Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 55732 |
|---|---|
| ensemblid | ENSG00000000460.17 |
| hgncid | 25565 |
| symbol | FIRRM |
| name | FIGNL1 interacting regulator of recombination and mitosis |
| refseq_nuc | NM_001320047.2 |
| refseq_prot | NP_001306976.1 |
| ensembl_nuc | ENST00000359326.9 |
| ensembl_prot | ENSP00000352276.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 169795040 |
| end | 169854080 |
| strand | + |
| ver | v1.2 |
| region | chr1:169795040-169854080 |
| region5000 | chr1:169790040-169859080 |
| regionname0 | FIRRM_chr1_169795040_169854080 |
| regionname5000 | FIRRM_chr1_169790040_169859080 |
| 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 | 853 | 385 | 82 | 61 | 188 | 13 | 39 | 145 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0002 | 0/0 | 853 | 15 | 0 | 5 | 5 | 2 | 3 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0003 | 0/0 | 853 | 10 | 10 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0004 | 0/0 | 853 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0005 | 0/0 | 853 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0006 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0007 | 0/0 | 853 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0008 | 0/0 | 853 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| 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 | 2562 | 328 | 78 | 45 | 159 | 13 | 31 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0002 | 0/0 | 2562 | 54 | 3 | 14 | 29 | 0 | 8 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0003 | 0/0 | 2562 | 14 | 0 | 5 | 4 | 2 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0004 | 0/0 | 2562 | 10 | 10 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0005 | 0/0 | 2562 | 6 | 0 | 0 | 6 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0006 | 0/0 | 2562 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0007 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0008 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0009 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0010 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0011 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| c0012 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| 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 | 1451 | 143 | 26 | 29 | 59 | 6 | 22 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0002 | 0/0 | 1451 | 106 | 19 | 13 | 67 | 3 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0003 | 0/0 | 1451 | 60 | 17 | 14 | 16 | 4 | 9 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0004 | 0/0 | 1460 | 58 | 3 | 2 | 48 | 1 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0005 | 0/0 | 1456 | 15 | 0 | 5 | 5 | 2 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0006 | 0/0 | 1456 | 9 | 9 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0007 | 0/0 | 1460 | 5 | 5 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0008 | 0/0 | 1451 | 5 | 5 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0009 | 0/0 | 1436 | 4 | 4 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0010 | 0/0 | 1460 | 4 | 4 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0011 | 1/0 | 1450 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0012 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0013 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0014 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0015 | 0/0 | 1451 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0016 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0017 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0018 | 0/0 | 1451 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0019 | 0/0 | 1451 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0020 | 0/0 | 1451 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| t0021 | 0/0 | 1451 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| 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 | 4 | 0 | 3 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0006 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| 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 | 2562 | 328 | 78 | 45 | 159 | 13 | 31 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0002 | 0/0 | 2562 | 54 | 3 | 14 | 29 | 0 | 8 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0006 | 0/0 | 2562 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0009 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0002c0003 | 0/0 | 2562 | 14 | 0 | 5 | 4 | 2 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0002c0012 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0003c0004 | 0/0 | 2562 | 10 | 10 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0004c0005 | 0/0 | 2562 | 6 | 0 | 0 | 6 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0005c0008 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0006c0007 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0007c0010 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0008c0011 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4012 | 82 | 21 | 15 | 25 | 6 | 14 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0002 | 0/0 | 4012 | 102 | 19 | 11 | 66 | 2 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0003 | 0/0 | 4012 | 50 | 7 | 14 | 16 | 4 | 9 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0004 | 0/0 | 4021 | 57 | 2 | 2 | 48 | 1 | 4 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0006 | 0/0 | 4017 | 9 | 9 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0007 | 0/0 | 4021 | 5 | 5 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0008 | 0/0 | 4012 | 5 | 5 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0009 | 0/0 | 3997 | 4 | 4 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0010 | 0/0 | 4021 | 4 | 4 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0011 | 1/0 | 4011 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0012 | 0/0 | 4012 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0013 | 0/0 | 4012 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0015 | 0/0 | 4012 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0016 | 0/0 | 4012 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0017 | 0/0 | 4012 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0018 | 0/0 | 4012 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0019 | 0/0 | 4012 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0020 | 0/0 | 4012 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0001t0021 | 0/0 | 4012 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0002t0001 | 0/0 | 4012 | 53 | 3 | 14 | 28 | 0 | 8 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0002t0014 | 0/0 | 4012 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0006t0002 | 0/0 | 4012 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0001c0009t0001 | 0/0 | 4012 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0002c0003t0005 | 0/0 | 4017 | 14 | 0 | 5 | 4 | 2 | 3 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0002c0012t0005 | 0/0 | 4017 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0003c0004t0003 | 0/0 | 4012 | 10 | 10 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0004c0005t0001 | 0/0 | 4012 | 6 | 0 | 0 | 6 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0005c0008t0002 | 0/0 | 4012 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0006c0007t0001 | 0/0 | 4012 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0007c0010t0004 | 0/0 | 4021 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| a0008c0011t0002 | 0/0 | 4012 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | copy fasta | chr1 | 169790040 | 169859080 |
| 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 | 4 | 0 | 3 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0002 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0006 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0010g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0010g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0011g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0012g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0013g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0015g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0016g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0017g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0018g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0019g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0020g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0001t0021g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0002t0014g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0006t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0006t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0001c0009t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0372 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0376 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0377 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0379 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0381 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0003t0005g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0002c0012t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0003c0004t0003g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0004c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0005c0008t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0006c0007t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0007c0010t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| a0008c0011t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0147 | EUR | GBR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0146 | EUR | GBR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0092 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0249 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | FIN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0328 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00423 | hp2 | a0004 | c0005 | t0001 | g0172 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0301 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00609 | hp2 | a0004 | c0005 | t0001 | g0168 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0290 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0297 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | CHS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0308 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0142 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00741 | hp1 | a0002 | c0003 | t0005 | g0377 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01069 | hp2 | a0001 | c0006 | t0002 | g0030 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01071 | hp2 | a0001 | c0006 | t0002 | g0031 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0124 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01109 | hp1 | a0001 | c0001 | t0018 | g0029 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0361 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0317 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0123 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01168 | hp2 | a0002 | c0003 | t0005 | g0373 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01169 | hp1 | a0002 | c0003 | t0005 | g0379 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0318 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01175 | hp2 | a0001 | c0001 | t0020 | g0153 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0346 | AMR | PUR | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0333 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0132 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0334 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0025 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0309 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01361 | hp2 | a0002 | c0003 | t0005 | g0380 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0144 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01516 | hp1 | a0002 | c0003 | t0005 | g0376 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01517 | hp2 | a0002 | c0003 | t0005 | g0371 | EUR | IBS | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01884 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01891 | hp1 | a0003 | c0004 | t0003 | g0137 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01891 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0250 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0338 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0315 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01981 | hp1 | a0002 | c0003 | t0005 | g0378 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0319 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0279 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02015 | hp2 | a0001 | c0001 | t0012 | g0214 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0311 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02027 | hp2 | a0008 | c0011 | t0002 | g0082 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0325 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02074 | hp1 | a0002 | c0003 | t0005 | g0382 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02129 | hp2 | a0001 | c0001 | t0004 | g0268 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0312 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0264 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0112 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0344 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CDX | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02257 | hp2 | a0001 | c0001 | t0013 | g0367 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02258 | hp1 | a0003 | c0004 | t0003 | g0155 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0343 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0316 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02280 | hp1 | a0001 | c0001 | t0006 | g0366 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0225 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02293 | hp1 | a0001 | c0001 | t0019 | g0099 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02451 | hp1 | a0001 | c0001 | t0010 | g0245 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0360 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02523 | hp1 | a0002 | c0003 | t0005 | g0374 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0362 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0272 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02615 | hp1 | a0007 | c0010 | t0004 | g0161 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02630 | hp1 | a0001 | c0001 | t0009 | g0228 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02630 | hp2 | a0003 | c0004 | t0003 | g0138 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02647 | hp2 | a0003 | c0004 | t0003 | g0150 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0241 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02717 | hp2 | a0006 | c0007 | t0001 | g0298 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02723 | hp1 | a0003 | c0004 | t0003 | g0133 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0336 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02818 | hp1 | a0003 | c0004 | t0003 | g0370 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02886 | hp1 | a0003 | c0004 | t0003 | g0159 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02895 | hp1 | a0003 | c0004 | t0003 | g0368 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0353 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0342 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02897 | hp1 | a0003 | c0004 | t0003 | g0369 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0350 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02965 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0348 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02970 | hp2 | a0001 | c0001 | t0007 | g0166 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0358 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0223 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0127 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0340 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0352 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0165 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03130 | hp2 | a0003 | c0004 | t0003 | g0154 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03139 | hp1 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0357 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03209 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03225 | hp2 | a0001 | c0009 | t0001 | g0006 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03239 | hp1 | a0002 | c0003 | t0005 | g0375 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0322 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0164 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0227 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0354 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03491 | hp2 | a0002 | c0003 | t0005 | g0381 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03516 | hp1 | a0001 | c0001 | t0007 | g0163 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0224 | AFR | ESN | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0113 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0363 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0115 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0111 | SAS | PJL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0321 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0335 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0300 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0339 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0117 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0313 | SAS | BEB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04199 | hp1 | a0002 | c0003 | t0005 | g0372 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0314 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0143 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0271 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | STU | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0222 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | CHB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18939 | hp1 | a0004 | c0005 | t0001 | g0170 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18943 | hp2 | a0002 | c0012 | t0005 | g0027 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18953 | hp1 | a0001 | c0002 | t0014 | g0295 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18953 | hp2 | a0002 | c0003 | t0005 | g0383 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0254 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18956 | hp2 | a0004 | c0005 | t0001 | g0169 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0292 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18961 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0310 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0280 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18972 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18973 | hp2 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18974 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0327 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0323 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0109 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18985 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0236 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18987 | hp2 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18989 | hp2 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18995 | hp1 | a0001 | c0002 | t0001 | g0337 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18997 | hp1 | a0001 | c0001 | t0016 | g0080 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0293 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0326 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19002 | hp2 | a0001 | c0001 | t0017 | g0060 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19005 | hp2 | a0001 | c0001 | t0021 | g0173 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0239 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0160 | AFR | LWK | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0324 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19056 | hp2 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19065 | hp1 | a0001 | c0001 | t0004 | g0253 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0329 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19066 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19070 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19072 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19075 | hp2 | a0004 | c0005 | t0001 | g0167 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0024 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0248 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0305 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0330 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19088 | hp2 | a0004 | c0005 | t0001 | g0171 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0303 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0157 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0136 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0187 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20805 | hp2 | a0005 | c0008 | t0002 | g0094 | EUR | TSI | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0097 | SAS | GIH | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0201 | SAS | GIH | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0320 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0140 | AMR | CLM | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0247 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02109 | hp2 | a0001 | c0001 | t0009 | g0226 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02486 | hp1 | a0001 | c0001 | t0006 | g0364 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02486 | hp2 | a0001 | c0001 | t0010 | g0238 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0359 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0365 | AFR | MSL | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18955 | hp1 | a0002 | c0003 | t0005 | g0027 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0356 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | USA | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0011 | g0090 | REF | REF | FIRRM_chr1_169790040_169859080 | FIRRM | chr1 | 169790040 | 169859080 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169804196
|
A | G | 1 | a0008 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.434A>G | p.Asp145Gly | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/25 | 790/4011 | 434/2562 | 145/853 | chr1 | 169804196 | ||
| chr1:169806067
|
A | G | 1 | a0007 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.542A>G | p.Asn181Ser | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/25 | 898/4011 | 542/2562 | 181/853 | chr1 | 169806067 | ||
| chr1:169807852
|
A | G | 1 | a0004 | 6 | HG00423.hp2 HG00609.hp2 NA18939.hp1 others(3): Show |
missense_variant | MODERATE | c.625A>G | p.Ser209Gly | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/25 | 981/4011 | 625/2562 | 209/853 | chr1 | 169807852 | ||
| chr1:169827056
|
T | C | 1 | a0003 | 10 | HG01891.hp1 HG02258.hp1 HG02630.hp2 others(7): Show |
missense_variant | MODERATE | c.854T>C | p.Phe285Ser | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/25 | 1210/4011 | 854/2562 | 285/853 | chr1 | 169827056 | ||
| chr1:169830739
|
G | T | 1 | a0002 | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
missense_variant | MODERATE | c.1441G>T | p.Ala481Ser | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/25 | 1797/4011 | 1441/2562 | 481/853 | chr1 | 169830739 | ||
| chr1:169837087
|
G | A | 1 | a0005 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.1700G>A | p.Arg567His | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/25 | 2056/4011 | 1700/2562 | 567/853 | chr1 | 169837087 | ||
| chr1:169851914
|
A | C | 1 | a0006 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.2342A>C | p.Glu781Ala | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/25 | 2698/4011 | 2342/2562 | 781/853 | chr1 | 169851914 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169803198
|
A | C | 1 | a0002c0012 | 1 | NA18943.hp2 | synonymous_variant | LOW | c.201A>C | p.Thr67Thr | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/25 | 557/4011 | 201/2562 | 67/853 | chr1 | 169803198 | ||
| chr1:169804176
|
G | A | 2 | a0001c0002a0006c0007 | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
synonymous_variant | LOW | c.414G>A | p.Leu138Leu | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/25 | 770/4011 | 414/2562 | 138/853 | chr1 | 169804176 | ||
| chr1:169827718
|
A | C | 1 | a0001c0009 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1005A>C | p.Pro335Pro | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/25 | 1361/4011 | 1005/2562 | 335/853 | chr1 | 169827718 | ||
| chr1:169851858
|
T | A | 1 | a0001c0006 | 2 | HG01069.hp2 HG01071.hp2 |
synonymous_variant | LOW | c.2286T>A | p.Arg762Arg | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/25 | 2642/4011 | 2286/2562 | 762/853 | chr1 | 169851858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169795041
|
C | T | 1 | a0001c0001t0021 | 1 | NA19005.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-355C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/25 | chr1 | 169795041 | ||||||
| chr1:169795851
|
T | TG | 30 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | 419 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(416): Show |
5_prime_UTR_variant | MODIFIER | c.-258_-257insG | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/25 | 5054 | chr1 | 169795851 | |||||
| chr1:169795875
|
A | G | 1 | a0001c0001t0008 | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-234A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/25 | 5031 | chr1 | 169795875 | |||||
| chr1:169795911
|
C | G | 6 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(3): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
5_prime_UTR_variant | MODIFIER | c.-198C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/25 | 4995 | chr1 | 169795911 | |||||
| chr1:169798892
|
T | C | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
5_prime_UTR_variant | MODIFIER | c.-90T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/25 | 2014 | chr1 | 169798892 | |||||
| chr1:169798897
|
G | A | 1 | a0001c0001t0015 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/25 | 2009 | chr1 | 169798897 | |||||
| chr1:169798939
|
C | A | 19 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
5_prime_UTR_variant | MODIFIER | c.-43C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/25 | 1967 | chr1 | 169798939 | |||||
| chr1:169852999
|
A | AGGCAGAA others(2): Show |
4 | a0001c0001t0004a0001c0001t0007a0001c0001t0010others(1): Show | 67 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*15_*23dupCAGAACTG others(1): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 24 | INFO_REALIGN_3_PRIME | chr1 | 169852999 | ||||
| chr1:169853231
|
A | G | 1 | a0001c0001t0009 | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*244A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 244 | chr1 | 169853231 | |||||
| chr1:169853312
|
A | G | 1 | a0001c0002t0014 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*325A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 325 | chr1 | 169853312 | |||||
| chr1:169853344
|
T | G | 1 | a0001c0001t0016 | 1 | NA18997.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 357 | chr1 | 169853344 | |||||
| chr1:169853347
|
T | TAAAGA | 2 | a0002c0003t0005a0002c0012t0005 | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*362_*366dupAAGAA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 367 | INFO_REALIGN_3_PRIME | chr1 | 169853347 | ||||
| chr1:169853402
|
A | G | 2 | a0002c0003t0005a0002c0012t0005 | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*415A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 415 | chr1 | 169853402 | |||||
| chr1:169853415
|
A | T | 1 | a0001c0001t0019 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*428A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 428 | chr1 | 169853415 | |||||
| chr1:169853709
|
A | G | 1 | a0001c0001t0010 | 4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*722A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 722 | chr1 | 169853709 | |||||
| chr1:169853751
|
C | G | 1 | a0001c0001t0018 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*764C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 764 | chr1 | 169853751 | |||||
| chr1:169853819
|
T | C | 1 | a0001c0001t0012 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 832 | chr1 | 169853819 | |||||
| chr1:169853842
|
A | T | 2 | a0001c0001t0009a0001c0001t0013 | 5 | HG02109.hp2 HG02257.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*855A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 855 | chr1 | 169853842 | |||||
| chr1:169853890
|
C | T | 1 | a0001c0001t0017 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*903C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 903 | chr1 | 169853890 | |||||
| chr1:169853905
|
AACTTAGA others(8): Show |
A | 1 | a0001c0001t0009 | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*920_*934delCTTAGA others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 920 | INFO_REALIGN_3_PRIME | chr1 | 169853905 | ||||
| chr1:169854007
|
T | G | 1 | a0001c0001t0020 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1020T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 1020 | chr1 | 169854007 | |||||
| chr1:169854036
|
T | TTTTTC | 1 | a0001c0001t0006 | 9 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1054_*1058dupCTTT others(1): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 25/25 | 1059 | INFO_REALIGN_3_PRIME | chr1 | 169854036 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:169795279
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-281+164C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795279 | ||||||
| chr1:169795361
|
A | AAAGTGAG others(12): Show |
3 | a0003c0004t0003g0368a0003c0004t0003g0369a0003c0004t0003g0370 | 3 | HG02818.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-281+250_-281+268d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr1 | 169795361 | |||||
| chr1:169795427
|
C | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-281+312C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795427 | ||||||
| chr1:169795448
|
C | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-281+333C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795448 | ||||||
| chr1:169795485
|
C | T | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-280-344C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795485 | ||||||
| chr1:169795747
|
A | G | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-280-82A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | chr1 | 169795747 | ||||||
| chr1:169795782
|
CTTCT | C | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-280-36_-280-33del others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr1 | 169795782 | |||||
| chr1:169795998
|
T | C | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.-126+15T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169795998 | ||||||
| chr1:169796098
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0006g0362 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.-126+115T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796098 | ||||||
| chr1:169796102
|
G | C | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-126+119G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796102 | ||||||
| chr1:169796170
|
C | A | 1 | a0001c0001t0002g0028 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-126+187C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796170 | ||||||
| chr1:169796186
|
A | G | 3 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0103 | 3 | NA18981.hp2 NA18991.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-126+203A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796186 | ||||||
| chr1:169796199
|
G | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(225): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.-126+216G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796199 | ||||||
| chr1:169796207
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-126+224C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796207 | ||||||
| chr1:169796292
|
G | A | 1 | a0001c0001t0018g0029 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-126+309G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796292 | ||||||
| chr1:169796321
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-126+338C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796321 | ||||||
| chr1:169796450
|
A | G | 2 | a0001c0001t0002g0100a0001c0001t0019g0099 | 2 | HG00735.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.-126+467A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796450 | ||||||
| chr1:169796582
|
T | A | 1 | a0001c0001t0003g0015 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-126+599T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796582 | ||||||
| chr1:169796635
|
A | G | 1 | a0001c0001t0002g0361 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-126+652A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796635 | ||||||
| chr1:169796758
|
G | A | 58 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(55): Show | 61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.-126+775G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796758 | ||||||
| chr1:169796861
|
T | G | 1 | a0001c0001t0003g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-126+878T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796861 | ||||||
| chr1:169796936
|
A | G | 2 | a0001c0002t0001g0359a0001c0002t0001g0360 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-126+953A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169796936 | ||||||
| chr1:169797137
|
C | T | 57 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(54): Show | 61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.-126+1154C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797137 | ||||||
| chr1:169797157
|
G | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-126+1174G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797157 | ||||||
| chr1:169797224
|
A | C | 4 | a0001c0001t0004g0284a0001c0001t0004g0285a0001c0001t0004g0286others(1): Show | 4 | NA18972.hp2 NA18973.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.-126+1241A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797224 | ||||||
| chr1:169797231
|
G | C | 2 | a0001c0006t0002g0030a0001c0006t0002g0031 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-126+1248G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797231 | ||||||
| chr1:169797474
|
T | A | 2 | a0001c0002t0001g0289a0001c0002t0001g0290 | 2 | HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.-125-1383T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797474 | ||||||
| chr1:169797487
|
G | A | 2 | a0001c0006t0002g0030a0001c0006t0002g0031 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-125-1370G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797487 | ||||||
| chr1:169797618
|
G | A | 1 | a0001c0001t0004g0235 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-125-1239G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797618 | ||||||
| chr1:169797670
|
G | A | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-125-1187G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797670 | ||||||
| chr1:169797741
|
A | C | 1 | a0003c0004t0003g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-125-1116A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797741 | ||||||
| chr1:169797822
|
G | A | 1 | a0001c0001t0002g0032 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-125-1035G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797822 | ||||||
| chr1:169797883
|
A | T | 6 | a0001c0001t0002g0095a0001c0001t0002g0096a0001c0001t0002g0097others(3): Show | 6 | HG00544.hp2 HG00735.hp2 HG02293.hp1 others(3): Show |
intron_variant | MODIFIER | c.-125-974A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797883 | ||||||
| chr1:169797884
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(284): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-125-973T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797884 | ||||||
| chr1:169797888
|
G | A | 6 | a0004c0005t0001g0167a0004c0005t0001g0168a0004c0005t0001g0169others(3): Show | 6 | HG00423.hp2 HG00609.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.-125-969G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169797888 | ||||||
| chr1:169798062
|
CTT | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.-125-794_-125-793d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798062 | ||||||
| chr1:169798237
|
T | C | 1 | a0001c0001t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-125-620T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798237 | ||||||
| chr1:169798268
|
G | T | 3 | a0001c0001t0004g0281a0001c0001t0004g0282a0001c0001t0004g0283 | 3 | NA18989.hp2 NA19005.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-125-589G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798268 | ||||||
| chr1:169798278
|
C | CT | 18 | a0001c0001t0002g0358a0001c0001t0018g0029a0002c0003t0005g0027others(15): Show | 18 | HG00741.hp1 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-125-564dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr1 | 169798278 | |||||
| chr1:169798280
|
T | C | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-125-577T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798280 | ||||||
| chr1:169798298
|
C | T | 2 | a0001c0001t0006g0008a0001c0001t0006g0234 | 4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-125-559C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798298 | ||||||
| chr1:169798320
|
T | G | 2 | a0001c0001t0001g0174a0001c0001t0021g0173 | 2 | NA18957.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-125-537T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798320 | ||||||
| chr1:169798345
|
G | A | 1 | a0001c0001t0019g0099 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-125-512G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798345 | ||||||
| chr1:169798485
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0175others(4): Show | 12 | HG00323.hp2 HG00741.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.-125-372G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798485 | ||||||
| chr1:169798561
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-125-296T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798561 | ||||||
| chr1:169798636
|
G | A | 1 | a0003c0004t0003g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-125-221G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798636 | ||||||
| chr1:169798683
|
G | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-125-174G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 2/24 | chr1 | 169798683 | ||||||
| chr1:169798990
|
C | T | 1 | a0002c0003t0005g0383 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-24+32C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169798990 | ||||||
| chr1:169799220
|
G | A | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-24+262G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799220 | ||||||
| chr1:169799227
|
G | T | 1 | a0001c0001t0001g0233 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-24+269G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799227 | ||||||
| chr1:169799231
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.-24+273C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799231 | ||||||
| chr1:169799338
|
G | A | 1 | a0001c0001t0002g0033 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-24+380G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799338 | ||||||
| chr1:169799338
|
G | T | 4 | a0001c0001t0002g0354a0001c0001t0002g0355a0001c0001t0002g0356others(1): Show | 4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24+380G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799338 | ||||||
| chr1:169799359
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24+401C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799359 | ||||||
| chr1:169799421
|
A | G | 6 | a0001c0001t0001g0131a0001c0001t0006g0362a0001c0001t0006g0363others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24+463A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799421 | ||||||
| chr1:169799424
|
C | G | 1 | a0001c0001t0003g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-24+466C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799424 | ||||||
| chr1:169799440
|
A | G | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-24+482A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799440 | ||||||
| chr1:169799708
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24+750C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799708 | ||||||
| chr1:169799744
|
G | T | 1 | a0001c0001t0001g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-24+786G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799744 | ||||||
| chr1:169799812
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-24+854A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799812 | ||||||
| chr1:169799833
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24+875G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799833 | ||||||
| chr1:169799840
|
G | A | 379 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(376): Show | 412 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.-24+882G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799840 | ||||||
| chr1:169799847
|
C | A | 1 | a0001c0002t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-24+889C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799847 | ||||||
| chr1:169799904
|
G | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-24+946G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799904 | ||||||
| chr1:169799935
|
C | G | 1 | a0001c0001t0001g0106 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-23-948C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799935 | ||||||
| chr1:169799969
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 5 | NA18944.hp1 NA18954.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-914C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169799969 | ||||||
| chr1:169800025
|
G | A | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(294): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.-23-858G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800025 | ||||||
| chr1:169800029
|
T | TTTTG | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-23-842_-23-839dup others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800029 | |||||
| chr1:169800092
|
C | T | 1 | a0001c0002t0001g0339 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-23-791C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800092 | ||||||
| chr1:169800173
|
G | A | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0015g0342 | 3 | HG02896.hp2 HG02922.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-23-710G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800173 | ||||||
| chr1:169800233
|
A | G | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23-650A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800233 | ||||||
| chr1:169800239
|
T | G | 1 | a0001c0001t0002g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-23-644T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800239 | ||||||
| chr1:169800259
|
G | A | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-23-624G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800259 | ||||||
| chr1:169800339
|
G | A | 2 | a0001c0001t0004g0236a0001c0001t0004g0237 | 2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-23-544G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800339 | ||||||
| chr1:169800425
|
G | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.-23-458G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800425 | ||||||
| chr1:169800613
|
T | C | 1 | a0001c0001t0007g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-23-270T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800613 | ||||||
| chr1:169800661
|
A | T | 1 | a0001c0001t0002g0353 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-23-222A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | chr1 | 169800661 | ||||||
| chr1:169800709
|
TTC | T | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-168_-23-167del others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800709 | |||||
| chr1:169800715
|
C | CT | 7 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0001g0180others(4): Show | 8 | HG02559.hp2 HG02809.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.-23-153dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | |||||
| chr1:169800715
|
C | CTT | 227 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(224): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.-23-154_-23-153dup others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | |||||
| chr1:169800715
|
C | CTTT | 5 | a0001c0001t0006g0362a0001c0001t0008g0020a0001c0001t0008g0222others(2): Show | 6 | HG01884.hp1 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-23-155_-23-153dup others(3): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | |||||
| chr1:169800715
|
C | CTTTT | 60 | a0001c0001t0002g0358a0001c0001t0004g0023a0001c0001t0004g0024others(57): Show | 64 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-23-156_-23-153dup others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr1 | 169800715 | |||||
| chr1:169801159
|
C | T | 1 | a0001c0001t0009g0228 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.66+188C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801159 | ||||||
| chr1:169801178
|
C | T | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+207C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801178 | ||||||
| chr1:169801336
|
T | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+365T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801336 | ||||||
| chr1:169801433
|
G | A | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+462G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801433 | ||||||
| chr1:169801445
|
C | CA | 161 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(158): Show | 174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.66+496dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801445 | |||||
| chr1:169801445
|
C | CAA | 24 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(21): Show | 25 | HG01884.hp1 HG01975.hp1 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.66+495_66+496dupAA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801445 | |||||
| chr1:169801445
|
CA | C | 14 | a0001c0001t0001g0131a0001c0001t0001g0221a0001c0001t0002g0033others(11): Show | 14 | HG02109.hp2 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+496delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801445 | |||||
| chr1:169801496
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.66+525C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801496 | ||||||
| chr1:169801505
|
C | T | 1 | a0001c0001t0004g0240 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.66+534C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801505 | ||||||
| chr1:169801597
|
C | CA | 14 | a0001c0001t0002g0040a0002c0003t0005g0027a0002c0003t0005g0371others(11): Show | 14 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.66+646dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801597 | |||||
| chr1:169801597
|
CAAA | C | 62 | a0001c0001t0001g0175a0001c0001t0003g0014a0001c0001t0003g0015others(59): Show | 65 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.66+644_66+646delAA others(1): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801597 | |||||
| chr1:169801597
|
CAAAA | C | 200 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(197): Show | 223 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.66+643_66+646delAA others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr1 | 169801597 | |||||
| chr1:169801679
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.66+708A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801679 | ||||||
| chr1:169801731
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.66+760A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801731 | ||||||
| chr1:169801810
|
T | C | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-811T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801810 | ||||||
| chr1:169801863
|
A | T | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-758A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169801863 | ||||||
| chr1:169802057
|
T | C | 3 | a0001c0001t0001g0174a0001c0001t0001g0186a0001c0001t0021g0173 | 3 | NA18957.hp1 NA18960.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.67-564T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802057 | ||||||
| chr1:169802068
|
A | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0129a0001c0001t0003g0130 | 3 | NA18964.hp1 NA18974.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.67-553A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802068 | ||||||
| chr1:169802109
|
A | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.67-512A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802109 | ||||||
| chr1:169802221
|
G | A | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-400G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802221 | ||||||
| chr1:169802236
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.67-385A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802236 | ||||||
| chr1:169802288
|
A | G | 2 | a0001c0001t0006g0008a0001c0001t0006g0234 | 4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-333A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802288 | ||||||
| chr1:169802295
|
T | G | 1 | a0001c0001t0001g0187 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.67-326T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802295 | ||||||
| chr1:169802477
|
G | A | 3 | a0001c0002t0001g0297a0001c0002t0001g0299a0006c0007t0001g0298 | 3 | HG00642.hp2 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.67-144G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 4/24 | chr1 | 169802477 | ||||||
| chr1:169802797
|
G | A | 1 | a0007c0010t0004g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.171+72G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802797 | ||||||
| chr1:169802824
|
C | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.171+99C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802824 | ||||||
| chr1:169802867
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0220others(1): Show | 7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+142A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802867 | ||||||
| chr1:169802883
|
A | G | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.171+158A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169802883 | ||||||
| chr1:169802898
|
TAAG | T | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(72): Show | 91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.171+178_171+180del others(3): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr1 | 169802898 | |||||
| chr1:169803093
|
C | T | 1 | a0001c0001t0002g0353 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.172-76C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169803093 | ||||||
| chr1:169803144
|
G | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.172-25G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 5/24 | chr1 | 169803144 | ||||||
| chr1:169803504
|
T | TG | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.312+199dupG | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr1 | 169803504 | |||||
| chr1:169803521
|
A | T | 1 | a0001c0001t0008g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.312+212A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | chr1 | 169803521 | ||||||
| chr1:169803651
|
TC | T | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.312+344delC | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr1 | 169803651 | |||||
| chr1:169803836
|
C | T | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.313-239C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | chr1 | 169803836 | ||||||
| chr1:169804019
|
T | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.313-56T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 6/24 | chr1 | 169804019 | ||||||
| chr1:169804294
|
A | G | 6 | a0001c0001t0001g0131a0001c0001t0006g0362a0001c0001t0006g0363others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+54A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804294 | ||||||
| chr1:169804344
|
A | C | 1 | a0001c0001t0002g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.478+104A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804344 | ||||||
| chr1:169804460
|
A | G | 1 | a0001c0001t0009g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.478+220A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804460 | ||||||
| chr1:169804475
|
A | G | 2 | a0001c0006t0002g0030a0001c0006t0002g0031 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.478+235A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804475 | ||||||
| chr1:169804524
|
AT | A | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.478+291delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr1 | 169804524 | |||||
| chr1:169804556
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.478+316G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804556 | ||||||
| chr1:169804589
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(72): Show | 91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.478+349G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804589 | ||||||
| chr1:169804722
|
A | C | 16 | a0001c0001t0002g0358a0002c0003t0005g0027a0002c0003t0005g0371others(13): Show | 16 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.478+482A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804722 | ||||||
| chr1:169804782
|
A | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.478+542A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804782 | ||||||
| chr1:169804863
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.478+623A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804863 | ||||||
| chr1:169804966
|
A | G | 6 | a0001c0001t0001g0131a0001c0001t0006g0362a0001c0001t0006g0363others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.478+726A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169804966 | ||||||
| chr1:169805143
|
C | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.479-861C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805143 | ||||||
| chr1:169805179
|
T | C | 2 | a0001c0001t0004g0241a0001c0001t0004g0242 | 2 | HG02683.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.479-825T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805179 | ||||||
| chr1:169805182
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.479-822A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805182 | ||||||
| chr1:169805193
|
A | G | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.479-811A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805193 | ||||||
| chr1:169805374
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.479-630T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805374 | ||||||
| chr1:169805375
|
A | G | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.479-629A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805375 | ||||||
| chr1:169805435
|
G | T | 1 | a0001c0001t0002g0086 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.479-569G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805435 | ||||||
| chr1:169805521
|
C | T | 2 | a0001c0002t0001g0296a0001c0002t0001g0337 | 2 | NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.479-483C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805521 | ||||||
| chr1:169805522
|
C | T | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.479-482C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805522 | ||||||
| chr1:169805628
|
T | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.479-376T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169805628 | ||||||
| chr1:169806001
|
C | T | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.479-3C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 7/24 | chr1 | 169806001 | ||||||
| chr1:169806176
|
A | G | 4 | a0001c0001t0004g0277a0001c0001t0004g0278a0001c0001t0004g0279others(1): Show | 4 | HG02015.hp1 HG02080.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.563+88A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806176 | ||||||
| chr1:169806483
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.563+395A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806483 | ||||||
| chr1:169806563
|
A | T | 1 | a0001c0001t0004g0240 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.563+475A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806563 | ||||||
| chr1:169806577
|
T | C | 11 | a0001c0001t0001g0188a0001c0001t0001g0189a0001c0001t0001g0190others(8): Show | 11 | HG00423.hp2 HG00609.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.563+489T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806577 | ||||||
| chr1:169806940
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.564-851A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169806940 | ||||||
| chr1:169807056
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.564-735T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807056 | ||||||
| chr1:169807094
|
T | A | 1 | a0001c0002t0001g0300 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.564-697T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807094 | ||||||
| chr1:169807234
|
T | A | 1 | a0001c0001t0002g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.564-557T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807234 | ||||||
| chr1:169807242
|
A | G | 1 | a0001c0001t0001g0210 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.564-549A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807242 | ||||||
| chr1:169807315
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0220others(1): Show | 7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.564-476A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807315 | ||||||
| chr1:169807485
|
A | C | 66 | a0001c0001t0001g0017a0001c0001t0001g0131a0001c0001t0001g0162others(63): Show | 68 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.564-306A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807485 | ||||||
| chr1:169807493
|
G | T | 1 | a0001c0001t0001g0219 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.564-298G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807493 | ||||||
| chr1:169807603
|
T | A | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.564-188T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 8/24 | chr1 | 169807603 | ||||||
| chr1:169808028
|
T | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+99T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808028 | ||||||
| chr1:169808030
|
T | C | 1 | a0001c0001t0002g0041 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.702+101T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808030 | ||||||
| chr1:169808284
|
A | G | 6 | a0001c0001t0001g0007a0001c0001t0001g0215a0001c0001t0001g0216others(3): Show | 8 | HG02015.hp2 HG02056.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.702+355A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808284 | ||||||
| chr1:169808438
|
T | A | 1 | a0001c0001t0004g0243 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.702+509T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808438 | ||||||
| chr1:169808608
|
G | GT | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(220): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.702+693dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169808608 | |||||
| chr1:169808608
|
G | GTT | 55 | a0001c0001t0001g0162a0001c0001t0002g0358a0001c0001t0003g0128others(52): Show | 56 | HG00408.hp1 HG00621.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.702+692_702+693dup others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169808608 | |||||
| chr1:169808660
|
A | G | 1 | a0001c0001t0004g0242 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.702+731A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808660 | ||||||
| chr1:169808971
|
A | G | 2 | a0001c0001t0002g0083a0001c0001t0002g0084 | 2 | HG02056.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.702+1042A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808971 | ||||||
| chr1:169808986
|
G | A | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.702+1057G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169808986 | ||||||
| chr1:169809014
|
C | T | 1 | a0001c0001t0002g0357 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.702+1085C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809014 | ||||||
| chr1:169809095
|
A | G | 1 | a0001c0001t0015g0342 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.702+1166A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809095 | ||||||
| chr1:169809292
|
C | T | 1 | a0001c0002t0001g0336 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.702+1363C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809292 | ||||||
| chr1:169809351
|
A | G | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+1422A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809351 | ||||||
| chr1:169809360
|
G | A | 1 | a0001c0002t0001g0304 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.702+1431G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809360 | ||||||
| chr1:169809376
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.702+1447C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809376 | ||||||
| chr1:169809413
|
A | C | 2 | a0001c0002t0001g0289a0001c0002t0001g0290 | 2 | HG00621.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.702+1484A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809413 | ||||||
| chr1:169809418
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.702+1489C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809418 | ||||||
| chr1:169809539
|
A | G | 1 | a0008c0011t0002g0082 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.702+1610A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809539 | ||||||
| chr1:169809604
|
A | G | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.702+1675A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809604 | ||||||
| chr1:169809615
|
A | G | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.702+1686A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809615 | ||||||
| chr1:169809872
|
A | C | 1 | a0001c0002t0001g0360 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.702+1943A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809872 | ||||||
| chr1:169809998
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.702+2069C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169809998 | ||||||
| chr1:169810116
|
G | A | 1 | a0001c0001t0002g0095 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.702+2187G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810116 | ||||||
| chr1:169810173
|
C | A | 1 | a0001c0001t0007g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.702+2244C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810173 | ||||||
| chr1:169810202
|
T | G | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+2273T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810202 | ||||||
| chr1:169810348
|
G | A | 3 | a0001c0002t0001g0305a0001c0002t0001g0306a0001c0002t0001g0307 | 3 | NA18940.hp2 NA19076.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.702+2419G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810348 | ||||||
| chr1:169810360
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.702+2431C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810360 | ||||||
| chr1:169810446
|
T | C | 6 | a0001c0001t0001g0131a0001c0001t0006g0362a0001c0001t0006g0363others(3): Show | 6 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+2517T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810446 | ||||||
| chr1:169810523
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+2594A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810523 | ||||||
| chr1:169810525
|
T | G | 1 | a0001c0001t0003g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2596T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810525 | ||||||
| chr1:169810583
|
G | T | 1 | a0001c0001t0003g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2654G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810583 | ||||||
| chr1:169810649
|
T | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+2720T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810649 | ||||||
| chr1:169810669
|
T | C | 52 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(49): Show | 53 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.702+2740T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810669 | ||||||
| chr1:169810703
|
C | G | 1 | a0001c0001t0003g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.702+2774C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810703 | ||||||
| chr1:169810731
|
A | T | 1 | a0001c0001t0003g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2802A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810731 | ||||||
| chr1:169810764
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.702+2835G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810764 | ||||||
| chr1:169810798
|
A | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+2869A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810798 | ||||||
| chr1:169810815
|
T | C | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.702+2886T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810815 | ||||||
| chr1:169810832
|
C | A | 1 | a0001c0001t0004g0244 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.702+2903C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810832 | ||||||
| chr1:169810834
|
A | AT | 43 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0021others(40): Show | 53 | HG00438.hp1 HG00621.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.702+2941dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATT | 23 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(20): Show | 23 | HG00408.hp2 HG00735.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.702+2940_702+2941d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTT | 7 | a0001c0001t0001g0106a0001c0001t0001g0209a0001c0001t0002g0098others(4): Show | 7 | HG00323.hp1 HG01884.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+2939_702+2941d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTT | 22 | a0001c0001t0001g0105a0001c0001t0002g0346a0001c0001t0004g0025others(19): Show | 23 | HG00423.hp1 HG00673.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.702+2938_702+2941d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTT | 20 | a0001c0001t0004g0235a0001c0001t0004g0240a0001c0001t0004g0243others(17): Show | 20 | HG00438.hp2 HG02015.hp1 HG02129.hp2 others(17): Show |
intron_variant | MODIFIER | c.702+2937_702+2941d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(1): Show |
9 | a0001c0001t0002g0347a0001c0001t0002g0354a0001c0001t0002g0355others(6): Show | 9 | HG02602.hp1 HG02647.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.702+2934_702+2941d others(10): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(3): Show |
7 | a0001c0001t0003g0108a0001c0001t0003g0109a0001c0001t0003g0118others(4): Show | 7 | HG02083.hp2 NA18964.hp2 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+2932_702+2941d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(4): Show |
9 | a0001c0001t0003g0014a0001c0001t0003g0110a0001c0001t0003g0119others(6): Show | 10 | HG03942.hp1 NA18959.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+2931_702+2941d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(5): Show |
4 | a0001c0001t0003g0121a0001c0002t0001g0328a0001c0002t0001g0329others(1): Show | 4 | HG00408.hp1 NA18994.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+2930_702+2941d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0122 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.702+2929_702+2941d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(7): Show |
4 | a0001c0001t0002g0348a0001c0001t0002g0358a0001c0001t0003g0129others(1): Show | 4 | HG02970.hp1 HG02976.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2928_702+2941d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(8): Show |
2 | a0001c0002t0001g0306a0001c0002t0001g0307 | 2 | NA18940.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.702+2927_702+2941d others(17): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0002t0001g0293others(1): Show | 4 | HG01074.hp1 HG01167.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+2926_702+2941d others(18): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0004g0287 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.702+2925_702+2941d others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(11): Show |
4 | a0001c0001t0003g0125a0001c0001t0003g0128a0001c0002t0001g0332others(1): Show | 4 | HG03471.hp1 NA18977.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2924_702+2941d others(20): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(12): Show |
1 | a0001c0002t0001g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.702+2923_702+2941d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(13): Show |
4 | a0001c0001t0002g0344a0001c0001t0002g0349a0001c0001t0003g0130others(1): Show | 4 | HG01258.hp2 HG02145.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2922_702+2941d others(22): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(14): Show |
1 | a0001c0002t0001g0335 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.702+2921_702+2941d others(23): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0003g0126 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.702+2920_702+2941d others(24): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0003g0127 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.702+2918_702+2941d others(26): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(19): Show |
1 | a0001c0001t0003g0107 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.702+2916_702+2941d others(28): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | ATTTTTTT others(25): Show |
1 | a0001c0002t0001g0290 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.702+2910_702+2941d others(34): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
A | T | 2 | a0001c0001t0002g0081a0001c0001t0004g0244 | 2 | HG00597.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.702+2905A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810834 | ||||||
| chr1:169810834
|
AT | A | 27 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0131others(24): Show | 32 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.702+2941delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATT | A | 13 | a0001c0001t0001g0019a0001c0001t0001g0180a0001c0001t0001g0193others(10): Show | 14 | HG01123.hp1 HG01981.hp2 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.702+2940_702+2941d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTT | A | 10 | a0001c0001t0001g0212a0001c0001t0002g0340a0001c0001t0002g0341others(7): Show | 11 | HG01167.hp1 HG01169.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+2939_702+2941d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTT | A | 7 | a0001c0001t0003g0151a0001c0001t0003g0152a0001c0001t0003g0156others(4): Show | 7 | HG01175.hp2 HG01978.hp2 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.702+2937_702+2941d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTT | A | 37 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(34): Show | 39 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.702+2936_702+2941d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT | A | 10 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0228others(7): Show | 10 | HG01168.hp2 HG01517.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+2935_702+2941d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(3): Show |
A | 7 | a0001c0001t0001g0192a0001c0001t0003g0115a0001c0001t0004g0246others(4): Show | 7 | HG00642.hp2 HG02717.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+2932_702+2941d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0001g0104a0001c0002t0001g0301 | 2 | HG00597.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.702+2931_702+2941d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0002t0001g0310a0001c0002t0001g0311a0001c0002t0001g0312 | 3 | HG02027.hp1 HG02132.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.702+2930_702+2941d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(6): Show |
A | 1 | a0001c0001t0002g0345 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.702+2929_702+2941d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(7): Show |
A | 8 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(5): Show | 9 | HG02280.hp1 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2928_702+2941d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(8): Show |
A | 2 | a0001c0001t0002g0043a0001c0001t0003g0114 | 2 | HG00544.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.702+2927_702+2941d others(17): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(9): Show |
A | 8 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0003g0112others(5): Show | 9 | HG02145.hp1 HG02559.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2926_702+2941d others(18): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810834
|
ATTTTTTT others(10): Show |
A | 2 | a0001c0002t0001g0308a0001c0002t0001g0309 | 2 | HG00733.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.702+2925_702+2941d others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169810834 | |||||
| chr1:169810845
|
T | A | 1 | a0001c0001t0003g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.702+2916T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810845 | ||||||
| chr1:169810871
|
G | T | 1 | a0001c0002t0001g0304 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.702+2942G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810871 | ||||||
| chr1:169810872
|
A | T | 1 | a0001c0002t0001g0304 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.702+2943A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810872 | ||||||
| chr1:169810887
|
C | G | 3 | a0001c0001t0004g0284a0001c0001t0004g0285a0001c0001t0004g0286 | 3 | NA18973.hp2 NA19062.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.702+2958C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810887 | ||||||
| chr1:169810892
|
G | A | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+2963G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810892 | ||||||
| chr1:169810926
|
C | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+2997C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810926 | ||||||
| chr1:169810985
|
G | A | 1 | a0001c0001t0006g0363 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.702+3056G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169810985 | ||||||
| chr1:169811014
|
C | T | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3085C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811014 | ||||||
| chr1:169811016
|
C | T | 1 | a0001c0002t0001g0292 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.702+3087C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811016 | ||||||
| chr1:169811020
|
C | T | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+3091C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811020 | ||||||
| chr1:169811349
|
A | C | 2 | a0001c0001t0003g0108a0001c0001t0003g0118 | 2 | NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.702+3420A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811349 | ||||||
| chr1:169811362
|
T | G | 1 | a0001c0001t0002g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.702+3433T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811362 | ||||||
| chr1:169811674
|
A | AATCTAAA others(17): Show |
10 | a0001c0001t0003g0112a0001c0001t0003g0119a0001c0001t0006g0363others(7): Show | 10 | HG02145.hp1 HG02280.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.702+3871_702+3894d others(26): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811674 | |||||
| chr1:169811674
|
AATCTAAA others(17): Show |
A | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(185): Show | 211 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.702+3871_702+3894d others(26): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811674 | |||||
| chr1:169811674
|
AATCTAAA others(41): Show |
A | 9 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(6): Show | 9 | HG00280.hp1 HG00673.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+3847_702+3894d others(50): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811674 | |||||
| chr1:169811693
|
C | T | 10 | a0002c0003t0005g0027a0002c0003t0005g0372a0002c0003t0005g0373others(7): Show | 10 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.702+3764C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811693 | ||||||
| chr1:169811704
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3775A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811704 | ||||||
| chr1:169811717
|
C | T | 1 | a0001c0002t0001g0296 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.702+3788C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811717 | ||||||
| chr1:169811722
|
T | A | 1 | a0001c0002t0001g0296 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.702+3793T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811722 | ||||||
| chr1:169811728
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3799A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811728 | ||||||
| chr1:169811752
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3823A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811752 | ||||||
| chr1:169811761
|
TAGACAGA others(21): Show |
T | 1 | a0001c0002t0001g0321 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.702+3836_702+3863d others(30): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811761 | |||||
| chr1:169811765
|
C | CAGATTAT others(61): Show |
2 | a0002c0003t0005g0378a0002c0003t0005g0380 | 2 | HG01361.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.702+3846_702+3847i others(70): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811765 | |||||
| chr1:169811765
|
C | CAGATTAT others(85): Show |
13 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(10): Show | 13 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.702+3846_702+3847i others(94): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811765 | |||||
| chr1:169811765
|
C | T | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3836C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811765 | ||||||
| chr1:169811766
|
A | T | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3837A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811766 | ||||||
| chr1:169811767
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3838G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811767 | ||||||
| chr1:169811768
|
A | T | 58 | a0001c0001t0002g0358a0001c0001t0004g0023a0001c0001t0004g0024others(55): Show | 62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.702+3839A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811768 | ||||||
| chr1:169811769
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3840T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811769 | ||||||
| chr1:169811776
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3847A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811776 | ||||||
| chr1:169811785
|
TAGACAGA others(21): Show |
T | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.702+3860_702+3887d others(30): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811785 | |||||
| chr1:169811789
|
C | T | 1 | a0001c0001t0004g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3860C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811789 | ||||||
| chr1:169811790
|
A | T | 1 | a0001c0001t0004g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3861A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811790 | ||||||
| chr1:169811791
|
G | A | 1 | a0001c0001t0004g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3862G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811791 | ||||||
| chr1:169811792
|
A | T | 1 | a0001c0001t0004g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3863A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811792 | ||||||
| chr1:169811793
|
T | C | 1 | a0001c0001t0004g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702+3864T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811793 | ||||||
| chr1:169811797
|
CTAAATAG others(37): Show |
C | 26 | a0001c0001t0002g0009a0001c0001t0002g0010a0001c0001t0002g0011others(23): Show | 30 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.702+3871_702+3914d others(46): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811797 | |||||
| chr1:169811800
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+3871A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811800 | ||||||
| chr1:169811811
|
G | GATTATCT others(13): Show |
1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+3883_702+3884i others(22): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(157): Show |
2 | a0001c0001t0004g0251a0007c0010t0004g0161 | 2 | HG00673.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.702+3883_702+3884i others(166): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(181): Show |
3 | a0001c0001t0010g0022a0001c0001t0010g0238a0001c0001t0010g0245 | 4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(190): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(205): Show |
6 | a0001c0001t0004g0236a0001c0001t0004g0237a0001c0001t0004g0249others(3): Show | 6 | HG00323.hp1 HG02155.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(214): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(229): Show |
11 | a0001c0001t0004g0235a0001c0001t0004g0239a0001c0001t0004g0246others(8): Show | 11 | HG01943.hp1 HG02135.hp2 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(238): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(253): Show |
16 | a0001c0001t0004g0023a0001c0001t0004g0025a0001c0001t0004g0240others(13): Show | 18 | HG00423.hp1 HG00438.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(262): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(277): Show |
5 | a0001c0001t0004g0024a0001c0001t0004g0260a0001c0001t0004g0268others(2): Show | 6 | HG02129.hp2 HG04204.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(286): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(301): Show |
5 | a0001c0001t0004g0244a0001c0001t0004g0261a0001c0001t0004g0269others(2): Show | 5 | HG02602.hp1 NA18959.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+3883_702+3884i others(310): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(325): Show |
2 | a0001c0001t0004g0242a0001c0001t0004g0273 | 2 | HG04228.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.702+3883_702+3884i others(334): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811811
|
G | GATTATCT others(349): Show |
3 | a0001c0001t0004g0241a0001c0001t0004g0248a0001c0001t0004g0274 | 3 | HG02683.hp2 NA18966.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.702+3883_702+3884i others(358): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811811 | |||||
| chr1:169811813
|
C | CAGATTAT others(109): Show |
1 | a0001c0001t0007g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.702+3894_702+3895i others(118): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811813 | |||||
| chr1:169811813
|
C | CAGTTTAT others(301): Show |
4 | a0001c0001t0004g0277a0001c0001t0004g0278a0001c0001t0004g0279others(1): Show | 4 | HG02015.hp1 HG02080.hp2 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+3886_702+3887i others(310): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811813 | |||||
| chr1:169811813
|
C | T | 54 | a0001c0001t0002g0358a0001c0001t0004g0023a0001c0001t0004g0024others(51): Show | 58 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.702+3884C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811813 | ||||||
| chr1:169811816
|
ATTATCTA others(16): Show |
A | 1 | a0001c0001t0002g0044 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.702+3888_702+3910d others(25): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811816 | ||||||
| chr1:169811821
|
C | CTAAATAG others(13): Show |
1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3894_702+3895i others(22): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811821 | |||||
| chr1:169811828
|
A | T | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3899A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811828 | ||||||
| chr1:169811829
|
A | C | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.702+3900A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169811829 | ||||||
| chr1:169811841
|
T | TTATC | 57 | a0001c0001t0002g0358a0001c0001t0004g0023a0001c0001t0004g0024others(54): Show | 61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.702+3915_702+3918d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811841 | |||||
| chr1:169811841
|
T | TTATCTAT others(257): Show |
1 | a0001c0001t0004g0263 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.702+3918_702+3919i others(266): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811841 | |||||
| chr1:169811869
|
T | TTAGA | 4 | a0001c0001t0003g0113a0001c0001t0003g0119a0001c0001t0003g0129others(1): Show | 4 | HG02572.hp2 HG03579.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+3961_702+3964d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169811869 | |||||
| chr1:169812100
|
G | A | 1 | a0003c0004t0003g0150 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.702+4171G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812100 | ||||||
| chr1:169812150
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+4221A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812150 | ||||||
| chr1:169812384
|
G | C | 1 | a0001c0001t0004g0241 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.702+4455G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812384 | ||||||
| chr1:169812400
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0220others(1): Show | 7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+4471G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812400 | ||||||
| chr1:169812436
|
C | G | 1 | a0001c0001t0004g0255 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.702+4507C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812436 | ||||||
| chr1:169812465
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.702+4536T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812465 | ||||||
| chr1:169812528
|
A | T | 1 | a0001c0001t0004g0283 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.702+4599A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812528 | ||||||
| chr1:169812547
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0197 | 3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+4618A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812547 | ||||||
| chr1:169812728
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0197 | 3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.702+4799G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812728 | ||||||
| chr1:169812856
|
C | CA | 6 | a0001c0001t0002g0098a0001c0001t0004g0283a0001c0002t0001g0304others(3): Show | 6 | HG01256.hp1 HG01258.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+4941dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169812856 | |||||
| chr1:169812968
|
T | G | 33 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(30): Show | 35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.702+5039T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812968 | ||||||
| chr1:169812972
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+5043A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169812972 | ||||||
| chr1:169813048
|
C | T | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.702+5119C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813048 | ||||||
| chr1:169813102
|
A | G | 26 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(23): Show | 27 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.702+5173A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813102 | ||||||
| chr1:169813265
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.702+5336T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813265 | ||||||
| chr1:169813268
|
A | G | 12 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0343others(9): Show | 12 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.702+5339A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813268 | ||||||
| chr1:169813424
|
G | A | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.702+5495G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813424 | ||||||
| chr1:169813451
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.702+5522C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813451 | ||||||
| chr1:169813486
|
G | A | 3 | a0001c0002t0001g0321a0001c0002t0001g0322a0001c0002t0001g0336 | 3 | HG02735.hp2 HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.702+5557G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813486 | ||||||
| chr1:169813706
|
A | G | 1 | a0001c0001t0004g0266 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.702+5777A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813706 | ||||||
| chr1:169813879
|
C | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+5950C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813879 | ||||||
| chr1:169813917
|
A | T | 1 | a0001c0001t0017g0060 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.702+5988A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813917 | ||||||
| chr1:169813927
|
C | T | 1 | a0004c0005t0001g0171 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.702+5998C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813927 | ||||||
| chr1:169813959
|
C | G | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+6030C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169813959 | ||||||
| chr1:169814105
|
G | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6176G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814105 | ||||||
| chr1:169814403
|
T | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6474T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814403 | ||||||
| chr1:169814407
|
A | G | 1 | a0001c0001t0001g0190 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.702+6478A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814407 | ||||||
| chr1:169814498
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.702+6569G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814498 | ||||||
| chr1:169814513
|
C | G | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.702+6584C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814513 | ||||||
| chr1:169814518
|
G | A | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.702+6589G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814518 | ||||||
| chr1:169814599
|
A | C | 1 | a0001c0001t0002g0343 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.702+6670A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814599 | ||||||
| chr1:169814604
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6675A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814604 | ||||||
| chr1:169814616
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.702+6687A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814616 | ||||||
| chr1:169814639
|
C | T | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+6710C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814639 | ||||||
| chr1:169814661
|
G | A | 65 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0006g0362others(62): Show | 67 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.702+6732G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814661 | ||||||
| chr1:169814847
|
C | A | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.703-6832C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169814847 | ||||||
| chr1:169815024
|
G | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-6655G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815024 | ||||||
| chr1:169815026
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.703-6653G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815026 | ||||||
| chr1:169815206
|
G | A | 1 | a0001c0001t0004g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.703-6473G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815206 | ||||||
| chr1:169815251
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.703-6428G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815251 | ||||||
| chr1:169815252
|
C | T | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.703-6427C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815252 | ||||||
| chr1:169815295
|
C | CA | 16 | a0001c0001t0002g0098a0002c0003t0005g0027a0002c0003t0005g0371others(13): Show | 16 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-6370dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169815295 | |||||
| chr1:169815422
|
C | G | 33 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(30): Show | 35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.703-6257C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815422 | ||||||
| chr1:169815562
|
A | T | 1 | a0001c0001t0002g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.703-6117A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815562 | ||||||
| chr1:169815563
|
T | A | 1 | a0001c0001t0002g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.703-6116T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815563 | ||||||
| chr1:169815593
|
C | T | 2 | a0001c0001t0002g0350a0001c0001t0002g0351 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.703-6086C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815593 | ||||||
| chr1:169815697
|
T | G | 1 | a0001c0001t0001g0203 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.703-5982T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815697 | ||||||
| chr1:169815739
|
A | C | 58 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(55): Show | 62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.703-5940A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815739 | ||||||
| chr1:169815933
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-5746A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169815933 | ||||||
| chr1:169816074
|
A | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-5605A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816074 | ||||||
| chr1:169816133
|
A | T | 58 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(55): Show | 62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.703-5546A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816133 | ||||||
| chr1:169816204
|
CT | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.703-5474delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816204 | ||||||
| chr1:169816363
|
A | T | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-5316A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816363 | ||||||
| chr1:169816437
|
A | G | 1 | a0001c0001t0001g0193 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703-5242A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816437 | ||||||
| chr1:169816446
|
TTCTC | T | 5 | a0001c0001t0002g0350a0001c0001t0002g0351a0001c0001t0002g0352others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.703-5228_703-5225d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169816446 | |||||
| chr1:169816793
|
A | T | 1 | a0001c0001t0002g0035 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.703-4886A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169816793 | ||||||
| chr1:169817022
|
A | G | 57 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(54): Show | 61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.703-4657A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817022 | ||||||
| chr1:169817096
|
A | C | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.703-4583A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817096 | ||||||
| chr1:169817163
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-4516A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817163 | ||||||
| chr1:169817206
|
T | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-4473T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817206 | ||||||
| chr1:169817337
|
C | G | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(70): Show | 89 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.703-4342C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817337 | ||||||
| chr1:169817380
|
C | T | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-4299C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817380 | ||||||
| chr1:169817386
|
T | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-4293T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817386 | ||||||
| chr1:169817776
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.703-3903T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817776 | ||||||
| chr1:169817781
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.703-3898A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817781 | ||||||
| chr1:169817891
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.703-3788G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169817891 | ||||||
| chr1:169817951
|
A | AT | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(266): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.703-3717dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169817951 | |||||
| chr1:169818067
|
C | T | 58 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(55): Show | 62 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.703-3612C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818067 | ||||||
| chr1:169818306
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.703-3373A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818306 | ||||||
| chr1:169818388
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.703-3291G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818388 | ||||||
| chr1:169818449
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-3230G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818449 | ||||||
| chr1:169818480
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.703-3199A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818480 | ||||||
| chr1:169818730
|
A | G | 4 | a0001c0001t0002g0061a0001c0001t0002g0062a0001c0001t0002g0073others(1): Show | 4 | HG00673.hp2 NA18950.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-2949A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818730 | ||||||
| chr1:169818743
|
A | G | 2 | a0001c0001t0004g0023a0001c0001t0004g0263 | 3 | NA18612.hp1 NA18963.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.703-2936A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818743 | ||||||
| chr1:169818764
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-2915G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818764 | ||||||
| chr1:169818793
|
T | A | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2886T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818793 | ||||||
| chr1:169818912
|
C | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-2767C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169818912 | ||||||
| chr1:169819058
|
C | T | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.703-2621C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819058 | ||||||
| chr1:169819060
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0220others(1): Show | 7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-2619G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819060 | ||||||
| chr1:169819121
|
G | A | 1 | a0001c0001t0004g0257 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.703-2558G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819121 | ||||||
| chr1:169819168
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-2511A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819168 | ||||||
| chr1:169819184
|
A | G | 1 | a0001c0001t0003g0119 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.703-2495A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819184 | ||||||
| chr1:169819266
|
G | T | 1 | a0001c0002t0001g0360 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703-2413G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819266 | ||||||
| chr1:169819282
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.703-2397G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819282 | ||||||
| chr1:169819311
|
C | T | 3 | a0001c0001t0002g0352a0001c0001t0002g0353a0001c0001t0002g0361 | 3 | HG01109.hp2 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.703-2368C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819311 | ||||||
| chr1:169819373
|
C | T | 1 | a0001c0001t0003g0117 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.703-2306C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819373 | ||||||
| chr1:169819424
|
A | T | 1 | a0007c0010t0004g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.703-2255A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819424 | ||||||
| chr1:169819443
|
T | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-2236T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819443 | ||||||
| chr1:169819613
|
C | T | 3 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG01081.hp1 HG01884.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.703-2066C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819613 | ||||||
| chr1:169819695
|
C | T | 59 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(56): Show | 60 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.703-1984C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819695 | ||||||
| chr1:169819702
|
AC | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(73): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.703-1974delC | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169819702 | |||||
| chr1:169819705
|
C | T | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-1974C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819705 | ||||||
| chr1:169819718
|
G | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-1961G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819718 | ||||||
| chr1:169819720
|
C | T | 1 | a0001c0001t0002g0361 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.703-1959C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819720 | ||||||
| chr1:169819740
|
C | T | 51 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(48): Show | 54 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.703-1939C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819740 | ||||||
| chr1:169819873
|
G | GC | 11 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0035others(8): Show | 13 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-1804dupC | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | INFO_REALIGN_3_PRIME | chr1 | 169819873 | |||||
| chr1:169819887
|
G | A | 1 | a0001c0001t0009g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.703-1792G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819887 | ||||||
| chr1:169819899
|
A | G | 1 | a0001c0001t0020g0153 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.703-1780A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169819899 | ||||||
| chr1:169820001
|
G | C | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-1678G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820001 | ||||||
| chr1:169820008
|
A | G | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 66 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.703-1671A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820008 | ||||||
| chr1:169820195
|
A | G | 2 | a0001c0001t0006g0008a0001c0001t0006g0234 | 4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-1484A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820195 | ||||||
| chr1:169820321
|
G | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.703-1358G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820321 | ||||||
| chr1:169820373
|
G | T | 1 | a0001c0001t0001g0221 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.703-1306G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820373 | ||||||
| chr1:169820483
|
C | T | 1 | a0001c0001t0002g0347 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.703-1196C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820483 | ||||||
| chr1:169820563
|
A | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-1116A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820563 | ||||||
| chr1:169820625
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.703-1054G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820625 | ||||||
| chr1:169820637
|
C | T | 1 | a0004c0005t0001g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.703-1042C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820637 | ||||||
| chr1:169820698
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.703-981A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820698 | ||||||
| chr1:169820743
|
C | T | 14 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0296others(11): Show | 14 | NA18940.hp2 NA18959.hp1 NA18979.hp2 others(11): Show |
intron_variant | MODIFIER | c.703-936C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169820743 | ||||||
| chr1:169821020
|
T | G | 59 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(56): Show | 62 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.703-659T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821020 | ||||||
| chr1:169821194
|
G | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-485G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821194 | ||||||
| chr1:169821210
|
A | G | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.703-469A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821210 | ||||||
| chr1:169821260
|
T | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-419T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821260 | ||||||
| chr1:169821404
|
A | G | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.703-275A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821404 | ||||||
| chr1:169821404
|
A | T | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.703-275A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821404 | ||||||
| chr1:169821451
|
C | G | 2 | a0001c0001t0002g0346a0001c0001t0002g0347 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.703-228C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821451 | ||||||
| chr1:169821527
|
G | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.703-152G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 9/24 | chr1 | 169821527 | ||||||
| chr1:169822073
|
A | G | 2 | a0001c0001t0006g0008a0001c0001t0006g0234 | 4 | HG01891.hp2 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+314A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822073 | ||||||
| chr1:169822121
|
G | A | 1 | a0001c0001t0002g0010 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.783+362G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822121 | ||||||
| chr1:169822190
|
C | T | 26 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(23): Show | 27 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.783+431C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822190 | ||||||
| chr1:169822191
|
C | G | 1 | a0001c0001t0003g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.783+432C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822191 | ||||||
| chr1:169822192
|
C | T | 14 | a0001c0002t0001g0292a0001c0002t0001g0293a0001c0002t0001g0296others(11): Show | 14 | NA18940.hp2 NA18959.hp1 NA18979.hp2 others(11): Show |
intron_variant | MODIFIER | c.783+433C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822192 | ||||||
| chr1:169822246
|
G | A | 2 | a0001c0001t0002g0350a0001c0001t0002g0351 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.783+487G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822246 | ||||||
| chr1:169822685
|
A | G | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.784-723A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822685 | ||||||
| chr1:169822796
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0197 | 3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.784-612G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822796 | ||||||
| chr1:169822846
|
C | T | 1 | a0001c0002t0001g0337 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.784-562C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822846 | ||||||
| chr1:169822897
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.784-511T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169822897 | ||||||
| chr1:169823049
|
C | T | 12 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0041others(9): Show | 14 | NA18941.hp2 NA18945.hp2 NA18949.hp2 others(11): Show |
intron_variant | MODIFIER | c.784-359C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823049 | ||||||
| chr1:169823156
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-252C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823156 | ||||||
| chr1:169823190
|
T | G | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(279): Show | 308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.784-218T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823190 | ||||||
| chr1:169823284
|
C | A | 1 | a0001c0001t0002g0077 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.784-124C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823284 | ||||||
| chr1:169823322
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0197 | 3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.784-86A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 10/24 | chr1 | 169823322 | ||||||
| chr1:169823501
|
A | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+29A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823501 | ||||||
| chr1:169823551
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+79T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823551 | ||||||
| chr1:169823692
|
T | TAATA | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+222_848+225dup others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169823692 | |||||
| chr1:169823749
|
A | G | 1 | a0001c0001t0002g0092 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.848+277A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823749 | ||||||
| chr1:169823752
|
CG | C | 32 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(29): Show | 34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.848+281delG | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823752 | ||||||
| chr1:169823961
|
A | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+489A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169823961 | ||||||
| chr1:169824061
|
A | G | 3 | a0001c0001t0003g0107a0001c0001t0003g0129a0001c0001t0003g0130 | 3 | NA18964.hp1 NA18974.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.848+589A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824061 | ||||||
| chr1:169824107
|
A | G | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.848+635A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824107 | ||||||
| chr1:169824158
|
GA | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+691delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169824158 | |||||
| chr1:169824170
|
C | T | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+698C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824170 | ||||||
| chr1:169824272
|
C | G | 13 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0180others(10): Show | 18 | HG01192.hp1 HG02015.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.848+800C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824272 | ||||||
| chr1:169824274
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0197a0001c0001t0001g0212 | 4 | HG02818.hp2 HG02965.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.848+802A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824274 | ||||||
| chr1:169824446
|
A | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.848+974A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824446 | ||||||
| chr1:169824495
|
C | T | 1 | a0001c0001t0002g0345 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.848+1023C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824495 | ||||||
| chr1:169824716
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+1244G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824716 | ||||||
| chr1:169824725
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.848+1253G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824725 | ||||||
| chr1:169824774
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.848+1302C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824774 | ||||||
| chr1:169824884
|
C | T | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.848+1412C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824884 | ||||||
| chr1:169824931
|
A | G | 1 | a0001c0002t0001g0307 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.848+1459A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824931 | ||||||
| chr1:169824942
|
T | A | 1 | a0001c0001t0002g0344 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.848+1470T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169824942 | ||||||
| chr1:169825196
|
C | T | 2 | a0001c0001t0003g0146a0001c0001t0003g0157 | 2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.848+1724C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825196 | ||||||
| chr1:169825218
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.848+1746A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825218 | ||||||
| chr1:169825357
|
C | T | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.849-1694C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825357 | ||||||
| chr1:169825364
|
A | G | 1 | a0002c0003t0005g0378 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.849-1687A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825364 | ||||||
| chr1:169825547
|
T | C | 58 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(55): Show | 61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.849-1504T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825547 | ||||||
| chr1:169825567
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.849-1484A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825567 | ||||||
| chr1:169825641
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.849-1410T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825641 | ||||||
| chr1:169825721
|
A | T | 58 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(55): Show | 61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.849-1330A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825721 | ||||||
| chr1:169825781
|
A | C | 1 | a0001c0001t0002g0034 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.849-1270A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825781 | ||||||
| chr1:169825989
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-1062A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169825989 | ||||||
| chr1:169826064
|
T | A | 7 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0044others(4): Show | 9 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.849-987T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826064 | ||||||
| chr1:169826073
|
CT | C | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(263): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.849-969delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826073 | |||||
| chr1:169826074
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.849-977T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826074 | ||||||
| chr1:169826103
|
G | A | 1 | a0001c0001t0003g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.849-948G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826103 | ||||||
| chr1:169826112
|
G | C | 1 | a0001c0001t0002g0353 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.849-939G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826112 | ||||||
| chr1:169826135
|
A | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.849-916A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826135 | ||||||
| chr1:169826180
|
C | A | 1 | a0001c0001t0002g0341 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.849-871C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826180 | ||||||
| chr1:169826189
|
C | G | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.849-862C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826189 | ||||||
| chr1:169826260
|
C | T | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.849-791C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826260 | ||||||
| chr1:169826305
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-746C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826305 | ||||||
| chr1:169826338
|
C | A | 2 | a0001c0001t0003g0112a0001c0001t0003g0113 | 2 | HG02145.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.849-713C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826338 | ||||||
| chr1:169826342
|
C | T | 1 | a0001c0001t0003g0145 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.849-709C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826342 | ||||||
| chr1:169826343
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.849-708G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826343 | ||||||
| chr1:169826358
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.849-693C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826358 | ||||||
| chr1:169826362
|
A | AT | 292 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(289): Show | 318 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.849-673dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826362 | |||||
| chr1:169826362
|
A | ATT | 9 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0001t0001g0233others(6): Show | 9 | HG02055.hp2 HG02074.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.849-674_849-673dup others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826362 | |||||
| chr1:169826401
|
C | T | 2 | a0001c0002t0001g0317a0001c0002t0001g0318 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.849-650C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826401 | ||||||
| chr1:169826414
|
G | A | 8 | a0003c0004t0003g0133a0003c0004t0003g0137a0003c0004t0003g0138others(5): Show | 8 | HG01891.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.849-637G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826414 | ||||||
| chr1:169826487
|
C | T | 1 | a0001c0001t0002g0356 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.849-564C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826487 | ||||||
| chr1:169826500
|
T | A | 2 | a0004c0005t0001g0168a0004c0005t0001g0172 | 2 | HG00423.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.849-551T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826500 | ||||||
| chr1:169826659
|
C | T | 4 | a0001c0001t0003g0107a0001c0001t0003g0129a0001c0001t0003g0130others(1): Show | 4 | NA18964.hp1 NA18974.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.849-392C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | chr1 | 169826659 | ||||||
| chr1:169826854
|
TGTTTA | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.849-190_849-186del others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr1 | 169826854 | |||||
| chr1:169827275
|
T | C | 1 | a0004c0005t0001g0168 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.997+76T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827275 | ||||||
| chr1:169827400
|
G | C | 1 | a0001c0001t0001g0199 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.997+201G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827400 | ||||||
| chr1:169827410
|
G | C | 1 | a0001c0001t0004g0262 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.997+211G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827410 | ||||||
| chr1:169827463
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.998-248C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827463 | ||||||
| chr1:169827555
|
T | G | 3 | a0001c0001t0002g0352a0001c0001t0002g0353a0001c0001t0002g0361 | 3 | HG01109.hp2 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.998-156T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827555 | ||||||
| chr1:169827666
|
T | A | 1 | a0001c0001t0001g0199 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.998-45T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827666 | ||||||
| chr1:169827688
|
A | G | 1 | a0001c0001t0004g0247 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.998-23A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 12/24 | chr1 | 169827688 | ||||||
| chr1:169827926
|
G | GT | 5 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0164others(2): Show | 6 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1127+96dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr1 | 169827926 | |||||
| chr1:169827965
|
G | A | 2 | a0001c0001t0007g0164a0001c0001t0007g0165 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1127+125G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169827965 | ||||||
| chr1:169827980
|
T | C | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+140T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169827980 | ||||||
| chr1:169827986
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(73): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1127+146G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169827986 | ||||||
| chr1:169828138
|
C | T | 1 | a0001c0001t0002g0072 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1127+298C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828138 | ||||||
| chr1:169828139
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+299G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828139 | ||||||
| chr1:169828163
|
A | G | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1127+323A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828163 | ||||||
| chr1:169828254
|
A | C | 2 | a0001c0002t0001g0321a0001c0002t0001g0322 | 2 | HG03239.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1127+414A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828254 | ||||||
| chr1:169828281
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0220others(1): Show | 7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1127+441C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828281 | ||||||
| chr1:169828371
|
T | G | 59 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(56): Show | 60 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1127+531T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828371 | ||||||
| chr1:169828409
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1127+569A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828409 | ||||||
| chr1:169828522
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1127+682A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828522 | ||||||
| chr1:169828623
|
A | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1128-640A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828623 | ||||||
| chr1:169828749
|
A | G | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-514A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828749 | ||||||
| chr1:169828781
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1128-482A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828781 | ||||||
| chr1:169828793
|
G | A | 4 | a0001c0001t0003g0109a0001c0001t0003g0110a0001c0001t0003g0120others(1): Show | 4 | NA18985.hp1 NA18985.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-470G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828793 | ||||||
| chr1:169828815
|
G | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1128-448G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828815 | ||||||
| chr1:169828883
|
C | CT | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1128-379dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | INFO_REALIGN_3_PRIME | chr1 | 169828883 | |||||
| chr1:169828894
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1128-369C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 13/24 | chr1 | 169828894 | ||||||
| chr1:169829591
|
G | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1314+142G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | chr1 | 169829591 | ||||||
| chr1:169829604
|
C | G | 32 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(29): Show | 34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1314+155C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | chr1 | 169829604 | ||||||
| chr1:169829928
|
AAG | A | 5 | a0002c0003t0005g0371a0002c0003t0005g0375a0002c0003t0005g0376others(2): Show | 5 | HG00741.hp1 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-328_1315-327d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr1 | 169829928 | |||||
| chr1:169830074
|
A | G | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1315-185A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 14/24 | chr1 | 169830074 | ||||||
| chr1:169830431
|
C | CTA | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1397+91_1397+92ins others(2): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr1 | 169830431 | |||||
| chr1:169830688
|
T | C | 2 | a0001c0001t0003g0139a0001c0001t0003g0151 | 2 | HG03831.hp2 HG06807.hp2 |
splice_region_variant&intron_variant | LOW | c.1398-8T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 15/24 | chr1 | 169830688 | ||||||
| chr1:169830689
|
A | G | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | splice_region_variant&intron_variant | LOW | c.1398-7A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 15/24 | chr1 | 169830689 | ||||||
| chr1:169830820
|
A | G | 1 | a0001c0002t0001g0337 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1449+73A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830820 | ||||||
| chr1:169830838
|
G | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1449+91G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830838 | ||||||
| chr1:169830860
|
G | A | 1 | a0001c0001t0003g0140 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1449+113G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830860 | ||||||
| chr1:169830921
|
C | T | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1449+174C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830921 | ||||||
| chr1:169830949
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449+202C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830949 | ||||||
| chr1:169830979
|
A | C | 2 | a0001c0002t0001g0359a0001c0002t0001g0360 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1449+232A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169830979 | ||||||
| chr1:169831013
|
A | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449+266A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831013 | ||||||
| chr1:169831164
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1449+417G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831164 | ||||||
| chr1:169831259
|
A | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1449+512A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831259 | ||||||
| chr1:169831272
|
C | A | 4 | a0001c0001t0002g0354a0001c0001t0002g0355a0001c0001t0002g0356others(1): Show | 4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1449+525C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831272 | ||||||
| chr1:169831294
|
A | C | 1 | a0001c0001t0001g0193 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1449+547A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831294 | ||||||
| chr1:169831549
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1449+802A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831549 | ||||||
| chr1:169831604
|
T | C | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1450-813T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831604 | ||||||
| chr1:169831621
|
A | T | 1 | a0001c0001t0010g0245 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1450-796A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831621 | ||||||
| chr1:169831877
|
C | G | 1 | a0001c0001t0002g0066 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1450-540C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169831877 | ||||||
| chr1:169832025
|
C | T | 1 | a0001c0001t0002g0344 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1450-392C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832025 | ||||||
| chr1:169832038
|
T | G | 1 | a0001c0001t0002g0345 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1450-379T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832038 | ||||||
| chr1:169832080
|
G | A | 1 | a0001c0001t0002g0051 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1450-337G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832080 | ||||||
| chr1:169832238
|
A | G | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1450-179A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 16/24 | chr1 | 169832238 | ||||||
| chr1:169832633
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0220others(1): Show | 7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+127C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832633 | ||||||
| chr1:169832634
|
G | A | 1 | a0001c0001t0004g0260 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1539+128G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832634 | ||||||
| chr1:169832839
|
C | T | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1539+333C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832839 | ||||||
| chr1:169832971
|
G | A | 32 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(29): Show | 34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1539+465G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169832971 | ||||||
| chr1:169833340
|
G | C | 1 | a0001c0001t0008g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1539+834G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833340 | ||||||
| chr1:169833370
|
C | T | 10 | a0002c0003t0005g0027a0002c0003t0005g0372a0002c0003t0005g0373others(7): Show | 10 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(7): Show |
intron_variant | MODIFIER | c.1539+864C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833370 | ||||||
| chr1:169833396
|
G | A | 1 | a0002c0003t0005g0380 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1539+890G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833396 | ||||||
| chr1:169833619
|
G | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(202): Show | 227 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1539+1113G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833619 | ||||||
| chr1:169833707
|
G | A | 6 | a0001c0001t0001g0018a0001c0001t0001g0192a0001c0001t0001g0199others(3): Show | 7 | HG01168.hp1 HG01515.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+1201G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833707 | ||||||
| chr1:169833737
|
C | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(299): Show | 328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1539+1231C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833737 | ||||||
| chr1:169833757
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1539+1251A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833757 | ||||||
| chr1:169833760
|
A | G | 7 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0044others(4): Show | 9 | HG01099.hp1 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1539+1254A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833760 | ||||||
| chr1:169833773
|
C | G | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1539+1267C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833773 | ||||||
| chr1:169833781
|
CT | C | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1539+1277delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833781 | |||||
| chr1:169833807
|
A | C | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1539+1301A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833807 | ||||||
| chr1:169833815
|
C | G | 58 | a0001c0001t0001g0189a0001c0001t0003g0014a0001c0001t0003g0015others(55): Show | 61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1539+1309C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833815 | ||||||
| chr1:169833846
|
C | CT | 19 | a0001c0001t0002g0085a0001c0001t0002g0101a0001c0001t0002g0340others(16): Show | 20 | HG01243.hp2 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1539+1365dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | |||||
| chr1:169833846
|
C | CTTT | 40 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(37): Show | 41 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1539+1363_1539+136 others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | |||||
| chr1:169833846
|
C | CTTTT | 7 | a0001c0002t0001g0296a0001c0002t0001g0300a0001c0002t0001g0303others(4): Show | 7 | HG01169.hp2 HG03831.hp1 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1539+1362_1539+136 others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | |||||
| chr1:169833846
|
CT | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(139): Show | 161 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1539+1365delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | |||||
| chr1:169833846
|
CTT | C | 21 | a0001c0001t0001g0200a0001c0001t0001g0219a0001c0001t0003g0109others(18): Show | 21 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1539+1364_1539+136 others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | |||||
| chr1:169833846
|
CTTT | C | 57 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(54): Show | 61 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.1539+1363_1539+136 others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | |||||
| chr1:169833846
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0012g0214 | 3 | HG02015.hp2 HG02056.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1539+1351_1539+136 others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169833846 | |||||
| chr1:169833928
|
C | T | 1 | a0001c0001t0003g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1539+1422C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833928 | ||||||
| chr1:169833978
|
A | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0175others(4): Show | 12 | HG00323.hp2 HG00741.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1539+1472A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169833978 | ||||||
| chr1:169834076
|
T | C | 1 | a0001c0002t0001g0321 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1539+1570T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834076 | ||||||
| chr1:169834266
|
A | C | 1 | a0001c0001t0007g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1539+1760A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834266 | ||||||
| chr1:169834443
|
C | T | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1539+1937C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834443 | ||||||
| chr1:169834473
|
C | CT | 73 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(70): Show | 89 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1539+1975dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169834473 | |||||
| chr1:169834549
|
A | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1539+2043A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834549 | ||||||
| chr1:169834576
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1539+2070C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834576 | ||||||
| chr1:169834640
|
C | T | 1 | a0001c0001t0006g0366 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1539+2134C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834640 | ||||||
| chr1:169834743
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0162 | 3 | HG02559.hp2 HG02809.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1540-2184C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834743 | ||||||
| chr1:169834982
|
A | G | 1 | a0001c0001t0018g0029 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1540-1945A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169834982 | ||||||
| chr1:169835014
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1540-1913G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835014 | ||||||
| chr1:169835221
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1540-1706G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835221 | ||||||
| chr1:169835258
|
A | G | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1540-1669A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835258 | ||||||
| chr1:169835338
|
C | G | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-1589C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835338 | ||||||
| chr1:169835485
|
A | C | 2 | a0001c0001t0003g0016a0001c0001t0003g0149 | 3 | HG01081.hp2 HG01099.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1540-1442A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835485 | ||||||
| chr1:169835579
|
T | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1540-1348T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835579 | ||||||
| chr1:169835611
|
A | G | 2 | a0001c0001t0003g0144a0001c0001t0003g0145 | 2 | HG00642.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1540-1316A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835611 | ||||||
| chr1:169835745
|
A | G | 1 | a0001c0001t0001g0212 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1540-1182A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835745 | ||||||
| chr1:169835980
|
A | G | 3 | a0001c0001t0010g0022a0001c0001t0010g0238a0001c0001t0010g0245 | 4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-947A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169835980 | ||||||
| chr1:169836053
|
AT | A | 64 | a0001c0001t0002g0052a0001c0001t0002g0346a0001c0001t0002g0358others(61): Show | 67 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1540-856delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169836053 | |||||
| chr1:169836053
|
ATT | A | 121 | a0001c0001t0002g0347a0001c0001t0004g0023a0001c0001t0004g0024others(118): Show | 127 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.1540-857_1540-856d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169836053 | |||||
| chr1:169836053
|
ATTT | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): Show | 115 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1540-858_1540-856d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr1 | 169836053 | |||||
| chr1:169836161
|
C | T | 1 | a0001c0001t0004g0283 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1540-766C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836161 | ||||||
| chr1:169836225
|
C | T | 58 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(55): Show | 61 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.1540-702C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836225 | ||||||
| chr1:169836228
|
T | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0213a0001c0001t0001g0215others(6): Show | 11 | HG02015.hp2 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1540-699T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836228 | ||||||
| chr1:169836347
|
G | C | 1 | a0003c0004t0003g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1540-580G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836347 | ||||||
| chr1:169836392
|
C | G | 1 | a0001c0001t0009g0226 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1540-535C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836392 | ||||||
| chr1:169836408
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1540-519T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836408 | ||||||
| chr1:169836422
|
C | T | 5 | a0001c0001t0001g0021a0001c0001t0001g0207a0001c0001t0001g0229others(2): Show | 6 | HG02735.hp1 NA18944.hp1 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.1540-505C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836422 | ||||||
| chr1:169836570
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1540-357T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836570 | ||||||
| chr1:169836641
|
T | A | 1 | a0001c0001t0003g0141 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1540-286T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836641 | ||||||
| chr1:169836794
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1540-133G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836794 | ||||||
| chr1:169836825
|
C | G | 1 | a0001c0001t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1540-102C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836825 | ||||||
| chr1:169836924
|
C | T | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | splice_region_variant&intron_variant | LOW | c.1540-3C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 17/24 | chr1 | 169836924 | ||||||
| chr1:169837313
|
T | C | 1 | a0004c0005t0001g0169 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1725+201T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837313 | ||||||
| chr1:169837395
|
G | T | 4 | a0001c0001t0003g0135a0001c0001t0003g0146a0001c0001t0003g0157others(1): Show | 4 | HG00140.hp2 HG01175.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+283G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837395 | ||||||
| chr1:169837448
|
A | G | 1 | a0001c0001t0004g0255 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1725+336A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837448 | ||||||
| chr1:169837487
|
C | G | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1725+375C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837487 | ||||||
| chr1:169837752
|
A | G | 1 | a0001c0002t0001g0339 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1725+640A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837752 | ||||||
| chr1:169837803
|
G | C | 2 | a0001c0001t0004g0258a0001c0001t0004g0259 | 2 | HG00423.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.1725+691G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837803 | ||||||
| chr1:169837931
|
C | G | 20 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0040others(17): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1725+819C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837931 | ||||||
| chr1:169837939
|
T | C | 9 | a0001c0001t0002g0013a0001c0001t0002g0040a0001c0001t0002g0052others(6): Show | 10 | HG00597.hp1 HG00609.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.1725+827T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837939 | ||||||
| chr1:169837954
|
G | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1725+842G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837954 | ||||||
| chr1:169837968
|
G | A | 1 | a0001c0001t0003g0111 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1725+856G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169837968 | ||||||
| chr1:169838031
|
G | A | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1725+919G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838031 | ||||||
| chr1:169838117
|
T | A | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+1005T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838117 | ||||||
| chr1:169838228
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1725+1116T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838228 | ||||||
| chr1:169838351
|
T | C | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1725+1239T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838351 | ||||||
| chr1:169838459
|
C | A | 1 | a0001c0001t0003g0145 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1725+1347C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838459 | ||||||
| chr1:169838480
|
T | C | 33 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(30): Show | 35 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1725+1368T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838480 | ||||||
| chr1:169838490
|
T | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1725+1378T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838490 | ||||||
| chr1:169838538
|
A | G | 1 | a0001c0001t0001g0187 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1725+1426A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838538 | ||||||
| chr1:169838559
|
G | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(73): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1725+1447G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838559 | ||||||
| chr1:169838608
|
G | A | 20 | a0001c0001t0002g0003a0001c0001t0002g0013a0001c0001t0002g0040others(17): Show | 23 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1725+1496G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838608 | ||||||
| chr1:169838720
|
C | T | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1725+1608C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838720 | ||||||
| chr1:169838848
|
C | T | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1725+1736C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169838848 | ||||||
| chr1:169838928
|
C | CATCT | 4 | a0001c0001t0002g0354a0001c0001t0002g0355a0001c0001t0002g0356others(1): Show | 4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+1817_1725+182 others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169838928 | |||||
| chr1:169839020
|
G | A | 2 | a0001c0001t0008g0223a0001c0001t0008g0224 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1725+1908G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839020 | ||||||
| chr1:169839259
|
C | T | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1725+2147C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839259 | ||||||
| chr1:169839510
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1725+2398C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839510 | ||||||
| chr1:169839528
|
G | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.1725+2416G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839528 | ||||||
| chr1:169839617
|
A | G | 3 | a0001c0001t0002g0101a0001c0001t0002g0102a0001c0001t0002g0103 | 3 | NA18981.hp2 NA18991.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1725+2505A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839617 | ||||||
| chr1:169839794
|
T | C | 1 | a0001c0001t0004g0250 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1726-2623T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839794 | ||||||
| chr1:169839825
|
C | T | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1726-2592C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839825 | ||||||
| chr1:169839897
|
T | A | 1 | a0001c0002t0001g0302 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1726-2520T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839897 | ||||||
| chr1:169839990
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-2427T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169839990 | ||||||
| chr1:169840040
|
T | C | 2 | a0001c0002t0001g0323a0001c0002t0001g0324 | 2 | NA18983.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1726-2377T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840040 | ||||||
| chr1:169840128
|
TTATAG | T | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-2282_1726-227 others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169840128 | |||||
| chr1:169840144
|
A | G | 2 | a0003c0004t0003g0154a0003c0004t0003g0155 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1726-2273A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840144 | ||||||
| chr1:169840192
|
C | G | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1726-2225C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840192 | ||||||
| chr1:169840335
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-2082C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840335 | ||||||
| chr1:169840389
|
A | G | 1 | a0001c0001t0003g0124 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1726-2028A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840389 | ||||||
| chr1:169840439
|
C | G | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1726-1978C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840439 | ||||||
| chr1:169840445
|
G | T | 1 | a0001c0001t0016g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1726-1972G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840445 | ||||||
| chr1:169840461
|
A | T | 1 | a0001c0001t0003g0115 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1726-1956A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840461 | ||||||
| chr1:169840472
|
T | C | 65 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0006g0362others(62): Show | 67 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1726-1945T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840472 | ||||||
| chr1:169840475
|
A | T | 1 | a0001c0001t0002g0097 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1726-1942A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840475 | ||||||
| chr1:169840511
|
C | CT | 24 | a0001c0001t0001g0218a0001c0001t0002g0352a0001c0001t0002g0353others(21): Show | 25 | HG00741.hp1 HG01109.hp2 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1726-1892dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169840511 | |||||
| chr1:169840533
|
C | T | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1726-1884C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840533 | ||||||
| chr1:169840542
|
G | A | 54 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 62 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1726-1875G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840542 | ||||||
| chr1:169840542
|
G | T | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-1875G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840542 | ||||||
| chr1:169840543
|
C | T | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1726-1874C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840543 | ||||||
| chr1:169840632
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1726-1785T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840632 | ||||||
| chr1:169840660
|
G | A | 3 | a0001c0001t0003g0146a0001c0001t0003g0157a0001c0001t0020g0153 | 3 | HG00140.hp2 HG01175.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1726-1757G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840660 | ||||||
| chr1:169840667
|
C | T | 1 | a0001c0001t0009g0227 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1726-1750C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840667 | ||||||
| chr1:169840700
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1726-1717T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840700 | ||||||
| chr1:169840731
|
C | T | 2 | a0001c0001t0004g0236a0001c0001t0004g0237 | 2 | NA18948.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.1726-1686C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840731 | ||||||
| chr1:169840751
|
C | G | 2 | a0001c0001t0007g0163a0001c0001t0007g0166 | 2 | HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1726-1666C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840751 | ||||||
| chr1:169840772
|
A | G | 1 | a0001c0001t0016g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1726-1645A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840772 | ||||||
| chr1:169840773
|
G | T | 1 | a0001c0001t0016g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1726-1644G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840773 | ||||||
| chr1:169840802
|
G | A | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(263): Show | 292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.1726-1615G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840802 | ||||||
| chr1:169840833
|
G | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-1584G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840833 | ||||||
| chr1:169840933
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-1484T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169840933 | ||||||
| chr1:169841027
|
C | T | 4 | a0002c0003t0005g0027a0002c0003t0005g0374a0002c0003t0005g0382others(1): Show | 4 | HG02074.hp1 HG02523.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-1390C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841027 | ||||||
| chr1:169841028
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-1389A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841028 | ||||||
| chr1:169841040
|
G | T | 3 | a0001c0001t0010g0022a0001c0001t0010g0238a0001c0001t0010g0245 | 4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-1377G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841040 | ||||||
| chr1:169841342
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1726-1075T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841342 | ||||||
| chr1:169841459
|
G | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1726-958G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841459 | ||||||
| chr1:169841745
|
C | T | 1 | a0007c0010t0004g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1726-672C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169841745 | ||||||
| chr1:169842069
|
G | A | 2 | a0001c0001t0002g0053a0001c0001t0002g0067 | 2 | HG02257.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1726-348G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842069 | ||||||
| chr1:169842124
|
C | T | 1 | a0001c0001t0006g0362 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1726-293C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842124 | ||||||
| chr1:169842166
|
T | C | 5 | a0001c0001t0002g0350a0001c0001t0002g0351a0001c0001t0002g0352others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-251T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842166 | ||||||
| chr1:169842174
|
C | CA | 18 | a0001c0001t0002g0085a0001c0001t0004g0287a0002c0003t0005g0027others(15): Show | 18 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.1726-228dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr1 | 169842174 | |||||
| chr1:169842358
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1726-59C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 18/24 | chr1 | 169842358 | ||||||
| chr1:169842701
|
T | A | 1 | a0001c0001t0016g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1848+162T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842701 | ||||||
| chr1:169842736
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1848+197C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842736 | ||||||
| chr1:169842799
|
A | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1848+260A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842799 | ||||||
| chr1:169842825
|
T | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1848+286T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842825 | ||||||
| chr1:169842855
|
T | A | 2 | a0001c0001t0004g0281a0001c0001t0004g0283 | 2 | NA18989.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1848+316T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842855 | ||||||
| chr1:169842887
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0106others(1): Show | 4 | HG01081.hp1 HG01884.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1848+348T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169842887 | ||||||
| chr1:169843090
|
T | C | 3 | a0001c0001t0002g0352a0001c0001t0002g0353a0001c0001t0002g0361 | 3 | HG01109.hp2 HG02895.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1848+551T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843090 | ||||||
| chr1:169843122
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1849-552A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843122 | ||||||
| chr1:169843186
|
A | G | 1 | a0001c0002t0014g0295 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1849-488A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843186 | ||||||
| chr1:169843260
|
T | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0208 | 2 | NA18950.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1849-414T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843260 | ||||||
| chr1:169843287
|
T | G | 1 | a0001c0001t0010g0238 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1849-387T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843287 | ||||||
| chr1:169843393
|
C | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1849-281C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843393 | ||||||
| chr1:169843442
|
T | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1849-232T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843442 | ||||||
| chr1:169843471
|
A | G | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1849-203A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843471 | ||||||
| chr1:169843524
|
C | T | 2 | a0001c0001t0004g0239a0001c0001t0004g0247 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1849-150C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843524 | ||||||
| chr1:169843575
|
A | G | 2 | a0002c0003t0005g0373a0002c0003t0005g0379 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1849-99A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | chr1 | 169843575 | ||||||
| chr1:169843624
|
ATTC | A | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1849-47_1849-45del others(3): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr1 | 169843624 | |||||
| chr1:169843778
|
A | G | 4 | a0001c0002t0001g0301a0001c0002t0001g0310a0001c0002t0001g0311others(1): Show | 4 | HG00597.hp2 HG02027.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944+9A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169843778 | ||||||
| chr1:169843797
|
T | C | 1 | a0001c0002t0001g0326 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1944+28T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169843797 | ||||||
| chr1:169844048
|
A | G | 1 | a0001c0001t0002g0067 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1944+279A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844048 | ||||||
| chr1:169844205
|
G | A | 2 | a0001c0002t0001g0359a0001c0002t0001g0360 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1944+436G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844205 | ||||||
| chr1:169844212
|
T | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1944+443T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844212 | ||||||
| chr1:169844228
|
A | G | 6 | a0001c0001t0004g0243a0001c0001t0004g0255a0001c0001t0004g0277others(3): Show | 6 | HG02015.hp1 HG02080.hp2 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1944+459A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844228 | ||||||
| chr1:169844246
|
A | G | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1944+477A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844246 | ||||||
| chr1:169844505
|
G | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1944+736G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844505 | ||||||
| chr1:169844619
|
A | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1944+850A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844619 | ||||||
| chr1:169844631
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1944+862A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844631 | ||||||
| chr1:169844850
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944+1081G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844850 | ||||||
| chr1:169844887
|
A | C | 1 | a0001c0002t0001g0291 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1944+1118A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844887 | ||||||
| chr1:169844920
|
T | C | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1944+1151T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169844920 | ||||||
| chr1:169845219
|
A | G | 1 | a0001c0001t0009g0225 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1944+1450A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845219 | ||||||
| chr1:169845392
|
C | T | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(194): Show | 218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.1944+1623C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845392 | ||||||
| chr1:169845407
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(73): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1944+1638A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845407 | ||||||
| chr1:169845591
|
G | A | 5 | a0001c0001t0006g0362a0001c0001t0006g0363a0001c0001t0006g0364others(2): Show | 5 | HG02280.hp1 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1944+1822G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845591 | ||||||
| chr1:169845687
|
C | CTTCCA | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1944+1921_1944+192 others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169845687 | |||||
| chr1:169845689
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1944+1920T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845689 | ||||||
| chr1:169845931
|
C | T | 297 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(294): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1945-1759C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169845931 | ||||||
| chr1:169846101
|
T | C | 77 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(74): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.1945-1589T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846101 | ||||||
| chr1:169846107
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0197 | 3 | HG02965.hp2 HG06807.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1945-1583T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846107 | ||||||
| chr1:169846120
|
C | G | 1 | a0001c0001t0002g0083 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1945-1570C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846120 | ||||||
| chr1:169846219
|
A | G | 4 | a0001c0001t0002g0354a0001c0001t0002g0355a0001c0001t0002g0356others(1): Show | 4 | HG03195.hp2 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1945-1471A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846219 | ||||||
| chr1:169846231
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0204 | 3 | HG03491.hp1 HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1945-1459A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846231 | ||||||
| chr1:169846670
|
C | T | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1945-1020C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846670 | ||||||
| chr1:169846971
|
G | A | 9 | a0001c0001t0003g0107a0001c0001t0003g0111a0001c0001t0003g0114others(6): Show | 9 | HG00544.hp1 HG03017.hp2 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.1945-719G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169846971 | ||||||
| chr1:169847032
|
C | T | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-658C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847032 | ||||||
| chr1:169847041
|
G | T | 32 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(29): Show | 34 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1945-649G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847041 | ||||||
| chr1:169847060
|
T | C | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-630T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847060 | ||||||
| chr1:169847163
|
A | G | 57 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(54): Show | 60 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.1945-527A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847163 | ||||||
| chr1:169847176
|
G | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.1945-514G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847176 | ||||||
| chr1:169847234
|
C | A | 1 | a0001c0001t0002g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1945-456C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847234 | ||||||
| chr1:169847290
|
A | G | 1 | a0001c0001t0002g0028 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1945-400A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847290 | ||||||
| chr1:169847313
|
T | TA | 6 | a0001c0001t0002g0055a0001c0001t0002g0068a0001c0001t0002g0081others(3): Show | 6 | HG00597.hp1 HG02647.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945-350dupA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | |||||
| chr1:169847313
|
TA | T | 6 | a0001c0001t0001g0183a0001c0001t0002g0033a0001c0001t0002g0035others(3): Show | 6 | HG01515.hp2 HG01975.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.1945-350delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | |||||
| chr1:169847313
|
TAAA | T | 58 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(55): Show | 67 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.1945-352_1945-350d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | |||||
| chr1:169847313
|
TAAAA | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0104others(79): Show | 93 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.1945-353_1945-350d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | |||||
| chr1:169847313
|
TAAAAA | T | 115 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0003g0014others(112): Show | 120 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.1945-354_1945-350d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | |||||
| chr1:169847313
|
TAAAAAA | T | 23 | a0001c0001t0003g0132a0001c0001t0009g0225a0001c0001t0009g0226others(20): Show | 23 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.1945-355_1945-350d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr1 | 169847313 | |||||
| chr1:169847317
|
A | T | 2 | a0001c0001t0008g0020a0001c0001t0008g0222 | 3 | HG01884.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1945-373A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847317 | ||||||
| chr1:169847318
|
A | T | 2 | a0001c0001t0008g0223a0001c0001t0008g0224 | 2 | HG02976.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1945-372A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847318 | ||||||
| chr1:169847340
|
A | G | 1 | a0001c0001t0001g0189 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1945-350A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847340 | ||||||
| chr1:169847484
|
G | A | 2 | a0001c0001t0003g0156a0001c0001t0003g0158 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1945-206G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847484 | ||||||
| chr1:169847521
|
T | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.1945-169T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847521 | ||||||
| chr1:169847560
|
T | A | 6 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0007g0163others(3): Show | 7 | HG02559.hp2 HG02809.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1945-130T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 20/24 | chr1 | 169847560 | ||||||
| chr1:169847850
|
A | G | 1 | a0007c0010t0004g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2058+47A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169847850 | ||||||
| chr1:169847882
|
T | C | 3 | a0001c0001t0003g0123a0001c0001t0003g0124a0001c0001t0003g0126 | 3 | HG00733.hp2 HG01074.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.2058+79T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169847882 | ||||||
| chr1:169848191
|
C | T | 1 | a0001c0001t0008g0224 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2058+388C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848191 | ||||||
| chr1:169848210
|
G | A | 4 | a0001c0001t0006g0363a0001c0001t0006g0364a0001c0001t0006g0365others(1): Show | 4 | HG02280.hp1 HG02486.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2058+407G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848210 | ||||||
| chr1:169848427
|
A | C | 54 | a0001c0002t0001g0026a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 55 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2058+624A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848427 | ||||||
| chr1:169848430
|
T | C | 4 | a0001c0001t0002g0044a0001c0001t0002g0049a0001c0001t0002g0050others(1): Show | 4 | NA18970.hp1 NA19058.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.2058+627T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848430 | ||||||
| chr1:169848495
|
T | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.2058+692T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848495 | ||||||
| chr1:169848638
|
G | A | 1 | a0001c0001t0002g0345 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2058+835G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848638 | ||||||
| chr1:169848953
|
C | T | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2059-547C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169848953 | ||||||
| chr1:169849049
|
A | G | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.2059-451A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849049 | ||||||
| chr1:169849051
|
G | T | 1 | a0002c0003t0005g0381 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2059-449G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849051 | ||||||
| chr1:169849053
|
T | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2059-447T>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849053 | ||||||
| chr1:169849077
|
T | C | 2 | a0001c0001t0007g0164a0001c0001t0007g0165 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2059-423T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849077 | ||||||
| chr1:169849215
|
G | A | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2059-285G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849215 | ||||||
| chr1:169849238
|
T | G | 2 | a0001c0001t0008g0020a0001c0001t0008g0222 | 3 | HG01884.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2059-262T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849238 | ||||||
| chr1:169849263
|
A | G | 6 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0343others(3): Show | 6 | HG02145.hp2 HG02258.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2059-237A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849263 | ||||||
| chr1:169849338
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2059-162G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 21/24 | chr1 | 169849338 | ||||||
| chr1:169849622
|
T | G | 5 | a0001c0001t0002g0350a0001c0001t0002g0351a0001c0001t0002g0352others(2): Show | 5 | HG01109.hp2 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.2163+18T>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849622 | ||||||
| chr1:169849717
|
T | C | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2163+113T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849717 | ||||||
| chr1:169849738
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2163+134C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849738 | ||||||
| chr1:169849739
|
G | A | 57 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(54): Show | 60 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.2163+135G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849739 | ||||||
| chr1:169849785
|
T | C | 25 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(22): Show | 26 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.2163+181T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849785 | ||||||
| chr1:169849924
|
A | G | 65 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0006g0362others(62): Show | 67 | HG00408.hp1 HG00597.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.2163+320A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849924 | ||||||
| chr1:169849976
|
C | G | 4 | a0001c0001t0009g0225a0001c0001t0009g0226a0001c0001t0009g0227others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.2164-289C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169849976 | ||||||
| chr1:169850035
|
C | T | 11 | a0001c0001t0003g0014a0001c0001t0003g0108a0001c0001t0003g0109others(8): Show | 12 | NA18973.hp1 NA18977.hp2 NA18978.hp2 others(9): Show |
intron_variant | MODIFIER | c.2164-230C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169850035 | ||||||
| chr1:169850143
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(73): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.2164-122G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 22/24 | chr1 | 169850143 | ||||||
| chr1:169850417
|
C | T | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2244+72C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850417 | ||||||
| chr1:169850464
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2244+119A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850464 | ||||||
| chr1:169850525
|
C | T | 2 | a0001c0001t0004g0261a0001c0001t0004g0270 | 2 | NA18974.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.2244+180C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850525 | ||||||
| chr1:169850529
|
G | A | 15 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(12): Show | 15 | HG00741.hp1 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.2244+184G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850529 | ||||||
| chr1:169850641
|
C | G | 1 | a0001c0001t0007g0160 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2244+296C>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850641 | ||||||
| chr1:169850689
|
G | A | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2244+344G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850689 | ||||||
| chr1:169850751
|
A | G | 308 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(305): Show | 334 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.2244+406A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850751 | ||||||
| chr1:169850870
|
A | G | 1 | a0001c0001t0004g0248 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2244+525A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850870 | ||||||
| chr1:169850912
|
T | C | 1 | a0001c0001t0002g0358 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2244+567T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850912 | ||||||
| chr1:169850936
|
G | GAGA | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2244+592_2244+594d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850936 | |||||
| chr1:169850974
|
G | A | 24 | a0001c0001t0003g0014a0001c0001t0003g0107a0001c0001t0003g0108others(21): Show | 25 | HG00544.hp1 HG00733.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.2244+629G>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850974 | ||||||
| chr1:169850980
|
C | CT | 6 | a0001c0001t0006g0365a0001c0001t0006g0366a0001c0001t0009g0225others(3): Show | 6 | HG01109.hp1 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244+661dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTT | 18 | a0001c0001t0002g0346a0001c0001t0002g0356a0001c0001t0003g0114others(15): Show | 18 | HG00408.hp1 HG00544.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.2244+658_2244+661d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTT | 22 | a0001c0001t0002g0347a0001c0001t0002g0349a0001c0001t0002g0354others(19): Show | 23 | HG00621.hp1 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.2244+657_2244+661d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTT | 13 | a0001c0001t0002g0340a0001c0001t0003g0130a0001c0001t0015g0342others(10): Show | 13 | HG00642.hp2 HG00733.hp1 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.2244+656_2244+661d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT | 10 | a0001c0001t0002g0341a0001c0001t0002g0343a0001c0001t0002g0344others(7): Show | 10 | HG01258.hp2 HG01261.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.2244+655_2244+661d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0310 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2244+652_2244+661d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0002g0348a0001c0001t0003g0014a0001c0001t0003g0109others(2): Show | 6 | HG02970.hp1 NA18973.hp1 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.2244+651_2244+661d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0003g0110a0001c0001t0003g0120 | 2 | NA19009.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2244+650_2244+661d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0003g0119 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2244+649_2244+661d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0108 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2244+646_2244+661d others(18): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0003g0128 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2244+643_2244+661d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(14): Show |
1 | a0001c0001t0006g0363 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2244+641_2244+661d others(23): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0003g0125a0001c0001t0006g0364 | 2 | HG02486.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2244+639_2244+661d others(25): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0116 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2244+661_2244+662i others(32): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
CTTTTTTT others(61): Show |
C | 1 | a0002c0003t0005g0377 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2244+661_2244+728d others(70): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850980
|
CTTTTTTT others(62): Show |
C | 14 | a0002c0003t0005g0027a0002c0003t0005g0371a0002c0003t0005g0372others(11): Show | 14 | HG01168.hp2 HG01169.hp1 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.2244+660_2244+728d others(71): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850980 | |||||
| chr1:169850982
|
TTTTTTTT others(56): Show |
T | 1 | a0001c0001t0003g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2244+662_2244+724d others(65): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850982 | |||||
| chr1:169850985
|
TTTTTTTT others(53): Show |
T | 9 | a0001c0001t0003g0015a0001c0001t0003g0016a0001c0001t0003g0132others(6): Show | 11 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2244+662_2244+721d others(62): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850985 | |||||
| chr1:169850986
|
TTTTTTTT others(52): Show |
T | 12 | a0001c0001t0003g0139a0001c0001t0003g0140a0001c0001t0003g0142others(9): Show | 12 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.2244+662_2244+720d others(61): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850986 | |||||
| chr1:169850987
|
TTTTTTTT others(51): Show |
T | 7 | a0001c0001t0003g0134a0001c0001t0003g0135a0001c0001t0003g0152others(4): Show | 7 | HG02055.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244+662_2244+719d others(60): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850987 | |||||
| chr1:169850988
|
TTTTTTTT others(50): Show |
T | 2 | a0001c0001t0003g0156a0003c0004t0003g0154 | 2 | HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2244+662_2244+718d others(59): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850988 | |||||
| chr1:169850989
|
TTTTTTTT others(49): Show |
T | 1 | a0001c0001t0003g0143 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2244+662_2244+717d others(58): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850989 | |||||
| chr1:169850990
|
TTTTTTTT others(48): Show |
T | 1 | a0003c0004t0003g0155 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2244+662_2244+716d others(57): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169850990 | |||||
| chr1:169850996
|
TTTTTTTT others(8): Show |
T | 4 | a0001c0001t0008g0020a0001c0001t0008g0222a0001c0001t0008g0223others(1): Show | 5 | HG01884.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2244+652_2244+666d others(17): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850996 | ||||||
| chr1:169850997
|
TTTTTTTT others(7): Show |
T | 2 | a0001c0001t0003g0118a0001c0002t0001g0332 | 2 | NA19063.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.2244+653_2244+666d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850997 | ||||||
| chr1:169850998
|
TTTTTTTT others(6): Show |
T | 1 | a0001c0002t0001g0360 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2244+654_2244+666d others(15): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169850998 | ||||||
| chr1:169851001
|
TTTTTTAT others(3): Show |
T | 1 | a0001c0001t0003g0123 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2244+657_2244+666d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851001 | ||||||
| chr1:169851003
|
TTTTA | T | 42 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(39): Show | 46 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.2244+662_2244+665d others(6): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851003 | |||||
| chr1:169851004
|
TTTA | T | 64 | a0001c0001t0002g0003a0001c0001t0002g0010a0001c0001t0002g0011others(61): Show | 70 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.2244+662_2244+664d others(5): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851004 | |||||
| chr1:169851004
|
TTTATTTG | T | 59 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(56): Show | 75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.2244+660_2244+666d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851004 | ||||||
| chr1:169851005
|
TTA | T | 29 | a0001c0001t0002g0009a0001c0001t0002g0038a0001c0001t0002g0039others(26): Show | 30 | HG01109.hp2 HG02071.hp2 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.2244+662_2244+663d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851005 | |||||
| chr1:169851005
|
TTATTTG | T | 15 | a0001c0001t0001g0105a0001c0001t0001g0174a0001c0001t0001g0175others(12): Show | 15 | HG01361.hp1 HG02004.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.2244+661_2244+666d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851005 | ||||||
| chr1:169851006
|
TA | T | 5 | a0001c0001t0002g0058a0001c0001t0002g0096a0001c0001t0002g0100others(2): Show | 5 | HG00544.hp2 HG00735.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+662delA | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851006 | ||||||
| chr1:169851007
|
A | T | 100 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0002g0340others(97): Show | 103 | HG00408.hp1 HG00544.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.2244+662A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851007 | ||||||
| chr1:169851011
|
G | T | 148 | a0001c0001t0001g0017a0001c0001t0001g0162a0001c0001t0002g0358others(145): Show | 155 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.2244+666G>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851011 | ||||||
| chr1:169851045
|
C | CT | 49 | a0001c0001t0002g0009a0001c0001t0002g0028a0001c0001t0002g0033others(46): Show | 50 | HG00280.hp2 HG00438.hp1 HG00544.hp2 others(47): Show |
intron_variant | MODIFIER | c.2244+728dupT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTT | 7 | a0001c0001t0002g0032a0001c0001t0002g0072a0001c0001t0019g0099others(4): Show | 7 | HG02040.hp2 HG02293.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.2244+727_2244+728d others(4): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0001g0312 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2244+719_2244+728d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(4): Show |
2 | a0001c0002t0001g0301a0001c0002t0001g0310 | 2 | HG00597.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.2244+718_2244+728d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(5): Show |
1 | a0001c0002t0001g0300 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2244+717_2244+728d others(14): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(7): Show |
1 | a0001c0002t0001g0311 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2244+715_2244+728d others(16): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(10): Show |
3 | a0001c0002t0001g0302a0001c0002t0001g0322a0001c0002t0001g0335 | 3 | HG03239.hp2 HG03834.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.2244+712_2244+728d others(19): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(11): Show |
3 | a0001c0002t0001g0308a0001c0002t0001g0309a0001c0002t0001g0321 | 3 | HG00733.hp1 HG01261.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2244+711_2244+728d others(20): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(12): Show |
1 | a0001c0002t0001g0299 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2244+710_2244+728d others(21): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(14): Show |
1 | a0001c0002t0001g0297 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2244+708_2244+728d others(23): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(18): Show |
1 | a0006c0007t0001g0298 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2244+704_2244+728d others(27): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(19): Show |
1 | a0001c0002t0001g0339 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2244+703_2244+728d others(28): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(25): Show |
1 | a0001c0002t0001g0333 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2244+728_2244+729i others(34): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(26): Show |
1 | a0001c0002t0001g0334 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.2244+728_2244+729i others(35): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
C | CTTTTTTT others(29): Show |
1 | a0001c0002t0001g0304 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2244+728_2244+729i others(38): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
CT | C | 23 | a0001c0001t0002g0057a0001c0001t0002g0074a0001c0001t0002g0340others(20): Show | 24 | HG00544.hp1 HG00733.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2244+728delT | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
CTTTTT | C | 14 | a0001c0001t0004g0263a0001c0001t0004g0285a0001c0001t0006g0363others(11): Show | 15 | HG00408.hp1 HG01123.hp1 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.2244+724_2244+728d others(7): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
CTTTTTT | C | 56 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(53): Show | 60 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.2244+723_2244+728d others(8): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
CTTTTTTT others(3): Show |
C | 57 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(54): Show | 66 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.2244+719_2244+728d others(12): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851045
|
CTTTTTTT others(4): Show |
C | 17 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0131others(14): Show | 24 | HG01192.hp1 HG01891.hp2 HG02015.hp2 others(21): Show |
intron_variant | MODIFIER | c.2244+718_2244+728d others(13): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr1 | 169851045 | |||||
| chr1:169851077
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2244+732A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851077 | ||||||
| chr1:169851173
|
C | A | 1 | a0001c0001t0003g0113 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2245-644C>A | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851173 | ||||||
| chr1:169851270
|
A | C | 1 | a0001c0001t0004g0266 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2245-547A>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851270 | ||||||
| chr1:169851374
|
G | C | 1 | a0001c0001t0013g0367 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2245-443G>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851374 | ||||||
| chr1:169851416
|
C | T | 2 | a0002c0003t0005g0371a0002c0003t0005g0376 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.2245-401C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851416 | ||||||
| chr1:169851499
|
A | G | 2 | a0001c0002t0001g0359a0001c0002t0001g0360 | 2 | HG02451.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2245-318A>G | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851499 | ||||||
| chr1:169851541
|
C | T | 3 | a0001c0001t0010g0022a0001c0001t0010g0238a0001c0001t0010g0245 | 4 | HG02451.hp1 HG02486.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2245-276C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851541 | ||||||
| chr1:169851569
|
A | T | 2 | a0001c0001t0002g0346a0001c0001t0002g0347 | 2 | HG01243.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2245-248A>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 23/24 | chr1 | 169851569 | ||||||
| chr1:169851994
|
C | T | 59 | a0001c0001t0004g0023a0001c0001t0004g0024a0001c0001t0004g0025others(56): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2364+58C>T | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169851994 | ||||||
| chr1:169852261
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0180a0001c0001t0001g0220others(1): Show | 7 | HG01192.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2364+325T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852261 | ||||||
| chr1:169852347
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(264): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2364+411T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852347 | ||||||
| chr1:169852395
|
ATAGTAAT | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0175others(4): Show | 12 | HG00323.hp2 HG00741.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.2365-389_2365-383d others(9): Show |
FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr1 | 169852395 | |||||
| chr1:169852527
|
T | C | 1 | a0001c0001t0002g0354 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2365-263T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852527 | ||||||
| chr1:169852709
|
T | C | 1 | a0001c0001t0002g0036 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2365-81T>C | FIRRM | ENSG00000000460.17 | transcript | ENST00000359326.9 | protein_coding | 24/24 | chr1 | 169852709 |