Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 57545 |
|---|---|
| ensemblid | ENSG00000048342.18 |
| hgncid | 29253 |
| symbol | CC2D2A |
| name | coiled-coil and C2 domain containing 2A |
| refseq_nuc | NM_001378615.1 |
| refseq_prot | NP_001365544.1 |
| ensembl_nuc | ENST00000424120.6 |
| ensembl_prot | ENSP00000403465.1 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 15469882 |
| end | 15601552 |
| strand | + |
| ver | v1.2 |
| region | chr4:15469882-15601552 |
| region5000 | chr4:15464882-15606552 |
| regionname0 | CC2D2A_chr4_15469882_15601552 |
| regionname5000 | CC2D2A_chr4_15464882_15606552 |
| 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 | 1620 | 262 | 73 | 42 | 99 | 12 | 34 | 77 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0002 | 0/0 | 1620 | 45 | 3 | 9 | 29 | 0 | 4 | 21 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0003 | 0/0 | 1619 | 11 | 1 | 5 | 0 | 2 | 3 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0004 | 0/0 | 1620 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0005 | 0/0 | 1620 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0006 | 0/0 | 1620 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0007 | 0/0 | 1620 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0008 | 0/0 | 1620 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0009 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0010 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0011 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0012 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0013 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0014 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0015 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0016 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0017 | 0/0 | 1620 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0018 | 0/0 | 1620 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0019 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0020 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0021 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0022 | 0/0 | 1620 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| 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 | 4863 | 177 | 58 | 34 | 44 | 10 | 29 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0002 | 0/0 | 4863 | 43 | 2 | 1 | 40 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0003 | 0/0 | 4863 | 34 | 2 | 8 | 22 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0004 | 0/0 | 4863 | 22 | 4 | 6 | 6 | 2 | 4 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0005 | 0/0 | 4863 | 11 | 1 | 1 | 7 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0006 | 0/0 | 4863 | 11 | 4 | 1 | 5 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0007 | 0/0 | 4860 | 9 | 1 | 4 | 0 | 2 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0008 | 0/0 | 4863 | 6 | 3 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0009 | 0/0 | 4863 | 3 | 0 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0010 | 0/0 | 4860 | 2 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0011 | 0/0 | 4863 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0012 | 0/0 | 4863 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0013 | 0/0 | 4863 | 2 | 1 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0014 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0015 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0016 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0017 | 0/0 | 4863 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0018 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0019 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0020 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0021 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0022 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0023 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0024 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0025 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0026 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0027 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0028 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0029 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0030 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0031 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0032 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| c0033 | 0/0 | 4863 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 322 | 191 | 44 | 34 | 74 | 8 | 31 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| t0002 | 1/1 | 322 | 151 | 45 | 23 | 64 | 6 | 11 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| t0003 | 0/0 | 322 | 2 | 1 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| 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 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| 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 | 4863 | 177 | 58 | 34 | 44 | 10 | 29 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0002 | 0/0 | 4863 | 43 | 2 | 1 | 40 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0004 | 0/0 | 4863 | 22 | 4 | 6 | 6 | 2 | 4 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0006 | 0/0 | 4863 | 11 | 4 | 1 | 5 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0008 | 0/0 | 4863 | 6 | 3 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0015 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0024 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0026 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0002c0003 | 0/0 | 4863 | 34 | 2 | 8 | 22 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0002c0005 | 0/0 | 4863 | 11 | 1 | 1 | 7 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0003c0007 | 0/0 | 4860 | 9 | 1 | 4 | 0 | 2 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0003c0010 | 0/0 | 4860 | 2 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0004c0013 | 0/0 | 4863 | 2 | 1 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0004c0022 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0005c0009 | 0/0 | 4863 | 3 | 0 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0006c0011 | 0/0 | 4863 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0006c0032 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0007c0012 | 0/0 | 4863 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0008c0033 | 0/0 | 4863 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0009c0018 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0010c0025 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0011c0023 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0012c0021 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0013c0020 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0014c0027 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0015c0031 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0016c0019 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0017c0017 | 0/0 | 4863 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0018c0016 | 0/0 | 4863 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0019c0028 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0020c0029 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0021c0030 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0022c0014 | 0/0 | 4863 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5184 | 138 | 34 | 28 | 41 | 8 | 27 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0001t0002 | 1/1 | 5184 | 39 | 24 | 6 | 3 | 2 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0002t0001 | 0/0 | 5184 | 3 | 0 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0002t0002 | 0/0 | 5184 | 40 | 2 | 1 | 37 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0004t0002 | 0/0 | 5184 | 22 | 4 | 6 | 6 | 2 | 4 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0006t0001 | 0/0 | 5184 | 8 | 2 | 0 | 5 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0006t0002 | 0/0 | 5184 | 3 | 2 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0008t0002 | 0/0 | 5184 | 6 | 3 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0015t0001 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0024t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0001c0026t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0002c0003t0001 | 0/0 | 5184 | 22 | 2 | 4 | 14 | 0 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0002c0003t0002 | 0/0 | 5184 | 12 | 0 | 4 | 8 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0002c0005t0001 | 0/0 | 5184 | 9 | 1 | 1 | 6 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0002c0005t0002 | 0/0 | 5184 | 2 | 0 | 0 | 1 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0003c0007t0002 | 0/0 | 5181 | 9 | 1 | 4 | 0 | 2 | 2 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0003c0010t0002 | 0/0 | 5181 | 2 | 0 | 1 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0004c0013t0003 | 0/0 | 5184 | 2 | 1 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0004c0022t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0005c0009t0002 | 0/0 | 5184 | 3 | 0 | 0 | 3 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0006c0011t0001 | 0/0 | 5184 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0006c0032t0001 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0007c0012t0002 | 0/0 | 5184 | 2 | 2 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0008c0033t0001 | 0/0 | 5184 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0009c0018t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0010c0025t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0011c0023t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0012c0021t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0013c0020t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0014c0027t0002 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0015c0031t0001 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0016c0019t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0017c0017t0002 | 0/0 | 5184 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0018c0016t0002 | 0/0 | 5184 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0019c0028t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0020c0029t0001 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0021c0030t0002 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| a0022c0014t0002 | 0/0 | 5184 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | copy fasta | chr4 | 15464882 | 15606552 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0001 | 0/1 | 2 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0215 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0001t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0004t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0006t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0008t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0008t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0008t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0008t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0008t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0008t0002g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0015t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0024t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0001c0026t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0003t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0002c0005t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0007t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0010t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0003c0010t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0004c0013t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0004c0013t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0004c0022t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0005c0009t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0005c0009t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0005c0009t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0006c0011t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0006c0011t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0006c0032t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0007c0012t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0007c0012t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0008c0033t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0009c0018t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0010c0025t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0011c0023t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0012c0021t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0013c0020t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0014c0027t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0015c0031t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0016c0019t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0017c0017t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0018c0016t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0019c0028t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0020c0029t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0021c0030t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| a0022c0014t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00140 | hp1 | a0003 | c0007 | t0002 | g0159 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0260 | EUR | GBR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0261 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00280 | hp2 | a0001 | c0004 | t0002 | g0256 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0206 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00408 | hp1 | a0001 | c0006 | t0001 | g0325 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0082 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00438 | hp1 | a0002 | c0003 | t0002 | g0330 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00438 | hp2 | a0001 | c0004 | t0002 | g0097 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0123 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00558 | hp2 | a0002 | c0003 | t0001 | g0302 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00597 | hp1 | a0002 | c0003 | t0001 | g0329 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0169 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00609 | hp2 | a0020 | c0029 | t0001 | g0002 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00735 | hp1 | a0001 | c0004 | t0002 | g0136 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01070 | hp2 | a0003 | c0007 | t0002 | g0163 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01081 | hp1 | a0001 | c0006 | t0002 | g0219 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0155 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01109 | hp1 | a0004 | c0013 | t0003 | g0135 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01109 | hp2 | a0003 | c0010 | t0002 | g0164 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01167 | hp2 | a0002 | c0003 | t0001 | g0321 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0259 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01243 | hp2 | a0001 | c0004 | t0002 | g0257 | AMR | PUR | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01255 | hp1 | a0002 | c0003 | t0002 | g0328 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01255 | hp2 | a0001 | c0004 | t0002 | g0202 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0276 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01346 | hp2 | a0001 | c0004 | t0002 | g0240 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01358 | hp1 | a0001 | c0004 | t0002 | g0177 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01358 | hp2 | a0002 | c0003 | t0002 | g0315 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01433 | hp1 | a0002 | c0003 | t0002 | g0326 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01433 | hp2 | a0002 | c0005 | t0001 | g0036 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01515 | hp1 | a0003 | c0007 | t0002 | g0191 | EUR | IBS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0103 | EUR | IBS | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0333 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01934 | hp1 | a0002 | c0003 | t0002 | g0275 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01952 | hp2 | a0002 | c0003 | t0001 | g0274 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01978 | hp1 | a0003 | c0007 | t0002 | g0165 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01978 | hp2 | a0008 | c0033 | t0001 | g0290 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01993 | hp2 | a0003 | c0007 | t0002 | g0162 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0322 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02015 | hp2 | a0016 | c0019 | t0001 | g0189 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02027 | hp2 | a0001 | c0004 | t0002 | g0133 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02040 | hp1 | a0002 | c0003 | t0001 | g0337 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02040 | hp2 | a0001 | c0006 | t0001 | g0294 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02055 | hp2 | a0001 | c0015 | t0001 | g0074 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02056 | hp1 | a0002 | c0003 | t0001 | g0334 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0086 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02071 | hp1 | a0001 | c0006 | t0001 | g0292 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02071 | hp2 | a0021 | c0030 | t0002 | g0222 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0283 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02132 | hp1 | a0002 | c0005 | t0001 | g0139 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02132 | hp2 | a0014 | c0027 | t0002 | g0168 | EAS | KHV | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02148 | hp1 | a0003 | c0007 | t0002 | g0236 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0308 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0232 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0127 | EAS | CDX | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02257 | hp2 | a0007 | c0012 | t0002 | g0015 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0291 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0285 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02602 | hp2 | a0003 | c0007 | t0002 | g0161 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0301 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02622 | hp1 | a0006 | c0032 | t0001 | g0252 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02647 | hp1 | a0001 | c0024 | t0002 | g0098 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02683 | hp1 | a0001 | c0004 | t0002 | g0241 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02698 | hp2 | a0002 | c0005 | t0002 | g0279 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0338 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02723 | hp1 | a0006 | c0011 | t0001 | g0253 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02809 | hp1 | a0001 | c0004 | t0002 | g0033 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02809 | hp2 | a0004 | c0022 | t0002 | g0030 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02818 | hp1 | a0002 | c0003 | t0001 | g0262 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02886 | hp2 | a0007 | c0012 | t0002 | g0026 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02895 | hp2 | a0001 | c0008 | t0002 | g0336 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02896 | hp1 | a0001 | c0008 | t0002 | g0331 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0311 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02897 | hp1 | a0001 | c0008 | t0002 | g0332 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02965 | hp2 | a0010 | c0025 | t0002 | g0019 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02976 | hp1 | a0002 | c0005 | t0001 | g0031 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02976 | hp2 | a0009 | c0018 | t0002 | g0043 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03017 | hp1 | a0001 | c0004 | t0002 | g0239 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03098 | hp1 | a0018 | c0016 | t0002 | g0223 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03130 | hp1 | a0001 | c0006 | t0002 | g0100 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0090 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03209 | hp2 | a0011 | c0023 | t0002 | g0021 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03239 | hp1 | a0003 | c0010 | t0002 | g0152 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03453 | hp1 | a0001 | c0006 | t0001 | g0278 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03516 | hp1 | a0001 | c0006 | t0002 | g0327 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03579 | hp1 | a0006 | c0011 | t0001 | g0281 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03654 | hp2 | a0017 | c0017 | t0002 | g0237 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03669 | hp1 | a0001 | c0004 | t0002 | g0158 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03710 | hp1 | a0001 | c0004 | t0002 | g0172 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03710 | hp2 | a0002 | c0005 | t0001 | g0339 | SAS | PJL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03831 | hp1 | a0001 | c0006 | t0001 | g0273 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0221 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0214 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04228 | hp1 | a0003 | c0007 | t0002 | g0251 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18522 | hp2 | a0012 | c0021 | t0002 | g0037 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0195 | EAS | CHB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18942 | hp1 | a0013 | c0020 | t0001 | g0120 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18942 | hp2 | a0001 | c0002 | t0002 | g0295 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18943 | hp1 | a0022 | c0014 | t0002 | g0124 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0296 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0194 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18951 | hp1 | a0002 | c0003 | t0002 | g0309 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18953 | hp2 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18960 | hp1 | a0002 | c0003 | t0001 | g0320 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18973 | hp1 | a0001 | c0002 | t0002 | g0126 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18974 | hp1 | a0002 | c0003 | t0002 | g0247 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18975 | hp2 | a0001 | c0008 | t0002 | g0269 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18977 | hp1 | a0001 | c0004 | t0002 | g0171 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18977 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0200 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0254 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0306 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18983 | hp1 | a0002 | c0003 | t0002 | g0270 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18985 | hp1 | a0002 | c0003 | t0002 | g0277 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0094 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18990 | hp1 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0198 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0199 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18994 | hp2 | a0001 | c0004 | t0002 | g0208 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19001 | hp2 | a0002 | c0003 | t0001 | g0318 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19004 | hp1 | a0002 | c0003 | t0001 | g0148 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19004 | hp2 | a0001 | c0002 | t0002 | g0149 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19005 | hp2 | a0002 | c0005 | t0001 | g0121 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19006 | hp1 | a0002 | c0005 | t0002 | g0107 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19006 | hp2 | a0002 | c0003 | t0001 | g0246 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19009 | hp1 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19009 | hp2 | a0002 | c0003 | t0001 | g0305 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19011 | hp2 | a0001 | c0002 | t0002 | g0153 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19030 | hp1 | a0001 | c0004 | t0002 | g0039 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0313 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19054 | hp2 | a0001 | c0002 | t0002 | g0157 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19056 | hp1 | a0001 | c0002 | t0002 | g0095 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19056 | hp2 | a0002 | c0005 | t0001 | g0116 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19057 | hp1 | a0005 | c0009 | t0002 | g0114 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19057 | hp2 | a0002 | c0003 | t0001 | g0304 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19058 | hp1 | a0002 | c0003 | t0002 | g0268 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19062 | hp1 | a0001 | c0002 | t0002 | g0128 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19064 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19066 | hp1 | a0001 | c0004 | t0002 | g0173 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19066 | hp2 | a0002 | c0003 | t0002 | g0293 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19067 | hp1 | a0002 | c0003 | t0002 | g0288 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19067 | hp2 | a0005 | c0009 | t0002 | g0113 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19068 | hp1 | a0005 | c0009 | t0002 | g0066 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19068 | hp2 | a0001 | c0002 | t0002 | g0193 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19078 | hp1 | a0002 | c0005 | t0001 | g0081 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19078 | hp2 | a0001 | c0004 | t0002 | g0174 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19080 | hp1 | a0002 | c0005 | t0001 | g0002 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19080 | hp2 | a0001 | c0002 | t0002 | g0284 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19082 | hp2 | a0001 | c0008 | t0002 | g0271 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19085 | hp1 | a0002 | c0003 | t0001 | g0303 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19088 | hp2 | a0002 | c0005 | t0001 | g0106 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19090 | hp2 | a0001 | c0026 | t0001 | g0115 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0230 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA19091 | hp2 | a0001 | c0006 | t0001 | g0004 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20129 | hp1 | a0004 | c0013 | t0003 | g0134 | AFR | ASW | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20129 | hp2 | a0001 | c0006 | t0001 | g0312 | AFR | ASW | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0248 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | GIH | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | GIH | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0207 | AMR | CLM | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02109 | hp1 | a0001 | c0004 | t0002 | g0087 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02486 | hp2 | a0003 | c0007 | t0002 | g0160 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02559 | hp1 | a0015 | c0031 | t0001 | g0316 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0300 | AFR | MSL | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18955 | hp1 | a0001 | c0008 | t0002 | g0263 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA18955 | hp2 | a0019 | c0028 | t0001 | g0088 | EAS | JPT | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0089 | AFR | USA | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0001 | REF | REF | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0215 | REF | REF | CC2D2A_chr4_15464882_15606552 | CC2D2A | chr4 | 15464882 | 15606552 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15480737
|
G | A | 1 | a0022 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.157G>A | p.Glu53Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/37 | 351/5184 | 157/4863 | 53/1620 | chr4 | 15480737 | ||
| chr4:15502513
|
C | T | 1 | a0021 | 1 | HG02071.hp2 | missense_variant | MODERATE | c.332C>T | p.Ala111Val | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/37 | 526/5184 | 332/4863 | 111/1620 | chr4 | 15502513 | ||
| chr4:15510159
|
G | T | 1 | a0020 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.459G>T | p.Arg153Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/37 | 653/5184 | 459/4863 | 153/1620 | chr4 | 15510159 | ||
| chr4:15511269
|
C | T | 1 | a0019 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.563C>T | p.Ala188Val | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/37 | 757/5184 | 563/4863 | 188/1620 | chr4 | 15511269 | ||
| chr4:15511381
|
GGAA | G | 1 | a0003 | 11 | HG00140.hp1 HG01070.hp2 HG01109.hp2 others(8): Show |
conservative_inframe_deletion | MODERATE | c.685_687delGAA | p.Glu229del | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/37 | 879/5184 | 685/4863 | 229/1620 | INFO_REALIGN_3_PRIME | chr4 | 15511381 | |
| chr4:15514710
|
G | A | 1 | a0018 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.721G>A | p.Glu241Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/37 | 915/5184 | 721/4863 | 241/1620 | chr4 | 15514710 | ||
| chr4:15515909
|
T | C | 1 | a0017 | 1 | HG03654.hp2 | missense_variant | MODERATE | c.922T>C | p.Phe308Leu | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/37 | 1116/5184 | 922/4863 | 308/1620 | chr4 | 15515909 | ||
| chr4:15516734
|
A | C | 3 | a0002a0008a0020 | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
missense_variant | MODERATE | c.1127A>C | p.Glu376Ala | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/37 | 1321/5184 | 1127/4863 | 376/1620 | chr4 | 15516734 | ||
| chr4:15538112
|
G | A | 1 | a0009 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1978G>A | p.Val660Ile | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/37 | 2172/5184 | 1978/4863 | 660/1620 | chr4 | 15538112 | ||
| chr4:15540848
|
C | T | 1 | a0008 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.2015C>T | p.Ser672Leu | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/37 | 2209/5184 | 2015/4863 | 672/1620 | chr4 | 15540848 | ||
| chr4:15540883
|
T | A | 1 | a0009 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.2050T>A | p.Leu684Ile | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/37 | 2244/5184 | 2050/4863 | 684/1620 | chr4 | 15540883 | ||
| chr4:15550839
|
G | A | 2 | a0015a0016 | 2 | HG02015.hp2 HG02559.hp1 |
missense_variant | MODERATE | c.2197G>A | p.Gly733Arg | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/37 | 2391/5184 | 2197/4863 | 733/1620 | chr4 | 15550839 | ||
| chr4:15550925
|
A | C | 1 | a0010 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.2283A>C | p.Glu761Asp | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/37 | 2477/5184 | 2283/4863 | 761/1620 | chr4 | 15550925 | ||
| chr4:15553256
|
G | A | 1 | a0014 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.2437G>A | p.Gly813Arg | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/37 | 2631/5184 | 2437/4863 | 813/1620 | chr4 | 15553256 | ||
| chr4:15559217
|
T | C | 1 | a0013 | 1 | NA18942.hp1 | missense_variant | MODERATE | c.2882T>C | p.Ile961Thr | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/37 | 3076/5184 | 2882/4863 | 961/1620 | chr4 | 15559217 | ||
| chr4:15559247
|
A | G | 1 | a0011 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.2912A>G | p.Tyr971Cys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/37 | 3106/5184 | 2912/4863 | 971/1620 | chr4 | 15559247 | ||
| chr4:15563386
|
G | A | 1 | a0006 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.3046G>A | p.Glu1016Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/37 | 3240/5184 | 3046/4863 | 1016/1620 | chr4 | 15563386 | ||
| chr4:15570411
|
G | A | 2 | a0004a0012 | 4 | HG01109.hp1 HG02809.hp2 NA18522.hp2 others(1): Show |
missense_variant | MODERATE | c.3509G>A | p.Arg1170Lys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/37 | 3703/5184 | 3509/4863 | 1170/1620 | chr4 | 15570411 | ||
| chr4:15580121
|
C | A | 1 | a0012 | 1 | NA18522.hp2 | missense_variant | MODERATE | c.3925C>A | p.Pro1309Thr | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/37 | 4119/5184 | 3925/4863 | 1309/1620 | chr4 | 15580121 | ||
| chr4:15589567
|
C | G | 1 | a0005 | 3 | NA19057.hp1 NA19067.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.4202C>G | p.Thr1401Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/37 | 4396/5184 | 4202/4863 | 1401/1620 | chr4 | 15589567 | ||
| chr4:15597428
|
C | T | 1 | a0007 | 2 | HG02257.hp2 HG02886.hp2 |
missense_variant | MODERATE | c.4459C>T | p.Arg1487Cys | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/37 | 4653/5184 | 4459/4863 | 1487/1620 | chr4 | 15597428 | ||
| chr4:15601264
|
T | A | 1 | a0015 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.4702T>A | p.Tyr1568Asn | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 37/37 | 4896/5184 | 4702/4863 | 1568/1620 | chr4 | 15601264 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15480736
|
C | T | 6 | a0001c0006a0001c0008a0002c0003others(3): Show | 54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
synonymous_variant | LOW | c.156C>T | p.Ser52Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/37 | 350/5184 | 156/4863 | 52/1620 | chr4 | 15480736 | ||
| chr4:15502840
|
T | C | 1 | a0001c0015 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.355T>C | p.Leu119Leu | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/37 | 549/5184 | 355/4863 | 119/1620 | chr4 | 15502840 | ||
| chr4:15514766
|
C | T | 6 | a0001c0002a0001c0008a0004c0013others(3): Show | 54 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
synonymous_variant | LOW | c.777C>T | p.His259His | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/37 | 971/5184 | 777/4863 | 259/1620 | chr4 | 15514766 | ||
| chr4:15514775
|
C | T | 1 | a0001c0026 | 1 | NA19090.hp2 | synonymous_variant | LOW | c.786C>T | p.Asp262Asp | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/37 | 980/5184 | 786/4863 | 262/1620 | chr4 | 15514775 | ||
| chr4:15553294
|
C | T | 1 | a0001c0024 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.2475C>T | p.Ile825Ile | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/37 | 2669/5184 | 2475/4863 | 825/1620 | chr4 | 15553294 | ||
| chr4:15567395
|
G | A | 8 | a0001c0004a0003c0007a0004c0013others(5): Show | 39 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(36): Show |
synonymous_variant | LOW | c.3201G>A | p.Ser1067Ser | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 25/37 | 3395/5184 | 3201/4863 | 1067/1620 | chr4 | 15567395 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15469989
|
G | A | 1 | a0004c0013t0003 | 2 | HG01109.hp1 NA20129.hp1 |
5_prime_UTR_variant | MODIFIER | c.-87G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/37 | 5944 | chr4 | 15469989 | |||||
| chr4:15601446
|
G | C | 15 | a0001c0001t0001a0001c0002t0001a0001c0006t0001others(12): Show | 191 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*21G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 37/37 | 21 | chr4 | 15601446 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:15470094
|
G | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 40 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.-19+37G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470094 | ||||||
| chr4:15470306
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-19+249C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470306 | ||||||
| chr4:15470457
|
A | G | 1 | a0009c0018t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-19+400A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470457 | ||||||
| chr4:15470602
|
C | G | 1 | a0001c0001t0001g0340 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-19+545C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470602 | ||||||
| chr4:15470649
|
A | ATC | 10 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0042others(7): Show | 10 | HG01106.hp1 HG01192.hp2 HG01993.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+632_-19+633dup others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | |||||
| chr4:15470649
|
A | ATCTC | 5 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0258others(2): Show | 5 | HG01123.hp1 HG02280.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+630_-19+633dup others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | |||||
| chr4:15470649
|
A | ATCTCTC | 5 | a0001c0001t0001g0028a0001c0001t0002g0016a0001c0001t0002g0017others(2): Show | 5 | HG01433.hp2 HG03195.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+628_-19+633dup others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | |||||
| chr4:15470649
|
A | ATCTCTCT others(3): Show |
2 | a0001c0001t0001g0027a0001c0001t0001g0035 | 2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-19+624_-19+633dup others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | |||||
| chr4:15470649
|
A | ATCTCTCT others(5): Show |
1 | a0001c0001t0001g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-19+622_-19+633dup others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | |||||
| chr4:15470649
|
A | ATCTCTCT others(7): Show |
1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+620_-19+633dup others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470649 | |||||
| chr4:15470671
|
CTCTCTCT others(35): Show |
C | 1 | a0001c0001t0001g0045 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-19+616_-19+657del others(42): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470671 | |||||
| chr4:15470673
|
CTCTCTCT others(29): Show |
C | 1 | a0001c0001t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-19+618_-19+653del others(36): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470673 | |||||
| chr4:15470675
|
CTCTCTCT others(27): Show |
C | 3 | a0001c0001t0001g0049a0001c0001t0002g0047a0001c0001t0002g0048 | 3 | HG01952.hp1 HG02293.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-19+620_-19+653del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470675 | |||||
| chr4:15470677
|
CTCTCTCT others(11): Show |
C | 1 | a0001c0002t0002g0050 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-19+622_-19+639del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470677 | |||||
| chr4:15470677
|
CTCTCTCT others(25): Show |
C | 8 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(5): Show | 8 | NA18945.hp2 NA18959.hp1 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+622_-19+653del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470677 | |||||
| chr4:15470677
|
CTCTCTCT others(27): Show |
C | 8 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(5): Show | 8 | HG00733.hp1 HG01099.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+622_-19+655del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470677 | |||||
| chr4:15470679
|
CTCTCTCT others(7): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-19+624_-19+637del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | |||||
| chr4:15470679
|
CTCTCTCT others(13): Show |
C | 1 | a0001c0002t0001g0068 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-19+624_-19+643del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | |||||
| chr4:15470679
|
CTCTCTCT others(15): Show |
C | 1 | a0001c0002t0002g0069 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-19+624_-19+645del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | |||||
| chr4:15470679
|
CTCTCTCT others(17): Show |
C | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01099.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-19+624_-19+647del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | |||||
| chr4:15470679
|
CTCTCTCT others(25): Show |
C | 5 | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0076others(2): Show | 5 | HG00735.hp2 HG02055.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+624_-19+655del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | |||||
| chr4:15470679
|
CTCTCTCT others(27): Show |
C | 15 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(12): Show | 16 | HG00099.hp2 HG00408.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+624_-19+657del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470679 | |||||
| chr4:15470681
|
CTCTCTCT others(7): Show |
C | 2 | a0001c0002t0002g0089a0001c0002t0002g0090 | 2 | HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-19+626_-19+639del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(11): Show |
C | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG03017.hp2 NA18906.hp2 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+626_-19+643del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(13): Show |
C | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-19+626_-19+645del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(15): Show |
C | 2 | a0001c0004t0002g0097a0001c0024t0002g0098 | 2 | HG00438.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-19+626_-19+647del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(17): Show |
C | 2 | a0001c0001t0001g0003a0001c0001t0001g0099 | 3 | HG01167.hp1 HG01169.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-19+626_-19+649del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(21): Show |
C | 1 | a0001c0006t0002g0100 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-19+626_-19+653del others(28): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(25): Show |
C | 8 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0104others(5): Show | 8 | HG01515.hp2 NA18948.hp1 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+626_-19+657del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(27): Show |
C | 13 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0111others(10): Show | 13 | HG03239.hp2 HG03942.hp2 HG04115.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+626_-19+659del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470681
|
CTCTCTCT others(29): Show |
C | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-19+626_-19+661del others(36): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470681 | |||||
| chr4:15470683
|
CTCTCTCT others(5): Show |
C | 2 | a0001c0001t0001g0005a0001c0002t0002g0123 | 2 | HG00558.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-19+628_-19+639del others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470683
|
CTCTCTCT others(7): Show |
C | 1 | a0022c0014t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-19+628_-19+641del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470683
|
CTCTCTCT others(11): Show |
C | 3 | a0001c0001t0001g0125a0001c0002t0002g0126a0001c0002t0002g0127 | 3 | HG02165.hp2 HG03486.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-19+628_-19+645del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470683
|
CTCTCTCT others(13): Show |
C | 4 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0002t0002g0128others(1): Show | 4 | HG02145.hp1 NA18954.hp2 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+628_-19+647del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470683
|
CTCTCTCT others(15): Show |
C | 4 | a0001c0001t0001g0132a0001c0004t0002g0133a0004c0013t0003g0134others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+628_-19+649del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470683
|
CTCTCTCT others(19): Show |
C | 1 | a0001c0004t0002g0136 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-19+628_-19+653del others(26): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470683
|
CTCTCTCT others(27): Show |
C | 10 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0140others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+628_-19+661del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470683
|
CTCTCTCT others(31): Show |
C | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-19+628_-19+665del others(38): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470683 | |||||
| chr4:15470685
|
CTCTCTAT others(5): Show |
C | 1 | a0002c0003t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-19+630_-19+641del others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(9): Show |
C | 2 | a0001c0002t0001g0150a0001c0002t0002g0149 | 2 | NA19004.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-19+630_-19+645del others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(11): Show |
C | 7 | a0001c0001t0002g0151a0001c0002t0002g0153a0001c0002t0002g0154others(4): Show | 7 | HG00597.hp2 HG01106.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+630_-19+647del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(13): Show |
C | 14 | a0001c0001t0001g0006a0001c0001t0001g0166a0001c0001t0002g0167others(11): Show | 14 | HG00140.hp1 HG00609.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+630_-19+649del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(15): Show |
C | 4 | a0001c0004t0002g0171a0001c0004t0002g0172a0001c0004t0002g0173others(1): Show | 4 | HG03710.hp1 NA18977.hp1 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+630_-19+651del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(17): Show |
C | 3 | a0001c0001t0001g0007a0001c0001t0001g0175a0001c0002t0002g0176 | 3 | HG00099.hp1 HG02109.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-19+630_-19+653del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(19): Show |
C | 1 | a0001c0004t0002g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19+630_-19+655del others(26): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(25): Show |
C | 4 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180others(1): Show | 4 | HG01081.hp2 HG01361.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+630_-19+661del others(32): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470685
|
CTCTCTAT others(27): Show |
C | 3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184 | 3 | HG02683.hp2 HG03834.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.-19+630_-19+663del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470685 | |||||
| chr4:15470687
|
CTCTA | C | 4 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0002g0186others(1): Show | 4 | HG02015.hp2 HG02165.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+632_-19+635del others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | |||||
| chr4:15470687
|
CTCTATAT others(7): Show |
C | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-19+632_-19+645del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | |||||
| chr4:15470687
|
CTCTATAT others(11): Show |
C | 11 | a0001c0001t0001g0190a0001c0001t0001g0196a0001c0001t0001g0197others(8): Show | 11 | HG01515.hp1 HG02698.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+632_-19+649del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | |||||
| chr4:15470687
|
CTCTATAT others(13): Show |
C | 2 | a0001c0001t0001g0201a0001c0004t0002g0202 | 2 | HG01255.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-19+632_-19+651del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | |||||
| chr4:15470687
|
CTCTATAT others(15): Show |
C | 6 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 6 | HG00323.hp1 HG00741.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+632_-19+653del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | |||||
| chr4:15470687
|
CTCTATAT others(27): Show |
C | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0211others(1): Show | 4 | NA18951.hp2 NA18953.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+632_-19+665del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470687 | |||||
| chr4:15470689
|
C | A | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19+632C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470689 | ||||||
| chr4:15470689
|
CTA | C | 8 | a0001c0001t0001g0217a0001c0001t0001g0340a0001c0001t0002g0022others(5): Show | 8 | HG00642.hp2 HG02257.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+676_-19+677del others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATA | C | 21 | a0001c0001t0001g0264a0001c0001t0001g0307a0001c0001t0001g0319others(18): Show | 21 | HG00438.hp1 HG00558.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.-19+674_-19+677del others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATA | C | 22 | a0001c0001t0001g0023a0001c0001t0001g0218a0001c0001t0001g0245others(19): Show | 23 | HG00639.hp2 HG01074.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-19+672_-19+677del others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(1): Show |
C | 22 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0220others(19): Show | 22 | HG00408.hp1 HG01257.hp1 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+670_-19+677del others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(3): Show |
C | 9 | a0001c0001t0001g0010a0001c0001t0001g0013a0001c0001t0001g0249others(6): Show | 9 | HG01255.hp1 HG02040.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+668_-19+677del others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(5): Show |
C | 6 | a0001c0001t0001g0250a0001c0001t0001g0314a0001c0006t0001g0278others(3): Show | 6 | HG01358.hp2 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+666_-19+677del others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(7): Show |
C | 4 | a0001c0001t0002g0280a0002c0005t0002g0279a0018c0016t0002g0223others(1): Show | 4 | HG02071.hp2 HG02486.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+664_-19+677del others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(9): Show |
C | 6 | a0001c0001t0001g0224a0001c0001t0001g0225a0001c0001t0001g0226others(3): Show | 6 | HG00621.hp1 HG02622.hp1 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+662_-19+677del others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(11): Show |
C | 16 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0282others(13): Show | 16 | HG00733.hp2 HG02080.hp2 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+660_-19+677del others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(13): Show |
C | 3 | a0001c0001t0001g0235a0001c0004t0002g0256a0003c0007t0002g0236 | 3 | HG00280.hp2 HG02055.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-19+658_-19+677del others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(15): Show |
C | 6 | a0001c0001t0001g0238a0001c0004t0002g0239a0001c0004t0002g0240others(3): Show | 6 | HG01243.hp2 HG01346.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+656_-19+677del others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(17): Show |
C | 1 | a0001c0001t0002g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-19+654_-19+677del others(24): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470689
|
CTATATAT others(27): Show |
C | 1 | a0001c0001t0001g0243 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-19+644_-19+677del others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15470689 | |||||
| chr4:15470691
|
A | C | 31 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0020others(28): Show | 31 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+634A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470691 | ||||||
| chr4:15470693
|
A | C | 32 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0028others(29): Show | 32 | HG00140.hp2 HG00280.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-19+636A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470693 | ||||||
| chr4:15470695
|
A | C | 46 | a0001c0001t0001g0020a0001c0001t0001g0029a0001c0001t0001g0042others(43): Show | 46 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-19+638A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470695 | ||||||
| chr4:15470697
|
A | C | 57 | a0001c0001t0001g0023a0001c0001t0001g0029a0001c0001t0001g0042others(54): Show | 58 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(55): Show |
intron_variant | MODIFIER | c.-19+640A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470697 | ||||||
| chr4:15470699
|
A | C | 70 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0042others(67): Show | 71 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19+642A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470699 | ||||||
| chr4:15470701
|
A | C | 61 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0042others(58): Show | 62 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.-19+644A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470701 | ||||||
| chr4:15470703
|
A | C | 49 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0042others(46): Show | 50 | HG00408.hp1 HG00438.hp1 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.-19+646A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470703 | ||||||
| chr4:15470705
|
A | C | 30 | a0001c0001t0001g0044a0001c0001t0001g0314a0001c0001t0001g0324others(27): Show | 30 | HG00408.hp1 HG00438.hp1 HG01255.hp1 others(27): Show |
intron_variant | MODIFIER | c.-19+648A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470705 | ||||||
| chr4:15470707
|
A | C | 24 | a0001c0001t0001g0044a0001c0001t0001g0314a0001c0001t0001g0324others(21): Show | 24 | HG00408.hp1 HG01255.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+650A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470707 | ||||||
| chr4:15470709
|
A | C | 15 | a0001c0001t0001g0282a0001c0001t0001g0314a0001c0001t0002g0333others(12): Show | 15 | HG01255.hp1 HG01358.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.-19+652A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470709 | ||||||
| chr4:15470711
|
A | C | 8 | a0001c0001t0001g0282a0001c0001t0002g0338a0001c0002t0001g0283others(5): Show | 8 | HG00280.hp2 HG02080.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+654A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470711 | ||||||
| chr4:15470713
|
A | C | 3 | a0001c0002t0002g0295a0001c0002t0002g0296a0001c0004t0002g0257 | 3 | HG01243.hp2 NA18942.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.-19+656A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470713 | ||||||
| chr4:15470729
|
A | C | 1 | a0005c0009t0002g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+672A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470729 | ||||||
| chr4:15470732
|
T | A | 1 | a0005c0009t0002g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+675T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470732 | ||||||
| chr4:15470733
|
A | C | 1 | a0005c0009t0002g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+676A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470733 | ||||||
| chr4:15470743
|
T | A | 1 | a0005c0009t0002g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-19+686T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470743 | ||||||
| chr4:15470804
|
T | C | 335 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(332): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.-19+747T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15470804 | ||||||
| chr4:15471235
|
G | A | 3 | a0001c0001t0001g0218a0006c0011t0001g0253a0006c0011t0001g0281 | 3 | HG02723.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19+1178G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471235 | ||||||
| chr4:15471242
|
A | G | 1 | a0001c0001t0002g0131 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-19+1185A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471242 | ||||||
| chr4:15471391
|
TG | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-19+1337delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15471391 | |||||
| chr4:15471551
|
A | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 40 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.-19+1494A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471551 | ||||||
| chr4:15471559
|
C | A | 3 | a0001c0001t0001g0218a0006c0011t0001g0253a0006c0011t0001g0281 | 3 | HG02723.hp1 HG02970.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-19+1502C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471559 | ||||||
| chr4:15471628
|
C | CA | 8 | a0001c0001t0001g0077a0001c0001t0001g0109a0001c0001t0001g0209others(5): Show | 8 | HG02257.hp1 HG02965.hp1 HG03942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+1585dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15471628 | |||||
| chr4:15471628
|
CA | C | 51 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.-19+1585delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15471628 | |||||
| chr4:15471782
|
T | C | 1 | a0001c0002t0002g0193 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-19+1725T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471782 | ||||||
| chr4:15471799
|
A | T | 1 | a0002c0005t0001g0339 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+1742A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471799 | ||||||
| chr4:15471839
|
C | T | 3 | a0001c0004t0002g0240a0001c0004t0002g0241a0001c0004t0002g0257 | 3 | HG01243.hp2 HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-19+1782C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471839 | ||||||
| chr4:15471845
|
A | G | 1 | a0018c0016t0002g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-19+1788A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15471845 | ||||||
| chr4:15472147
|
A | G | 231 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(228): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.-19+2090A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472147 | ||||||
| chr4:15472332
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-19+2275G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472332 | ||||||
| chr4:15472531
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-19+2474T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472531 | ||||||
| chr4:15472647
|
GT | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-19+2604delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15472647 | |||||
| chr4:15472842
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0002g0072a0001c0001t0002g0103 | 3 | HG00735.hp2 HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-19+2785T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15472842 | ||||||
| chr4:15473090
|
A | T | 1 | a0001c0001t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-18-2825A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473090 | ||||||
| chr4:15473158
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-18-2757T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473158 | ||||||
| chr4:15473372
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(42): Show | 46 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.-18-2543C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473372 | ||||||
| chr4:15473470
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18-2445G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473470 | ||||||
| chr4:15473476
|
A | G | 293 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.-18-2439A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473476 | ||||||
| chr4:15473506
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-18-2409G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473506 | ||||||
| chr4:15473539
|
A | G | 1 | a0002c0005t0001g0339 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18-2376A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473539 | ||||||
| chr4:15473581
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18-2334G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15473581 | ||||||
| chr4:15473830
|
GA | G | 3 | a0001c0001t0002g0024a0001c0004t0002g0033a0001c0004t0002g0039 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-2082delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | INFO_REALIGN_3_PRIME | chr4 | 15473830 | |||||
| chr4:15474164
|
C | T | 1 | a0001c0004t0002g0239 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-18-1751C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474164 | ||||||
| chr4:15474304
|
G | A | 1 | a0001c0002t0001g0068 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-18-1611G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474304 | ||||||
| chr4:15474507
|
A | G | 1 | a0002c0005t0001g0031 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-18-1408A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474507 | ||||||
| chr4:15474620
|
A | C | 50 | a0001c0001t0001g0093a0001c0001t0001g0181a0001c0001t0001g0196others(47): Show | 50 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-1295A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474620 | ||||||
| chr4:15474704
|
A | G | 50 | a0001c0001t0001g0093a0001c0001t0001g0181a0001c0001t0001g0196others(47): Show | 50 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-1211A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474704 | ||||||
| chr4:15474875
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-18-1040C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474875 | ||||||
| chr4:15474980
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18-935A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15474980 | ||||||
| chr4:15475051
|
G | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-18-864G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475051 | ||||||
| chr4:15475100
|
C | A | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-18-815C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475100 | ||||||
| chr4:15475135
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-18-780G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475135 | ||||||
| chr4:15475187
|
T | A | 1 | a0001c0001t0001g0289 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-18-728T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475187 | ||||||
| chr4:15475222
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-693C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475222 | ||||||
| chr4:15475246
|
C | T | 8 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0002g0025others(5): Show | 8 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18-669C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475246 | ||||||
| chr4:15475295
|
A | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 96 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.-18-620A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475295 | ||||||
| chr4:15475298
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-18-617G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475298 | ||||||
| chr4:15475327
|
C | A | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.-18-588C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475327 | ||||||
| chr4:15475458
|
C | A | 1 | a0001c0001t0002g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-457C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475458 | ||||||
| chr4:15475564
|
C | T | 1 | a0013c0020t0001g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-18-351C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475564 | ||||||
| chr4:15475778
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-18-137G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 1/36 | chr4 | 15475778 | ||||||
| chr4:15476031
|
C | T | 1 | a0001c0004t0002g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.39+60C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476031 | ||||||
| chr4:15476188
|
C | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0070others(51): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.39+217C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476188 | ||||||
| chr4:15476406
|
C | G | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.39+435C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476406 | ||||||
| chr4:15476477
|
G | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0070others(51): Show | 55 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.39+506G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476477 | ||||||
| chr4:15476593
|
G | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(36): Show | 39 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.39+622G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476593 | ||||||
| chr4:15476925
|
G | T | 3 | a0002c0003t0001g0304a0002c0003t0001g0305a0002c0003t0001g0306 | 3 | NA18981.hp2 NA19009.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.39+954G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15476925 | ||||||
| chr4:15477000
|
C | A | 2 | a0001c0001t0002g0266a0001c0001t0002g0280 | 2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.39+1029C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477000 | ||||||
| chr4:15477068
|
C | T | 53 | a0001c0006t0001g0004a0001c0006t0001g0273a0001c0006t0001g0278others(50): Show | 54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.39+1097C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477068 | ||||||
| chr4:15477230
|
T | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(194): Show | 199 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.39+1259T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477230 | ||||||
| chr4:15477242
|
C | T | 1 | a0001c0006t0002g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.39+1271C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477242 | ||||||
| chr4:15477290
|
A | C | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 40 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.39+1319A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477290 | ||||||
| chr4:15477301
|
C | CA | 10 | a0001c0001t0001g0079a0001c0001t0001g0209a0001c0001t0001g0314others(7): Show | 10 | HG02293.hp1 HG02293.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.39+1347dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | INFO_REALIGN_3_PRIME | chr4 | 15477301 | |||||
| chr4:15477356
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.40-1367T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477356 | ||||||
| chr4:15477775
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | NA18612.hp2 NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.40-948C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477775 | ||||||
| chr4:15477920
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40-803C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15477920 | ||||||
| chr4:15478017
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.40-706A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478017 | ||||||
| chr4:15478159
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.40-564C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478159 | ||||||
| chr4:15478412
|
C | A | 1 | a0001c0006t0001g0325 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.40-311C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478412 | ||||||
| chr4:15478449
|
T | C | 293 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.40-274T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478449 | ||||||
| chr4:15478544
|
A | C | 3 | a0001c0001t0002g0024a0001c0004t0002g0033a0001c0004t0002g0039 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.40-179A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478544 | ||||||
| chr4:15478601
|
A | C | 293 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(290): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.40-122A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 2/36 | chr4 | 15478601 | ||||||
| chr4:15478858
|
G | A | 54 | a0001c0001t0001g0324a0001c0006t0001g0004a0001c0006t0001g0273others(51): Show | 55 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.123+52G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15478858 | ||||||
| chr4:15478938
|
G | T | 5 | a0001c0001t0001g0008a0001c0001t0002g0025a0001c0001t0002g0032others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.123+132G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15478938 | ||||||
| chr4:15479019
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.123+213C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479019 | ||||||
| chr4:15479024
|
G | T | 1 | a0002c0003t0001g0303 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.123+218G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479024 | ||||||
| chr4:15479041
|
T | G | 53 | a0001c0006t0001g0004a0001c0006t0001g0273a0001c0006t0001g0278others(50): Show | 54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.123+235T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479041 | ||||||
| chr4:15479049
|
T | C | 50 | a0001c0001t0001g0093a0001c0001t0001g0181a0001c0001t0001g0196others(47): Show | 50 | HG00597.hp2 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.123+243T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479049 | ||||||
| chr4:15479161
|
T | C | 1 | a0001c0001t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.123+355T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479161 | ||||||
| chr4:15479460
|
C | G | 6 | a0001c0001t0001g0008a0001c0001t0001g0228a0001c0001t0002g0025others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.123+654C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479460 | ||||||
| chr4:15479485
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0002g0017a0001c0001t0002g0022 | 3 | HG02622.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.123+679G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479485 | ||||||
| chr4:15479601
|
T | A | 2 | a0001c0006t0001g0273a0001c0006t0001g0292 | 2 | HG02071.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.123+795T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479601 | ||||||
| chr4:15479613
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.123+807G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15479613 | ||||||
| chr4:15480036
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.124-668C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480036 | ||||||
| chr4:15480214
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.124-490G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480214 | ||||||
| chr4:15480352
|
A | G | 198 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(195): Show | 200 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.124-352A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480352 | ||||||
| chr4:15480452
|
C | G | 25 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(22): Show | 25 | HG01243.hp1 HG01433.hp2 HG02280.hp2 others(22): Show |
intron_variant | MODIFIER | c.124-252C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480452 | ||||||
| chr4:15480589
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.124-115C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480589 | ||||||
| chr4:15480698
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(85): Show | 89 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
splice_region_variant&intron_variant | LOW | c.124-6C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 3/36 | chr4 | 15480698 | ||||||
| chr4:15480853
|
A | G | 294 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(291): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.247+26A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15480853 | ||||||
| chr4:15480874
|
G | A | 1 | a0001c0006t0001g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.247+47G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15480874 | ||||||
| chr4:15481044
|
A | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(86): Show | 90 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.247+217A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481044 | ||||||
| chr4:15481086
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.247+259A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481086 | ||||||
| chr4:15481113
|
T | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013 | 3 | HG02109.hp2 HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.247+286T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481113 | ||||||
| chr4:15481185
|
G | A | 148 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.247+358G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481185 | ||||||
| chr4:15481279
|
C | T | 4 | a0001c0001t0001g0006a0001c0004t0002g0240a0001c0004t0002g0241others(1): Show | 4 | HG01243.hp2 HG01346.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+452C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481279 | ||||||
| chr4:15481280
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.247+453G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481280 | ||||||
| chr4:15481372
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.247+545G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481372 | ||||||
| chr4:15481380
|
G | A | 34 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.247+553G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481380 | ||||||
| chr4:15481466
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0044others(57): Show | 61 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.247+639G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481466 | ||||||
| chr4:15481470
|
C | A | 2 | a0002c0005t0001g0031a0002c0005t0001g0036 | 2 | HG01433.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.247+643C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481470 | ||||||
| chr4:15481664
|
T | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.247+837T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481664 | ||||||
| chr4:15481873
|
G | C | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+1046G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15481873 | ||||||
| chr4:15482186
|
G | C | 28 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(25): Show | 28 | HG01243.hp1 HG01433.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.247+1359G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482186 | ||||||
| chr4:15482228
|
G | C | 1 | a0013c0020t0001g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.247+1401G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482228 | ||||||
| chr4:15482262
|
T | C | 1 | a0001c0001t0002g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.247+1435T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482262 | ||||||
| chr4:15482527
|
C | T | 290 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(287): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.247+1700C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482527 | ||||||
| chr4:15482562
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247+1735A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482562 | ||||||
| chr4:15482699
|
C | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0228a0001c0001t0002g0025others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+1872C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482699 | ||||||
| chr4:15482872
|
T | C | 1 | a0002c0005t0001g0081 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.247+2045T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482872 | ||||||
| chr4:15482875
|
AT | A | 53 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(50): Show | 54 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.247+2050delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15482875 | |||||
| chr4:15482879
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.247+2052G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482879 | ||||||
| chr4:15482899
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247+2072C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482899 | ||||||
| chr4:15482900
|
G | A | 1 | a0002c0005t0001g0339 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.247+2073G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15482900 | ||||||
| chr4:15483127
|
A | T | 1 | a0001c0001t0002g0300 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.247+2300A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483127 | ||||||
| chr4:15483391
|
T | G | 1 | a0001c0024t0002g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.247+2564T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483391 | ||||||
| chr4:15483560
|
T | C | 5 | a0001c0001t0001g0122a0001c0001t0001g0137a0001c0001t0001g0138others(2): Show | 5 | HG00323.hp2 HG01074.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+2733T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483560 | ||||||
| chr4:15483614
|
C | T | 53 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(50): Show | 54 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.247+2787C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483614 | ||||||
| chr4:15483761
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.247+2934G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483761 | ||||||
| chr4:15483880
|
T | C | 3 | a0001c0001t0002g0024a0001c0004t0002g0033a0001c0004t0002g0039 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.247+3053T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483880 | ||||||
| chr4:15483986
|
G | C | 1 | a0001c0001t0002g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.247+3159G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15483986 | ||||||
| chr4:15484061
|
A | AGTTTATA others(10): Show |
1 | a0001c0001t0001g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.247+3235_247+3236i others(19): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15484061 | |||||
| chr4:15484111
|
T | C | 6 | a0002c0003t0001g0274a0002c0003t0001g0276a0002c0003t0002g0275others(3): Show | 6 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+3284T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484111 | ||||||
| chr4:15484383
|
T | C | 4 | a0001c0002t0002g0050a0001c0002t0002g0123a0001c0002t0002g0194others(1): Show | 4 | HG00558.hp1 NA18747.hp2 NA18948.hp2 others(1): Show |
intron_variant | MODIFIER | c.247+3556T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484383 | ||||||
| chr4:15484455
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.247+3628G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484455 | ||||||
| chr4:15484460
|
C | T | 6 | a0001c0001t0002g0024a0001c0004t0002g0033a0001c0004t0002g0039others(3): Show | 6 | HG01891.hp2 HG02809.hp1 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+3633C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484460 | ||||||
| chr4:15484545
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.247+3718G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484545 | ||||||
| chr4:15484670
|
A | G | 1 | a0001c0004t0002g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.247+3843A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484670 | ||||||
| chr4:15484694
|
T | G | 1 | a0001c0004t0002g0256 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.247+3867T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15484694 | ||||||
| chr4:15485149
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247+4322G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485149 | ||||||
| chr4:15485174
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+4347A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485174 | ||||||
| chr4:15485192
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.247+4365A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485192 | ||||||
| chr4:15485211
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.247+4384A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485211 | ||||||
| chr4:15485228
|
C | G | 12 | a0001c0001t0001g0092a0001c0001t0001g0224a0001c0001t0001g0229others(9): Show | 12 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+4401C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485228 | ||||||
| chr4:15485705
|
T | C | 53 | a0001c0006t0001g0004a0001c0006t0001g0273a0001c0006t0001g0278others(50): Show | 54 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.247+4878T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485705 | ||||||
| chr4:15485739
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.247+4912C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485739 | ||||||
| chr4:15485808
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+4981A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15485808 | ||||||
| chr4:15486030
|
G | A | 12 | a0001c0001t0001g0092a0001c0001t0001g0224a0001c0001t0001g0229others(9): Show | 12 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+5203G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15486030 | ||||||
| chr4:15486372
|
GT | G | 12 | a0001c0001t0001g0092a0001c0001t0001g0224a0001c0001t0001g0229others(9): Show | 12 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+5548delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15486372 | |||||
| chr4:15486525
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0228a0001c0001t0002g0025others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+5698G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15486525 | ||||||
| chr4:15486588
|
T | C | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.247+5761T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15486588 | ||||||
| chr4:15487137
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.247+6310T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487137 | ||||||
| chr4:15487331
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0002g0017a0001c0001t0002g0022 | 3 | HG02622.hp2 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.247+6504G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487331 | ||||||
| chr4:15487370
|
T | C | 3 | a0001c0001t0002g0024a0001c0004t0002g0033a0001c0004t0002g0039 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.247+6543T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487370 | ||||||
| chr4:15487448
|
C | T | 295 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(292): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.247+6621C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487448 | ||||||
| chr4:15487505
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.247+6678C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487505 | ||||||
| chr4:15487506
|
C | T | 1 | a0018c0016t0002g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.247+6679C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487506 | ||||||
| chr4:15487536
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+6709C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487536 | ||||||
| chr4:15487572
|
G | A | 5 | a0001c0001t0001g0008a0001c0001t0002g0025a0001c0001t0002g0032others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+6745G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487572 | ||||||
| chr4:15487652
|
G | A | 8 | a0001c0001t0002g0266a0001c0001t0002g0272a0001c0001t0002g0280others(5): Show | 8 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.247+6825G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487652 | ||||||
| chr4:15487665
|
G | A | 4 | a0001c0006t0001g0004a0002c0003t0001g0303a0002c0003t0001g0318others(1): Show | 5 | NA18960.hp1 NA18990.hp1 NA19001.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+6838G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487665 | ||||||
| chr4:15487780
|
T | A | 3 | a0001c0001t0001g0020a0001c0001t0002g0012a0010c0025t0002g0019 | 3 | HG02965.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.247+6953T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487780 | ||||||
| chr4:15487785
|
T | TA | 5 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0059others(2): Show | 5 | HG01099.hp2 HG01192.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+6965dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15487785 | |||||
| chr4:15487789
|
A | AT | 12 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(9): Show | 12 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.247+6962_247+6963i others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487789 | ||||||
| chr4:15487789
|
A | ATT | 78 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.247+6962_247+6963i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487789 | ||||||
| chr4:15487789
|
A | ATTT | 52 | a0001c0006t0001g0004a0001c0006t0001g0273a0001c0006t0001g0278others(49): Show | 53 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.247+6962_247+6963i others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487789 | ||||||
| chr4:15487790
|
A | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+6963A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487790 | ||||||
| chr4:15487791
|
A | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+6964A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487791 | ||||||
| chr4:15487792
|
A | AT | 142 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0046others(139): Show | 143 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.247+6976dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15487792 | |||||
| chr4:15487792
|
A | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(140): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.247+6965A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487792 | ||||||
| chr4:15487831
|
A | G | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+7004A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15487831 | ||||||
| chr4:15487957
|
T | TC | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+7136dupC | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15487957 | |||||
| chr4:15488019
|
G | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(138): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.247+7192G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488019 | ||||||
| chr4:15488098
|
G | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(104): Show | 109 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.247+7271G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488098 | ||||||
| chr4:15488168
|
G | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.247+7341G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488168 | ||||||
| chr4:15488491
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.247+7664T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488491 | ||||||
| chr4:15488512
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.247+7685G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488512 | ||||||
| chr4:15488614
|
C | T | 7 | a0001c0001t0001g0166a0001c0004t0002g0097a0001c0004t0002g0133others(4): Show | 7 | HG00438.hp2 HG02027.hp2 NA18977.hp1 others(4): Show |
intron_variant | MODIFIER | c.247+7787C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488614 | ||||||
| chr4:15488645
|
C | G | 1 | a0016c0019t0001g0189 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.247+7818C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488645 | ||||||
| chr4:15488728
|
G | A | 3 | a0001c0008t0002g0331a0001c0008t0002g0332a0001c0008t0002g0336 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.247+7901G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488728 | ||||||
| chr4:15488809
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0249 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.247+7982G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488809 | ||||||
| chr4:15488934
|
C | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+8107C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15488934 | ||||||
| chr4:15489015
|
C | A | 1 | a0001c0001t0002g0186 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.247+8188C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489015 | ||||||
| chr4:15489128
|
A | T | 142 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.247+8301A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489128 | ||||||
| chr4:15489218
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.247+8391T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489218 | ||||||
| chr4:15489226
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.247+8399A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489226 | ||||||
| chr4:15489329
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.247+8502C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489329 | ||||||
| chr4:15489585
|
C | T | 1 | a0001c0001t0002g0151 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.247+8758C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489585 | ||||||
| chr4:15489586
|
G | A | 2 | a0006c0011t0001g0253a0006c0011t0001g0281 | 2 | HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.247+8759G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489586 | ||||||
| chr4:15489706
|
T | C | 11 | a0001c0001t0001g0092a0001c0001t0001g0224a0001c0001t0001g0229others(8): Show | 11 | HG00558.hp1 HG00733.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.247+8879T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15489706 | ||||||
| chr4:15490227
|
C | T | 203 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0009others(200): Show | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.247+9400C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490227 | ||||||
| chr4:15490389
|
A | G | 1 | a0001c0002t0002g0157 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.247+9562A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490389 | ||||||
| chr4:15490414
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.247+9587C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490414 | ||||||
| chr4:15490448
|
G | C | 1 | a0001c0001t0001g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.247+9621G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490448 | ||||||
| chr4:15490554
|
C | T | 271 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(268): Show | 274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.247+9727C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490554 | ||||||
| chr4:15490644
|
A | G | 13 | a0001c0001t0001g0190a0002c0005t0002g0279a0003c0007t0002g0159others(10): Show | 13 | HG00140.hp1 HG01070.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.247+9817A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490644 | ||||||
| chr4:15490779
|
T | C | 52 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(49): Show | 53 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.247+9952T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490779 | ||||||
| chr4:15490820
|
G | C | 21 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049others(18): Show | 22 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.247+9993G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490820 | ||||||
| chr4:15490853
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.247+10026G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490853 | ||||||
| chr4:15490867
|
CCTGTT | C | 43 | a0001c0001t0001g0007a0001c0001t0001g0051a0001c0001t0001g0052others(40): Show | 43 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(40): Show |
intron_variant | MODIFIER | c.247+10053_247+1005 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15490867 | |||||
| chr4:15490918
|
C | G | 1 | a0001c0006t0001g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.247+10091C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490918 | ||||||
| chr4:15490921
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.247+10094T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490921 | ||||||
| chr4:15490934
|
G | A | 25 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0067others(22): Show | 25 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.247+10107G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15490934 | ||||||
| chr4:15491003
|
G | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0028others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+10176G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491003 | ||||||
| chr4:15491037
|
G | A | 1 | a0002c0003t0002g0277 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.247+10210G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491037 | ||||||
| chr4:15491048
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.247+10221C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491048 | ||||||
| chr4:15491098
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.247+10271C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491098 | ||||||
| chr4:15491099
|
G | A | 1 | a0001c0004t0002g0097 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.247+10272G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491099 | ||||||
| chr4:15491126
|
G | C | 53 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(50): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.247+10299G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491126 | ||||||
| chr4:15491147
|
C | T | 46 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0051others(43): Show | 46 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(43): Show |
intron_variant | MODIFIER | c.247+10320C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491147 | ||||||
| chr4:15491252
|
T | C | 49 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(46): Show | 50 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.247+10425T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491252 | ||||||
| chr4:15491366
|
T | G | 5 | a0001c0001t0001g0092a0001c0001t0001g0224a0001c0001t0001g0282others(2): Show | 5 | HG02615.hp2 HG03017.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+10539T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491366 | ||||||
| chr4:15491397
|
C | G | 1 | a0001c0002t0002g0195 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.247+10570C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491397 | ||||||
| chr4:15491415
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(25): Show | 28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.247+10588C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491415 | ||||||
| chr4:15491849
|
T | A | 1 | a0001c0001t0002g0310 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.248-10580T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491849 | ||||||
| chr4:15491947
|
T | A | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(25): Show | 28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.248-10482T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15491947 | ||||||
| chr4:15492030
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.248-10399A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492030 | ||||||
| chr4:15492058
|
A | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(25): Show | 28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.248-10371A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492058 | ||||||
| chr4:15492131
|
C | T | 69 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049others(66): Show | 70 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.248-10298C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492131 | ||||||
| chr4:15492164
|
A | G | 1 | a0001c0001t0002g0310 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.248-10265A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492164 | ||||||
| chr4:15492198
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248-10231C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492198 | ||||||
| chr4:15492491
|
CTT | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0067others(23): Show | 26 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.248-9931_248-9930d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15492491 | |||||
| chr4:15492500
|
G | T | 55 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(52): Show | 56 | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.248-9929G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492500 | ||||||
| chr4:15492513
|
GT | G | 28 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0044others(25): Show | 28 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.248-9905delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15492513 | |||||
| chr4:15492544
|
G | A | 2 | a0003c0007t0002g0159a0003c0007t0002g0160 | 2 | HG00140.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.248-9885G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492544 | ||||||
| chr4:15492571
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.248-9858T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492571 | ||||||
| chr4:15492696
|
C | G | 3 | a0001c0004t0002g0202a0001c0004t0002g0206a0001c0004t0002g0207 | 3 | HG00323.hp1 HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.248-9733C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492696 | ||||||
| chr4:15492704
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.248-9725G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492704 | ||||||
| chr4:15492788
|
C | A | 1 | a0001c0004t0002g0136 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.248-9641C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15492788 | ||||||
| chr4:15493059
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.248-9370A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493059 | ||||||
| chr4:15493130
|
T | C | 53 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(50): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-9299T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493130 | ||||||
| chr4:15493142
|
T | G | 53 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(50): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-9287T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493142 | ||||||
| chr4:15493188
|
C | T | 3 | a0001c0001t0002g0024a0001c0004t0002g0033a0001c0004t0002g0039 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.248-9241C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493188 | ||||||
| chr4:15493191
|
C | A | 1 | a0001c0001t0001g0051 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.248-9238C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493191 | ||||||
| chr4:15493245
|
A | ATTAT | 53 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(50): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-9160_248-9157d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493245 | |||||
| chr4:15493245
|
A | ATTATTTA others(1): Show |
6 | a0001c0001t0001g0057a0001c0001t0001g0062a0001c0001t0001g0102others(3): Show | 7 | HG00099.hp2 HG00733.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-9164_248-9157d others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493245 | |||||
| chr4:15493245
|
A | ATTATTTA others(5): Show |
15 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049others(12): Show | 15 | HG01099.hp2 HG01192.hp1 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.248-9168_248-9157d others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493245 | |||||
| chr4:15493265
|
T | TTTAC | 30 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.248-9161_248-9160i others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493265 | |||||
| chr4:15493269
|
T | C | 30 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(27): Show | 30 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(27): Show |
intron_variant | MODIFIER | c.248-9160T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493269 | ||||||
| chr4:15493269
|
T | TTTAC | 45 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(42): Show | 45 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(42): Show |
intron_variant | MODIFIER | c.248-9146_248-9143d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15493269 | |||||
| chr4:15493576
|
T | C | 1 | a0001c0001t0002g0041 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.248-8853T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493576 | ||||||
| chr4:15493686
|
A | G | 148 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(145): Show | 149 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(146): Show |
intron_variant | MODIFIER | c.248-8743A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493686 | ||||||
| chr4:15493688
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.248-8741T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493688 | ||||||
| chr4:15493724
|
T | C | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.248-8705T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15493724 | ||||||
| chr4:15494021
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.248-8408C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494021 | ||||||
| chr4:15494088
|
G | A | 1 | a0010c0025t0002g0019 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.248-8341G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494088 | ||||||
| chr4:15494089
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.248-8340T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494089 | ||||||
| chr4:15494202
|
G | A | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248-8227G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494202 | ||||||
| chr4:15494270
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.248-8159A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494270 | ||||||
| chr4:15494379
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.248-8050G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494379 | ||||||
| chr4:15494396
|
G | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(24): Show | 27 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(24): Show |
intron_variant | MODIFIER | c.248-8033G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494396 | ||||||
| chr4:15494646
|
G | A | 53 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(50): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.248-7783G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494646 | ||||||
| chr4:15494686
|
T | C | 120 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0045others(117): Show | 121 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.248-7743T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494686 | ||||||
| chr4:15494963
|
A | G | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.248-7466A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15494963 | ||||||
| chr4:15495005
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.248-7424G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495005 | ||||||
| chr4:15495006
|
A | T | 1 | a0001c0001t0002g0001 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.248-7423A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495006 | ||||||
| chr4:15495093
|
C | G | 42 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(39): Show | 42 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.248-7336C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495093 | ||||||
| chr4:15495161
|
T | C | 1 | a0001c0001t0001g0166 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.248-7268T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495161 | ||||||
| chr4:15495297
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.248-7132C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495297 | ||||||
| chr4:15495355
|
C | G | 1 | a0001c0001t0001g0056 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-7074C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495355 | ||||||
| chr4:15495356
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-7073A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495356 | ||||||
| chr4:15495357
|
C | A | 1 | a0001c0001t0001g0056 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-7072C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495357 | ||||||
| chr4:15495750
|
G | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.248-6679G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495750 | ||||||
| chr4:15495873
|
C | A | 2 | a0001c0001t0002g0244a0001c0001t0002g0286 | 2 | HG03834.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.248-6556C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15495873 | ||||||
| chr4:15496137
|
T | G | 1 | a0009c0018t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-6292T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496137 | ||||||
| chr4:15496166
|
T | C | 4 | a0001c0001t0001g0005a0002c0003t0001g0313a0002c0005t0001g0031others(1): Show | 4 | HG01433.hp2 HG02976.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-6263T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496166 | ||||||
| chr4:15496312
|
A | T | 1 | a0001c0001t0001g0056 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.248-6117A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496312 | ||||||
| chr4:15496485
|
C | T | 48 | a0001c0006t0002g0219a0001c0008t0002g0263a0001c0008t0002g0269others(45): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.248-5944C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496485 | ||||||
| chr4:15496586
|
C | T | 1 | a0001c0002t0002g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.248-5843C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496586 | ||||||
| chr4:15496980
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.248-5449C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496980 | ||||||
| chr4:15496991
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.248-5438A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15496991 | ||||||
| chr4:15497093
|
C | A | 44 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 44 | HG00733.hp2 HG01081.hp2 HG01169.hp1 others(41): Show |
intron_variant | MODIFIER | c.248-5336C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497093 | ||||||
| chr4:15497177
|
G | A | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-5252G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497177 | ||||||
| chr4:15497612
|
A | G | 1 | a0001c0001t0001g0299 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.248-4817A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497612 | ||||||
| chr4:15497627
|
T | C | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(180): Show | 185 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(182): Show |
intron_variant | MODIFIER | c.248-4802T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497627 | ||||||
| chr4:15497719
|
T | C | 60 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049others(57): Show | 62 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.248-4710T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497719 | ||||||
| chr4:15497848
|
C | A | 1 | a0001c0004t0002g0136 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.248-4581C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15497848 | ||||||
| chr4:15497857
|
A | AT | 60 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049others(57): Show | 62 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.248-4571dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15497857 | |||||
| chr4:15498097
|
G | T | 1 | a0009c0018t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-4332G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498097 | ||||||
| chr4:15498147
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.248-4282A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498147 | ||||||
| chr4:15498462
|
G | A | 1 | a0002c0003t0002g0293 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.248-3967G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498462 | ||||||
| chr4:15498501
|
C | A | 1 | a0017c0017t0002g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.248-3928C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498501 | ||||||
| chr4:15498654
|
ACT | A | 6 | a0002c0003t0001g0276a0002c0003t0002g0275a0002c0003t0002g0315others(3): Show | 6 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-3774_248-3773d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498654 | ||||||
| chr4:15498798
|
T | C | 3 | a0002c0003t0001g0303a0002c0003t0001g0318a0002c0003t0001g0320 | 3 | NA18960.hp1 NA19001.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.248-3631T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498798 | ||||||
| chr4:15498897
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0002g0130 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.248-3532C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498897 | ||||||
| chr4:15498939
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0002g0130 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.248-3490A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15498939 | ||||||
| chr4:15499211
|
A | C | 1 | a0001c0001t0001g0298 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.248-3218A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499211 | ||||||
| chr4:15499267
|
G | A | 2 | a0005c0009t0002g0113a0005c0009t0002g0114 | 2 | NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.248-3162G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499267 | ||||||
| chr4:15499276
|
G | A | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.248-3153G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499276 | ||||||
| chr4:15499397
|
T | A | 1 | a0009c0018t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-3032T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499397 | ||||||
| chr4:15499621
|
T | C | 7 | a0001c0001t0002g0151a0001c0001t0002g0272a0001c0001t0002g0310others(4): Show | 7 | HG01891.hp1 HG02559.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-2808T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499621 | ||||||
| chr4:15499631
|
T | C | 15 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0023others(12): Show | 15 | HG02109.hp2 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.248-2798T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499631 | ||||||
| chr4:15499880
|
A | G | 54 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0001t0001g0226others(51): Show | 54 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.248-2549A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15499880 | ||||||
| chr4:15499928
|
GGGA | G | 121 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(118): Show | 122 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.248-2494_248-2492d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15499928 | |||||
| chr4:15500075
|
T | TTG | 7 | a0001c0001t0001g0209a0001c0001t0001g0212a0002c0003t0001g0246others(4): Show | 7 | HG00597.hp1 NA18951.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-2322_248-2321d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | |||||
| chr4:15500075
|
T | TTGTG | 39 | a0001c0002t0001g0150a0001c0002t0002g0154a0001c0004t0002g0208others(36): Show | 39 | HG00438.hp1 HG00558.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.248-2324_248-2321d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | |||||
| chr4:15500075
|
T | TTGTGTG | 5 | a0001c0008t0002g0271a0002c0003t0001g0259a0002c0003t0002g0247others(2): Show | 5 | HG01192.hp2 NA18974.hp1 NA19058.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-2326_248-2321d others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | |||||
| chr4:15500075
|
TTGTG | T | 14 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0023others(11): Show | 14 | HG01243.hp1 HG02451.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.248-2324_248-2321d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | |||||
| chr4:15500075
|
TTGTGTG | T | 6 | a0001c0001t0001g0092a0001c0001t0001g0282a0001c0001t0001g0324others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-2326_248-2321d others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | |||||
| chr4:15500075
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0001g0007a0007c0012t0002g0026a0009c0018t0002g0043 | 3 | HG02109.hp2 HG02886.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.248-2328_248-2321d others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | |||||
| chr4:15500075
|
TTGTGTGT others(3): Show |
T | 1 | a0001c0006t0002g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.248-2330_248-2321d others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500075 | |||||
| chr4:15500089
|
G | A | 1 | a0001c0002t0002g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.248-2340G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500089 | ||||||
| chr4:15500097
|
G | A | 8 | a0001c0001t0001g0067a0001c0001t0002g0024a0001c0001t0002g0025others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-2332G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500097 | ||||||
| chr4:15500099
|
G | A | 8 | a0001c0001t0001g0067a0001c0001t0002g0024a0001c0001t0002g0025others(5): Show | 8 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-2330G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500099 | ||||||
| chr4:15500099
|
G | GTATACA | 3 | a0001c0001t0002g0272a0001c0001t0002g0311a0001c0001t0002g0323 | 3 | HG02896.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.248-2329_248-2328i others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATACAT others(3): Show |
1 | a0001c0001t0002g0266 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.248-2329_248-2328i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATACAT others(7): Show |
4 | a0001c0001t0002g0151a0001c0001t0002g0280a0001c0001t0002g0333others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATACAT others(9): Show |
1 | a0001c0001t0002g0310 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.248-2329_248-2328i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATATA | 5 | a0001c0001t0001g0061a0001c0001t0001g0109a0001c0001t0001g0178others(2): Show | 5 | HG01081.hp2 HG01169.hp1 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0055a0001c0001t0001g0079a0001c0001t0001g0101others(1): Show | 4 | HG00735.hp1 HG02293.hp2 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATATAT others(3): Show |
7 | a0001c0001t0001g0051a0001c0001t0001g0053a0001c0001t0001g0054others(4): Show | 7 | HG02055.hp2 HG03486.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATATAT others(5): Show |
5 | a0001c0001t0001g0052a0001c0001t0001g0073a0001c0001t0001g0229others(2): Show | 5 | HG00733.hp2 HG02258.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-2329_248-2328i others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATATAT others(7): Show |
3 | a0001c0001t0001g0056a0001c0001t0002g0022a0016c0019t0001g0189 | 3 | HG02015.hp2 HG02622.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.248-2329_248-2328i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0267 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-2329_248-2328i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500099
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0001g0225 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.248-2328_248-2315d others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500099 | |||||
| chr4:15500101
|
G | A | 48 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0051others(45): Show | 49 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.248-2328G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500101 | ||||||
| chr4:15500101
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0001g0091 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.248-2327_248-2326i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | |||||
| chr4:15500101
|
G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0188a0001c0001t0001g0217 | 2 | HG03654.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.248-2327_248-2326i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | |||||
| chr4:15500101
|
G | GTATATAT others(9): Show |
1 | a0001c0001t0001g0250 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-2327_248-2326i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | |||||
| chr4:15500101
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0001g0213 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.248-2327_248-2326i others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | |||||
| chr4:15500101
|
GTGTGTGT others(11): Show |
G | 2 | a0001c0006t0001g0278a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.248-2326_248-2309d others(20): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500101 | |||||
| chr4:15500103
|
G | A | 64 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0051others(61): Show | 65 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.248-2326G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500103 | ||||||
| chr4:15500103
|
GTGTGTAT others(1): Show |
G | 11 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0027others(8): Show | 11 | HG02630.hp2 HG02723.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.248-2324_248-2317d others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500103 | |||||
| chr4:15500103
|
GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.248-2324_248-2315d others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500103 | |||||
| chr4:15500105
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0023others(63): Show | 67 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.248-2324G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500105 | ||||||
| chr4:15500107
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0023others(64): Show | 68 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.248-2322G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500107 | ||||||
| chr4:15500107
|
G | GTGTGTA | 3 | a0001c0001t0001g0006a0002c0003t0002g0315a0002c0005t0001g0139 | 3 | HG01358.hp2 HG02132.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.248-2321_248-2320i others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTAT others(3): Show |
1 | a0001c0006t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.248-2321_248-2320i others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTAT others(5): Show |
4 | a0001c0001t0002g0048a0001c0001t0002g0059a0001c0001t0002g0060others(1): Show | 4 | HG01099.hp2 HG01192.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2321_248-2320i others(14): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTGT others(7): Show |
4 | a0001c0001t0001g0083a0001c0001t0002g0047a0005c0009t0002g0066others(1): Show | 4 | HG02293.hp1 NA18747.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2321_248-2320i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTGT others(9): Show |
1 | a0001c0006t0001g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.248-2321_248-2320i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTGT others(7): Show |
6 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0057others(3): Show | 6 | HG02080.hp1 NA18612.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-2321_248-2320i others(16): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTGT others(9): Show |
1 | a0001c0001t0002g0072 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.248-2321_248-2320i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.248-2321_248-2320i others(22): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
G | GTGTGTGT others(9): Show |
2 | a0001c0001t0001g0102a0001c0001t0002g0103 | 2 | HG01515.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.248-2321_248-2320i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
GTA | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(127): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.248-2298_248-2297d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500107
|
GTATA | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0110a0001c0001t0001g0190others(14): Show | 17 | HG00642.hp2 HG01515.hp1 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.248-2300_248-2297d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500107 | |||||
| chr4:15500109
|
A | G | 33 | a0001c0001t0001g0063a0001c0001t0001g0122a0001c0001t0001g0146others(30): Show | 33 | HG00280.hp1 HG01433.hp1 HG01433.hp2 others(30): Show |
intron_variant | MODIFIER | c.248-2320A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500109 | ||||||
| chr4:15500111
|
A | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0013others(131): Show | 136 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.248-2318A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500111 | ||||||
| chr4:15500113
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0063others(137): Show | 142 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.248-2316A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500113 | ||||||
| chr4:15500115
|
A | G | 62 | a0001c0001t0001g0075a0001c0001t0001g0096a0001c0001t0001g0105others(59): Show | 62 | HG00323.hp2 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.248-2314A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500115 | ||||||
| chr4:15500117
|
A | G | 4 | a0001c0002t0002g0095a0001c0002t0002g0192a0001c0002t0002g0227others(1): Show | 4 | HG00621.hp1 NA18953.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-2312A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500117 | ||||||
| chr4:15500129
|
A | ATG | 3 | a0001c0001t0002g0024a0001c0001t0002g0032a0001c0004t0002g0039 | 3 | HG01891.hp2 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.248-2299_248-2298i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15500129 | |||||
| chr4:15500129
|
A | G | 19 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0023others(16): Show | 19 | HG02109.hp2 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.248-2300A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500129 | ||||||
| chr4:15500182
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.248-2247T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500182 | ||||||
| chr4:15500343
|
T | C | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-2086T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500343 | ||||||
| chr4:15500350
|
G | A | 1 | a0001c0004t0002g0208 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.248-2079G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500350 | ||||||
| chr4:15500492
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.248-1937T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500492 | ||||||
| chr4:15500684
|
T | C | 24 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(21): Show | 25 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.248-1745T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500684 | ||||||
| chr4:15500951
|
C | T | 1 | a0002c0005t0002g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.248-1478C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15500951 | ||||||
| chr4:15501286
|
T | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-1143T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15501286 | ||||||
| chr4:15501745
|
T | G | 69 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0010others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.248-684T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15501745 | ||||||
| chr4:15501797
|
T | C | 1 | a0001c0006t0001g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248-632T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15501797 | ||||||
| chr4:15502073
|
A | T | 52 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(49): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.248-356A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15502073 | ||||||
| chr4:15502091
|
A | G | 6 | a0001c0002t0002g0128a0001c0002t0002g0129a0001c0002t0002g0169others(3): Show | 6 | HG00609.hp1 HG02132.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-338A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | chr4 | 15502091 | ||||||
| chr4:15502371
|
T | TTTTTC | 95 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(92): Show | 96 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.248-48_248-44dupCT others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 4/36 | INFO_REALIGN_3_PRIME | chr4 | 15502371 | |||||
| chr4:15502526
|
A | T | 1 | a0001c0002t0002g0231 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.336+9A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/36 | chr4 | 15502526 | ||||||
| chr4:15502617
|
C | T | 1 | a0015c0031t0001g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.336+100C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/36 | chr4 | 15502617 | ||||||
| chr4:15502637
|
G | C | 2 | a0004c0013t0003g0134a0004c0013t0003g0135 | 2 | HG01109.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.336+120G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 5/36 | chr4 | 15502637 | ||||||
| chr4:15503184
|
T | A | 1 | a0009c0018t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.438+261T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503184 | ||||||
| chr4:15503196
|
G | A | 50 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(47): Show | 50 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.438+273G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503196 | ||||||
| chr4:15503272
|
C | A | 3 | a0001c0008t0002g0331a0001c0008t0002g0332a0001c0008t0002g0336 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.438+349C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503272 | ||||||
| chr4:15503397
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.438+474C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503397 | ||||||
| chr4:15503634
|
A | AG | 258 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(255): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.438+713dupG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | INFO_REALIGN_3_PRIME | chr4 | 15503634 | |||||
| chr4:15503634
|
A | G | 1 | a0001c0026t0001g0115 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.438+711A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503634 | ||||||
| chr4:15503771
|
A | C | 2 | a0004c0022t0002g0030a0012c0021t0002g0037 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.438+848A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503771 | ||||||
| chr4:15503820
|
C | T | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.438+897C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503820 | ||||||
| chr4:15503933
|
G | C | 317 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.438+1010G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503933 | ||||||
| chr4:15503991
|
C | G | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.438+1068C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15503991 | ||||||
| chr4:15504419
|
G | A | 1 | a0002c0003t0001g0337 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.438+1496G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504419 | ||||||
| chr4:15504496
|
A | G | 4 | a0001c0001t0001g0137a0001c0001t0001g0182a0001c0001t0001g0183others(1): Show | 4 | HG00323.hp2 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.438+1573A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504496 | ||||||
| chr4:15504947
|
G | C | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+2024G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504947 | ||||||
| chr4:15504955
|
C | G | 1 | a0022c0014t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.438+2032C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15504955 | ||||||
| chr4:15505085
|
G | A | 44 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.438+2162G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505085 | ||||||
| chr4:15505173
|
A | G | 1 | a0001c0001t0001g0003 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.438+2250A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505173 | ||||||
| chr4:15505188
|
T | A | 44 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.438+2265T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505188 | ||||||
| chr4:15505409
|
T | C | 211 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(208): Show | 212 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(209): Show |
intron_variant | MODIFIER | c.438+2486T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505409 | ||||||
| chr4:15505431
|
C | A | 1 | a0001c0006t0002g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.438+2508C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505431 | ||||||
| chr4:15505545
|
G | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(77): Show | 81 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.438+2622G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505545 | ||||||
| chr4:15505688
|
C | T | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.438+2765C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505688 | ||||||
| chr4:15505842
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.438+2919C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505842 | ||||||
| chr4:15505873
|
G | C | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.438+2950G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15505873 | ||||||
| chr4:15506068
|
G | A | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+3145G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506068 | ||||||
| chr4:15506082
|
A | T | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+3159A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506082 | ||||||
| chr4:15506150
|
T | C | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.438+3227T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506150 | ||||||
| chr4:15506207
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.438+3284C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506207 | ||||||
| chr4:15506222
|
A | T | 1 | a0001c0004t0002g0256 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.438+3299A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506222 | ||||||
| chr4:15506224
|
T | C | 3 | a0001c0004t0002g0240a0001c0004t0002g0241a0001c0004t0002g0257 | 3 | HG01243.hp2 HG01346.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.438+3301T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506224 | ||||||
| chr4:15506246
|
A | T | 1 | a0001c0004t0002g0136 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.438+3323A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506246 | ||||||
| chr4:15506727
|
A | G | 1 | a0001c0004t0002g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.439-3412A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506727 | ||||||
| chr4:15506812
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.439-3327G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506812 | ||||||
| chr4:15506848
|
C | T | 28 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(25): Show | 29 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.439-3291C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506848 | ||||||
| chr4:15506858
|
G | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 76 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.439-3281G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15506858 | ||||||
| chr4:15507119
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.439-3020C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507119 | ||||||
| chr4:15507152
|
T | G | 1 | a0001c0001t0001g0204 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.439-2987T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507152 | ||||||
| chr4:15507244
|
T | A | 2 | a0001c0001t0001g0044a0001c0001t0002g0130 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439-2895T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507244 | ||||||
| chr4:15507344
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.439-2795T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507344 | ||||||
| chr4:15507374
|
T | C | 1 | a0001c0004t0002g0206 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.439-2765T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507374 | ||||||
| chr4:15507447
|
A | G | 2 | a0007c0012t0002g0015a0007c0012t0002g0026 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.439-2692A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507447 | ||||||
| chr4:15507599
|
G | A | 57 | a0001c0001t0001g0146a0001c0001t0001g0181a0001c0002t0001g0068others(54): Show | 57 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(54): Show |
intron_variant | MODIFIER | c.439-2540G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507599 | ||||||
| chr4:15507668
|
G | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(71): Show | 75 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.439-2471G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507668 | ||||||
| chr4:15507723
|
T | C | 3 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0067 | 3 | HG03195.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.439-2416T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507723 | ||||||
| chr4:15507764
|
G | A | 74 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(71): Show | 75 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.439-2375G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507764 | ||||||
| chr4:15507771
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.439-2368T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507771 | ||||||
| chr4:15507777
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.439-2362C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507777 | ||||||
| chr4:15507996
|
A | G | 1 | a0001c0002t0001g0068 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.439-2143A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15507996 | ||||||
| chr4:15508112
|
T | G | 2 | a0001c0001t0001g0044a0001c0001t0002g0130 | 2 | HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.439-2027T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508112 | ||||||
| chr4:15508331
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.439-1808A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508331 | ||||||
| chr4:15508344
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.439-1795A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508344 | ||||||
| chr4:15508375
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0146others(62): Show | 65 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.439-1764T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508375 | ||||||
| chr4:15508399
|
G | A | 1 | a0002c0003t0001g0334 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.439-1740G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508399 | ||||||
| chr4:15508455
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.439-1684A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15508455 | ||||||
| chr4:15509031
|
G | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.439-1108G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509031 | ||||||
| chr4:15509237
|
C | G | 1 | a0001c0006t0002g0100 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.439-902C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509237 | ||||||
| chr4:15509252
|
T | C | 2 | a0002c0003t0002g0315a0002c0003t0002g0328 | 2 | HG01255.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.439-887T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509252 | ||||||
| chr4:15509277
|
C | CT | 181 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0011others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.439-848dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | INFO_REALIGN_3_PRIME | chr4 | 15509277 | |||||
| chr4:15509277
|
C | CTT | 9 | a0001c0001t0001g0062a0001c0001t0001g0144a0001c0001t0001g0203others(6): Show | 9 | HG00642.hp1 HG00733.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.439-849_439-848dup others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | INFO_REALIGN_3_PRIME | chr4 | 15509277 | |||||
| chr4:15509421
|
C | T | 1 | a0009c0018t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.439-718C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509421 | ||||||
| chr4:15509431
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.439-708G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509431 | ||||||
| chr4:15509599
|
G | A | 54 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(51): Show | 54 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(51): Show |
intron_variant | MODIFIER | c.439-540G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509599 | ||||||
| chr4:15509660
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.439-479C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509660 | ||||||
| chr4:15509703
|
G | T | 74 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(71): Show | 75 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.439-436G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509703 | ||||||
| chr4:15509764
|
G | T | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.439-375G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509764 | ||||||
| chr4:15509945
|
G | A | 3 | a0002c0003t0001g0313a0002c0005t0001g0031a0002c0005t0001g0036 | 3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.439-194G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15509945 | ||||||
| chr4:15510032
|
G | A | 12 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0023others(9): Show | 12 | HG02109.hp2 HG02145.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.439-107G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 6/36 | chr4 | 15510032 | ||||||
| chr4:15510407
|
A | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.540+167A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510407 | ||||||
| chr4:15510705
|
A | G | 1 | a0001c0001t0002g0242 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.540+465A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510705 | ||||||
| chr4:15510767
|
A | AAG | 3 | a0001c0001t0002g0024a0001c0004t0002g0033a0001c0004t0002g0039 | 3 | HG01891.hp2 HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.541-478_541-477dup others(2): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | INFO_REALIGN_3_PRIME | chr4 | 15510767 | |||||
| chr4:15510767
|
A | G | 119 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0051others(116): Show | 119 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.541-480A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510767 | ||||||
| chr4:15510917
|
A | G | 212 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(209): Show | 213 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.541-330A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15510917 | ||||||
| chr4:15511222
|
G | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0023others(7): Show | 10 | HG02109.hp2 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.541-25G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 7/36 | chr4 | 15511222 | ||||||
| chr4:15511446
|
T | C | 1 | a0001c0001t0002g0038 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.717+23T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15511446 | ||||||
| chr4:15511524
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.717+101C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15511524 | ||||||
| chr4:15511742
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.717+319T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15511742 | ||||||
| chr4:15512143
|
A | G | 1 | a0017c0017t0002g0237 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.717+720A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15512143 | ||||||
| chr4:15512493
|
A | C | 76 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(73): Show | 77 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.717+1070A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15512493 | ||||||
| chr4:15512727
|
G | A | 1 | a0001c0002t0002g0157 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.717+1304G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15512727 | ||||||
| chr4:15512951
|
C | CA | 6 | a0001c0001t0001g0145a0001c0004t0002g0240a0001c0004t0002g0241others(3): Show | 6 | HG01243.hp2 HG01346.hp2 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.717+1542dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr4 | 15512951 | |||||
| chr4:15512951
|
CA | C | 196 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(193): Show | 197 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(194): Show |
intron_variant | MODIFIER | c.717+1542delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | INFO_REALIGN_3_PRIME | chr4 | 15512951 | |||||
| chr4:15513006
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.717+1583A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513006 | ||||||
| chr4:15513224
|
C | T | 51 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0224others(48): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.718-1483C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513224 | ||||||
| chr4:15513363
|
C | T | 1 | a0002c0005t0002g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.718-1344C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513363 | ||||||
| chr4:15513427
|
C | T | 202 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(199): Show | 203 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(200): Show |
intron_variant | MODIFIER | c.718-1280C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513427 | ||||||
| chr4:15513730
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0002g0025a0001c0001t0002g0032others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.718-977G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513730 | ||||||
| chr4:15513805
|
T | C | 1 | a0001c0004t0002g0172 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.718-902T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15513805 | ||||||
| chr4:15514168
|
C | T | 203 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(200): Show | 204 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(201): Show |
intron_variant | MODIFIER | c.718-539C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15514168 | ||||||
| chr4:15514536
|
C | T | 3 | a0001c0001t0001g0218a0001c0001t0001g0228a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.718-171C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 8/36 | chr4 | 15514536 | ||||||
| chr4:15515194
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.880+325A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/36 | chr4 | 15515194 | ||||||
| chr4:15515370
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.881-498G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/36 | chr4 | 15515370 | ||||||
| chr4:15515514
|
A | G | 9 | a0001c0001t0001g0044a0001c0001t0002g0025a0001c0001t0002g0032others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.881-354A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 9/36 | chr4 | 15515514 | ||||||
| chr4:15516005
|
G | A | 1 | a0001c0001t0001g0040 | 1 | HG01243.hp1 | splice_donor_variant&intron_variant | HIGH | c.1017+1G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | chr4 | 15516005 | ||||||
| chr4:15516133
|
AT | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 76 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.1017+142delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | INFO_REALIGN_3_PRIME | chr4 | 15516133 | |||||
| chr4:15516248
|
C | G | 1 | a0001c0002t0002g0157 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1017+244C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | chr4 | 15516248 | ||||||
| chr4:15516313
|
C | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 76 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1017+309C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 10/36 | chr4 | 15516313 | ||||||
| chr4:15516864
|
A | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112 | 3 | NA18975.hp1 NA18995.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1149+108A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15516864 | ||||||
| chr4:15516944
|
C | CT | 8 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0067others(5): Show | 8 | HG02071.hp1 HG02738.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1149+211dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | |||||
| chr4:15516944
|
CT | C | 119 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(116): Show | 120 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.1149+211delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | |||||
| chr4:15516944
|
CTT | C | 53 | a0001c0001t0001g0076a0001c0001t0001g0218a0001c0001t0001g0228others(50): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1149+210_1149+211d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | |||||
| chr4:15516944
|
CTTT | C | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1149+209_1149+211d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15516944 | |||||
| chr4:15516972
|
C | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(70): Show | 74 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1149+216C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15516972 | ||||||
| chr4:15517009
|
G | A | 7 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+253G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517009 | ||||||
| chr4:15517011
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0002g0242 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1149+255G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517011 | ||||||
| chr4:15517040
|
C | T | 1 | a0001c0002t0002g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1149+284C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517040 | ||||||
| chr4:15517097
|
G | A | 1 | a0001c0002t0002g0155 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1149+341G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517097 | ||||||
| chr4:15517104
|
C | A | 9 | a0001c0001t0001g0044a0001c0001t0002g0025a0001c0001t0002g0032others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+348C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517104 | ||||||
| chr4:15517109
|
G | A | 5 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0001g0140others(2): Show | 5 | HG00741.hp2 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+353G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517109 | ||||||
| chr4:15517324
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0002g0025a0001c0001t0002g0032others(6): Show | 9 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+568G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517324 | ||||||
| chr4:15517915
|
G | A | 2 | a0001c0001t0001g0249a0001c0001t0002g0242 | 2 | HG02451.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1149+1159G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517915 | ||||||
| chr4:15517951
|
C | A | 7 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+1195C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517951 | ||||||
| chr4:15517970
|
G | T | 1 | a0001c0002t0002g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1149+1214G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15517970 | ||||||
| chr4:15518008
|
G | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01099.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1149+1252G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518008 | ||||||
| chr4:15518036
|
G | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149+1280G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518036 | ||||||
| chr4:15518457
|
C | T | 2 | a0007c0012t0002g0015a0007c0012t0002g0026 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1149+1701C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518457 | ||||||
| chr4:15518791
|
C | T | 1 | a0002c0003t0001g0337 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1149+2035C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518791 | ||||||
| chr4:15518824
|
G | A | 51 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(49): Show |
intron_variant | MODIFIER | c.1149+2068G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518824 | ||||||
| chr4:15518848
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1149+2092C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518848 | ||||||
| chr4:15518980
|
A | G | 1 | a0001c0001t0001g0104 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1149+2224A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15518980 | ||||||
| chr4:15519776
|
C | T | 1 | a0001c0001t0002g0017 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1149+3020C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519776 | ||||||
| chr4:15519779
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1149+3023C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519779 | ||||||
| chr4:15519780
|
G | A | 73 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(70): Show | 74 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1149+3024G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519780 | ||||||
| chr4:15519977
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1149+3221G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15519977 | ||||||
| chr4:15520121
|
G | T | 1 | a0001c0002t0002g0255 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1149+3365G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520121 | ||||||
| chr4:15520352
|
C | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(70): Show | 74 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.1149+3596C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520352 | ||||||
| chr4:15520379
|
C | A | 1 | a0002c0005t0001g0081 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1149+3623C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520379 | ||||||
| chr4:15520586
|
T | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(77): Show | 81 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1149+3830T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520586 | ||||||
| chr4:15520659
|
C | T | 44 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1149+3903C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520659 | ||||||
| chr4:15520745
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1149+3989C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520745 | ||||||
| chr4:15520749
|
T | G | 1 | a0001c0001t0001g0224 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1149+3993T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520749 | ||||||
| chr4:15520797
|
G | A | 3 | a0001c0001t0001g0249a0001c0001t0002g0242a0001c0001t0002g0338 | 3 | HG02451.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1149+4041G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15520797 | ||||||
| chr4:15521170
|
A | C | 1 | a0002c0005t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1149+4414A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521170 | ||||||
| chr4:15521191
|
A | G | 1 | a0008c0033t0001g0290 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1149+4435A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521191 | ||||||
| chr4:15521192
|
C | T | 44 | a0002c0003t0001g0148a0002c0003t0001g0214a0002c0003t0001g0221others(41): Show | 44 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1149+4436C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521192 | ||||||
| chr4:15521324
|
T | C | 47 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1149+4568T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521324 | ||||||
| chr4:15521445
|
C | G | 1 | a0001c0006t0002g0327 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1149+4689C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521445 | ||||||
| chr4:15521513
|
T | A | 5 | a0001c0001t0001g0267a0001c0001t0001g0319a0001c0001t0002g0022others(2): Show | 5 | HG02258.hp2 HG02615.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1149+4757T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521513 | ||||||
| chr4:15521585
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1149+4829G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15521585 | ||||||
| chr4:15522106
|
C | T | 1 | a0001c0008t0002g0269 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1150-5341C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522106 | ||||||
| chr4:15522155
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1150-5292C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522155 | ||||||
| chr4:15522167
|
C | T | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1150-5280C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522167 | ||||||
| chr4:15522176
|
G | A | 8 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-5271G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522176 | ||||||
| chr4:15522230
|
C | T | 8 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(5): Show | 8 | HG02145.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-5217C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522230 | ||||||
| chr4:15522292
|
G | A | 3 | a0001c0001t0001g0249a0001c0001t0002g0242a0001c0001t0002g0338 | 3 | HG02451.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-5155G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522292 | ||||||
| chr4:15522343
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1150-5104C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522343 | ||||||
| chr4:15522415
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1150-5032A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522415 | ||||||
| chr4:15522508
|
G | GT | 6 | a0001c0001t0001g0299a0001c0001t0002g0025a0001c0001t0002g0032others(3): Show | 6 | HG01106.hp1 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-4927dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15522508 | |||||
| chr4:15522508
|
GT | G | 55 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(52): Show | 56 | HG00099.hp2 HG00733.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.1150-4927delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15522508 | |||||
| chr4:15522540
|
G | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1150-4907G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522540 | ||||||
| chr4:15522632
|
T | A | 1 | a0001c0002t0002g0227 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1150-4815T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522632 | ||||||
| chr4:15522901
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1150-4546C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522901 | ||||||
| chr4:15522947
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1150-4500G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522947 | ||||||
| chr4:15522985
|
A | G | 185 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0045others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1150-4462A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15522985 | ||||||
| chr4:15523031
|
T | G | 1 | a0002c0003t0002g0293 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1150-4416T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15523031 | ||||||
| chr4:15523114
|
CA | C | 46 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(43): Show | 46 | HG00323.hp1 HG00733.hp2 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1150-4318delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15523114 | |||||
| chr4:15523180
|
G | GTCCT | 52 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(49): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1150-4245_1150-424 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15523180 | |||||
| chr4:15523180
|
GTCCT | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0029others(1): Show | 4 | HG02630.hp2 HG03471.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-4245_1150-424 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15523180 | |||||
| chr4:15523248
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1150-4199G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15523248 | ||||||
| chr4:15523487
|
C | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0282 | 2 | HG02615.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1150-3960C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15523487 | ||||||
| chr4:15524171
|
T | G | 1 | a0019c0028t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1150-3276T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524171 | ||||||
| chr4:15524229
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1150-3218G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524229 | ||||||
| chr4:15524281
|
C | T | 1 | a0001c0001t0001g0181 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1150-3166C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524281 | ||||||
| chr4:15524295
|
G | A | 2 | a0007c0012t0002g0015a0007c0012t0002g0026 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1150-3152G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524295 | ||||||
| chr4:15524428
|
G | GCCTTCTG others(334): Show |
1 | a0001c0001t0001g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1150-3002_1150-300 others(345): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524428 | |||||
| chr4:15524447
|
A | AT | 8 | a0001c0001t0001g0166a0001c0001t0001g0216a0001c0001t0002g0130others(5): Show | 8 | HG01978.hp1 HG02027.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-2979dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | |||||
| chr4:15524447
|
A | ATTTTTTT | 46 | a0001c0001t0001g0006a0001c0001t0001g0063a0001c0001t0001g0282others(43): Show | 46 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.1150-2985_1150-297 others(11): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | |||||
| chr4:15524447
|
A | ATTTTTTT others(1): Show |
10 | a0001c0001t0001g0078a0001c0001t0001g0084a0001c0001t0001g0105others(7): Show | 10 | HG00621.hp2 HG01952.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150-2986_1150-297 others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | |||||
| chr4:15524447
|
AT | A | 52 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(49): Show | 52 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.1150-2979delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | |||||
| chr4:15524447
|
ATTTT | A | 23 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049others(20): Show | 24 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1150-2982_1150-297 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | INFO_REALIGN_3_PRIME | chr4 | 15524447 | |||||
| chr4:15524512
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1150-2935G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524512 | ||||||
| chr4:15524543
|
C | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0146others(59): Show | 62 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1150-2904C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524543 | ||||||
| chr4:15524595
|
T | C | 7 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150-2852T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524595 | ||||||
| chr4:15524610
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1150-2837T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524610 | ||||||
| chr4:15524652
|
C | T | 3 | a0001c0002t0002g0284a0001c0002t0002g0295a0001c0002t0002g0296 | 3 | NA18942.hp2 NA18945.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1150-2795C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524652 | ||||||
| chr4:15524653
|
G | A | 87 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(84): Show | 88 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1150-2794G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524653 | ||||||
| chr4:15524663
|
G | A | 255 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.1150-2784G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524663 | ||||||
| chr4:15524672
|
C | A | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-2775C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524672 | ||||||
| chr4:15524673
|
G | A | 50 | a0001c0001t0001g0005a0001c0001t0002g0024a0001c0004t0002g0033others(47): Show | 50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1150-2774G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524673 | ||||||
| chr4:15524702
|
T | C | 1 | a0001c0001t0001g0340 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1150-2745T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524702 | ||||||
| chr4:15524740
|
C | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0071 | 2 | HG01099.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1150-2707C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524740 | ||||||
| chr4:15524743
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1150-2704A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15524743 | ||||||
| chr4:15525420
|
A | T | 52 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(49): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1150-2027A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525420 | ||||||
| chr4:15525423
|
C | G | 1 | a0001c0004t0002g0133 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1150-2024C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525423 | ||||||
| chr4:15525453
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1150-1994G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525453 | ||||||
| chr4:15525474
|
A | T | 183 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0045others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1150-1973A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525474 | ||||||
| chr4:15525475
|
A | C | 183 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0045others(180): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1150-1972A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525475 | ||||||
| chr4:15525476
|
T | G | 22 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0049others(19): Show | 23 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150-1971T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525476 | ||||||
| chr4:15525555
|
T | G | 1 | a0002c0003t0001g0318 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1150-1892T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525555 | ||||||
| chr4:15525726
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1150-1721C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525726 | ||||||
| chr4:15525865
|
T | C | 2 | a0001c0004t0002g0087a0001c0004t0002g0285 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1150-1582T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15525865 | ||||||
| chr4:15526185
|
A | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1150-1262A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526185 | ||||||
| chr4:15526274
|
AC | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1150-1172delC | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526274 | ||||||
| chr4:15526440
|
C | A | 1 | a0001c0002t0002g0227 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1150-1007C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526440 | ||||||
| chr4:15526656
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1150-791A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526656 | ||||||
| chr4:15526741
|
C | T | 47 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(44): Show | 47 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(44): Show |
intron_variant | MODIFIER | c.1150-706C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526741 | ||||||
| chr4:15526764
|
C | A | 44 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1150-683C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526764 | ||||||
| chr4:15526833
|
C | A | 44 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(41): Show | 44 | HG00733.hp2 HG00735.hp1 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.1150-614C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15526833 | ||||||
| chr4:15527106
|
T | G | 1 | a0002c0003t0001g0308 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1150-341T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15527106 | ||||||
| chr4:15527171
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1150-276G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15527171 | ||||||
| chr4:15527289
|
C | T | 3 | a0001c0001t0001g0249a0001c0001t0002g0242a0001c0001t0002g0338 | 3 | HG02451.hp1 HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1150-158C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 11/36 | chr4 | 15527289 | ||||||
| chr4:15527682
|
T | A | 1 | a0001c0006t0002g0327 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1359+26T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15527682 | ||||||
| chr4:15527760
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1359+104C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15527760 | ||||||
| chr4:15528468
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1360-152A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528468 | ||||||
| chr4:15528501
|
C | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1360-119C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528501 | ||||||
| chr4:15528505
|
C | T | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1360-115C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528505 | ||||||
| chr4:15528528
|
A | G | 1 | a0002c0003t0001g0320 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1360-92A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 12/36 | chr4 | 15528528 | ||||||
| chr4:15528957
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0042 | 3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1466+231C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15528957 | ||||||
| chr4:15529163
|
T | C | 1 | a0001c0001t0002g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1466+437T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529163 | ||||||
| chr4:15529262
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1466+536G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529262 | ||||||
| chr4:15529378
|
A | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1466+652A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529378 | ||||||
| chr4:15529381
|
C | CA | 9 | a0001c0001t0001g0143a0001c0001t0001g0203a0001c0001t0002g0025others(6): Show | 9 | HG00741.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1466+668dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529381 | |||||
| chr4:15529483
|
A | G | 1 | a0001c0001t0001g0218 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1466+757A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529483 | ||||||
| chr4:15529650
|
T | C | 2 | a0005c0009t0002g0113a0005c0009t0002g0114 | 2 | NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1466+924T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529650 | ||||||
| chr4:15529673
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1466+947G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529673 | ||||||
| chr4:15529685
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1466+959T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529685 | ||||||
| chr4:15529816
|
C | CT | 6 | a0001c0001t0001g0201a0001c0001t0001g0205a0001c0001t0001g0226others(3): Show | 6 | HG00280.hp2 HG01978.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.1466+1102dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529816 | |||||
| chr4:15529843
|
CATTT | C | 63 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0146others(60): Show | 63 | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1466+1127_1466+113 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529843 | |||||
| chr4:15529878
|
ATTTTTTA others(8): Show |
A | 1 | a0001c0001t0002g0280 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1466+1159_1466+117 others(19): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529878 | |||||
| chr4:15529892
|
AT | A | 75 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 76 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.1466+1174delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529892 | |||||
| chr4:15529900
|
T | A | 3 | a0001c0006t0001g0278a0001c0006t0001g0325a0001c0024t0002g0098 | 3 | HG00408.hp1 HG02647.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1466+1174T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15529900 | ||||||
| chr4:15529904
|
TTTATTA | T | 48 | a0001c0001t0001g0108a0002c0003t0001g0148a0002c0003t0001g0214others(45): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1466+1185_1466+119 others(10): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15529904 | |||||
| chr4:15530003
|
ACT | A | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1466+1280_1466+128 others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15530003 | |||||
| chr4:15530038
|
T | C | 2 | a0001c0002t0002g0069a0001c0002t0002g0155 | 2 | HG01106.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.1466+1312T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530038 | ||||||
| chr4:15530041
|
G | C | 1 | a0001c0002t0002g0155 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1466+1315G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530041 | ||||||
| chr4:15530083
|
C | T | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1466+1357C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530083 | ||||||
| chr4:15530086
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1466+1360C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530086 | ||||||
| chr4:15530113
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1466+1387A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530113 | ||||||
| chr4:15530164
|
C | G | 2 | a0007c0012t0002g0015a0007c0012t0002g0026 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1466+1438C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530164 | ||||||
| chr4:15530183
|
A | G | 3 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0002g0130 | 3 | HG02145.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1466+1457A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530183 | ||||||
| chr4:15530207
|
G | A | 2 | a0001c0001t0001g0298a0001c0001t0001g0314 | 2 | HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1466+1481G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530207 | ||||||
| chr4:15530933
|
C | A | 1 | a0002c0003t0001g0308 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1466+2207C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15530933 | ||||||
| chr4:15531241
|
G | A | 40 | a0001c0001t0001g0224a0001c0001t0001g0282a0002c0003t0001g0148others(37): Show | 40 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1467-1952G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531241 | ||||||
| chr4:15531342
|
C | G | 26 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(23): Show | 27 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1467-1851C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531342 | ||||||
| chr4:15531414
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1467-1779C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531414 | ||||||
| chr4:15531446
|
C | T | 40 | a0001c0001t0001g0224a0001c0001t0001g0282a0002c0003t0001g0148others(37): Show | 40 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1467-1747C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531446 | ||||||
| chr4:15531646
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1467-1547C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531646 | ||||||
| chr4:15531713
|
C | T | 5 | a0002c0003t0001g0276a0002c0003t0002g0275a0002c0003t0002g0315others(2): Show | 5 | HG01255.hp1 HG01257.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1467-1480C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531713 | ||||||
| chr4:15531900
|
G | A | 4 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0212others(1): Show | 4 | NA18612.hp1 NA18953.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467-1293G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15531900 | ||||||
| chr4:15532218
|
G | T | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1467-975G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532218 | ||||||
| chr4:15532348
|
C | T | 65 | a0001c0001t0001g0146a0001c0002t0001g0068a0001c0002t0001g0150others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.1467-845C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532348 | ||||||
| chr4:15532489
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1467-704T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532489 | ||||||
| chr4:15532492
|
A | T | 1 | a0002c0003t0001g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1467-701A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532492 | ||||||
| chr4:15532668
|
G | A | 1 | a0001c0001t0002g0333 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1467-525G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15532668 | ||||||
| chr4:15533023
|
C | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1467-170C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15533023 | ||||||
| chr4:15533029
|
GACATCCT others(9): Show |
G | 7 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(4): Show | 7 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1467-159_1467-144d others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | INFO_REALIGN_3_PRIME | chr4 | 15533029 | |||||
| chr4:15533090
|
G | A | 40 | a0001c0001t0001g0224a0001c0001t0001g0282a0002c0003t0001g0148others(37): Show | 40 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1467-103G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 13/36 | chr4 | 15533090 | ||||||
| chr4:15533373
|
T | C | 1 | a0003c0007t0002g0191 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1607+40T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15533373 | ||||||
| chr4:15533472
|
A | G | 313 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(310): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.1607+139A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15533472 | ||||||
| chr4:15533598
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1607+265A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15533598 | ||||||
| chr4:15534114
|
G | A | 1 | a0001c0004t0002g0177 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1607+781G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534114 | ||||||
| chr4:15534216
|
T | C | 2 | a0001c0004t0002g0087a0001c0004t0002g0285 | 2 | HG02109.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1607+883T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534216 | ||||||
| chr4:15534589
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1607+1256G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534589 | ||||||
| chr4:15534628
|
T | C | 5 | a0001c0001t0001g0220a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG00639.hp2 HG01070.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1607+1295T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534628 | ||||||
| chr4:15534883
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1607+1550A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15534883 | ||||||
| chr4:15535005
|
G | GA | 11 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0067others(8): Show | 11 | HG02027.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1607+1682dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | INFO_REALIGN_3_PRIME | chr4 | 15535005 | |||||
| chr4:15535155
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1608-1765T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15535155 | ||||||
| chr4:15535218
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1608-1702C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15535218 | ||||||
| chr4:15535401
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1608-1519C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15535401 | ||||||
| chr4:15536084
|
C | T | 1 | a0001c0001t0001g0184 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1608-836C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536084 | ||||||
| chr4:15536089
|
G | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1608-831G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536089 | ||||||
| chr4:15536144
|
C | A | 2 | a0004c0022t0002g0030a0012c0021t0002g0037 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1608-776C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536144 | ||||||
| chr4:15536307
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1608-613G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536307 | ||||||
| chr4:15536341
|
G | A | 49 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.1608-579G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536341 | ||||||
| chr4:15536349
|
C | T | 1 | a0001c0002t0002g0254 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1608-571C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536349 | ||||||
| chr4:15536354
|
T | C | 43 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(40): Show | 43 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1608-566T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536354 | ||||||
| chr4:15536563
|
T | C | 1 | a0001c0001t0001g0183 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1608-357T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536563 | ||||||
| chr4:15536761
|
A | C | 10 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0067others(7): Show | 10 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.1608-159A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536761 | ||||||
| chr4:15536768
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1608-152T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536768 | ||||||
| chr4:15536800
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1608-120T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 14/36 | chr4 | 15536800 | ||||||
| chr4:15537121
|
T | G | 262 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1764+45T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537121 | ||||||
| chr4:15537299
|
G | T | 144 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0051others(141): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1764+223G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537299 | ||||||
| chr4:15537576
|
G | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1765-323G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537576 | ||||||
| chr4:15537579
|
T | C | 43 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(40): Show | 43 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1765-320T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537579 | ||||||
| chr4:15537830
|
A | G | 45 | a0001c0001t0001g0063a0001c0001t0001g0078a0001c0001t0001g0084others(42): Show | 45 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.1765-69A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537830 | ||||||
| chr4:15537875
|
A | G | 146 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0051others(143): Show | 147 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1765-24A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 15/36 | chr4 | 15537875 | ||||||
| chr4:15538156
|
C | T | 26 | a0001c0001t0001g0006a0001c0001t0001g0045a0001c0001t0001g0046others(23): Show | 27 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2003+19C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538156 | ||||||
| chr4:15538234
|
C | T | 3 | a0002c0003t0001g0313a0002c0005t0001g0031a0002c0005t0001g0036 | 3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2003+97C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538234 | ||||||
| chr4:15538521
|
C | T | 1 | a0001c0001t0002g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2003+384C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538521 | ||||||
| chr4:15538663
|
A | T | 314 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(311): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2003+526A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538663 | ||||||
| chr4:15538857
|
G | A | 8 | a0001c0002t0002g0192a0001c0002t0002g0233a0001c0002t0002g0284others(5): Show | 8 | NA18942.hp2 NA18945.hp1 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.2003+720G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538857 | ||||||
| chr4:15538867
|
A | G | 262 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(259): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2003+730A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538867 | ||||||
| chr4:15538915
|
C | G | 50 | a0001c0001t0001g0003a0001c0001t0001g0062a0001c0001t0001g0070others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.2003+778C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15538915 | ||||||
| chr4:15539099
|
A | G | 1 | a0001c0002t0002g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2003+962A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539099 | ||||||
| chr4:15539458
|
C | T | 1 | a0001c0001t0002g0333 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2003+1321C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539458 | ||||||
| chr4:15539522
|
C | G | 1 | a0001c0001t0001g0110 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2004-1315C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539522 | ||||||
| chr4:15539553
|
T | G | 3 | a0001c0008t0002g0331a0001c0008t0002g0332a0001c0008t0002g0336 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2004-1284T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539553 | ||||||
| chr4:15539772
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2004-1065T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539772 | ||||||
| chr4:15539969
|
A | C | 1 | a0022c0014t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2004-868A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539969 | ||||||
| chr4:15539986
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.2004-851G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15539986 | ||||||
| chr4:15540045
|
A | C | 1 | a0003c0007t0002g0236 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2004-792A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540045 | ||||||
| chr4:15540101
|
T | C | 5 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0028others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.2004-736T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540101 | ||||||
| chr4:15540136
|
A | C | 6 | a0001c0001t0001g0224a0001c0001t0001g0282a0001c0001t0002g0130others(3): Show | 6 | HG01433.hp2 HG02145.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.2004-701A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540136 | ||||||
| chr4:15540159
|
A | C | 1 | a0009c0018t0002g0043 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2004-678A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540159 | ||||||
| chr4:15540288
|
G | GT | 6 | a0001c0001t0001g0077a0001c0001t0002g0130a0002c0003t0001g0148others(3): Show | 6 | HG01433.hp2 HG02145.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2004-538dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | INFO_REALIGN_3_PRIME | chr4 | 15540288 | |||||
| chr4:15540574
|
A | G | 78 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(75): Show | 78 | HG00733.hp2 HG00741.hp2 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.2004-263A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540574 | ||||||
| chr4:15540623
|
A | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0044a0001c0001t0002g0016others(1): Show | 4 | HG03195.hp1 HG03209.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2004-214A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540623 | ||||||
| chr4:15540788
|
T | A | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2004-49T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540788 | ||||||
| chr4:15540825
|
C | A | 1 | a0002c0003t0001g0337 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2004-12C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 16/36 | chr4 | 15540825 | ||||||
| chr4:15541159
|
A | G | 63 | a0001c0001t0002g0244a0001c0001t0002g0286a0001c0002t0001g0150others(60): Show | 63 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.2181+145A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541159 | ||||||
| chr4:15541212
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2181+198G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541212 | ||||||
| chr4:15541297
|
C | T | 1 | a0003c0010t0002g0152 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2181+283C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541297 | ||||||
| chr4:15541339
|
T | A | 26 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0029others(23): Show | 26 | HG00639.hp1 HG01891.hp1 HG02258.hp2 others(23): Show |
intron_variant | MODIFIER | c.2181+325T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541339 | ||||||
| chr4:15541388
|
C | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(112): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2181+374C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541388 | ||||||
| chr4:15541601
|
G | A | 1 | a0015c0031t0001g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2181+587G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541601 | ||||||
| chr4:15541668
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2181+654A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541668 | ||||||
| chr4:15541744
|
A | G | 2 | a0001c0001t0001g0228a0015c0031t0001g0316 | 2 | HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2181+730A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15541744 | ||||||
| chr4:15542045
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0001g0249 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2181+1031C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542045 | ||||||
| chr4:15542282
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1268G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542282 | ||||||
| chr4:15542299
|
A | G | 1 | a0002c0005t0001g0081 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2181+1285A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542299 | ||||||
| chr4:15542437
|
C | A | 1 | a0001c0001t0002g0001 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2181+1423C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542437 | ||||||
| chr4:15542540
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1526A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542540 | ||||||
| chr4:15542777
|
G | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2181+1763G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542777 | ||||||
| chr4:15542853
|
C | T | 312 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(309): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2181+1839C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542853 | ||||||
| chr4:15542917
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2181+1903C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15542917 | ||||||
| chr4:15543093
|
C | T | 1 | a0001c0001t0001g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2181+2079C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543093 | ||||||
| chr4:15543172
|
A | T | 1 | a0002c0003t0001g0303 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2181+2158A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543172 | ||||||
| chr4:15543316
|
G | A | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+2302G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543316 | ||||||
| chr4:15543693
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2181+2679C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543693 | ||||||
| chr4:15543787
|
G | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(51): Show | 55 | HG00323.hp2 HG00741.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.2181+2773G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543787 | ||||||
| chr4:15543908
|
C | T | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+2894C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15543908 | ||||||
| chr4:15544043
|
T | C | 5 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(2): Show | 5 | NA18945.hp2 NA18994.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.2181+3029T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544043 | ||||||
| chr4:15544060
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2181+3046A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544060 | ||||||
| chr4:15544073
|
GAAGCCTC others(7): Show |
G | 1 | a0001c0001t0001g0184 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2181+3060_2181+307 others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544073 | ||||||
| chr4:15544107
|
C | T | 1 | a0001c0024t0002g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2181+3093C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544107 | ||||||
| chr4:15544118
|
G | A | 1 | a0001c0006t0002g0327 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2181+3104G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544118 | ||||||
| chr4:15544239
|
C | T | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2181+3225C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544239 | ||||||
| chr4:15544443
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2181+3429C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544443 | ||||||
| chr4:15544471
|
A | T | 1 | a0001c0001t0001g0297 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2181+3457A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544471 | ||||||
| chr4:15544586
|
A | G | 1 | a0001c0004t0002g0158 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2181+3572A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544586 | ||||||
| chr4:15544590
|
C | A | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2181+3576C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544590 | ||||||
| chr4:15544643
|
C | A | 1 | a0001c0001t0002g0286 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2181+3629C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544643 | ||||||
| chr4:15544790
|
A | T | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2181+3776A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544790 | ||||||
| chr4:15544926
|
T | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 19 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2181+3912T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15544926 | ||||||
| chr4:15545042
|
G | A | 1 | a0001c0002t0002g0050 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2181+4028G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545042 | ||||||
| chr4:15545511
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0029others(1): Show | 4 | HG02630.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2181+4497G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545511 | ||||||
| chr4:15545514
|
T | A | 1 | a0001c0004t0002g0239 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2181+4500T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545514 | ||||||
| chr4:15545514
|
T | C | 1 | a0001c0004t0002g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2181+4500T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545514 | ||||||
| chr4:15545691
|
C | A | 106 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0244others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2181+4677C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545691 | ||||||
| chr4:15545710
|
AATGGGAA others(1): Show |
A | 151 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.2181+4706_2181+471 others(12): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15545710 | |||||
| chr4:15545715
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2181+4701G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545715 | ||||||
| chr4:15545752
|
A | G | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2181+4738A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545752 | ||||||
| chr4:15545869
|
G | T | 1 | a0002c0003t0001g0320 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2181+4855G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545869 | ||||||
| chr4:15545890
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2181+4876C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545890 | ||||||
| chr4:15545985
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2182-4839C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15545985 | ||||||
| chr4:15546086
|
G | C | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-4738G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546086 | ||||||
| chr4:15546281
|
C | T | 3 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0042 | 3 | HG02970.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2182-4543C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546281 | ||||||
| chr4:15546636
|
G | A | 1 | a0001c0015t0001g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2182-4188G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546636 | ||||||
| chr4:15546688
|
C | T | 35 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(32): Show | 35 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2182-4136C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546688 | ||||||
| chr4:15546792
|
C | T | 40 | a0001c0001t0001g0096a0001c0004t0002g0033a0001c0004t0002g0039others(37): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.2182-4032C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546792 | ||||||
| chr4:15546793
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2182-4031G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546793 | ||||||
| chr4:15546892
|
A | C | 3 | a0002c0003t0001g0313a0002c0005t0001g0031a0002c0005t0001g0036 | 3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2182-3932A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546892 | ||||||
| chr4:15546905
|
T | G | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2182-3919T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546905 | ||||||
| chr4:15546927
|
T | C | 111 | a0001c0001t0001g0096a0001c0001t0001g0220a0001c0001t0001g0264others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2182-3897T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15546927 | ||||||
| chr4:15547093
|
A | C | 156 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2182-3731A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547093 | ||||||
| chr4:15547340
|
T | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2182-3484T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547340 | ||||||
| chr4:15547362
|
G | T | 18 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(15): Show | 19 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.2182-3462G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547362 | ||||||
| chr4:15547611
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2182-3213C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547611 | ||||||
| chr4:15547628
|
T | C | 156 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(153): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.2182-3196T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547628 | ||||||
| chr4:15547630
|
G | A | 5 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2182-3194G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547630 | ||||||
| chr4:15547646
|
A | C | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2182-3178A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547646 | ||||||
| chr4:15547672
|
A | T | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-3152A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547672 | ||||||
| chr4:15547757
|
T | C | 5 | a0002c0003t0002g0247a0002c0003t0002g0268a0002c0003t0002g0288others(2): Show | 5 | NA18951.hp1 NA18974.hp1 NA19006.hp1 others(2): Show |
intron_variant | MODIFIER | c.2182-3067T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547757 | ||||||
| chr4:15547988
|
G | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-2836G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15547988 | ||||||
| chr4:15548070
|
G | T | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2182-2754G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548070 | ||||||
| chr4:15548121
|
A | AT | 117 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(114): Show | 118 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2182-2690dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15548121 | |||||
| chr4:15548145
|
G | C | 4 | a0001c0001t0001g0188a0001c0001t0001g0213a0001c0001t0001g0217others(1): Show | 4 | HG02602.hp1 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2182-2679G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548145 | ||||||
| chr4:15548147
|
T | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2182-2677T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548147 | ||||||
| chr4:15548148
|
A | G | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2182-2676A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548148 | ||||||
| chr4:15548155
|
G | A | 66 | a0001c0001t0002g0024a0001c0001t0002g0244a0001c0001t0002g0286others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2182-2669G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548155 | ||||||
| chr4:15548161
|
T | A | 1 | a0001c0006t0001g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2182-2663T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548161 | ||||||
| chr4:15548179
|
G | A | 1 | a0001c0024t0002g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2182-2645G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548179 | ||||||
| chr4:15548187
|
T | C | 1 | a0001c0001t0001g0201 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2182-2637T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548187 | ||||||
| chr4:15548281
|
C | T | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-2543C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548281 | ||||||
| chr4:15548362
|
C | T | 106 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0244others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2182-2462C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548362 | ||||||
| chr4:15548487
|
A | C | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-2337A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15548487 | ||||||
| chr4:15548570
|
C | CA | 74 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(71): Show | 75 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2182-2240dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15548570 | |||||
| chr4:15548570
|
CA | C | 7 | a0001c0001t0001g0104a0001c0001t0001g0228a0001c0001t0001g0324others(4): Show | 7 | HG02559.hp1 HG02683.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2182-2240delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | INFO_REALIGN_3_PRIME | chr4 | 15548570 | |||||
| chr4:15549041
|
T | C | 1 | a0019c0028t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2182-1783T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549041 | ||||||
| chr4:15549484
|
G | T | 1 | a0001c0001t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2182-1340G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549484 | ||||||
| chr4:15549506
|
A | C | 6 | a0004c0013t0003g0134a0004c0013t0003g0135a0004c0022t0002g0030others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2182-1318A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549506 | ||||||
| chr4:15549664
|
G | A | 16 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0022others(13): Show | 16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2182-1160G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549664 | ||||||
| chr4:15549675
|
C | T | 65 | a0001c0001t0002g0244a0001c0001t0002g0286a0001c0002t0001g0283others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.2182-1149C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549675 | ||||||
| chr4:15549693
|
C | T | 106 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0244others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2182-1131C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549693 | ||||||
| chr4:15549732
|
G | A | 2 | a0002c0003t0001g0303a0002c0003t0001g0320 | 2 | NA18960.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2182-1092G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15549732 | ||||||
| chr4:15550159
|
G | T | 1 | a0001c0024t0002g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2182-665G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550159 | ||||||
| chr4:15550176
|
G | A | 3 | a0001c0001t0002g0012a0001c0001t0002g0022a0010c0025t0002g0019 | 3 | HG02622.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2182-648G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550176 | ||||||
| chr4:15550335
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2182-489C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550335 | ||||||
| chr4:15550443
|
T | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2182-381T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550443 | ||||||
| chr4:15550495
|
G | A | 39 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(36): Show | 39 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2182-329G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550495 | ||||||
| chr4:15550575
|
T | C | 115 | a0001c0001t0001g0096a0001c0001t0001g0220a0001c0001t0001g0228others(112): Show | 115 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.2182-249T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550575 | ||||||
| chr4:15550672
|
A | G | 39 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(36): Show | 39 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2182-152A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550672 | ||||||
| chr4:15550800
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(37): Show | 40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2182-24C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 17/36 | chr4 | 15550800 | ||||||
| chr4:15551396
|
A | G | 40 | a0001c0001t0001g0096a0001c0004t0002g0033a0001c0004t0002g0039others(37): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.2338+416A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551396 | ||||||
| chr4:15551403
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2338+423C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551403 | ||||||
| chr4:15551448
|
T | C | 5 | a0001c0001t0001g0085a0001c0001t0001g0117a0001c0001t0001g0140others(2): Show | 5 | HG00741.hp2 HG03239.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338+468T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551448 | ||||||
| chr4:15551496
|
T | A | 8 | a0003c0007t0002g0159a0003c0007t0002g0160a0003c0007t0002g0161others(5): Show | 8 | HG00140.hp1 HG01070.hp2 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.2338+516T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551496 | ||||||
| chr4:15551505
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2338+525T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551505 | ||||||
| chr4:15551520
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2338+540C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551520 | ||||||
| chr4:15551608
|
C | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2338+628C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551608 | ||||||
| chr4:15551652
|
T | C | 2 | a0001c0002t0002g0082a0001c0002t0002g0094 | 2 | HG00408.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2338+672T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551652 | ||||||
| chr4:15551829
|
T | C | 1 | a0002c0003t0001g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2338+849T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15551829 | ||||||
| chr4:15552127
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2339-1031G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552127 | ||||||
| chr4:15552148
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2339-1010G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552148 | ||||||
| chr4:15552246
|
T | G | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2339-912T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552246 | ||||||
| chr4:15552344
|
A | C | 1 | a0001c0004t0002g0174 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2339-814A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552344 | ||||||
| chr4:15552345
|
G | A | 1 | a0001c0001t0001g0101 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2339-813G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552345 | ||||||
| chr4:15552403
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2339-755A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552403 | ||||||
| chr4:15552458
|
T | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2339-700T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552458 | ||||||
| chr4:15552534
|
A | G | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2339-624A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552534 | ||||||
| chr4:15552596
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2339-562T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15552596 | ||||||
| chr4:15553077
|
G | C | 1 | a0001c0006t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2339-81G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 18/36 | chr4 | 15553077 | ||||||
| chr4:15553445
|
GGTAAAAA others(8): Show |
G | 9 | a0001c0001t0001g0093a0002c0003t0001g0246a0002c0005t0001g0002others(6): Show | 9 | HG00609.hp2 HG02132.hp1 NA19005.hp2 others(6): Show |
intron_variant | MODIFIER | c.2486+143_2486+157d others(17): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | INFO_REALIGN_3_PRIME | chr4 | 15553445 | |||||
| chr4:15553474
|
C | T | 1 | a0001c0006t0002g0327 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2486+169C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553474 | ||||||
| chr4:15553528
|
G | A | 1 | a0002c0003t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2486+223G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553528 | ||||||
| chr4:15553919
|
T | C | 1 | a0022c0014t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2486+614T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553919 | ||||||
| chr4:15553934
|
C | T | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2486+629C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15553934 | ||||||
| chr4:15554034
|
G | A | 1 | a0001c0006t0002g0100 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2486+729G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554034 | ||||||
| chr4:15554057
|
A | G | 14 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2486+752A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554057 | ||||||
| chr4:15554063
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2486+758A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554063 | ||||||
| chr4:15554360
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2487-712G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554360 | ||||||
| chr4:15554361
|
C | T | 1 | a0001c0001t0001g0282 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2487-711C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554361 | ||||||
| chr4:15554422
|
G | A | 66 | a0001c0001t0002g0024a0001c0001t0002g0244a0001c0001t0002g0286others(63): Show | 66 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.2487-650G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554422 | ||||||
| chr4:15554573
|
G | A | 16 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0022others(13): Show | 16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2487-499G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554573 | ||||||
| chr4:15554607
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2487-465T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554607 | ||||||
| chr4:15554630
|
C | T | 7 | a0001c0002t0001g0283a0001c0002t0002g0050a0001c0002t0002g0123others(4): Show | 7 | HG00558.hp1 HG02080.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.2487-442C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554630 | ||||||
| chr4:15554641
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2487-431G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554641 | ||||||
| chr4:15554780
|
A | G | 112 | a0001c0001t0001g0096a0001c0001t0001g0220a0001c0001t0001g0264others(109): Show | 112 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.2487-292A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15554780 | ||||||
| chr4:15555061
|
C | G | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2487-11C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 19/36 | chr4 | 15555061 | ||||||
| chr4:15555413
|
C | T | 2 | a0001c0001t0002g0130a0001c0002t0002g0233 | 2 | HG02145.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.2625+203C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555413 | ||||||
| chr4:15555414
|
G | A | 1 | a0001c0024t0002g0098 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2625+204G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555414 | ||||||
| chr4:15555477
|
G | C | 7 | a0002c0003t0001g0274a0002c0003t0001g0302a0002c0003t0001g0308others(4): Show | 7 | HG00558.hp2 HG00597.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.2625+267G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555477 | ||||||
| chr4:15555486
|
T | C | 6 | a0001c0004t0002g0097a0001c0004t0002g0133a0001c0004t0002g0171others(3): Show | 6 | HG00438.hp2 HG02027.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.2625+276T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555486 | ||||||
| chr4:15555721
|
G | C | 1 | a0019c0028t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2625+511G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555721 | ||||||
| chr4:15555819
|
C | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(37): Show | 40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2625+609C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555819 | ||||||
| chr4:15555868
|
A | T | 106 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0244others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2625+658A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15555868 | ||||||
| chr4:15556015
|
T | G | 16 | a0001c0001t0002g0012a0001c0001t0002g0017a0001c0001t0002g0022others(13): Show | 16 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.2625+805T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556015 | ||||||
| chr4:15556290
|
C | T | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-1014C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556290 | ||||||
| chr4:15556332
|
C | T | 1 | a0001c0001t0001g0005 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2626-972C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556332 | ||||||
| chr4:15556454
|
T | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | NA18612.hp2 NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.2626-850T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556454 | ||||||
| chr4:15556497
|
T | C | 2 | a0001c0001t0002g0131a0001c0001t0002g0167 | 2 | NA18974.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.2626-807T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556497 | ||||||
| chr4:15556563
|
C | T | 40 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(37): Show | 40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2626-741C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556563 | ||||||
| chr4:15556609
|
C | G | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-695C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556609 | ||||||
| chr4:15556720
|
C | T | 106 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0244others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2626-584C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556720 | ||||||
| chr4:15556729
|
A | C | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-575A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556729 | ||||||
| chr4:15556744
|
G | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2626-560G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556744 | ||||||
| chr4:15556784
|
T | C | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2626-520T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556784 | ||||||
| chr4:15556895
|
G | T | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2626-409G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15556895 | ||||||
| chr4:15557044
|
G | A | 10 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | HG02055.hp2 NA18945.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.2626-260G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15557044 | ||||||
| chr4:15557045
|
T | C | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-259T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15557045 | ||||||
| chr4:15557223
|
T | A | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2626-81T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | chr4 | 15557223 | ||||||
| chr4:15557262
|
TCTGA | T | 3 | a0001c0002t0002g0157a0001c0002t0002g0230a0001c0002t0002g0231 | 3 | NA19054.hp2 NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.2626-38_2626-35del others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 20/36 | INFO_REALIGN_3_PRIME | chr4 | 15557262 | |||||
| chr4:15557552
|
A | G | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+45A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557552 | ||||||
| chr4:15557748
|
A | C | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+241A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557748 | ||||||
| chr4:15557761
|
A | G | 2 | a0007c0012t0002g0015a0007c0012t0002g0026 | 2 | HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2829+254A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557761 | ||||||
| chr4:15557831
|
G | C | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+324G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557831 | ||||||
| chr4:15557840
|
T | C | 35 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(32): Show | 35 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2829+333T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557840 | ||||||
| chr4:15557884
|
G | T | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+377G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557884 | ||||||
| chr4:15557896
|
A | G | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+389A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557896 | ||||||
| chr4:15557975
|
T | G | 165 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(162): Show | 165 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.2829+468T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15557975 | ||||||
| chr4:15558009
|
C | T | 2 | a0001c0001t0002g0130a0011c0023t0002g0021 | 2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2829+502C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558009 | ||||||
| chr4:15558075
|
T | C | 108 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0130others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.2829+568T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558075 | ||||||
| chr4:15558201
|
A | G | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.2829+694A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558201 | ||||||
| chr4:15558374
|
G | A | 15 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(12): Show | 16 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.2830-791G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558374 | ||||||
| chr4:15558475
|
C | A | 40 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(37): Show | 40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.2830-690C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558475 | ||||||
| chr4:15558702
|
A | C | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2830-463A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558702 | ||||||
| chr4:15558719
|
G | C | 1 | a0001c0001t0001g0265 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2830-446G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558719 | ||||||
| chr4:15558821
|
G | T | 43 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(40): Show | 43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.2830-344G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558821 | ||||||
| chr4:15558881
|
T | C | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2830-284T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558881 | ||||||
| chr4:15558950
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2830-215C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15558950 | ||||||
| chr4:15559008
|
C | G | 155 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(152): Show | 155 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.2830-157C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15559008 | ||||||
| chr4:15559068
|
A | G | 1 | a0001c0006t0002g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2830-97A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15559068 | ||||||
| chr4:15559127
|
G | T | 39 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(36): Show | 39 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.2830-38G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 21/36 | chr4 | 15559127 | ||||||
| chr4:15559469
|
C | A | 14 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.2922+212C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559469 | ||||||
| chr4:15559473
|
A | G | 150 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(147): Show | 150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.2922+216A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559473 | ||||||
| chr4:15559563
|
T | A | 1 | a0002c0005t0001g0116 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2922+306T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559563 | ||||||
| chr4:15559630
|
A | G | 106 | a0001c0001t0001g0096a0001c0001t0002g0024a0001c0001t0002g0244others(103): Show | 106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2922+373A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559630 | ||||||
| chr4:15559660
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2922+403G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559660 | ||||||
| chr4:15559667
|
C | CTGTTTCC others(9): Show |
2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+411_2922+412i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | INFO_REALIGN_3_PRIME | chr4 | 15559667 | |||||
| chr4:15559669
|
T | G | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+412T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559669 | ||||||
| chr4:15559669
|
T | TTTTCCTT others(9): Show |
59 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(56): Show | 59 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.2922+423_2922+424i others(18): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | INFO_REALIGN_3_PRIME | chr4 | 15559669 | |||||
| chr4:15559720
|
A | AC | 61 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(58): Show | 61 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.2922+463_2922+464i others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559720 | ||||||
| chr4:15559865
|
C | T | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+608C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559865 | ||||||
| chr4:15559882
|
A | G | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2922+625A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15559882 | ||||||
| chr4:15560033
|
C | T | 1 | a0001c0002t0002g0157 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2923-498C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15560033 | ||||||
| chr4:15560091
|
C | CA | 111 | a0001c0001t0001g0096a0001c0001t0001g0220a0001c0001t0001g0264others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2923-437dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | INFO_REALIGN_3_PRIME | chr4 | 15560091 | |||||
| chr4:15560390
|
C | T | 13 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(10): Show | 14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2923-141C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 22/36 | chr4 | 15560390 | ||||||
| chr4:15560719
|
C | T | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(40): Show | 43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.3014+97C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560719 | ||||||
| chr4:15560830
|
T | C | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(40): Show | 43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.3014+208T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560830 | ||||||
| chr4:15560844
|
C | G | 43 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(40): Show | 43 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.3014+222C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560844 | ||||||
| chr4:15560903
|
C | T | 4 | a0001c0001t0001g0091a0001c0001t0001g0125a0001c0001t0001g0225others(1): Show | 4 | HG03486.hp1 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3014+281C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15560903 | ||||||
| chr4:15561061
|
T | G | 2 | a0004c0022t0002g0030a0012c0021t0002g0037 | 2 | HG02809.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3014+439T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561061 | ||||||
| chr4:15561084
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3014+462G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561084 | ||||||
| chr4:15561200
|
C | A | 15 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(12): Show | 16 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.3014+578C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561200 | ||||||
| chr4:15561203
|
A | T | 15 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(12): Show | 16 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.3014+581A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561203 | ||||||
| chr4:15561348
|
C | A | 1 | a0007c0012t0002g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3014+726C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561348 | ||||||
| chr4:15561477
|
C | A | 2 | a0001c0001t0001g0146a0011c0023t0002g0021 | 2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3014+855C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561477 | ||||||
| chr4:15561507
|
C | T | 1 | a0019c0028t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3014+885C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561507 | ||||||
| chr4:15561537
|
G | GT | 19 | a0001c0001t0001g0003a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 20 | HG00099.hp1 HG00639.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.3014+925dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | INFO_REALIGN_3_PRIME | chr4 | 15561537 | |||||
| chr4:15561690
|
T | C | 1 | a0001c0002t0001g0150 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.3014+1068T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561690 | ||||||
| chr4:15561747
|
G | A | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3014+1125G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561747 | ||||||
| chr4:15561787
|
T | A | 126 | a0001c0001t0001g0096a0001c0001t0002g0012a0001c0001t0002g0016others(123): Show | 126 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.3014+1165T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561787 | ||||||
| chr4:15561992
|
C | T | 167 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(164): Show | 167 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.3015-1363C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15561992 | ||||||
| chr4:15562258
|
A | G | 1 | a0002c0005t0002g0279 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3015-1097A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562258 | ||||||
| chr4:15562337
|
A | G | 4 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(1): Show | 4 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.3015-1018A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562337 | ||||||
| chr4:15562415
|
A | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3015-940A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562415 | ||||||
| chr4:15562460
|
A | C | 324 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3015-895A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562460 | ||||||
| chr4:15562476
|
G | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3015-879G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562476 | ||||||
| chr4:15562560
|
T | C | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3015-795T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562560 | ||||||
| chr4:15562835
|
C | A | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3015-520C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15562835 | ||||||
| chr4:15563060
|
T | C | 2 | a0001c0001t0002g0072a0001c0001t0002g0103 | 2 | HG00735.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.3015-295T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15563060 | ||||||
| chr4:15563086
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3015-269G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15563086 | ||||||
| chr4:15563192
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3015-163C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 23/36 | chr4 | 15563192 | ||||||
| chr4:15563545
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3182+23G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563545 | ||||||
| chr4:15563585
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3182+63T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563585 | ||||||
| chr4:15563657
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.3182+135A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563657 | ||||||
| chr4:15563961
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3182+439C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15563961 | ||||||
| chr4:15564113
|
A | T | 81 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(78): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.3182+591A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564113 | ||||||
| chr4:15564135
|
C | T | 209 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(206): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.3182+613C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564135 | ||||||
| chr4:15564212
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.3182+690A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564212 | ||||||
| chr4:15564236
|
C | A | 1 | a0001c0001t0001g0298 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3182+714C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564236 | ||||||
| chr4:15564251
|
G | C | 67 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0023others(64): Show | 68 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.3182+729G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564251 | ||||||
| chr4:15564447
|
A | T | 1 | a0001c0006t0002g0219 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3182+925A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564447 | ||||||
| chr4:15564520
|
A | C | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3182+998A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564520 | ||||||
| chr4:15564630
|
C | G | 1 | a0001c0001t0001g0307 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.3182+1108C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564630 | ||||||
| chr4:15564668
|
C | G | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3182+1146C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564668 | ||||||
| chr4:15564812
|
G | A | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3182+1290G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564812 | ||||||
| chr4:15564836
|
C | T | 3 | a0001c0001t0002g0024a0001c0006t0002g0100a0001c0006t0002g0327 | 3 | HG01891.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.3182+1314C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564836 | ||||||
| chr4:15564947
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3182+1425G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15564947 | ||||||
| chr4:15565024
|
G | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.3182+1502G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565024 | ||||||
| chr4:15565070
|
T | C | 2 | a0001c0002t0002g0086a0001c0002t0002g0255 | 2 | HG02056.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3182+1548T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565070 | ||||||
| chr4:15565282
|
T | C | 324 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3182+1760T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565282 | ||||||
| chr4:15565399
|
G | GT | 138 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(135): Show | 140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.3182+1892dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | INFO_REALIGN_3_PRIME | chr4 | 15565399 | |||||
| chr4:15565399
|
G | GTT | 8 | a0001c0001t0001g0040a0001c0001t0001g0209a0001c0001t0001g0226others(5): Show | 8 | HG01123.hp1 HG01243.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.3182+1891_3182+189 others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | INFO_REALIGN_3_PRIME | chr4 | 15565399 | |||||
| chr4:15565399
|
GT | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(34): Show | 37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.3182+1892delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | INFO_REALIGN_3_PRIME | chr4 | 15565399 | |||||
| chr4:15565728
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3183-1649C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565728 | ||||||
| chr4:15565988
|
A | G | 2 | a0001c0002t0001g0283a0001c0002t0002g0234 | 2 | HG02080.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3183-1389A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15565988 | ||||||
| chr4:15566260
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3183-1117C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566260 | ||||||
| chr4:15566286
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3183-1091G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566286 | ||||||
| chr4:15566642
|
C | T | 1 | a0001c0004t0002g0202 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3183-735C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566642 | ||||||
| chr4:15566701
|
G | C | 1 | a0001c0004t0002g0158 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3183-676G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566701 | ||||||
| chr4:15566834
|
G | C | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3183-543G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566834 | ||||||
| chr4:15566968
|
C | T | 5 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3183-409C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566968 | ||||||
| chr4:15566979
|
A | T | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3183-398A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15566979 | ||||||
| chr4:15567084
|
A | C | 1 | a0001c0001t0001g0104 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3183-293A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15567084 | ||||||
| chr4:15567262
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3183-115C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15567262 | ||||||
| chr4:15567369
|
T | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
splice_region_variant&intron_variant | LOW | c.3183-8T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 24/36 | chr4 | 15567369 | ||||||
| chr4:15567523
|
A | C | 216 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(213): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.3288+41A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 25/36 | chr4 | 15567523 | ||||||
| chr4:15567617
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0023 | 2 | HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3289-60G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 25/36 | chr4 | 15567617 | ||||||
| chr4:15567917
|
C | T | 1 | a0001c0001t0002g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3398+131C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15567917 | ||||||
| chr4:15568180
|
T | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3398+394T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15568180 | ||||||
| chr4:15568566
|
C | T | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3399-727C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15568566 | ||||||
| chr4:15568648
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3399-645T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 26/36 | chr4 | 15568648 | ||||||
| chr4:15569480
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3495+91G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569480 | ||||||
| chr4:15569597
|
A | G | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.3495+208A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569597 | ||||||
| chr4:15569600
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3495+211G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569600 | ||||||
| chr4:15569811
|
C | T | 324 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3495+422C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15569811 | ||||||
| chr4:15570141
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3496-257A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 27/36 | chr4 | 15570141 | ||||||
| chr4:15570582
|
C | T | 1 | a0001c0002t0002g0090 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3594+86C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15570582 | ||||||
| chr4:15570748
|
CGGGAGGC others(25): Show |
C | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0146 | 3 | HG02145.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3594+273_3594+304d others(34): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15570748 | |||||
| chr4:15570883
|
A | C | 40 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0013others(37): Show | 40 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.3594+387A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15570883 | ||||||
| chr4:15570909
|
A | C | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3594+413A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15570909 | ||||||
| chr4:15571021
|
C | T | 324 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3594+525C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571021 | ||||||
| chr4:15571092
|
T | A | 1 | a0001c0001t0001g0260 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3594+596T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571092 | ||||||
| chr4:15571430
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3594+934G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571430 | ||||||
| chr4:15571446
|
G | C | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3594+950G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571446 | ||||||
| chr4:15571497
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0143 | 2 | HG00741.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3594+1001C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571497 | ||||||
| chr4:15571606
|
C | CA | 181 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(178): Show | 184 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.3594+1124dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15571606 | |||||
| chr4:15571606
|
C | CAA | 38 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(35): Show | 38 | HG00642.hp1 HG00741.hp1 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.3594+1123_3594+112 others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15571606 | |||||
| chr4:15571884
|
A | G | 2 | a0002c0003t0001g0308a0002c0003t0001g0322 | 2 | HG02015.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.3594+1388A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571884 | ||||||
| chr4:15571895
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3594+1399C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571895 | ||||||
| chr4:15571910
|
C | T | 37 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(34): Show | 37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.3594+1414C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571910 | ||||||
| chr4:15571987
|
C | T | 13 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(10): Show | 14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3594+1491C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15571987 | ||||||
| chr4:15572413
|
T | C | 1 | a0002c0003t0001g0329 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3595-1737T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572413 | ||||||
| chr4:15572433
|
C | T | 3 | a0002c0003t0001g0313a0002c0005t0001g0031a0002c0005t0001g0036 | 3 | HG01433.hp2 HG02976.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3595-1717C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572433 | ||||||
| chr4:15572794
|
G | A | 10 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | HG02055.hp2 NA18945.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.3595-1356G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572794 | ||||||
| chr4:15572843
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3595-1307T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572843 | ||||||
| chr4:15572878
|
G | A | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3595-1272G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15572878 | ||||||
| chr4:15573042
|
T | C | 113 | a0001c0001t0001g0220a0001c0001t0001g0264a0001c0001t0001g0265others(110): Show | 113 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.3595-1108T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573042 | ||||||
| chr4:15573139
|
C | CAAGTT | 324 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3595-1011_3595-101 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573139 | ||||||
| chr4:15573334
|
AGGCTGGA others(18): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.3595-811_3595-787d others(27): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | INFO_REALIGN_3_PRIME | chr4 | 15573334 | |||||
| chr4:15573571
|
G | A | 5 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3595-579G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573571 | ||||||
| chr4:15573598
|
G | A | 1 | a0001c0006t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3595-552G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573598 | ||||||
| chr4:15573801
|
C | T | 13 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(10): Show | 14 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.3595-349C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573801 | ||||||
| chr4:15573893
|
G | A | 3 | a0001c0001t0001g0220a0001c0001t0001g0265a0001c0001t0001g0289 | 3 | HG00639.hp2 HG01074.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.3595-257G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15573893 | ||||||
| chr4:15574039
|
A | T | 1 | a0005c0009t0002g0113 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3595-111A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15574039 | ||||||
| chr4:15574095
|
C | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(211): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.3595-55C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15574095 | ||||||
| chr4:15574128
|
C | T | 108 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0244others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3595-22C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 28/36 | chr4 | 15574128 | ||||||
| chr4:15574581
|
T | G | 1 | a0022c0014t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3771+255T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574581 | ||||||
| chr4:15574641
|
A | G | 173 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.3771+315A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574641 | ||||||
| chr4:15574737
|
C | T | 2 | a0001c0001t0002g0311a0001c0001t0002g0323 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.3771+411C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574737 | ||||||
| chr4:15574762
|
T | G | 6 | a0004c0013t0003g0134a0004c0013t0003g0135a0004c0022t0002g0030others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.3771+436T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574762 | ||||||
| chr4:15574791
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3771+465A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574791 | ||||||
| chr4:15574808
|
T | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3771+482T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574808 | ||||||
| chr4:15574903
|
T | C | 1 | a0001c0002t0002g0169 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3771+577T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574903 | ||||||
| chr4:15574922
|
G | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.3771+596G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15574922 | ||||||
| chr4:15575065
|
T | C | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3771+739T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575065 | ||||||
| chr4:15575341
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3771+1015C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575341 | ||||||
| chr4:15575669
|
T | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+1343T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575669 | ||||||
| chr4:15575702
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 94 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3771+1376A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575702 | ||||||
| chr4:15575726
|
T | A | 1 | a0003c0007t0002g0162 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3771+1400T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575726 | ||||||
| chr4:15575791
|
T | C | 324 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(321): Show | 327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.3771+1465T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575791 | ||||||
| chr4:15575804
|
A | T | 1 | a0002c0005t0001g0139 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.3771+1478A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575804 | ||||||
| chr4:15575893
|
G | A | 1 | a0001c0006t0001g0294 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3771+1567G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575893 | ||||||
| chr4:15575939
|
G | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(167): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.3771+1613G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575939 | ||||||
| chr4:15575964
|
A | G | 173 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.3771+1638A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15575964 | ||||||
| chr4:15576115
|
G | A | 108 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0244others(105): Show | 108 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.3771+1789G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576115 | ||||||
| chr4:15576445
|
T | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(170): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.3771+2119T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576445 | ||||||
| chr4:15576458
|
A | T | 1 | a0005c0009t0002g0113 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.3771+2132A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576458 | ||||||
| chr4:15576622
|
A | G | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(7): Show | 10 | HG01243.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3771+2296A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576622 | ||||||
| chr4:15576623
|
A | T | 10 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(7): Show | 10 | HG01243.hp1 HG02280.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.3771+2297A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576623 | ||||||
| chr4:15576781
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.3771+2455T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576781 | ||||||
| chr4:15576865
|
G | A | 1 | a0002c0003t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3771+2539G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15576865 | ||||||
| chr4:15577122
|
TACTG | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+2797_3771+280 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577122 | ||||||
| chr4:15577128
|
G | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+2802G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577128 | ||||||
| chr4:15577129
|
A | G | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3771+2803A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577129 | ||||||
| chr4:15577428
|
CTTAAT | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3772-2537_3772-253 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15577428 | |||||
| chr4:15577505
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3772-2463T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577505 | ||||||
| chr4:15577577
|
A | G | 4 | a0001c0001t0002g0024a0001c0001t0002g0300a0001c0006t0002g0100others(1): Show | 4 | HG01891.hp2 HG03130.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.3772-2391A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15577577 | ||||||
| chr4:15578093
|
T | G | 1 | a0001c0006t0001g0292 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3772-1875T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578093 | ||||||
| chr4:15578379
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3772-1589G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578379 | ||||||
| chr4:15578395
|
G | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3772-1573G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578395 | ||||||
| chr4:15578787
|
GGTTT | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0137a0002c0003t0001g0308others(1): Show | 4 | HG00323.hp2 HG02015.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.3772-1152_3772-114 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578787 | |||||
| chr4:15578799
|
TG | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0146 | 3 | HG02109.hp2 HG02145.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3772-1168delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578799 | ||||||
| chr4:15578803
|
TGTTTG | T | 3 | a0001c0001t0001g0144a0001c0001t0001g0204a0001c0001t0001g0238 | 3 | HG00642.hp1 HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.3772-1164_3772-116 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578803 | ||||||
| chr4:15578804
|
G | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.3772-1164G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578804 | ||||||
| chr4:15578807
|
TG | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(86): Show | 89 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.3772-1160delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578807 | ||||||
| chr4:15578808
|
G | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0013others(2): Show | 5 | HG02109.hp2 HG02145.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3772-1160G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578808 | ||||||
| chr4:15578811
|
TG | T | 10 | a0001c0001t0001g0229a0001c0001t0002g0286a0001c0002t0002g0089others(7): Show | 10 | HG00438.hp1 HG00597.hp2 HG00733.hp2 others(7): Show |
intron_variant | MODIFIER | c.3772-1156delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578811 | ||||||
| chr4:15578812
|
G | GT | 10 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0062others(7): Show | 11 | HG00099.hp1 HG00733.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.3772-1153dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578812 | |||||
| chr4:15578812
|
G | T | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(94): Show | 97 | HG00408.hp2 HG00558.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.3772-1156G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578812 | ||||||
| chr4:15578815
|
TG | T | 40 | a0001c0001t0001g0324a0001c0001t0002g0016a0001c0004t0002g0039others(37): Show | 40 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.3772-1152delG | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578815 | ||||||
| chr4:15578816
|
G | GT | 19 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0045others(16): Show | 19 | HG00639.hp1 HG02080.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3772-1147dupT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578816 | |||||
| chr4:15578816
|
G | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(129): Show | 134 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.3772-1152G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15578816 | ||||||
| chr4:15578816
|
GT | G | 5 | a0001c0001t0001g0228a0001c0004t0002g0033a0001c0004t0002g0239others(2): Show | 5 | HG00280.hp2 HG02559.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.3772-1147delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15578816 | |||||
| chr4:15579024
|
C | CA | 318 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.3772-936dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | INFO_REALIGN_3_PRIME | chr4 | 15579024 | |||||
| chr4:15579131
|
T | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(90): Show | 94 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.3772-837T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579131 | ||||||
| chr4:15579275
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3772-693G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579275 | ||||||
| chr4:15579635
|
C | T | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.3772-333C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579635 | ||||||
| chr4:15579929
|
T | C | 3 | a0001c0001t0002g0012a0001c0001t0002g0022a0010c0025t0002g0019 | 3 | HG02622.hp2 HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.3772-39T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 29/36 | chr4 | 15579929 | ||||||
| chr4:15580256
|
G | A | 1 | a0001c0004t0002g0087 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3975+85G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580256 | ||||||
| chr4:15580362
|
A | G | 215 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(212): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.3975+191A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580362 | ||||||
| chr4:15580415
|
A | T | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3975+244A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580415 | ||||||
| chr4:15580593
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(169): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.3975+422G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580593 | ||||||
| chr4:15580637
|
C | CA | 69 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 70 | HG00099.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.3975+488dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15580637 | |||||
| chr4:15580637
|
CA | C | 12 | a0001c0001t0001g0042a0001c0001t0001g0188a0001c0001t0001g0235others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.3975+488delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15580637 | |||||
| chr4:15580637
|
CAA | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(134): Show | 137 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.3975+487_3975+488d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15580637 | |||||
| chr4:15580743
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3975+572A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580743 | ||||||
| chr4:15580885
|
A | G | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3975+714A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580885 | ||||||
| chr4:15580994
|
C | T | 2 | a0001c0004t0002g0033a0001c0004t0002g0039 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3975+823C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15580994 | ||||||
| chr4:15581019
|
T | C | 5 | a0001c0001t0001g0220a0001c0001t0001g0264a0001c0001t0001g0265others(2): Show | 5 | HG00639.hp2 HG01070.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.3975+848T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581019 | ||||||
| chr4:15581100
|
A | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0258a0001c0001t0001g0260others(1): Show | 4 | HG00140.hp2 HG00280.hp1 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.3975+929A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581100 | ||||||
| chr4:15581159
|
A | C | 1 | a0001c0001t0001g0261 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.3975+988A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581159 | ||||||
| chr4:15581453
|
C | T | 1 | a0001c0001t0002g0186 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.3975+1282C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581453 | ||||||
| chr4:15581808
|
T | C | 3 | a0001c0002t0002g0089a0001c0002t0002g0090a0001c0002t0002g0155 | 3 | HG01106.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.3975+1637T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15581808 | ||||||
| chr4:15582040
|
A | G | 1 | a0002c0003t0001g0148 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3975+1869A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582040 | ||||||
| chr4:15582224
|
TTAAA | T | 31 | a0001c0004t0002g0087a0001c0004t0002g0097a0001c0004t0002g0133others(28): Show | 31 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.3975+2057_3975+206 others(8): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15582224 | |||||
| chr4:15582292
|
G | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0070a0001c0001t0001g0071others(2): Show | 6 | HG00099.hp1 HG01099.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.3975+2121G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582292 | ||||||
| chr4:15582520
|
G | C | 1 | a0001c0002t0002g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3975+2349G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582520 | ||||||
| chr4:15582562
|
T | C | 40 | a0001c0004t0002g0033a0001c0004t0002g0039a0001c0004t0002g0087others(37): Show | 40 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.3975+2391T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582562 | ||||||
| chr4:15582631
|
C | T | 1 | a0001c0001t0001g0020 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3975+2460C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582631 | ||||||
| chr4:15582960
|
A | G | 4 | a0001c0001t0001g0091a0001c0001t0001g0125a0001c0001t0001g0225others(1): Show | 4 | HG03486.hp1 NA18906.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.3975+2789A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15582960 | ||||||
| chr4:15583185
|
T | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3976-2972T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583185 | ||||||
| chr4:15583328
|
T | C | 1 | a0002c0003t0001g0322 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3976-2829T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583328 | ||||||
| chr4:15583456
|
AACTGTTA others(4): Show |
A | 1 | a0001c0002t0002g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.3976-2700_3976-269 others(15): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583456 | ||||||
| chr4:15583509
|
A | G | 1 | a0001c0001t0002g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3976-2648A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583509 | ||||||
| chr4:15583599
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3976-2558T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583599 | ||||||
| chr4:15583702
|
C | G | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.3976-2455C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583702 | ||||||
| chr4:15583721
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3976-2436G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583721 | ||||||
| chr4:15583724
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0013 | 2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.3976-2433C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583724 | ||||||
| chr4:15583731
|
C | T | 82 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(79): Show | 83 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.3976-2426C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583731 | ||||||
| chr4:15583776
|
C | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3976-2381C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583776 | ||||||
| chr4:15583808
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3976-2349G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583808 | ||||||
| chr4:15583837
|
G | A | 9 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0014others(6): Show | 9 | HG01243.hp1 HG02280.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.3976-2320G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15583837 | ||||||
| chr4:15583950
|
C | CA | 7 | a0001c0001t0001g0023a0001c0001t0002g0024a0001c0001t0002g0130others(4): Show | 7 | HG01891.hp2 HG02132.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.3976-2193dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15583950 | |||||
| chr4:15583960
|
AAAAAG | A | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3976-2182_3976-217 others(9): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | INFO_REALIGN_3_PRIME | chr4 | 15583960 | |||||
| chr4:15584004
|
G | A | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3976-2153G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584004 | ||||||
| chr4:15584032
|
T | C | 3 | a0003c0007t0002g0159a0003c0007t0002g0160a0003c0007t0002g0161 | 3 | HG00140.hp1 HG02486.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.3976-2125T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584032 | ||||||
| chr4:15584124
|
G | A | 14 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.3976-2033G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584124 | ||||||
| chr4:15584198
|
T | A | 1 | a0019c0028t0001g0088 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3976-1959T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584198 | ||||||
| chr4:15584324
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.3976-1833T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584324 | ||||||
| chr4:15584385
|
G | A | 1 | a0001c0001t0002g0025 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3976-1772G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584385 | ||||||
| chr4:15584602
|
G | A | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.3976-1555G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584602 | ||||||
| chr4:15584653
|
A | G | 22 | a0001c0001t0001g0093a0001c0001t0001g0102a0001c0001t0001g0110others(19): Show | 22 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.3976-1504A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584653 | ||||||
| chr4:15584757
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3976-1400G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584757 | ||||||
| chr4:15584971
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3976-1186C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584971 | ||||||
| chr4:15584986
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3976-1171A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15584986 | ||||||
| chr4:15585910
|
A | G | 1 | a0002c0003t0001g0214 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3976-247A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 30/36 | chr4 | 15585910 | ||||||
| chr4:15586274
|
A | T | 323 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.4065+28A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586274 | ||||||
| chr4:15586475
|
A | C | 3 | a0001c0008t0002g0331a0001c0008t0002g0332a0001c0008t0002g0336 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4065+229A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586475 | ||||||
| chr4:15586632
|
T | A | 3 | a0001c0001t0002g0024a0001c0006t0002g0100a0001c0006t0002g0327 | 3 | HG01891.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.4065+386T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586632 | ||||||
| chr4:15586850
|
G | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0146 | 3 | HG02145.hp2 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.4065+604G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15586850 | ||||||
| chr4:15587267
|
C | T | 116 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0025others(113): Show | 116 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.4066-549C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587267 | ||||||
| chr4:15587341
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4066-475T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587341 | ||||||
| chr4:15587567
|
G | A | 6 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(3): Show | 6 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.4066-249G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587567 | ||||||
| chr4:15587648
|
T | C | 1 | a0002c0003t0002g0326 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4066-168T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587648 | ||||||
| chr4:15587691
|
C | G | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.4066-125C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587691 | ||||||
| chr4:15587692
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4066-124G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587692 | ||||||
| chr4:15587722
|
C | T | 111 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0142others(108): Show | 111 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.4066-94C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 31/36 | chr4 | 15587722 | ||||||
| chr4:15588176
|
G | A | 2 | a0001c0004t0002g0033a0001c0004t0002g0039 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4179+247G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588176 | ||||||
| chr4:15588621
|
A | G | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4179+692A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588621 | ||||||
| chr4:15588637
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4179+708T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588637 | ||||||
| chr4:15588744
|
C | G | 37 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(34): Show | 37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.4180-801C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588744 | ||||||
| chr4:15588843
|
G | T | 1 | a0001c0001t0001g0229 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.4180-702G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588843 | ||||||
| chr4:15588979
|
G | A | 5 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4180-566G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15588979 | ||||||
| chr4:15589234
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4180-311C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589234 | ||||||
| chr4:15589288
|
T | C | 1 | a0001c0006t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4180-257T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589288 | ||||||
| chr4:15589348
|
G | C | 1 | a0001c0002t0002g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.4180-197G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589348 | ||||||
| chr4:15589472
|
G | A | 1 | a0001c0002t0002g0231 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.4180-73G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589472 | ||||||
| chr4:15589508
|
T | C | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4180-37T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 32/36 | chr4 | 15589508 | ||||||
| chr4:15589784
|
A | AAT | 139 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(136): Show | 140 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.4314+119_4314+120d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15589784 | |||||
| chr4:15589784
|
A | AATAT | 72 | a0001c0001t0001g0078a0001c0001t0002g0142a0001c0002t0002g0086others(69): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.4314+117_4314+120d others(6): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15589784 | |||||
| chr4:15589800
|
C | T | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.4314+121C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15589800 | ||||||
| chr4:15589821
|
TA | T | 337 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(334): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.4314+146delA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15589821 | |||||
| chr4:15589842
|
C | T | 114 | a0001c0001t0002g0016a0001c0001t0002g0024a0001c0001t0002g0142others(111): Show | 114 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.4314+163C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15589842 | ||||||
| chr4:15589858
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4314+179T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15589858 | ||||||
| chr4:15590091
|
C | A | 1 | a0005c0009t0002g0066 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.4314+412C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590091 | ||||||
| chr4:15590259
|
A | C | 1 | a0002c0003t0001g0334 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4314+580A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590259 | ||||||
| chr4:15590313
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4314+634G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590313 | ||||||
| chr4:15590328
|
A | T | 1 | a0001c0006t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4314+649A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590328 | ||||||
| chr4:15590360
|
C | T | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4314+681C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590360 | ||||||
| chr4:15590475
|
A | G | 1 | a0001c0001t0001g0073 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.4314+796A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590475 | ||||||
| chr4:15590636
|
G | A | 1 | a0001c0001t0001g0007 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4314+957G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590636 | ||||||
| chr4:15590898
|
G | A | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4314+1219G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15590898 | ||||||
| chr4:15591008
|
G | A | 4 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0029others(1): Show | 4 | HG02630.hp2 HG03471.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.4314+1329G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591008 | ||||||
| chr4:15591168
|
T | C | 1 | a0001c0004t0002g0285 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4314+1489T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591168 | ||||||
| chr4:15591219
|
AT | A | 303 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(300): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.4314+1557delT | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | INFO_REALIGN_3_PRIME | chr4 | 15591219 | |||||
| chr4:15591241
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(140): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.4314+1562C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591241 | ||||||
| chr4:15591295
|
A | G | 119 | a0001c0001t0001g0220a0001c0001t0001g0264a0001c0001t0001g0265others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4314+1616A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591295 | ||||||
| chr4:15591313
|
G | A | 1 | a0001c0001t0001g0145 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.4314+1634G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591313 | ||||||
| chr4:15591449
|
C | A | 2 | a0002c0003t0001g0259a0002c0003t0001g0262 | 2 | HG01192.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.4314+1770C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591449 | ||||||
| chr4:15591453
|
A | C | 87 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(84): Show | 88 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.4314+1774A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591453 | ||||||
| chr4:15591509
|
G | A | 1 | a0002c0003t0002g0326 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4314+1830G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591509 | ||||||
| chr4:15591546
|
C | G | 1 | a0001c0001t0002g0001 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.4314+1867C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591546 | ||||||
| chr4:15591569
|
T | C | 1 | a0001c0004t0002g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4314+1890T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591569 | ||||||
| chr4:15591708
|
A | G | 5 | a0001c0001t0002g0025a0001c0001t0002g0032a0001c0001t0002g0038others(2): Show | 5 | HG02257.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4314+2029A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591708 | ||||||
| chr4:15591758
|
A | T | 2 | a0001c0002t0002g0050a0001c0002t0002g0194 | 2 | NA18948.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.4314+2079A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591758 | ||||||
| chr4:15591837
|
T | C | 1 | a0002c0003t0002g0330 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4314+2158T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15591837 | ||||||
| chr4:15592069
|
C | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(140): Show | 145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.4314+2390C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592069 | ||||||
| chr4:15592292
|
A | G | 1 | a0001c0002t0002g0232 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4314+2613A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592292 | ||||||
| chr4:15592339
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.4314+2660A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592339 | ||||||
| chr4:15592676
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0002g0338 | 2 | HG02717.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.4314+2997A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592676 | ||||||
| chr4:15592685
|
T | G | 15 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(12): Show | 16 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(13): Show |
intron_variant | MODIFIER | c.4314+3006T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592685 | ||||||
| chr4:15592920
|
T | C | 26 | a0001c0001t0001g0111a0002c0003t0001g0148a0002c0003t0001g0214others(23): Show | 26 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.4315-3165T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592920 | ||||||
| chr4:15592930
|
G | A | 1 | a0001c0001t0002g0038 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4315-3155G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15592930 | ||||||
| chr4:15593153
|
G | T | 41 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(38): Show | 41 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.4315-2932G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593153 | ||||||
| chr4:15593275
|
T | C | 42 | a0001c0001t0001g0005a0001c0001t0001g0063a0001c0001t0001g0075others(39): Show | 43 | HG00323.hp2 HG00621.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.4315-2810T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593275 | ||||||
| chr4:15593338
|
C | A | 1 | a0001c0006t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4315-2747C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593338 | ||||||
| chr4:15593675
|
T | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4315-2410T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593675 | ||||||
| chr4:15593791
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0238 | 2 | HG00741.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.4315-2294G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593791 | ||||||
| chr4:15593967
|
G | C | 1 | a0001c0006t0001g0278 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4315-2118G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15593967 | ||||||
| chr4:15594251
|
G | T | 1 | a0002c0003t0002g0293 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.4315-1834G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15594251 | ||||||
| chr4:15594401
|
G | C | 283 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0008others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.4315-1684G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15594401 | ||||||
| chr4:15594830
|
A | T | 264 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(261): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.4315-1255A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15594830 | ||||||
| chr4:15595256
|
T | C | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4315-829T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15595256 | ||||||
| chr4:15595607
|
G | T | 1 | a0001c0006t0001g0312 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4315-478G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15595607 | ||||||
| chr4:15595660
|
G | A | 1 | a0011c0023t0002g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.4315-425G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 33/36 | chr4 | 15595660 | ||||||
| chr4:15596276
|
A | G | 2 | a0005c0009t0002g0113a0005c0009t0002g0114 | 2 | NA19057.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.4437+69A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596276 | ||||||
| chr4:15596361
|
C | T | 318 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.4437+154C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596361 | ||||||
| chr4:15596407
|
G | A | 1 | a0001c0002t0002g0170 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4437+200G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596407 | ||||||
| chr4:15596428
|
T | TAA | 76 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(73): Show | 78 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(75): Show |
intron_variant | MODIFIER | c.4437+223_4437+224d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | INFO_REALIGN_3_PRIME | chr4 | 15596428 | |||||
| chr4:15596493
|
C | A | 1 | a0001c0001t0001g0008 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4437+286C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596493 | ||||||
| chr4:15596758
|
C | T | 11 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0059others(8): Show | 11 | HG00735.hp2 HG01081.hp1 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.4437+551C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596758 | ||||||
| chr4:15596855
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4438-552C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596855 | ||||||
| chr4:15596914
|
A | G | 119 | a0001c0001t0001g0220a0001c0001t0001g0264a0001c0001t0001g0265others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4438-493A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596914 | ||||||
| chr4:15596985
|
C | T | 318 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.4438-422C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15596985 | ||||||
| chr4:15597017
|
ATGT | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4438-385_4438-383d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | INFO_REALIGN_3_PRIME | chr4 | 15597017 | |||||
| chr4:15597169
|
G | C | 2 | a0001c0001t0002g0016a0001c0024t0002g0098 | 2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.4438-238G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15597169 | ||||||
| chr4:15597270
|
T | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0324a0015c0031t0001g0316 | 3 | HG02559.hp1 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4438-137T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15597270 | ||||||
| chr4:15597398
|
C | A | 2 | a0002c0003t0001g0303a0002c0003t0001g0320 | 2 | NA18960.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.4438-9C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 34/36 | chr4 | 15597398 | ||||||
| chr4:15597513
|
A | C | 1 | a0001c0002t0002g0233 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.4496+48A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597513 | ||||||
| chr4:15597531
|
A | G | 1 | a0001c0001t0001g0147 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4496+66A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597531 | ||||||
| chr4:15597607
|
G | T | 3 | a0006c0011t0001g0253a0006c0011t0001g0281a0006c0032t0001g0252 | 3 | HG02622.hp1 HG02723.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4496+142G>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597607 | ||||||
| chr4:15597628
|
T | G | 10 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | HG02055.hp2 NA18945.hp2 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.4496+163T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597628 | ||||||
| chr4:15597730
|
T | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0249 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4496+265T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597730 | ||||||
| chr4:15597938
|
C | T | 1 | a0001c0002t0002g0155 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.4496+473C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15597938 | ||||||
| chr4:15598049
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4496+584T>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598049 | ||||||
| chr4:15598188
|
A | C | 3 | a0001c0001t0001g0109a0001c0001t0001g0187a0001c0001t0001g0297 | 3 | HG03942.hp2 HG04199.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.4496+723A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598188 | ||||||
| chr4:15598222
|
C | T | 119 | a0001c0001t0001g0220a0001c0001t0001g0264a0001c0001t0001g0265others(116): Show | 119 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.4496+757C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598222 | ||||||
| chr4:15598234
|
C | G | 1 | a0001c0001t0002g0186 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.4496+769C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598234 | ||||||
| chr4:15598476
|
G | A | 1 | a0001c0001t0001g0061 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.4496+1011G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598476 | ||||||
| chr4:15598494
|
G | A | 1 | a0013c0020t0001g0120 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.4496+1029G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598494 | ||||||
| chr4:15598582
|
C | T | 264 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(261): Show | 266 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(263): Show |
intron_variant | MODIFIER | c.4497-947C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598582 | ||||||
| chr4:15598707
|
C | G | 3 | a0001c0001t0001g0049a0001c0001t0001g0064a0001c0001t0001g0065 | 3 | NA18612.hp2 NA19062.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.4497-822C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598707 | ||||||
| chr4:15598738
|
T | G | 1 | a0001c0001t0002g0130 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4497-791T>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598738 | ||||||
| chr4:15598740
|
A | G | 16 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(13): Show | 17 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.4497-789A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598740 | ||||||
| chr4:15598827
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4497-702T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15598827 | ||||||
| chr4:15599176
|
A | G | 128 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(125): Show | 129 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.4497-353A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15599176 | ||||||
| chr4:15599367
|
G | A | 1 | a0018c0016t0002g0223 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4497-162G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15599367 | ||||||
| chr4:15599430
|
T | C | 2 | a0001c0004t0002g0033a0001c0004t0002g0039 | 2 | HG02809.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.4497-99T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 35/36 | chr4 | 15599430 | ||||||
| chr4:15600138
|
T | C | 33 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0067others(30): Show | 33 | HG00558.hp2 HG00597.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.4674+432T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600138 | ||||||
| chr4:15600184
|
C | G | 1 | a0002c0003t0001g0334 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4674+478C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600184 | ||||||
| chr4:15600484
|
C | T | 1 | a0001c0002t0002g0230 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.4675-753C>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600484 | ||||||
| chr4:15600593
|
T | C | 37 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(34): Show | 37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.4675-644T>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600593 | ||||||
| chr4:15600625
|
G | A | 1 | a0001c0001t0001g0181 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4675-612G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600625 | ||||||
| chr4:15600629
|
G | C | 123 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.4675-608G>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600629 | ||||||
| chr4:15600635
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4675-602G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600635 | ||||||
| chr4:15600793
|
C | G | 1 | a0001c0002t0002g0176 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.4675-444C>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600793 | ||||||
| chr4:15600873
|
G | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(57): Show | 61 | HG00099.hp1 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.4675-364G>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600873 | ||||||
| chr4:15600896
|
C | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0020 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.4675-341C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600896 | ||||||
| chr4:15600903
|
C | CA | 49 | a0001c0001t0001g0010a0001c0001t0001g0023a0001c0001t0001g0067others(46): Show | 50 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.4675-316dupA | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600903 | |||||
| chr4:15600903
|
C | CAA | 87 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(84): Show | 88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.4675-317_4675-316d others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600903 | |||||
| chr4:15600903
|
C | CAAA | 51 | a0001c0001t0001g0062a0001c0001t0001g0220a0001c0001t0001g0264others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.4675-318_4675-316d others(5): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600903 | |||||
| chr4:15600913
|
A | AAG | 85 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(82): Show | 86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.4675-323_4675-322i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600913 | |||||
| chr4:15600915
|
A | G | 1 | a0001c0001t0002g0338 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4675-322A>G | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15600915 | ||||||
| chr4:15600917
|
A | AAG | 37 | a0001c0001t0001g0006a0001c0001t0001g0051a0001c0001t0001g0052others(34): Show | 37 | HG00642.hp1 HG00733.hp2 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.4675-319_4675-318i others(4): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15600917 | |||||
| chr4:15601068
|
A | C | 2 | a0001c0001t0002g0291a0001c0001t0002g0301 | 2 | HG02258.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.4675-169A>C | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601068 | ||||||
| chr4:15601148
|
C | CT | 14 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.4675-89_4675-88ins others(1): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601148 | ||||||
| chr4:15601149
|
A | T | 14 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.4675-88A>T | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601149 | ||||||
| chr4:15601150
|
C | A | 14 | a0001c0001t0002g0001a0001c0001t0002g0047a0001c0001t0002g0048others(11): Show | 15 | HG00099.hp2 HG00735.hp2 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.4675-87C>A | CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | chr4 | 15601150 | ||||||
| chr4:15601150
|
C | CTTA | 305 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(302): Show | 307 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(304): Show |
intron_variant | MODIFIER | c.4675-85_4675-83dup others(3): Show |
CC2D2A | ENSG00000048342.18 | transcript | ENST00000424120.6 | protein_coding | 36/36 | INFO_REALIGN_3_PRIME | chr4 | 15601150 |