Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 8634 |
|---|---|
| ensemblid | ENSG00000137996.13 |
| hgncid | 17981 |
| symbol | RTCA |
| name | RNA 3'-terminal phosphate cyclase |
| refseq_nuc | NM_003729.4 |
| refseq_prot | NP_003720.1 |
| ensembl_nuc | ENST00000370128.9 |
| ensembl_prot | ENSP00000359146.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 100266216 |
| end | 100292769 |
| strand | + |
| ver | v1.2 |
| region | chr1:100266216-100292769 |
| region5000 | chr1:100261216-100297769 |
| regionname0 | RTCA_chr1_100266216_100292769 |
| regionname5000 | RTCA_chr1_100261216_100297769 |
| 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 | 366 | 291 | 85 | 51 | 111 | 12 | 30 | 74 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0002 | 0/0 | 366 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0003 | 0/0 | 366 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0004 | 0/0 | 366 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| 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 | 1101 | 287 | 84 | 50 | 111 | 10 | 30 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| c0002 | 0/0 | 1101 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| c0003 | 0/0 | 1101 | 2 | 0 | 1 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| c0004 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| c0005 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| c0006 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| c0007 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1427 | 195 | 45 | 38 | 82 | 7 | 22 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0002 | 0/0 | 1427 | 35 | 17 | 6 | 8 | 2 | 2 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0003 | 1/0 | 1426 | 18 | 13 | 0 | 3 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0004 | 0/0 | 1426 | 14 | 2 | 0 | 9 | 0 | 3 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0005 | 0/0 | 1428 | 8 | 1 | 1 | 6 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0006 | 0/0 | 1427 | 6 | 0 | 4 | 0 | 2 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0007 | 0/0 | 1427 | 3 | 0 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0008 | 0/0 | 1427 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0009 | 0/0 | 1416 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0010 | 0/0 | 1444 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0011 | 0/0 | 1427 | 2 | 0 | 0 | 0 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0012 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0013 | 0/0 | 1427 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0014 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0015 | 0/0 | 1427 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0016 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0017 | 0/0 | 1427 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| t0018 | 0/0 | 1444 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| 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 | 14 | 1 | 6 | 4 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0002 | 0/0 | 11 | 0 | 2 | 6 | 0 | 3 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0003 | 0/0 | 9 | 3 | 1 | 5 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0004 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0005 | 0/0 | 6 | 1 | 1 | 0 | 0 | 4 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0006 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0008 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0009 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0027 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0028 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| 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 | 1101 | 287 | 84 | 50 | 111 | 10 | 30 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0003 | 0/0 | 1101 | 2 | 0 | 1 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0005 | 0/0 | 1101 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0007 | 0/0 | 1101 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0002c0002 | 0/0 | 1101 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0003c0006 | 0/0 | 1101 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0004c0004 | 0/0 | 1101 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2527 | 187 | 41 | 36 | 82 | 5 | 22 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0002 | 0/0 | 2527 | 35 | 17 | 6 | 8 | 2 | 2 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0003 | 1/0 | 2526 | 18 | 13 | 0 | 3 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0004 | 0/0 | 2526 | 14 | 2 | 0 | 9 | 0 | 3 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0005 | 0/0 | 2528 | 7 | 1 | 1 | 5 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0006 | 0/0 | 2527 | 6 | 0 | 4 | 0 | 2 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0007 | 0/0 | 2527 | 3 | 0 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0008 | 0/0 | 2527 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0009 | 0/0 | 2516 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0010 | 0/0 | 2544 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0011 | 0/0 | 2527 | 2 | 0 | 0 | 0 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0012 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0013 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0014 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0015 | 0/0 | 2527 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0016 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0017 | 0/0 | 2527 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0001t0018 | 0/0 | 2544 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0003t0001 | 0/0 | 2527 | 2 | 0 | 1 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0005t0001 | 0/0 | 2527 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0001c0007t0001 | 0/0 | 2527 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0002c0002t0001 | 0/0 | 2527 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0003c0006t0005 | 0/0 | 2528 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| a0004c0004t0001 | 0/0 | 2527 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | copy fasta | chr1 | 100261216 | 100297769 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 13 | 1 | 5 | 4 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 2 | 6 | 0 | 3 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0003 | 0/0 | 8 | 3 | 1 | 4 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0006 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0005 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0006g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0006g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0007g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0008g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0008g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0009g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0010g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0010g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0011g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0012g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0013g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0014g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0015g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0016g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0017g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0001t0018g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0005t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0001c0007t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0003c0006t0005g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| a0004c0004t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0005 | t0001 | g0028 | EUR | GBR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0010 | EUR | GBR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00323 | hp2 | a0001 | c0001 | t0006 | g0055 | EUR | FIN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0202 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01074 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01099 | hp2 | a0001 | c0001 | t0006 | g0030 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0005 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01261 | hp2 | a0001 | c0001 | t0015 | g0008 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01358 | hp1 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01515 | hp2 | a0001 | c0001 | t0007 | g0118 | EUR | IBS | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0174 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01891 | hp1 | a0001 | c0001 | t0010 | g0188 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02015 | hp1 | a0003 | c0006 | t0005 | g0006 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | CDX | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02280 | hp1 | a0001 | c0001 | t0013 | g0054 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02293 | hp1 | a0004 | c0004 | t0001 | g0009 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02572 | hp2 | a0001 | c0001 | t0018 | g0186 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0184 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02630 | hp2 | a0001 | c0001 | t0008 | g0117 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02647 | hp1 | a0001 | c0001 | t0008 | g0024 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02723 | hp1 | a0001 | c0001 | t0009 | g0181 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0156 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0187 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0177 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0185 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03490 | hp1 | a0001 | c0001 | t0011 | g0005 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03492 | hp2 | a0001 | c0001 | t0011 | g0005 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0161 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0034 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0163 | SAS | STU | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18522 | hp1 | a0001 | c0007 | t0001 | g0050 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18612 | hp2 | a0001 | c0001 | t0005 | g0139 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0003 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18939 | hp2 | a0001 | c0001 | t0017 | g0096 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18953 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0034 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18994 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18995 | hp1 | a0001 | c0001 | t0012 | g0009 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19062 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19067 | hp2 | a0001 | c0001 | t0016 | g0027 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19072 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | YRI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ASW | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ASW | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0015 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0201 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0189 | EUR | TSI | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01123 | hp1 | a0001 | c0001 | t0007 | g0065 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0166 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0100 | AFR | ACB | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0024 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | USA | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0152 | REF | REF | RTCA_chr1_100261216_100297769 | RTCA | chr1 | 100261216 | 100297769 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100266412
|
A | G | 1 | a0002 | 3 | HG02258.hp1 HG02559.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.37A>G | p.Met13Val | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 197/2526 | 37/1101 | 13/366 | chr1 | 100266412 | ||
| chr1:100266569
|
G | A | 1 | a0004 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.91G>A | p.Gly31Ser | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/11 | 251/2526 | 91/1101 | 31/366 | chr1 | 100266569 | ||
| chr1:100287174
|
G | A | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.970G>A | p.Ala324Thr | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/11 | 1130/2526 | 970/1101 | 324/366 | chr1 | 100287174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100270665
|
C | T | 1 | a0001c0003 | 2 | HG00738.hp2 NA20752.hp2 |
synonymous_variant | LOW | c.399C>T | p.Ile133Ile | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/11 | 559/2526 | 399/1101 | 133/366 | chr1 | 100270665 | ||
| chr1:100274929
|
T | C | 1 | a0001c0005 | 1 | HG00140.hp1 | synonymous_variant | LOW | c.579T>C | p.Tyr193Tyr | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/11 | 739/2526 | 579/1101 | 193/366 | chr1 | 100274929 | ||
| chr1:100287176
|
G | A | 1 | a0001c0007 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.972G>A | p.Ala324Ala | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/11 | 1132/2526 | 972/1101 | 324/366 | chr1 | 100287176 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100266248
|
C | T | 1 | a0001c0001t0018 | 1 | HG02572.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 128 | chr1 | 100266248 | |||||
| chr1:100266259
|
C | A | 1 | a0001c0001t0012 | 1 | NA18995.hp1 | 5_prime_UTR_variant | MODIFIER | c.-117C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 117 | chr1 | 100266259 | |||||
| chr1:100266263
|
C | CA | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(14): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
5_prime_UTR_variant | MODIFIER | c.-113_-112insA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 112 | chr1 | 100266263 | |||||
| chr1:100266264
|
G | A | 17 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(14): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
5_prime_UTR_variant | MODIFIER | c.-112G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 1/11 | 112 | chr1 | 100266264 | |||||
| chr1:100291620
|
T | G | 1 | a0001c0001t0007 | 3 | HG01074.hp1 HG01123.hp1 HG01515.hp2 |
3_prime_UTR_variant | MODIFIER | c.*116T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 116 | chr1 | 100291620 | |||||
| chr1:100291863
|
T | C | 1 | a0001c0001t0013 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*359T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 359 | chr1 | 100291863 | |||||
| chr1:100291912
|
A | T | 1 | a0001c0001t0017 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*408A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 408 | chr1 | 100291912 | |||||
| chr1:100291929
|
C | CT | 4 | a0001c0001t0002a0001c0001t0005a0001c0001t0011others(1): Show | 45 | HG00140.hp2 HG00597.hp1 HG00642.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*443dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 444 | INFO_REALIGN_3_PRIME | chr1 | 100291929 | ||||
| chr1:100291929
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0009 | 3 | HG02622.hp1 HG02723.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*434_*443delTTTTTT others(4): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 434 | INFO_REALIGN_3_PRIME | chr1 | 100291929 | ||||
| chr1:100291959
|
G | C | 1 | a0001c0001t0014 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*455G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 455 | chr1 | 100291959 | |||||
| chr1:100292068
|
C | T | 1 | a0001c0001t0004 | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*564C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 564 | chr1 | 100292068 | |||||
| chr1:100292197
|
C | T | 1 | a0001c0001t0016 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*693C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 693 | chr1 | 100292197 | |||||
| chr1:100292198
|
G | A | 2 | a0001c0001t0008a0001c0001t0011 | 5 | HG02630.hp2 HG02647.hp1 HG03490.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*694G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 694 | chr1 | 100292198 | |||||
| chr1:100292207
|
T | C | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(15): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*703T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 703 | chr1 | 100292207 | |||||
| chr1:100292213
|
C | T | 1 | a0001c0001t0015 | 1 | HG01261.hp2 | 3_prime_UTR_variant | MODIFIER | c.*709C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 709 | chr1 | 100292213 | |||||
| chr1:100292268
|
C | T | 1 | a0001c0001t0006 | 6 | HG00323.hp2 HG01070.hp2 HG01099.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*764C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 764 | chr1 | 100292268 | |||||
| chr1:100292427
|
C | T | 1 | a0001c0001t0004 | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*923C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 923 | chr1 | 100292427 | |||||
| chr1:100292543
|
C | T | 1 | a0001c0001t0004 | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1039C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 1039 | chr1 | 100292543 | |||||
| chr1:100292599
|
T | C | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(15): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
3_prime_UTR_variant | MODIFIER | c.*1095T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 1095 | chr1 | 100292599 | |||||
| chr1:100292641
|
T | TATGTTTT others(11): Show |
2 | a0001c0001t0010a0001c0001t0018 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1139_*1156dupTGTT others(14): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 11/11 | 1157 | INFO_REALIGN_3_PRIME | chr1 | 100292641 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:100266670
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.146+46G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266670 | ||||||
| chr1:100266766
|
T | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.146+142T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266766 | ||||||
| chr1:100266848
|
A | G | 2 | a0001c0003t0001g0201a0001c0003t0001g0202 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.146+224A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266848 | ||||||
| chr1:100266877
|
G | A | 1 | a0001c0001t0003g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.146+253G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266877 | ||||||
| chr1:100266894
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.146+270T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266894 | ||||||
| chr1:100266947
|
A | G | 5 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(2): Show | 8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.146+323A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266947 | ||||||
| chr1:100266964
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.146+340T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266964 | ||||||
| chr1:100266970
|
C | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.146+346C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100266970 | ||||||
| chr1:100267045
|
A | C | 11 | a0001c0001t0002g0005a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.146+421A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267045 | ||||||
| chr1:100267125
|
A | G | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.146+501A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267125 | ||||||
| chr1:100267141
|
G | T | 8 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(5): Show | 11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.146+517G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267141 | ||||||
| chr1:100267299
|
T | C | 5 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(2): Show | 5 | HG00323.hp2 HG01928.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.146+675T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267299 | ||||||
| chr1:100267460
|
CAG | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(10): Show | 14 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.147-689_147-688del others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 100267460 | |||||
| chr1:100267651
|
G | GT | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 282 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.147-487dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 100267651 | |||||
| chr1:100267651
|
G | GTT | 8 | a0001c0001t0001g0032a0001c0001t0001g0151a0001c0001t0002g0182others(5): Show | 9 | HG02055.hp1 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.147-488_147-487dup others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr1 | 100267651 | |||||
| chr1:100267709
|
A | G | 5 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(2): Show | 8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.147-443A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267709 | ||||||
| chr1:100267725
|
G | T | 2 | a0001c0001t0004g0178a0001c0001t0004g0179 | 2 | NA18969.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.147-427G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267725 | ||||||
| chr1:100267779
|
A | G | 6 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG00438.hp1 HG00609.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-373A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267779 | ||||||
| chr1:100267996
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.147-156T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 2/10 | chr1 | 100267996 | ||||||
| chr1:100268328
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.290+33C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268328 | ||||||
| chr1:100268403
|
G | GT | 86 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(83): Show | 130 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.290+120dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100268403 | |||||
| chr1:100268571
|
T | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 5 | HG02055.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+276T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268571 | ||||||
| chr1:100268615
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0007t0001g0050 | 3 | HG03486.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.290+320G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268615 | ||||||
| chr1:100268810
|
G | C | 1 | a0001c0001t0003g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.290+515G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268810 | ||||||
| chr1:100268913
|
G | T | 1 | a0001c0001t0001g0092 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.290+618G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268913 | ||||||
| chr1:100268927
|
G | A | 19 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0038others(16): Show | 22 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.290+632G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100268927 | ||||||
| chr1:100269005
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.290+710A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269005 | ||||||
| chr1:100269048
|
T | C | 1 | a0001c0001t0008g0024 | 2 | HG02647.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.290+753T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269048 | ||||||
| chr1:100269049
|
A | ATG | 16 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.290+755_290+756ins others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100269049 | |||||
| chr1:100269052
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.290+757A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269052 | ||||||
| chr1:100269191
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.290+896C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269191 | ||||||
| chr1:100269222
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.290+927G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269222 | ||||||
| chr1:100269328
|
C | T | 14 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0035others(11): Show | 21 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.290+1033C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269328 | ||||||
| chr1:100269337
|
C | T | 6 | a0001c0001t0001g0008a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 9 | HG00639.hp1 HG01255.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.290+1042C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269337 | ||||||
| chr1:100269362
|
TC | T | 3 | a0001c0001t0005g0137a0001c0001t0005g0138a0001c0001t0005g0139 | 3 | NA18612.hp2 NA18956.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.290+1068delC | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269362 | ||||||
| chr1:100269363
|
C | CT | 16 | a0001c0001t0002g0005a0001c0001t0002g0036a0001c0001t0002g0174others(13): Show | 20 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.290+1086dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100269363 | |||||
| chr1:100269363
|
CT | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.290+1086delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100269363 | |||||
| chr1:100269364
|
T | G | 3 | a0001c0001t0005g0137a0001c0001t0005g0138a0001c0001t0005g0139 | 3 | NA18612.hp2 NA18956.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.290+1069T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269364 | ||||||
| chr1:100269400
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.290+1105G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269400 | ||||||
| chr1:100269739
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.291-818C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269739 | ||||||
| chr1:100269843
|
T | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0063 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.291-714T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269843 | ||||||
| chr1:100269875
|
C | G | 3 | a0001c0001t0002g0176a0001c0001t0002g0177a0001c0001t0003g0175 | 3 | HG02809.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.291-682C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269875 | ||||||
| chr1:100269983
|
A | T | 1 | a0001c0001t0001g0136 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.291-574A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100269983 | ||||||
| chr1:100270035
|
C | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.291-522C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270035 | ||||||
| chr1:100270180
|
G | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.291-377G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270180 | ||||||
| chr1:100270200
|
TGAA | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.291-352_291-350del others(3): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr1 | 100270200 | |||||
| chr1:100270208
|
G | A | 4 | a0001c0001t0003g0040a0001c0001t0003g0155a0001c0001t0003g0156others(1): Show | 4 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.291-349G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270208 | ||||||
| chr1:100270320
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.291-237T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270320 | ||||||
| chr1:100270347
|
A | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(134): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.291-210A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270347 | ||||||
| chr1:100270352
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.291-205G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 3/10 | chr1 | 100270352 | ||||||
| chr1:100270696
|
G | C | 1 | a0001c0001t0002g0017 | 3 | HG02257.hp1 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.414+16G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270696 | ||||||
| chr1:100270815
|
C | CT | 14 | a0001c0001t0001g0150a0001c0001t0004g0034a0001c0001t0004g0158others(11): Show | 15 | HG00609.hp1 HG02109.hp1 HG02717.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+146dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr1 | 100270815 | |||||
| chr1:100270821
|
T | A | 1 | a0001c0001t0002g0189 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.414+141T>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270821 | ||||||
| chr1:100270932
|
C | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.414+252C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270932 | ||||||
| chr1:100270961
|
T | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.414+281T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100270961 | ||||||
| chr1:100271041
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | HG00408.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.414+361C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271041 | ||||||
| chr1:100271131
|
T | C | 2 | a0001c0003t0001g0201a0001c0003t0001g0202 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.414+451T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271131 | ||||||
| chr1:100271215
|
A | G | 1 | a0001c0001t0002g0189 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.414+535A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271215 | ||||||
| chr1:100271275
|
C | A | 2 | a0001c0001t0001g0014a0001c0001t0001g0025 | 5 | HG02451.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+595C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271275 | ||||||
| chr1:100271287
|
AT | A | 4 | a0001c0001t0003g0040a0001c0001t0003g0155a0001c0001t0003g0156others(1): Show | 4 | HG02622.hp2 HG03130.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+608delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271287 | ||||||
| chr1:100271561
|
A | T | 1 | a0001c0001t0002g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.414+881A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271561 | ||||||
| chr1:100271576
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG02129.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.414+896A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271576 | ||||||
| chr1:100271614
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.414+934A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271614 | ||||||
| chr1:100271632
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.414+952G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271632 | ||||||
| chr1:100271637
|
C | T | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.414+957C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271637 | ||||||
| chr1:100271672
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.414+992C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271672 | ||||||
| chr1:100271856
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.414+1176C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100271856 | ||||||
| chr1:100272226
|
C | T | 1 | a0001c0001t0001g0023 | 2 | HG02630.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.415-1168C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272226 | ||||||
| chr1:100272565
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.415-829G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272565 | ||||||
| chr1:100272572
|
T | C | 1 | a0001c0003t0001g0201 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.415-822T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272572 | ||||||
| chr1:100272642
|
T | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.415-752T>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272642 | ||||||
| chr1:100272676
|
A | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0007t0001g0050 | 3 | HG03486.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.415-718A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272676 | ||||||
| chr1:100272894
|
G | A | 1 | a0001c0001t0017g0096 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.415-500G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100272894 | ||||||
| chr1:100273083
|
A | C | 1 | a0001c0001t0001g0085 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.415-311A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273083 | ||||||
| chr1:100273117
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.415-277C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273117 | ||||||
| chr1:100273167
|
G | A | 5 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(2): Show | 8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.415-227G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273167 | ||||||
| chr1:100273228
|
T | C | 1 | a0001c0001t0009g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.415-166T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273228 | ||||||
| chr1:100273317
|
G | A | 9 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(6): Show | 10 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-77G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 4/10 | chr1 | 100273317 | ||||||
| chr1:100273639
|
C | T | 5 | a0001c0001t0002g0192a0001c0001t0002g0193a0001c0001t0002g0194others(2): Show | 5 | HG00597.hp1 HG02071.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.473+187C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100273639 | ||||||
| chr1:100273973
|
C | T | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.473+521C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100273973 | ||||||
| chr1:100273990
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.473+538C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100273990 | ||||||
| chr1:100274090
|
C | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.473+638C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274090 | ||||||
| chr1:100274169
|
A | G | 1 | a0001c0001t0001g0084 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.474-655A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274169 | ||||||
| chr1:100274251
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.474-573T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274251 | ||||||
| chr1:100274277
|
C | A | 1 | a0001c0001t0001g0097 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.474-547C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274277 | ||||||
| chr1:100274278
|
G | A | 3 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0018g0186 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.474-546G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274278 | ||||||
| chr1:100274508
|
A | G | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.474-316A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274508 | ||||||
| chr1:100274524
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.474-300T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274524 | ||||||
| chr1:100274649
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.474-175C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274649 | ||||||
| chr1:100274741
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.474-83T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 5/10 | chr1 | 100274741 | ||||||
| chr1:100274976
|
T | C | 1 | a0001c0001t0007g0065 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.615+11T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100274976 | ||||||
| chr1:100275050
|
GAACTT | G | 14 | a0001c0001t0002g0010a0001c0001t0002g0017a0001c0001t0002g0035others(11): Show | 21 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.615+89_615+93delTT others(3): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 100275050 | |||||
| chr1:100275104
|
C | T | 1 | a0001c0001t0001g0022 | 2 | HG00280.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.615+139C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275104 | ||||||
| chr1:100275138
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.615+173G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275138 | ||||||
| chr1:100275228
|
C | G | 3 | a0001c0001t0010g0187a0001c0001t0010g0188a0001c0001t0018g0186 | 3 | HG01891.hp1 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.615+263C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275228 | ||||||
| chr1:100275310
|
A | G | 2 | a0001c0001t0004g0166a0001c0001t0004g0167 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.616-289A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | chr1 | 100275310 | ||||||
| chr1:100275391
|
AATATATG others(1): Show |
A | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.616-205_616-198del others(8): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr1 | 100275391 | |||||
| chr1:100275867
|
G | A | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.740+144G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100275867 | ||||||
| chr1:100275980
|
C | T | 1 | a0001c0001t0003g0197 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.740+257C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100275980 | ||||||
| chr1:100276037
|
G | A | 2 | a0001c0001t0009g0184a0001c0001t0009g0185 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.740+314G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276037 | ||||||
| chr1:100276231
|
T | C | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044 | 3 | HG02572.hp1 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.740+508T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276231 | ||||||
| chr1:100276352
|
G | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(207): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.740+629G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276352 | ||||||
| chr1:100276417
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.740+694A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276417 | ||||||
| chr1:100276432
|
A | G | 1 | a0001c0001t0001g0022 | 2 | HG00280.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.740+709A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276432 | ||||||
| chr1:100276478
|
A | G | 11 | a0001c0001t0002g0005a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.740+755A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276478 | ||||||
| chr1:100276609
|
G | A | 5 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(2): Show | 8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.741-649G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276609 | ||||||
| chr1:100276648
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG04184.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.741-610G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276648 | ||||||
| chr1:100276843
|
C | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.741-415C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276843 | ||||||
| chr1:100276866
|
C | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0082others(3): Show | 6 | HG00408.hp1 HG00597.hp2 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.741-392C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276866 | ||||||
| chr1:100276937
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.741-321A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100276937 | ||||||
| chr1:100277114
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.741-144A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 7/10 | chr1 | 100277114 | ||||||
| chr1:100277436
|
T | C | 1 | a0001c0003t0001g0202 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.799+120T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277436 | ||||||
| chr1:100277522
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.799+206A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277522 | ||||||
| chr1:100277659
|
A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0047 | 3 | HG02055.hp2 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.799+343A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277659 | ||||||
| chr1:100277802
|
T | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0005g0100 | 3 | HG02559.hp2 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.799+486T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277802 | ||||||
| chr1:100277802
|
T | TG | 24 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0047others(21): Show | 31 | HG00738.hp2 HG01257.hp1 HG01261.hp1 others(28): Show |
intron_variant | MODIFIER | c.799+495dupG | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100277802 | |||||
| chr1:100277828
|
CT | C | 2 | a0001c0001t0003g0011a0001c0001t0003g0198 | 5 | HG02486.hp1 HG03579.hp1 NA19043.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+513delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100277828 | ||||||
| chr1:100278044
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.799+728C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278044 | ||||||
| chr1:100278549
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.799+1233T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278549 | ||||||
| chr1:100278864
|
C | T | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.799+1548C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278864 | ||||||
| chr1:100278898
|
C | T | 1 | a0001c0001t0001g0064 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.799+1582C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278898 | ||||||
| chr1:100278899
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.799+1583G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100278899 | ||||||
| chr1:100279094
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.799+1778A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279094 | ||||||
| chr1:100279242
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.799+1926G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279242 | ||||||
| chr1:100279326
|
T | C | 8 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(5): Show | 11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.799+2010T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279326 | ||||||
| chr1:100279591
|
A | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0153a0001c0001t0002g0154 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+2275A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279591 | ||||||
| chr1:100279614
|
A | AT | 28 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(25): Show | 43 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.799+2311dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100279614 | |||||
| chr1:100279614
|
A | T | 1 | a0001c0001t0002g0154 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.799+2298A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279614 | ||||||
| chr1:100279675
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.799+2359A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279675 | ||||||
| chr1:100279729
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.799+2413A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279729 | ||||||
| chr1:100279752
|
T | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.799+2436T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279752 | ||||||
| chr1:100279873
|
C | G | 12 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0032others(9): Show | 22 | HG00438.hp2 HG00735.hp1 HG02717.hp2 others(19): Show |
intron_variant | MODIFIER | c.799+2557C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279873 | ||||||
| chr1:100279933
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.799+2617T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100279933 | ||||||
| chr1:100280083
|
A | G | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0086 | 3 | HG02280.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.799+2767A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280083 | ||||||
| chr1:100280095
|
A | G | 5 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(2): Show | 8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.799+2779A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280095 | ||||||
| chr1:100280218
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.799+2902C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280218 | ||||||
| chr1:100280236
|
G | T | 1 | a0001c0001t0003g0200 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.799+2920G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280236 | ||||||
| chr1:100280400
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.799+3084G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280400 | ||||||
| chr1:100280500
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.799+3184A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280500 | ||||||
| chr1:100280510
|
T | A | 16 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.799+3194T>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280510 | ||||||
| chr1:100280603
|
T | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(27): Show | 45 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.799+3287T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280603 | ||||||
| chr1:100280736
|
G | T | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.799+3420G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280736 | ||||||
| chr1:100280823
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.799+3507G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100280823 | ||||||
| chr1:100281167
|
G | C | 1 | a0001c0001t0002g0157 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.799+3851G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281167 | ||||||
| chr1:100281322
|
TAGAG | T | 13 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(10): Show | 14 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.800-3903_800-3900d others(6): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100281322 | |||||
| chr1:100281516
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.800-3712G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281516 | ||||||
| chr1:100281635
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.800-3593A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281635 | ||||||
| chr1:100281871
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.800-3357C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100281871 | ||||||
| chr1:100282362
|
T | G | 2 | a0001c0001t0002g0017a0001c0001t0002g0168 | 4 | HG01109.hp1 HG02257.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-2866T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282362 | ||||||
| chr1:100282569
|
A | T | 34 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0017others(31): Show | 45 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.800-2659A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282569 | ||||||
| chr1:100282578
|
G | T | 1 | a0001c0001t0002g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.800-2650G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282578 | ||||||
| chr1:100282658
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.800-2570A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282658 | ||||||
| chr1:100282727
|
C | CA | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.800-2497dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100282727 | |||||
| chr1:100282956
|
G | A | 3 | a0001c0001t0002g0033a0001c0001t0002g0153a0001c0001t0002g0154 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-2272G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100282956 | ||||||
| chr1:100283077
|
G | A | 12 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(9): Show | 13 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.800-2151G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283077 | ||||||
| chr1:100283160
|
C | CT | 28 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0002g0005others(25): Show | 39 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.800-2045dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283160 | |||||
| chr1:100283160
|
CT | C | 129 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(126): Show | 192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.800-2045delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283160 | |||||
| chr1:100283160
|
CTT | C | 22 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0041others(19): Show | 25 | HG00323.hp2 HG00609.hp1 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.800-2046_800-2045d others(4): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283160 | |||||
| chr1:100283203
|
A | G | 1 | a0001c0001t0008g0117 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.800-2025A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283203 | ||||||
| chr1:100283234
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.800-1994G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283234 | ||||||
| chr1:100283237
|
C | T | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.800-1991C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283237 | ||||||
| chr1:100283239
|
C | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.800-1989C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283239 | ||||||
| chr1:100283352
|
G | A | 12 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(9): Show | 13 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(10): Show |
intron_variant | MODIFIER | c.800-1876G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283352 | ||||||
| chr1:100283437
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.800-1791T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283437 | ||||||
| chr1:100283572
|
G | C | 1 | a0001c0001t0001g0126 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.800-1656G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283572 | ||||||
| chr1:100283633
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.800-1595A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283633 | ||||||
| chr1:100283827
|
C | A | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.800-1401C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283827 | ||||||
| chr1:100283931
|
AAAAGAAA others(12): Show |
A | 10 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0161others(7): Show | 11 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-1293_800-1275d others(21): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283931 | |||||
| chr1:100283932
|
AAAGAAAA others(11): Show |
A | 2 | a0001c0001t0004g0160a0001c0001t0004g0165 | 2 | NA18969.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.800-1293_800-1276d others(20): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283932 | |||||
| chr1:100283933
|
AAGAAAAA others(10): Show |
A | 1 | a0001c0001t0004g0159 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.800-1293_800-1277d others(19): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283933 | |||||
| chr1:100283935
|
G | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.800-1293G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283935 | ||||||
| chr1:100283935
|
G | GA | 5 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(2): Show | 8 | HG02257.hp2 HG02486.hp1 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.800-1279dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283935 | |||||
| chr1:100283935
|
G | GAA | 29 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0017others(26): Show | 40 | HG00140.hp2 HG00597.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.800-1280_800-1279d others(4): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283935 | |||||
| chr1:100283935
|
G | GAAA | 7 | a0001c0001t0002g0154a0001c0001t0002g0171a0001c0001t0002g0182others(4): Show | 7 | HG00642.hp2 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.800-1281_800-1279d others(5): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283935 | |||||
| chr1:100283943
|
AAAAAAAG others(7): Show |
A | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.800-1282_800-1269d others(16): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283943 | |||||
| chr1:100283944
|
AAAAAAGA others(6): Show |
A | 14 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 15 | HG01891.hp2 HG02280.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.800-1281_800-1269d others(15): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283944 | |||||
| chr1:100283945
|
AAAAAGAA others(5): Show |
A | 4 | a0001c0001t0001g0047a0001c0001t0001g0116a0001c0003t0001g0202others(1): Show | 4 | HG00323.hp1 HG00738.hp2 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-1280_800-1269d others(14): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283945 | |||||
| chr1:100283946
|
AAAAGAAA others(4): Show |
A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 160 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.800-1279_800-1269d others(13): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283946 | |||||
| chr1:100283947
|
AAAGAAAA others(3): Show |
A | 36 | a0001c0001t0001g0009a0001c0001t0001g0019a0001c0001t0001g0027others(33): Show | 38 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.800-1262_800-1253d others(12): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100283947 | |||||
| chr1:100283949
|
AGAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0102 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.800-1278_800-1268d others(13): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283949 | ||||||
| chr1:100283957
|
C | A | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.800-1271C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283957 | ||||||
| chr1:100283999
|
C | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0047 | 3 | HG02055.hp2 HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.800-1229C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100283999 | ||||||
| chr1:100284350
|
C | CT | 14 | a0001c0001t0001g0077a0001c0001t0004g0034a0001c0001t0004g0158others(11): Show | 15 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(12): Show |
intron_variant | MODIFIER | c.800-871dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100284350 | |||||
| chr1:100284397
|
A | AT | 32 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0009others(29): Show | 50 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.800-815dupT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100284397 | |||||
| chr1:100284467
|
C | A | 1 | a0001c0001t0001g0107 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.800-761C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284467 | ||||||
| chr1:100284699
|
C | A | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.800-529C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284699 | ||||||
| chr1:100284747
|
T | C | 1 | a0001c0001t0001g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.800-481T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284747 | ||||||
| chr1:100284814
|
C | G | 2 | a0001c0001t0006g0015a0001c0001t0006g0030 | 5 | HG01070.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-414C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284814 | ||||||
| chr1:100284890
|
G | A | 1 | a0001c0001t0003g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.800-338G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284890 | ||||||
| chr1:100284998
|
A | G | 16 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.800-230A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | chr1 | 100284998 | ||||||
| chr1:100285177
|
AGTTTT | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.800-25_800-21delGT others(3): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100285177 | |||||
| chr1:100285177
|
AGTTTTGT others(3): Show |
A | 1 | a0001c0001t0001g0045 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.800-30_800-21delGT others(8): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr1 | 100285177 | |||||
| chr1:100285387
|
A | T | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.894+65A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285387 | ||||||
| chr1:100285428
|
C | T | 8 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(5): Show | 11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.894+106C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285428 | ||||||
| chr1:100285499
|
G | C | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(163): Show | 234 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.894+177G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285499 | ||||||
| chr1:100285505
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.894+183A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285505 | ||||||
| chr1:100285516
|
C | G | 1 | a0001c0001t0004g0163 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.894+194C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285516 | ||||||
| chr1:100285517
|
G | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0043 | 2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.894+195G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285517 | ||||||
| chr1:100285556
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.894+234C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285556 | ||||||
| chr1:100285705
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.894+383G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285705 | ||||||
| chr1:100285720
|
A | G | 1 | a0001c0001t0004g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.894+398A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285720 | ||||||
| chr1:100285723
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.894+401G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100285723 | ||||||
| chr1:100286002
|
C | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0006g0015others(1): Show | 7 | HG00323.hp1 HG01070.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.894+680C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286002 | ||||||
| chr1:100286249
|
G | A | 16 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.895-850G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286249 | ||||||
| chr1:100286315
|
G | A | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.895-784G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286315 | ||||||
| chr1:100286315
|
G | C | 1 | a0001c0001t0001g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.895-784G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286315 | ||||||
| chr1:100286322
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.895-777C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286322 | ||||||
| chr1:100286346
|
C | T | 2 | a0001c0003t0001g0201a0001c0003t0001g0202 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.895-753C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286346 | ||||||
| chr1:100286352
|
G | T | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.895-747G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286352 | ||||||
| chr1:100286386
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.895-713G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286386 | ||||||
| chr1:100286450
|
G | A | 3 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0086 | 3 | HG02280.hp2 HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.895-649G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286450 | ||||||
| chr1:100286454
|
C | CA | 72 | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0018others(69): Show | 90 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.895-623dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 100286454 | |||||
| chr1:100286454
|
C | CAA | 17 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0047others(14): Show | 18 | HG00642.hp2 HG01109.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.895-624_895-623dup others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 100286454 | |||||
| chr1:100286484
|
C | CA | 4 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(1): Show | 7 | HG02257.hp2 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.895-607dupA | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr1 | 100286484 | |||||
| chr1:100286876
|
A | G | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.895-223A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100286876 | ||||||
| chr1:100287018
|
T | G | 3 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0007t0001g0050 | 3 | HG03486.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.895-81T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 9/10 | chr1 | 100287018 | ||||||
| chr1:100287385
|
G | A | 11 | a0001c0001t0002g0005a0001c0001t0002g0189a0001c0001t0002g0190others(8): Show | 14 | HG00597.hp1 HG01257.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.999+182G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287385 | ||||||
| chr1:100287435
|
A | T | 1 | a0001c0001t0003g0200 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.999+232A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287435 | ||||||
| chr1:100287436
|
T | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.999+233T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287436 | ||||||
| chr1:100287586
|
A | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.999+383A>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287586 | ||||||
| chr1:100287642
|
CATTTT | C | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+445_999+449del others(5): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100287642 | |||||
| chr1:100287794
|
CT | C | 54 | a0001c0001t0001g0060a0001c0001t0002g0005a0001c0001t0002g0010others(51): Show | 69 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.999+608delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100287794 | |||||
| chr1:100287794
|
CTT | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 220 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(217): Show |
intron_variant | MODIFIER | c.999+607_999+608del others(2): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100287794 | |||||
| chr1:100287825
|
A | G | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(206): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.999+622A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287825 | ||||||
| chr1:100287859
|
T | C | 1 | a0001c0001t0004g0164 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.999+656T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100287859 | ||||||
| chr1:100288049
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.999+846C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288049 | ||||||
| chr1:100288079
|
C | T | 8 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(5): Show | 11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.999+876C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288079 | ||||||
| chr1:100288171
|
A | G | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0002c0002t0001g0051others(2): Show | 5 | HG01891.hp2 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.999+968A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288171 | ||||||
| chr1:100288245
|
C | T | 2 | a0001c0001t0009g0184a0001c0001t0009g0185 | 2 | HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.999+1042C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288245 | ||||||
| chr1:100288285
|
C | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.999+1082C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288285 | ||||||
| chr1:100288347
|
A | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0039 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.999+1144A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288347 | ||||||
| chr1:100288514
|
C | T | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+1311C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288514 | ||||||
| chr1:100288534
|
G | A | 6 | a0001c0001t0002g0005a0001c0001t0002g0189a0001c0001t0002g0190others(3): Show | 9 | HG01257.hp1 HG01261.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.999+1331G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288534 | ||||||
| chr1:100288538
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.999+1335T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288538 | ||||||
| chr1:100288546
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG00438.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.999+1343C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288546 | ||||||
| chr1:100288634
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.999+1431T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288634 | ||||||
| chr1:100288640
|
C | G | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.999+1437C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288640 | ||||||
| chr1:100288688
|
G | A | 2 | a0001c0003t0001g0201a0001c0003t0001g0202 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.999+1485G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288688 | ||||||
| chr1:100288690
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.999+1487C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288690 | ||||||
| chr1:100288815
|
TTTTTC | T | 3 | a0001c0001t0002g0033a0001c0001t0002g0153a0001c0001t0002g0154 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.999+1622_999+1626d others(7): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100288815 | |||||
| chr1:100288825
|
C | A | 3 | a0001c0001t0002g0193a0001c0001t0002g0195a0001c0001t0002g0196 | 3 | HG02071.hp1 HG02074.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.999+1622C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288825 | ||||||
| chr1:100288878
|
A | G | 34 | a0001c0001t0002g0005a0001c0001t0002g0010a0001c0001t0002g0017others(31): Show | 45 | HG00140.hp2 HG00597.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.999+1675A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288878 | ||||||
| chr1:100288926
|
A | G | 154 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(151): Show | 221 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.999+1723A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100288926 | ||||||
| chr1:100289027
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.999+1824T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289027 | ||||||
| chr1:100289104
|
A | G | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 235 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.999+1901A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289104 | ||||||
| chr1:100289304
|
T | G | 7 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0001g0074others(4): Show | 7 | HG00558.hp1 HG01255.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-2099T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289304 | ||||||
| chr1:100289306
|
G | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1000-2097G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289306 | ||||||
| chr1:100289308
|
T | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.1000-2095T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289308 | ||||||
| chr1:100289376
|
C | T | 4 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(1): Show | 7 | HG02257.hp2 HG02486.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-2027C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289376 | ||||||
| chr1:100289475
|
T | G | 1 | a0001c0001t0001g0105 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1000-1928T>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289475 | ||||||
| chr1:100289946
|
T | C | 16 | a0001c0001t0001g0018a0001c0001t0001g0038a0001c0001t0001g0039others(13): Show | 17 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1000-1457T>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100289946 | ||||||
| chr1:100290387
|
C | T | 2 | a0001c0001t0004g0166a0001c0001t0004g0167 | 2 | HG02109.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1000-1016C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290387 | ||||||
| chr1:100290523
|
C | T | 8 | a0001c0001t0003g0011a0001c0001t0003g0197a0001c0001t0003g0198others(5): Show | 11 | HG01891.hp1 HG02257.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1000-880C>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290523 | ||||||
| chr1:100290670
|
G | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0109a0001c0001t0001g0119 | 3 | HG01167.hp1 HG01169.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.1000-733G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290670 | ||||||
| chr1:100290696
|
G | A | 3 | a0001c0001t0009g0181a0001c0001t0009g0184a0001c0001t0009g0185 | 3 | HG02622.hp1 HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1000-707G>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290696 | ||||||
| chr1:100290715
|
G | T | 2 | a0001c0003t0001g0201a0001c0003t0001g0202 | 2 | HG00738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1000-688G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290715 | ||||||
| chr1:100290765
|
C | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 5 | HG02055.hp2 HG02451.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000-638C>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100290765 | ||||||
| chr1:100291245
|
ATTAAGTT | A | 13 | a0001c0001t0004g0034a0001c0001t0004g0158a0001c0001t0004g0159others(10): Show | 14 | HG02109.hp1 HG02717.hp1 HG03942.hp2 others(11): Show |
intron_variant | MODIFIER | c.1000-156_1000-150d others(9): Show |
RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr1 | 100291245 | |||||
| chr1:100291249
|
A | C | 3 | a0002c0002t0001g0051a0002c0002t0001g0052a0002c0002t0001g0053 | 3 | HG02258.hp1 HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1000-154A>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291249 | ||||||
| chr1:100291306
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1000-97G>T | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291306 | ||||||
| chr1:100291309
|
C | A | 1 | a0001c0001t0002g0168 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1000-94C>A | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291309 | ||||||
| chr1:100291328
|
CT | C | 3 | a0001c0001t0001g0020a0001c0001t0001g0078a0001c0001t0005g0020 | 3 | HG00642.hp1 HG01255.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.1000-74delT | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291328 | ||||||
| chr1:100291332
|
A | G | 3 | a0001c0001t0002g0033a0001c0001t0002g0153a0001c0001t0002g0154 | 4 | HG02895.hp1 HG02897.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000-71A>G | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291332 | ||||||
| chr1:100291371
|
G | C | 1 | a0001c0001t0001g0032 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1000-32G>C | RTCA | ENSG00000137996.13 | transcript | ENST00000370128.9 | protein_coding | 10/10 | chr1 | 100291371 |