| geneid | 123036 |
|---|---|
| ensemblid | ENSG00000165929.13 |
| hgncid | 19859 |
| symbol | TC2N |
| name | tandem C2 domains, nuclear |
| refseq_nuc | NM_001128596.3 |
| refseq_prot | NP_001122068.2 |
| ensembl_nuc | ENST00000435962.7 |
| ensembl_prot | ENSP00000387882.2 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 91779746 |
| end | 91867536 |
| strand | - |
| ver | v1.2 |
| region | chr14:91779746-91867536 |
| region5000 | chr14:91774746-91872536 |
| regionname0 | TC2N_chr14_91779746_91867536 |
| regionname5000 | TC2N_chr14_91774746_91872536 |
| 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 | 0/1 | 490 | 331 | 86 | 58 | 136 | 14 | 36 | 98 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0002 | 1/0 | 490 | 8 | 7 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0003 | 0/0 | 490 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0004 | 0/0 | 490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0005 | 0/0 | 490 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 1473 | 274 | 79 | 46 | 108 | 12 | 29 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| c0002 | 0/1 | 1473 | 56 | 7 | 12 | 27 | 2 | 7 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| c0003 | 1/0 | 1473 | 8 | 7 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| c0004 | 0/0 | 1473 | 3 | 3 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| c0005 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| c0006 | 0/0 | 1473 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| c0007 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| 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 | 3686 | 107 | 20 | 27 | 41 | 6 | 12 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0002 | 0/0 | 3686 | 105 | 13 | 25 | 57 | 3 | 7 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0003 | 0/0 | 3686 | 33 | 5 | 1 | 14 | 3 | 10 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0004 | 0/0 | 3686 | 14 | 0 | 0 | 10 | 0 | 4 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0005 | 0/0 | 3686 | 13 | 12 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0006 | 0/0 | 3686 | 11 | 11 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0007 | 1/0 | 3686 | 7 | 6 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0008 | 0/0 | 3686 | 7 | 6 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0009 | 0/0 | 3686 | 7 | 6 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0010 | 0/0 | 3686 | 5 | 3 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0011 | 0/0 | 3686 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0012 | 0/0 | 3686 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0013 | 0/0 | 4004 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0014 | 0/0 | 3686 | 2 | 0 | 0 | 0 | 2 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0015 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0016 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0017 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0018 | 0/0 | 4017 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0019 | 0/0 | 4018 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0020 | 0/0 | 4004 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0021 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0022 | 0/0 | 3686 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0023 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0024 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0025 | 0/0 | 4005 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0026 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0027 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0028 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0029 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0030 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0031 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0032 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0033 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0034 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0035 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0036 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0037 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0038 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| t0039 | 0/0 | 4000 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1473 | 274 | 79 | 46 | 108 | 12 | 29 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0002 | 0/1 | 1473 | 56 | 7 | 12 | 27 | 2 | 7 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0006 | 0/0 | 1473 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0002c0003 | 1/0 | 1473 | 8 | 7 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0003c0004 | 0/0 | 1473 | 3 | 3 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0004c0005 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0005c0007 | 0/0 | 1473 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5158 | 52 | 11 | 15 | 17 | 4 | 5 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0002 | 0/0 | 5158 | 102 | 11 | 25 | 56 | 3 | 7 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0003 | 0/0 | 5158 | 33 | 5 | 1 | 14 | 3 | 10 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0004 | 0/0 | 5158 | 14 | 0 | 0 | 10 | 0 | 4 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0005 | 0/0 | 5158 | 13 | 12 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0006 | 0/0 | 5158 | 11 | 11 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0008 | 0/0 | 5158 | 7 | 6 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0009 | 0/0 | 5158 | 7 | 6 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0010 | 0/0 | 5158 | 5 | 3 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0012 | 0/0 | 5158 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0013 | 0/0 | 5476 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0014 | 0/0 | 5158 | 2 | 0 | 0 | 0 | 2 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0016 | 0/0 | 5158 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0017 | 0/0 | 5489 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0018 | 0/0 | 5489 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0019 | 0/0 | 5490 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0020 | 0/0 | 5476 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0021 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0022 | 0/0 | 5158 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0023 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0024 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0025 | 0/0 | 5477 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0026 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0027 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0029 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0030 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0031 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0032 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0033 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0034 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0035 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0036 | 0/0 | 5158 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0037 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0038 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0001t0039 | 0/0 | 5472 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0002t0001 | 0/1 | 5158 | 53 | 7 | 12 | 24 | 2 | 7 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0002t0011 | 0/0 | 5158 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0001c0006t0002 | 0/0 | 5158 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0002c0003t0007 | 1/0 | 5158 | 7 | 6 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0002c0003t0015 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0003c0004t0001 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0003c0004t0002 | 0/0 | 5158 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0004c0005t0001 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| a0005c0007t0028 | 0/0 | 5158 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | copy fasta | chr14 | 91774746 | 91872536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0005g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0006g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0008g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0010g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0012g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0012g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0012g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0013g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0014g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0014g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0016g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0017g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0018g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0019g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0020g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0021g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0022g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0023g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0024g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0025g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0026g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0027g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0029g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0030g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0031g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0032g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0033g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0034g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0035g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0036g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0037g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0038g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0001t0039g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0011g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0002t0011g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0001c0006t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0007g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0002c0003t0015g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0003c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0003c0004t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0003c0004t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0004c0005t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| a0005c0007t0028g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0182 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0185 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0285 | EUR | GBR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00423 | hp1 | a0001 | c0001 | t0012 | g0321 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0101 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0147 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0136 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0148 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0139 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0157 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0279 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01167 | hp2 | a0001 | c0001 | t0016 | g0067 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0295 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01175 | hp2 | a0001 | c0001 | t0036 | g0293 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0082 | AMR | PUR | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0263 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0150 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | CLM | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0242 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0198 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01516 | hp2 | a0001 | c0001 | t0014 | g0308 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01517 | hp1 | a0001 | c0001 | t0014 | g0248 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0014 | EUR | IBS | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01884 | hp2 | a0001 | c0001 | t0008 | g0080 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01891 | hp2 | a0001 | c0001 | t0009 | g0155 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0105 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02040 | hp2 | a0001 | c0001 | t0033 | g0247 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02055 | hp2 | a0001 | c0001 | t0006 | g0073 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02083 | hp2 | a0001 | c0001 | t0024 | g0124 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0270 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0264 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02155 | hp2 | a0001 | c0001 | t0032 | g0192 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02257 | hp2 | a0001 | c0001 | t0008 | g0085 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02258 | hp1 | a0002 | c0003 | t0007 | g0164 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02258 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02280 | hp1 | a0001 | c0001 | t0009 | g0130 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PEL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0144 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02572 | hp1 | a0003 | c0004 | t0002 | g0283 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0219 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0324 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0146 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02622 | hp2 | a0001 | c0001 | t0009 | g0153 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02630 | hp2 | a0001 | c0001 | t0025 | g0021 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0149 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0178 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02717 | hp2 | a0002 | c0003 | t0007 | g0011 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02723 | hp1 | a0001 | c0001 | t0031 | g0168 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0059 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0197 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0173 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02809 | hp1 | a0001 | c0001 | t0026 | g0158 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02809 | hp2 | a0001 | c0001 | t0030 | g0145 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0003 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02818 | hp2 | a0001 | c0001 | t0027 | g0074 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02886 | hp1 | a0002 | c0003 | t0007 | g0166 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02895 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02896 | hp1 | a0001 | c0001 | t0006 | g0069 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02922 | hp1 | a0003 | c0004 | t0001 | g0070 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0161 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02970 | hp1 | a0002 | c0003 | t0007 | g0162 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0003 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0084 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02976 | hp2 | a0002 | c0003 | t0007 | g0165 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03041 | hp1 | a0001 | c0001 | t0019 | g0083 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0079 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03098 | hp1 | a0001 | c0001 | t0010 | g0133 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0142 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03130 | hp2 | a0001 | c0001 | t0009 | g0156 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03139 | hp1 | a0004 | c0005 | t0001 | g0047 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03195 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0081 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03209 | hp2 | a0001 | c0001 | t0029 | g0199 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03225 | hp2 | a0001 | c0001 | t0018 | g0088 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0177 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03486 | hp1 | a0002 | c0003 | t0015 | g0092 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0093 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0318 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03516 | hp1 | a0001 | c0001 | t0006 | g0062 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03516 | hp2 | a0003 | c0004 | t0002 | g0282 | AFR | ESN | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03540 | hp1 | a0001 | c0001 | t0020 | g0087 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0232 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03688 | hp2 | a0001 | c0001 | t0010 | g0132 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0186 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0126 | SAS | PJL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0312 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0224 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0138 | SAS | BEB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0137 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04199 | hp2 | a0001 | c0001 | t0004 | g0311 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04204 | hp1 | a0001 | c0001 | t0022 | g0016 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0122 | SAS | STU | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18522 | hp1 | a0001 | c0001 | t0006 | g0054 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18612 | hp1 | a0001 | c0006 | t0002 | g0258 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18747 | hp1 | a0001 | c0001 | t0012 | g0320 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | CHB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18906 | hp2 | a0001 | c0001 | t0013 | g0022 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18960 | hp1 | a0001 | c0001 | t0012 | g0319 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18962 | hp1 | a0001 | c0001 | t0023 | g0052 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18964 | hp2 | a0001 | c0001 | t0034 | g0223 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18966 | hp2 | a0001 | c0002 | t0011 | g0007 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0314 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18970 | hp2 | a0001 | c0001 | t0037 | g0317 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0322 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18983 | hp1 | a0001 | c0002 | t0011 | g0007 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18993 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19001 | hp1 | a0001 | c0001 | t0038 | g0325 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19030 | hp2 | a0001 | c0002 | t0001 | g0096 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19043 | hp1 | a0002 | c0003 | t0007 | g0011 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19054 | hp2 | a0001 | c0001 | t0021 | g0075 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0151 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19065 | hp2 | a0001 | c0002 | t0011 | g0111 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0326 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0099 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19087 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19240 | hp1 | a0001 | c0001 | t0035 | g0277 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | YRI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20129 | hp1 | a0001 | c0001 | t0039 | g0327 | AFR | ASW | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0131 | AFR | ASW | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0116 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0287 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0117 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | TSI | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0072 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0134 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0160 | AFR | ACB | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03471 | hp1 | a0001 | c0001 | t0017 | g0086 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0269 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0095 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0078 | AFR | USA | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA21309 | hp1 | a0001 | c0001 | t0013 | g0020 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| NA21309 | hp2 | a0005 | c0007 | t0028 | g0090 | AFR | LWK | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0114 | REF | REF | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0007 | g0163 | REF | REF | TC2N_chr14_91774746_91872536 | TC2N | chr14 | 91774746 | 91872536 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91800327
|
C | T | 1 | a0003 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.515G>A | p.Ser172Asn | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/12 | 846/5158 | 515/1473 | 172/490 | chr14 | 91800327 | ||
| chr14:91802271
|
T | A | 1 | a0005 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.452A>T | p.Lys151Met | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/12 | 783/5158 | 452/1473 | 151/490 | chr14 | 91802271 | ||
| chr14:91802271
|
T | G | 3 | a0001a0003a0004 | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
missense_variant | MODERATE | c.452A>C | p.Lys151Thr | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/12 | 783/5158 | 452/1473 | 151/490 | chr14 | 91802271 | ||
| chr14:91812485
|
A | G | 1 | a0004 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.128T>C | p.Val43Ala | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/12 | 459/5158 | 128/1473 | 43/490 | chr14 | 91812485 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91783169
|
G | A | 1 | a0001c0006 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1404C>T | p.Asn468Asn | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1735/5158 | 1404/1473 | 468/490 | chr14 | 91783169 | ||
| chr14:91785243
|
A | G | 1 | a0001c0002 | 56 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(53): Show |
synonymous_variant | LOW | c.1281T>C | p.Leu427Leu | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/12 | 1612/5158 | 1281/1473 | 427/490 | chr14 | 91785243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91779793
|
C | T | 1 | a0001c0001t0023 | 1 | NA18962.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3307G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3307 | chr14 | 91779793 | |||||
| chr14:91779821
|
C | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*3279G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3279 | chr14 | 91779821 | |||||
| chr14:91780090
|
T | A | 1 | a0001c0001t0038 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3010A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3010 | chr14 | 91780090 | |||||
| chr14:91780098
|
G | A | 1 | a0001c0001t0029 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3002C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 3002 | chr14 | 91780098 | |||||
| chr14:91780280
|
A | T | 2 | a0001c0001t0005a0001c0001t0030 | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2820T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2820 | chr14 | 91780280 | |||||
| chr14:91780610
|
A | G | 1 | a0001c0001t0022 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2490T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2490 | chr14 | 91780610 | |||||
| chr14:91780905
|
T | TAAAACAT others(311): Show |
1 | a0001c0001t0020 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(314): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | |||||
| chr14:91780905
|
T | TAAAACAT others(325): Show |
1 | a0001c0001t0019 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(328): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | |||||
| chr14:91780905
|
T | TAAAACAT others(324): Show |
1 | a0001c0001t0018 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(327): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | |||||
| chr14:91780905
|
T | TAAAACAT others(324): Show |
1 | a0001c0001t0017 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(327): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | |||||
| chr14:91780905
|
T | TAAAACAT others(307): Show |
1 | a0001c0001t0039 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(310): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | |||||
| chr14:91780905
|
T | TAAAACAT others(311): Show |
1 | a0001c0001t0013 | 2 | NA18906.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(314): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | |||||
| chr14:91780905
|
T | TAAAACAT others(312): Show |
1 | a0001c0001t0025 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2195insTTTT others(315): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2194 | chr14 | 91780905 | |||||
| chr14:91780939
|
C | T | 2 | a0001c0001t0009a0001c0001t0026 | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2161G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2161 | chr14 | 91780939 | |||||
| chr14:91780946
|
T | G | 2 | a0001c0001t0010a0001c0001t0035 | 6 | HG02559.hp1 HG02738.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2154A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2154 | chr14 | 91780946 | |||||
| chr14:91781004
|
A | G | 1 | a0001c0001t0021 | 1 | NA19054.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2096T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 2096 | chr14 | 91781004 | |||||
| chr14:91781110
|
T | C | 1 | a0001c0001t0024 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1990A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1990 | chr14 | 91781110 | |||||
| chr14:91781133
|
A | C | 1 | a0005c0007t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1967T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1967 | chr14 | 91781133 | |||||
| chr14:91781174
|
A | T | 4 | a0001c0001t0017a0001c0001t0018a0001c0001t0019others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1926T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1926 | chr14 | 91781174 | |||||
| chr14:91781338
|
T | A | 1 | a0001c0002t0011 | 3 | NA18966.hp2 NA18983.hp1 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1762A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1762 | chr14 | 91781338 | |||||
| chr14:91781470
|
G | T | 1 | a0001c0001t0031 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1630C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1630 | chr14 | 91781470 | |||||
| chr14:91781616
|
A | G | 1 | a0001c0001t0016 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1484T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1484 | chr14 | 91781616 | |||||
| chr14:91781715
|
G | C | 3 | a0001c0001t0013a0001c0001t0025a0001c0001t0039 | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1385C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1385 | chr14 | 91781715 | |||||
| chr14:91781999
|
A | T | 1 | a0001c0001t0038 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1101T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1101 | chr14 | 91781999 | |||||
| chr14:91782083
|
G | T | 1 | a0001c0001t0034 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1017C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 1017 | chr14 | 91782083 | |||||
| chr14:91782120
|
C | T | 1 | a0005c0007t0028 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*980G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 980 | chr14 | 91782120 | |||||
| chr14:91782268
|
C | T | 1 | a0001c0001t0027 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*832G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 832 | chr14 | 91782268 | |||||
| chr14:91782406
|
A | G | 1 | a0001c0001t0008 | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*694T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 694 | chr14 | 91782406 | |||||
| chr14:91782475
|
T | A | 1 | a0001c0001t0026 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*625A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 625 | chr14 | 91782475 | |||||
| chr14:91782512
|
A | C | 1 | a0001c0001t0030 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*588T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 588 | chr14 | 91782512 | |||||
| chr14:91782541
|
T | C | 8 | a0001c0001t0004a0001c0001t0005a0001c0001t0006others(5): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*559A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 559 | chr14 | 91782541 | |||||
| chr14:91782608
|
C | G | 1 | a0001c0001t0014 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*492G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 492 | chr14 | 91782608 | |||||
| chr14:91782628
|
A | G | 1 | a0001c0001t0033 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*472T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 472 | chr14 | 91782628 | |||||
| chr14:91782695
|
G | A | 2 | a0001c0001t0005a0001c0001t0030 | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*405C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 405 | chr14 | 91782695 | |||||
| chr14:91782757
|
T | C | 5 | a0001c0001t0003a0001c0001t0012a0001c0001t0031others(2): Show | 39 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*343A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 343 | chr14 | 91782757 | |||||
| chr14:91782782
|
G | A | 42 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(39): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*318C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 12/12 | 318 | chr14 | 91782782 | |||||
| chr14:91867267
|
T | C | 8 | a0001c0001t0002a0001c0001t0014a0001c0001t0033others(5): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
5_prime_UTR_variant | MODIFIER | c.-62A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/12 | 53498 | chr14 | 91867267 | |||||
| chr14:91867428
|
G | A | 4 | a0001c0001t0004a0001c0001t0012a0001c0001t0037others(1): Show | 19 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-223C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/12 | chr14 | 91867428 | ||||||
| chr14:91867492
|
G | A | 1 | a0001c0001t0039 | 1 | NA20129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-287C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/12 | 53723 | chr14 | 91867492 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:91783227
|
G | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1363-17C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783227 | ||||||
| chr14:91783260
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1363-50G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783260 | ||||||
| chr14:91783510
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1363-300G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783510 | ||||||
| chr14:91783623
|
T | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1363-413A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91783623 | ||||||
| chr14:91784068
|
T | C | 1 | a0001c0001t0004g0315 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1363-858A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784068 | ||||||
| chr14:91784100
|
G | A | 1 | a0001c0001t0019g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1363-890C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784100 | ||||||
| chr14:91784122
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1363-912G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784122 | ||||||
| chr14:91784292
|
T | C | 46 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(43): Show | 51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1362+870A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784292 | ||||||
| chr14:91784301
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1362+861A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784301 | ||||||
| chr14:91784529
|
T | C | 8 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1362+633A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784529 | ||||||
| chr14:91784545
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1362+617C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784545 | ||||||
| chr14:91784887
|
A | C | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1362+275T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91784887 | ||||||
| chr14:91785019
|
C | T | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1362+143G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785019 | ||||||
| chr14:91785034
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1362+128A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785034 | ||||||
| chr14:91785120
|
A | G | 2 | a0001c0001t0002g0222a0001c0001t0034g0223 | 2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1362+42T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785120 | ||||||
| chr14:91785135
|
T | C | 46 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(43): Show | 51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1362+27A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 11/11 | chr14 | 91785135 | ||||||
| chr14:91785403
|
A | T | 1 | a0001c0001t0019g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1163-42T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785403 | ||||||
| chr14:91785507
|
C | T | 1 | a0001c0001t0031g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1163-146G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785507 | ||||||
| chr14:91785574
|
A | C | 2 | a0001c0001t0003g0059a0001c0001t0003g0167 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1163-213T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785574 | ||||||
| chr14:91785603
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1163-242G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785603 | ||||||
| chr14:91785685
|
A | G | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1163-324T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785685 | ||||||
| chr14:91785820
|
G | A | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1163-459C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785820 | ||||||
| chr14:91785935
|
C | T | 1 | a0001c0001t0002g0266 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1163-574G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91785935 | ||||||
| chr14:91786066
|
G | C | 4 | a0001c0001t0003g0013a0001c0001t0003g0057a0001c0001t0003g0058others(1): Show | 4 | NA18968.hp2 NA18998.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1163-705C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786066 | ||||||
| chr14:91786201
|
A | G | 1 | a0001c0001t0013g0020 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1163-840T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786201 | ||||||
| chr14:91786300
|
C | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1163-939G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786300 | ||||||
| chr14:91786363
|
T | C | 1 | a0001c0001t0003g0015 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1163-1002A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786363 | ||||||
| chr14:91786495
|
T | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1162+1018A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786495 | ||||||
| chr14:91786695
|
T | C | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1162+818A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786695 | ||||||
| chr14:91786716
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1162+797A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786716 | ||||||
| chr14:91786718
|
G | T | 1 | a0004c0005t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1162+795C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786718 | ||||||
| chr14:91786731
|
T | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1162+782A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786731 | ||||||
| chr14:91786746
|
T | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162+767A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786746 | ||||||
| chr14:91786791
|
A | G | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1162+722T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786791 | ||||||
| chr14:91786906
|
G | A | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1162+607C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786906 | ||||||
| chr14:91786953
|
T | A | 1 | a0001c0001t0005g0144 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1162+560A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91786953 | ||||||
| chr14:91787011
|
T | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1162+502A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787011 | ||||||
| chr14:91787141
|
A | T | 2 | a0001c0001t0002g0306a0001c0001t0002g0309 | 2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1162+372T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787141 | ||||||
| chr14:91787212
|
A | G | 1 | a0001c0001t0009g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1162+301T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787212 | ||||||
| chr14:91787262
|
T | G | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | NA18947.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1162+251A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 10/11 | chr14 | 91787262 | ||||||
| chr14:91787649
|
T | C | 2 | a0001c0001t0001g0071a0001c0001t0021g0075 | 2 | NA19000.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1048-22A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91787649 | ||||||
| chr14:91787728
|
T | G | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1048-101A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91787728 | ||||||
| chr14:91787818
|
T | A | 313 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(310): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.1048-191A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91787818 | ||||||
| chr14:91788232
|
G | A | 326 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(323): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1048-605C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788232 | ||||||
| chr14:91788359
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1048-732A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788359 | ||||||
| chr14:91788428
|
A | C | 17 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(14): Show | 19 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.1048-801T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788428 | ||||||
| chr14:91788510
|
A | G | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1048-883T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788510 | ||||||
| chr14:91788659
|
T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1048-1032A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788659 | ||||||
| chr14:91788715
|
A | C | 1 | a0001c0001t0033g0247 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1048-1088T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788715 | ||||||
| chr14:91788961
|
TA | T | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.1048-1335delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91788961 | ||||||
| chr14:91789022
|
T | G | 38 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(35): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1048-1395A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789022 | ||||||
| chr14:91789136
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1048-1509C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789136 | ||||||
| chr14:91789197
|
A | T | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.1048-1570T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789197 | ||||||
| chr14:91789304
|
G | T | 46 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(43): Show | 51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1048-1677C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789304 | ||||||
| chr14:91789363
|
G | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0044 | 2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1048-1736C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789363 | ||||||
| chr14:91789429
|
TA | T | 10 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(7): Show | 10 | HG02630.hp2 HG02723.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.1048-1803delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789429 | ||||||
| chr14:91789440
|
AAAG | A | 36 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(33): Show | 41 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1048-1816_1048-181 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789440 | ||||||
| chr14:91789592
|
CAGAG | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048-1969_1048-196 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789592 | ||||||
| chr14:91789609
|
T | A | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1048-1982A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789609 | ||||||
| chr14:91789623
|
C | CA | 22 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(19): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1048-1997dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789623 | ||||||
| chr14:91789630
|
A | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1048-2003T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789630 | ||||||
| chr14:91789806
|
T | G | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1048-2179A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789806 | ||||||
| chr14:91789813
|
C | A | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1048-2186G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789813 | ||||||
| chr14:91789888
|
C | A | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1048-2261G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91789888 | ||||||
| chr14:91790037
|
C | G | 38 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(35): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1047+2330G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790037 | ||||||
| chr14:91790040
|
A | C | 2 | a0001c0001t0001g0036a0001c0001t0016g0067 | 2 | HG01109.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1047+2327T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790040 | ||||||
| chr14:91790080
|
T | G | 1 | a0001c0001t0030g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1047+2287A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790080 | ||||||
| chr14:91790391
|
A | G | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+1976T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790391 | ||||||
| chr14:91790407
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1047+1960G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790407 | ||||||
| chr14:91790572
|
T | C | 5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047+1795A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790572 | ||||||
| chr14:91790618
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1047+1749G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790618 | ||||||
| chr14:91790687
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+1680A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790687 | ||||||
| chr14:91790719
|
T | C | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1047+1648A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790719 | ||||||
| chr14:91790842
|
T | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+1525A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790842 | ||||||
| chr14:91790950
|
A | G | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+1417T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91790950 | ||||||
| chr14:91791064
|
G | A | 6 | a0001c0001t0010g0131a0001c0001t0010g0132a0001c0001t0010g0133others(3): Show | 6 | HG02559.hp1 HG02738.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1047+1303C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791064 | ||||||
| chr14:91791114
|
G | C | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+1253C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791114 | ||||||
| chr14:91791176
|
A | AGGAGG | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(89): Show | 102 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1047+1186_1047+119 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791176 | ||||||
| chr14:91791176
|
AGGAGG | A | 121 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(118): Show | 121 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1047+1186_1047+119 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791176 | ||||||
| chr14:91791415
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1047+952G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791415 | ||||||
| chr14:91791485
|
A | G | 7 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1047+882T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791485 | ||||||
| chr14:91791514
|
T | A | 1 | a0001c0001t0009g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1047+853A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791514 | ||||||
| chr14:91791535
|
T | TGA | 38 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(35): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1047+830_1047+831d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791535 | ||||||
| chr14:91791562
|
G | A | 1 | a0001c0001t0009g0130 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1047+805C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791562 | ||||||
| chr14:91791593
|
A | G | 38 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(35): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.1047+774T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791593 | ||||||
| chr14:91791639
|
T | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1047+728A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791639 | ||||||
| chr14:91791757
|
T | TA | 24 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(21): Show | 27 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1047+609dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791757 | ||||||
| chr14:91791757
|
T | TAA | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.1047+608_1047+609d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791757 | ||||||
| chr14:91791758
|
A | T | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1047+609T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791758 | ||||||
| chr14:91791836
|
G | A | 2 | a0001c0001t0002g0238a0001c0001t0037g0317 | 2 | NA18970.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1047+531C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791836 | ||||||
| chr14:91791913
|
G | A | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.1047+454C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91791913 | ||||||
| chr14:91792011
|
C | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1047+356G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792011 | ||||||
| chr14:91792030
|
A | G | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1047+337T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792030 | ||||||
| chr14:91792118
|
C | CA | 5 | a0001c0001t0001g0051a0001c0001t0013g0020a0001c0001t0013g0022others(2): Show | 5 | HG02630.hp2 HG03471.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1047+248dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792118 | ||||||
| chr14:91792121
|
AG | A | 4 | a0001c0002t0001g0114a0001c0002t0001g0115a0001c0002t0001g0116others(1): Show | 4 | HG00733.hp2 HG03710.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+245delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792121 | ||||||
| chr14:91792122
|
G | A | 316 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(313): Show | 332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.1047+245C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792122 | ||||||
| chr14:91792155
|
G | T | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1047+212C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792155 | ||||||
| chr14:91792221
|
T | TA | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1047+145dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792221 | ||||||
| chr14:91792353
|
C | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1047+14G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 9/11 | chr14 | 91792353 | ||||||
| chr14:91792793
|
C | T | 1 | a0001c0002t0001g0106 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.856-235G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91792793 | ||||||
| chr14:91793082
|
A | G | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-524T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793082 | ||||||
| chr14:91793139
|
T | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0023others(17): Show | 22 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.856-581A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793139 | ||||||
| chr14:91793165
|
A | G | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-607T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793165 | ||||||
| chr14:91793356
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.856-798T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793356 | ||||||
| chr14:91793441
|
T | C | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.856-883A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793441 | ||||||
| chr14:91793463
|
T | A | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-905A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793463 | ||||||
| chr14:91793559
|
A | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.856-1001T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793559 | ||||||
| chr14:91793595
|
C | T | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1037G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793595 | ||||||
| chr14:91793846
|
T | C | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1288A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793846 | ||||||
| chr14:91793850
|
C | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0296 | 2 | NA18968.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.856-1292G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793850 | ||||||
| chr14:91793930
|
CT | C | 3 | a0001c0001t0003g0170a0001c0001t0003g0177a0001c0001t0003g0178 | 3 | HG02683.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.856-1373delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91793930 | ||||||
| chr14:91794447
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.856-1889C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794447 | ||||||
| chr14:91794509
|
G | A | 2 | a0001c0001t0001g0027a0001c0001t0001g0040 | 2 | HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.856-1951C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794509 | ||||||
| chr14:91794602
|
TG | T | 47 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(44): Show | 47 | HG00642.hp2 HG00673.hp1 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.856-2045delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794602 | ||||||
| chr14:91794656
|
CA | C | 9 | a0001c0001t0002g0289a0001c0001t0013g0020a0001c0001t0013g0022others(6): Show | 9 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.856-2099delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794656 | ||||||
| chr14:91794748
|
A | G | 1 | a0001c0001t0002g0303 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.856-2190T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794748 | ||||||
| chr14:91794876
|
T | C | 8 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-2318A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91794876 | ||||||
| chr14:91795098
|
G | A | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856-2540C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795098 | ||||||
| chr14:91795153
|
C | T | 2 | a0001c0001t0003g0059a0001c0001t0003g0167 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.856-2595G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795153 | ||||||
| chr14:91795447
|
G | A | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+2338C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795447 | ||||||
| chr14:91795564
|
T | C | 46 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(43): Show | 51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.855+2221A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795564 | ||||||
| chr14:91795839
|
C | G | 1 | a0001c0001t0002g0222 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.855+1946G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795839 | ||||||
| chr14:91795846
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(241): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.855+1939T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795846 | ||||||
| chr14:91795980
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.855+1805A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91795980 | ||||||
| chr14:91796066
|
T | C | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.855+1719A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796066 | ||||||
| chr14:91796358
|
C | G | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.855+1427G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796358 | ||||||
| chr14:91796585
|
C | CT | 326 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(323): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.855+1199dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796585 | ||||||
| chr14:91796614
|
G | A | 36 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(33): Show | 41 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.855+1171C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796614 | ||||||
| chr14:91796659
|
T | C | 7 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+1126A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796659 | ||||||
| chr14:91796878
|
C | T | 1 | a0001c0001t0003g0015 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.855+907G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796878 | ||||||
| chr14:91796913
|
A | G | 3 | a0001c0001t0002g0200a0001c0001t0002g0234a0001c0001t0002g0302 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.855+872T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796913 | ||||||
| chr14:91796971
|
T | TTTTG | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.855+810_855+813dup others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91796971 | ||||||
| chr14:91797103
|
T | C | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.855+682A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797103 | ||||||
| chr14:91797324
|
T | C | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.855+461A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797324 | ||||||
| chr14:91797327
|
A | C | 196 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(193): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.855+458T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797327 | ||||||
| chr14:91797557
|
C | A | 1 | a0004c0005t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.855+228G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797557 | ||||||
| chr14:91797724
|
A | C | 39 | a0001c0001t0001g0091a0001c0001t0003g0012a0001c0001t0003g0013others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.855+61T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797724 | ||||||
| chr14:91797735
|
AT | A | 39 | a0001c0001t0001g0091a0001c0001t0003g0012a0001c0001t0003g0013others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.855+49delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797735 | ||||||
| chr14:91797736
|
TA | T | 240 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(237): Show | 250 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.855+48delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797736 | ||||||
| chr14:91797737
|
A | C | 39 | a0001c0001t0001g0091a0001c0001t0003g0012a0001c0001t0003g0013others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.855+48T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 8/11 | chr14 | 91797737 | ||||||
| chr14:91797955
|
C | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-54G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91797955 | ||||||
| chr14:91798037
|
C | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.739-136G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798037 | ||||||
| chr14:91798039
|
C | T | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.739-138G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798039 | ||||||
| chr14:91798087
|
C | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.739-186G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798087 | ||||||
| chr14:91798187
|
A | C | 1 | a0001c0001t0004g0324 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.738+112T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 7/11 | chr14 | 91798187 | ||||||
| chr14:91798413
|
G | C | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.638-14C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798413 | ||||||
| chr14:91798681
|
T | G | 1 | a0001c0001t0003g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.638-282A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798681 | ||||||
| chr14:91798816
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.637+173C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798816 | ||||||
| chr14:91798922
|
T | C | 5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.637+67A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 6/11 | chr14 | 91798922 | ||||||
| chr14:91799182
|
A | G | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.562-118T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799182 | ||||||
| chr14:91799213
|
G | GA | 17 | a0001c0001t0001g0097a0001c0001t0002g0201a0001c0001t0002g0270others(14): Show | 17 | HG02145.hp1 HG02145.hp2 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.562-150dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799213 | ||||||
| chr14:91799213
|
GA | G | 42 | a0001c0001t0001g0091a0001c0001t0003g0012a0001c0001t0003g0013others(39): Show | 43 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(40): Show |
intron_variant | MODIFIER | c.562-150delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799213 | ||||||
| chr14:91799322
|
A | C | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.562-258T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799322 | ||||||
| chr14:91799668
|
A | T | 2 | a0001c0001t0003g0059a0001c0001t0003g0167 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.562-604T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799668 | ||||||
| chr14:91799761
|
A | G | 1 | a0001c0001t0005g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.561+520T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799761 | ||||||
| chr14:91799863
|
A | G | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.561+418T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799863 | ||||||
| chr14:91799908
|
A | C | 1 | a0001c0001t0031g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.561+373T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799908 | ||||||
| chr14:91799917
|
A | G | 3 | a0001c0001t0002g0200a0001c0001t0002g0234a0001c0001t0002g0302 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.561+364T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91799917 | ||||||
| chr14:91800088
|
T | G | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.561+193A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800088 | ||||||
| chr14:91800143
|
A | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.561+138T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800143 | ||||||
| chr14:91800154
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.561+127A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800154 | ||||||
| chr14:91800168
|
C | A | 1 | a0001c0001t0035g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.561+113G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800168 | ||||||
| chr14:91800216
|
C | T | 1 | a0001c0001t0006g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.561+65G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 5/11 | chr14 | 91800216 | ||||||
| chr14:91800443
|
A | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-71T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800443 | ||||||
| chr14:91800727
|
A | G | 1 | a0001c0001t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.470-355T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800727 | ||||||
| chr14:91800941
|
GATAT | G | 3 | a0001c0001t0003g0170a0001c0001t0003g0177a0001c0001t0003g0178 | 3 | HG02683.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.470-573_470-570del others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800941 | ||||||
| chr14:91800943
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.470-571A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800943 | ||||||
| chr14:91800953
|
T | C | 1 | a0001c0001t0002g0225 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.470-581A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800953 | ||||||
| chr14:91800955
|
C | CACACACA others(27): Show |
60 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.470-617_470-584dup others(34): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800955 | ||||||
| chr14:91800955
|
C | CACACACA others(61): Show |
2 | a0001c0001t0002g0295a0001c0001t0039g0327 | 2 | HG01175.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.470-651_470-584dup others(68): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800955 | ||||||
| chr14:91800957
|
C | CACACACA others(25): Show |
2 | a0001c0001t0013g0022a0001c0001t0025g0021 | 2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.470-617_470-586dup others(32): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91800957 | ||||||
| chr14:91801070
|
ATG | A | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.470-700_470-699del others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801070 | ||||||
| chr14:91801080
|
G | GTA | 9 | a0001c0001t0002g0260a0001c0001t0002g0297a0001c0001t0013g0020others(6): Show | 9 | HG01081.hp2 HG01175.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.470-710_470-709dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801080 | ||||||
| chr14:91801080
|
G | GTGTA | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.470-709_470-708ins others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801080 | ||||||
| chr14:91801082
|
A | G | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.470-710T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801082 | ||||||
| chr14:91801690
|
A | G | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.469+564T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801690 | ||||||
| chr14:91801735
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.469+519A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801735 | ||||||
| chr14:91801752
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(97): Show | 109 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.469+502G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801752 | ||||||
| chr14:91801893
|
G | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.469+361C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91801893 | ||||||
| chr14:91802132
|
C | T | 7 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.469+122G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91802132 | ||||||
| chr14:91802161
|
A | G | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.469+93T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91802161 | ||||||
| chr14:91802187
|
C | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(97): Show | 109 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.469+67G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 4/11 | chr14 | 91802187 | ||||||
| chr14:91802543
|
T | C | 38 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(35): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.302-122A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802543 | ||||||
| chr14:91802565
|
C | T | 1 | a0002c0003t0007g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.302-144G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802565 | ||||||
| chr14:91802708
|
C | G | 1 | a0001c0001t0009g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.302-287G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802708 | ||||||
| chr14:91802744
|
T | TGG | 31 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(28): Show | 36 | HG02109.hp1 HG02451.hp2 HG02602.hp2 others(33): Show |
intron_variant | MODIFIER | c.302-325_302-324dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802744 | ||||||
| chr14:91802746
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0045 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.302-325C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802746 | ||||||
| chr14:91802776
|
G | A | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.302-355C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802776 | ||||||
| chr14:91802788
|
T | C | 1 | a0001c0001t0036g0293 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.302-367A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802788 | ||||||
| chr14:91802817
|
G | A | 1 | a0001c0001t0030g0145 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.302-396C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802817 | ||||||
| chr14:91802859
|
C | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-438G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91802859 | ||||||
| chr14:91803084
|
G | A | 54 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(51): Show | 59 | HG01081.hp1 HG01109.hp1 HG01891.hp2 others(56): Show |
intron_variant | MODIFIER | c.302-663C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803084 | ||||||
| chr14:91803097
|
T | G | 1 | a0001c0002t0011g0111 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.302-676A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803097 | ||||||
| chr14:91803380
|
T | C | 1 | a0001c0001t0003g0176 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.302-959A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | ||||||
| chr14:91803380
|
T | TAC | 61 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(58): Show | 64 | HG00099.hp1 HG00099.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.302-961_302-960dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | ||||||
| chr14:91803380
|
T | TACAC | 14 | a0001c0001t0001g0066a0001c0001t0004g0322a0001c0001t0005g0003others(11): Show | 17 | HG01081.hp1 HG01975.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.302-963_302-960dup others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | ||||||
| chr14:91803380
|
T | TACACAC | 20 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(17): Show | 22 | HG02602.hp2 HG02647.hp1 HG02818.hp2 others(19): Show |
intron_variant | MODIFIER | c.302-965_302-960dup others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | ||||||
| chr14:91803380
|
T | TATAC | 8 | a0001c0001t0006g0072a0001c0001t0006g0073a0001c0001t0006g0159others(5): Show | 8 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.302-960_302-959ins others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | ||||||
| chr14:91803380
|
TAC | T | 7 | a0001c0001t0002g0239a0001c0001t0002g0306a0001c0001t0002g0309others(4): Show | 7 | HG00423.hp1 NA18747.hp1 NA18960.hp1 others(4): Show |
intron_variant | MODIFIER | c.302-961_302-960del others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803380 | ||||||
| chr14:91803382
|
C | T | 7 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(4): Show | 7 | HG02572.hp1 HG02630.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.302-961G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803382 | ||||||
| chr14:91803403
|
G | A | 1 | a0001c0001t0002g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.302-982C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803403 | ||||||
| chr14:91803412
|
T | C | 2 | a0001c0001t0002g0251a0005c0007t0028g0090 | 2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.302-991A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803412 | ||||||
| chr14:91803412
|
T | TAC | 3 | a0001c0002t0001g0135a0001c0002t0001g0147a0002c0003t0015g0092 | 3 | HG00738.hp1 HG01069.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.302-993_302-992dup others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803412 | ||||||
| chr14:91803412
|
TAC | T | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.302-993_302-992del others(2): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803412 | ||||||
| chr14:91803428
|
C | CACACACA others(1): Show |
11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.302-1008_302-1007i others(10): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | ||||||
| chr14:91803428
|
C | CACACAT | 26 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(23): Show | 28 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(25): Show |
intron_variant | MODIFIER | c.302-1008_302-1007i others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | ||||||
| chr14:91803428
|
C | CACAT | 4 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(1): Show | 4 | HG02145.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-1008_302-1007i others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | ||||||
| chr14:91803428
|
C | CAT | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.302-1009_302-1008d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | ||||||
| chr14:91803428
|
C | CATAT | 11 | a0001c0001t0001g0032a0001c0001t0002g0232a0001c0001t0009g0130others(8): Show | 11 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.302-1011_302-1008d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | ||||||
| chr14:91803428
|
C | T | 1 | a0001c0001t0002g0251 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.302-1007G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803428 | ||||||
| chr14:91803509
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.302-1088C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803509 | ||||||
| chr14:91803515
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.302-1094A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803515 | ||||||
| chr14:91803557
|
A | T | 1 | a0001c0001t0004g0322 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.302-1136T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803557 | ||||||
| chr14:91803560
|
C | T | 2 | a0001c0001t0003g0169a0001c0001t0003g0174 | 2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.302-1139G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803560 | ||||||
| chr14:91803577
|
G | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.302-1156C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803577 | ||||||
| chr14:91803609
|
C | T | 2 | a0001c0002t0001g0114a0001c0002t0001g0115 | 2 | HG00733.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.302-1188G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803609 | ||||||
| chr14:91803767
|
A | T | 1 | a0001c0001t0002g0228 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.302-1346T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803767 | ||||||
| chr14:91803836
|
A | C | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.302-1415T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803836 | ||||||
| chr14:91803908
|
C | A | 1 | a0001c0001t0002g0210 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.302-1487G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803908 | ||||||
| chr14:91803909
|
C | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-1488G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803909 | ||||||
| chr14:91803963
|
T | C | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.302-1542A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803963 | ||||||
| chr14:91803997
|
G | A | 38 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(35): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.302-1576C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91803997 | ||||||
| chr14:91804102
|
A | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.302-1681T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804102 | ||||||
| chr14:91804142
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.302-1721G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804142 | ||||||
| chr14:91804221
|
C | T | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-1800G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804221 | ||||||
| chr14:91804265
|
T | C | 1 | a0002c0003t0007g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.302-1844A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804265 | ||||||
| chr14:91804270
|
A | G | 5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.302-1849T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804270 | ||||||
| chr14:91804470
|
T | C | 1 | a0001c0001t0023g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.302-2049A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804470 | ||||||
| chr14:91804633
|
G | C | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-2212C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804633 | ||||||
| chr14:91804744
|
G | T | 1 | a0001c0002t0001g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.302-2323C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804744 | ||||||
| chr14:91804884
|
G | A | 1 | a0001c0001t0004g0324 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.302-2463C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804884 | ||||||
| chr14:91804943
|
C | T | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-2522G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91804943 | ||||||
| chr14:91805260
|
AG | A | 2 | a0001c0002t0001g0008a0001c0002t0001g0118 | 3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.302-2840delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805260 | ||||||
| chr14:91805407
|
G | A | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.302-2986C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805407 | ||||||
| chr14:91805421
|
C | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0016g0067 | 3 | HG01109.hp2 HG01167.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.302-3000G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805421 | ||||||
| chr14:91805450
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035 | 3 | HG01261.hp2 HG02004.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.302-3029G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805450 | ||||||
| chr14:91805523
|
T | A | 1 | a0001c0001t0002g0253 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.302-3102A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805523 | ||||||
| chr14:91805658
|
C | T | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.302-3237G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805658 | ||||||
| chr14:91805749
|
T | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.302-3328A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805749 | ||||||
| chr14:91805791
|
G | A | 2 | a0001c0001t0003g0182a0001c0001t0003g0198 | 2 | HG00099.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.302-3370C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805791 | ||||||
| chr14:91805818
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.302-3397A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805818 | ||||||
| chr14:91805933
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0030a0001c0001t0001g0040 | 3 | HG00673.hp2 HG02071.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.302-3512G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91805933 | ||||||
| chr14:91806111
|
GC | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-3691delG | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806111 | ||||||
| chr14:91806390
|
T | G | 1 | a0001c0001t0004g0326 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.302-3969A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806390 | ||||||
| chr14:91806497
|
G | C | 4 | a0001c0001t0006g0072a0001c0001t0006g0073a0001c0001t0006g0159others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-4076C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806497 | ||||||
| chr14:91806585
|
C | T | 1 | a0001c0001t0004g0312 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.302-4164G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806585 | ||||||
| chr14:91806671
|
G | T | 1 | a0001c0001t0002g0235 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.302-4250C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806671 | ||||||
| chr14:91806729
|
G | A | 1 | a0001c0001t0002g0264 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.302-4308C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806729 | ||||||
| chr14:91806829
|
A | G | 1 | a0001c0001t0001g0049 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.302-4408T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806829 | ||||||
| chr14:91806971
|
C | T | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-4550G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91806971 | ||||||
| chr14:91807003
|
A | T | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.302-4582T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807003 | ||||||
| chr14:91807063
|
C | T | 1 | a0001c0001t0006g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.302-4642G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807063 | ||||||
| chr14:91807085
|
G | C | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.302-4664C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807085 | ||||||
| chr14:91807172
|
C | T | 2 | a0001c0001t0013g0020a0001c0001t0032g0192 | 2 | HG02155.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.302-4751G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807172 | ||||||
| chr14:91807247
|
C | T | 4 | a0001c0001t0003g0170a0001c0001t0003g0176a0001c0001t0003g0177others(1): Show | 4 | HG02683.hp2 HG03239.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.302-4826G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807247 | ||||||
| chr14:91807340
|
T | C | 7 | a0001c0001t0002g0245a0001c0001t0002g0261a0001c0001t0002g0268others(4): Show | 7 | HG00544.hp2 HG00609.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.302-4919A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807340 | ||||||
| chr14:91807634
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.301+4678A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807634 | ||||||
| chr14:91807926
|
G | A | 1 | a0001c0001t0002g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.301+4386C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807926 | ||||||
| chr14:91807932
|
T | C | 2 | a0001c0001t0002g0245a0001c0002t0001g0093 | 2 | HG00544.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.301+4380A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91807932 | ||||||
| chr14:91808160
|
C | T | 1 | a0001c0001t0021g0075 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.301+4152G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808160 | ||||||
| chr14:91808291
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.301+4021T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808291 | ||||||
| chr14:91808351
|
G | A | 2 | a0001c0001t0002g0306a0001c0001t0002g0309 | 2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.301+3961C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808351 | ||||||
| chr14:91808837
|
T | C | 4 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0271others(1): Show | 4 | HG00423.hp2 NA18960.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.301+3475A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808837 | ||||||
| chr14:91808978
|
T | A | 1 | a0002c0003t0007g0164 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.301+3334A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91808978 | ||||||
| chr14:91809377
|
C | A | 44 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(41): Show | 47 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.301+2935G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809377 | ||||||
| chr14:91809602
|
T | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+2710A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809602 | ||||||
| chr14:91809775
|
A | G | 1 | a0001c0001t0002g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.301+2537T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809775 | ||||||
| chr14:91809881
|
A | T | 1 | a0001c0001t0005g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.301+2431T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91809881 | ||||||
| chr14:91810040
|
A | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.301+2272T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810040 | ||||||
| chr14:91810041
|
T | C | 1 | a0001c0002t0011g0111 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.301+2271A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810041 | ||||||
| chr14:91810138
|
C | T | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+2174G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810138 | ||||||
| chr14:91810316
|
TG | T | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.301+1995delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810316 | ||||||
| chr14:91810333
|
C | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+1979G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810333 | ||||||
| chr14:91810477
|
A | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+1835T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810477 | ||||||
| chr14:91810496
|
T | C | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+1816A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810496 | ||||||
| chr14:91810558
|
T | C | 11 | a0001c0001t0002g0207a0001c0001t0002g0217a0001c0001t0002g0222others(8): Show | 11 | HG00673.hp1 HG02071.hp2 HG02074.hp2 others(8): Show |
intron_variant | MODIFIER | c.301+1754A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810558 | ||||||
| chr14:91810573
|
A | G | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+1739T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810573 | ||||||
| chr14:91810581
|
C | T | 1 | a0001c0001t0002g0256 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.301+1731G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810581 | ||||||
| chr14:91810681
|
A | C | 1 | a0001c0001t0009g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.301+1631T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810681 | ||||||
| chr14:91810734
|
C | A | 1 | a0001c0001t0009g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.301+1578G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810734 | ||||||
| chr14:91810841
|
C | G | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.301+1471G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810841 | ||||||
| chr14:91810868
|
G | GA | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+1443dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810868 | ||||||
| chr14:91810909
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.301+1403C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810909 | ||||||
| chr14:91810991
|
T | A | 1 | a0001c0001t0002g0281 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.301+1321A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91810991 | ||||||
| chr14:91811041
|
C | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.301+1271G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811041 | ||||||
| chr14:91811150
|
C | T | 3 | a0001c0001t0005g0003a0001c0001t0005g0146a0001c0001t0005g0149 | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.301+1162G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811150 | ||||||
| chr14:91811151
|
G | A | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+1161C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811151 | ||||||
| chr14:91811248
|
A | AT | 38 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(35): Show | 43 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(40): Show |
intron_variant | MODIFIER | c.301+1063dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811248 | ||||||
| chr14:91811360
|
G | GT | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.301+951dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811360 | ||||||
| chr14:91811504
|
TTCTC | T | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+804_301+807del others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811504 | ||||||
| chr14:91811587
|
T | C | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.301+725A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811587 | ||||||
| chr14:91811639
|
T | C | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.301+673A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811639 | ||||||
| chr14:91811754
|
G | C | 1 | a0001c0001t0024g0124 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.301+558C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811754 | ||||||
| chr14:91811873
|
T | A | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.301+439A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811873 | ||||||
| chr14:91811974
|
T | C | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.301+338A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91811974 | ||||||
| chr14:91812014
|
T | A | 2 | a0001c0001t0002g0222a0001c0001t0034g0223 | 2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.301+298A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91812014 | ||||||
| chr14:91812296
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0044 | 2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.301+16G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91812296 | ||||||
| chr14:91812298
|
A | G | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.301+14T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 3/11 | chr14 | 91812298 | ||||||
| chr14:91812686
|
C | G | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.68-141G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91812686 | ||||||
| chr14:91812838
|
T | C | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.68-293A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91812838 | ||||||
| chr14:91813386
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67+317A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813386 | ||||||
| chr14:91813412
|
C | T | 1 | a0001c0001t0002g0253 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67+291G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813412 | ||||||
| chr14:91813437
|
C | G | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67+266G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813437 | ||||||
| chr14:91813639
|
T | G | 51 | a0001c0001t0024g0124a0001c0002t0001g0001a0001c0002t0001g0008others(48): Show | 57 | HG00544.hp1 HG00558.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.67+64A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813639 | ||||||
| chr14:91813693
|
T | C | 111 | a0001c0001t0001g0017a0001c0001t0001g0023a0001c0001t0001g0034others(108): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.67+10A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 2/11 | chr14 | 91813693 | ||||||
| chr14:91813893
|
A | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-68T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91813893 | ||||||
| chr14:91813993
|
T | C | 1 | a0001c0001t0002g0300 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-56-168A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91813993 | ||||||
| chr14:91814056
|
GA | G | 6 | a0001c0001t0010g0131a0001c0001t0010g0132a0001c0001t0010g0133others(3): Show | 6 | HG02559.hp1 HG02738.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-232delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814056 | ||||||
| chr14:91814310
|
T | C | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-485A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814310 | ||||||
| chr14:91814331
|
G | A | 47 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(44): Show | 47 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.-56-506C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814331 | ||||||
| chr14:91814357
|
CA | C | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-533delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814357 | ||||||
| chr14:91814391
|
T | C | 36 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(33): Show | 41 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(38): Show |
intron_variant | MODIFIER | c.-56-566A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814391 | ||||||
| chr14:91814944
|
TATACAAT others(6): Show |
T | 3 | a0001c0001t0002g0200a0001c0001t0002g0234a0001c0001t0002g0302 | 3 | HG00735.hp2 HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-56-1132_-56-1120d others(15): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91814944 | ||||||
| chr14:91815042
|
T | C | 7 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-1217A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815042 | ||||||
| chr14:91815161
|
C | T | 1 | a0001c0001t0002g0212 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-56-1336G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815161 | ||||||
| chr14:91815200
|
G | A | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1375C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815200 | ||||||
| chr14:91815248
|
C | A | 2 | a0001c0001t0002g0225a0001c0001t0002g0226 | 2 | NA18947.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-56-1423G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815248 | ||||||
| chr14:91815347
|
A | ATGAAT | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1523_-56-1522i others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815347 | ||||||
| chr14:91815348
|
C | A | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1523G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815348 | ||||||
| chr14:91815349
|
T | A | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-1524A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815349 | ||||||
| chr14:91815429
|
C | A | 1 | a0001c0001t0002g0201 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-56-1604G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815429 | ||||||
| chr14:91815434
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-1609G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815434 | ||||||
| chr14:91815447
|
G | A | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-56-1622C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815447 | ||||||
| chr14:91815765
|
T | C | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-1940A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815765 | ||||||
| chr14:91815772
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-56-1947A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815772 | ||||||
| chr14:91815932
|
T | C | 266 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(263): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-56-2107A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91815932 | ||||||
| chr14:91816011
|
A | G | 1 | a0001c0001t0031g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-2186T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816011 | ||||||
| chr14:91816039
|
A | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-2214T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816039 | ||||||
| chr14:91816189
|
T | C | 7 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-2364A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816189 | ||||||
| chr14:91816378
|
G | A | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-2553C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816378 | ||||||
| chr14:91816482
|
T | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-2657A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816482 | ||||||
| chr14:91816526
|
G | T | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-2701C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816526 | ||||||
| chr14:91816649
|
T | C | 1 | a0001c0001t0002g0278 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-56-2824A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816649 | ||||||
| chr14:91816779
|
T | A | 1 | a0001c0001t0031g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-2954A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816779 | ||||||
| chr14:91816959
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-56-3134G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91816959 | ||||||
| chr14:91817008
|
C | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-3183G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817008 | ||||||
| chr14:91817338
|
T | C | 1 | a0001c0001t0002g0236 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-56-3513A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817338 | ||||||
| chr14:91817818
|
G | A | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-3993C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817818 | ||||||
| chr14:91817828
|
T | G | 39 | a0001c0001t0001g0091a0001c0001t0003g0012a0001c0001t0003g0013others(36): Show | 40 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.-56-4003A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91817828 | ||||||
| chr14:91818089
|
T | C | 149 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(146): Show | 150 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.-56-4264A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818089 | ||||||
| chr14:91818168
|
C | T | 1 | a0001c0001t0002g0207 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-56-4343G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818168 | ||||||
| chr14:91818169
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-4344C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818169 | ||||||
| chr14:91818179
|
A | G | 3 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0038g0325 | 3 | NA18969.hp2 NA19001.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-56-4354T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818179 | ||||||
| chr14:91818441
|
A | G | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-4616T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818441 | ||||||
| chr14:91818476
|
T | A | 42 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(39): Show | 47 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(44): Show |
intron_variant | MODIFIER | c.-56-4651A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818476 | ||||||
| chr14:91818799
|
C | T | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-56-4974G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818799 | ||||||
| chr14:91818825
|
C | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-56-5000G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818825 | ||||||
| chr14:91818865
|
A | G | 1 | a0001c0001t0003g0197 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-56-5040T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818865 | ||||||
| chr14:91818897
|
A | T | 1 | a0001c0001t0003g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-56-5072T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818897 | ||||||
| chr14:91818947
|
G | C | 2 | a0001c0001t0001g0091a0001c0002t0001g0120 | 2 | NA19030.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-56-5122C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818947 | ||||||
| chr14:91818982
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-56-5157A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818982 | ||||||
| chr14:91818995
|
A | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-5170T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91818995 | ||||||
| chr14:91819028
|
C | G | 42 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(39): Show | 47 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(44): Show |
intron_variant | MODIFIER | c.-56-5203G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819028 | ||||||
| chr14:91819040
|
C | A | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-5215G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819040 | ||||||
| chr14:91819528
|
C | T | 3 | a0001c0002t0001g0102a0001c0002t0001g0104a0001c0002t0001g0106 | 3 | NA19079.hp1 NA19080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-56-5703G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819528 | ||||||
| chr14:91819756
|
C | T | 10 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-5931G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819756 | ||||||
| chr14:91819765
|
C | T | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-5940G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819765 | ||||||
| chr14:91819766
|
G | A | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-5941C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819766 | ||||||
| chr14:91819884
|
T | C | 1 | a0001c0001t0009g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-56-6059A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819884 | ||||||
| chr14:91819918
|
A | C | 38 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0015others(35): Show | 39 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(36): Show |
intron_variant | MODIFIER | c.-56-6093T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819918 | ||||||
| chr14:91819943
|
T | A | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-6118A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91819943 | ||||||
| chr14:91820131
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-56-6306T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820131 | ||||||
| chr14:91820196
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-56-6371G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820196 | ||||||
| chr14:91820283
|
A | G | 1 | a0001c0001t0031g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-56-6458T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820283 | ||||||
| chr14:91820297
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-56-6472G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820297 | ||||||
| chr14:91820380
|
A | T | 4 | a0001c0001t0001g0175a0001c0001t0002g0269a0001c0001t0002g0270others(1): Show | 4 | HG02145.hp2 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-6555T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820380 | ||||||
| chr14:91820387
|
CAATA | C | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-6566_-56-6563d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820387 | ||||||
| chr14:91820513
|
G | C | 156 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(153): Show | 161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-6688C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820513 | ||||||
| chr14:91820545
|
G | A | 1 | a0001c0001t0002g0246 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-56-6720C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820545 | ||||||
| chr14:91820688
|
A | G | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-6863T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820688 | ||||||
| chr14:91820703
|
T | TA | 149 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(146): Show | 154 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.-56-6879dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820703 | ||||||
| chr14:91820729
|
C | T | 1 | a0001c0001t0002g0228 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-56-6904G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820729 | ||||||
| chr14:91820931
|
A | G | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-7106T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91820931 | ||||||
| chr14:91821173
|
A | C | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-56-7348T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821173 | ||||||
| chr14:91821399
|
G | C | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(97): Show | 109 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-56-7574C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821399 | ||||||
| chr14:91821471
|
C | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-56-7646G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821471 | ||||||
| chr14:91821662
|
A | G | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-7837T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821662 | ||||||
| chr14:91821672
|
C | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0043a0001c0001t0001g0055others(1): Show | 5 | HG00099.hp2 HG02683.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-7847G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821672 | ||||||
| chr14:91821917
|
G | C | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-8092C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91821917 | ||||||
| chr14:91822232
|
A | T | 1 | a0001c0002t0001g0122 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-56-8407T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822232 | ||||||
| chr14:91822235
|
T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(34): Show | 40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-56-8410A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822235 | ||||||
| chr14:91822466
|
G | GTTC | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-56-8644_-56-8642d others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822466 | ||||||
| chr14:91822668
|
G | C | 1 | a0001c0001t0010g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-8843C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822668 | ||||||
| chr14:91822694
|
G | C | 1 | a0001c0001t0002g0265 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-56-8869C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822694 | ||||||
| chr14:91822714
|
C | CT | 155 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(152): Show | 160 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.-56-8890dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822714 | ||||||
| chr14:91822802
|
T | C | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-56-8977A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822802 | ||||||
| chr14:91822874
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-56-9049T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822874 | ||||||
| chr14:91822916
|
C | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-9091G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822916 | ||||||
| chr14:91822957
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(92): Show | 104 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.-56-9132G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91822957 | ||||||
| chr14:91823023
|
T | C | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-56-9198A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823023 | ||||||
| chr14:91823212
|
C | T | 1 | a0001c0001t0002g0216 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-56-9387G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823212 | ||||||
| chr14:91823394
|
C | CTGG | 5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-9570_-56-9569i others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823394 | ||||||
| chr14:91823395
|
C | G | 5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-9570G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823395 | ||||||
| chr14:91823396
|
T | A | 5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-9571A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823396 | ||||||
| chr14:91823530
|
A | G | 118 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(115): Show | 118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-9705T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823530 | ||||||
| chr14:91823535
|
A | AAG | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-9711_-56-9710i others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823535 | ||||||
| chr14:91823535
|
A | G | 2 | a0001c0001t0008g0081a0001c0002t0001g0112 | 2 | HG03195.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.-56-9710T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823535 | ||||||
| chr14:91823536
|
G | A | 10 | a0001c0001t0008g0081a0001c0001t0009g0130a0001c0001t0009g0153others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-9711C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823536 | ||||||
| chr14:91823536
|
G | GA | 310 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(307): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-56-9712dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823536 | ||||||
| chr14:91823579
|
A | G | 8 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-9754T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823579 | ||||||
| chr14:91823768
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-56-9943T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823768 | ||||||
| chr14:91823840
|
T | C | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-10015A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823840 | ||||||
| chr14:91823890
|
A | AAAC | 13 | a0001c0001t0001g0024a0001c0001t0002g0214a0001c0001t0002g0215others(10): Show | 13 | HG02015.hp1 HG02523.hp1 NA18947.hp1 others(10): Show |
intron_variant | MODIFIER | c.-56-10068_-56-1006 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823890 | ||||||
| chr14:91823890
|
A | C | 2 | a0001c0001t0013g0022a0001c0001t0025g0021 | 2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-56-10065T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91823890 | ||||||
| chr14:91824337
|
A | G | 156 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(153): Show | 161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-10512T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824337 | ||||||
| chr14:91824400
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(97): Show | 109 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.-56-10575T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824400 | ||||||
| chr14:91824511
|
A | T | 3 | a0001c0001t0003g0170a0001c0001t0003g0177a0001c0001t0003g0178 | 3 | HG02683.hp2 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-56-10686T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824511 | ||||||
| chr14:91824536
|
C | T | 4 | a0001c0001t0002g0200a0001c0001t0002g0234a0001c0001t0002g0235others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-10711G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824536 | ||||||
| chr14:91824639
|
G | T | 9 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(6): Show | 9 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-10814C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824639 | ||||||
| chr14:91824682
|
G | A | 1 | a0001c0001t0002g0244 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-56-10857C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824682 | ||||||
| chr14:91824840
|
G | C | 1 | a0001c0001t0002g0260 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-56-11015C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824840 | ||||||
| chr14:91824950
|
G | C | 1 | a0001c0001t0001g0040 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-56-11125C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91824950 | ||||||
| chr14:91825026
|
CT | C | 232 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(229): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.-56-11202delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | ||||||
| chr14:91825026
|
CTT | C | 10 | a0001c0001t0001g0039a0001c0001t0002g0239a0001c0001t0002g0300others(7): Show | 10 | HG01981.hp2 HG02647.hp1 HG03704.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-11203_-56-1120 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | ||||||
| chr14:91825026
|
CTTT | C | 41 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(38): Show | 46 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(43): Show |
intron_variant | MODIFIER | c.-56-11204_-56-1120 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | ||||||
| chr14:91825026
|
CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-56-11217_-56-1120 others(20): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825026 | ||||||
| chr14:91825027
|
T | C | 1 | a0002c0003t0007g0165 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-56-11202A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825027 | ||||||
| chr14:91825035
|
T | C | 2 | a0001c0001t0013g0022a0001c0001t0025g0021 | 2 | HG02630.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-56-11210A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825035 | ||||||
| chr14:91825036
|
T | C | 1 | a0001c0001t0010g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-11211A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825036 | ||||||
| chr14:91825267
|
C | T | 1 | a0001c0001t0002g0202 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-56-11442G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825267 | ||||||
| chr14:91825283
|
C | T | 1 | a0001c0001t0016g0067 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-56-11458G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825283 | ||||||
| chr14:91825284
|
G | A | 1 | a0001c0001t0026g0158 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-56-11459C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825284 | ||||||
| chr14:91825338
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-11513C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825338 | ||||||
| chr14:91825544
|
T | C | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-11719A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825544 | ||||||
| chr14:91825646
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-56-11821A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825646 | ||||||
| chr14:91825667
|
C | T | 1 | a0001c0001t0010g0173 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-56-11842G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825667 | ||||||
| chr14:91825700
|
T | C | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-11875A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825700 | ||||||
| chr14:91825764
|
A | T | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-56-11939T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825764 | ||||||
| chr14:91825862
|
T | C | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-12037A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825862 | ||||||
| chr14:91825893
|
G | A | 22 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(19): Show | 23 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.-56-12068C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91825893 | ||||||
| chr14:91826144
|
C | A | 1 | a0001c0001t0002g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-56-12319G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826144 | ||||||
| chr14:91826198
|
T | C | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-12373A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826198 | ||||||
| chr14:91826212
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-12387G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826212 | ||||||
| chr14:91826213
|
G | T | 4 | a0001c0001t0002g0211a0001c0001t0002g0255a0001c0001t0002g0266others(1): Show | 4 | NA18995.hp2 NA19077.hp2 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-12388C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826213 | ||||||
| chr14:91826231
|
G | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0023others(16): Show | 21 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-12406C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826231 | ||||||
| chr14:91826313
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-56-12488A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826313 | ||||||
| chr14:91826315
|
G | T | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-12490C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826315 | ||||||
| chr14:91826318
|
T | TG | 4 | a0001c0001t0002g0200a0001c0001t0002g0234a0001c0001t0002g0235others(1): Show | 4 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-12494dupC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826318 | ||||||
| chr14:91826319
|
G | GA | 294 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(291): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-56-12495dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826319 | ||||||
| chr14:91826319
|
G | GAA | 21 | a0001c0001t0001g0030a0001c0001t0002g0209a0001c0001t0002g0220others(18): Show | 21 | HG00673.hp2 HG01175.hp1 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.-56-12496_-56-1249 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826319 | ||||||
| chr14:91826425
|
T | G | 118 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(115): Show | 118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-12600A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826425 | ||||||
| chr14:91826861
|
C | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-13036G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826861 | ||||||
| chr14:91826877
|
T | C | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-13052A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91826877 | ||||||
| chr14:91827111
|
T | C | 1 | a0001c0001t0002g0220 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-56-13286A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827111 | ||||||
| chr14:91827174
|
A | G | 156 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(153): Show | 161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-56-13349T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827174 | ||||||
| chr14:91827210
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-56-13385G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827210 | ||||||
| chr14:91827787
|
C | A | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-13962G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827787 | ||||||
| chr14:91827795
|
T | G | 1 | a0001c0001t0002g0229 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-56-13970A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827795 | ||||||
| chr14:91827930
|
T | G | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-14105A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91827930 | ||||||
| chr14:91828165
|
T | C | 1 | a0001c0001t0009g0156 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-56-14340A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828165 | ||||||
| chr14:91828250
|
A | G | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-56-14425T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828250 | ||||||
| chr14:91828347
|
A | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-14522T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828347 | ||||||
| chr14:91828357
|
T | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(34): Show | 40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-56-14532A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828357 | ||||||
| chr14:91828363
|
T | C | 118 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(115): Show | 118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-14538A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828363 | ||||||
| chr14:91828459
|
TTA | T | 3 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0272 | 3 | HG02145.hp2 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-56-14636_-56-1463 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828459 | ||||||
| chr14:91828500
|
C | A | 1 | a0004c0005t0001g0047 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-56-14675G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828500 | ||||||
| chr14:91828508
|
C | T | 156 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(153): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(164): Show |
intron_variant | MODIFIER | c.-56-14683G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828508 | ||||||
| chr14:91828797
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-14972A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91828797 | ||||||
| chr14:91829051
|
T | TA | 6 | a0001c0001t0002g0233a0001c0001t0002g0261a0001c0001t0006g0061others(3): Show | 6 | HG02040.hp1 HG02040.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-56-15227dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829051 | ||||||
| chr14:91829051
|
TA | T | 47 | a0001c0001t0001g0014a0001c0001t0001g0076a0001c0001t0002g0279others(44): Show | 48 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.-56-15227delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829051 | ||||||
| chr14:91829056
|
A | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-56-15231T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829056 | ||||||
| chr14:91829091
|
T | C | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-15266A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829091 | ||||||
| chr14:91829280
|
T | G | 13 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(10): Show | 15 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(12): Show |
intron_variant | MODIFIER | c.-56-15455A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829280 | ||||||
| chr14:91829530
|
T | C | 1 | a0001c0001t0025g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-56-15705A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829530 | ||||||
| chr14:91829727
|
T | C | 118 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(115): Show | 118 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.-56-15902A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829727 | ||||||
| chr14:91829789
|
C | T | 2 | a0001c0001t0003g0059a0001c0001t0003g0167 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-56-15964G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91829789 | ||||||
| chr14:91830167
|
T | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-16342A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830167 | ||||||
| chr14:91830344
|
C | T | 1 | a0001c0002t0001g0096 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-56-16519G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830344 | ||||||
| chr14:91830569
|
C | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-16744G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830569 | ||||||
| chr14:91830655
|
C | CA | 137 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(134): Show | 139 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-56-16831dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830655 | ||||||
| chr14:91830664
|
A | C | 1 | a0001c0001t0001g0030 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-56-16839T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830664 | ||||||
| chr14:91830681
|
A | G | 110 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(107): Show | 110 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-56-16856T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830681 | ||||||
| chr14:91830738
|
A | AT | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-16914_-56-1691 others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830738 | ||||||
| chr14:91830908
|
G | C | 2 | a0001c0001t0005g0010a0001c0001t0005g0144 | 3 | HG02451.hp2 HG02922.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-56-17083C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830908 | ||||||
| chr14:91830965
|
T | C | 1 | a0001c0001t0002g0210 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-56-17140A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91830965 | ||||||
| chr14:91831022
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-56-17197A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831022 | ||||||
| chr14:91831088
|
G | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-17263C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831088 | ||||||
| chr14:91831135
|
G | C | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17310C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831135 | ||||||
| chr14:91831137
|
TAA | T | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17314_-56-1731 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831137 | ||||||
| chr14:91831142
|
C | G | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17317G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831142 | ||||||
| chr14:91831143
|
C | A | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17318G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831143 | ||||||
| chr14:91831145
|
A | T | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17320T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831145 | ||||||
| chr14:91831147
|
C | G | 3 | a0003c0004t0001g0070a0003c0004t0002g0282a0003c0004t0002g0283 | 3 | HG02572.hp1 HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-56-17322G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831147 | ||||||
| chr14:91831227
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-56-17402G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831227 | ||||||
| chr14:91831575
|
T | C | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-17750A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831575 | ||||||
| chr14:91831602
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-56-17777T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831602 | ||||||
| chr14:91831885
|
G | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-18060C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831885 | ||||||
| chr14:91831902
|
G | A | 1 | a0001c0001t0003g0064 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-56-18077C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831902 | ||||||
| chr14:91831924
|
C | G | 9 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(6): Show | 9 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-18099G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91831924 | ||||||
| chr14:91832173
|
G | A | 5 | a0001c0001t0002g0213a0001c0001t0002g0224a0001c0001t0002g0231others(2): Show | 5 | HG00642.hp2 HG00738.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.-56-18348C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832173 | ||||||
| chr14:91832203
|
A | G | 7 | a0001c0001t0009g0130a0001c0001t0009g0154a0001c0001t0009g0155others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-18378T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832203 | ||||||
| chr14:91832390
|
C | CA | 31 | a0001c0001t0002g0274a0001c0001t0004g0004a0001c0001t0004g0311others(28): Show | 36 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-56-18566dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832390 | ||||||
| chr14:91832390
|
C | CAA | 268 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0014others(265): Show | 278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.-56-18567_-56-1856 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832390 | ||||||
| chr14:91832390
|
C | CAAA | 21 | a0001c0001t0001g0005a0001c0001t0001g0055a0001c0001t0002g0201others(18): Show | 22 | HG00099.hp2 HG01109.hp1 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.-56-18568_-56-1856 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832390 | ||||||
| chr14:91832547
|
C | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-18722G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832547 | ||||||
| chr14:91832566
|
A | G | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-18741T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832566 | ||||||
| chr14:91832592
|
G | A | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-56-18767C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832592 | ||||||
| chr14:91832737
|
A | G | 1 | a0001c0002t0001g0121 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-56-18912T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832737 | ||||||
| chr14:91832755
|
T | C | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-18930A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832755 | ||||||
| chr14:91832853
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-56-19028T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832853 | ||||||
| chr14:91832893
|
G | A | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-19068C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91832893 | ||||||
| chr14:91833166
|
C | T | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-19341G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833166 | ||||||
| chr14:91833524
|
A | T | 7 | a0001c0001t0009g0130a0001c0001t0009g0154a0001c0001t0009g0155others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-56-19699T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833524 | ||||||
| chr14:91833629
|
C | T | 1 | a0001c0001t0004g0311 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-56-19804G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833629 | ||||||
| chr14:91833754
|
A | T | 8 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-19929T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833754 | ||||||
| chr14:91833825
|
C | T | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-20000G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833825 | ||||||
| chr14:91833867
|
C | A | 1 | a0001c0001t0001g0029 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-56-20042G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833867 | ||||||
| chr14:91833918
|
G | C | 1 | a0001c0001t0010g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-56-20093C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833918 | ||||||
| chr14:91833920
|
G | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-20095C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91833920 | ||||||
| chr14:91834080
|
T | G | 1 | a0001c0001t0002g0310 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-56-20255A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834080 | ||||||
| chr14:91834276
|
T | G | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-20451A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834276 | ||||||
| chr14:91834368
|
G | A | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-20543C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834368 | ||||||
| chr14:91834444
|
C | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-20619G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834444 | ||||||
| chr14:91834494
|
A | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-20669T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834494 | ||||||
| chr14:91834703
|
C | T | 2 | a0001c0001t0002g0212a0001c0001t0002g0221 | 2 | NA19060.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-56-20878G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834703 | ||||||
| chr14:91834848
|
T | G | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-21023A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834848 | ||||||
| chr14:91834850
|
G | T | 37 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(34): Show | 42 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-56-21025C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91834850 | ||||||
| chr14:91835205
|
G | T | 1 | a0001c0001t0004g0326 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-56-21380C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835205 | ||||||
| chr14:91835307
|
A | C | 2 | a0001c0001t0002g0246a0001c0001t0033g0247 | 2 | HG02040.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-56-21482T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835307 | ||||||
| chr14:91835802
|
C | A | 1 | a0001c0001t0002g0237 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-56-21977G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835802 | ||||||
| chr14:91835813
|
A | G | 8 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-21988T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835813 | ||||||
| chr14:91835815
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-56-21990C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835815 | ||||||
| chr14:91835918
|
C | T | 4 | a0001c0001t0003g0013a0001c0001t0003g0057a0001c0001t0003g0058others(1): Show | 4 | NA18968.hp2 NA18998.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-22093G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91835918 | ||||||
| chr14:91836217
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(301): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-56-22392T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836217 | ||||||
| chr14:91836350
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-56-22525G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836350 | ||||||
| chr14:91836376
|
G | A | 4 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021others(1): Show | 4 | HG02630.hp2 NA18906.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-22551C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836376 | ||||||
| chr14:91836405
|
C | T | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-22580G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836405 | ||||||
| chr14:91836484
|
C | G | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-22659G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836484 | ||||||
| chr14:91836550
|
G | A | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-56-22725C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836550 | ||||||
| chr14:91836574
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-56-22749C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836574 | ||||||
| chr14:91836577
|
A | AGGCGAGG others(13): Show |
5 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(2): Show | 5 | HG02145.hp1 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836577
|
A | AGGCGAGG others(13): Show |
124 | a0001c0001t0001g0006a0001c0001t0001g0017a0001c0001t0001g0034others(121): Show | 125 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-56-22772_-56-2275 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836577
|
A | AGGCGAGG others(33): Show |
49 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0002g0214others(46): Show | 50 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.-56-22792_-56-2275 others(44): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836577
|
A | AGGCGAGG others(53): Show |
48 | a0001c0001t0001g0018a0001c0001t0003g0015a0001c0001t0003g0189others(45): Show | 53 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(50): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(64): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836577
|
A | AGGCGAGG others(73): Show |
34 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0019others(31): Show | 37 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(84): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836577
|
A | AGGCGAGG others(93): Show |
11 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0046others(8): Show | 11 | HG01074.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(104): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836577
|
A | AGGCGAGG others(113): Show |
2 | a0001c0001t0010g0134a0004c0005t0001g0047 | 2 | HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-56-22753_-56-2275 others(124): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836577
|
AGGCGAGG others(13): Show |
A | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-22772_-56-2275 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836577 | ||||||
| chr14:91836607
|
A | AGGCGGGG others(13): Show |
1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-22802_-56-2278 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836607 | ||||||
| chr14:91836628
|
G | A | 163 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(160): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.-56-22803C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836628 | ||||||
| chr14:91836635
|
C | A | 9 | a0001c0001t0002g0216a0001c0001t0002g0262a0001c0001t0002g0263others(6): Show | 9 | HG00609.hp2 HG01258.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.-56-22810G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836635 | ||||||
| chr14:91836820
|
G | A | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-56-22995C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91836820 | ||||||
| chr14:91837132
|
G | C | 1 | a0001c0001t0012g0320 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-56-23307C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837132 | ||||||
| chr14:91837219
|
A | G | 2 | a0001c0001t0002g0306a0001c0001t0002g0309 | 2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-56-23394T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837219 | ||||||
| chr14:91837246
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-23421C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837246 | ||||||
| chr14:91837270
|
T | C | 320 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(317): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-56-23445A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837270 | ||||||
| chr14:91837298
|
C | T | 8 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0017g0086others(5): Show | 8 | HG02630.hp2 HG03041.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-56-23473G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837298 | ||||||
| chr14:91837368
|
A | C | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-56-23543T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837368 | ||||||
| chr14:91837525
|
A | T | 1 | a0001c0002t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-23700T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837525 | ||||||
| chr14:91837533
|
A | G | 157 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(154): Show | 162 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-56-23708T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837533 | ||||||
| chr14:91837534
|
G | T | 1 | a0001c0002t0001g0008 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-56-23709C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837534 | ||||||
| chr14:91837788
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-23963T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91837788 | ||||||
| chr14:91838065
|
A | G | 1 | a0001c0001t0002g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-56-24240T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838065 | ||||||
| chr14:91838072
|
CA | C | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-24248delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838072 | ||||||
| chr14:91838074
|
A | T | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-56-24249T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838074 | ||||||
| chr14:91838146
|
C | CT | 46 | a0001c0001t0001g0036a0001c0001t0002g0205a0001c0001t0002g0253others(43): Show | 51 | HG01081.hp1 HG01109.hp2 HG02055.hp2 others(48): Show |
intron_variant | MODIFIER | c.-56-24322dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838146 | ||||||
| chr14:91838146
|
C | CTT | 10 | a0001c0001t0004g0322a0001c0001t0005g0149a0001c0001t0009g0130others(7): Show | 10 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-56-24323_-56-2432 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838146 | ||||||
| chr14:91838146
|
CT | C | 7 | a0001c0001t0001g0091a0001c0001t0003g0059a0001c0001t0003g0167others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.-56-24322delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838146 | ||||||
| chr14:91838358
|
C | G | 1 | a0002c0003t0007g0162 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-56-24533G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838358 | ||||||
| chr14:91838376
|
C | A | 2 | a0001c0001t0004g0004a0001c0001t0004g0313 | 4 | NA18945.hp1 NA19057.hp1 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.-56-24551G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838376 | ||||||
| chr14:91838528
|
C | A | 5 | a0001c0002t0001g0009a0001c0002t0001g0137a0001c0002t0001g0138others(2): Show | 6 | HG01106.hp1 HG03490.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.-56-24703G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838528 | ||||||
| chr14:91838728
|
C | A | 1 | a0001c0001t0002g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-56-24903G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838728 | ||||||
| chr14:91838973
|
A | G | 164 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(161): Show | 169 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-56-25148T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91838973 | ||||||
| chr14:91839112
|
C | A | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-56-25287G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839112 | ||||||
| chr14:91839241
|
G | A | 1 | a0001c0002t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-56-25416C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839241 | ||||||
| chr14:91839370
|
C | T | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-56-25545G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839370 | ||||||
| chr14:91839461
|
C | G | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-56-25636G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839461 | ||||||
| chr14:91839704
|
C | T | 1 | a0001c0001t0006g0073 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-56-25879G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91839704 | ||||||
| chr14:91840457
|
A | G | 1 | a0001c0001t0002g0244 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-56-26632T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91840457 | ||||||
| chr14:91840561
|
T | A | 60 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(57): Show | 60 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.-57+26701A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91840561 | ||||||
| chr14:91840613
|
G | A | 8 | a0001c0001t0009g0130a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+26649C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91840613 | ||||||
| chr14:91841033
|
G | A | 310 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(307): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.-57+26229C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841033 | ||||||
| chr14:91841226
|
G | T | 1 | a0001c0001t0002g0224 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-57+26036C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841226 | ||||||
| chr14:91841432
|
A | C | 14 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(11): Show | 16 | HG02602.hp2 HG03491.hp1 HG03831.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+25830T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841432 | ||||||
| chr14:91841701
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0013g0022others(1): Show | 4 | HG02071.hp1 HG02523.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+25561G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841701 | ||||||
| chr14:91841763
|
G | A | 1 | a0001c0001t0002g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-57+25499C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841763 | ||||||
| chr14:91841908
|
A | G | 1 | a0001c0001t0031g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-57+25354T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841908 | ||||||
| chr14:91841909
|
T | G | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+25353A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841909 | ||||||
| chr14:91841916
|
T | C | 1 | a0001c0001t0002g0289 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-57+25346A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841916 | ||||||
| chr14:91841976
|
C | CT | 199 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(196): Show | 203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.-57+25285dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841976 | ||||||
| chr14:91841976
|
C | CTT | 81 | a0001c0001t0001g0006a0001c0001t0001g0039a0001c0001t0001g0044others(78): Show | 88 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-57+25284_-57+2528 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91841976 | ||||||
| chr14:91842022
|
G | A | 1 | a0001c0001t0004g0311 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+25240C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842022 | ||||||
| chr14:91842193
|
C | A | 31 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(28): Show | 36 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-57+25069G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842193 | ||||||
| chr14:91842237
|
G | A | 1 | a0002c0003t0007g0166 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-57+25025C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842237 | ||||||
| chr14:91842348
|
T | A | 2 | a0001c0001t0003g0197a0001c0001t0003g0198 | 2 | HG01516.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-57+24914A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842348 | ||||||
| chr14:91842441
|
G | T | 1 | a0001c0001t0002g0267 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-57+24821C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842441 | ||||||
| chr14:91842482
|
T | C | 2 | a0001c0001t0001g0038a0001c0001t0001g0044 | 2 | HG04115.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-57+24780A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842482 | ||||||
| chr14:91842729
|
C | T | 4 | a0001c0001t0006g0072a0001c0001t0006g0073a0001c0001t0006g0159others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+24533G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842729 | ||||||
| chr14:91842742
|
A | T | 46 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(43): Show | 51 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(48): Show |
intron_variant | MODIFIER | c.-57+24520T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842742 | ||||||
| chr14:91842885
|
A | G | 156 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(153): Show | 161 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-57+24377T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842885 | ||||||
| chr14:91842896
|
C | T | 1 | a0001c0001t0002g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-57+24366G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842896 | ||||||
| chr14:91842911
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+24351G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842911 | ||||||
| chr14:91842914
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-57+24348G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842914 | ||||||
| chr14:91842935
|
A | C | 1 | a0001c0001t0002g0297 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-57+24327T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842935 | ||||||
| chr14:91842981
|
A | G | 164 | a0001c0001t0001g0017a0001c0001t0001g0034a0001c0001t0001g0035others(161): Show | 169 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(166): Show |
intron_variant | MODIFIER | c.-57+24281T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91842981 | ||||||
| chr14:91843223
|
AT | A | 50 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(47): Show | 50 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.-57+24038delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843223 | ||||||
| chr14:91843259
|
G | C | 1 | a0001c0001t0002g0297 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-57+24003C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843259 | ||||||
| chr14:91843394
|
A | G | 1 | a0001c0001t0002g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-57+23868T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843394 | ||||||
| chr14:91843440
|
C | G | 1 | a0001c0001t0001g0048 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-57+23822G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843440 | ||||||
| chr14:91843500
|
A | G | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-57+23762T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843500 | ||||||
| chr14:91843617
|
C | G | 8 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(5): Show | 8 | HG02818.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+23645G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843617 | ||||||
| chr14:91843649
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | NA19002.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-57+23613G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843649 | ||||||
| chr14:91843687
|
G | A | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+23575C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843687 | ||||||
| chr14:91843720
|
T | C | 1 | a0001c0001t0002g0294 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-57+23542A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843720 | ||||||
| chr14:91843762
|
C | T | 1 | a0001c0001t0008g0084 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-57+23500G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843762 | ||||||
| chr14:91843882
|
AT | A | 45 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(42): Show | 50 | HG01081.hp1 HG01109.hp1 HG01891.hp2 others(47): Show |
intron_variant | MODIFIER | c.-57+23379delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843882 | ||||||
| chr14:91843910
|
C | T | 1 | a0001c0001t0006g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57+23352G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843910 | ||||||
| chr14:91843946
|
T | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 18 | HG01192.hp2 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-57+23316A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91843946 | ||||||
| chr14:91844053
|
G | GA | 138 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(135): Show | 143 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(140): Show |
intron_variant | MODIFIER | c.-57+23208dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844053 | ||||||
| chr14:91844130
|
G | C | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+23132C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844130 | ||||||
| chr14:91844140
|
T | C | 4 | a0001c0001t0003g0064a0001c0001t0012g0319a0001c0001t0012g0320others(1): Show | 4 | HG00423.hp1 NA18747.hp1 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+23122A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844140 | ||||||
| chr14:91844186
|
G | T | 26 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(23): Show | 28 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-57+23076C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844186 | ||||||
| chr14:91844206
|
G | A | 1 | a0001c0001t0006g0065 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-57+23056C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844206 | ||||||
| chr14:91844355
|
G | T | 139 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(136): Show | 144 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.-57+22907C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844355 | ||||||
| chr14:91844521
|
T | C | 7 | a0001c0001t0009g0153a0001c0001t0009g0154a0001c0001t0009g0155others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+22741A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844521 | ||||||
| chr14:91844534
|
C | T | 1 | a0001c0001t0002g0208 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-57+22728G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844534 | ||||||
| chr14:91844535
|
G | A | 1 | a0001c0001t0006g0062 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-57+22727C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844535 | ||||||
| chr14:91844693
|
G | A | 9 | a0001c0002t0001g0008a0001c0002t0001g0100a0001c0002t0001g0101others(6): Show | 10 | HG00733.hp2 HG00735.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+22569C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844693 | ||||||
| chr14:91844740
|
G | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(155): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.-57+22522C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844740 | ||||||
| chr14:91844760
|
C | CA | 55 | a0001c0001t0001g0019a0001c0001t0001g0039a0001c0001t0001g0040others(52): Show | 58 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.-57+22501dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | ||||||
| chr14:91844760
|
C | CAA | 17 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0003g0170others(14): Show | 17 | HG00642.hp1 HG01109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-57+22500_-57+2250 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | ||||||
| chr14:91844760
|
CA | C | 11 | a0001c0001t0003g0012a0001c0001t0008g0079a0001c0001t0008g0080others(8): Show | 12 | HG01192.hp2 HG01884.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+22501delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | ||||||
| chr14:91844760
|
CAAAAAAA others(3): Show |
C | 7 | a0001c0001t0002g0217a0001c0001t0002g0230a0001c0001t0002g0231others(4): Show | 7 | HG00642.hp2 HG02109.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+22492_-57+2250 others(14): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | ||||||
| chr14:91844760
|
CAAAAAAA others(4): Show |
C | 132 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(129): Show | 137 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.-57+22491_-57+2250 others(15): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91844760 | ||||||
| chr14:91845066
|
G | A | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+22196C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845066 | ||||||
| chr14:91845085
|
G | A | 1 | a0001c0001t0009g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+22177C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845085 | ||||||
| chr14:91845121
|
G | A | 1 | a0001c0001t0002g0297 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-57+22141C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845121 | ||||||
| chr14:91845232
|
A | AAAAT | 98 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(95): Show | 98 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.-57+22026_-57+2202 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | ||||||
| chr14:91845232
|
A | AAAATAAA others(1): Show |
21 | a0001c0001t0002g0212a0001c0001t0002g0213a0001c0001t0002g0217others(18): Show | 21 | HG00609.hp2 HG00738.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-57+22022_-57+2202 others(12): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | ||||||
| chr14:91845232
|
AAAAT | A | 46 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0183others(43): Show | 46 | HG00099.hp1 HG00423.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-57+22026_-57+2202 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | ||||||
| chr14:91845232
|
AAAATAAA others(1): Show |
A | 109 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 119 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.-57+22022_-57+2202 others(12): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | ||||||
| chr14:91845232
|
AAAATAAA others(5): Show |
A | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+22018_-57+2202 others(16): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | ||||||
| chr14:91845232
|
AAAATAAA others(13): Show |
A | 6 | a0001c0001t0010g0131a0001c0001t0010g0132a0001c0001t0010g0133others(3): Show | 6 | HG02559.hp1 HG03098.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+22010_-57+2202 others(24): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845232 | ||||||
| chr14:91845269
|
A | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(7): Show | 11 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+21993T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845269 | ||||||
| chr14:91845274
|
T | A | 1 | a0001c0001t0002g0286 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-57+21988A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845274 | ||||||
| chr14:91845442
|
T | G | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+21820A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845442 | ||||||
| chr14:91845454
|
T | C | 4 | a0001c0001t0002g0284a0001c0001t0002g0285a0001c0001t0002g0287others(1): Show | 4 | HG00140.hp2 HG01175.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+21808A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845454 | ||||||
| chr14:91845561
|
G | T | 48 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(45): Show | 48 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.-57+21701C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91845561 | ||||||
| chr14:91846015
|
T | C | 108 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(105): Show | 108 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-57+21247A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846015 | ||||||
| chr14:91846025
|
A | G | 142 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(139): Show | 147 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-57+21237T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846025 | ||||||
| chr14:91846128
|
GC | G | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+21133delG | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846128 | ||||||
| chr14:91846130
|
T | A | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+21132A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846130 | ||||||
| chr14:91846551
|
G | A | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+20711C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846551 | ||||||
| chr14:91846984
|
G | A | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+20278C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846984 | ||||||
| chr14:91846986
|
G | A | 1 | a0001c0001t0037g0317 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-57+20276C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91846986 | ||||||
| chr14:91847006
|
C | T | 1 | a0001c0001t0010g0131 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-57+20256G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847006 | ||||||
| chr14:91847033
|
G | A | 14 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(11): Show | 14 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+20229C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847033 | ||||||
| chr14:91847166
|
G | A | 1 | a0001c0001t0002g0232 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-57+20096C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847166 | ||||||
| chr14:91847207
|
G | A | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+20055C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847207 | ||||||
| chr14:91847259
|
G | GA | 8 | a0001c0001t0009g0153a0001c0001t0009g0154a0001c0001t0009g0155others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+20002dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847259 | ||||||
| chr14:91847259
|
G | GAA | 11 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(8): Show | 11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+20001_-57+2000 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847259 | ||||||
| chr14:91847259
|
G | GAAA | 42 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(39): Show | 47 | HG01081.hp1 HG01192.hp2 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.-57+20000_-57+2000 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847259 | ||||||
| chr14:91847347
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-57+19915G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847347 | ||||||
| chr14:91847362
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+19900G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847362 | ||||||
| chr14:91847363
|
T | A | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+19899A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847363 | ||||||
| chr14:91847557
|
C | T | 1 | a0001c0002t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-57+19705G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847557 | ||||||
| chr14:91847792
|
T | C | 1 | a0001c0001t0002g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-57+19470A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847792 | ||||||
| chr14:91847828
|
G | A | 14 | a0001c0001t0002g0200a0001c0001t0002g0207a0001c0001t0002g0217others(11): Show | 14 | HG00673.hp1 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+19434C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847828 | ||||||
| chr14:91847873
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-57+19389T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91847873 | ||||||
| chr14:91848031
|
G | A | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+19231C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848031 | ||||||
| chr14:91848051
|
T | C | 39 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(36): Show | 42 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.-57+19211A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848051 | ||||||
| chr14:91848098
|
A | T | 1 | a0001c0001t0006g0060 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-57+19164T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848098 | ||||||
| chr14:91848174
|
A | G | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203 | 3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+19088T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848174 | ||||||
| chr14:91848313
|
G | A | 29 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(26): Show | 34 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+18949C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848313 | ||||||
| chr14:91848356
|
G | C | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203 | 3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+18906C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848356 | ||||||
| chr14:91848432
|
C | A | 259 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(256): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-57+18830G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848432 | ||||||
| chr14:91848548
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-57+18714G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848548 | ||||||
| chr14:91848574
|
C | T | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+18688G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848574 | ||||||
| chr14:91848599
|
T | G | 1 | a0001c0001t0004g0318 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-57+18663A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848599 | ||||||
| chr14:91848605
|
G | T | 1 | a0001c0001t0002g0303 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-57+18657C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848605 | ||||||
| chr14:91848897
|
T | C | 29 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(26): Show | 34 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+18365A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91848897 | ||||||
| chr14:91849158
|
A | C | 1 | a0001c0001t0034g0223 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-57+18104T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849158 | ||||||
| chr14:91849230
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-57+18032C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849230 | ||||||
| chr14:91849288
|
T | C | 7 | a0001c0001t0009g0153a0001c0001t0009g0154a0001c0001t0009g0155others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+17974A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849288 | ||||||
| chr14:91849399
|
T | G | 2 | a0001c0001t0001g0014a0001c0001t0001g0045 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-57+17863A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849399 | ||||||
| chr14:91849595
|
T | A | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+17667A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849595 | ||||||
| chr14:91849684
|
G | A | 4 | a0001c0001t0031g0168a0003c0004t0001g0070a0003c0004t0002g0282others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+17578C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849684 | ||||||
| chr14:91849786
|
C | G | 318 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(315): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.-57+17476G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849786 | ||||||
| chr14:91849830
|
C | T | 31 | a0001c0001t0002g0208a0001c0001t0004g0004a0001c0001t0004g0311others(28): Show | 36 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.-57+17432G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849830 | ||||||
| chr14:91849941
|
C | T | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+17321G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849941 | ||||||
| chr14:91849971
|
C | A | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+17291G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91849971 | ||||||
| chr14:91850004
|
A | G | 30 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(27): Show | 35 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-57+17258T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850004 | ||||||
| chr14:91850049
|
C | CA | 9 | a0001c0001t0002g0276a0001c0001t0009g0153a0001c0001t0009g0154others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+17212dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | ||||||
| chr14:91850049
|
CA | C | 251 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(248): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.-57+17212delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | ||||||
| chr14:91850049
|
CAAA | C | 29 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(26): Show | 34 | HG01081.hp1 HG02055.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-57+17210_-57+1721 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | ||||||
| chr14:91850049
|
CAAAAA | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+17208_-57+1721 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850049 | ||||||
| chr14:91850180
|
C | T | 40 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0183others(37): Show | 41 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.-57+17082G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850180 | ||||||
| chr14:91850182
|
T | TA | 267 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(264): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-57+17079dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850182 | ||||||
| chr14:91850324
|
A | G | 1 | a0001c0001t0002g0301 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-57+16938T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850324 | ||||||
| chr14:91850348
|
T | C | 11 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(8): Show | 11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+16914A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850348 | ||||||
| chr14:91850411
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+16851C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850411 | ||||||
| chr14:91850490
|
A | C | 1 | a0001c0001t0001g0024 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-57+16772T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850490 | ||||||
| chr14:91850496
|
A | G | 2 | a0001c0002t0001g0135a0001c0002t0001g0147 | 2 | HG00738.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.-57+16766T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850496 | ||||||
| chr14:91850603
|
G | A | 1 | a0001c0001t0035g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-57+16659C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850603 | ||||||
| chr14:91850659
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-57+16603T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850659 | ||||||
| chr14:91850736
|
G | T | 1 | a0001c0001t0002g0305 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-57+16526C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850736 | ||||||
| chr14:91850794
|
G | A | 2 | a0001c0001t0002g0215a0001c0001t0002g0240 | 2 | HG02523.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-57+16468C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850794 | ||||||
| chr14:91850835
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-57+16427T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850835 | ||||||
| chr14:91850836
|
G | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-57+16426C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850836 | ||||||
| chr14:91850966
|
G | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+16296C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91850966 | ||||||
| chr14:91851012
|
A | G | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-57+16250T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851012 | ||||||
| chr14:91851197
|
G | A | 1 | a0001c0002t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-57+16065C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851197 | ||||||
| chr14:91851213
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+16049C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851213 | ||||||
| chr14:91851312
|
G | A | 6 | a0001c0001t0002g0241a0001c0001t0002g0242a0001c0001t0002g0243others(3): Show | 6 | HG00639.hp1 HG00733.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+15950C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851312 | ||||||
| chr14:91851435
|
G | T | 319 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(316): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-57+15827C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851435 | ||||||
| chr14:91851438
|
G | T | 2 | a0001c0001t0002g0269a0001c0001t0002g0270 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-57+15824C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851438 | ||||||
| chr14:91851511
|
T | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(43): Show | 49 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.-57+15751A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851511 | ||||||
| chr14:91851522
|
C | T | 7 | a0001c0001t0009g0153a0001c0001t0009g0154a0001c0001t0009g0155others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+15740G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851522 | ||||||
| chr14:91851807
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0077 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-57+15455T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851807 | ||||||
| chr14:91851828
|
C | T | 179 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(176): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.-57+15434G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851828 | ||||||
| chr14:91851990
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+15272C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91851990 | ||||||
| chr14:91852111
|
T | C | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.-57+15151A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852111 | ||||||
| chr14:91852154
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+15108C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852154 | ||||||
| chr14:91852191
|
G | A | 2 | a0001c0001t0003g0169a0001c0001t0003g0174 | 2 | HG02647.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-57+15071C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852191 | ||||||
| chr14:91852198
|
C | T | 1 | a0005c0007t0028g0090 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-57+15064G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852198 | ||||||
| chr14:91852287
|
C | T | 2 | a0001c0001t0003g0059a0001c0001t0003g0167 | 2 | HG02622.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-57+14975G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852287 | ||||||
| chr14:91852315
|
C | T | 49 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(46): Show | 49 | HG00639.hp1 HG00642.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.-57+14947G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852315 | ||||||
| chr14:91852345
|
C | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+14917G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852345 | ||||||
| chr14:91852472
|
A | G | 151 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-57+14790T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852472 | ||||||
| chr14:91852485
|
C | T | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+14777G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852485 | ||||||
| chr14:91852591
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(207): Show | 226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.-57+14671C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852591 | ||||||
| chr14:91852699
|
T | C | 1 | a0001c0001t0010g0134 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-57+14563A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852699 | ||||||
| chr14:91852779
|
T | G | 1 | a0001c0001t0002g0200 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-57+14483A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852779 | ||||||
| chr14:91852815
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+14447C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852815 | ||||||
| chr14:91852935
|
G | A | 11 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+14327C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852935 | ||||||
| chr14:91852948
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+14314C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91852948 | ||||||
| chr14:91853028
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+14234C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853028 | ||||||
| chr14:91853136
|
GCTACT | G | 11 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+14121_-57+1412 others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853136 | ||||||
| chr14:91853375
|
T | C | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+13887A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853375 | ||||||
| chr14:91853380
|
A | G | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+13882T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853380 | ||||||
| chr14:91853381
|
C | T | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+13881G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853381 | ||||||
| chr14:91853397
|
G | T | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+13865C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853397 | ||||||
| chr14:91853435
|
G | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+13827C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853435 | ||||||
| chr14:91853539
|
A | G | 1 | a0001c0001t0009g0153 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-57+13723T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853539 | ||||||
| chr14:91853558
|
A | G | 1 | a0001c0001t0002g0249 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-57+13704T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853558 | ||||||
| chr14:91853629
|
ATTT | A | 164 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(161): Show | 174 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.-57+13630_-57+1363 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853629 | ||||||
| chr14:91853629
|
ATTTT | A | 5 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0185others(2): Show | 6 | HG00140.hp1 HG03490.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-57+13629_-57+1363 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853629 | ||||||
| chr14:91853642
|
TTTA | T | 11 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(8): Show | 11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+13617_-57+1361 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853642 | ||||||
| chr14:91853649
|
TACAC | T | 16 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0244others(13): Show | 16 | HG00423.hp2 HG02145.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.-57+13609_-57+1361 others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853649 | ||||||
| chr14:91853649
|
TACACAC | T | 119 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(116): Show | 124 | HG00140.hp2 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.-57+13607_-57+1361 others(10): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853649 | ||||||
| chr14:91853649
|
TACACACA others(5): Show |
T | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+13601_-57+1361 others(16): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853649 | ||||||
| chr14:91853665
|
C | A | 7 | a0001c0001t0009g0153a0001c0001t0009g0154a0001c0001t0009g0155others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+13597G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853665 | ||||||
| chr14:91853675
|
C | A | 180 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.-57+13587G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853675 | ||||||
| chr14:91853951
|
C | T | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-57+13311G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91853951 | ||||||
| chr14:91854010
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+13252G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854010 | ||||||
| chr14:91854061
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(152): Show | 166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.-57+13201C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854061 | ||||||
| chr14:91854178
|
G | A | 11 | a0001c0001t0006g0054a0001c0001t0006g0060a0001c0001t0006g0061others(8): Show | 11 | HG02630.hp2 HG02818.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-57+13084C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854178 | ||||||
| chr14:91854413
|
A | G | 1 | a0001c0001t0004g0326 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-57+12849T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854413 | ||||||
| chr14:91854420
|
G | GGAGGGGG others(26): Show |
7 | a0001c0001t0009g0153a0001c0001t0009g0154a0001c0001t0009g0155others(4): Show | 7 | HG01109.hp1 HG01891.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+12809_-57+1284 others(37): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854420 | ||||||
| chr14:91854508
|
TGGA | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+12751_-57+1275 others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854508 | ||||||
| chr14:91854508
|
TGGAGGA | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(172): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-57+12748_-57+1275 others(10): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854508 | ||||||
| chr14:91854649
|
G | A | 3 | a0001c0001t0013g0020a0001c0001t0013g0022a0001c0001t0025g0021 | 3 | HG02630.hp2 NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-57+12613C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854649 | ||||||
| chr14:91854674
|
A | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG00558.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-57+12588T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854674 | ||||||
| chr14:91854817
|
C | G | 1 | a0001c0001t0002g0300 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-57+12445G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854817 | ||||||
| chr14:91854866
|
A | G | 110 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(107): Show | 110 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-57+12396T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91854866 | ||||||
| chr14:91855009
|
C | T | 1 | a0001c0001t0009g0154 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-57+12253G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855009 | ||||||
| chr14:91855176
|
C | T | 11 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(8): Show | 14 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-57+12086G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855176 | ||||||
| chr14:91855241
|
C | G | 319 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(316): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.-57+12021G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855241 | ||||||
| chr14:91855414
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-57+11848G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855414 | ||||||
| chr14:91855782
|
C | T | 1 | a0001c0001t0004g0311 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+11480G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855782 | ||||||
| chr14:91855787
|
G | T | 11 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+11475C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855787 | ||||||
| chr14:91855811
|
G | A | 4 | a0001c0001t0006g0072a0001c0001t0006g0073a0001c0001t0006g0159others(1): Show | 4 | HG02055.hp2 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+11451C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91855811 | ||||||
| chr14:91856072
|
T | C | 111 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0002g0200others(108): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-57+11190A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856072 | ||||||
| chr14:91856214
|
C | T | 1 | a0001c0002t0001g0187 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-57+11048G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856214 | ||||||
| chr14:91856215
|
G | A | 7 | a0001c0001t0003g0015a0001c0001t0009g0130a0001c0001t0010g0131others(4): Show | 7 | HG02280.hp1 HG02559.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+11047C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856215 | ||||||
| chr14:91856270
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 6 | HG01891.hp1 HG02055.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-57+10992G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856270 | ||||||
| chr14:91856442
|
G | A | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+10820C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856442 | ||||||
| chr14:91856486
|
CA | C | 143 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(140): Show | 155 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.-57+10775delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856486 | ||||||
| chr14:91856486
|
CAA | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(41): Show | 47 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-57+10774_-57+1077 others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856486 | ||||||
| chr14:91856672
|
C | T | 9 | a0001c0001t0006g0159a0001c0001t0006g0161a0001c0001t0009g0153others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+10590G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856672 | ||||||
| chr14:91856699
|
C | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(13): Show | 20 | HG01081.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+10563G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91856699 | ||||||
| chr14:91857095
|
G | C | 17 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 21 | HG01081.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-57+10167C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857095 | ||||||
| chr14:91857096
|
C | T | 9 | a0001c0001t0006g0159a0001c0001t0006g0161a0001c0001t0009g0153others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+10166G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857096 | ||||||
| chr14:91857109
|
T | A | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+10153A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857109 | ||||||
| chr14:91857298
|
A | G | 1 | a0001c0001t0002g0221 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-57+9964T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857298 | ||||||
| chr14:91857422
|
G | A | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+9840C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857422 | ||||||
| chr14:91857520
|
A | T | 1 | a0001c0002t0001g0110 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-57+9742T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857520 | ||||||
| chr14:91857566
|
G | A | 37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(34): Show | 40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-57+9696C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857566 | ||||||
| chr14:91857609
|
G | A | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+9653C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857609 | ||||||
| chr14:91857742
|
C | T | 2 | a0001c0001t0014g0248a0001c0001t0014g0308 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-57+9520G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857742 | ||||||
| chr14:91857893
|
G | T | 1 | a0001c0002t0001g0128 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-57+9369C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857893 | ||||||
| chr14:91857965
|
CTTTG | C | 37 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(34): Show | 40 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-57+9293_-57+9296d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91857965 | ||||||
| chr14:91858008
|
C | G | 8 | a0001c0001t0003g0059a0001c0001t0006g0054a0001c0001t0006g0060others(5): Show | 8 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+9254G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858008 | ||||||
| chr14:91858114
|
C | T | 204 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0091others(201): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-57+9148G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858114 | ||||||
| chr14:91858140
|
T | TTTC | 3 | a0001c0001t0003g0013a0001c0001t0003g0169a0001c0002t0001g0094 | 3 | HG02965.hp2 NA19054.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-57+9119_-57+9121d others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858140 | ||||||
| chr14:91858152
|
C | CT | 21 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(18): Show | 22 | HG01891.hp1 HG01928.hp1 HG02015.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57+9109dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | ||||||
| chr14:91858152
|
C | CTT | 18 | a0001c0001t0006g0159a0001c0001t0008g0078a0001c0001t0008g0079others(15): Show | 18 | HG01109.hp1 HG01192.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.-57+9108_-57+9109d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | ||||||
| chr14:91858152
|
C | CTTCT | 88 | a0001c0001t0001g0068a0001c0001t0001g0091a0001c0001t0001g0175others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.-57+9109_-57+9110i others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | ||||||
| chr14:91858152
|
C | CTTCTT | 55 | a0001c0001t0001g0071a0001c0001t0002g0204a0001c0001t0002g0205others(52): Show | 55 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-57+9109_-57+9110i others(7): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | ||||||
| chr14:91858152
|
C | T | 2 | a0001c0001t0002g0284a0001c0001t0002g0285 | 2 | HG00140.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-57+9110G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858152 | ||||||
| chr14:91858155
|
T | C | 2 | a0001c0001t0002g0245a0001c0002t0001g0093 | 2 | HG00544.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-57+9107A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858155 | ||||||
| chr14:91858271
|
C | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(37): Show | 43 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.-57+8991G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858271 | ||||||
| chr14:91858535
|
T | C | 33 | a0001c0001t0003g0064a0001c0001t0004g0004a0001c0001t0004g0311others(30): Show | 35 | HG00423.hp1 HG01192.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.-57+8727A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858535 | ||||||
| chr14:91858747
|
C | T | 8 | a0001c0001t0003g0059a0001c0001t0006g0054a0001c0001t0006g0060others(5): Show | 8 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.-57+8515G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858747 | ||||||
| chr14:91858850
|
C | T | 50 | a0001c0001t0001g0097a0001c0001t0024g0124a0001c0002t0001g0001others(47): Show | 56 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.-57+8412G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858850 | ||||||
| chr14:91858898
|
G | T | 310 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(307): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-57+8364C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91858898 | ||||||
| chr14:91859053
|
T | C | 22 | a0001c0001t0003g0064a0001c0001t0004g0004a0001c0001t0004g0311others(19): Show | 24 | HG00423.hp1 HG02055.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57+8209A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859053 | ||||||
| chr14:91859078
|
C | T | 9 | a0001c0001t0006g0159a0001c0001t0006g0161a0001c0001t0009g0153others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+8184G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859078 | ||||||
| chr14:91859084
|
G | A | 11 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+8178C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859084 | ||||||
| chr14:91859305
|
A | T | 5 | a0001c0001t0001g0175a0001c0001t0003g0170a0001c0001t0003g0176others(2): Show | 5 | HG02683.hp2 HG03239.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.-57+7957T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859305 | ||||||
| chr14:91859351
|
C | T | 30 | a0001c0001t0003g0064a0001c0001t0004g0004a0001c0001t0004g0311others(27): Show | 32 | HG00423.hp1 HG01109.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.-57+7911G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859351 | ||||||
| chr14:91859410
|
C | T | 20 | a0001c0001t0003g0064a0001c0001t0004g0004a0001c0001t0004g0311others(17): Show | 22 | HG00423.hp1 HG02055.hp2 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57+7852G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859410 | ||||||
| chr14:91859412
|
T | C | 7 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+7850A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859412 | ||||||
| chr14:91859670
|
C | T | 1 | a0001c0002t0001g0127 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-57+7592G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859670 | ||||||
| chr14:91859754
|
T | C | 7 | a0001c0001t0002g0218a0001c0001t0002g0246a0001c0001t0002g0284others(4): Show | 7 | HG00140.hp2 HG01175.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+7508A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859754 | ||||||
| chr14:91859926
|
A | G | 148 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0091others(145): Show | 149 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(146): Show |
intron_variant | MODIFIER | c.-57+7336T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859926 | ||||||
| chr14:91859968
|
A | C | 3 | a0001c0001t0005g0003a0001c0001t0005g0146a0001c0001t0005g0149 | 5 | HG02615.hp1 HG02630.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-57+7294T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859968 | ||||||
| chr14:91859970
|
G | T | 1 | a0001c0001t0002g0219 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-57+7292C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91859970 | ||||||
| chr14:91860071
|
G | T | 41 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(38): Show | 44 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.-57+7191C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860071 | ||||||
| chr14:91860074
|
C | G | 2 | a0001c0001t0006g0072a0001c0001t0006g0073 | 2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-57+7188G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860074 | ||||||
| chr14:91860287
|
G | T | 321 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(318): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-57+6975C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860287 | ||||||
| chr14:91860331
|
C | CA | 24 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(21): Show | 27 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.-57+6930dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860331 | ||||||
| chr14:91860331
|
CA | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(90): Show | 96 | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.-57+6930delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860331 | ||||||
| chr14:91860735
|
C | T | 9 | a0001c0001t0006g0159a0001c0001t0006g0161a0001c0001t0009g0153others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+6527G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860735 | ||||||
| chr14:91860765
|
T | C | 9 | a0001c0001t0003g0059a0001c0001t0006g0054a0001c0001t0006g0060others(6): Show | 9 | HG02723.hp2 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-57+6497A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860765 | ||||||
| chr14:91860891
|
C | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0048a0001c0001t0001g0049others(70): Show | 83 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.-57+6371G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91860891 | ||||||
| chr14:91861105
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-57+6157A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861105 | ||||||
| chr14:91861136
|
T | C | 1 | a0001c0001t0003g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-57+6126A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861136 | ||||||
| chr14:91861138
|
C | T | 18 | a0001c0001t0003g0064a0001c0001t0004g0004a0001c0001t0004g0311others(15): Show | 20 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+6124G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861138 | ||||||
| chr14:91861440
|
C | T | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+5822G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861440 | ||||||
| chr14:91861515
|
G | C | 1 | a0001c0001t0003g0195 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-57+5747C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861515 | ||||||
| chr14:91861533
|
C | T | 1 | a0001c0002t0001g0109 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-57+5729G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861533 | ||||||
| chr14:91861558
|
G | A | 31 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0183others(28): Show | 32 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.-57+5704C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861558 | ||||||
| chr14:91861705
|
C | T | 2 | a0001c0001t0039g0327a0002c0003t0015g0092 | 2 | HG03486.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-57+5557G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861705 | ||||||
| chr14:91861721
|
G | A | 1 | a0001c0001t0002g0202 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-57+5541C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861721 | ||||||
| chr14:91861734
|
C | T | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+5528G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861734 | ||||||
| chr14:91861765
|
A | G | 32 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0183others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-57+5497T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861765 | ||||||
| chr14:91861814
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-57+5448T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861814 | ||||||
| chr14:91861823
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-57+5439C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861823 | ||||||
| chr14:91861827
|
G | A | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+5435C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861827 | ||||||
| chr14:91861845
|
T | C | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+5417A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861845 | ||||||
| chr14:91861913
|
A | AAT | 255 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(252): Show | 269 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.-57+5347_-57+5348d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861913 | ||||||
| chr14:91861958
|
GTA | G | 10 | a0001c0001t0001g0097a0001c0002t0001g0094a0001c0002t0001g0098others(7): Show | 10 | HG01928.hp2 NA18989.hp1 NA19001.hp2 others(7): Show |
intron_variant | MODIFIER | c.-57+5302_-57+5303d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91861958 | ||||||
| chr14:91862142
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(135): Show | 151 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(148): Show |
intron_variant | MODIFIER | c.-57+5120C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862142 | ||||||
| chr14:91862255
|
G | A | 4 | a0001c0001t0017g0086a0001c0001t0018g0088a0001c0001t0019g0083others(1): Show | 4 | HG03041.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+5007C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862255 | ||||||
| chr14:91862339
|
C | CA | 12 | a0001c0001t0001g0077a0001c0001t0002g0288a0001c0001t0002g0289others(9): Show | 12 | HG00597.hp1 HG02055.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57+4922dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | ||||||
| chr14:91862339
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0008g0078a0001c0001t0008g0080a0001c0001t0008g0081others(6): Show | 9 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+4914_-57+4922d others(11): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | ||||||
| chr14:91862339
|
CAAAAAA | C | 12 | a0001c0001t0005g0003a0001c0001t0005g0010a0001c0001t0005g0095others(9): Show | 15 | HG01081.hp1 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-57+4917_-57+4922d others(8): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | ||||||
| chr14:91862339
|
CAAAAAAA | C | 118 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 128 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.-57+4916_-57+4922d others(9): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862339 | ||||||
| chr14:91862418
|
G | C | 1 | a0001c0001t0001g0053 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-57+4844C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862418 | ||||||
| chr14:91862485
|
T | A | 11 | a0001c0001t0003g0172a0001c0001t0003g0188a0001c0001t0003g0189others(8): Show | 11 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+4777A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862485 | ||||||
| chr14:91862509
|
G | A | 18 | a0001c0001t0003g0064a0001c0001t0004g0004a0001c0001t0004g0311others(15): Show | 20 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(17): Show |
intron_variant | MODIFIER | c.-57+4753C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862509 | ||||||
| chr14:91862605
|
G | A | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203 | 3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+4657C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862605 | ||||||
| chr14:91862669
|
G | A | 1 | a0001c0001t0006g0159 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-57+4593C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862669 | ||||||
| chr14:91862760
|
G | A | 12 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+4502C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862760 | ||||||
| chr14:91862856
|
A | C | 1 | a0001c0001t0003g0174 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-57+4406T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862856 | ||||||
| chr14:91862858
|
A | G | 1 | a0001c0001t0006g0054 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-57+4404T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862858 | ||||||
| chr14:91862971
|
T | C | 12 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203others(9): Show | 12 | HG01109.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-57+4291A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91862971 | ||||||
| chr14:91863113
|
C | G | 2 | a0001c0002t0001g0089a0005c0007t0028g0090 | 2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+4149G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863113 | ||||||
| chr14:91863273
|
G | A | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+3989C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863273 | ||||||
| chr14:91863323
|
G | A | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203 | 3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+3939C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863323 | ||||||
| chr14:91863404
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-57+3858T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863404 | ||||||
| chr14:91863519
|
G | A | 9 | a0001c0001t0006g0159a0001c0001t0006g0161a0001c0001t0009g0153others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+3743C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863519 | ||||||
| chr14:91863711
|
C | A | 66 | a0001c0001t0001g0097a0001c0001t0005g0003a0001c0001t0005g0010others(63): Show | 75 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-57+3551G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863711 | ||||||
| chr14:91863772
|
C | T | 69 | a0001c0001t0001g0097a0001c0001t0002g0201a0001c0001t0002g0202others(66): Show | 78 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.-57+3490G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863772 | ||||||
| chr14:91863829
|
C | CA | 73 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0097others(70): Show | 79 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(76): Show |
intron_variant | MODIFIER | c.-57+3432dupT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863829 | ||||||
| chr14:91863829
|
CA | C | 56 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(53): Show | 60 | HG00099.hp2 HG00673.hp2 HG01074.hp2 others(57): Show |
intron_variant | MODIFIER | c.-57+3432delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863829 | ||||||
| chr14:91863884
|
C | A | 78 | a0001c0001t0001g0097a0001c0001t0002g0201a0001c0001t0002g0202others(75): Show | 87 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.-57+3378G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863884 | ||||||
| chr14:91863889
|
A | G | 32 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0183others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-57+3373T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91863889 | ||||||
| chr14:91864069
|
C | T | 78 | a0001c0001t0001g0097a0001c0001t0002g0201a0001c0001t0002g0202others(75): Show | 87 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.-57+3193G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864069 | ||||||
| chr14:91864182
|
C | G | 1 | a0001c0001t0005g0141 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-57+3080G>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864182 | ||||||
| chr14:91864446
|
T | C | 66 | a0001c0001t0001g0097a0001c0001t0005g0003a0001c0001t0005g0010others(63): Show | 75 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-57+2816A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864446 | ||||||
| chr14:91864475
|
G | A | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 166 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.-57+2787C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864475 | ||||||
| chr14:91864509
|
A | G | 1 | a0001c0001t0019g0083 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-57+2753T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864509 | ||||||
| chr14:91864522
|
G | T | 17 | a0001c0001t0004g0004a0001c0001t0004g0311a0001c0001t0004g0312others(14): Show | 19 | HG00423.hp1 HG02602.hp2 HG03491.hp1 others(16): Show |
intron_variant | MODIFIER | c.-57+2740C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864522 | ||||||
| chr14:91864596
|
A | C | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+2666T>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864596 | ||||||
| chr14:91864709
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-57+2553T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864709 | ||||||
| chr14:91864739
|
CT | C | 9 | a0001c0001t0006g0159a0001c0001t0006g0161a0001c0001t0009g0153others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+2522delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864739 | ||||||
| chr14:91864777
|
CT | C | 264 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(261): Show | 277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-57+2484delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864777 | ||||||
| chr14:91864777
|
CTT | C | 19 | a0001c0001t0002g0297a0001c0001t0002g0298a0001c0001t0003g0197others(16): Show | 22 | HG01069.hp1 HG01081.hp1 HG01081.hp2 others(19): Show |
intron_variant | MODIFIER | c.-57+2483_-57+2484d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864777 | ||||||
| chr14:91864777
|
CTTT | C | 11 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-57+2482_-57+2484d others(5): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864777 | ||||||
| chr14:91864805
|
A | T | 1 | a0001c0001t0002g0211 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-57+2457T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864805 | ||||||
| chr14:91864814
|
C | A | 1 | a0001c0002t0001g0126 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-57+2448G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864814 | ||||||
| chr14:91864821
|
G | T | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+2441C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864821 | ||||||
| chr14:91864868
|
G | T | 2 | a0001c0002t0001g0127a0001c0002t0001g0128 | 2 | HG00642.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-57+2394C>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864868 | ||||||
| chr14:91864969
|
C | T | 4 | a0001c0001t0008g0079a0001c0001t0008g0080a0001c0001t0008g0081others(1): Show | 4 | HG01192.hp2 HG01884.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-57+2293G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91864969 | ||||||
| chr14:91865031
|
C | T | 2 | a0001c0002t0001g0089a0005c0007t0028g0090 | 2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+2231G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865031 | ||||||
| chr14:91865075
|
G | A | 1 | a0001c0001t0001g0091 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-57+2187C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865075 | ||||||
| chr14:91865144
|
A | G | 2 | a0001c0002t0001g0089a0005c0007t0028g0090 | 2 | HG01261.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+2118T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865144 | ||||||
| chr14:91865217
|
T | C | 1 | a0001c0001t0002g0299 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-57+2045A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865217 | ||||||
| chr14:91865221
|
GATTT | G | 73 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 77 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.-57+2037_-57+2040d others(6): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865221 | ||||||
| chr14:91865303
|
TC | T | 37 | a0001c0001t0001g0097a0001c0001t0024g0124a0001c0002t0001g0001others(34): Show | 42 | HG00544.hp1 HG00733.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.-57+1958delG | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865303 | ||||||
| chr14:91865367
|
TG | T | 8 | a0001c0001t0006g0159a0001c0001t0009g0153a0001c0001t0009g0154others(5): Show | 8 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-57+1894delC | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865367 | ||||||
| chr14:91865369
|
G | GT | 7 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0207others(4): Show | 7 | HG00438.hp2 HG00735.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.-57+1892dupA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865369 | ||||||
| chr14:91865369
|
GT | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(64): Show | 71 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.-57+1892delA | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865369 | ||||||
| chr14:91865369
|
GTT | G | 16 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0002g0309others(13): Show | 16 | HG01167.hp2 HG01192.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.-57+1891_-57+1892d others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865369 | ||||||
| chr14:91865377
|
T | G | 1 | a0002c0003t0015g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-57+1885A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865377 | ||||||
| chr14:91865390
|
T | A | 3 | a0001c0001t0029g0199a0001c0002t0001g0089a0005c0007t0028g0090 | 3 | HG01261.hp1 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-57+1872A>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865390 | ||||||
| chr14:91865390
|
TA | T | 62 | a0001c0001t0001g0097a0001c0001t0002g0204a0001c0001t0004g0326others(59): Show | 71 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(68): Show |
intron_variant | MODIFIER | c.-57+1871delT | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865390 | ||||||
| chr14:91865391
|
A | T | 22 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0003g0169others(19): Show | 24 | HG00423.hp1 HG02602.hp2 HG02965.hp2 others(21): Show |
intron_variant | MODIFIER | c.-57+1871T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865391 | ||||||
| chr14:91865392
|
A | T | 1 | a0001c0002t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-57+1870T>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865392 | ||||||
| chr14:91865566
|
C | T | 12 | a0001c0001t0008g0078a0001c0001t0008g0079a0001c0001t0008g0080others(9): Show | 12 | HG01192.hp2 HG01884.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-57+1696G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865566 | ||||||
| chr14:91865572
|
T | G | 1 | a0001c0001t0031g0168 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-57+1690A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865572 | ||||||
| chr14:91865670
|
A | G | 1 | a0001c0001t0039g0327 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-57+1592T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865670 | ||||||
| chr14:91865671
|
C | T | 153 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(150): Show | 166 | HG00099.hp2 HG00544.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.-57+1591G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865671 | ||||||
| chr14:91865740
|
T | G | 32 | a0001c0001t0001g0175a0001c0001t0001g0179a0001c0001t0001g0183others(29): Show | 33 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-57+1522A>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91865740 | ||||||
| chr14:91866129
|
A | G | 9 | a0001c0001t0006g0159a0001c0001t0006g0161a0001c0001t0009g0153others(6): Show | 9 | HG01109.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-57+1133T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866129 | ||||||
| chr14:91866204
|
C | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 79 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.-57+1058G>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866204 | ||||||
| chr14:91866311
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-57+951G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866311 | ||||||
| chr14:91866378
|
T | C | 80 | a0001c0001t0001g0091a0001c0001t0001g0097a0001c0001t0005g0003others(77): Show | 89 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(86): Show |
intron_variant | MODIFIER | c.-57+884A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866378 | ||||||
| chr14:91866459
|
A | G | 3 | a0001c0001t0002g0201a0001c0001t0002g0202a0001c0001t0002g0203 | 3 | HG02145.hp1 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-57+803T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866459 | ||||||
| chr14:91866472
|
T | C | 66 | a0001c0001t0001g0097a0001c0001t0005g0003a0001c0001t0005g0010others(63): Show | 75 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-57+790A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866472 | ||||||
| chr14:91866506
|
G | A | 288 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(285): Show | 303 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(300): Show |
intron_variant | MODIFIER | c.-57+756C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866506 | ||||||
| chr14:91866524
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(71): Show | 78 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.-57+738G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866524 | ||||||
| chr14:91866605
|
G | C | 4 | a0001c0001t0001g0091a0001c0002t0001g0089a0002c0003t0015g0092others(1): Show | 4 | HG01261.hp1 HG03486.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-57+657C>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866605 | ||||||
| chr14:91866657
|
G | A | 66 | a0001c0001t0001g0097a0001c0001t0005g0003a0001c0001t0005g0010others(63): Show | 75 | HG00544.hp1 HG00642.hp1 HG00733.hp2 others(72): Show |
intron_variant | MODIFIER | c.-57+605C>T | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866657 | ||||||
| chr14:91866691
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-57+571G>A | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866691 | ||||||
| chr14:91866852
|
A | G | 1 | a0001c0001t0004g0311 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-57+410T>C | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91866852 | ||||||
| chr14:91867067
|
T | C | 1 | a0001c0001t0002g0310 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-57+195A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91867067 | ||||||
| chr14:91867087
|
C | CCTCT | 279 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 294 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(291): Show |
intron_variant | MODIFIER | c.-57+174_-57+175ins others(4): Show |
TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91867087 | ||||||
| chr14:91867184
|
T | C | 1 | a0001c0001t0029g0199 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-57+78A>G | TC2N | ENSG00000165929.13 | transcript | ENST00000435962.7 | protein_coding | 1/11 | chr14 | 91867184 |