HG02622.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.284+6537A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737851 | ||||||
| chr12:45737902
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.284+6588T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737902 | ||||||
| chr12:45737904
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284+6590T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45737904 | ||||||
| chr12:45738281
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+6967T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738281 | ||||||
| chr12:45738391
|
T | A | 10 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.284+7077T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738391 | ||||||
| chr12:45738725
|
G | T | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+7411G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738725 | ||||||
| chr12:45738779
|
C | CT | 28 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0029others(25): Show | 28 | HG00280.hp1 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.284+7499dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
C | CTT | 20 | a0001c0001t0001g0032a0001c0001t0001g0069a0001c0001t0001g0070others(17): Show | 20 | HG00621.hp1 HG00621.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.284+7498_284+7499d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
C | CTTTT | 13 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0110others(10): Show | 14 | HG01071.hp1 HG01109.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.284+7496_284+7499d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
C | CTTTTT | 45 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(42): Show | 45 | HG00609.hp2 HG01168.hp1 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.284+7495_284+7499d others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
C | CTTTTTT | 26 | a0001c0001t0001g0088a0001c0001t0001g0124a0001c0001t0001g0125others(23): Show | 26 | HG00408.hp2 HG00673.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.284+7494_284+7499d others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0180a0001c0001t0001g0208a0001c0001t0003g0280others(3): Show | 6 | HG02738.hp2 HG03704.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.284+7492_284+7499d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0301 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.284+7489_284+7499d others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.284+7486_284+7499d others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CT | C | 21 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0009others(18): Show | 21 | HG00140.hp2 HG00408.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.284+7499delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTT | C | 7 | a0001c0001t0001g0016a0001c0001t0001g0316a0001c0001t0005g0286others(4): Show | 7 | HG01257.hp1 HG01891.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+7498_284+7499d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTTTTTTT others(2): Show |
C | 43 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.284+7491_284+7499d others(11): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTTTTTTT others(3): Show |
C | 3 | a0001c0001t0001g0240a0001c0001t0009g0211a0001c0001t0009g0212 | 3 | HG01074.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.284+7490_284+7499d others(12): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0009g0112 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.284+7489_284+7499d others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0035a0001c0011t0019g0272 | 2 | HG01884.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.284+7488_284+7499d others(14): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0001g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.284+7484_284+7499d others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTTTTTTT others(10): Show |
C | 32 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(29): Show | 32 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.284+7483_284+7499d others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738779
|
CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0152a0001c0001t0001g0154 | 2 | HG03490.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.284+7482_284+7499d others(20): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45738779 | |||||
| chr12:45738952
|
T | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+7638T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45738952 | ||||||
| chr12:45739019
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.284+7705A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739019 | ||||||
| chr12:45739143
|
G | GT | 8 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0148others(5): Show | 8 | HG01167.hp2 HG02602.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+7836dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739143 | |||||
| chr12:45739322
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.284+8008A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739322 | ||||||
| chr12:45739355
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.284+8041A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739355 | ||||||
| chr12:45739383
|
G | C | 1 | a0001c0001t0001g0038 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.284+8069G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739383 | ||||||
| chr12:45739401
|
T | G | 111 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(108): Show | 112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.284+8087T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739401 | ||||||
| chr12:45739438
|
C | CT | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 203 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.284+8148dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739438 | |||||
| chr12:45739438
|
C | CTT | 83 | a0001c0001t0001g0014a0001c0001t0001g0061a0001c0001t0001g0068others(80): Show | 83 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.284+8147_284+8148d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739438 | |||||
| chr12:45739438
|
C | CTTT | 10 | a0001c0001t0001g0256a0001c0001t0001g0268a0001c0001t0001g0278others(7): Show | 10 | HG00099.hp1 HG01257.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+8146_284+8148d others(5): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45739438 | |||||
| chr12:45739470
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+8156C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739470 | ||||||
| chr12:45739663
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+8349G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739663 | ||||||
| chr12:45739737
|
T | A | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.284+8423T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45739737 | ||||||
| chr12:45740371
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0290 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+9057T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740371 | ||||||
| chr12:45740517
|
G | A | 2 | a0001c0001t0001g0069a0001c0001t0001g0102 | 2 | HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.284+9203G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740517 | ||||||
| chr12:45740595
|
A | T | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+9281A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740595 | ||||||
| chr12:45740692
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.284+9378T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740692 | ||||||
| chr12:45740799
|
G | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+9485G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740799 | ||||||
| chr12:45740850
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0001g0029 | 2 | HG02083.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.284+9536T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740850 | ||||||
| chr12:45740909
|
G | T | 1 | a0001c0001t0001g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.284+9595G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45740909 | ||||||
| chr12:45741002
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0204 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.284+9688C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741002 | ||||||
| chr12:45741029
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.284+9715T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741029 | ||||||
| chr12:45741184
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+9870A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741184 | ||||||
| chr12:45741342
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.284+10028C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741342 | ||||||
| chr12:45741384
|
G | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+10070G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741384 | ||||||
| chr12:45741591
|
ATT | A | 47 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.284+10278_284+1027 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45741591 | ||||||
| chr12:45742360
|
G | A | 1 | a0001c0001t0001g0160 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.284+11046G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742360 | ||||||
| chr12:45742379
|
G | A | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+11065G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742379 | ||||||
| chr12:45742498
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+11184A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742498 | ||||||
| chr12:45742570
|
A | T | 1 | a0001c0001t0001g0129 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.284+11256A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742570 | ||||||
| chr12:45742853
|
C | T | 47 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.284+11539C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742853 | ||||||
| chr12:45742999
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+11685A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45742999 | ||||||
| chr12:45743026
|
T | C | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+11712T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743026 | ||||||
| chr12:45743045
|
T | G | 1 | a0001c0001t0017g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.284+11731T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743045 | ||||||
| chr12:45743197
|
T | TA | 9 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0235others(6): Show | 9 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+11895dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45743197 | |||||
| chr12:45743262
|
G | A | 3 | a0001c0002t0002g0225a0001c0002t0002g0228a0001c0002t0002g0305 | 3 | HG01884.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.284+11948G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743262 | ||||||
| chr12:45743450
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284+12136C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743450 | ||||||
| chr12:45743538
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+12224T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45743538 | ||||||
| chr12:45744490
|
T | G | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.284+13176T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744490 | ||||||
| chr12:45744561
|
T | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+13247T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744561 | ||||||
| chr12:45744622
|
C | T | 1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284+13308C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744622 | ||||||
| chr12:45744811
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+13497A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744811 | ||||||
| chr12:45744853
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+13539G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744853 | ||||||
| chr12:45744941
|
T | A | 107 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(104): Show | 108 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.284+13627T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744941 | ||||||
| chr12:45744944
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.284+13630C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45744944 | ||||||
| chr12:45745482
|
T | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+14168T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745482 | ||||||
| chr12:45745582
|
A | G | 3 | a0001c0001t0001g0201a0001c0001t0001g0231a0001c0001t0001g0235 | 3 | HG01109.hp2 HG02129.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.284+14268A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745582 | ||||||
| chr12:45745612
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+14298A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745612 | ||||||
| chr12:45745672
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+14358T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745672 | ||||||
| chr12:45745715
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+14401T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745715 | ||||||
| chr12:45745763
|
G | A | 5 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0260others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+14449G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745763 | ||||||
| chr12:45745807
|
C | T | 1 | a0001c0001t0007g0184 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.284+14493C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45745807 | ||||||
| chr12:45746100
|
A | AT | 52 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0130others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.284+14801dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746100 | |||||
| chr12:45746100
|
A | ATTTTTTT others(2): Show |
8 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(5): Show | 8 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.284+14793_284+1480 others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746100 | |||||
| chr12:45746100
|
A | ATTTTTTT others(3): Show |
2 | a0001c0001t0003g0283a0001c0001t0003g0314 | 2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.284+14792_284+1480 others(14): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746100 | |||||
| chr12:45746214
|
GATC | G | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+14901_284+1490 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746214 | ||||||
| chr12:45746338
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+15024T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746338 | ||||||
| chr12:45746377
|
T | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+15063T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746377 | ||||||
| chr12:45746481
|
A | G | 1 | a0008c0015t0001g0294 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.284+15167A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746481 | ||||||
| chr12:45746491
|
G | GT | 40 | a0001c0001t0001g0292a0001c0001t0003g0280a0001c0001t0003g0281others(37): Show | 40 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.284+15187dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45746491 | |||||
| chr12:45746632
|
C | T | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.284+15318C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746632 | ||||||
| chr12:45746720
|
A | G | 1 | a0001c0006t0008g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.284+15406A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746720 | ||||||
| chr12:45746738
|
C | G | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.284+15424C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746738 | ||||||
| chr12:45746789
|
C | T | 9 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+15475C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746789 | ||||||
| chr12:45746853
|
G | A | 1 | a0001c0001t0001g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.284+15539G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746853 | ||||||
| chr12:45746859
|
C | T | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG01099.hp2 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+15545C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746859 | ||||||
| chr12:45746891
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0060 | 2 | HG04199.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.284+15577C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746891 | ||||||
| chr12:45746907
|
C | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.284+15593C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746907 | ||||||
| chr12:45746930
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.284+15616C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746930 | ||||||
| chr12:45746969
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+15655C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746969 | ||||||
| chr12:45746990
|
C | T | 2 | a0001c0001t0003g0282a0001c0001t0003g0314 | 2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.284+15676C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45746990 | ||||||
| chr12:45747003
|
T | C | 3 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212 | 3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.284+15689T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747003 | ||||||
| chr12:45747011
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+15697C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747011 | ||||||
| chr12:45747209
|
AT | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+15897delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45747209 | |||||
| chr12:45747512
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0278 | 2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.284+16198A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747512 | ||||||
| chr12:45747557
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.284+16243C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747557 | ||||||
| chr12:45747589
|
C | T | 44 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(41): Show | 44 | HG00099.hp2 HG00609.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.284+16275C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747589 | ||||||
| chr12:45747759
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0309 | 2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.284+16445A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747759 | ||||||
| chr12:45747791
|
A | G | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.284+16477A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747791 | ||||||
| chr12:45747943
|
C | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+16629C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45747943 | ||||||
| chr12:45748116
|
A | G | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+16802A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748116 | ||||||
| chr12:45748120
|
T | G | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.284+16806T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748120 | ||||||
| chr12:45748344
|
T | G | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.284+17030T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748344 | ||||||
| chr12:45748352
|
C | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0094 | 2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.284+17038C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748352 | ||||||
| chr12:45748536
|
A | AG | 47 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.284+17223dupG | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45748536 | |||||
| chr12:45748572
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.284+17258A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748572 | ||||||
| chr12:45748607
|
C | T | 1 | a0001c0001t0001g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.284+17293C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748607 | ||||||
| chr12:45748681
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.284+17367C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748681 | ||||||
| chr12:45748715
|
T | G | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.284+17401T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748715 | ||||||
| chr12:45748844
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+17530T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748844 | ||||||
| chr12:45748855
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.284+17541G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748855 | ||||||
| chr12:45748888
|
A | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+17574A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748888 | ||||||
| chr12:45748888
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.284+17574A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45748888 | ||||||
| chr12:45749141
|
T | C | 3 | a0001c0001t0001g0152a0001c0001t0012g0182a0001c0001t0012g0183 | 3 | HG01358.hp1 HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.284+17827T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749141 | ||||||
| chr12:45749412
|
TACAG | T | 3 | a0004c0005t0001g0111a0004c0005t0001g0147a0004c0005t0001g0169 | 3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.284+18104_284+1810 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45749412 | |||||
| chr12:45749469
|
A | G | 1 | a0001c0001t0001g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.284+18155A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749469 | ||||||
| chr12:45749470
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.284+18156T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749470 | ||||||
| chr12:45749541
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.284+18227A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749541 | ||||||
| chr12:45749661
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+18347A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749661 | ||||||
| chr12:45749778
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.284+18464C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45749778 | ||||||
| chr12:45750045
|
T | C | 3 | a0004c0005t0001g0111a0004c0005t0001g0147a0004c0005t0001g0169 | 3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.284+18731T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750045 | ||||||
| chr12:45750202
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.284+18888G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750202 | ||||||
| chr12:45750480
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.284+19166T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750480 | ||||||
| chr12:45750500
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+19186C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750500 | ||||||
| chr12:45750534
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+19220A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45750534 | ||||||
| chr12:45751044
|
A | G | 2 | a0001c0001t0001g0002a0001c0001t0001g0018 | 2 | HG00140.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.284+19730A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751044 | ||||||
| chr12:45751072
|
C | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0110others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.284+19758C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751072 | ||||||
| chr12:45751429
|
A | G | 311 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(308): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.284+20115A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751429 | ||||||
| chr12:45751629
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.284+20315C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751629 | ||||||
| chr12:45751683
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.284+20369T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751683 | ||||||
| chr12:45751820
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+20506G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751820 | ||||||
| chr12:45751938
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0268a0001c0001t0001g0310 | 3 | HG01168.hp2 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.284+20624G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45751938 | ||||||
| chr12:45752153
|
A | G | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.284+20839A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752153 | ||||||
| chr12:45752394
|
A | G | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+21080A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752394 | ||||||
| chr12:45752683
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0029 | 2 | HG02083.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.284+21369G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752683 | ||||||
| chr12:45752776
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.284+21462G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45752776 | ||||||
| chr12:45753131
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0091a0007c0017t0001g0008 | 3 | HG02280.hp1 HG03490.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.284+21817C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753131 | ||||||
| chr12:45753268
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284+21954C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753268 | ||||||
| chr12:45753340
|
G | A | 1 | a0001c0001t0005g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284+22026G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753340 | ||||||
| chr12:45753594
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.284+22280T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753594 | ||||||
| chr12:45753666
|
G | A | 1 | a0013c0018t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.284+22352G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753666 | ||||||
| chr12:45753963
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.284+22649C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45753963 | ||||||
| chr12:45754183
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.284+22869T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754183 | ||||||
| chr12:45754241
|
T | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+22927T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754241 | ||||||
| chr12:45754333
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.284+23019A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754333 | ||||||
| chr12:45754398
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.284+23084G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754398 | ||||||
| chr12:45754408
|
T | G | 1 | a0005c0008t0001g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.284+23094T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754408 | ||||||
| chr12:45754469
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.284+23155A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754469 | ||||||
| chr12:45754536
|
T | C | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+23222T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754536 | ||||||
| chr12:45754637
|
C | G | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+23323C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45754637 | ||||||
| chr12:45755175
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+23861A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755175 | ||||||
| chr12:45755233
|
T | G | 1 | a0001c0002t0002g0258 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284+23919T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755233 | ||||||
| chr12:45755386
|
G | T | 1 | a0001c0001t0001g0002 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.284+24072G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755386 | ||||||
| chr12:45755485
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+24171A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755485 | ||||||
| chr12:45755569
|
T | C | 5 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0260others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.284+24255T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755569 | ||||||
| chr12:45755730
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.284+24416T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755730 | ||||||
| chr12:45755760
|
C | G | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+24446C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755760 | ||||||
| chr12:45755804
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284+24490A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45755804 | ||||||
| chr12:45756235
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.284+24921C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756235 | ||||||
| chr12:45756242
|
C | A | 1 | a0001c0001t0001g0021 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.284+24928C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756242 | ||||||
| chr12:45756375
|
TG | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+25062delG | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756375 | ||||||
| chr12:45756718
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.284+25404G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756718 | ||||||
| chr12:45756803
|
G | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+25489G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756803 | ||||||
| chr12:45756813
|
C | T | 1 | a0001c0006t0008g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.284+25499C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45756813 | ||||||
| chr12:45757075
|
T | G | 1 | a0001c0001t0015g0149 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.284+25761T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757075 | ||||||
| chr12:45757342
|
C | T | 39 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.284+26028C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757342 | ||||||
| chr12:45757347
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+26033T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757347 | ||||||
| chr12:45757482
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+26168A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757482 | ||||||
| chr12:45757552
|
G | A | 4 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0297others(1): Show | 4 | HG02602.hp2 HG04199.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+26238G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757552 | ||||||
| chr12:45757564
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.284+26250A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757564 | ||||||
| chr12:45757620
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0278 | 2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.284+26306A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757620 | ||||||
| chr12:45757761
|
C | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+26447C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757761 | ||||||
| chr12:45757914
|
C | T | 1 | a0001c0001t0004g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284+26600C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45757914 | ||||||
| chr12:45758056
|
C | T | 18 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 18 | HG00438.hp2 HG00621.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.284+26742C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758056 | ||||||
| chr12:45758167
|
TAGG | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+26854_284+2685 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758167 | ||||||
| chr12:45758335
|
A | G | 1 | a0013c0018t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.284+27021A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758335 | ||||||
| chr12:45758513
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+27199T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758513 | ||||||
| chr12:45758548
|
T | C | 1 | a0001c0001t0001g0202 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.284+27234T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758548 | ||||||
| chr12:45758613
|
C | T | 1 | a0003c0004t0006g0108 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.284+27299C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758613 | ||||||
| chr12:45758627
|
A | G | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.284+27313A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758627 | ||||||
| chr12:45758960
|
A | G | 44 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0122others(41): Show | 44 | HG00438.hp1 HG00738.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.284+27646A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758960 | ||||||
| chr12:45758992
|
A | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0069a0001c0001t0001g0102others(1): Show | 4 | HG00597.hp1 HG00621.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+27678A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45758992 | ||||||
| chr12:45759132
|
C | T | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.284+27818C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759132 | ||||||
| chr12:45759150
|
C | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0099 | 2 | HG00621.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.284+27836C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759150 | ||||||
| chr12:45759845
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+28531C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759845 | ||||||
| chr12:45759966
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+28652A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45759966 | ||||||
| chr12:45760352
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.284+29038T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760352 | ||||||
| chr12:45760392
|
T | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.284+29078T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760392 | ||||||
| chr12:45760407
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.284+29093A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760407 | ||||||
| chr12:45760487
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.284+29173G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760487 | ||||||
| chr12:45760491
|
G | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.284+29177G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760491 | ||||||
| chr12:45760493
|
G | GT | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+29186dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45760493 | |||||
| chr12:45760873
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284+29559G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760873 | ||||||
| chr12:45760896
|
C | T | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.284+29582C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760896 | ||||||
| chr12:45760925
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.284+29611G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45760925 | ||||||
| chr12:45761136
|
AT | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+29823delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761136 | ||||||
| chr12:45761199
|
G | A | 1 | a0001c0002t0002g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.284+29885G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761199 | ||||||
| chr12:45761362
|
T | C | 202 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0094others(199): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.284+30048T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761362 | ||||||
| chr12:45761724
|
T | C | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+30410T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761724 | ||||||
| chr12:45761859
|
C | A | 1 | a0001c0001t0001g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.284+30545C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761859 | ||||||
| chr12:45761887
|
G | A | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+30573G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761887 | ||||||
| chr12:45761994
|
C | A | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+30680C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45761994 | ||||||
| chr12:45762011
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.284+30697A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762011 | ||||||
| chr12:45762267
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284+30953A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762267 | ||||||
| chr12:45762476
|
A | G | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+31162A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762476 | ||||||
| chr12:45762504
|
T | C | 1 | a0008c0015t0001g0294 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.284+31190T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762504 | ||||||
| chr12:45762852
|
C | T | 1 | a0001c0001t0003g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.284+31538C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762852 | ||||||
| chr12:45762875
|
G | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+31561G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762875 | ||||||
| chr12:45762918
|
A | G | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+31604A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45762918 | ||||||
| chr12:45763073
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+31759A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763073 | ||||||
| chr12:45763109
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+31795T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763109 | ||||||
| chr12:45763127
|
A | G | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.284+31813A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763127 | ||||||
| chr12:45763353
|
C | A | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.284+32039C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763353 | ||||||
| chr12:45763401
|
C | T | 1 | a0001c0001t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.284+32087C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763401 | ||||||
| chr12:45763428
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.284+32114C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763428 | ||||||
| chr12:45763639
|
C | CA | 6 | a0001c0001t0001g0034a0001c0001t0001g0077a0001c0001t0001g0098others(3): Show | 6 | HG02135.hp1 HG02135.hp2 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+32338dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45763639 | |||||
| chr12:45763652
|
A | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0241a0001c0001t0001g0306 | 3 | HG01346.hp1 HG02132.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+32338A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763652 | ||||||
| chr12:45763653
|
T | A | 145 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0044others(142): Show | 146 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.284+32339T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763653 | ||||||
| chr12:45763654
|
T | A | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.284+32340T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763654 | ||||||
| chr12:45763660
|
T | A | 6 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0001t0001g0097others(3): Show | 6 | HG01346.hp1 HG02809.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+32346T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763660 | ||||||
| chr12:45763660
|
TA | T | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+32350delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45763660 | |||||
| chr12:45763661
|
A | T | 58 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0044others(55): Show | 58 | HG00438.hp1 HG00673.hp2 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.284+32347A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763661 | ||||||
| chr12:45763699
|
C | T | 3 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG00673.hp1 NA18944.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.284+32385C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763699 | ||||||
| chr12:45763729
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+32415G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763729 | ||||||
| chr12:45763784
|
C | T | 1 | a0001c0001t0003g0281 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.284+32470C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763784 | ||||||
| chr12:45763840
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+32526A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45763840 | ||||||
| chr12:45764125
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+32811A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764125 | ||||||
| chr12:45764612
|
C | T | 39 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.284+33298C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764612 | ||||||
| chr12:45764682
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+33368C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764682 | ||||||
| chr12:45764735
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.284+33421A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45764735 | ||||||
| chr12:45765200
|
GTTTTCTT others(4): Show |
G | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0067 | 3 | NA18947.hp1 NA18970.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.284+33897_284+3390 others(15): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45765200 | |||||
| chr12:45765232
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+33918A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765232 | ||||||
| chr12:45765279
|
C | T | 3 | a0001c0001t0007g0184a0001c0001t0007g0237a0001c0001t0007g0269 | 3 | HG02630.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.284+33965C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765279 | ||||||
| chr12:45765348
|
A | G | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.284+34034A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765348 | ||||||
| chr12:45765514
|
G | GT | 17 | a0001c0001t0001g0038a0001c0001t0001g0069a0001c0001t0001g0126others(14): Show | 17 | HG00621.hp2 HG00673.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.284+34215dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45765514 | |||||
| chr12:45765811
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.284+34497A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765811 | ||||||
| chr12:45765814
|
G | A | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.284+34500G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45765814 | ||||||
| chr12:45766093
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284+34779A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766093 | ||||||
| chr12:45766123
|
G | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.284+34809G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766123 | ||||||
| chr12:45766164
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+34850A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766164 | ||||||
| chr12:45766194
|
G | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0102a0014c0019t0001g0079 | 3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.284+34880G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766194 | ||||||
| chr12:45766376
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.284+35062C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766376 | ||||||
| chr12:45766377
|
G | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35063G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766377 | ||||||
| chr12:45766468
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.284+35154A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766468 | ||||||
| chr12:45766659
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35345A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766659 | ||||||
| chr12:45766713
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.284+35399A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766713 | ||||||
| chr12:45766805
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.284+35491C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766805 | ||||||
| chr12:45766825
|
A | C | 4 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0297others(1): Show | 4 | HG02602.hp2 HG04199.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.284+35511A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766825 | ||||||
| chr12:45766848
|
ATCCTAGC others(60): Show |
A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35535_284+3560 others(71): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766848 | ||||||
| chr12:45766915
|
C | T | 9 | a0002c0003t0001g0210a0002c0003t0001g0248a0002c0003t0001g0249others(6): Show | 9 | HG00597.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.284+35601C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766915 | ||||||
| chr12:45766917
|
A | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35603A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766917 | ||||||
| chr12:45766918
|
A | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+35604A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766918 | ||||||
| chr12:45766919
|
G | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35605G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766919 | ||||||
| chr12:45766921
|
T | TTA | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35607_284+3560 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766921 | ||||||
| chr12:45766923
|
G | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35609G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766923 | ||||||
| chr12:45766925
|
G | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35611G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766925 | ||||||
| chr12:45766926
|
C | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35612C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45766926 | ||||||
| chr12:45767057
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.284+35743C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767057 | ||||||
| chr12:45767084
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+35770C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767084 | ||||||
| chr12:45767162
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.284+35848T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767162 | ||||||
| chr12:45767477
|
T | C | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.284+36163T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767477 | ||||||
| chr12:45767645
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(106): Show | 110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.284+36331A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767645 | ||||||
| chr12:45767689
|
A | G | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+36375A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767689 | ||||||
| chr12:45767910
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.284+36596C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767910 | ||||||
| chr12:45767995
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.284+36681T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45767995 | ||||||
| chr12:45768142
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+36828A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768142 | ||||||
| chr12:45768468
|
T | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+37154T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768468 | ||||||
| chr12:45768506
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.284+37192C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768506 | ||||||
| chr12:45768596
|
G | C | 9 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+37282G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768596 | ||||||
| chr12:45768810
|
A | G | 1 | a0001c0001t0001g0050 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.284+37496A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768810 | ||||||
| chr12:45768841
|
CA | C | 5 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+37529delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45768841 | |||||
| chr12:45768843
|
A | G | 3 | a0001c0001t0001g0296a0001c0009t0011g0207a0001c0009t0011g0209 | 3 | HG01975.hp1 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.284+37529A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768843 | ||||||
| chr12:45768873
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.284+37559C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768873 | ||||||
| chr12:45768914
|
C | T | 1 | a0001c0001t0001g0003 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.284+37600C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45768914 | ||||||
| chr12:45769021
|
G | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+37707G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769021 | ||||||
| chr12:45769065
|
A | G | 9 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.284+37751A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769065 | ||||||
| chr12:45769195
|
A | G | 2 | a0001c0001t0001g0026a0001c0001t0001g0029 | 2 | HG02083.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.284+37881A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769195 | ||||||
| chr12:45769218
|
A | T | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.284+37904A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769218 | ||||||
| chr12:45769285
|
T | TTAAA | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.284+37974_284+3797 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45769285 | |||||
| chr12:45769574
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+38260C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769574 | ||||||
| chr12:45769902
|
G | GA | 6 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | NA18959.hp2 NA18973.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+38594dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45769902 | |||||
| chr12:45769980
|
C | T | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.284+38666C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45769980 | ||||||
| chr12:45770063
|
G | T | 1 | a0002c0003t0001g0254 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.284+38749G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770063 | ||||||
| chr12:45770174
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.284+38860A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770174 | ||||||
| chr12:45770178
|
G | A | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+38864G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770178 | ||||||
| chr12:45770192
|
G | A | 2 | a0001c0001t0001g0161a0003c0004t0018g0205 | 2 | HG02451.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.284+38878G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770192 | ||||||
| chr12:45770644
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.284+39330C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770644 | ||||||
| chr12:45770711
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.284+39397C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770711 | ||||||
| chr12:45770759
|
A | C | 1 | a0001c0001t0001g0078 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.284+39445A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770759 | ||||||
| chr12:45770850
|
A | G | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.284+39536A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770850 | ||||||
| chr12:45770882
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0094 | 2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.284+39568A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45770882 | ||||||
| chr12:45771027
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.284+39713C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771027 | ||||||
| chr12:45771352
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.284+40038A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771352 | ||||||
| chr12:45771356
|
C | CA | 38 | a0001c0001t0001g0067a0001c0001t0001g0242a0001c0001t0001g0264others(35): Show | 38 | HG00140.hp1 HG01175.hp1 HG01884.hp2 others(35): Show |
intron_variant | MODIFIER | c.285-40045dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771356 | |||||
| chr12:45771468
|
C | T | 4 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0001g0311others(1): Show | 4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-39950C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771468 | ||||||
| chr12:45771501
|
C | CA | 6 | a0001c0001t0001g0241a0001c0001t0001g0306a0001c0001t0003g0314others(3): Show | 6 | HG01346.hp1 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-39902dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771501 | |||||
| chr12:45771501
|
CA | C | 26 | a0001c0001t0001g0274a0001c0001t0009g0112a0001c0001t0009g0211others(23): Show | 26 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.285-39902delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771501 | |||||
| chr12:45771639
|
C | T | 1 | a0001c0001t0012g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.285-39779C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771639 | ||||||
| chr12:45771692
|
C | CTA | 25 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0157others(22): Show | 25 | HG00140.hp1 HG00673.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.285-39709_285-3970 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771692 | |||||
| chr12:45771692
|
CTA | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-39709_285-3970 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771692 | |||||
| chr12:45771951
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-39467T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45771951 | ||||||
| chr12:45771991
|
AAGG | A | 9 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.285-39422_285-3942 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45771991 | |||||
| chr12:45772012
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-39406C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772012 | ||||||
| chr12:45772073
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0066a0001c0001t0001g0100 | 3 | HG02486.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.285-39345A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772073 | ||||||
| chr12:45772150
|
T | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-39268T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772150 | ||||||
| chr12:45772209
|
A | T | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-39209A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772209 | ||||||
| chr12:45772405
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-39013C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772405 | ||||||
| chr12:45772552
|
A | G | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.285-38866A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772552 | ||||||
| chr12:45772621
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.285-38797T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772621 | ||||||
| chr12:45772653
|
A | G | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.285-38765A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45772653 | ||||||
| chr12:45773516
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.285-37902A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45773516 | ||||||
| chr12:45773692
|
A | C | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-37726A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45773692 | ||||||
| chr12:45773906
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285-37512G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45773906 | ||||||
| chr12:45774163
|
T | A | 1 | a0001c0009t0011g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285-37255T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774163 | ||||||
| chr12:45774284
|
AGTGTGAA others(5): Show |
A | 108 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(105): Show | 109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.285-37131_285-3712 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45774284 | |||||
| chr12:45774509
|
A | G | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.285-36909A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774509 | ||||||
| chr12:45774511
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-36907G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774511 | ||||||
| chr12:45774612
|
G | A | 1 | a0001c0001t0001g0023 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.285-36806G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774612 | ||||||
| chr12:45774647
|
C | T | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-36771C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774647 | ||||||
| chr12:45774741
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.285-36677T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774741 | ||||||
| chr12:45774890
|
A | C | 4 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-36528A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774890 | ||||||
| chr12:45774932
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-36486T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774932 | ||||||
| chr12:45774967
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-36451C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45774967 | ||||||
| chr12:45775046
|
C | A | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-36372C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775046 | ||||||
| chr12:45775217
|
C | T | 1 | a0002c0020t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285-36201C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775217 | ||||||
| chr12:45775248
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-36170G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775248 | ||||||
| chr12:45775311
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-36107A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775311 | ||||||
| chr12:45775459
|
G | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-35959G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775459 | ||||||
| chr12:45775847
|
A | G | 1 | a0001c0001t0015g0149 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.285-35571A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775847 | ||||||
| chr12:45775860
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-35558A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45775860 | ||||||
| chr12:45776442
|
G | A | 11 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0125others(8): Show | 11 | HG00609.hp2 HG00673.hp1 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-34976G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776442 | ||||||
| chr12:45776513
|
A | G | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-34905A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776513 | ||||||
| chr12:45776629
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.285-34789T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776629 | ||||||
| chr12:45776724
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-34694C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776724 | ||||||
| chr12:45776766
|
A | T | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-34652A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776766 | ||||||
| chr12:45776781
|
C | CT | 23 | a0001c0001t0001g0020a0001c0001t0001g0034a0001c0001t0001g0037others(20): Show | 23 | HG00741.hp1 HG01106.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.285-34616dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45776781 | |||||
| chr12:45776781
|
CT | C | 38 | a0001c0001t0001g0052a0001c0001t0001g0187a0001c0001t0003g0280others(35): Show | 38 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.285-34616delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45776781 | |||||
| chr12:45776840
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.285-34578C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776840 | ||||||
| chr12:45776958
|
G | T | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-34460G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776958 | ||||||
| chr12:45776970
|
A | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(237): Show | 241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.285-34448A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45776970 | ||||||
| chr12:45777199
|
T | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0087a0001c0001t0001g0088others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.285-34219T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777199 | ||||||
| chr12:45777292
|
A | C | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-34126A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777292 | ||||||
| chr12:45777527
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-33891C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777527 | ||||||
| chr12:45777550
|
T | G | 1 | a0001c0001t0001g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.285-33868T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777550 | ||||||
| chr12:45777705
|
G | T | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.285-33713G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777705 | ||||||
| chr12:45777706
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.285-33712C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777706 | ||||||
| chr12:45777932
|
C | G | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.285-33486C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45777932 | ||||||
| chr12:45778101
|
G | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-33317G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778101 | ||||||
| chr12:45778121
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-33297C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778121 | ||||||
| chr12:45778123
|
C | T | 5 | a0001c0001t0001g0033a0001c0001t0001g0056a0001c0001t0001g0071others(2): Show | 5 | HG01071.hp1 HG01358.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-33295C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778123 | ||||||
| chr12:45778185
|
G | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-33233G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778185 | ||||||
| chr12:45778251
|
C | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0116a0001c0001t0001g0117others(122): Show | 126 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.285-33167C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778251 | ||||||
| chr12:45778255
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-33163C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778255 | ||||||
| chr12:45778259
|
C | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-33159C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778259 | ||||||
| chr12:45778294
|
T | A | 4 | a0001c0001t0005g0273a0001c0001t0005g0286a0001c0001t0005g0288others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-33124T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778294 | ||||||
| chr12:45778298
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.285-33120A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778298 | ||||||
| chr12:45778307
|
G | A | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.285-33111G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778307 | ||||||
| chr12:45778380
|
G | A | 10 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(7): Show | 10 | HG02647.hp2 HG02738.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.285-33038G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778380 | ||||||
| chr12:45778421
|
T | C | 1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.285-32997T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778421 | ||||||
| chr12:45778424
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-32994A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778424 | ||||||
| chr12:45778461
|
GA | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-32956delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778461 | ||||||
| chr12:45778585
|
A | G | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-32833A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778585 | ||||||
| chr12:45778759
|
T | C | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.285-32659T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778759 | ||||||
| chr12:45778828
|
A | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-32590A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45778828 | ||||||
| chr12:45779161
|
C | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-32257C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779161 | ||||||
| chr12:45779551
|
A | G | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-31867A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779551 | ||||||
| chr12:45779746
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.285-31672T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779746 | ||||||
| chr12:45779756
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.285-31662A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45779756 | ||||||
| chr12:45780086
|
A | G | 2 | a0004c0005t0001g0147a0004c0005t0001g0169 | 2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.285-31332A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780086 | ||||||
| chr12:45780205
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.285-31213C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780205 | ||||||
| chr12:45780207
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0290 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-31211A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780207 | ||||||
| chr12:45780229
|
G | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-31189G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780229 | ||||||
| chr12:45780384
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.285-31034T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780384 | ||||||
| chr12:45780610
|
A | AATT | 3 | a0001c0001t0001g0096a0001c0001t0001g0271a0001c0011t0019g0272 | 3 | HG01884.hp1 HG02257.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.285-30789_285-3078 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45780610 | |||||
| chr12:45780728
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.285-30690C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780728 | ||||||
| chr12:45780864
|
C | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0180 | 2 | NA18950.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.285-30554C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780864 | ||||||
| chr12:45780973
|
A | C | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-30445A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45780973 | ||||||
| chr12:45781114
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.285-30304C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781114 | ||||||
| chr12:45781160
|
T | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-30258T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781160 | ||||||
| chr12:45781256
|
A | G | 3 | a0001c0001t0001g0264a0001c0001t0001g0270a0009c0014t0021g0213 | 3 | HG02559.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-30162A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781256 | ||||||
| chr12:45781322
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.285-30096A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781322 | ||||||
| chr12:45781334
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-30084C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781334 | ||||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0007g0237 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0007g0184 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1032): Show |
1 | a0001c0001t0001g0176 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0003g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0003g0281 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0003g0280 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0003g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0003g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1004): Show |
1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1015): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(999): Show |
1 | a0001c0001t0001g0306 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1010): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1039): Show |
2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1050): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0013c0018t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1032): Show |
1 | a0001c0001t0001g0133 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1027): Show |
1 | a0001c0001t0001g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1038): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0007g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0073 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0238 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0151 | 2 | HG04199.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0239 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0015 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
2 | a0001c0001t0001g0067a0005c0008t0001g0080 | 2 | NA19001.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0020g0030 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
1 | a0001c0009t0011g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0090a0001c0001t0001g0144 | 3 | HG02129.hp1 HG02976.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 2 | HG01106.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1002): Show |
1 | a0001c0001t0001g0041 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1013): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0062 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(999): Show |
1 | a0001c0001t0001g0040 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1010): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1036): Show |
1 | a0001c0001t0001g0168 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1027): Show |
1 | a0001c0001t0015g0149 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1038): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1028): Show |
2 | a0001c0001t0001g0160a0001c0001t0001g0199 | 2 | NA18953.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0010g0191 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0298 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0299 | 2 | HG01109.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
2 | a0001c0001t0001g0044a0001c0001t0001g0179 | 2 | HG01981.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0150 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
1 | a0008c0015t0001g0294 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
1 | a0004c0005t0001g0147 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(994): Show |
1 | a0001c0001t0001g0019 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1005): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1037): Show |
1 | a0001c0001t0001g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1048): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1036): Show |
1 | a0001c0006t0008g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
1 | a0001c0006t0008g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1028): Show |
1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1028): Show |
2 | a0001c0001t0001g0110a0001c0001t0001g0116 | 2 | HG01346.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0070 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
4 | a0001c0001t0001g0185a0001c0001t0001g0236a0001c0001t0001g0290others(1): Show | 4 | HG02896.hp1 HG02897.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1030): Show |
1 | a0001c0001t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0014 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
2 | a0001c0001t0001g0032a0001c0001t0001g0085 | 2 | HG02683.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
4 | a0001c0001t0001g0069a0001c0001t0001g0074a0001c0001t0001g0099others(1): Show | 4 | HG00621.hp2 HG01433.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
4 | a0001c0001t0001g0046a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02083.hp1 HG02602.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0117 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0103 | 2 | HG02135.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1017): Show |
1 | a0001c0001t0001g0078 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0028 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
5 | a0001c0001t0001g0084a0001c0001t0001g0096a0001c0001t0001g0134others(2): Show | 5 | HG01074.hp2 HG01106.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0061 | 2 | HG04184.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0152 | 2 | HG03704.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0293 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1009): Show |
1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
6 | a0001c0001t0001g0058a0001c0001t0001g0066a0001c0001t0001g0071others(3): Show | 6 | HG01168.hp1 HG01169.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
3 | a0001c0001t0001g0035a0001c0001t0001g0050a0005c0008t0001g0043 | 3 | HG00099.hp2 HG02135.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1017): Show |
3 | a0001c0001t0001g0034a0001c0001t0001g0064a0001c0001t0001g0095 | 3 | HG00438.hp2 NA18956.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1018): Show |
6 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0029others(3): Show | 7 | HG01993.hp2 HG02083.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | HG00639.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
3 | a0001c0001t0001g0138a0001c0001t0001g0232a0001c0001t0012g0183 | 3 | HG01515.hp2 HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
2 | a0001c0001t0001g0139a0001c0001t0012g0182 | 2 | HG01358.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1008): Show |
1 | a0001c0001t0001g0033 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1019): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1012): Show |
1 | a0001c0001t0001g0025 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1013): Show |
3 | a0001c0001t0001g0060a0006c0007t0001g0010a0006c0007t0001g0012 | 3 | NA18941.hp2 NA18957.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
1 | a0001c0009t0011g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
3 | a0001c0001t0001g0047a0001c0001t0001g0063a0001c0002t0002g0225 | 3 | HG00280.hp1 NA18906.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
3 | a0001c0001t0001g0036a0001c0001t0001g0072a0001c0001t0001g0089 | 3 | HG00621.hp1 NA18747.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1017): Show |
4 | a0001c0001t0001g0009a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG01257.hp1 HG01258.hp2 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1018): Show |
7 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0023others(4): Show | 7 | HG00140.hp2 HG01256.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
2 | a0001c0001t0001g0094a0001c0016t0001g0302 | 2 | HG02809.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
2 | a0001c0001t0001g0120a0001c0001t0001g0148 | 2 | HG01167.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0017g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1012): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0037 | 2 | NA18980.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
1 | a0001c0001t0001g0241 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1008): Show |
1 | a0001c0001t0001g0022 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1019): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1009): Show |
1 | a0001c0001t0005g0285 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0048 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1000): Show |
1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1011): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(997): Show |
1 | a0001c0001t0001g0038 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1008): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1038): Show |
1 | a0001c0001t0001g0174 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1049): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1030): Show |
1 | a0012c0012t0001g0127 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1032): Show |
1 | a0001c0001t0001g0161 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0158 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0122 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0123 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0165 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
2 | a0001c0001t0001g0303a0001c0001t0010g0109 | 2 | HG03927.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1025): Show |
1 | a0001c0001t0001g0190 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1029): Show |
1 | a0001c0001t0001g0301 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0171a0001c0001t0001g0204 | 3 | HG00673.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1025): Show |
2 | a0001c0001t0001g0203a0001c0001t0001g0309 | 2 | HG00609.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0128 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1012): Show |
2 | a0001c0001t0001g0159a0001c0001t0001g0177 | 2 | NA18950.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
1 | a0001c0001t0001g0193 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
1 | a0001c0001t0001g0200 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
6 | a0001c0001t0001g0088a0001c0001t0001g0146a0001c0001t0001g0166others(3): Show | 6 | HG01975.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
5 | a0001c0001t0001g0124a0001c0001t0001g0163a0001c0001t0001g0167others(2): Show | 5 | HG01934.hp2 HG02273.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
3 | a0001c0001t0001g0175a0001c0001t0001g0201a0001c0001t0001g0315 | 3 | HG02129.hp2 NA18959.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
4 | a0001c0001t0001g0045a0001c0001t0001g0087a0001c0001t0001g0121others(1): Show | 4 | NA18944.hp1 NA18977.hp2 NA19072.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0129 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0162 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1021): Show |
2 | a0001c0001t0001g0202a0004c0005t0001g0169 | 2 | NA19077.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1032): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1029): Show |
1 | a0001c0001t0001g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
1 | a0001c0001t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0003 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0054 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0065 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1010): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0055 | 2 | HG02165.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1021): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1012): Show |
1 | a0001c0001t0001g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1011): Show |
1 | a0001c0001t0001g0083 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1022): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1044): Show |
1 | a0001c0002t0002g0259 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1055): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1036): Show |
1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1032): Show |
1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1039): Show |
1 | a0001c0006t0008g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1050): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1036): Show |
3 | a0001c0001t0004g0194a0001c0002t0002g0214a0001c0002t0002g0260 | 3 | HG02630.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1034): Show |
1 | a0001c0002t0002g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1045): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1035): Show |
1 | a0001c0002t0002g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1046): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1036): Show |
1 | a0001c0002t0002g0215 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1031): Show |
1 | a0001c0002t0002g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
2 | a0001c0002t0002g0216a0001c0002t0002g0218 | 2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1035): Show |
1 | a0001c0002t0002g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1046): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1025): Show |
1 | a0001c0002t0002g0261 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1036): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1030): Show |
1 | a0001c0001t0004g0195 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1032): Show |
1 | a0001c0002t0002g0217 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1043): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1028): Show |
1 | a0001c0001t0004g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1030): Show |
1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1041): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
1 | a0001c0002t0002g0226 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
2 | a0001c0001t0004g0196a0001c0001t0004g0197 | 2 | HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
1 | a0001c0001t0001g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1017): Show |
1 | a0014c0019t0001g0079 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1028): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
1 | a0001c0002t0002g0229 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1005): Show |
1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1016): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1006): Show |
1 | a0001c0001t0014g0287 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1017): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
1 | a0001c0002t0002g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
1 | a0001c0002t0002g0305 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1001): Show |
1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1012): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0005g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1005): Show |
1 | a0001c0002t0002g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1016): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1009): Show |
1 | a0009c0014t0021g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1008): Show |
1 | a0001c0001t0009g0211 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1019): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1009): Show |
2 | a0001c0001t0009g0112a0001c0001t0009g0212 | 2 | HG01167.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1020): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
1 | a0001c0001t0001g0270 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
1 | a0001c0001t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(996): Show |
2 | a0003c0004t0006g0105a0003c0004t0006g0108 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1007): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(994): Show |
1 | a0003c0004t0006g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1005): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(995): Show |
1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1006): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1028): Show |
1 | a0001c0001t0001g0242 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1039): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1002): Show |
1 | a0001c0001t0001g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1013): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1003): Show |
1 | a0001c0001t0001g0311 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1014): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1006): Show |
1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1017): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1036): Show |
1 | a0002c0003t0001g0262 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1047): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1039): Show |
1 | a0010c0013t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1050): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1035): Show |
1 | a0002c0003t0001g0254 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1046): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1031): Show |
1 | a0001c0001t0001g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0244 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1029): Show |
2 | a0001c0001t0001g0275a0002c0003t0001g0143 | 2 | HG01934.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1031): Show |
1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
2 | a0001c0001t0001g0141a0001c0001t0001g0257 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1029): Show |
2 | a0001c0001t0001g0130a0001c0001t0013g0266 | 2 | HG02293.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1040): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1033): Show |
1 | a0001c0001t0001g0291 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1044): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1026): Show |
1 | a0001c0001t0001g0245 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1037): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1024): Show |
1 | a0001c0001t0001g0233 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1035): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1023): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0246 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1034): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1031): Show |
1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1042): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1013): Show |
1 | a0001c0001t0001g0276 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1018): Show |
1 | a0001c0001t0001g0310 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1029): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1019): Show |
1 | a0002c0003t0001g0253 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1030): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1020): Show |
1 | a0001c0001t0001g0142 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1031): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
1 | a0002c0020t0001g0251 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1022): Show |
1 | a0001c0001t0001g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1033): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
1 | a0002c0003t0001g0248 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1016): Show |
2 | a0001c0001t0001g0268a0002c0003t0001g0210 | 2 | NA19060.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1027): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1011): Show |
1 | a0001c0001t0013g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1022): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1013): Show |
2 | a0002c0003t0001g0249a0002c0003t0001g0308 | 2 | NA18945.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1024): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
2 | a0002c0003t0001g0250a0002c0003t0001g0307 | 2 | HG00597.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1015): Show |
1 | a0001c0001t0001g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1026): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1014): Show |
1 | a0002c0003t0001g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1025): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1010): Show |
1 | a0001c0001t0001g0256 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1021): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1006): Show |
1 | a0001c0001t0001g0317 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1017): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1007): Show |
1 | a0001c0001t0001g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1018): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1012): Show |
1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1023): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1001): Show |
2 | a0001c0001t0001g0296a0001c0001t0001g0304 | 2 | HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.285-30035_285-3003 others(1012): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781372
|
T | TTGGCCAG others(1002): Show |
1 | a0001c0001t0001g0312 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.285-30035_285-3003 others(1013): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45781372 | |||||
| chr12:45781508
|
G | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0243others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-29910G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781508 | ||||||
| chr12:45781686
|
A | G | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-29732A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781686 | ||||||
| chr12:45781776
|
T | C | 1 | a0001c0001t0010g0191 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.285-29642T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781776 | ||||||
| chr12:45781820
|
T | C | 1 | a0001c0001t0001g0289 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.285-29598T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781820 | ||||||
| chr12:45781959
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0309 | 2 | NA18966.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.285-29459A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45781959 | ||||||
| chr12:45782093
|
A | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(96): Show | 100 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.285-29325A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782093 | ||||||
| chr12:45782120
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-29298A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782120 | ||||||
| chr12:45782137
|
T | TA | 3 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096 | 3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.285-29278dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45782137 | |||||
| chr12:45782168
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-29250A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782168 | ||||||
| chr12:45782486
|
G | A | 9 | a0002c0003t0001g0210a0002c0003t0001g0248a0002c0003t0001g0249others(6): Show | 9 | HG00597.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.285-28932G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782486 | ||||||
| chr12:45782487
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.285-28931G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782487 | ||||||
| chr12:45782578
|
G | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-28840G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782578 | ||||||
| chr12:45782610
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.285-28808C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782610 | ||||||
| chr12:45782809
|
C | T | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-28609C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45782809 | ||||||
| chr12:45783044
|
A | T | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG00140.hp1 HG01934.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.285-28374A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783044 | ||||||
| chr12:45783111
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01168.hp1 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.285-28307A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783111 | ||||||
| chr12:45783166
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-28252T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783166 | ||||||
| chr12:45783654
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-27764G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783654 | ||||||
| chr12:45783704
|
A | C | 3 | a0001c0002t0002g0225a0001c0002t0002g0228a0001c0002t0002g0305 | 3 | HG01884.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.285-27714A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783704 | ||||||
| chr12:45783751
|
A | T | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-27667A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783751 | ||||||
| chr12:45783886
|
TAAGTTA | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(159): Show | 163 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.285-27529_285-2752 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45783886 | |||||
| chr12:45783913
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-27505A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783913 | ||||||
| chr12:45783939
|
A | G | 1 | a0001c0001t0001g0003 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.285-27479A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45783939 | ||||||
| chr12:45784190
|
G | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-27228G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45784190 | ||||||
| chr12:45784375
|
T | A | 23 | a0001c0001t0001g0129a0001c0001t0001g0159a0001c0001t0001g0160others(20): Show | 23 | HG01109.hp1 HG01934.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.285-27043T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45784375 | ||||||
| chr12:45784613
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-26805G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45784613 | ||||||
| chr12:45785202
|
C | T | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0067others(1): Show | 4 | NA18940.hp1 NA18947.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-26216C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785202 | ||||||
| chr12:45785391
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0279 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.285-26027C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785391 | ||||||
| chr12:45785392
|
G | A | 3 | a0001c0006t0008g0113a0001c0006t0008g0114a0001c0006t0008g0115 | 3 | HG02622.hp2 HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.285-26026G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785392 | ||||||
| chr12:45785499
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.285-25919G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785499 | ||||||
| chr12:45785617
|
A | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0077a0001c0001t0001g0099 | 3 | HG00621.hp1 HG02135.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.285-25801A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785617 | ||||||
| chr12:45785714
|
C | A | 1 | a0001c0001t0001g0067 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.285-25704C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785714 | ||||||
| chr12:45785764
|
A | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-25654A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785764 | ||||||
| chr12:45785862
|
G | C | 1 | a0001c0001t0001g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.285-25556G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785862 | ||||||
| chr12:45785913
|
G | A | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.285-25505G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785913 | ||||||
| chr12:45785954
|
A | G | 1 | a0001c0001t0001g0311 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.285-25464A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785954 | ||||||
| chr12:45785998
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0062 | 2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.285-25420T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45785998 | ||||||
| chr12:45786095
|
A | C | 8 | a0001c0001t0001g0240a0001c0001t0001g0245a0001c0001t0001g0246others(5): Show | 8 | HG00642.hp1 HG01074.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.285-25323A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786095 | ||||||
| chr12:45786113
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-25305A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786113 | ||||||
| chr12:45786137
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.285-25281A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786137 | ||||||
| chr12:45786238
|
TTAAAG | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-25177_285-2517 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45786238 | |||||
| chr12:45786280
|
A | T | 1 | a0001c0001t0001g0162 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.285-25138A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786280 | ||||||
| chr12:45786370
|
C | G | 1 | a0009c0014t0021g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.285-25048C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786370 | ||||||
| chr12:45786401
|
A | G | 1 | a0001c0002t0002g0219 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.285-25017A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786401 | ||||||
| chr12:45786525
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.285-24893G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786525 | ||||||
| chr12:45786644
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.285-24774T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786644 | ||||||
| chr12:45786902
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-24516G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786902 | ||||||
| chr12:45786959
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.285-24459A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45786959 | ||||||
| chr12:45787209
|
A | G | 1 | a0003c0004t0006g0105 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.285-24209A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787209 | ||||||
| chr12:45787218
|
C | CTTTT | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-24187_285-2418 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45787218 | |||||
| chr12:45787282
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.285-24136A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787282 | ||||||
| chr12:45787573
|
C | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-23845C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787573 | ||||||
| chr12:45787713
|
A | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-23705A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45787713 | ||||||
| chr12:45788026
|
G | A | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(22): Show | 25 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-23392G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788026 | ||||||
| chr12:45788029
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.285-23389T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788029 | ||||||
| chr12:45788209
|
A | G | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-23209A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788209 | ||||||
| chr12:45788484
|
A | C | 1 | a0001c0001t0001g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.285-22934A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788484 | ||||||
| chr12:45788609
|
G | A | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-22809G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788609 | ||||||
| chr12:45788632
|
T | C | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.285-22786T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788632 | ||||||
| chr12:45788665
|
A | T | 1 | a0001c0001t0001g0126 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.285-22753A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788665 | ||||||
| chr12:45788907
|
A | C | 40 | a0001c0001t0001g0292a0001c0001t0003g0280a0001c0001t0003g0281others(37): Show | 40 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.285-22511A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45788907 | ||||||
| chr12:45789047
|
A | G | 1 | a0001c0001t0001g0011 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.285-22371A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789047 | ||||||
| chr12:45789049
|
CA | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(162): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.285-22368delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789049 | ||||||
| chr12:45789068
|
A | G | 47 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(44): Show | 47 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.285-22350A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789068 | ||||||
| chr12:45789742
|
G | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-21676G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45789742 | ||||||
| chr12:45790004
|
T | A | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.285-21414T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790004 | ||||||
| chr12:45790005
|
C | G | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.285-21413C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790005 | ||||||
| chr12:45790006
|
A | C | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.285-21412A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790006 | ||||||
| chr12:45790341
|
TTGTA | T | 9 | a0002c0003t0001g0210a0002c0003t0001g0248a0002c0003t0001g0249others(6): Show | 9 | HG00597.hp2 HG02155.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.285-21074_285-2107 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45790341 | |||||
| chr12:45790351
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-21067T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790351 | ||||||
| chr12:45790376
|
A | G | 1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.285-21042A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790376 | ||||||
| chr12:45790487
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-20931C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790487 | ||||||
| chr12:45790488
|
A | C | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-20930A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790488 | ||||||
| chr12:45790690
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0003g0281 | 2 | NA20752.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.285-20728C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790690 | ||||||
| chr12:45790840
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-20578A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790840 | ||||||
| chr12:45790940
|
G | A | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-20478G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45790940 | ||||||
| chr12:45791066
|
T | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-20352T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791066 | ||||||
| chr12:45791204
|
C | CTG | 8 | a0001c0001t0001g0068a0001c0001t0001g0118a0001c0001t0001g0145others(5): Show | 8 | HG00738.hp2 HG01099.hp2 HG02132.hp2 others(5): Show |
intron_variant | MODIFIER | c.285-20185_285-2018 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | |||||
| chr12:45791204
|
C | CTGTG | 3 | a0001c0001t0001g0022a0001c0001t0001g0292a0001c0011t0019g0272 | 3 | HG01884.hp1 HG02300.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.285-20187_285-2018 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | |||||
| chr12:45791204
|
CTG | C | 92 | a0001c0001t0001g0057a0001c0001t0001g0110a0001c0001t0001g0120others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.285-20185_285-2018 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | |||||
| chr12:45791204
|
CTGTG | C | 19 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(16): Show | 19 | HG01167.hp1 HG01169.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.285-20187_285-2018 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45791204 | |||||
| chr12:45791373
|
A | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-20045A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791373 | ||||||
| chr12:45791384
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-20034C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791384 | ||||||
| chr12:45791483
|
C | A | 6 | a0001c0001t0001g0140a0001c0001t0001g0142a0001c0001t0001g0233others(3): Show | 6 | HG00639.hp2 HG01081.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-19935C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791483 | ||||||
| chr12:45791607
|
T | G | 1 | a0001c0001t0001g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.285-19811T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791607 | ||||||
| chr12:45791646
|
T | C | 29 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(26): Show | 29 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.285-19772T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791646 | ||||||
| chr12:45791662
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0094 | 2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.285-19756C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791662 | ||||||
| chr12:45791782
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.285-19636A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45791782 | ||||||
| chr12:45792010
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0306a0001c0001t0003g0283 | 3 | HG01346.hp1 HG02809.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.285-19408C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792010 | ||||||
| chr12:45792493
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-18925G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792493 | ||||||
| chr12:45792520
|
C | T | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-18898C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792520 | ||||||
| chr12:45792528
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-18890C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792528 | ||||||
| chr12:45792610
|
GAGAT | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-18805_285-1880 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45792610 | |||||
| chr12:45792942
|
T | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.285-18476T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45792942 | ||||||
| chr12:45793037
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.285-18381G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793037 | ||||||
| chr12:45793121
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.285-18297G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793121 | ||||||
| chr12:45793157
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-18261G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793157 | ||||||
| chr12:45793159
|
G | C | 4 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0187others(1): Show | 4 | NA18966.hp2 NA19001.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.285-18259G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793159 | ||||||
| chr12:45793205
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.285-18213C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793205 | ||||||
| chr12:45793216
|
C | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-18202C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793216 | ||||||
| chr12:45793227
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-18191G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793227 | ||||||
| chr12:45793346
|
C | CT | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.285-18065dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793346 | |||||
| chr12:45793543
|
C | CTG | 5 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0148others(2): Show | 5 | HG01167.hp2 HG01346.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-17855_285-1785 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793543 | |||||
| chr12:45793543
|
C | CTGTG | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-17857_285-1785 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793543 | |||||
| chr12:45793543
|
CTGTG | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-17857_285-1785 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793543 | |||||
| chr12:45793565
|
A | G | 3 | a0001c0002t0002g0225a0001c0002t0002g0228a0001c0002t0002g0305 | 3 | HG01884.hp2 HG02922.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.285-17853A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793565 | ||||||
| chr12:45793602
|
A | C | 1 | a0001c0006t0008g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.285-17816A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793602 | ||||||
| chr12:45793730
|
C | CAT | 5 | a0002c0003t0001g0250a0003c0004t0006g0105a0003c0004t0006g0106others(2): Show | 5 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-17676_285-1767 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45793730 | |||||
| chr12:45793826
|
A | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.285-17592A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793826 | ||||||
| chr12:45793837
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.285-17581T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793837 | ||||||
| chr12:45793960
|
G | T | 6 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | NA18959.hp2 NA18973.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-17458G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793960 | ||||||
| chr12:45793971
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.285-17447T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45793971 | ||||||
| chr12:45794143
|
C | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-17275C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794143 | ||||||
| chr12:45794282
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-17136T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794282 | ||||||
| chr12:45794328
|
G | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-17090G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794328 | ||||||
| chr12:45794343
|
G | A | 215 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.285-17075G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794343 | ||||||
| chr12:45794362
|
T | C | 3 | a0001c0001t0001g0078a0001c0001t0001g0081a0001c0001t0001g0089 | 3 | NA18979.hp1 NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.285-17056T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794362 | ||||||
| chr12:45794709
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-16709C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794709 | ||||||
| chr12:45794734
|
T | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-16684T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794734 | ||||||
| chr12:45794772
|
G | A | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-16646G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794772 | ||||||
| chr12:45794927
|
C | G | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.285-16491C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45794927 | ||||||
| chr12:45795084
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0279 | 2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.285-16334T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795084 | ||||||
| chr12:45795411
|
C | T | 3 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212 | 3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.285-16007C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795411 | ||||||
| chr12:45795445
|
T | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-15973T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795445 | ||||||
| chr12:45795452
|
G | A | 1 | a0001c0001t0005g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.285-15966G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795452 | ||||||
| chr12:45795471
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.285-15947G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795471 | ||||||
| chr12:45795501
|
G | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(22): Show | 25 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-15917G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795501 | ||||||
| chr12:45795519
|
G | A | 1 | a0001c0001t0009g0212 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.285-15899G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795519 | ||||||
| chr12:45795542
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-15876C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795542 | ||||||
| chr12:45795577
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.285-15841C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795577 | ||||||
| chr12:45795702
|
C | CTG | 112 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(109): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.285-15715_285-1571 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45795702 | |||||
| chr12:45795918
|
A | T | 1 | a0001c0002t0002g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.285-15500A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45795918 | ||||||
| chr12:45796081
|
AC | A | 5 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0260others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.285-15335delC | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45796081 | |||||
| chr12:45796217
|
C | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-15201C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796217 | ||||||
| chr12:45796231
|
G | A | 1 | a0001c0001t0017g0131 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.285-15187G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796231 | ||||||
| chr12:45796444
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285-14974A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796444 | ||||||
| chr12:45796502
|
G | GTTTATTT others(13): Show |
4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-14907_285-1488 others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45796502 | |||||
| chr12:45796593
|
A | G | 23 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(20): Show | 23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.285-14825A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796593 | ||||||
| chr12:45796786
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.285-14632A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45796786 | ||||||
| chr12:45797080
|
C | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096 | 3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.285-14338C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797080 | ||||||
| chr12:45797295
|
C | T | 2 | a0001c0001t0001g0240a0001c0001t0001g0246 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.285-14123C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797295 | ||||||
| chr12:45797309
|
A | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-14109A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797309 | ||||||
| chr12:45797526
|
T | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(202): Show | 206 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.285-13892T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797526 | ||||||
| chr12:45797564
|
A | C | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.285-13854A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797564 | ||||||
| chr12:45797591
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.285-13827A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797591 | ||||||
| chr12:45797865
|
T | A | 2 | a0001c0001t0003g0282a0001c0001t0003g0314 | 2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.285-13553T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45797865 | ||||||
| chr12:45798208
|
GT | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(98): Show | 102 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.285-13200delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45798208 | |||||
| chr12:45798383
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0060 | 2 | NA18941.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.285-13035T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798383 | ||||||
| chr12:45798443
|
A | G | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.285-12975A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798443 | ||||||
| chr12:45798574
|
A | T | 213 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(210): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.285-12844A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798574 | ||||||
| chr12:45798732
|
AC | A | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-12685delC | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798732 | ||||||
| chr12:45798799
|
A | G | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-12619A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798799 | ||||||
| chr12:45798869
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-12549T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798869 | ||||||
| chr12:45798904
|
C | T | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-12514C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45798904 | ||||||
| chr12:45799444
|
G | A | 39 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-11974G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45799444 | ||||||
| chr12:45799596
|
C | G | 39 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-11822C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45799596 | ||||||
| chr12:45799788
|
G | A | 1 | a0001c0002t0002g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.285-11630G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45799788 | ||||||
| chr12:45800070
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.285-11348G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800070 | ||||||
| chr12:45800128
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.285-11290G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800128 | ||||||
| chr12:45800162
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.285-11256G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800162 | ||||||
| chr12:45800521
|
C | CAT | 214 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(211): Show | 215 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.285-10897_285-1089 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800521 | ||||||
| chr12:45800650
|
A | AAAG | 218 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.285-10767_285-1076 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45800650 | |||||
| chr12:45800799
|
A | C | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.285-10619A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45800799 | ||||||
| chr12:45800978
|
GAA | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-10438_285-1043 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45800978 | |||||
| chr12:45801051
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0257 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.285-10367G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801051 | ||||||
| chr12:45801073
|
G | C | 1 | a0001c0001t0001g0082 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.285-10345G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801073 | ||||||
| chr12:45801185
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.285-10233G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801185 | ||||||
| chr12:45801306
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-10112C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801306 | ||||||
| chr12:45801319
|
G | GA | 28 | a0001c0001t0001g0015a0001c0001t0001g0061a0001c0001t0001g0234others(25): Show | 28 | HG00544.hp2 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.285-10086dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45801319 | |||||
| chr12:45801332
|
A | AAG | 45 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0140others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-10086_285-1008 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801332 | ||||||
| chr12:45801333
|
G | T | 45 | a0001c0001t0001g0128a0001c0001t0001g0130a0001c0001t0001g0140others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-10085G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801333 | ||||||
| chr12:45801334
|
T | G | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.285-10084T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801334 | ||||||
| chr12:45801370
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0064others(4): Show | 7 | HG00438.hp2 HG00621.hp1 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.285-10048G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801370 | ||||||
| chr12:45801378
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.285-10040A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801378 | ||||||
| chr12:45801505
|
C | G | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-9913C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801505 | ||||||
| chr12:45801968
|
G | A | 2 | a0001c0001t0001g0055a0001c0001t0001g0083 | 2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.285-9450G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801968 | ||||||
| chr12:45801971
|
T | C | 2 | a0001c0001t0001g0119a0001c0001t0017g0131 | 2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.285-9447T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45801971 | ||||||
| chr12:45802066
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.285-9352A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45802066 | ||||||
| chr12:45802473
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.285-8945G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45802473 | ||||||
| chr12:45802978
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.285-8440C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45802978 | ||||||
| chr12:45803084
|
A | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-8334A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803084 | ||||||
| chr12:45803189
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0187a0001c0001t0001g0309 | 3 | NA18966.hp2 NA19001.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.285-8229T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803189 | ||||||
| chr12:45803243
|
A | G | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285-8175A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803243 | ||||||
| chr12:45803479
|
A | C | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.285-7939A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803479 | ||||||
| chr12:45803535
|
A | G | 1 | a0001c0002t0002g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.285-7883A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803535 | ||||||
| chr12:45803540
|
G | A | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.285-7878G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803540 | ||||||
| chr12:45803612
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0192 | 2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.285-7806C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803612 | ||||||
| chr12:45803693
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.285-7725G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803693 | ||||||
| chr12:45803704
|
G | T | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-7714G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803704 | ||||||
| chr12:45803973
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.285-7445A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45803973 | ||||||
| chr12:45804042
|
A | G | 6 | a0001c0001t0001g0013a0001c0001t0001g0078a0001c0001t0001g0081others(3): Show | 6 | HG02135.hp1 NA18612.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-7376A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804042 | ||||||
| chr12:45804251
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0208a0001c0009t0011g0207others(1): Show | 4 | HG02717.hp1 HG02965.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-7167A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804251 | ||||||
| chr12:45804481
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.285-6937T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804481 | ||||||
| chr12:45804728
|
A | C | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.285-6690A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804728 | ||||||
| chr12:45804812
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.285-6606T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804812 | ||||||
| chr12:45804867
|
T | G | 1 | a0001c0001t0001g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.285-6551T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45804867 | ||||||
| chr12:45805429
|
G | T | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.285-5989G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805429 | ||||||
| chr12:45805600
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.285-5818G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805600 | ||||||
| chr12:45805806
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.285-5612T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805806 | ||||||
| chr12:45805822
|
C | T | 44 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.285-5596C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45805822 | ||||||
| chr12:45806015
|
T | C | 2 | a0001c0001t0013g0265a0001c0001t0013g0266 | 2 | HG00741.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.285-5403T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806015 | ||||||
| chr12:45806203
|
A | AT | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-5203dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45806203 | |||||
| chr12:45806226
|
A | G | 39 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-5192A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806226 | ||||||
| chr12:45806245
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0001g0178a0001c0001t0001g0204 | 3 | HG00738.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.285-5173T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806245 | ||||||
| chr12:45806613
|
G | T | 25 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(22): Show | 25 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-4805G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806613 | ||||||
| chr12:45806792
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.285-4626G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45806792 | ||||||
| chr12:45807407
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(112): Show | 116 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.285-4011A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45807407 | ||||||
| chr12:45807596
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-3822A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45807596 | ||||||
| chr12:45807693
|
AAC | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-3723_285-3722d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45807693 | |||||
| chr12:45807987
|
C | T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-3431C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45807987 | ||||||
| chr12:45808038
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-3380A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808038 | ||||||
| chr12:45808117
|
T | G | 66 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0087others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.285-3301T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808117 | ||||||
| chr12:45808119
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.285-3299C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808119 | ||||||
| chr12:45808167
|
A | G | 39 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(36): Show | 39 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.285-3251A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808167 | ||||||
| chr12:45808316
|
A | G | 45 | a0001c0001t0001g0055a0001c0001t0001g0130a0001c0001t0001g0140others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.285-3102A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808316 | ||||||
| chr12:45808358
|
A | T | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-3060A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808358 | ||||||
| chr12:45808413
|
A | G | 27 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.285-3005A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808413 | ||||||
| chr12:45808567
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2851A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808567 | ||||||
| chr12:45808688
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.285-2730C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808688 | ||||||
| chr12:45808690
|
A | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG00140.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.285-2728A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808690 | ||||||
| chr12:45808732
|
C | CGTGT | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2683_285-2682i others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808732 | |||||
| chr12:45808736
|
C | T | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2682C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808736 | ||||||
| chr12:45808736
|
CGT | C | 54 | a0001c0001t0001g0049a0001c0001t0001g0055a0001c0001t0001g0090others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.285-2659_285-2658d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808736 | |||||
| chr12:45808736
|
CGTGT | C | 8 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.285-2661_285-2658d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808736 | |||||
| chr12:45808753
|
GTGTGTGT others(1): Show |
G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-2657_285-2650d others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45808753 | |||||
| chr12:45808801
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.285-2617G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808801 | ||||||
| chr12:45808835
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.285-2583G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808835 | ||||||
| chr12:45808898
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.285-2520G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808898 | ||||||
| chr12:45808932
|
T | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-2486T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45808932 | ||||||
| chr12:45809235
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.285-2183A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809235 | ||||||
| chr12:45809285
|
C | G | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-2133C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809285 | ||||||
| chr12:45809305
|
A | G | 1 | a0010c0013t0001g0263 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.285-2113A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809305 | ||||||
| chr12:45809494
|
CCTT | C | 25 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.285-1920_285-1918d others(5): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr12 | 45809494 | |||||
| chr12:45809875
|
A | G | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.285-1543A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45809875 | ||||||
| chr12:45810131
|
T | G | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.285-1287T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810131 | ||||||
| chr12:45810207
|
G | T | 1 | a0001c0001t0001g0009 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.285-1211G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810207 | ||||||
| chr12:45810686
|
C | G | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.285-732C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810686 | ||||||
| chr12:45810693
|
G | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-725G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810693 | ||||||
| chr12:45810694
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.285-724C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810694 | ||||||
| chr12:45810937
|
C | T | 7 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(4): Show | 7 | HG02559.hp1 HG02738.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.285-481C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810937 | ||||||
| chr12:45810983
|
G | A | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.285-435G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45810983 | ||||||
| chr12:45811025
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.285-393C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811025 | ||||||
| chr12:45811131
|
C | T | 4 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0001g0311others(1): Show | 4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.285-287C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811131 | ||||||
| chr12:45811147
|
T | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.285-271T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811147 | ||||||
| chr12:45811247
|
C | T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.285-171C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811247 | ||||||
| chr12:45811349
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.285-69T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 3/20 | chr12 | 45811349 | ||||||
| chr12:45811908
|
C | T | 3 | a0001c0006t0008g0113a0001c0006t0008g0114a0001c0006t0008g0115 | 3 | HG02622.hp2 HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.418+357C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45811908 | ||||||
| chr12:45812058
|
A | G | 1 | a0001c0001t0001g0013 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.418+507A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812058 | ||||||
| chr12:45812145
|
A | T | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.418+594A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812145 | ||||||
| chr12:45812310
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.418+759G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812310 | ||||||
| chr12:45812346
|
C | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.418+795C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812346 | ||||||
| chr12:45812354
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.418+803G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812354 | ||||||
| chr12:45812509
|
TCTG | T | 3 | a0001c0001t0001g0069a0001c0001t0001g0102a0014c0019t0001g0079 | 3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.418+959_418+961del others(3): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812509 | ||||||
| chr12:45812513
|
A | G | 3 | a0001c0001t0001g0069a0001c0001t0001g0102a0014c0019t0001g0079 | 3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.418+962A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812513 | ||||||
| chr12:45812766
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1215C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45812766 | ||||||
| chr12:45813039
|
G | C | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.418+1488G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813039 | ||||||
| chr12:45813218
|
CTG | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.418+1668_418+1669d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813218 | ||||||
| chr12:45813458
|
T | TA | 61 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.418+1923dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45813458 | |||||
| chr12:45813458
|
T | TAA | 24 | a0001c0001t0001g0271a0001c0002t0002g0214a0001c0002t0002g0216others(21): Show | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.418+1922_418+1923d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45813458 | |||||
| chr12:45813458
|
TA | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(105): Show | 109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.418+1923delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45813458 | |||||
| chr12:45813548
|
G | A | 2 | a0001c0001t0009g0112a0001c0001t0009g0211 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.418+1997G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813548 | ||||||
| chr12:45813573
|
C | T | 2 | a0001c0002t0002g0226a0001c0002t0002g0229 | 2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.418+2022C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45813573 | ||||||
| chr12:45814073
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.418+2522G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814073 | ||||||
| chr12:45814151
|
C | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0174 | 2 | NA18962.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.418+2600C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814151 | ||||||
| chr12:45814263
|
C | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.418+2712C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814263 | ||||||
| chr12:45814371
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.418+2820C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814371 | ||||||
| chr12:45814539
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.418+2988A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814539 | ||||||
| chr12:45814581
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.418+3030C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814581 | ||||||
| chr12:45814588
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.418+3037T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814588 | ||||||
| chr12:45814599
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.418+3048G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814599 | ||||||
| chr12:45814636
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.419-3034A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814636 | ||||||
| chr12:45814655
|
A | G | 108 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(105): Show | 109 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.419-3015A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814655 | ||||||
| chr12:45814890
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.419-2780G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45814890 | ||||||
| chr12:45815286
|
A | C | 1 | a0001c0001t0001g0168 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.419-2384A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815286 | ||||||
| chr12:45815475
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.419-2195G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815475 | ||||||
| chr12:45815599
|
T | TTG | 36 | a0001c0001t0001g0041a0001c0001t0001g0062a0001c0001t0001g0065others(33): Show | 36 | HG01109.hp2 HG01175.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.419-2049_419-2048d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45815599 | |||||
| chr12:45815599
|
TTG | T | 3 | a0001c0001t0001g0133a0001c0001t0004g0194a0001c0006t0008g0115 | 3 | HG00642.hp2 HG02647.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.419-2049_419-2048d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45815599 | |||||
| chr12:45815654
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.419-2016G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815654 | ||||||
| chr12:45815698
|
G | A | 8 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0148others(5): Show | 8 | HG01167.hp2 HG02602.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.419-1972G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815698 | ||||||
| chr12:45815737
|
C | T | 2 | a0001c0001t0013g0265a0001c0001t0013g0266 | 2 | HG00741.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.419-1933C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815737 | ||||||
| chr12:45815849
|
C | G | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.419-1821C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45815849 | ||||||
| chr12:45816341
|
A | G | 1 | a0001c0006t0008g0114 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.419-1329A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816341 | ||||||
| chr12:45816383
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.419-1287T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816383 | ||||||
| chr12:45816674
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.419-996C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816674 | ||||||
| chr12:45816805
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.419-865A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816805 | ||||||
| chr12:45816960
|
C | T | 1 | a0008c0015t0001g0294 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.419-710C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45816960 | ||||||
| chr12:45817128
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.419-542G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817128 | ||||||
| chr12:45817294
|
C | T | 1 | a0001c0002t0002g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.419-376C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817294 | ||||||
| chr12:45817431
|
T | A | 46 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(43): Show | 46 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.419-239T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817431 | ||||||
| chr12:45817506
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.419-164G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817506 | ||||||
| chr12:45817526
|
T | TTATATTT others(32): Show |
4 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.419-137_419-99dupT others(38): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr12 | 45817526 | |||||
| chr12:45817613
|
T | C | 43 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(40): Show | 43 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.419-57T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 4/20 | chr12 | 45817613 | ||||||
| chr12:45817967
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.637+79T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45817967 | ||||||
| chr12:45818157
|
T | C | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.637+269T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818157 | ||||||
| chr12:45818390
|
C | A | 23 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(20): Show | 23 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.637+502C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818390 | ||||||
| chr12:45818392
|
A | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.637+504A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818392 | ||||||
| chr12:45818761
|
T | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.637+873T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818761 | ||||||
| chr12:45818908
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.637+1020A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45818908 | ||||||
| chr12:45819093
|
A | G | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0004c0005t0001g0111others(2): Show | 5 | NA18747.hp1 NA18956.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1205A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819093 | ||||||
| chr12:45819130
|
T | A | 5 | a0001c0002t0002g0258a0001c0002t0002g0259a0001c0002t0002g0260others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.637+1242T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819130 | ||||||
| chr12:45819251
|
C | G | 28 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.637+1363C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819251 | ||||||
| chr12:45819510
|
T | C | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.637+1622T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819510 | ||||||
| chr12:45819656
|
A | G | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1764A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819656 | ||||||
| chr12:45819684
|
C | A | 1 | a0001c0002t0002g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.638-1736C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819684 | ||||||
| chr12:45819808
|
G | A | 204 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(201): Show | 205 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.638-1612G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819808 | ||||||
| chr12:45819930
|
G | C | 2 | a0001c0001t0005g0285a0001c0001t0005g0286 | 2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.638-1490G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819930 | ||||||
| chr12:45819967
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.638-1453C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45819967 | ||||||
| chr12:45820035
|
T | A | 1 | a0001c0001t0001g0018 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.638-1385T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820035 | ||||||
| chr12:45820084
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.638-1336A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820084 | ||||||
| chr12:45820208
|
A | G | 4 | a0001c0001t0001g0054a0001c0001t0001g0065a0001c0001t0001g0093others(1): Show | 4 | NA18966.hp1 NA18969.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.638-1212A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820208 | ||||||
| chr12:45820321
|
T | C | 1 | a0001c0006t0008g0113 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.638-1099T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820321 | ||||||
| chr12:45820526
|
C | T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.638-894C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820526 | ||||||
| chr12:45820616
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0268 | 2 | HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.638-804T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820616 | ||||||
| chr12:45820717
|
T | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.638-703T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820717 | ||||||
| chr12:45820775
|
T | C | 1 | a0001c0001t0013g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.638-645T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45820775 | ||||||
| chr12:45821018
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.638-402T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45821018 | ||||||
| chr12:45821364
|
A | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.638-56A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45821364 | ||||||
| chr12:45821380
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(162): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.638-40G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 5/20 | chr12 | 45821380 | ||||||
| chr12:45821585
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.705+98A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45821585 | ||||||
| chr12:45821611
|
T | C | 1 | a0005c0008t0001g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.705+124T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45821611 | ||||||
| chr12:45821673
|
C | T | 3 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0067 | 3 | NA18947.hp1 NA18970.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.705+186C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45821673 | ||||||
| chr12:45822112
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+625T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822112 | ||||||
| chr12:45822135
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.705+648A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822135 | ||||||
| chr12:45822377
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.705+890T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822377 | ||||||
| chr12:45822623
|
T | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.705+1136T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822623 | ||||||
| chr12:45822876
|
C | T | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.705+1389C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45822876 | ||||||
| chr12:45823180
|
A | G | 1 | a0002c0003t0001g0143 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.705+1693A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823180 | ||||||
| chr12:45823256
|
T | C | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.705+1769T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823256 | ||||||
| chr12:45823580
|
CAAAT | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+2097_705+2100d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45823580 | |||||
| chr12:45823688
|
G | GA | 24 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(21): Show | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.705+2207dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45823688 | |||||
| chr12:45823722
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.705+2235C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823722 | ||||||
| chr12:45823889
|
A | G | 5 | a0001c0001t0001g0245a0001c0001t0001g0296a0001c0001t0001g0304others(2): Show | 5 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+2402A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45823889 | ||||||
| chr12:45824012
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.705+2525G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824012 | ||||||
| chr12:45824096
|
T | C | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.705+2609T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824096 | ||||||
| chr12:45824125
|
A | G | 3 | a0001c0001t0001g0158a0001c0001t0001g0190a0012c0012t0001g0127 | 3 | NA18940.hp2 NA18947.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.705+2638A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824125 | ||||||
| chr12:45824331
|
GGAAAAAC others(15): Show |
G | 1 | a0001c0001t0001g0090 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.705+2857_705+2878d others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45824331 | |||||
| chr12:45824427
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+2940A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824427 | ||||||
| chr12:45824491
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0062 | 2 | HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.705+3004A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824491 | ||||||
| chr12:45824540
|
A | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.705+3053A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824540 | ||||||
| chr12:45824689
|
T | G | 2 | a0001c0001t0007g0184a0001c0001t0007g0237 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.705+3202T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824689 | ||||||
| chr12:45824713
|
C | T | 24 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(21): Show | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.705+3226C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824713 | ||||||
| chr12:45824758
|
A | G | 1 | a0001c0009t0011g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.705+3271A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824758 | ||||||
| chr12:45824840
|
G | A | 24 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(21): Show | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.705+3353G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45824840 | ||||||
| chr12:45824866
|
C | CAT | 12 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(9): Show | 13 | HG00438.hp1 HG02056.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.705+3394_705+3395d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45824866 | |||||
| chr12:45824866
|
CAT | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0145a0001c0001t0001g0292others(1): Show | 4 | HG02132.hp2 HG02559.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+3394_705+3395d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45824866 | |||||
| chr12:45825022
|
G | T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.705+3535G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825022 | ||||||
| chr12:45825161
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+3674A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825161 | ||||||
| chr12:45825735
|
A | G | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.705+4248A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825735 | ||||||
| chr12:45825837
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+4350A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825837 | ||||||
| chr12:45825871
|
A | G | 1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.705+4384A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825871 | ||||||
| chr12:45825911
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.705+4424A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825911 | ||||||
| chr12:45825930
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.705+4443G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825930 | ||||||
| chr12:45825992
|
C | T | 1 | a0009c0014t0021g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.705+4505C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45825992 | ||||||
| chr12:45826327
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+4840G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826327 | ||||||
| chr12:45826361
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.705+4874G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826361 | ||||||
| chr12:45826425
|
T | C | 4 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0001g0311others(1): Show | 4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.705+4938T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826425 | ||||||
| chr12:45826458
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.705+4971T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826458 | ||||||
| chr12:45826569
|
C | CA | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+5083dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45826569 | |||||
| chr12:45826617
|
A | T | 1 | a0001c0001t0001g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.705+5130A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826617 | ||||||
| chr12:45826671
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.705+5184G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826671 | ||||||
| chr12:45826684
|
G | A | 2 | a0002c0003t0001g0210a0002c0003t0001g0250 | 2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.705+5197G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826684 | ||||||
| chr12:45826727
|
A | G | 1 | a0001c0001t0013g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.705+5240A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45826727 | ||||||
| chr12:45827091
|
C | A | 5 | a0001c0001t0001g0130a0001c0001t0001g0141a0001c0001t0001g0243others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.705+5604C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827091 | ||||||
| chr12:45827110
|
T | G | 1 | a0001c0002t0002g0215 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.705+5623T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827110 | ||||||
| chr12:45827149
|
A | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.705+5662A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827149 | ||||||
| chr12:45827811
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.705+6324T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45827811 | ||||||
| chr12:45828113
|
G | A | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.705+6626G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828113 | ||||||
| chr12:45828143
|
A | C | 1 | a0001c0001t0001g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.705+6656A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828143 | ||||||
| chr12:45828143
|
A | G | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.705+6656A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828143 | ||||||
| chr12:45828339
|
G | T | 4 | a0001c0001t0005g0273a0001c0001t0005g0286a0001c0001t0005g0288others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.705+6852G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828339 | ||||||
| chr12:45828540
|
T | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.705+7053T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828540 | ||||||
| chr12:45828564
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.705+7077G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828564 | ||||||
| chr12:45828595
|
C | T | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.705+7108C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828595 | ||||||
| chr12:45828662
|
G | C | 1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.705+7175G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828662 | ||||||
| chr12:45828686
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.705+7199G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828686 | ||||||
| chr12:45828746
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0095 | 2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.705+7259A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828746 | ||||||
| chr12:45828945
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.705+7458A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45828945 | ||||||
| chr12:45829365
|
T | C | 115 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(112): Show | 116 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.706-7224T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829365 | ||||||
| chr12:45829600
|
T | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-6989T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829600 | ||||||
| chr12:45829638
|
T | A | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.706-6951T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829638 | ||||||
| chr12:45829792
|
T | TTTC | 75 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.706-6788_706-6786d others(5): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45829792 | |||||
| chr12:45829802
|
T | TTC | 137 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0087others(134): Show | 138 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.706-6786_706-6785i others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45829802 | |||||
| chr12:45829803
|
T | TC | 5 | a0001c0001t0001g0045a0001c0001t0001g0123a0001c0001t0001g0156others(2): Show | 5 | HG01069.hp2 HG01256.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.706-6786_706-6785i others(3): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829803 | ||||||
| chr12:45829898
|
G | C | 28 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.706-6691G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829898 | ||||||
| chr12:45829991
|
G | T | 215 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.706-6598G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45829991 | ||||||
| chr12:45830136
|
G | A | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-6453G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830136 | ||||||
| chr12:45830195
|
T | G | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.706-6394T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830195 | ||||||
| chr12:45830280
|
A | G | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.706-6309A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830280 | ||||||
| chr12:45830356
|
T | G | 3 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG00140.hp1 HG01934.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.706-6233T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830356 | ||||||
| chr12:45830358
|
C | T | 6 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0163others(3): Show | 6 | NA18959.hp2 NA18973.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-6231C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830358 | ||||||
| chr12:45830368
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-6221G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830368 | ||||||
| chr12:45830831
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0095 | 2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.706-5758A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830831 | ||||||
| chr12:45830912
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.706-5677G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830912 | ||||||
| chr12:45830913
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.706-5676C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830913 | ||||||
| chr12:45830988
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.706-5601G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45830988 | ||||||
| chr12:45831031
|
C | T | 23 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(20): Show | 23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.706-5558C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831031 | ||||||
| chr12:45831236
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-5353C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831236 | ||||||
| chr12:45831250
|
C | A | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.706-5339C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831250 | ||||||
| chr12:45831364
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0072 | 2 | HG00621.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.706-5225C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831364 | ||||||
| chr12:45831369
|
GTTAT | G | 6 | a0001c0001t0001g0134a0001c0001t0001g0158a0001c0001t0001g0161others(3): Show | 6 | HG01074.hp2 NA18940.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.706-5212_706-5209d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45831369 | |||||
| chr12:45831536
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.706-5053T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831536 | ||||||
| chr12:45831627
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.706-4962A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831627 | ||||||
| chr12:45831724
|
A | G | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.706-4865A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831724 | ||||||
| chr12:45831811
|
C | G | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-4778C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45831811 | ||||||
| chr12:45832414
|
G | A | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-4175G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832414 | ||||||
| chr12:45832702
|
C | T | 111 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(108): Show | 112 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.706-3887C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832702 | ||||||
| chr12:45832760
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.706-3829C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832760 | ||||||
| chr12:45832957
|
A | G | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-3632A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45832957 | ||||||
| chr12:45833867
|
A | G | 24 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(21): Show | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.706-2722A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45833867 | ||||||
| chr12:45833883
|
T | C | 1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.706-2706T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45833883 | ||||||
| chr12:45834199
|
A | G | 3 | a0001c0001t0001g0013a0005c0008t0001g0043a0005c0008t0001g0080 | 3 | HG02135.hp1 NA18612.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.706-2390A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834199 | ||||||
| chr12:45834260
|
C | CT | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-2317dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45834260 | |||||
| chr12:45834272
|
T | C | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.706-2317T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834272 | ||||||
| chr12:45834458
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.706-2131T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834458 | ||||||
| chr12:45834464
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.706-2125G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834464 | ||||||
| chr12:45834487
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-2102A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834487 | ||||||
| chr12:45834697
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(111): Show | 115 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.706-1892G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834697 | ||||||
| chr12:45834843
|
C | G | 1 | a0001c0001t0001g0243 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.706-1746C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45834843 | ||||||
| chr12:45835083
|
T | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.706-1506T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835083 | ||||||
| chr12:45835289
|
G | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.706-1300G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835289 | ||||||
| chr12:45835346
|
A | G | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.706-1243A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835346 | ||||||
| chr12:45835499
|
C | CA | 26 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.706-1080dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45835499 | |||||
| chr12:45835628
|
G | A | 2 | a0001c0001t0001g0036a0001c0001t0001g0053 | 2 | NA18747.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.706-961G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835628 | ||||||
| chr12:45835684
|
A | G | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-905A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835684 | ||||||
| chr12:45835900
|
C | CA | 7 | a0001c0001t0001g0045a0001c0001t0003g0280a0001c0001t0003g0281others(4): Show | 7 | HG02486.hp2 HG02738.hp2 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.706-678dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45835900 | |||||
| chr12:45835906
|
A | C | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.706-683A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835906 | ||||||
| chr12:45835912
|
C | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-677C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835912 | ||||||
| chr12:45835912
|
C | CAAA | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.706-674_706-672dup others(3): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr12 | 45835912 | |||||
| chr12:45835918
|
C | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-671C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835918 | ||||||
| chr12:45835925
|
G | C | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.706-664G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835925 | ||||||
| chr12:45835949
|
TTA | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.706-639_706-638del others(2): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45835949 | ||||||
| chr12:45836248
|
C | T | 98 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(95): Show | 99 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.706-341C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45836248 | ||||||
| chr12:45836556
|
A | C | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.706-33A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 6/20 | chr12 | 45836556 | ||||||
| chr12:45836727
|
A | C | 5 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.773-14A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 7/20 | chr12 | 45836727 | ||||||
| chr12:45837141
|
A | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1023+150A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 8/20 | chr12 | 45837141 | ||||||
| chr12:45838102
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1330+395T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838102 | ||||||
| chr12:45838170
|
C | T | 23 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(20): Show | 23 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1330+463C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838170 | ||||||
| chr12:45838322
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1330+615A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838322 | ||||||
| chr12:45838389
|
T | C | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1330+682T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838389 | ||||||
| chr12:45838868
|
G | GT | 41 | a0001c0001t0001g0068a0001c0001t0001g0074a0001c0001t0001g0075others(38): Show | 41 | HG00544.hp2 HG01167.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.1331-446dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 45838868 | |||||
| chr12:45838868
|
G | GTT | 7 | a0001c0001t0003g0314a0001c0002t0002g0215a0003c0004t0006g0105others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1331-447_1331-446d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr12 | 45838868 | |||||
| chr12:45838868
|
G | T | 2 | a0001c0001t0007g0184a0001c0001t0007g0237 | 2 | HG02630.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1331-461G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838868 | ||||||
| chr12:45838873
|
T | G | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1331-456T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838873 | ||||||
| chr12:45838965
|
A | G | 1 | a0013c0018t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1331-364A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45838965 | ||||||
| chr12:45839020
|
G | A | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1331-309G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839020 | ||||||
| chr12:45839110
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1331-219C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839110 | ||||||
| chr12:45839217
|
T | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1331-112T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839217 | ||||||
| chr12:45839259
|
T | C | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1331-70T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 10/20 | chr12 | 45839259 | ||||||
| chr12:45839753
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1498+257T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839753 | ||||||
| chr12:45839814
|
G | A | 1 | a0001c0001t0015g0149 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1498+318G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839814 | ||||||
| chr12:45839847
|
A | G | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1498+351A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839847 | ||||||
| chr12:45839946
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1498+450G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45839946 | ||||||
| chr12:45840196
|
C | A | 1 | a0002c0003t0001g0255 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1498+700C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840196 | ||||||
| chr12:45840228
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1498+732A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840228 | ||||||
| chr12:45840262
|
A | G | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+766A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840262 | ||||||
| chr12:45840684
|
A | G | 4 | a0001c0001t0005g0285a0001c0001t0007g0184a0001c0001t0007g0237others(1): Show | 4 | HG02258.hp1 HG02630.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498+1188A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840684 | ||||||
| chr12:45840738
|
T | C | 1 | a0013c0018t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1498+1242T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840738 | ||||||
| chr12:45840788
|
C | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0146 | 3 | HG02056.hp2 NA18612.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1498+1292C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45840788 | ||||||
| chr12:45841019
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0001g0310 | 2 | HG01168.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1498+1523C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841019 | ||||||
| chr12:45841087
|
G | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1498+1591G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841087 | ||||||
| chr12:45841211
|
A | G | 5 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(2): Show | 5 | HG03239.hp2 HG03704.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.1498+1715A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841211 | ||||||
| chr12:45841211
|
A | T | 1 | a0001c0001t0003g0314 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1498+1715A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841211 | ||||||
| chr12:45841404
|
G | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1498+1908G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841404 | ||||||
| chr12:45841884
|
C | T | 1 | a0001c0001t0001g0140 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1498+2388C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45841884 | ||||||
| chr12:45842085
|
C | T | 2 | a0001c0001t0001g0271a0001c0011t0019g0272 | 2 | HG01884.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1498+2589C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842085 | ||||||
| chr12:45842109
|
A | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1498+2613A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842109 | ||||||
| chr12:45842234
|
C | CA | 23 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096others(20): Show | 23 | HG01175.hp1 HG02109.hp1 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.1498+2753dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45842234 | |||||
| chr12:45842234
|
CA | C | 13 | a0001c0001t0001g0236a0001c0001t0001g0264a0001c0001t0001g0270others(10): Show | 13 | HG02615.hp2 HG02738.hp2 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.1498+2753delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45842234 | |||||
| chr12:45842250
|
T | A | 1 | a0001c0002t0002g0259 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1498+2754T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842250 | ||||||
| chr12:45842295
|
GTGTATAT others(17): Show |
G | 3 | a0001c0001t0001g0136a0001c0001t0001g0171a0001c0001t0001g0204 | 3 | HG01192.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1498+2833_1498+285 others(28): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45842295 | |||||
| chr12:45842481
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1498+2985G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842481 | ||||||
| chr12:45842574
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0192 | 2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1498+3078T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842574 | ||||||
| chr12:45842683
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+3187G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842683 | ||||||
| chr12:45842847
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498+3351A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45842847 | ||||||
| chr12:45843137
|
G | C | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1498+3641G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843137 | ||||||
| chr12:45843279
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1499-3577C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843279 | ||||||
| chr12:45843286
|
T | TTTAGCTA others(507): Show |
5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-3570_1499-356 others(518): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843286 | ||||||
| chr12:45843329
|
A | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0136a0001c0001t0001g0137others(5): Show | 8 | HG00280.hp2 HG00639.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.1499-3527A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843329 | ||||||
| chr12:45843375
|
C | CT | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-3466dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | INFO_REALIGN_3_PRIME | chr12 | 45843375 | |||||
| chr12:45843378
|
T | C | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-3478T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843378 | ||||||
| chr12:45843401
|
C | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-3455C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843401 | ||||||
| chr12:45843471
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-3385A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843471 | ||||||
| chr12:45843750
|
T | G | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1499-3106T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843750 | ||||||
| chr12:45843754
|
T | C | 2 | a0001c0001t0001g0081a0001c0001t0001g0089 | 2 | NA19064.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1499-3102T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843754 | ||||||
| chr12:45843841
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1499-3015C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843841 | ||||||
| chr12:45843850
|
C | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1499-3006C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843850 | ||||||
| chr12:45843938
|
C | T | 7 | a0001c0001t0001g0236a0001c0001t0001g0241a0001c0001t0001g0289others(4): Show | 7 | HG01346.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1499-2918C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843938 | ||||||
| chr12:45843982
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1499-2874C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45843982 | ||||||
| chr12:45844141
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1499-2715G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844141 | ||||||
| chr12:45844141
|
G | C | 1 | a0001c0001t0001g0047 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1499-2715G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844141 | ||||||
| chr12:45844258
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1499-2598A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844258 | ||||||
| chr12:45844378
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1499-2478G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844378 | ||||||
| chr12:45844576
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1499-2280G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844576 | ||||||
| chr12:45844728
|
C | G | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1499-2128C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844728 | ||||||
| chr12:45844781
|
C | T | 1 | a0001c0001t0001g0172 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1499-2075C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844781 | ||||||
| chr12:45844857
|
C | T | 44 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.1499-1999C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844857 | ||||||
| chr12:45844891
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0290 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1499-1965C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45844891 | ||||||
| chr12:45845161
|
C | T | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1499-1695C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845161 | ||||||
| chr12:45845229
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1499-1627G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845229 | ||||||
| chr12:45845317
|
T | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0192 | 2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1499-1539T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845317 | ||||||
| chr12:45845346
|
T | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0066a0001c0001t0001g0100 | 3 | HG02486.hp1 HG04199.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1499-1510T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845346 | ||||||
| chr12:45845369
|
T | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1499-1487T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845369 | ||||||
| chr12:45845635
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1499-1221G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845635 | ||||||
| chr12:45845742
|
A | G | 2 | a0001c0001t0009g0112a0001c0001t0009g0211 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1499-1114A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845742 | ||||||
| chr12:45845826
|
G | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1499-1030G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845826 | ||||||
| chr12:45845934
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1499-922T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45845934 | ||||||
| chr12:45846378
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1499-478G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846378 | ||||||
| chr12:45846397
|
C | T | 2 | a0001c0002t0002g0226a0001c0002t0002g0229 | 2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1499-459C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846397 | ||||||
| chr12:45846480
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1499-376T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846480 | ||||||
| chr12:45846505
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1499-351C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846505 | ||||||
| chr12:45846615
|
T | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1499-241T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846615 | ||||||
| chr12:45846679
|
A | G | 1 | a0002c0003t0001g0186 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1499-177A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846679 | ||||||
| chr12:45846744
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1499-112C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846744 | ||||||
| chr12:45846775
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1499-81G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 11/20 | chr12 | 45846775 | ||||||
| chr12:45847039
|
T | C | 3 | a0004c0005t0001g0111a0004c0005t0001g0147a0004c0005t0001g0169 | 3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1580+102T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847039 | ||||||
| chr12:45847380
|
T | A | 314 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(311): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.1580+443T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847380 | ||||||
| chr12:45847397
|
T | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1580+460T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847397 | ||||||
| chr12:45847436
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1580+499A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847436 | ||||||
| chr12:45847483
|
C | G | 1 | a0008c0015t0001g0294 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1580+546C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847483 | ||||||
| chr12:45847636
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1580+699C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847636 | ||||||
| chr12:45847687
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0204 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1580+750C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847687 | ||||||
| chr12:45847703
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1580+766G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847703 | ||||||
| chr12:45847911
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1581-925A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45847911 | ||||||
| chr12:45848114
|
T | A | 3 | a0001c0001t0001g0015a0001c0009t0011g0207a0001c0009t0011g0209 | 3 | HG02056.hp1 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1581-722T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848114 | ||||||
| chr12:45848400
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1581-436C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848400 | ||||||
| chr12:45848412
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1581-424G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848412 | ||||||
| chr12:45848632
|
T | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1581-204T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848632 | ||||||
| chr12:45848658
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1581-178C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848658 | ||||||
| chr12:45848701
|
C | T | 2 | a0001c0002t0002g0226a0001c0002t0002g0229 | 2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1581-135C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 12/20 | chr12 | 45848701 | ||||||
| chr12:45849099
|
G | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1715+129G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849099 | ||||||
| chr12:45849106
|
T | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1715+136T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849106 | ||||||
| chr12:45849336
|
T | G | 3 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212 | 3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1716-244T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849336 | ||||||
| chr12:45849411
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0051 | 2 | HG00609.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1716-169G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 13/20 | chr12 | 45849411 | ||||||
| chr12:45853204
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4773+308G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853204 | ||||||
| chr12:45853286
|
G | A | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4773+390G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853286 | ||||||
| chr12:45853515
|
A | G | 7 | a0001c0001t0001g0264a0001c0001t0001g0270a0003c0004t0006g0105others(4): Show | 7 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.4773+619A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853515 | ||||||
| chr12:45853807
|
A | G | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4773+911A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853807 | ||||||
| chr12:45853870
|
G | A | 40 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(37): Show | 40 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(37): Show |
intron_variant | MODIFIER | c.4773+974G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853870 | ||||||
| chr12:45853888
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4773+992C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853888 | ||||||
| chr12:45853961
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0095 | 2 | HG00438.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.4773+1065C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45853961 | ||||||
| chr12:45854004
|
C | T | 2 | a0001c0001t0001g0236a0001c0001t0001g0290 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4773+1108C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854004 | ||||||
| chr12:45854005
|
G | A | 6 | a0002c0003t0001g0255a0003c0004t0006g0105a0003c0004t0006g0106others(3): Show | 6 | HG02155.hp1 HG02451.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.4773+1109G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854005 | ||||||
| chr12:45854021
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+1125G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854021 | ||||||
| chr12:45854125
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0007 | 2 | HG00544.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.4773+1229C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854125 | ||||||
| chr12:45854145
|
C | T | 1 | a0001c0001t0012g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4773+1249C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854145 | ||||||
| chr12:45854308
|
G | A | 3 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0148 | 3 | HG01167.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4773+1412G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854308 | ||||||
| chr12:45854383
|
G | A | 2 | a0004c0005t0001g0147a0004c0005t0001g0169 | 2 | NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.4773+1487G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45854383 | ||||||
| chr12:45855017
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0003g0280a0001c0001t0003g0281others(42): Show | 45 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(42): Show |
intron_variant | MODIFIER | c.4773+2121T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855017 | ||||||
| chr12:45855036
|
T | G | 3 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212 | 3 | HG01167.hp1 HG01169.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.4773+2140T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855036 | ||||||
| chr12:45855104
|
G | A | 23 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(20): Show | 23 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.4773+2208G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855104 | ||||||
| chr12:45855271
|
C | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+2375C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855271 | ||||||
| chr12:45855376
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0001g0268 | 2 | HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4773+2480A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855376 | ||||||
| chr12:45855563
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4773+2667A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855563 | ||||||
| chr12:45855644
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.4773+2748T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855644 | ||||||
| chr12:45855670
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4773+2774A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855670 | ||||||
| chr12:45855731
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4773+2835G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855731 | ||||||
| chr12:45855859
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4773+2963C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855859 | ||||||
| chr12:45855889
|
T | C | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+2993T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855889 | ||||||
| chr12:45855904
|
T | G | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4773+3008T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855904 | ||||||
| chr12:45855909
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4773+3013G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855909 | ||||||
| chr12:45855947
|
T | C | 1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4773+3051T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45855947 | ||||||
| chr12:45856004
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4773+3108T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45856004 | ||||||
| chr12:45856067
|
C | CT | 46 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0024others(43): Show | 46 | HG01106.hp2 HG01109.hp2 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.4773+3196dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | |||||
| chr12:45856067
|
C | CTT | 36 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(33): Show | 36 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.4773+3195_4773+319 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | |||||
| chr12:45856067
|
CT | C | 13 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0086others(10): Show | 13 | HG01167.hp1 HG01256.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.4773+3196delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | |||||
| chr12:45856067
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4773+3186_4773+319 others(15): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | |||||
| chr12:45856067
|
CTTTTTTT others(5): Show |
C | 7 | a0001c0001t0001g0022a0001c0001t0001g0051a0003c0004t0006g0105others(4): Show | 7 | HG00609.hp1 HG02300.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4773+3185_4773+319 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | |||||
| chr12:45856067
|
CTTTTTTT others(6): Show |
C | 4 | a0001c0001t0005g0273a0001c0001t0005g0286a0001c0001t0005g0288others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4773+3184_4773+319 others(17): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45856067 | |||||
| chr12:45856075
|
T | C | 5 | a0001c0001t0003g0280a0001c0001t0003g0282a0001c0001t0003g0283others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.4773+3179T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45856075 | ||||||
| chr12:45856076
|
T | C | 1 | a0001c0001t0003g0281 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4773+3180T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45856076 | ||||||
| chr12:45857018
|
A | G | 1 | a0001c0001t0001g0064 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4774-3783A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857018 | ||||||
| chr12:45857049
|
T | C | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4774-3752T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857049 | ||||||
| chr12:45857228
|
A | C | 1 | a0001c0001t0001g0270 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4774-3573A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857228 | ||||||
| chr12:45857406
|
A | T | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-3395A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857406 | ||||||
| chr12:45857435
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4774-3366A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857435 | ||||||
| chr12:45857486
|
T | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-3315T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857486 | ||||||
| chr12:45857791
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4774-3010G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45857791 | ||||||
| chr12:45858049
|
C | T | 29 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(26): Show | 29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4774-2752C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45858049 | ||||||
| chr12:45858454
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4774-2347G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45858454 | ||||||
| chr12:45858946
|
A | C | 8 | a0001c0001t0001g0036a0001c0001t0001g0053a0001c0001t0001g0082others(5): Show | 8 | HG02129.hp1 NA18747.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.4774-1855A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45858946 | ||||||
| chr12:45859188
|
A | C | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-1613A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859188 | ||||||
| chr12:45859253
|
A | G | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4774-1548A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859253 | ||||||
| chr12:45859283
|
G | A | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4774-1518G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859283 | ||||||
| chr12:45859540
|
C | G | 1 | a0001c0002t0002g0220 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4774-1261C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859540 | ||||||
| chr12:45859608
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4774-1193A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859608 | ||||||
| chr12:45859675
|
T | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4774-1126T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859675 | ||||||
| chr12:45859879
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4774-922G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45859879 | ||||||
| chr12:45860175
|
T | C | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-626T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860175 | ||||||
| chr12:45860310
|
A | T | 1 | a0001c0001t0001g0042 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4774-491A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860310 | ||||||
| chr12:45860612
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4774-189T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860612 | ||||||
| chr12:45860660
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4774-141G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860660 | ||||||
| chr12:45860665
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.4774-136C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860665 | ||||||
| chr12:45860716
|
CAT | C | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.4774-83_4774-82del others(2): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr12 | 45860716 | |||||
| chr12:45860722
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.4774-79C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 15/20 | chr12 | 45860722 | ||||||
| chr12:45861176
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.4922+227C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861176 | ||||||
| chr12:45861212
|
A | G | 28 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4922+263A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861212 | ||||||
| chr12:45861253
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4922+304G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861253 | ||||||
| chr12:45861264
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | NA18974.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.4922+315C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861264 | ||||||
| chr12:45861296
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4922+347A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861296 | ||||||
| chr12:45861329
|
A | T | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4922+380A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861329 | ||||||
| chr12:45861554
|
T | C | 2 | a0002c0003t0001g0210a0002c0003t0001g0250 | 2 | NA19060.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.4922+605T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861554 | ||||||
| chr12:45861580
|
C | CT | 8 | a0001c0001t0001g0264a0001c0001t0001g0270a0001c0001t0003g0280others(5): Show | 8 | HG02738.hp2 HG03098.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.4922+652dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45861580 | |||||
| chr12:45861580
|
CT | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0026others(198): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.4922+652delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45861580 | |||||
| chr12:45861750
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4922+801A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861750 | ||||||
| chr12:45861890
|
A | G | 7 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0170others(4): Show | 7 | HG01109.hp1 HG01934.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.4922+941A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45861890 | ||||||
| chr12:45862067
|
T | C | 1 | a0001c0001t0007g0269 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4922+1118T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862067 | ||||||
| chr12:45862161
|
T | A | 3 | a0001c0001t0007g0184a0001c0001t0007g0237a0001c0001t0007g0269 | 3 | HG02630.hp1 HG03195.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.4922+1212T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862161 | ||||||
| chr12:45862166
|
G | T | 1 | a0004c0005t0001g0111 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4922+1217G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862166 | ||||||
| chr12:45862167
|
GT | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0020g0030 | 3 | HG00280.hp1 HG01993.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.4922+1223delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45862167 | |||||
| chr12:45862170
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0174 | 2 | NA18962.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.4922+1221T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862170 | ||||||
| chr12:45862646
|
C | G | 1 | a0001c0001t0012g0182 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4922+1697C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862646 | ||||||
| chr12:45862892
|
A | AT | 165 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0044others(162): Show | 166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.4922+1953dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45862892 | |||||
| chr12:45862955
|
A | T | 1 | a0001c0001t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4922+2006A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45862955 | ||||||
| chr12:45863082
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+2133G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863082 | ||||||
| chr12:45863313
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4922+2364A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863313 | ||||||
| chr12:45863391
|
G | A | 1 | a0001c0001t0003g0284 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.4922+2442G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863391 | ||||||
| chr12:45863592
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4922+2643A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863592 | ||||||
| chr12:45863669
|
ATTGTAAA others(5): Show |
A | 1 | a0001c0001t0001g0232 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.4922+2726_4922+273 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863669 | |||||
| chr12:45863703
|
C | T | 28 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4922+2754C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863703 | ||||||
| chr12:45863818
|
CT | C | 5 | a0001c0002t0002g0225a0001c0002t0002g0258a0001c0002t0002g0260others(2): Show | 5 | HG02630.hp2 HG03130.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+2878delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863818 | |||||
| chr12:45863855
|
TTG | T | 23 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(20): Show | 23 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.4922+2908_4922+290 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863855 | |||||
| chr12:45863856
|
TG | T | 5 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+2908delG | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863856 | ||||||
| chr12:45863857
|
G | T | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4922+2908G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863857 | ||||||
| chr12:45863857
|
GT | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.4922+2918delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45863857 | |||||
| chr12:45863901
|
A | G | 4 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0001g0187others(1): Show | 4 | NA18966.hp2 NA19001.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.4922+2952A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863901 | ||||||
| chr12:45863929
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4922+2980C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45863929 | ||||||
| chr12:45864031
|
T | A | 24 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(21): Show | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.4922+3082T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864031 | ||||||
| chr12:45864118
|
A | G | 1 | a0005c0008t0001g0080 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4922+3169A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864118 | ||||||
| chr12:45864289
|
A | G | 2 | a0001c0009t0011g0207a0001c0009t0011g0209 | 2 | HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4922+3340A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864289 | ||||||
| chr12:45864522
|
G | GA | 6 | a0001c0001t0003g0283a0003c0004t0006g0105a0003c0004t0006g0106others(3): Show | 6 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+3585dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45864522 | |||||
| chr12:45864534
|
A | C | 109 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(106): Show | 110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.4922+3585A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864534 | ||||||
| chr12:45864591
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4922+3642A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864591 | ||||||
| chr12:45864713
|
T | C | 1 | a0005c0008t0001g0043 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4922+3764T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864713 | ||||||
| chr12:45864799
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4922+3850A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864799 | ||||||
| chr12:45864835
|
T | C | 1 | a0001c0001t0010g0109 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.4922+3886T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45864835 | ||||||
| chr12:45865405
|
C | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+4456C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45865405 | ||||||
| chr12:45865633
|
A | G | 1 | a0002c0003t0001g0143 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4922+4684A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45865633 | ||||||
| chr12:45865914
|
A | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+4965A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45865914 | ||||||
| chr12:45866065
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0192 | 2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.4922+5116A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866065 | ||||||
| chr12:45866250
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+5301G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866250 | ||||||
| chr12:45866293
|
C | T | 2 | a0001c0001t0001g0097a0001c0001t0001g0252 | 2 | HG00738.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.4922+5344C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866293 | ||||||
| chr12:45866554
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4922+5605T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866554 | ||||||
| chr12:45866736
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4922+5787A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866736 | ||||||
| chr12:45866827
|
A | G | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4922+5878A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866827 | ||||||
| chr12:45866836
|
T | C | 4 | a0001c0001t0005g0273a0001c0001t0005g0286a0001c0001t0005g0288others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4922+5887T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866836 | ||||||
| chr12:45866881
|
A | T | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4922+5932A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866881 | ||||||
| chr12:45866926
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4922+5977A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45866926 | ||||||
| chr12:45866928
|
T | TTTG | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0014others(72): Show | 75 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.4922+6015_4922+601 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | |||||
| chr12:45866928
|
T | TTTGTTG | 13 | a0001c0001t0001g0031a0001c0001t0001g0036a0001c0001t0001g0053others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.4922+6012_4922+601 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | |||||
| chr12:45866928
|
TTTG | T | 13 | a0001c0001t0001g0082a0001c0001t0001g0094a0001c0001t0001g0241others(10): Show | 13 | HG01346.hp1 HG02273.hp2 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4922+6015_4922+601 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | |||||
| chr12:45866928
|
TTTGTTGT others(2): Show |
T | 4 | a0001c0001t0005g0273a0001c0001t0005g0286a0001c0001t0005g0288others(1): Show | 4 | HG01891.hp1 HG02818.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4922+6009_4922+601 others(13): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | |||||
| chr12:45866928
|
TTTGTTGT others(5): Show |
T | 29 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(26): Show | 29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4922+6006_4922+601 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45866928 | |||||
| chr12:45867002
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.4922+6053G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867002 | ||||||
| chr12:45867025
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4922+6076A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867025 | ||||||
| chr12:45867031
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4922+6082A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867031 | ||||||
| chr12:45867229
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+6280A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867229 | ||||||
| chr12:45867365
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4922+6416C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867365 | ||||||
| chr12:45867518
|
T | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.4922+6569T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867518 | ||||||
| chr12:45867538
|
C | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+6589C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867538 | ||||||
| chr12:45867599
|
C | T | 28 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4922+6650C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867599 | ||||||
| chr12:45867870
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4922+6921C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867870 | ||||||
| chr12:45867890
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+6941C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45867890 | ||||||
| chr12:45868369
|
A | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0094 | 2 | NA18977.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4922+7420A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868369 | ||||||
| chr12:45868434
|
C | CT | 3 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096 | 3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4922+7486dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45868434 | |||||
| chr12:45868642
|
T | C | 1 | a0013c0018t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4922+7693T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868642 | ||||||
| chr12:45868749
|
T | C | 9 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236others(6): Show | 9 | HG01109.hp2 HG01346.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.4922+7800T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868749 | ||||||
| chr12:45868793
|
C | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+7844C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868793 | ||||||
| chr12:45868883
|
C | T | 1 | a0008c0015t0001g0294 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.4922+7934C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45868883 | ||||||
| chr12:45869026
|
GT | G | 201 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(198): Show | 202 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.4922+8088delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45869026 | |||||
| chr12:45869076
|
T | G | 44 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(41): Show | 44 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.4922+8127T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869076 | ||||||
| chr12:45869128
|
G | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+8179G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869128 | ||||||
| chr12:45869450
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4922+8501G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869450 | ||||||
| chr12:45869672
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4922+8723C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869672 | ||||||
| chr12:45869756
|
G | C | 1 | a0001c0001t0001g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4922+8807G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45869756 | ||||||
| chr12:45869883
|
A | AAAAAC | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+8949_4922+895 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45869883 | |||||
| chr12:45869900
|
AAAAC | A | 5 | a0001c0001t0003g0280a0001c0001t0003g0282a0001c0001t0003g0283others(2): Show | 5 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+8962_4922+896 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45869900 | |||||
| chr12:45870071
|
C | T | 3 | a0001c0001t0001g0065a0001c0001t0001g0093a0001c0001t0001g0097 | 3 | NA18966.hp1 NA18969.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.4922+9122C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870071 | ||||||
| chr12:45870134
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4922+9185C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870134 | ||||||
| chr12:45870150
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4922+9201T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870150 | ||||||
| chr12:45870152
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.4922+9203A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870152 | ||||||
| chr12:45870168
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.4922+9219T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870168 | ||||||
| chr12:45870364
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4922+9415C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870364 | ||||||
| chr12:45870870
|
C | T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4922+9921C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870870 | ||||||
| chr12:45870979
|
G | A | 1 | a0001c0001t0001g0137 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4922+10030G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870979 | ||||||
| chr12:45870987
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0290 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4922+10038T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870987 | ||||||
| chr12:45870997
|
A | G | 2 | a0001c0001t0001g0208a0002c0020t0001g0251 | 2 | HG02165.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4922+10048A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45870997 | ||||||
| chr12:45871105
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4922+10156A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871105 | ||||||
| chr12:45871717
|
A | T | 3 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0197 | 3 | HG02647.hp1 HG03453.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4922+10768A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871717 | ||||||
| chr12:45871847
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4922+10898G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871847 | ||||||
| chr12:45871865
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4922+10916C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871865 | ||||||
| chr12:45871941
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4922+10992G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45871941 | ||||||
| chr12:45872133
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.4922+11184C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872133 | ||||||
| chr12:45872136
|
T | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4922+11187T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872136 | ||||||
| chr12:45872180
|
C | T | 158 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.4922+11231C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872180 | ||||||
| chr12:45872228
|
T | C | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4922+11279T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872228 | ||||||
| chr12:45872245
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4922+11296T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872245 | ||||||
| chr12:45872338
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0001g0185 | 2 | NA18969.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.4922+11389C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872338 | ||||||
| chr12:45872480
|
A | T | 29 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(26): Show | 29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4922+11531A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872480 | ||||||
| chr12:45872569
|
A | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0306 | 2 | HG01346.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4922+11620A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872569 | ||||||
| chr12:45872614
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4922+11665C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872614 | ||||||
| chr12:45872648
|
C | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+11699C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872648 | ||||||
| chr12:45872980
|
A | G | 1 | a0002c0003t0001g0307 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4922+12031A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45872980 | ||||||
| chr12:45873081
|
A | G | 1 | a0001c0001t0001g0077 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.4922+12132A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873081 | ||||||
| chr12:45873100
|
T | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.4922+12151T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873100 | ||||||
| chr12:45873302
|
C | G | 1 | a0001c0001t0001g0165 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4922+12353C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873302 | ||||||
| chr12:45873302
|
C | T | 17 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(14): Show | 17 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.4922+12353C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873302 | ||||||
| chr12:45873477
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(1): Show | 4 | HG00140.hp2 HG01256.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.4922+12528G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873477 | ||||||
| chr12:45873507
|
T | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01168.hp1 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.4922+12558T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873507 | ||||||
| chr12:45873936
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4922+12987C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873936 | ||||||
| chr12:45873966
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4922+13017G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45873966 | ||||||
| chr12:45874348
|
T | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+13399T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874348 | ||||||
| chr12:45874436
|
C | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4922+13487C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874436 | ||||||
| chr12:45874455
|
G | A | 8 | a0001c0001t0001g0240a0001c0001t0001g0245a0001c0001t0001g0246others(5): Show | 8 | HG00642.hp1 HG01074.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.4922+13506G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874455 | ||||||
| chr12:45874468
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4922+13519C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874468 | ||||||
| chr12:45874517
|
T | C | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.4922+13568T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874517 | ||||||
| chr12:45874913
|
T | C | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4922+13964T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874913 | ||||||
| chr12:45874967
|
A | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(215): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.4922+14018A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874967 | ||||||
| chr12:45874983
|
G | C | 215 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(212): Show | 216 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.4922+14034G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45874983 | ||||||
| chr12:45875150
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4922+14201G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875150 | ||||||
| chr12:45875301
|
A | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4922+14352A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875301 | ||||||
| chr12:45875435
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0001g0053 | 2 | NA18747.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.4922+14486A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875435 | ||||||
| chr12:45875780
|
G | A | 1 | a0001c0001t0012g0183 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4922+14831G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45875780 | ||||||
| chr12:45876302
|
G | A | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.4922+15353G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876302 | ||||||
| chr12:45876333
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096 | 3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.4922+15384G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876333 | ||||||
| chr12:45876353
|
C | T | 1 | a0001c0002t0002g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4922+15404C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876353 | ||||||
| chr12:45876382
|
T | G | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4923-15398T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876382 | ||||||
| chr12:45876569
|
GA | G | 112 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(109): Show | 113 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.4923-15198delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45876569 | |||||
| chr12:45876627
|
A | T | 1 | a0001c0002t0002g0228 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.4923-15153A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876627 | ||||||
| chr12:45876628
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-15152A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876628 | ||||||
| chr12:45876707
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4923-15073G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876707 | ||||||
| chr12:45876793
|
TA | T | 8 | a0001c0001t0001g0075a0001c0001t0001g0271a0001c0001t0003g0280others(5): Show | 8 | HG01168.hp1 HG02257.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.4923-14973delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45876793 | |||||
| chr12:45876846
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.4923-14934T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876846 | ||||||
| chr12:45876885
|
C | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4923-14895C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876885 | ||||||
| chr12:45876917
|
A | G | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4923-14863A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876917 | ||||||
| chr12:45876960
|
T | C | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.4923-14820T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45876960 | ||||||
| chr12:45877091
|
C | CA | 35 | a0001c0001t0001g0100a0001c0001t0001g0129a0001c0001t0001g0164others(32): Show | 35 | HG01175.hp1 HG01175.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.4923-14670dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45877091 | |||||
| chr12:45877091
|
CA | C | 13 | a0001c0001t0001g0060a0001c0001t0001g0075a0001c0001t0001g0084others(10): Show | 13 | HG01168.hp1 HG02451.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.4923-14670delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45877091 | |||||
| chr12:45877219
|
G | C | 1 | a0001c0001t0001g0139 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.4923-14561G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877219 | ||||||
| chr12:45877321
|
C | G | 1 | a0001c0001t0001g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4923-14459C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877321 | ||||||
| chr12:45877341
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.4923-14439G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877341 | ||||||
| chr12:45877343
|
A | G | 33 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(30): Show | 33 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.4923-14437A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877343 | ||||||
| chr12:45877385
|
T | C | 8 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0148others(5): Show | 8 | HG01167.hp2 HG02602.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.4923-14395T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877385 | ||||||
| chr12:45877573
|
G | A | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4923-14207G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877573 | ||||||
| chr12:45877953
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4923-13827G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877953 | ||||||
| chr12:45877991
|
G | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4923-13789G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45877991 | ||||||
| chr12:45878292
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4923-13488C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45878292 | ||||||
| chr12:45878776
|
G | T | 5 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.4923-13004G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45878776 | ||||||
| chr12:45878800
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4923-12980C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45878800 | ||||||
| chr12:45879063
|
C | G | 44 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4923-12717C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879063 | ||||||
| chr12:45879295
|
T | C | 4 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(1): Show | 4 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-12485T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879295 | ||||||
| chr12:45879354
|
C | T | 1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4923-12426C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879354 | ||||||
| chr12:45879419
|
A | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-12361A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879419 | ||||||
| chr12:45879572
|
A | G | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4923-12208A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879572 | ||||||
| chr12:45879955
|
G | A | 1 | a0001c0001t0005g0288 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4923-11825G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45879955 | ||||||
| chr12:45879986
|
AGT | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0176others(1): Show | 4 | HG02074.hp2 HG02523.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-11791_4923-11 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45879986 | |||||
| chr12:45880002
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.4923-11778G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880002 | ||||||
| chr12:45880099
|
T | G | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.4923-11681T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880099 | ||||||
| chr12:45880172
|
G | A | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4923-11608G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880172 | ||||||
| chr12:45880411
|
T | G | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4923-11369T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880411 | ||||||
| chr12:45880427
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0235 | 2 | HG01109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.4923-11353C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880427 | ||||||
| chr12:45880534
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4923-11246T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880534 | ||||||
| chr12:45880554
|
C | G | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.4923-11226C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880554 | ||||||
| chr12:45880608
|
A | T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4923-11172A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880608 | ||||||
| chr12:45880638
|
A | T | 1 | a0001c0001t0001g0084 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4923-11142A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880638 | ||||||
| chr12:45880654
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4923-11126C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45880654 | ||||||
| chr12:45881075
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.4923-10705G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881075 | ||||||
| chr12:45881513
|
A | G | 1 | a0001c0001t0001g0208 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.4923-10267A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881513 | ||||||
| chr12:45881564
|
A | G | 2 | a0006c0007t0001g0010a0006c0007t0001g0012 | 2 | NA18957.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.4923-10216A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881564 | ||||||
| chr12:45881654
|
GTCT | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-10120_4923-10 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45881654 | |||||
| chr12:45881968
|
G | A | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-9812G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45881968 | ||||||
| chr12:45882154
|
A | G | 115 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(112): Show | 116 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.4923-9626A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45882154 | ||||||
| chr12:45882315
|
C | T | 2 | a0001c0001t0003g0282a0001c0001t0003g0314 | 2 | HG02738.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.4923-9465C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45882315 | ||||||
| chr12:45882906
|
G | T | 3 | a0004c0005t0001g0111a0004c0005t0001g0147a0004c0005t0001g0169 | 3 | NA18747.hp1 NA18956.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.4923-8874G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45882906 | ||||||
| chr12:45883003
|
C | T | 1 | a0001c0001t0001g0256 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.4923-8777C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883003 | ||||||
| chr12:45883212
|
T | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0056a0001c0001t0001g0063others(1): Show | 4 | HG00280.hp1 HG01993.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-8568T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883212 | ||||||
| chr12:45883875
|
C | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4923-7905C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883875 | ||||||
| chr12:45883943
|
T | C | 29 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(26): Show | 29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.4923-7837T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45883943 | ||||||
| chr12:45884028
|
T | C | 1 | a0001c0001t0001g0050 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.4923-7752T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884028 | ||||||
| chr12:45884224
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.4923-7556C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884224 | ||||||
| chr12:45884394
|
T | TCAAA | 12 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(9): Show | 12 | HG02451.hp1 HG02647.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.4923-7365_4923-736 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45884394 | |||||
| chr12:45884401
|
A | G | 1 | a0002c0003t0001g0253 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.4923-7379A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884401 | ||||||
| chr12:45884594
|
T | C | 1 | a0001c0001t0001g0301 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4923-7186T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884594 | ||||||
| chr12:45884603
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4923-7177C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884603 | ||||||
| chr12:45884879
|
C | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4923-6901C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884879 | ||||||
| chr12:45884886
|
A | T | 10 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(7): Show | 10 | HG00438.hp2 HG00621.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.4923-6894A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884886 | ||||||
| chr12:45884976
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4923-6804C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45884976 | ||||||
| chr12:45885116
|
G | T | 1 | a0001c0001t0001g0009 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.4923-6664G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885116 | ||||||
| chr12:45885285
|
C | T | 44 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4923-6495C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885285 | ||||||
| chr12:45885319
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-6461A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885319 | ||||||
| chr12:45885371
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.4923-6409G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885371 | ||||||
| chr12:45885530
|
T | C | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4923-6250T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885530 | ||||||
| chr12:45885554
|
T | C | 1 | a0001c0001t0001g0188 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4923-6226T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885554 | ||||||
| chr12:45885596
|
T | C | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-6184T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885596 | ||||||
| chr12:45885600
|
G | A | 24 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(21): Show | 24 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.4923-6180G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885600 | ||||||
| chr12:45885641
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0148 | 3 | HG01167.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4923-6139A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885641 | ||||||
| chr12:45885775
|
G | A | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.4923-6005G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885775 | ||||||
| chr12:45885883
|
A | C | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-5897A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885883 | ||||||
| chr12:45885983
|
C | A | 1 | a0001c0001t0001g0034 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.4923-5797C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45885983 | ||||||
| chr12:45886104
|
A | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.4923-5676A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886104 | ||||||
| chr12:45886132
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.4923-5648A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886132 | ||||||
| chr12:45886146
|
GTGGGATA others(30): Show |
G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-5628_4923-559 others(41): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45886146 | |||||
| chr12:45886228
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-5552A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886228 | ||||||
| chr12:45886385
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(88): Show | 92 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.4923-5395C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886385 | ||||||
| chr12:45886456
|
T | G | 4 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(1): Show | 4 | HG01099.hp2 HG01175.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.4923-5324T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886456 | ||||||
| chr12:45886731
|
G | A | 66 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0087others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.4923-5049G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886731 | ||||||
| chr12:45886766
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4923-5014G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886766 | ||||||
| chr12:45886832
|
A | C | 3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4923-4948A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886832 | ||||||
| chr12:45886995
|
A | C | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4923-4785A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45886995 | ||||||
| chr12:45887251
|
T | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0241 | 2 | HG01346.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4923-4529T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887251 | ||||||
| chr12:45887254
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4923-4526A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887254 | ||||||
| chr12:45887445
|
A | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(107): Show | 111 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.4923-4335A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887445 | ||||||
| chr12:45887452
|
T | C | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4923-4328T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887452 | ||||||
| chr12:45887494
|
AAG | A | 5 | a0001c0001t0001g0236a0001c0001t0001g0271a0001c0001t0001g0289others(2): Show | 5 | HG02257.hp2 HG02615.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-4283_4923-428 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45887494 | |||||
| chr12:45887548
|
C | A | 1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4923-4232C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887548 | ||||||
| chr12:45887813
|
C | T | 44 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.4923-3967C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45887813 | ||||||
| chr12:45888119
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4923-3661T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888119 | ||||||
| chr12:45888194
|
C | CA | 39 | a0001c0001t0001g0014a0001c0001t0001g0021a0001c0001t0001g0034others(36): Show | 39 | HG00408.hp1 HG00597.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.4923-3571dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45888194 | |||||
| chr12:45888223
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(210): Show | 214 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.4923-3557G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888223 | ||||||
| chr12:45888260
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4923-3520A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888260 | ||||||
| chr12:45888475
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4923-3305C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888475 | ||||||
| chr12:45888509
|
T | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0037 | 3 | NA18950.hp1 NA18980.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.4923-3271T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888509 | ||||||
| chr12:45888825
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.4923-2955T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45888825 | ||||||
| chr12:45889058
|
C | T | 3 | a0001c0001t0001g0120a0001c0001t0001g0144a0001c0001t0001g0148 | 3 | HG01167.hp2 HG02896.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.4923-2722C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889058 | ||||||
| chr12:45889182
|
AAATAAT | A | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.4923-2588_4923-258 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45889182 | |||||
| chr12:45889247
|
A | G | 1 | a0001c0001t0001g0178 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4923-2533A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889247 | ||||||
| chr12:45889348
|
A | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4923-2432A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889348 | ||||||
| chr12:45889430
|
T | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-2350T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889430 | ||||||
| chr12:45889653
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4923-2127C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889653 | ||||||
| chr12:45889711
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.4923-2069G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889711 | ||||||
| chr12:45889806
|
C | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.4923-1974C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45889806 | ||||||
| chr12:45890214
|
A | G | 28 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4923-1566A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890214 | ||||||
| chr12:45890660
|
A | G | 1 | a0002c0003t0001g0250 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4923-1120A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890660 | ||||||
| chr12:45890927
|
G | C | 3 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0076 | 3 | HG01168.hp1 HG01169.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.4923-853G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890927 | ||||||
| chr12:45890937
|
C | T | 1 | a0001c0001t0001g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4923-843C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45890937 | ||||||
| chr12:45891001
|
C | A | 1 | a0001c0001t0001g0027 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4923-779C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891001 | ||||||
| chr12:45891041
|
T | C | 3 | a0001c0001t0001g0069a0001c0001t0001g0102a0014c0019t0001g0079 | 3 | HG00597.hp1 HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.4923-739T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891041 | ||||||
| chr12:45891058
|
G | A | 5 | a0001c0002t0002g0225a0001c0002t0002g0259a0001c0002t0002g0260others(2): Show | 5 | HG02630.hp2 HG02922.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-722G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891058 | ||||||
| chr12:45891163
|
C | CA | 6 | a0001c0001t0001g0021a0001c0001t0001g0119a0001c0001t0001g0271others(3): Show | 6 | HG02074.hp1 HG02257.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.4923-600dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45891163 | |||||
| chr12:45891163
|
CA | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 105 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.4923-600delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr12 | 45891163 | |||||
| chr12:45891441
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0020g0030 | 2 | HG02738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.4923-339T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891441 | ||||||
| chr12:45891538
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4923-242G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891538 | ||||||
| chr12:45891553
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4923-227G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 16/20 | chr12 | 45891553 | ||||||
| chr12:45891966
|
A | G | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.5062-45A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 17/20 | chr12 | 45891966 | ||||||
| chr12:45892181
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.5147+85T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892181 | ||||||
| chr12:45892479
|
C | CAT | 210 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(207): Show | 211 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.5147+397_5147+398d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 45892479 | |||||
| chr12:45892479
|
C | CATAT | 4 | a0001c0001t0001g0139a0001c0001t0001g0236a0001c0001t0001g0289others(1): Show | 4 | HG02615.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.5147+395_5147+398d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr12 | 45892479 | |||||
| chr12:45892567
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5147+471T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892567 | ||||||
| chr12:45892719
|
A | G | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5147+623A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892719 | ||||||
| chr12:45892723
|
C | T | 2 | a0001c0001t0001g0256a0001c0001t0001g0278 | 2 | HG00099.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.5147+627C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892723 | ||||||
| chr12:45892829
|
G | A | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5148-591G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892829 | ||||||
| chr12:45892900
|
A | G | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5148-520A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45892900 | ||||||
| chr12:45893116
|
C | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5148-304C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893116 | ||||||
| chr12:45893184
|
T | C | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5148-236T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893184 | ||||||
| chr12:45893313
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5148-107G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893313 | ||||||
| chr12:45893375
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.5148-45G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 18/20 | chr12 | 45893375 | ||||||
| chr12:45893732
|
T | C | 1 | a0001c0001t0001g0270 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.5363+11T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45893732 | ||||||
| chr12:45893828
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.5363+107A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45893828 | ||||||
| chr12:45894153
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+432A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894153 | ||||||
| chr12:45894397
|
G | GGCCC | 8 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0163others(5): Show | 8 | HG02129.hp2 NA18959.hp2 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.5363+677_5363+680d others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45894397 | |||||
| chr12:45894554
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5363+833G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894554 | ||||||
| chr12:45894650
|
T | C | 3 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0096 | 3 | HG04184.hp2 NA19077.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5363+929T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894650 | ||||||
| chr12:45894699
|
G | A | 216 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(213): Show | 217 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.5363+978G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894699 | ||||||
| chr12:45894833
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5363+1112C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894833 | ||||||
| chr12:45894840
|
A | ACCTCTTT others(281): Show |
1 | a0001c0001t0014g0287 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5363+1129_5363+113 others(292): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45894840 | |||||
| chr12:45894876
|
A | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | NA18950.hp1 NA18980.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+1155A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894876 | ||||||
| chr12:45894955
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.5363+1234T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45894955 | ||||||
| chr12:45895321
|
T | C | 11 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(8): Show | 11 | HG02451.hp1 HG02647.hp2 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.5363+1600T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895321 | ||||||
| chr12:45895387
|
A | G | 5 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(2): Show | 5 | HG02615.hp1 HG02647.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.5363+1666A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895387 | ||||||
| chr12:45895541
|
C | G | 29 | a0001c0001t0004g0194a0001c0001t0004g0195a0001c0001t0004g0196others(26): Show | 29 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(26): Show |
intron_variant | MODIFIER | c.5363+1820C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895541 | ||||||
| chr12:45895604
|
G | T | 3 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0188 | 3 | HG02523.hp1 NA18952.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.5363+1883G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895604 | ||||||
| chr12:45895695
|
G | A | 10 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5363+1974G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45895695 | ||||||
| chr12:45896099
|
T | A | 2 | a0001c0001t0001g0061a0001c0001t0001g0096 | 2 | HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.5363+2378T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896099 | ||||||
| chr12:45896165
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(106): Show | 110 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.5363+2444G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896165 | ||||||
| chr12:45896191
|
A | G | 4 | a0001c0001t0001g0296a0001c0001t0001g0304a0001c0001t0001g0311others(1): Show | 4 | HG01975.hp1 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+2470A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896191 | ||||||
| chr12:45896282
|
G | C | 2 | a0001c0002t0002g0258a0001c0002t0002g0305 | 2 | HG01884.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5363+2561G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896282 | ||||||
| chr12:45896403
|
A | G | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+2682A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896403 | ||||||
| chr12:45896449
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5363+2728C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896449 | ||||||
| chr12:45896459
|
G | C | 1 | a0001c0001t0001g0153 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5363+2738G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896459 | ||||||
| chr12:45896627
|
C | CT | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5363+2909dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45896627 | |||||
| chr12:45896674
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0146 | 3 | HG02056.hp2 NA18612.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.5363+2953G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896674 | ||||||
| chr12:45896682
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.5363+2961G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896682 | ||||||
| chr12:45896827
|
G | A | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5363+3106G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896827 | ||||||
| chr12:45896976
|
A | C | 1 | a0001c0001t0001g0031 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.5363+3255A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45896976 | ||||||
| chr12:45897107
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0073 | 2 | HG01071.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.5363+3386G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897107 | ||||||
| chr12:45897354
|
C | T | 1 | a0001c0006t0008g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5363+3633C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897354 | ||||||
| chr12:45897360
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.5363+3639C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897360 | ||||||
| chr12:45897382
|
A | G | 1 | a0001c0001t0001g0022 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5363+3661A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897382 | ||||||
| chr12:45897867
|
C | T | 1 | a0001c0001t0004g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.5363+4146C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45897867 | ||||||
| chr12:45898462
|
G | A | 28 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(25): Show | 28 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.5363+4741G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898462 | ||||||
| chr12:45898644
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0064 | 2 | HG02083.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.5363+4923G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898644 | ||||||
| chr12:45898829
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5363+5108G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898829 | ||||||
| chr12:45898911
|
C | A | 1 | a0001c0002t0002g0227 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.5363+5190C>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898911 | ||||||
| chr12:45898981
|
T | A | 1 | a0001c0001t0001g0300 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5363+5260T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898981 | ||||||
| chr12:45898994
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.5363+5273C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45898994 | ||||||
| chr12:45899068
|
T | C | 4 | a0002c0003t0001g0248a0002c0003t0001g0249a0002c0003t0001g0307others(1): Show | 4 | HG00597.hp2 NA18945.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.5363+5347T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899068 | ||||||
| chr12:45899212
|
C | T | 45 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(42): Show | 45 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.5363+5491C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899212 | ||||||
| chr12:45899249
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0001g0073others(1): Show | 4 | HG01071.hp1 HG01358.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.5363+5528C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899249 | ||||||
| chr12:45899270
|
C | CA | 52 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0020others(49): Show | 52 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.5363+5576dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | |||||
| chr12:45899270
|
CA | C | 7 | a0001c0001t0001g0076a0001c0001t0001g0136a0001c0001t0001g0138others(4): Show | 7 | HG00544.hp2 HG01169.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.5363+5576delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | |||||
| chr12:45899270
|
CAAAAAAA others(4): Show |
C | 44 | a0001c0001t0001g0130a0001c0001t0001g0140a0001c0001t0001g0141others(41): Show | 44 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.5363+5566_5363+557 others(15): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | |||||
| chr12:45899270
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0303 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.5363+5562_5363+557 others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899270 | |||||
| chr12:45899367
|
G | C | 4 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.5364-5567G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899367 | ||||||
| chr12:45899401
|
A | G | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5364-5533A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899401 | ||||||
| chr12:45899421
|
A | G | 1 | a0001c0001t0005g0286 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.5364-5513A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899421 | ||||||
| chr12:45899432
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.5364-5502A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899432 | ||||||
| chr12:45899462
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.5364-5472T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899462 | ||||||
| chr12:45899474
|
C | T | 2 | a0001c0001t0001g0171a0001c0001t0001g0204 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5364-5460C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899474 | ||||||
| chr12:45899478
|
C | T | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5364-5456C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899478 | ||||||
| chr12:45899516
|
G | C | 1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5364-5418G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899516 | ||||||
| chr12:45899592
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5364-5342C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899592 | ||||||
| chr12:45899597
|
T | C | 52 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0054others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.5364-5337T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899597 | ||||||
| chr12:45899621
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0231a0001c0001t0001g0235a0013c0018t0001g0230 | 3 | HG01109.hp2 HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.5364-5305_5364-528 others(22): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899621 | |||||
| chr12:45899633
|
T | TTA | 3 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107 | 3 | HG02647.hp2 HG02886.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.5364-5287_5364-528 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899633 | |||||
| chr12:45899649
|
TTGGTTAT others(21): Show |
T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5364-5269_5364-524 others(32): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899649 | |||||
| chr12:45899653
|
T | TTA | 3 | a0001c0001t0001g0110a0001c0001t0001g0264a0001c0001t0001g0270 | 3 | HG02965.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5364-5267_5364-526 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899653 | |||||
| chr12:45899655
|
ATATATAT others(33): Show |
A | 7 | a0001c0001t0001g0129a0001c0001t0001g0162a0001c0001t0001g0163others(4): Show | 7 | HG02886.hp1 HG02965.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.5364-5255_5364-521 others(44): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899655 | |||||
| chr12:45899657
|
ATATATAT others(17): Show |
A | 48 | a0001c0001t0001g0001a0001c0001t0001g0116a0001c0001t0001g0117others(45): Show | 49 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.5364-5255_5364-523 others(28): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899657 | |||||
| chr12:45899657
|
ATATATAT others(47): Show |
A | 1 | a0003c0004t0006g0107 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5364-5255_5364-520 others(58): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899657 | |||||
| chr12:45899661
|
ATATATAT others(3): Show |
A | 134 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(131): Show | 134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.5364-5255_5364-524 others(14): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899661 | |||||
| chr12:45899671
|
T | TTATA | 9 | a0001c0001t0001g0005a0001c0001t0001g0144a0001c0001t0001g0148others(6): Show | 9 | HG00738.hp1 HG01891.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.5364-5259_5364-525 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATA | 27 | a0001c0001t0001g0072a0001c0001t0001g0130a0001c0001t0001g0140others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.5364-5261_5364-525 others(10): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(13): Show |
1 | a0001c0001t0004g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(95): Show |
1 | a0001c0001t0013g0265 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(106): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(40): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(59): Show |
1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(70): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(89): Show |
1 | a0001c0001t0001g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5364-5256_5364-525 others(100): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(91): Show |
17 | a0001c0001t0001g0099a0001c0001t0001g0233a0001c0001t0001g0244others(14): Show | 17 | HG01071.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(102): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(93): Show |
2 | a0001c0001t0001g0240a0001c0001t0001g0246 | 2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(104): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(13): Show |
5 | a0001c0001t0001g0034a0001c0001t0001g0042a0001c0001t0001g0060others(2): Show | 5 | HG01978.hp2 HG01981.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(24): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(27): Show |
2 | a0001c0001t0001g0090a0001c0002t0002g0227 | 2 | HG02129.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(38): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
T | TTATATAT others(119): Show |
2 | a0001c0001t0001g0069a0001c0001t0001g0102 | 2 | HG00621.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.5364-5256_5364-525 others(130): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899671
|
TTATATAT others(7): Show |
T | 1 | a0001c0001t0001g0021 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.5364-5241_5364-522 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899671 | |||||
| chr12:45899673
|
ATATATGG others(1): Show |
A | 14 | a0001c0001t0009g0112a0001c0001t0009g0211a0001c0001t0009g0212others(11): Show | 14 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.5364-5255_5364-524 others(12): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899673 | |||||
| chr12:45899673
|
ATATATGG others(31): Show |
A | 6 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0003g0280others(3): Show | 6 | HG03516.hp2 HG03704.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.5364-5255_5364-521 others(42): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899673 | |||||
| chr12:45899673
|
ATATATGG others(45): Show |
A | 1 | a0001c0001t0004g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5364-5255_5364-520 others(56): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899673 | |||||
| chr12:45899694
|
G | GTT | 23 | a0001c0001t0001g0069a0001c0001t0001g0099a0001c0001t0001g0102others(20): Show | 23 | HG00621.hp2 HG00642.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.5364-5239_5364-523 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | |||||
| chr12:45899694
|
G | GTTATATA others(85): Show |
1 | a0001c0001t0001g0276 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(96): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | |||||
| chr12:45899694
|
G | GTTATATA others(87): Show |
20 | a0001c0001t0001g0072a0001c0001t0001g0140a0001c0001t0001g0141others(17): Show | 20 | HG00597.hp2 HG00621.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.5364-5198_5364-519 others(98): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | |||||
| chr12:45899694
|
G | GTTATATA others(85): Show |
1 | a0001c0001t0001g0275 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(96): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | |||||
| chr12:45899694
|
G | GTTATATA others(87): Show |
1 | a0001c0001t0001g0130 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(98): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899694 | |||||
| chr12:45899695
|
TTA | T | 15 | a0001c0001t0001g0005a0001c0001t0009g0112a0001c0001t0009g0211others(12): Show | 15 | HG01167.hp1 HG01169.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5364-5227_5364-522 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899695 | |||||
| chr12:45899697
|
A | ATATATAT others(7): Show |
7 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0005g0273others(4): Show | 7 | HG01891.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.5364-5207_5364-519 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | |||||
| chr12:45899697
|
A | ATATATAT others(101): Show |
1 | a0001c0001t0001g0278 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(112): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | |||||
| chr12:45899697
|
A | ATATATAT others(5): Show |
1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5364-5228_5364-522 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | |||||
| chr12:45899697
|
A | ATATATAT others(35): Show |
1 | a0003c0004t0018g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5364-5228_5364-522 others(46): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | |||||
| chr12:45899697
|
A | T | 1 | a0001c0001t0001g0013 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5364-5237A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899697 | ||||||
| chr12:45899697
|
ATATATAT others(7): Show |
A | 5 | a0001c0001t0001g0041a0001c0001t0001g0062a0001c0001t0001g0121others(2): Show | 5 | HG00673.hp1 HG01192.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-5207_5364-519 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899697 | |||||
| chr12:45899699
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0013 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.5364-5225_5364-521 others(16): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899699 | |||||
| chr12:45899711
|
T | TTA | 4 | a0001c0001t0001g0005a0001c0001t0001g0231a0001c0001t0001g0235others(1): Show | 4 | HG01109.hp2 HG02258.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.5364-5213_5364-521 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899711 | |||||
| chr12:45899711
|
T | TTATATAT others(41): Show |
1 | a0001c0001t0001g0234 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.5364-5198_5364-519 others(52): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899711 | |||||
| chr12:45899711
|
T | TTTTA | 10 | a0001c0002t0002g0214a0001c0002t0002g0215a0001c0002t0002g0216others(7): Show | 10 | HG02109.hp1 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.5364-5222_5364-522 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899711 | |||||
| chr12:45899727
|
ATATATAT others(7): Show |
A | 1 | a0001c0001t0001g0005 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.5364-5197_5364-518 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45899727 | |||||
| chr12:45899740
|
T | TATATATA others(83): Show |
1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5364-5194_5364-519 others(94): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899740 | ||||||
| chr12:45899741
|
T | A | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5364-5193T>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899741 | ||||||
| chr12:45899743
|
A | T | 1 | a0001c0001t0001g0274 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.5364-5191A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899743 | ||||||
| chr12:45899785
|
C | T | 1 | a0001c0001t0001g0292 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5364-5149C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899785 | ||||||
| chr12:45899786
|
CT | C | 37 | a0001c0001t0001g0001a0001c0001t0001g0110a0001c0001t0001g0116others(34): Show | 38 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(35): Show |
intron_variant | MODIFIER | c.5364-5147delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899786 | ||||||
| chr12:45899787
|
T | C | 7 | a0001c0001t0001g0138a0001c0001t0001g0153a0001c0001t0001g0192others(4): Show | 7 | HG00280.hp2 HG01358.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.5364-5147T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45899787 | ||||||
| chr12:45900083
|
CAG | C | 5 | a0003c0004t0006g0105a0003c0004t0006g0106a0003c0004t0006g0107others(2): Show | 5 | HG02451.hp1 HG02647.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.5364-4848_5364-484 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45900083 | |||||
| chr12:45900091
|
C | T | 1 | a0001c0016t0001g0302 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.5364-4843C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900091 | ||||||
| chr12:45900092
|
G | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0125a0001c0001t0001g0126 | 3 | HG00673.hp1 NA18944.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.5364-4842G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900092 | ||||||
| chr12:45900144
|
T | G | 1 | a0001c0001t0001g0006 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5364-4790T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900144 | ||||||
| chr12:45900160
|
A | T | 2 | a0001c0001t0001g0264a0001c0001t0001g0270 | 2 | HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.5364-4774A>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900160 | ||||||
| chr12:45900230
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5364-4704T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900230 | ||||||
| chr12:45900423
|
C | T | 1 | a0001c0001t0001g0009 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.5364-4511C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900423 | ||||||
| chr12:45900540
|
A | G | 1 | a0001c0002t0002g0221 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5364-4394A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900540 | ||||||
| chr12:45900909
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5364-4025C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900909 | ||||||
| chr12:45900911
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0289a0001c0001t0001g0290 | 3 | HG02615.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5364-4023C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45900911 | ||||||
| chr12:45901089
|
TTTTTC | T | 6 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(3): Show | 6 | HG02738.hp2 HG03239.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.5364-3838_5364-383 others(9): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901089 | |||||
| chr12:45901125
|
G | C | 158 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(155): Show | 159 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.5364-3809G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901125 | ||||||
| chr12:45901150
|
CTTAATTT others(7): Show |
C | 2 | a0001c0001t0003g0284a0001c0001t0003g0314 | 2 | HG02738.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.5364-3781_5364-376 others(18): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901150 | |||||
| chr12:45901150
|
CTTAATTT others(8): Show |
C | 4 | a0001c0001t0003g0280a0001c0001t0003g0281a0001c0001t0003g0282others(1): Show | 4 | HG03704.hp1 HG04115.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.5364-3781_5364-376 others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901150 | |||||
| chr12:45901154
|
A | AT | 18 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0070others(15): Show | 18 | HG00140.hp1 HG00639.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.5364-3746dupT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901154
|
A | ATT | 6 | a0001c0001t0001g0067a0001c0001t0001g0231a0001c0001t0001g0242others(3): Show | 6 | HG01109.hp2 HG01433.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.5364-3747_5364-374 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901154
|
AT | A | 63 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(60): Show | 63 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.5364-3746delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901154
|
ATT | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 57 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(54): Show |
intron_variant | MODIFIER | c.5364-3747_5364-374 others(6): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901154
|
ATTT | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0024others(22): Show | 25 | HG01167.hp2 HG01168.hp1 HG01346.hp1 others(22): Show |
intron_variant | MODIFIER | c.5364-3748_5364-374 others(7): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901154
|
ATTTT | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0208a0001c0001t0001g0297others(4): Show | 7 | HG02451.hp1 HG02602.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.5364-3749_5364-374 others(8): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901154
|
ATTTTTTT others(8): Show |
A | 3 | a0001c0001t0001g0126a0001c0001t0001g0170a0001c0001t0001g0179 | 3 | HG00673.hp1 HG01981.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.5364-3760_5364-374 others(19): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901154
|
ATTTTTTT others(9): Show |
A | 89 | a0001c0001t0001g0001a0001c0001t0001g0044a0001c0001t0001g0045others(86): Show | 90 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.5364-3761_5364-374 others(20): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45901154 | |||||
| chr12:45901316
|
G | T | 1 | a0001c0002t0002g0223 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.5364-3618G>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901316 | ||||||
| chr12:45901695
|
C | G | 1 | a0001c0001t0003g0282 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.5364-3239C>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901695 | ||||||
| chr12:45901748
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5364-3186A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45901748 | ||||||
| chr12:45902100
|
A | G | 4 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0146others(1): Show | 4 | HG00438.hp1 HG02056.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.5364-2834A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902100 | ||||||
| chr12:45902109
|
A | G | 1 | a0001c0001t0001g0277 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.5364-2825A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902109 | ||||||
| chr12:45902240
|
A | G | 1 | a0001c0001t0013g0266 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5364-2694A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902240 | ||||||
| chr12:45902295
|
A | G | 66 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0087others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.5364-2639A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902295 | ||||||
| chr12:45902422
|
A | C | 1 | a0013c0018t0001g0230 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5364-2512A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902422 | ||||||
| chr12:45902446
|
A | G | 1 | a0009c0014t0021g0213 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5364-2488A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902446 | ||||||
| chr12:45902527
|
T | G | 13 | a0002c0003t0001g0143a0002c0003t0001g0186a0002c0003t0001g0210others(10): Show | 13 | HG00597.hp2 HG00673.hp2 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.5364-2407T>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902527 | ||||||
| chr12:45902535
|
AT | A | 9 | a0001c0001t0001g0110a0001c0001t0001g0134a0001c0001t0001g0159others(6): Show | 9 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.5364-2385delT | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45902535 | |||||
| chr12:45902779
|
G | A | 2 | a0001c0001t0001g0236a0001c0001t0001g0290 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5364-2155G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902779 | ||||||
| chr12:45902807
|
C | T | 1 | a0001c0011t0019g0272 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.5364-2127C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902807 | ||||||
| chr12:45902861
|
A | G | 1 | a0001c0001t0016g0313 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5364-2073A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45902861 | ||||||
| chr12:45903269
|
G | A | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-1665G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45903269 | ||||||
| chr12:45903812
|
T | C | 5 | a0001c0001t0005g0273a0001c0001t0005g0285a0001c0001t0005g0286others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-1122T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45903812 | ||||||
| chr12:45904155
|
A | C | 1 | a0001c0001t0001g0004 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.5364-779A>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904155 | ||||||
| chr12:45904233
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0178a0001c0001t0001g0204 | 3 | HG00738.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5364-701G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904233 | ||||||
| chr12:45904495
|
G | A | 1 | a0001c0001t0003g0283 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.5364-439G>A | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904495 | ||||||
| chr12:45904507
|
A | G | 1 | a0011c0010t0002g0206 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.5364-427A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904507 | ||||||
| chr12:45904560
|
A | G | 2 | a0001c0001t0001g0316a0001c0001t0001g0317 | 2 | HG03516.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.5364-374A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904560 | ||||||
| chr12:45904563
|
C | T | 25 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0002t0002g0214others(22): Show | 25 | HG01175.hp1 HG01884.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.5364-371C>T | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904563 | ||||||
| chr12:45904652
|
T | C | 220 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0044others(217): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.5364-282T>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904652 | ||||||
| chr12:45904654
|
A | G | 220 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0001g0044others(217): Show | 221 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.5364-280A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904654 | ||||||
| chr12:45904689
|
C | CA | 39 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0021others(36): Show | 39 | HG00544.hp1 HG00639.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.5364-220dupA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45904689 | |||||
| chr12:45904689
|
C | CAA | 7 | a0001c0001t0001g0091a0001c0001t0001g0134a0001c0001t0001g0231others(4): Show | 7 | HG01074.hp2 HG01109.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.5364-221_5364-220d others(4): Show |
ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45904689 | |||||
| chr12:45904689
|
CA | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0042a0001c0001t0001g0161others(33): Show | 36 | HG01175.hp1 HG01256.hp1 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.5364-220delA | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr12 | 45904689 | |||||
| chr12:45904726
|
G | C | 5 | a0001c0001t0001g0231a0001c0001t0001g0235a0001c0001t0001g0236others(2): Show | 5 | HG01109.hp2 HG02258.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.5364-208G>C | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904726 | ||||||
| chr12:45904911
|
A | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0290 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5364-23A>G | ARID2 | ENSG00000189079.18 | transcript | ENST00000334344.11 | protein_coding | 20/20 | chr12 | 45904911 |