| geneid | 7039 |
|---|---|
| ensemblid | ENSG00000163235.16 |
| hgncid | 11765 |
| symbol | TGFA |
| name | transforming growth factor alpha |
| refseq_nuc | NM_003236.4 |
| refseq_prot | NP_003227.1 |
| ensembl_nuc | ENST00000295400.11 |
| ensembl_prot | ENSP00000295400.6 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 70447284 |
| end | 70553826 |
| strand | - |
| ver | v1.2 |
| region | chr2:70447284-70553826 |
| region5000 | chr2:70442284-70558826 |
| regionname0 | TGFA_chr2_70447284_70553826 |
| regionname5000 | TGFA_chr2_70442284_70558826 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 160 | 333 | 84 | 66 | 139 | 8 | 34 | 99 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0002 | 0/0 | 160 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0003 | 0/0 | 160 | 5 | 0 | 0 | 5 | 0 | 0 | 5 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 483 | 259 | 67 | 53 | 103 | 7 | 27 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| c0002 | 0/0 | 483 | 69 | 14 | 12 | 36 | 1 | 6 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| c0003 | 0/0 | 483 | 6 | 6 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| c0004 | 0/0 | 483 | 5 | 0 | 0 | 5 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| c0005 | 0/0 | 483 | 4 | 3 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| c0006 | 0/0 | 483 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| 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 | 3635 | 88 | 15 | 17 | 42 | 3 | 10 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0002 | 0/0 | 3631 | 58 | 8 | 19 | 25 | 2 | 4 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0003 | 0/0 | 3635 | 52 | 5 | 7 | 33 | 1 | 6 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0004 | 0/0 | 3635 | 28 | 2 | 3 | 17 | 1 | 5 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0005 | 1/0 | 3635 | 15 | 11 | 2 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0006 | 0/0 | 3635 | 14 | 3 | 3 | 3 | 0 | 5 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0007 | 0/0 | 3635 | 13 | 1 | 4 | 8 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0008 | 0/0 | 3635 | 10 | 8 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0009 | 0/0 | 3635 | 5 | 1 | 4 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0010 | 0/0 | 3635 | 5 | 0 | 0 | 5 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0011 | 0/0 | 3635 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0012 | 0/0 | 3635 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0013 | 0/0 | 3635 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0014 | 0/0 | 3636 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0015 | 0/0 | 3635 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0016 | 0/0 | 3636 | 3 | 3 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0017 | 0/0 | 3645 | 3 | 3 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0018 | 0/0 | 3631 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0019 | 0/0 | 3632 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0020 | 0/0 | 3632 | 2 | 0 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0021 | 0/0 | 3636 | 2 | 1 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0022 | 0/0 | 3635 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0023 | 0/0 | 3635 | 2 | 0 | 0 | 0 | 0 | 2 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0024 | 0/0 | 3635 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0025 | 0/0 | 3635 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0026 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0027 | 0/0 | 3635 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0028 | 0/0 | 3635 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0029 | 0/0 | 3631 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0030 | 0/0 | 3636 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0031 | 0/0 | 3635 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0032 | 0/0 | 3635 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0033 | 0/0 | 3635 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0034 | 0/0 | 3635 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0035 | 0/0 | 3634 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0036 | 0/0 | 3649 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0037 | 0/0 | 3635 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0038 | 0/0 | 3635 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| t0039 | 0/0 | 3635 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 483 | 259 | 67 | 53 | 103 | 7 | 27 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002 | 0/0 | 483 | 69 | 14 | 12 | 36 | 1 | 6 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0005 | 0/0 | 483 | 4 | 3 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0006 | 0/0 | 483 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0002c0003 | 0/0 | 483 | 6 | 6 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0003c0004 | 0/0 | 483 | 5 | 0 | 0 | 5 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4117 | 85 | 12 | 17 | 42 | 3 | 10 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0002 | 0/0 | 4113 | 56 | 6 | 19 | 25 | 2 | 4 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0004 | 0/0 | 4117 | 28 | 2 | 3 | 17 | 1 | 5 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0005 | 1/0 | 4117 | 15 | 11 | 2 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0006 | 0/0 | 4117 | 14 | 3 | 3 | 3 | 0 | 5 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0007 | 0/0 | 4117 | 13 | 1 | 4 | 8 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0008 | 0/0 | 4117 | 10 | 8 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0013 | 0/0 | 4117 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0014 | 0/0 | 4118 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0016 | 0/0 | 4118 | 3 | 3 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0017 | 0/0 | 4127 | 3 | 3 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0018 | 0/0 | 4113 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0019 | 0/0 | 4114 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0020 | 0/0 | 4114 | 2 | 0 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0021 | 0/0 | 4118 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0022 | 0/0 | 4117 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0023 | 0/0 | 4117 | 2 | 0 | 0 | 0 | 0 | 2 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0024 | 0/0 | 4117 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0025 | 0/0 | 4117 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0026 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0027 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0028 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0029 | 0/0 | 4113 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0030 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0031 | 0/0 | 4117 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0032 | 0/0 | 4117 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0033 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0001t0034 | 0/0 | 4117 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0003 | 0/0 | 4117 | 52 | 5 | 7 | 33 | 1 | 6 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0009 | 0/0 | 4117 | 5 | 1 | 4 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0011 | 0/0 | 4117 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0015 | 0/0 | 4117 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0035 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0037 | 0/0 | 4117 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0038 | 0/0 | 4117 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0002t0039 | 0/0 | 4117 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0005t0001 | 0/0 | 4117 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0005t0002 | 0/0 | 4113 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0005t0021 | 0/0 | 4118 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0001c0006t0036 | 0/0 | 4131 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0002c0003t0001 | 0/0 | 4117 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0002c0003t0012 | 0/0 | 4117 | 4 | 4 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| a0003c0004t0010 | 0/0 | 4117 | 5 | 0 | 0 | 5 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | copy fasta | chr2 | 70442284 | 70558826 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0066 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0005g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0006g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0007g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0013g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0013g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0013g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0014g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0014g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0014g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0014g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0016g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0016g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0016g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0017g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0017g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0018g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0018g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0019g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0019g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0020g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0021g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0022g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0022g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0023g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0023g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0024g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0024g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0025g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0025g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0026g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0027g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0028g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0029g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0030g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0031g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0032g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0033g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0001t0034g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0009g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0009g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0009g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0009g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0011g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0011g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0011g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0011g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0015g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0015g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0015g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0015g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0035g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0037g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0038g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0002t0039g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0005t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0005t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0005t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0005t0021g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0001c0006t0036g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0002c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0002c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0002c0003t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0002c0003t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0002c0003t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0002c0003t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0003c0004t0010g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0003c0004t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0003c0004t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0003c0004t0010g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| a0003c0004t0010g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0319 | EUR | GBR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0321 | EUR | GBR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0180 | EUR | FIN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00323 | hp2 | a0001 | c0002 | t0003 | g0213 | EUR | FIN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00423 | hp1 | a0001 | c0002 | t0003 | g0148 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0234 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00544 | hp2 | a0001 | c0002 | t0003 | g0027 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00558 | hp2 | a0001 | c0002 | t0003 | g0219 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00597 | hp1 | a0001 | c0002 | t0003 | g0019 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0131 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00621 | hp1 | a0001 | c0002 | t0038 | g0284 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00621 | hp2 | a0001 | c0001 | t0006 | g0243 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00639 | hp1 | a0001 | c0001 | t0006 | g0324 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00639 | hp2 | a0001 | c0002 | t0003 | g0214 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00642 | hp2 | a0001 | c0002 | t0039 | g0206 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0297 | EAS | CHS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00733 | hp2 | a0001 | c0002 | t0009 | g0311 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00735 | hp1 | a0001 | c0001 | t0030 | g0266 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00735 | hp2 | a0001 | c0001 | t0007 | g0188 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01069 | hp1 | a0001 | c0002 | t0003 | g0006 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0166 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01071 | hp1 | a0001 | c0001 | t0006 | g0165 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01071 | hp2 | a0001 | c0002 | t0003 | g0006 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0312 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01074 | hp2 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01081 | hp2 | a0001 | c0002 | t0003 | g0220 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01099 | hp2 | a0001 | c0001 | t0007 | g0119 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01106 | hp2 | a0001 | c0002 | t0009 | g0237 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0049 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01167 | hp2 | a0001 | c0001 | t0020 | g0002 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01169 | hp2 | a0001 | c0001 | t0020 | g0002 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0164 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01243 | hp1 | a0001 | c0005 | t0021 | g0136 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0200 | AMR | PUR | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01256 | hp2 | a0001 | c0002 | t0009 | g0173 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0318 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01258 | hp2 | a0001 | c0002 | t0009 | g0091 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01261 | hp1 | a0001 | c0001 | t0007 | g0057 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0310 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01433 | hp1 | a0001 | c0002 | t0003 | g0313 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0035 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01496 | hp1 | a0001 | c0002 | t0003 | g0303 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0226 | EUR | IBS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01517 | hp2 | a0001 | c0001 | t0031 | g0170 | EUR | IBS | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01884 | hp1 | a0001 | c0001 | t0014 | g0175 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01891 | hp1 | a0001 | c0001 | t0008 | g0079 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0338 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02015 | hp1 | a0001 | c0002 | t0003 | g0251 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02027 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02027 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02040 | hp1 | a0001 | c0001 | t0018 | g0329 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02040 | hp2 | a0001 | c0001 | t0026 | g0126 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02055 | hp1 | a0001 | c0005 | t0001 | g0177 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02055 | hp2 | a0001 | c0002 | t0011 | g0115 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02056 | hp1 | a0001 | c0002 | t0003 | g0330 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0331 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0254 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02071 | hp2 | a0001 | c0002 | t0003 | g0161 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02135 | hp1 | a0001 | c0001 | t0007 | g0109 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02145 | hp2 | a0001 | c0001 | t0024 | g0081 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CDX | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02165 | hp2 | a0001 | c0002 | t0003 | g0158 | EAS | CDX | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02257 | hp1 | a0001 | c0002 | t0015 | g0113 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02257 | hp2 | a0001 | c0002 | t0003 | g0202 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02258 | hp1 | a0001 | c0005 | t0002 | g0274 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02258 | hp2 | a0001 | c0002 | t0009 | g0087 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02280 | hp2 | a0001 | c0001 | t0021 | g0271 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0256 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0323 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02300 | hp2 | a0001 | c0001 | t0007 | g0187 | AMR | PEL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02572 | hp1 | a0001 | c0001 | t0033 | g0103 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02572 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0052 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02615 | hp1 | a0001 | c0001 | t0008 | g0001 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0336 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02622 | hp2 | a0001 | c0001 | t0008 | g0249 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0099 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02630 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02647 | hp2 | a0001 | c0002 | t0015 | g0076 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02717 | hp1 | a0002 | c0003 | t0001 | g0102 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02723 | hp1 | a0001 | c0001 | t0008 | g0050 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02723 | hp2 | a0001 | c0002 | t0015 | g0075 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0247 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02809 | hp2 | a0001 | c0001 | t0028 | g0122 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02818 | hp2 | a0001 | c0002 | t0011 | g0290 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0004 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0100 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0121 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02897 | hp2 | a0001 | c0001 | t0017 | g0004 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0074 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02922 | hp2 | a0001 | c0005 | t0002 | g0176 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02965 | hp1 | a0002 | c0003 | t0012 | g0250 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0097 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02970 | hp2 | a0001 | c0002 | t0011 | g0257 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02976 | hp1 | a0002 | c0003 | t0012 | g0104 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0141 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03017 | hp1 | a0001 | c0001 | t0006 | g0210 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0001 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03098 | hp2 | a0001 | c0001 | t0019 | g0139 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03130 | hp1 | a0001 | c0001 | t0022 | g0082 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03130 | hp2 | a0001 | c0001 | t0013 | g0261 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0048 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03139 | hp2 | a0001 | c0002 | t0015 | g0272 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03195 | hp1 | a0001 | c0002 | t0003 | g0085 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0248 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03225 | hp1 | a0001 | c0001 | t0017 | g0078 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03225 | hp2 | a0001 | c0001 | t0013 | g0260 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03486 | hp1 | a0001 | c0001 | t0019 | g0140 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0291 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03490 | hp1 | a0001 | c0002 | t0003 | g0009 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0184 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03492 | hp1 | a0001 | c0002 | t0003 | g0008 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0185 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0114 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0108 | AFR | ESN | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03540 | hp1 | a0001 | c0001 | t0014 | g0124 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03540 | hp2 | a0001 | c0001 | t0024 | g0289 | AFR | GWD | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03579 | hp1 | a0002 | c0003 | t0012 | g0105 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03579 | hp2 | a0001 | c0002 | t0003 | g0094 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0046 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03688 | hp2 | a0001 | c0002 | t0003 | g0034 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0259 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03831 | hp1 | a0001 | c0001 | t0023 | g0045 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0309 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0191 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03834 | hp2 | a0001 | c0001 | t0023 | g0065 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0047 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03927 | hp2 | a0001 | c0001 | t0034 | g0092 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04115 | hp1 | a0001 | c0002 | t0003 | g0033 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0162 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04184 | hp2 | a0001 | c0001 | t0006 | g0262 | SAS | BEB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04199 | hp1 | a0001 | c0006 | t0036 | g0038 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0212 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG04204 | hp2 | a0001 | c0002 | t0003 | g0071 | SAS | STU | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18522 | hp2 | a0001 | c0002 | t0003 | g0073 | AFR | YRI | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | CHB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CHB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | CHB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18941 | hp2 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18942 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0287 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18945 | hp2 | a0001 | c0002 | t0003 | g0244 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0299 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18946 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18953 | hp1 | a0001 | c0001 | t0018 | g0021 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18953 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18964 | hp2 | a0001 | c0002 | t0003 | g0144 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18965 | hp2 | a0001 | c0002 | t0037 | g0285 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18966 | hp1 | a0001 | c0002 | t0003 | g0242 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18967 | hp2 | a0001 | c0002 | t0003 | g0145 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18969 | hp2 | a0003 | c0004 | t0010 | g0252 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0298 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18972 | hp1 | a0001 | c0002 | t0003 | g0128 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18973 | hp2 | a0003 | c0004 | t0010 | g0253 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18975 | hp1 | a0001 | c0002 | t0035 | g0154 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18978 | hp1 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18979 | hp1 | a0001 | c0001 | t0025 | g0215 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18980 | hp1 | a0001 | c0002 | t0003 | g0129 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18982 | hp1 | a0001 | c0002 | t0003 | g0300 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0288 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18986 | hp2 | a0001 | c0002 | t0003 | g0042 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18991 | hp2 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18992 | hp2 | a0001 | c0002 | t0003 | g0143 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18993 | hp1 | a0003 | c0004 | t0010 | g0205 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18993 | hp2 | a0001 | c0002 | t0003 | g0111 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0282 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18997 | hp1 | a0001 | c0001 | t0006 | g0326 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19001 | hp1 | a0001 | c0002 | t0003 | g0263 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19002 | hp1 | a0003 | c0004 | t0010 | g0178 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0332 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19009 | hp2 | a0001 | c0001 | t0032 | g0316 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19010 | hp1 | a0001 | c0002 | t0003 | g0152 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19011 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0233 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19030 | hp2 | a0001 | c0002 | t0011 | g0080 | AFR | LWK | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | LWK | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0096 | AFR | LWK | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0283 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19055 | hp2 | a0001 | c0002 | t0003 | g0110 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19063 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19070 | hp1 | a0001 | c0001 | t0007 | g0294 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19074 | hp1 | a0001 | c0002 | t0003 | g0328 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19074 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19077 | hp1 | a0001 | c0001 | t0025 | g0292 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19077 | hp2 | a0001 | c0002 | t0003 | g0194 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19082 | hp1 | a0001 | c0001 | t0029 | g0296 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19082 | hp2 | a0001 | c0002 | t0003 | g0146 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19085 | hp2 | a0003 | c0004 | t0010 | g0255 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19086 | hp1 | a0001 | c0002 | t0003 | g0029 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0072 | AFR | YRI | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA19240 | hp2 | a0001 | c0001 | t0027 | g0112 | AFR | YRI | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0335 | AFR | ASW | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | ASW | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02109 | hp1 | a0002 | c0003 | t0012 | g0133 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0217 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG02559 | hp2 | a0001 | c0001 | t0008 | g0134 | AFR | ACB | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0138 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0239 | AFR | MSL | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | USA | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | USA | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA18955 | hp2 | a0001 | c0002 | t0003 | g0037 | EAS | JPT | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA20300 | hp1 | a0001 | c0001 | t0016 | g0101 | AFR | USA | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| NA20300 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | USA | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0066 | REF | REF | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0005 | g0265 | REF | REF | TGFA_chr2_70442284_70558826 | TGFA | chr2 | 70442284 | 70558826 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70453278
|
G | A | 1 | a0003 | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
missense_variant | MODERATE | c.415C>T | p.Arg139Trp | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/6 | 474/4117 | 415/483 | 139/160 | chr2 | 70453278 | ||
| chr2:70456379
|
C | T | 1 | a0002 | 6 | HG02109.hp1 HG02717.hp1 HG02965.hp1 others(3): Show |
missense_variant | MODERATE | c.325G>A | p.Val109Met | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/6 | 384/4117 | 325/483 | 109/160 | chr2 | 70456379 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70450862
|
G | A | 2 | a0001c0002a0001c0006 | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
synonymous_variant | LOW | c.480C>T | p.Val160Val | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 539/4117 | 480/483 | 160/160 | chr2 | 70450862 | ||
| chr2:70453240
|
G | C | 1 | a0001c0006 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.453C>G | p.Thr151Thr | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/6 | 512/4117 | 453/483 | 151/160 | chr2 | 70453240 | ||
| chr2:70514890
|
C | T | 1 | a0001c0005 | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
synonymous_variant | LOW | c.63G>A | p.Gln21Gln | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/6 | 122/4117 | 63/483 | 21/160 | chr2 | 70514890 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70447450
|
A | T | 9 | a0001c0001t0002a0001c0001t0014a0001c0001t0018others(6): Show | 71 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*3409T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 3409 | chr2 | 70447450 | |||||
| chr2:70447544
|
T | TA | 4 | a0001c0001t0019a0001c0001t0020a0001c0001t0021others(1): Show | 6 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3314dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 3314 | chr2 | 70447544 | |||||
| chr2:70447617
|
G | C | 14 | a0001c0001t0001a0001c0001t0008a0001c0001t0017others(11): Show | 117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3242C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 3242 | chr2 | 70447617 | |||||
| chr2:70447654
|
G | C | 1 | a0001c0001t0007 | 13 | HG00438.hp2 HG00609.hp2 HG00735.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3205C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 3205 | chr2 | 70447654 | |||||
| chr2:70447855
|
C | T | 1 | a0001c0001t0024 | 2 | HG02145.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3004G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 3004 | chr2 | 70447855 | |||||
| chr2:70447870
|
A | G | 1 | a0003c0004t0010 | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2989T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2989 | chr2 | 70447870 | |||||
| chr2:70447890
|
C | T | 1 | a0001c0001t0029 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2969G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2969 | chr2 | 70447890 | |||||
| chr2:70447920
|
A | G | 1 | a0001c0002t0035 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2939T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2939 | chr2 | 70447920 | |||||
| chr2:70447921
|
C | A | 1 | a0001c0002t0035 | 1 | NA18975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2938G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2938 | chr2 | 70447921 | |||||
| chr2:70447931
|
C | T | 1 | a0001c0001t0027 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2928G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2928 | chr2 | 70447931 | |||||
| chr2:70448150
|
C | T | 1 | a0001c0002t0011 | 4 | HG02055.hp2 HG02818.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2709G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2709 | chr2 | 70448150 | |||||
| chr2:70448266
|
G | C | 2 | a0001c0001t0008a0001c0001t0022 | 12 | HG01167.hp1 HG01192.hp1 HG01891.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2593C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2593 | chr2 | 70448266 | |||||
| chr2:70448372
|
G | A | 1 | a0001c0001t0032 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2487C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2487 | chr2 | 70448372 | |||||
| chr2:70448449
|
C | G | 10 | a0001c0001t0001a0001c0001t0023a0001c0001t0025others(7): Show | 97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*2410G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2410 | chr2 | 70448449 | |||||
| chr2:70448575
|
T | G | 2 | a0001c0002t0009a0001c0002t0039 | 6 | HG00642.hp2 HG00733.hp2 HG01106.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2284A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2284 | chr2 | 70448575 | |||||
| chr2:70448644
|
G | A | 1 | a0001c0001t0013 | 4 | HG02630.hp2 HG02976.hp2 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2215C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2215 | chr2 | 70448644 | |||||
| chr2:70448722
|
G | A | 1 | a0001c0001t0023 | 2 | HG03831.hp1 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2137C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2137 | chr2 | 70448722 | |||||
| chr2:70448775
|
A | G | 1 | a0001c0001t0031 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2084T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2084 | chr2 | 70448775 | |||||
| chr2:70448782
|
T | C | 2 | a0001c0001t0021a0001c0005t0021 | 2 | HG01243.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2077A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 2077 | chr2 | 70448782 | |||||
| chr2:70448966
|
G | A | 7 | a0001c0002t0003a0001c0002t0009a0001c0002t0011others(4): Show | 65 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1893C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1893 | chr2 | 70448966 | |||||
| chr2:70448994
|
A | AGTCAAGC others(3): Show |
1 | a0001c0001t0017 | 3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1855_*1864dupGAGG others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1864 | chr2 | 70448994 | |||||
| chr2:70449062
|
C | T | 1 | a0003c0004t0010 | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1797G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1797 | chr2 | 70449062 | |||||
| chr2:70449087
|
T | A | 2 | a0001c0001t0016a0001c0001t0030 | 4 | HG00735.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1772A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1772 | chr2 | 70449087 | |||||
| chr2:70449110
|
C | T | 1 | a0003c0004t0010 | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1749G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1749 | chr2 | 70449110 | |||||
| chr2:70449186
|
T | TA | 8 | a0001c0001t0014a0001c0001t0016a0001c0001t0030others(5): Show | 71 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1672dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1672 | chr2 | 70449186 | |||||
| chr2:70449186
|
T | TATTGTCT others(8): Show |
1 | a0001c0006t0036 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1672_*1673insTATA others(11): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1672 | chr2 | 70449186 | |||||
| chr2:70449196
|
TAAAG | T | 7 | a0001c0001t0002a0001c0001t0018a0001c0001t0019others(4): Show | 66 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1659_*1662delCTTT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1659 | chr2 | 70449196 | |||||
| chr2:70449469
|
T | C | 1 | a0001c0002t0037 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1390A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1390 | chr2 | 70449469 | |||||
| chr2:70449505
|
C | G | 1 | a0001c0001t0018 | 2 | HG02040.hp1 NA18953.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1354G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1354 | chr2 | 70449505 | |||||
| chr2:70449507
|
A | G | 10 | a0001c0001t0001a0001c0001t0023a0001c0001t0025others(7): Show | 97 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*1352T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1352 | chr2 | 70449507 | |||||
| chr2:70449637
|
GA | G | 7 | a0001c0002t0003a0001c0002t0009a0001c0002t0011others(4): Show | 65 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1221delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1221 | chr2 | 70449637 | |||||
| chr2:70449672
|
C | T | 2 | a0001c0001t0016a0001c0001t0030 | 4 | HG00735.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1187G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1187 | chr2 | 70449672 | |||||
| chr2:70449673
|
G | A | 1 | a0001c0001t0020 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1186C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1186 | chr2 | 70449673 | |||||
| chr2:70449829
|
C | T | 1 | a0001c0001t0022 | 2 | HG02922.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1030G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 1030 | chr2 | 70449829 | |||||
| chr2:70449995
|
G | A | 1 | a0001c0001t0025 | 2 | NA18979.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*864C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 864 | chr2 | 70449995 | |||||
| chr2:70450023
|
T | C | 1 | a0001c0001t0033 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*836A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 836 | chr2 | 70450023 | |||||
| chr2:70450250
|
A | G | 2 | a0001c0001t0021a0001c0005t0021 | 2 | HG01243.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*609T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 609 | chr2 | 70450250 | |||||
| chr2:70450262
|
C | G | 1 | a0002c0003t0012 | 4 | HG02109.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*597G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 597 | chr2 | 70450262 | |||||
| chr2:70450279
|
T | C | 1 | a0001c0002t0039 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*580A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 580 | chr2 | 70450279 | |||||
| chr2:70450307
|
A | G | 1 | a0001c0001t0004 | 28 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*552T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 552 | chr2 | 70450307 | |||||
| chr2:70450330
|
G | A | 1 | a0001c0001t0034 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*529C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 529 | chr2 | 70450330 | |||||
| chr2:70450331
|
G | A | 9 | a0001c0002t0003a0001c0002t0009a0001c0002t0011others(6): Show | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*528C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 528 | chr2 | 70450331 | |||||
| chr2:70450336
|
C | T | 7 | a0001c0001t0002a0001c0001t0018a0001c0001t0019others(4): Show | 66 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*523G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 523 | chr2 | 70450336 | |||||
| chr2:70450469
|
G | A | 1 | a0003c0004t0010 | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*390C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 390 | chr2 | 70450469 | |||||
| chr2:70450680
|
C | T | 1 | a0001c0002t0011 | 4 | HG02055.hp2 HG02818.hp2 HG02970.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*179G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 179 | chr2 | 70450680 | |||||
| chr2:70450687
|
A | C | 3 | a0001c0001t0006a0001c0001t0027a0001c0001t0028 | 16 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*172T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 172 | chr2 | 70450687 | |||||
| chr2:70450823
|
C | T | 1 | a0001c0001t0026 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*36G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 6/6 | 36 | chr2 | 70450823 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:70450907
|
C | A | 1 | a0001c0001t0002g0192 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.476-41G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70450907 | ||||||
| chr2:70450968
|
A | T | 10 | a0001c0001t0002g0007a0001c0001t0002g0041a0001c0001t0002g0054others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.476-102T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70450968 | ||||||
| chr2:70451040
|
C | T | 16 | a0001c0001t0006g0026a0001c0001t0006g0047a0001c0001t0006g0097others(13): Show | 16 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.476-174G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451040 | ||||||
| chr2:70451041
|
C | A | 89 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(86): Show | 92 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.476-175G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451041 | ||||||
| chr2:70451044
|
G | A | 68 | a0001c0002t0003g0005a0001c0002t0003g0006a0001c0002t0003g0008others(65): Show | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.476-178C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451044 | ||||||
| chr2:70451083
|
AAGTGAGT others(1): Show |
A | 4 | a0001c0002t0015g0075a0001c0002t0015g0076a0001c0002t0015g0113others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-225_476-218del others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451083 | ||||||
| chr2:70451090
|
T | TGAGTGAG others(16): Show |
7 | a0001c0001t0017g0004a0001c0001t0017g0078a0003c0004t0010g0178others(4): Show | 8 | HG02895.hp2 HG02897.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-247_476-225dup others(23): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451090 | ||||||
| chr2:70451126
|
G | C | 21 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(18): Show | 22 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.476-260C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451126 | ||||||
| chr2:70451133
|
C | G | 2 | a0001c0002t0003g0330a0001c0002t0037g0285 | 2 | HG02056.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.476-267G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451133 | ||||||
| chr2:70451133
|
C | T | 66 | a0001c0002t0003g0005a0001c0002t0003g0006a0001c0002t0003g0008others(63): Show | 68 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.476-267G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451133 | ||||||
| chr2:70451448
|
G | T | 1 | a0001c0001t0002g0180 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.476-582C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451448 | ||||||
| chr2:70451767
|
G | A | 1 | a0001c0002t0003g0018 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.476-901C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451767 | ||||||
| chr2:70451873
|
C | T | 3 | a0001c0001t0016g0099a0001c0001t0016g0100a0001c0001t0016g0101 | 3 | HG02630.hp1 HG02896.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.476-1007G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451873 | ||||||
| chr2:70451915
|
A | G | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.476-1049T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451915 | ||||||
| chr2:70451935
|
G | A | 68 | a0001c0002t0003g0005a0001c0002t0003g0006a0001c0002t0003g0008others(65): Show | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.476-1069C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451935 | ||||||
| chr2:70451996
|
C | T | 8 | a0001c0001t0005g0200a0001c0001t0005g0273a0001c0001t0005g0278others(5): Show | 8 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.476-1130G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70451996 | ||||||
| chr2:70452065
|
C | A | 2 | a0001c0001t0005g0072a0001c0001t0005g0291 | 2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.475+1153G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452065 | ||||||
| chr2:70452105
|
A | C | 89 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(86): Show | 92 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.475+1113T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452105 | ||||||
| chr2:70452235
|
T | C | 2 | a0001c0001t0021g0271a0001c0005t0021g0136 | 2 | HG01243.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.475+983A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452235 | ||||||
| chr2:70452281
|
C | T | 13 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0049others(10): Show | 14 | HG01167.hp1 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+937G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452281 | ||||||
| chr2:70452369
|
G | A | 1 | a0001c0002t0003g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.475+849C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452369 | ||||||
| chr2:70452475
|
CATTA | C | 29 | a0001c0001t0004g0011a0001c0001t0004g0017a0001c0001t0004g0030others(26): Show | 29 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(26): Show |
intron_variant | MODIFIER | c.475+739_475+742del others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452475 | ||||||
| chr2:70452627
|
C | T | 66 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(63): Show | 67 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(64): Show |
intron_variant | MODIFIER | c.475+591G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452627 | ||||||
| chr2:70452652
|
C | T | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.475+566G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452652 | ||||||
| chr2:70452697
|
T | C | 1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.475+521A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452697 | ||||||
| chr2:70452762
|
C | T | 5 | a0003c0004t0010g0178a0003c0004t0010g0205a0003c0004t0010g0252others(2): Show | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.475+456G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452762 | ||||||
| chr2:70452763
|
G | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+455C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452763 | ||||||
| chr2:70452771
|
G | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+447C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452771 | ||||||
| chr2:70452850
|
G | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0270 | 2 | NA18942.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.475+368C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70452850 | ||||||
| chr2:70453079
|
CT | C | 75 | a0001c0001t0017g0004a0001c0001t0017g0078a0001c0002t0003g0005others(72): Show | 78 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.475+138delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 5/5 | chr2 | 70453079 | ||||||
| chr2:70453426
|
TAAACCAG others(4): Show |
T | 28 | a0001c0001t0004g0011a0001c0001t0004g0017a0001c0001t0004g0030others(25): Show | 28 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.366-110_366-100del others(11): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453426 | ||||||
| chr2:70453467
|
G | A | 1 | a0001c0001t0005g0273 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.366-140C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453467 | ||||||
| chr2:70453473
|
G | A | 1 | a0001c0002t0003g0148 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.366-146C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453473 | ||||||
| chr2:70453476
|
C | T | 1 | a0001c0001t0005g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.366-149G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453476 | ||||||
| chr2:70453479
|
T | C | 13 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0049others(10): Show | 14 | HG01167.hp1 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-152A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453479 | ||||||
| chr2:70453481
|
G | A | 3 | a0001c0001t0004g0017a0001c0001t0004g0245a0001c0001t0004g0258 | 3 | HG00558.hp1 HG02080.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.366-154C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453481 | ||||||
| chr2:70453798
|
A | T | 4 | a0001c0002t0011g0080a0001c0002t0011g0115a0001c0002t0011g0257others(1): Show | 4 | HG02055.hp2 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-471T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453798 | ||||||
| chr2:70453818
|
A | G | 67 | a0001c0002t0003g0005a0001c0002t0003g0006a0001c0002t0003g0008others(64): Show | 69 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.366-491T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453818 | ||||||
| chr2:70453869
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.366-542G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70453869 | ||||||
| chr2:70454005
|
G | GA | 78 | a0001c0001t0001g0227a0001c0001t0002g0120a0001c0001t0002g0203others(75): Show | 80 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.366-679dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454005 | ||||||
| chr2:70454013
|
A | T | 13 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0049others(10): Show | 14 | HG01167.hp1 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-686T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454013 | ||||||
| chr2:70454159
|
G | A | 2 | a0001c0001t0017g0004a0001c0001t0017g0078 | 3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.366-832C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454159 | ||||||
| chr2:70454164
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.366-837C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454164 | ||||||
| chr2:70454196
|
C | T | 1 | a0001c0001t0004g0130 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.366-869G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454196 | ||||||
| chr2:70454264
|
C | T | 2 | a0001c0001t0002g0192a0001c0001t0002g0270 | 2 | NA18942.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.366-937G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454264 | ||||||
| chr2:70454274
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.366-947G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454274 | ||||||
| chr2:70454278
|
G | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-951C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454278 | ||||||
| chr2:70454364
|
G | T | 65 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(62): Show | 66 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.366-1037C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454364 | ||||||
| chr2:70454441
|
G | A | 1 | a0001c0002t0003g0242 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.366-1114C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454441 | ||||||
| chr2:70454517
|
A | G | 68 | a0001c0002t0003g0005a0001c0002t0003g0006a0001c0002t0003g0008others(65): Show | 70 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.366-1190T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454517 | ||||||
| chr2:70454694
|
C | A | 14 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-1367G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454694 | ||||||
| chr2:70454775
|
G | A | 7 | a0001c0001t0017g0004a0001c0001t0017g0078a0003c0004t0010g0178others(4): Show | 8 | HG02895.hp2 HG02897.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.366-1448C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454775 | ||||||
| chr2:70454813
|
A | G | 5 | a0003c0004t0010g0178a0003c0004t0010g0205a0003c0004t0010g0252others(2): Show | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.366-1486T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454813 | ||||||
| chr2:70454831
|
C | T | 14 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.366-1504G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454831 | ||||||
| chr2:70454838
|
C | T | 13 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0049others(10): Show | 14 | HG01167.hp1 HG01192.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+1501G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454838 | ||||||
| chr2:70454876
|
A | G | 5 | a0003c0004t0010g0178a0003c0004t0010g0205a0003c0004t0010g0252others(2): Show | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+1463T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454876 | ||||||
| chr2:70454878
|
G | A | 7 | a0001c0001t0017g0004a0001c0001t0017g0078a0003c0004t0010g0178others(4): Show | 8 | HG02895.hp2 HG02897.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+1461C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70454878 | ||||||
| chr2:70455035
|
C | T | 14 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.365+1304G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455035 | ||||||
| chr2:70455224
|
GA | G | 15 | a0001c0001t0006g0026a0001c0001t0006g0047a0001c0001t0006g0097others(12): Show | 15 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.365+1114delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455224 | ||||||
| chr2:70455511
|
G | C | 10 | a0001c0001t0004g0077a0001c0001t0005g0200a0001c0001t0005g0273others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+828C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455511 | ||||||
| chr2:70455582
|
G | A | 5 | a0003c0004t0010g0178a0003c0004t0010g0205a0003c0004t0010g0252others(2): Show | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.365+757C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455582 | ||||||
| chr2:70455833
|
C | G | 1 | a0001c0002t0037g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.365+506G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455833 | ||||||
| chr2:70455866
|
A | G | 1 | a0001c0001t0007g0331 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.365+473T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455866 | ||||||
| chr2:70455925
|
T | C | 7 | a0001c0001t0017g0004a0001c0001t0017g0078a0003c0004t0010g0178others(4): Show | 8 | HG02895.hp2 HG02897.hp2 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.365+414A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455925 | ||||||
| chr2:70455972
|
C | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0193 | 2 | NA18952.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.365+367G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70455972 | ||||||
| chr2:70456131
|
G | T | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.365+208C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70456131 | ||||||
| chr2:70456175
|
C | T | 17 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(14): Show | 18 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.365+164G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70456175 | ||||||
| chr2:70456218
|
A | G | 19 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(16): Show | 19 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.365+121T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70456218 | ||||||
| chr2:70456229
|
A | T | 1 | a0001c0002t0003g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.365+110T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70456229 | ||||||
| chr2:70456279
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0132 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.365+60C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 4/5 | chr2 | 70456279 | ||||||
| chr2:70456582
|
T | C | 10 | a0001c0001t0002g0007a0001c0001t0002g0041a0001c0001t0002g0054others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.216-94A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70456582 | ||||||
| chr2:70456621
|
T | C | 101 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(98): Show | 105 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.216-133A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70456621 | ||||||
| chr2:70456732
|
C | T | 2 | a0001c0001t0017g0004a0001c0001t0017g0078 | 3 | HG02895.hp2 HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.216-244G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70456732 | ||||||
| chr2:70456861
|
G | GT | 235 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(232): Show | 240 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.216-374_216-373ins others(1): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70456861 | ||||||
| chr2:70456905
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.216-417T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70456905 | ||||||
| chr2:70456932
|
T | C | 67 | a0001c0002t0003g0005a0001c0002t0003g0006a0001c0002t0003g0008others(64): Show | 69 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.216-444A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70456932 | ||||||
| chr2:70457280
|
T | C | 2 | a0001c0001t0005g0239a0001c0001t0005g0280 | 2 | HG02647.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.216-792A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457280 | ||||||
| chr2:70457319
|
A | G | 237 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(234): Show | 242 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.216-831T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457319 | ||||||
| chr2:70457499
|
G | A | 1 | a0001c0001t0006g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.216-1011C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457499 | ||||||
| chr2:70457545
|
C | CT | 86 | a0001c0001t0001g0032a0001c0001t0001g0044a0001c0001t0001g0106others(83): Show | 88 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.216-1058dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457545 | ||||||
| chr2:70457545
|
C | CTT | 25 | a0001c0001t0004g0017a0001c0001t0004g0030a0001c0001t0004g0031others(22): Show | 25 | HG00099.hp1 HG00558.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.216-1059_216-1058d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457545 | ||||||
| chr2:70457662
|
C | T | 4 | a0001c0002t0015g0075a0001c0002t0015g0076a0001c0002t0015g0113others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-1174G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457662 | ||||||
| chr2:70457730
|
C | T | 3 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108 | 3 | HG01433.hp2 HG02486.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.216-1242G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457730 | ||||||
| chr2:70457731
|
G | A | 10 | a0001c0001t0006g0026a0001c0001t0006g0047a0001c0001t0006g0162others(7): Show | 10 | HG00621.hp2 HG00639.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.216-1243C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457731 | ||||||
| chr2:70457805
|
G | C | 1 | a0001c0001t0006g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.216-1317C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457805 | ||||||
| chr2:70457946
|
T | G | 1 | a0001c0001t0005g0239 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.216-1458A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70457946 | ||||||
| chr2:70458102
|
G | GT | 7 | a0001c0001t0001g0269a0001c0001t0002g0135a0001c0001t0002g0327others(4): Show | 7 | HG01884.hp1 HG03516.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.216-1615dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458102 | ||||||
| chr2:70458129
|
A | C | 10 | a0001c0001t0002g0201a0001c0001t0014g0175a0001c0001t0017g0004others(7): Show | 12 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.216-1641T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458129 | ||||||
| chr2:70458341
|
C | T | 8 | a0001c0001t0005g0200a0001c0001t0005g0273a0001c0001t0005g0278others(5): Show | 8 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.216-1853G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458341 | ||||||
| chr2:70458525
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.216-2037G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458525 | ||||||
| chr2:70458565
|
C | A | 2 | a0001c0001t0001g0160a0001c0001t0001g0293 | 2 | HG00408.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.216-2077G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458565 | ||||||
| chr2:70458594
|
A | G | 6 | a0001c0001t0001g0137a0001c0001t0004g0142a0001c0001t0024g0289others(3): Show | 6 | HG01884.hp2 HG02818.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.216-2106T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458594 | ||||||
| chr2:70458638
|
T | C | 8 | a0001c0001t0002g0083a0001c0001t0002g0117a0001c0001t0002g0121others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.216-2150A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458638 | ||||||
| chr2:70458783
|
A | AC | 7 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(4): Show | 7 | HG01433.hp2 HG02486.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.216-2296dupG | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458783 | ||||||
| chr2:70458872
|
C | G | 1 | a0001c0001t0008g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.216-2384G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70458872 | ||||||
| chr2:70459029
|
C | T | 1 | a0001c0002t0003g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.216-2541G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459029 | ||||||
| chr2:70459082
|
G | A | 1 | a0001c0001t0004g0282 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.216-2594C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459082 | ||||||
| chr2:70459094
|
G | C | 1 | a0001c0001t0006g0324 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.216-2606C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459094 | ||||||
| chr2:70459103
|
A | T | 1 | a0001c0001t0002g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.216-2615T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459103 | ||||||
| chr2:70459140
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.216-2652T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459140 | ||||||
| chr2:70459369
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0281a0001c0001t0007g0057others(1): Show | 4 | HG00408.hp1 HG01261.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-2881G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459369 | ||||||
| chr2:70459516
|
C | CAAATCTG others(14): Show |
1 | a0001c0001t0002g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.216-3049_216-3029d others(23): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459516 | ||||||
| chr2:70459551
|
T | C | 26 | a0001c0001t0005g0072a0001c0001t0005g0233a0001c0001t0005g0239others(23): Show | 26 | HG00438.hp2 HG00609.hp2 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.216-3063A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459551 | ||||||
| chr2:70459562
|
G | A | 55 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(52): Show | 56 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.216-3074C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459562 | ||||||
| chr2:70459613
|
C | T | 11 | a0001c0001t0006g0279a0001c0001t0008g0001a0001c0001t0008g0048others(8): Show | 12 | HG01167.hp1 HG01192.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.216-3125G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459613 | ||||||
| chr2:70459647
|
C | G | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.216-3159G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459647 | ||||||
| chr2:70459826
|
C | T | 3 | a0001c0002t0003g0029a0001c0002t0003g0152a0001c0002t0003g0153 | 3 | NA18941.hp2 NA19010.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.216-3338G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459826 | ||||||
| chr2:70459855
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.216-3367C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459855 | ||||||
| chr2:70459920
|
A | G | 60 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(57): Show | 61 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.216-3432T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459920 | ||||||
| chr2:70459964
|
C | T | 4 | a0001c0001t0004g0077a0001c0001t0013g0095a0001c0001t0013g0141others(1): Show | 4 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-3476G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70459964 | ||||||
| chr2:70460007
|
G | A | 1 | a0001c0001t0001g0223 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.216-3519C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460007 | ||||||
| chr2:70460347
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.216-3859G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460347 | ||||||
| chr2:70460382
|
T | A | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.216-3894A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460382 | ||||||
| chr2:70460382
|
T | TA | 139 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(136): Show | 142 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.216-3895dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460382 | ||||||
| chr2:70460382
|
T | TAA | 78 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0135others(75): Show | 80 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.216-3896_216-3895d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460382 | ||||||
| chr2:70460393
|
C | A | 1 | a0001c0001t0002g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.216-3905G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460393 | ||||||
| chr2:70460394
|
T | C | 1 | a0001c0001t0002g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.216-3906A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460394 | ||||||
| chr2:70460396
|
C | T | 1 | a0001c0001t0002g0307 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.216-3908G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70460396 | ||||||
| chr2:70461084
|
G | C | 1 | a0001c0001t0002g0301 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.215+4532C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70461084 | ||||||
| chr2:70461230
|
A | G | 5 | a0001c0001t0001g0218a0001c0001t0001g0221a0001c0001t0023g0045others(2): Show | 5 | HG00099.hp2 HG01517.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+4386T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70461230 | ||||||
| chr2:70461249
|
C | G | 55 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(52): Show | 56 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.215+4367G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70461249 | ||||||
| chr2:70461475
|
G | T | 222 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(219): Show | 227 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.215+4141C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70461475 | ||||||
| chr2:70461611
|
C | T | 4 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(1): Show | 4 | HG01433.hp2 HG02486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+4005G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70461611 | ||||||
| chr2:70461734
|
C | G | 62 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(59): Show | 63 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.215+3882G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70461734 | ||||||
| chr2:70462008
|
T | A | 1 | a0001c0001t0004g0212 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.215+3608A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462008 | ||||||
| chr2:70462028
|
A | T | 1 | a0001c0001t0017g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.215+3588T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462028 | ||||||
| chr2:70462112
|
G | A | 97 | a0001c0001t0001g0137a0001c0001t0002g0024a0001c0001t0002g0025others(94): Show | 101 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.215+3504C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462112 | ||||||
| chr2:70462160
|
C | T | 216 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(213): Show | 220 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.215+3456G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462160 | ||||||
| chr2:70462224
|
G | T | 1 | a0001c0001t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.215+3392C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462224 | ||||||
| chr2:70462319
|
A | T | 56 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.215+3297T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462319 | ||||||
| chr2:70462486
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215+3130G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462486 | ||||||
| chr2:70462498
|
G | A | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+3118C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462498 | ||||||
| chr2:70462539
|
C | T | 2 | a0001c0001t0004g0287a0001c0001t0004g0288 | 2 | NA18943.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.215+3077G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462539 | ||||||
| chr2:70462597
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.215+3019G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462597 | ||||||
| chr2:70462657
|
C | G | 336 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0016others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.215+2959G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462657 | ||||||
| chr2:70462781
|
A | G | 62 | a0001c0001t0001g0337a0001c0001t0002g0007a0001c0001t0002g0014others(59): Show | 62 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.215+2835T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462781 | ||||||
| chr2:70462879
|
G | T | 1 | a0001c0001t0021g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.215+2737C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70462879 | ||||||
| chr2:70463002
|
G | C | 57 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(54): Show | 57 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.215+2614C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463002 | ||||||
| chr2:70463205
|
G | C | 86 | a0001c0001t0001g0137a0001c0001t0001g0337a0001c0001t0002g0007others(83): Show | 89 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.215+2411C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463205 | ||||||
| chr2:70463321
|
G | A | 1 | a0001c0002t0015g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.215+2295C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463321 | ||||||
| chr2:70463442
|
C | T | 1 | a0001c0002t0003g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.215+2174G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463442 | ||||||
| chr2:70463623
|
G | C | 2 | a0001c0001t0019g0139a0001c0001t0019g0140 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.215+1993C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463623 | ||||||
| chr2:70463634
|
C | A | 1 | a0001c0001t0001g0156 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.215+1982G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463634 | ||||||
| chr2:70463637
|
T | G | 4 | a0001c0001t0001g0137a0001c0002t0011g0080a0001c0002t0011g0257others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+1979A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463637 | ||||||
| chr2:70463870
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0021g0271 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.215+1746C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463870 | ||||||
| chr2:70463912
|
A | G | 2 | a0001c0001t0019g0139a0001c0001t0019g0140 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.215+1704T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463912 | ||||||
| chr2:70463978
|
T | A | 1 | a0001c0001t0005g0035 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.215+1638A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70463978 | ||||||
| chr2:70464204
|
C | T | 8 | a0001c0002t0003g0027a0001c0002t0003g0128a0001c0002t0003g0129others(5): Show | 8 | HG00544.hp2 HG00558.hp2 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.215+1412G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464204 | ||||||
| chr2:70464210
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0132 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.215+1406G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464210 | ||||||
| chr2:70464384
|
G | A | 80 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0016others(77): Show | 81 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.215+1232C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464384 | ||||||
| chr2:70464545
|
C | T | 1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.215+1071G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464545 | ||||||
| chr2:70464634
|
T | C | 68 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(65): Show | 68 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.215+982A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464634 | ||||||
| chr2:70464784
|
T | A | 79 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0135others(76): Show | 81 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.215+832A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464784 | ||||||
| chr2:70464790
|
G | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0277a0001c0001t0033g0103 | 3 | HG01109.hp1 HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.215+826C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464790 | ||||||
| chr2:70464963
|
C | T | 9 | a0001c0001t0001g0137a0001c0001t0004g0077a0001c0001t0013g0260others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+653G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464963 | ||||||
| chr2:70464996
|
C | T | 55 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(52): Show | 55 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.215+620G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70464996 | ||||||
| chr2:70465103
|
T | C | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.215+513A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465103 | ||||||
| chr2:70465167
|
A | G | 336 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0016others(333): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.215+449T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465167 | ||||||
| chr2:70465210
|
C | T | 9 | a0001c0001t0001g0137a0001c0001t0004g0077a0001c0001t0013g0260others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+406G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465210 | ||||||
| chr2:70465222
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0021g0271 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.215+394C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465222 | ||||||
| chr2:70465280
|
A | G | 2 | a0001c0001t0014g0175a0001c0001t0017g0078 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.215+336T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465280 | ||||||
| chr2:70465392
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0179a0001c0001t0001g0186others(1): Show | 4 | HG00140.hp2 HG00738.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+224G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465392 | ||||||
| chr2:70465393
|
G | A | 1 | a0001c0001t0004g0142 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.215+223C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465393 | ||||||
| chr2:70465397
|
T | C | 14 | a0001c0001t0006g0279a0001c0001t0008g0001a0001c0001t0008g0048others(11): Show | 16 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.215+219A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465397 | ||||||
| chr2:70465417
|
G | A | 1 | a0001c0001t0005g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.215+199C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465417 | ||||||
| chr2:70465425
|
C | T | 79 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0135others(76): Show | 81 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.215+191G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465425 | ||||||
| chr2:70465553
|
T | C | 1 | a0001c0001t0001g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.215+63A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 3/5 | chr2 | 70465553 | ||||||
| chr2:70465797
|
C | T | 4 | a0001c0001t0001g0137a0001c0002t0011g0080a0001c0002t0011g0257others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-61G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70465797 | ||||||
| chr2:70465834
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0021g0271 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.95-98C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70465834 | ||||||
| chr2:70465888
|
T | C | 1 | a0001c0001t0027g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.95-152A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70465888 | ||||||
| chr2:70465970
|
C | T | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-234G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70465970 | ||||||
| chr2:70466078
|
G | T | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-342C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466078 | ||||||
| chr2:70466335
|
G | A | 1 | a0001c0001t0001g0314 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.95-599C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466335 | ||||||
| chr2:70466364
|
G | C | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-628C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466364 | ||||||
| chr2:70466520
|
A | C | 79 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(76): Show | 79 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.95-784T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466520 | ||||||
| chr2:70466522
|
C | CA | 3 | a0001c0001t0014g0175a0001c0001t0017g0078a0001c0001t0020g0002 | 4 | HG01167.hp2 HG01169.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-787dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466522 | ||||||
| chr2:70466526
|
A | C | 2 | a0001c0001t0001g0246a0001c0001t0001g0314 | 2 | HG02615.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.95-790T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466526 | ||||||
| chr2:70466630
|
G | A | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-894C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466630 | ||||||
| chr2:70466663
|
C | T | 69 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(66): Show | 69 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.95-927G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466663 | ||||||
| chr2:70466752
|
A | G | 1 | a0001c0002t0003g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.95-1016T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466752 | ||||||
| chr2:70466768
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.95-1032T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466768 | ||||||
| chr2:70466838
|
A | G | 1 | a0001c0001t0008g0001 | 2 | HG02615.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.95-1102T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466838 | ||||||
| chr2:70466864
|
G | A | 2 | a0001c0001t0004g0309a0001c0001t0004g0318 | 2 | HG01257.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.95-1128C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466864 | ||||||
| chr2:70466926
|
G | A | 4 | a0001c0001t0001g0137a0001c0002t0011g0080a0001c0002t0011g0257others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1190C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466926 | ||||||
| chr2:70466930
|
G | A | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-1194C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70466930 | ||||||
| chr2:70467029
|
C | A | 14 | a0001c0001t0006g0279a0001c0001t0008g0001a0001c0001t0008g0048others(11): Show | 16 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-1293G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467029 | ||||||
| chr2:70467032
|
T | C | 240 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(237): Show | 245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.95-1296A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467032 | ||||||
| chr2:70467041
|
G | T | 1 | a0001c0002t0011g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.95-1305C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467041 | ||||||
| chr2:70467077
|
A | T | 14 | a0001c0001t0006g0279a0001c0001t0008g0001a0001c0001t0008g0048others(11): Show | 16 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-1341T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467077 | ||||||
| chr2:70467087
|
G | A | 77 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.95-1351C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467087 | ||||||
| chr2:70467133
|
C | T | 69 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(66): Show | 69 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.95-1397G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467133 | ||||||
| chr2:70467199
|
A | G | 2 | a0001c0001t0001g0246a0001c0001t0008g0134 | 2 | HG02559.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.95-1463T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467199 | ||||||
| chr2:70467213
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.95-1477T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467213 | ||||||
| chr2:70467222
|
A | G | 1 | a0001c0002t0009g0311 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.95-1486T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467222 | ||||||
| chr2:70467305
|
G | A | 240 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(237): Show | 245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.95-1569C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467305 | ||||||
| chr2:70467367
|
C | T | 14 | a0001c0001t0006g0279a0001c0001t0008g0001a0001c0001t0008g0048others(11): Show | 16 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-1631G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467367 | ||||||
| chr2:70467402
|
T | C | 9 | a0001c0001t0001g0137a0001c0001t0004g0077a0001c0001t0013g0260others(6): Show | 10 | HG02280.hp2 HG02451.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.95-1666A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467402 | ||||||
| chr2:70467471
|
C | A | 2 | a0001c0001t0005g0336a0001c0001t0005g0338 | 2 | HG01891.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.95-1735G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467471 | ||||||
| chr2:70467577
|
A | G | 3 | a0003c0004t0010g0178a0003c0004t0010g0205a0003c0004t0010g0255 | 3 | NA18993.hp1 NA19002.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.95-1841T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467577 | ||||||
| chr2:70467653
|
G | GT | 91 | a0001c0001t0001g0137a0001c0001t0002g0024a0001c0001t0002g0025others(88): Show | 94 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.95-1918dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467653 | ||||||
| chr2:70467688
|
T | A | 1 | a0002c0003t0001g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.95-1952A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467688 | ||||||
| chr2:70467751
|
A | G | 66 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(63): Show | 66 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.95-2015T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467751 | ||||||
| chr2:70467834
|
A | G | 1 | a0001c0001t0005g0239 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.95-2098T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467834 | ||||||
| chr2:70467947
|
C | T | 2 | a0001c0002t0003g0145a0001c0002t0003g0158 | 2 | HG02165.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.95-2211G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467947 | ||||||
| chr2:70467994
|
A | G | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.95-2258T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70467994 | ||||||
| chr2:70468057
|
G | A | 14 | a0001c0001t0006g0279a0001c0001t0008g0001a0001c0001t0008g0048others(11): Show | 16 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-2321C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468057 | ||||||
| chr2:70468057
|
G | C | 2 | a0001c0001t0001g0116a0001c0001t0001g0132 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.95-2321C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468057 | ||||||
| chr2:70468221
|
G | T | 4 | a0001c0001t0001g0137a0001c0002t0011g0080a0001c0002t0011g0257others(1): Show | 4 | HG02818.hp2 HG02970.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2485C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468221 | ||||||
| chr2:70468228
|
A | G | 2 | a0001c0001t0005g0217a0001c0001t0024g0289 | 2 | HG02109.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.95-2492T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468228 | ||||||
| chr2:70468430
|
C | T | 56 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(53): Show | 56 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.95-2694G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468430 | ||||||
| chr2:70468548
|
G | A | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-2812C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468548 | ||||||
| chr2:70468620
|
C | T | 14 | a0001c0001t0001g0137a0001c0001t0004g0077a0001c0001t0005g0072others(11): Show | 15 | HG02280.hp2 HG02451.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-2884G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468620 | ||||||
| chr2:70468718
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.95-2982C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468718 | ||||||
| chr2:70468816
|
C | T | 1 | a0001c0001t0005g0035 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-3080G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468816 | ||||||
| chr2:70468843
|
A | G | 1 | a0001c0002t0003g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.95-3107T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468843 | ||||||
| chr2:70468854
|
C | T | 2 | a0001c0001t0005g0200a0001c0001t0005g0273 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.95-3118G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70468854 | ||||||
| chr2:70469011
|
T | G | 1 | a0001c0001t0021g0271 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.95-3275A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469011 | ||||||
| chr2:70469013
|
G | A | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-3277C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469013 | ||||||
| chr2:70469027
|
A | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3291T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469027 | ||||||
| chr2:70469313
|
GTAAT | G | 14 | a0001c0001t0006g0279a0001c0001t0008g0001a0001c0001t0008g0048others(11): Show | 16 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-3581_95-3578del others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469313 | ||||||
| chr2:70469335
|
A | T | 28 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(25): Show | 28 | HG00438.hp2 HG00609.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.95-3599T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469335 | ||||||
| chr2:70469371
|
A | G | 77 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.95-3635T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469371 | ||||||
| chr2:70469398
|
G | A | 1 | a0001c0001t0005g0233 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.95-3662C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469398 | ||||||
| chr2:70469588
|
C | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-3852G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469588 | ||||||
| chr2:70469642
|
C | T | 4 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(1): Show | 4 | HG01433.hp2 HG02486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-3906G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469642 | ||||||
| chr2:70469674
|
C | T | 1 | a0001c0001t0008g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.95-3938G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469674 | ||||||
| chr2:70469697
|
C | T | 79 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0135others(76): Show | 81 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.95-3961G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469697 | ||||||
| chr2:70469727
|
A | G | 2 | a0001c0001t0023g0045a0001c0001t0023g0065 | 2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.95-3991T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469727 | ||||||
| chr2:70469734
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.95-3998T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469734 | ||||||
| chr2:70469821
|
A | G | 76 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(73): Show | 76 | HG00099.hp1 HG00438.hp2 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.95-4085T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70469821 | ||||||
| chr2:70470047
|
G | A | 2 | a0001c0001t0004g0077a0001c0001t0021g0271 | 2 | HG02280.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.95-4311C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70470047 | ||||||
| chr2:70470535
|
G | A | 103 | a0001c0001t0001g0137a0001c0001t0002g0007a0001c0001t0002g0014others(100): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.95-4799C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70470535 | ||||||
| chr2:70470588
|
C | A | 78 | a0001c0001t0001g0218a0001c0001t0001g0221a0001c0001t0002g0024others(75): Show | 80 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.95-4852G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70470588 | ||||||
| chr2:70470825
|
G | A | 1 | a0001c0001t0005g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.95-5089C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70470825 | ||||||
| chr2:70471102
|
T | C | 174 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(171): Show | 176 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.95-5366A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471102 | ||||||
| chr2:70471103
|
C | T | 81 | a0001c0001t0001g0151a0001c0001t0001g0218a0001c0001t0001g0221others(78): Show | 83 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.95-5367G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471103 | ||||||
| chr2:70471109
|
A | AC | 18 | a0001c0001t0001g0157a0001c0001t0001g0232a0001c0001t0005g0338others(15): Show | 18 | HG00558.hp2 HG00597.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.95-5374dupG | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471109 | ||||||
| chr2:70471117
|
C | A | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.95-5381G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471117 | ||||||
| chr2:70471117
|
CA | C | 69 | a0001c0001t0001g0116a0001c0001t0001g0132a0001c0001t0001g0246others(66): Show | 69 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(66): Show |
intron_variant | MODIFIER | c.95-5382delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471117 | ||||||
| chr2:70471118
|
A | C | 109 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(106): Show | 112 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.95-5382T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471118 | ||||||
| chr2:70471175
|
G | A | 82 | a0001c0001t0001g0044a0001c0001t0001g0116a0001c0001t0001g0132others(79): Show | 82 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.95-5439C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471175 | ||||||
| chr2:70471322
|
G | A | 5 | a0001c0001t0013g0260a0001c0001t0013g0261a0001c0002t0011g0115others(2): Show | 5 | HG02055.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-5586C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471322 | ||||||
| chr2:70471334
|
G | A | 1 | a0001c0001t0005g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.95-5598C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471334 | ||||||
| chr2:70471399
|
T | G | 185 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.95-5663A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471399 | ||||||
| chr2:70471441
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01496.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.95-5705G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471441 | ||||||
| chr2:70471443
|
C | T | 185 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.95-5707G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471443 | ||||||
| chr2:70471458
|
A | G | 206 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.95-5722T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471458 | ||||||
| chr2:70471459
|
C | T | 2 | a0001c0001t0001g0116a0001c0001t0001g0132 | 2 | HG02559.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.95-5723G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471459 | ||||||
| chr2:70471627
|
C | A | 97 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(94): Show | 97 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.95-5891G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471627 | ||||||
| chr2:70471634
|
G | A | 227 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(224): Show | 230 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.95-5898C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471634 | ||||||
| chr2:70471635
|
A | C | 92 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-5899T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471635 | ||||||
| chr2:70471635
|
A | T | 5 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(2): Show | 5 | HG01433.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-5899T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471635 | ||||||
| chr2:70471645
|
G | T | 10 | a0001c0001t0004g0077a0001c0001t0005g0072a0001c0001t0005g0239others(7): Show | 10 | HG02109.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-5909C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471645 | ||||||
| chr2:70471683
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.95-5947A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471683 | ||||||
| chr2:70471683
|
T | TTGAGTGC | 6 | a0001c0001t0004g0077a0001c0001t0005g0072a0001c0001t0005g0239others(3): Show | 6 | HG02280.hp2 HG02451.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-5954_95-5948dup others(7): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471683 | ||||||
| chr2:70471724
|
C | T | 200 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(197): Show | 203 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.95-5988G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471724 | ||||||
| chr2:70471747
|
G | A | 6 | a0001c0001t0001g0032a0001c0001t0001g0238a0001c0001t0001g0269others(3): Show | 6 | HG00408.hp1 HG01261.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-6011C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471747 | ||||||
| chr2:70471913
|
A | G | 1 | a0001c0002t0003g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.95-6177T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70471913 | ||||||
| chr2:70472027
|
T | C | 209 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(206): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.95-6291A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472027 | ||||||
| chr2:70472032
|
C | T | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-6296G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472032 | ||||||
| chr2:70472191
|
A | G | 21 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(18): Show | 22 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.95-6455T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472191 | ||||||
| chr2:70472193
|
A | T | 1 | a0001c0001t0002g0201 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-6457T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472193 | ||||||
| chr2:70472233
|
C | T | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.95-6497G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472233 | ||||||
| chr2:70472254
|
C | T | 1 | a0001c0002t0003g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.95-6518G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472254 | ||||||
| chr2:70472333
|
C | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0231 | 2 | HG01169.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.95-6597G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472333 | ||||||
| chr2:70472527
|
G | A | 4 | a0001c0002t0015g0075a0001c0002t0015g0076a0001c0002t0015g0113others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-6791C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472527 | ||||||
| chr2:70472677
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0004g0055 | 2 | HG01074.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.95-6941C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472677 | ||||||
| chr2:70472784
|
T | A | 1 | a0001c0001t0008g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.95-7048A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70472784 | ||||||
| chr2:70473055
|
G | A | 2 | a0001c0001t0006g0279a0001c0002t0003g0073 | 2 | NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.95-7319C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473055 | ||||||
| chr2:70473104
|
T | C | 213 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(210): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.95-7368A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473104 | ||||||
| chr2:70473149
|
A | C | 48 | a0001c0001t0002g0007a0001c0001t0002g0014a0001c0001t0002g0022others(45): Show | 48 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.95-7413T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473149 | ||||||
| chr2:70473183
|
G | C | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.95-7447C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473183 | ||||||
| chr2:70473259
|
T | C | 3 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-7523A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473259 | ||||||
| chr2:70473292
|
G | A | 1 | a0001c0001t0006g0248 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.95-7556C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473292 | ||||||
| chr2:70473680
|
G | GA | 90 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(87): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-7945dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473680 | ||||||
| chr2:70473681
|
A | AG | 128 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(125): Show | 129 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.95-7946dupC | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473681 | ||||||
| chr2:70473804
|
G | T | 6 | a0001c0001t0008g0098a0001c0001t0013g0260a0001c0001t0013g0261others(3): Show | 6 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-8068C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473804 | ||||||
| chr2:70473837
|
G | A | 4 | a0001c0001t0008g0098a0001c0002t0011g0115a0002c0003t0001g0102others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-8101C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473837 | ||||||
| chr2:70473880
|
A | G | 4 | a0001c0002t0015g0075a0001c0002t0015g0076a0001c0002t0015g0113others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-8144T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473880 | ||||||
| chr2:70473944
|
T | C | 219 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(216): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.95-8208A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473944 | ||||||
| chr2:70473989
|
G | A | 3 | a0001c0001t0006g0259a0001c0001t0017g0004a0001c0001t0022g0074 | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-8253C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70473989 | ||||||
| chr2:70474149
|
G | A | 3 | a0001c0001t0006g0097a0001c0001t0006g0248a0001c0001t0027g0112 | 3 | HG02970.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.95-8413C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474149 | ||||||
| chr2:70474255
|
T | C | 1 | a0001c0001t0006g0324 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.95-8519A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474255 | ||||||
| chr2:70474267
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.95-8531A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474267 | ||||||
| chr2:70474338
|
G | A | 3 | a0001c0001t0006g0097a0001c0001t0006g0248a0001c0001t0027g0112 | 3 | HG02970.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.95-8602C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474338 | ||||||
| chr2:70474637
|
G | A | 4 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0317others(1): Show | 4 | NA18747.hp1 NA18961.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-8901C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474637 | ||||||
| chr2:70474680
|
C | A | 1 | a0001c0001t0020g0002 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.95-8944G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474680 | ||||||
| chr2:70474791
|
G | A | 91 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(88): Show | 93 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.95-9055C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474791 | ||||||
| chr2:70474910
|
AACAC | A | 3 | a0001c0001t0016g0099a0001c0001t0016g0100a0001c0001t0016g0101 | 3 | HG02630.hp1 HG02896.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.95-9178_95-9175del others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474910 | ||||||
| chr2:70474964
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.95-9228C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474964 | ||||||
| chr2:70474969
|
C | CGT | 25 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0068others(22): Show | 26 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.95-9235_95-9234dup others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474969 | ||||||
| chr2:70474969
|
C | CGTGT | 54 | a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0093others(51): Show | 55 | HG00099.hp1 HG00735.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.95-9237_95-9234dup others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474969 | ||||||
| chr2:70474969
|
C | CGTGTGT | 60 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0137others(57): Show | 60 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.95-9239_95-9234dup others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474969 | ||||||
| chr2:70474969
|
C | CGTGTGTG others(1): Show |
6 | a0001c0001t0002g0307a0001c0001t0004g0245a0001c0001t0005g0072others(3): Show | 6 | HG03471.hp2 HG03486.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-9241_95-9234dup others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474969 | ||||||
| chr2:70474969
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0168a0001c0001t0014g0138 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.95-9243_95-9234dup others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474969 | ||||||
| chr2:70474969
|
CGT | C | 24 | a0001c0001t0001g0195a0001c0001t0002g0207a0001c0001t0004g0155others(21): Show | 24 | HG00597.hp1 HG00673.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.95-9235_95-9234del others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474969 | ||||||
| chr2:70474969
|
CGTGT | C | 96 | a0001c0001t0001g0090a0001c0001t0001g0118a0001c0001t0001g0125others(93): Show | 99 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.95-9237_95-9234del others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70474969 | ||||||
| chr2:70475073
|
C | T | 39 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(36): Show | 39 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.95-9337G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475073 | ||||||
| chr2:70475101
|
C | T | 208 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.95-9365G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475101 | ||||||
| chr2:70475224
|
G | C | 1 | a0001c0001t0008g0079 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.95-9488C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475224 | ||||||
| chr2:70475245
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.95-9509T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475245 | ||||||
| chr2:70475670
|
T | A | 1 | a0001c0001t0008g0134 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.95-9934A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475670 | ||||||
| chr2:70475725
|
C | G | 2 | a0001c0001t0004g0184a0001c0001t0004g0185 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.95-9989G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475725 | ||||||
| chr2:70475823
|
C | T | 5 | a0001c0001t0001g0137a0001c0001t0014g0175a0001c0001t0033g0103others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.95-10087G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475823 | ||||||
| chr2:70475998
|
C | A | 1 | a0001c0001t0022g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.95-10262G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70475998 | ||||||
| chr2:70476019
|
A | G | 1 | a0001c0002t0003g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.95-10283T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476019 | ||||||
| chr2:70476069
|
G | A | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-10333C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476069 | ||||||
| chr2:70476080
|
C | CA | 7 | a0001c0001t0001g0043a0001c0001t0001g0051a0001c0001t0001g0093others(4): Show | 7 | HG00423.hp2 HG02080.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-10345dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476080
|
C | CAA | 15 | a0001c0001t0001g0132a0001c0001t0002g0058a0001c0001t0002g0083others(12): Show | 15 | HG01243.hp1 HG01975.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.95-10346_95-10345d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476080
|
C | CAAA | 46 | a0001c0001t0001g0116a0001c0001t0002g0022a0001c0001t0002g0023others(43): Show | 46 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.95-10347_95-10345d others(5): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476080
|
C | CAAAA | 22 | a0001c0001t0001g0090a0001c0001t0002g0007a0001c0001t0002g0014others(19): Show | 22 | HG00735.hp2 HG01099.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-10348_95-10345d others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476080
|
C | CAAAAA | 73 | a0001c0001t0001g0125a0001c0001t0001g0137a0001c0001t0001g0151others(70): Show | 74 | HG00099.hp2 HG00423.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.95-10349_95-10345d others(7): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476080
|
C | CAAAAAA | 25 | a0001c0001t0001g0218a0001c0001t0002g0208a0001c0001t0002g0307others(22): Show | 26 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.95-10350_95-10345d others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476080
|
CA | C | 7 | a0001c0001t0006g0047a0001c0001t0006g0210a0001c0001t0006g0326others(4): Show | 8 | HG02055.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-10345delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476080
|
CAA | C | 17 | a0001c0001t0001g0118a0001c0001t0004g0077a0001c0001t0006g0162others(14): Show | 18 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-10346_95-10345d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476080 | ||||||
| chr2:70476108
|
T | A | 94 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(91): Show | 94 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.95-10372A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476108 | ||||||
| chr2:70476109
|
T | A | 31 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(28): Show | 31 | HG00735.hp2 HG01099.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-10373A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476109 | ||||||
| chr2:70476250
|
A | C | 3 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-10514T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476250 | ||||||
| chr2:70476349
|
C | G | 90 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(87): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-10613G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476349 | ||||||
| chr2:70476385
|
T | C | 1 | a0001c0001t0004g0286 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.95-10649A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476385 | ||||||
| chr2:70476627
|
G | A | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-10891C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476627 | ||||||
| chr2:70476689
|
T | C | 1 | a0001c0002t0015g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.95-10953A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476689 | ||||||
| chr2:70476715
|
C | A | 208 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.95-10979G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476715 | ||||||
| chr2:70476738
|
C | T | 21 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(18): Show | 22 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.95-11002G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476738 | ||||||
| chr2:70476774
|
T | C | 1 | a0001c0001t0004g0155 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.95-11038A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476774 | ||||||
| chr2:70476898
|
C | G | 198 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.95-11162G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476898 | ||||||
| chr2:70476980
|
C | G | 4 | a0001c0001t0008g0098a0001c0002t0011g0115a0002c0003t0001g0102others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-11244G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476980 | ||||||
| chr2:70476987
|
AT | A | 6 | a0001c0001t0005g0338a0001c0001t0006g0047a0001c0001t0006g0162others(3): Show | 6 | HG01891.hp2 HG02922.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-11252delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70476987 | ||||||
| chr2:70477379
|
A | G | 222 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.95-11643T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70477379 | ||||||
| chr2:70477489
|
G | C | 4 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(1): Show | 4 | NA18940.hp2 NA18956.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-11753C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70477489 | ||||||
| chr2:70477568
|
C | T | 2 | a0001c0001t0005g0200a0001c0001t0005g0273 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.95-11832G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70477568 | ||||||
| chr2:70477774
|
T | C | 90 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(87): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-12038A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70477774 | ||||||
| chr2:70478032
|
C | T | 9 | a0001c0001t0002g0007a0001c0001t0002g0041a0001c0001t0002g0060others(6): Show | 9 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-12296G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478032 | ||||||
| chr2:70478084
|
TCCCCAG | T | 86 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(83): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.95-12354_95-12349d others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478084 | ||||||
| chr2:70478270
|
C | T | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-12534G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478270 | ||||||
| chr2:70478307
|
A | T | 11 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0014g0138others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-12571T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478307 | ||||||
| chr2:70478425
|
T | C | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-12689A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478425 | ||||||
| chr2:70478500
|
GA | G | 190 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.95-12765delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478500 | ||||||
| chr2:70478565
|
C | T | 3 | a0001c0001t0002g0197a0001c0001t0007g0015a0001c0001t0007g0020 | 3 | HG02027.hp2 NA18970.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.95-12829G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478565 | ||||||
| chr2:70478736
|
C | A | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.95-13000G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478736 | ||||||
| chr2:70478855
|
G | A | 1 | a0001c0001t0001g0059 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.95-13119C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478855 | ||||||
| chr2:70478864
|
G | C | 2 | a0001c0001t0007g0015a0001c0001t0007g0020 | 2 | HG02027.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.95-13128C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478864 | ||||||
| chr2:70478899
|
A | T | 208 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.95-13163T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478899 | ||||||
| chr2:70478976
|
G | A | 208 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.95-13240C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70478976 | ||||||
| chr2:70479413
|
T | C | 11 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0014g0138others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-13677A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70479413 | ||||||
| chr2:70479456
|
T | C | 1 | a0001c0002t0011g0115 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.95-13720A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70479456 | ||||||
| chr2:70479605
|
A | C | 6 | a0001c0001t0008g0098a0001c0001t0013g0260a0001c0001t0013g0261others(3): Show | 6 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-13869T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70479605 | ||||||
| chr2:70479743
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0245 | 2 | HG02080.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.95-14007A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70479743 | ||||||
| chr2:70479902
|
T | C | 1 | a0001c0001t0007g0254 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.95-14166A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70479902 | ||||||
| chr2:70480064
|
CTAGA | C | 89 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(86): Show | 91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.95-14332_95-14329d others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70480064 | ||||||
| chr2:70480082
|
G | A | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.95-14346C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70480082 | ||||||
| chr2:70480235
|
T | C | 222 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(219): Show | 225 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.95-14499A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70480235 | ||||||
| chr2:70480283
|
G | A | 2 | a0001c0001t0013g0095a0001c0001t0013g0141 | 2 | HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.95-14547C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70480283 | ||||||
| chr2:70480762
|
G | C | 1 | a0001c0002t0011g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.95-15026C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70480762 | ||||||
| chr2:70481029
|
C | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-15293G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481029 | ||||||
| chr2:70481064
|
C | G | 21 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(18): Show | 22 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.95-15328G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481064 | ||||||
| chr2:70481128
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.95-15392C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481128 | ||||||
| chr2:70481129
|
G | A | 208 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(205): Show | 211 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.95-15393C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481129 | ||||||
| chr2:70481225
|
T | C | 187 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.95-15489A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481225 | ||||||
| chr2:70481666
|
A | G | 1 | a0001c0002t0003g0330 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.95-15930T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481666 | ||||||
| chr2:70481685
|
G | T | 89 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(86): Show | 91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.95-15949C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481685 | ||||||
| chr2:70481707
|
C | T | 11 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0014g0138others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-15971G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481707 | ||||||
| chr2:70481768
|
A | C | 16 | a0001c0001t0002g0197a0001c0001t0004g0198a0001c0001t0007g0013others(13): Show | 16 | HG00735.hp2 HG01099.hp2 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-16032T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70481768 | ||||||
| chr2:70482111
|
AT | A | 194 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.95-16376delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482111 | ||||||
| chr2:70482256
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.95-16520A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482256 | ||||||
| chr2:70482420
|
A | G | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-16684T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482420 | ||||||
| chr2:70482587
|
T | C | 1 | a0001c0001t0005g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.95-16851A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482587 | ||||||
| chr2:70482598
|
C | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-16862G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482598 | ||||||
| chr2:70482638
|
A | T | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-16902T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482638 | ||||||
| chr2:70482715
|
CT | C | 22 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(19): Show | 23 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.95-16980delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482715 | ||||||
| chr2:70482888
|
C | G | 1 | a0001c0001t0022g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.95-17152G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482888 | ||||||
| chr2:70482966
|
A | G | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-17230T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70482966 | ||||||
| chr2:70483043
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.95-17307G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483043 | ||||||
| chr2:70483119
|
G | A | 2 | a0001c0001t0004g0030a0001c0001t0004g0031 | 2 | NA18964.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.95-17383C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483119 | ||||||
| chr2:70483135
|
C | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-17399G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483135 | ||||||
| chr2:70483256
|
T | C | 1 | a0001c0001t0014g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.95-17520A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483256 | ||||||
| chr2:70483274
|
G | C | 19 | a0001c0001t0001g0160a0001c0001t0001g0293a0001c0001t0004g0011others(16): Show | 20 | HG00099.hp1 HG00408.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-17538C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483274 | ||||||
| chr2:70483288
|
A | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0044a0001c0001t0001g0051others(199): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.95-17552T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483288 | ||||||
| chr2:70483472
|
T | C | 1 | a0001c0001t0004g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.95-17736A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483472 | ||||||
| chr2:70483564
|
G | C | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-17828C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483564 | ||||||
| chr2:70483574
|
A | G | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-17838T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483574 | ||||||
| chr2:70483632
|
C | T | 11 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0014g0138others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-17896G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483632 | ||||||
| chr2:70483704
|
T | C | 2 | a0001c0001t0017g0078a0001c0001t0020g0002 | 3 | HG01167.hp2 HG01169.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.95-17968A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70483704 | ||||||
| chr2:70484016
|
T | A | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-18280A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484016 | ||||||
| chr2:70484051
|
T | C | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-18315A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484051 | ||||||
| chr2:70484093
|
A | T | 1 | a0001c0001t0005g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.95-18357T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484093 | ||||||
| chr2:70484130
|
T | C | 2 | a0001c0001t0002g0306a0001c0001t0002g0307 | 2 | NA18972.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.95-18394A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484130 | ||||||
| chr2:70484164
|
G | T | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-18428C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484164 | ||||||
| chr2:70484312
|
T | C | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-18576A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484312 | ||||||
| chr2:70484394
|
A | G | 1 | a0001c0001t0004g0030 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.95-18658T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484394 | ||||||
| chr2:70484405
|
C | A | 2 | a0001c0001t0017g0078a0001c0001t0020g0002 | 3 | HG01167.hp2 HG01169.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.95-18669G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484405 | ||||||
| chr2:70484475
|
T | C | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-18739A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484475 | ||||||
| chr2:70484589
|
T | A | 211 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(208): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.95-18853A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484589 | ||||||
| chr2:70484598
|
G | A | 90 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(87): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-18862C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484598 | ||||||
| chr2:70484784
|
G | A | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-19048C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484784 | ||||||
| chr2:70484863
|
G | A | 1 | a0001c0001t0032g0316 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.95-19127C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484863 | ||||||
| chr2:70484873
|
T | C | 259 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(256): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.95-19137A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70484873 | ||||||
| chr2:70485017
|
G | A | 1 | a0001c0001t0004g0319 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.95-19281C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485017 | ||||||
| chr2:70485109
|
A | G | 187 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.95-19373T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485109 | ||||||
| chr2:70485175
|
T | C | 2 | a0001c0001t0019g0139a0001c0001t0019g0140 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.95-19439A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485175 | ||||||
| chr2:70485221
|
C | T | 1 | a0001c0001t0008g0134 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.95-19485G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485221 | ||||||
| chr2:70485301
|
C | T | 3 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-19565G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485301 | ||||||
| chr2:70485364
|
A | G | 19 | a0001c0001t0001g0160a0001c0001t0001g0293a0001c0001t0004g0011others(16): Show | 20 | HG00099.hp1 HG00408.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-19628T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485364 | ||||||
| chr2:70485381
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.95-19645C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485381 | ||||||
| chr2:70485387
|
G | A | 11 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0014g0138others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-19651C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485387 | ||||||
| chr2:70485458
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0014g0138 | 2 | HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.95-19722C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485458 | ||||||
| chr2:70485488
|
G | A | 1 | a0001c0001t0008g0049 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.95-19752C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485488 | ||||||
| chr2:70485670
|
T | C | 227 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(224): Show | 230 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.95-19934A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485670 | ||||||
| chr2:70485728
|
C | T | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.95-19992G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485728 | ||||||
| chr2:70485883
|
A | G | 1 | a0001c0001t0022g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.95-20147T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70485883 | ||||||
| chr2:70486486
|
C | CT | 23 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(20): Show | 24 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.95-20751dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486486 | ||||||
| chr2:70486527
|
G | C | 93 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(90): Show | 95 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.95-20791C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486527 | ||||||
| chr2:70486609
|
G | T | 3 | a0001c0001t0004g0142a0001c0001t0006g0279a0001c0002t0003g0073 | 3 | HG01884.hp2 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.95-20873C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486609 | ||||||
| chr2:70486613
|
T | C | 6 | a0001c0001t0004g0155a0001c0001t0004g0283a0001c0001t0004g0297others(3): Show | 6 | HG00673.hp2 NA18946.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-20877A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486613 | ||||||
| chr2:70486699
|
C | A | 1 | a0001c0001t0002g0333 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.95-20963G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486699 | ||||||
| chr2:70486825
|
C | T | 1 | a0001c0001t0007g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.95-21089G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486825 | ||||||
| chr2:70486913
|
G | A | 1 | a0001c0002t0003g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.95-21177C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486913 | ||||||
| chr2:70486948
|
G | T | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.95-21212C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70486948 | ||||||
| chr2:70487076
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.95-21340A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487076 | ||||||
| chr2:70487168
|
G | A | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-21432C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487168 | ||||||
| chr2:70487175
|
C | T | 1 | a0001c0002t0003g0012 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.95-21439G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487175 | ||||||
| chr2:70487269
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.95-21533G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487269 | ||||||
| chr2:70487366
|
T | C | 188 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(185): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.95-21630A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487366 | ||||||
| chr2:70487486
|
T | G | 2 | a0001c0001t0014g0124a0001c0002t0003g0094 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.95-21750A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487486 | ||||||
| chr2:70487496
|
T | C | 254 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(251): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.95-21760A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487496 | ||||||
| chr2:70487661
|
T | C | 224 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(221): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.95-21925A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487661 | ||||||
| chr2:70487681
|
T | C | 2 | a0001c0001t0008g0249a0001c0001t0021g0271 | 2 | HG02280.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.95-21945A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487681 | ||||||
| chr2:70487906
|
A | C | 3 | a0001c0001t0016g0099a0001c0001t0016g0100a0001c0001t0016g0101 | 3 | HG02630.hp1 HG02896.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.95-22170T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487906 | ||||||
| chr2:70487930
|
C | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-22194G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70487930 | ||||||
| chr2:70488021
|
G | C | 3 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-22285C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488021 | ||||||
| chr2:70488254
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.95-22518G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488254 | ||||||
| chr2:70488595
|
TTTACA | T | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-22864_95-22860d others(7): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488595 | ||||||
| chr2:70488625
|
A | G | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.95-22889T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488625 | ||||||
| chr2:70488656
|
C | T | 232 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(229): Show | 235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.95-22920G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488656 | ||||||
| chr2:70488683
|
G | A | 4 | a0001c0002t0015g0075a0001c0002t0015g0076a0001c0002t0015g0113others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-22947C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488683 | ||||||
| chr2:70488692
|
A | C | 19 | a0001c0001t0001g0160a0001c0001t0001g0293a0001c0001t0004g0011others(16): Show | 20 | HG00099.hp1 HG00408.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.95-22956T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488692 | ||||||
| chr2:70488916
|
G | A | 187 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.95-23180C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70488916 | ||||||
| chr2:70489041
|
C | T | 4 | a0001c0002t0015g0075a0001c0002t0015g0076a0001c0002t0015g0113others(1): Show | 4 | HG02257.hp1 HG02647.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-23305G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489041 | ||||||
| chr2:70489085
|
C | T | 3 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.95-23349G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489085 | ||||||
| chr2:70489182
|
G | A | 1 | a0001c0001t0014g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.95-23446C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489182 | ||||||
| chr2:70489414
|
T | C | 21 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(18): Show | 22 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.95-23678A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489414 | ||||||
| chr2:70489467
|
T | C | 224 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(221): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.95-23731A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489467 | ||||||
| chr2:70489574
|
C | T | 6 | a0001c0001t0008g0098a0001c0001t0013g0260a0001c0001t0013g0261others(3): Show | 6 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-23838G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489574 | ||||||
| chr2:70489704
|
T | C | 1 | a0001c0002t0039g0206 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.95-23968A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489704 | ||||||
| chr2:70489727
|
A | G | 2 | a0001c0002t0003g0037a0001c0002t0035g0154 | 2 | NA18955.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.95-23991T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489727 | ||||||
| chr2:70489741
|
A | C | 1 | a0001c0001t0002g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.95-24005T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489741 | ||||||
| chr2:70489829
|
C | T | 1 | a0001c0001t0023g0045 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.95-24093G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489829 | ||||||
| chr2:70489863
|
T | G | 21 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(18): Show | 22 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.95-24127A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489863 | ||||||
| chr2:70489895
|
A | G | 21 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(18): Show | 22 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.95-24159T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489895 | ||||||
| chr2:70489946
|
C | T | 90 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0125others(87): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-24210G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489946 | ||||||
| chr2:70489955
|
G | A | 233 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(230): Show | 236 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.95-24219C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489955 | ||||||
| chr2:70489983
|
G | A | 188 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(185): Show | 190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.95-24247C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70489983 | ||||||
| chr2:70490100
|
T | C | 11 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0014g0138others(8): Show | 11 | HG01884.hp1 HG02257.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-24364A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490100 | ||||||
| chr2:70490201
|
T | C | 1 | a0001c0002t0003g0182 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.95-24465A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490201 | ||||||
| chr2:70490363
|
C | T | 24 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(21): Show | 25 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.94+24496G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490363 | ||||||
| chr2:70490375
|
A | G | 98 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(95): Show | 98 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.94+24484T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490375 | ||||||
| chr2:70490489
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.94+24370G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490489 | ||||||
| chr2:70490521
|
A | G | 234 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(231): Show | 237 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.94+24338T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490521 | ||||||
| chr2:70490584
|
C | T | 1 | a0001c0001t0008g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.94+24275G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490584 | ||||||
| chr2:70490653
|
A | G | 2 | a0001c0002t0003g0018a0001c0002t0003g0019 | 2 | HG00597.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.94+24206T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70490653 | ||||||
| chr2:70491010
|
C | T | 1 | a0001c0001t0001g0189 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.94+23849G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491010 | ||||||
| chr2:70491288
|
C | T | 1 | a0001c0002t0003g0182 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.94+23571G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491288 | ||||||
| chr2:70491318
|
G | C | 1 | a0001c0006t0036g0038 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.94+23541C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491318 | ||||||
| chr2:70491563
|
T | C | 212 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(209): Show | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.94+23296A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491563 | ||||||
| chr2:70491615
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.94+23244G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491615 | ||||||
| chr2:70491888
|
C | G | 231 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(228): Show | 235 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.94+22971G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491888 | ||||||
| chr2:70491944
|
C | T | 1 | a0001c0005t0002g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.94+22915G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491944 | ||||||
| chr2:70491954
|
T | A | 3 | a0001c0001t0005g0336a0001c0001t0005g0338a0001c0002t0003g0202 | 3 | HG01891.hp2 HG02257.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.94+22905A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491954 | ||||||
| chr2:70491995
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.94+22864T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70491995 | ||||||
| chr2:70492051
|
T | C | 1 | a0001c0002t0003g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.94+22808A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492051 | ||||||
| chr2:70492332
|
C | G | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+22527G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492332 | ||||||
| chr2:70492370
|
G | A | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+22489C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492370 | ||||||
| chr2:70492383
|
A | G | 23 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(20): Show | 24 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.94+22476T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492383 | ||||||
| chr2:70492430
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0167a0001c0001t0001g0171others(2): Show | 5 | HG00733.hp1 HG01070.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+22429C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492430 | ||||||
| chr2:70492787
|
G | A | 95 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(92): Show | 95 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.94+22072C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492787 | ||||||
| chr2:70492886
|
A | G | 5 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(2): Show | 5 | HG01433.hp2 HG02486.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+21973T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492886 | ||||||
| chr2:70492903
|
A | C | 17 | a0001c0001t0001g0160a0001c0001t0001g0293a0001c0001t0004g0011others(14): Show | 17 | HG00099.hp1 HG00408.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+21956T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492903 | ||||||
| chr2:70492938
|
C | T | 211 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(208): Show | 214 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.94+21921G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70492938 | ||||||
| chr2:70493113
|
A | C | 93 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0125others(90): Show | 95 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.94+21746T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493113 | ||||||
| chr2:70493237
|
C | T | 23 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(20): Show | 24 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.94+21622G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493237 | ||||||
| chr2:70493313
|
A | G | 1 | a0001c0001t0005g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.94+21546T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493313 | ||||||
| chr2:70493318
|
G | A | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+21541C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493318 | ||||||
| chr2:70493342
|
C | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+21517G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493342 | ||||||
| chr2:70493469
|
G | C | 23 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(20): Show | 24 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.94+21390C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493469 | ||||||
| chr2:70493471
|
C | T | 89 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0125others(86): Show | 91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.94+21388G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493471 | ||||||
| chr2:70493492
|
G | A | 1 | a0001c0001t0008g0249 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.94+21367C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493492 | ||||||
| chr2:70493519
|
A | T | 4 | a0001c0001t0005g0278a0002c0003t0012g0104a0002c0003t0012g0133others(1): Show | 4 | HG02109.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+21340T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493519 | ||||||
| chr2:70493570
|
T | A | 1 | a0001c0001t0030g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.94+21289A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493570 | ||||||
| chr2:70493874
|
A | G | 190 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.94+20985T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70493874 | ||||||
| chr2:70494029
|
C | CAA | 23 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(20): Show | 24 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.94+20828_94+20829d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494029 | ||||||
| chr2:70494059
|
C | T | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+20800G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494059 | ||||||
| chr2:70494060
|
T | C | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+20799A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494060 | ||||||
| chr2:70494313
|
A | T | 1 | a0001c0001t0024g0289 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+20546T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494313 | ||||||
| chr2:70494314
|
T | A | 1 | a0001c0001t0024g0289 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+20545A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494314 | ||||||
| chr2:70494360
|
A | G | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.94+20499T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494360 | ||||||
| chr2:70494632
|
C | T | 1 | a0001c0001t0004g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.94+20227G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494632 | ||||||
| chr2:70494652
|
G | A | 1 | a0001c0001t0024g0289 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+20207C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494652 | ||||||
| chr2:70494853
|
T | G | 256 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(253): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.94+20006A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494853 | ||||||
| chr2:70494923
|
G | T | 96 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(93): Show | 96 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.94+19936C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70494923 | ||||||
| chr2:70495046
|
C | T | 1 | a0001c0001t0001g0281 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.94+19813G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70495046 | ||||||
| chr2:70495448
|
G | T | 2 | a0001c0001t0019g0139a0001c0001t0019g0140 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.94+19411C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70495448 | ||||||
| chr2:70495631
|
G | A | 88 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(85): Show | 88 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.94+19228C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70495631 | ||||||
| chr2:70495706
|
G | A | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+19153C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70495706 | ||||||
| chr2:70495814
|
G | A | 92 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(89): Show | 92 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.94+19045C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70495814 | ||||||
| chr2:70495916
|
C | T | 86 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(83): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.94+18943G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70495916 | ||||||
| chr2:70495969
|
G | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0002c0003t0012g0105 | 3 | HG02818.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.94+18890C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70495969 | ||||||
| chr2:70496032
|
A | G | 92 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0125others(89): Show | 94 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.94+18827T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496032 | ||||||
| chr2:70496063
|
G | A | 2 | a0001c0001t0006g0259a0001c0001t0022g0074 | 2 | HG02922.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.94+18796C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496063 | ||||||
| chr2:70496413
|
A | C | 253 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(250): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.94+18446T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496413 | ||||||
| chr2:70496429
|
G | GA | 14 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(11): Show | 14 | HG01433.hp2 HG02055.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+18429dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496429 | ||||||
| chr2:70496429
|
GA | G | 218 | a0001c0001t0001g0044a0001c0001t0001g0090a0001c0001t0001g0106others(215): Show | 221 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.94+18429delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496429 | ||||||
| chr2:70496438
|
A | C | 4 | a0001c0001t0004g0011a0001c0001t0004g0286a0001c0001t0004g0287others(1): Show | 4 | NA18943.hp2 NA18982.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+18421T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496438 | ||||||
| chr2:70496754
|
G | A | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+18105C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496754 | ||||||
| chr2:70496764
|
C | T | 86 | a0001c0001t0001g0010a0001c0001t0001g0090a0001c0001t0001g0125others(83): Show | 88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.94+18095G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496764 | ||||||
| chr2:70496879
|
C | G | 111 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(108): Show | 111 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.94+17980G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496879 | ||||||
| chr2:70496906
|
C | A | 1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+17953G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70496906 | ||||||
| chr2:70497017
|
G | A | 1 | a0001c0001t0022g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.94+17842C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70497017 | ||||||
| chr2:70497301
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.94+17558C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70497301 | ||||||
| chr2:70497389
|
C | A | 24 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(21): Show | 25 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.94+17470G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70497389 | ||||||
| chr2:70497528
|
A | T | 1 | a0001c0001t0005g0233 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.94+17331T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70497528 | ||||||
| chr2:70497699
|
C | T | 27 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(24): Show | 28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.94+17160G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70497699 | ||||||
| chr2:70497859
|
C | A | 1 | a0001c0001t0005g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.94+17000G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70497859 | ||||||
| chr2:70498124
|
AAC | A | 24 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(21): Show | 25 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.94+16733_94+16734d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498124 | ||||||
| chr2:70498154
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.94+16705C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498154 | ||||||
| chr2:70498212
|
G | A | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+16647C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498212 | ||||||
| chr2:70498220
|
A | G | 139 | a0001c0001t0001g0044a0001c0001t0001g0088a0001c0001t0001g0106others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.94+16639T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498220 | ||||||
| chr2:70498442
|
A | G | 27 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(24): Show | 28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.94+16417T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498442 | ||||||
| chr2:70498462
|
A | G | 1 | a0001c0001t0007g0294 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.94+16397T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498462 | ||||||
| chr2:70498463
|
C | T | 84 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(81): Show | 86 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.94+16396G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498463 | ||||||
| chr2:70498500
|
G | A | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+16359C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498500 | ||||||
| chr2:70498552
|
A | G | 27 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(24): Show | 28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.94+16307T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498552 | ||||||
| chr2:70498750
|
C | T | 21 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(18): Show | 22 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.94+16109G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498750 | ||||||
| chr2:70498860
|
A | G | 1 | a0001c0001t0006g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.94+15999T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70498860 | ||||||
| chr2:70499015
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.94+15844A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499015 | ||||||
| chr2:70499062
|
T | A | 27 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(24): Show | 28 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.94+15797A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499062 | ||||||
| chr2:70499072
|
C | G | 3 | a0002c0003t0012g0104a0002c0003t0012g0133a0002c0003t0012g0250 | 3 | HG02109.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+15787G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499072 | ||||||
| chr2:70499153
|
T | A | 5 | a0001c0001t0001g0137a0001c0001t0014g0175a0001c0001t0033g0103others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+15706A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499153 | ||||||
| chr2:70499615
|
G | A | 1 | a0001c0001t0017g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94+15244C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499615 | ||||||
| chr2:70499720
|
C | T | 93 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(90): Show | 93 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.94+15139G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499720 | ||||||
| chr2:70499881
|
G | T | 3 | a0002c0003t0012g0104a0002c0003t0012g0133a0002c0003t0012g0250 | 3 | HG02109.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+14978C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499881 | ||||||
| chr2:70499946
|
C | G | 3 | a0002c0003t0012g0104a0002c0003t0012g0133a0002c0003t0012g0250 | 3 | HG02109.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+14913G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70499946 | ||||||
| chr2:70500083
|
C | T | 7 | a0001c0002t0003g0005a0001c0002t0003g0012a0001c0002t0003g0110others(4): Show | 8 | HG00621.hp1 HG02015.hp1 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+14776G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500083 | ||||||
| chr2:70500408
|
C | T | 4 | a0001c0001t0001g0051a0001c0001t0001g0193a0001c0001t0001g0264others(1): Show | 4 | HG00544.hp1 HG02080.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+14451G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500408 | ||||||
| chr2:70500418
|
G | A | 3 | a0001c0001t0007g0119a0001c0001t0007g0187a0001c0001t0007g0188 | 3 | HG00735.hp2 HG01099.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.94+14441C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500418 | ||||||
| chr2:70500459
|
T | TA | 139 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(136): Show | 140 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(137): Show |
intron_variant | MODIFIER | c.94+14399dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500459 | ||||||
| chr2:70500578
|
T | A | 6 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(3): Show | 6 | HG01433.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+14281A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500578 | ||||||
| chr2:70500692
|
C | G | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+14167G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500692 | ||||||
| chr2:70500725
|
C | G | 1 | a0001c0001t0002g0053 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.94+14134G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500725 | ||||||
| chr2:70500896
|
T | C | 140 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(137): Show | 142 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.94+13963A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500896 | ||||||
| chr2:70500952
|
T | C | 1 | a0001c0001t0014g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94+13907A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500952 | ||||||
| chr2:70500970
|
CA | C | 40 | a0001c0001t0001g0068a0001c0001t0001g0116a0001c0001t0001g0132others(37): Show | 42 | HG00099.hp2 HG01081.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.94+13888delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500970 | ||||||
| chr2:70500970
|
CAA | C | 163 | a0001c0001t0001g0090a0001c0001t0001g0106a0001c0001t0001g0107others(160): Show | 165 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.94+13887_94+13888d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500970 | ||||||
| chr2:70500970
|
CAAA | C | 10 | a0001c0001t0001g0044a0001c0001t0001g0171a0001c0001t0002g0007others(7): Show | 10 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+13886_94+13888d others(5): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500970 | ||||||
| chr2:70500992
|
G | A | 28 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(25): Show | 29 | HG00621.hp2 HG00735.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.94+13867C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70500992 | ||||||
| chr2:70501102
|
G | A | 84 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(81): Show | 86 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.94+13757C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501102 | ||||||
| chr2:70501169
|
A | G | 6 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(3): Show | 6 | HG01433.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+13690T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501169 | ||||||
| chr2:70501227
|
A | C | 93 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(90): Show | 93 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.94+13632T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501227 | ||||||
| chr2:70501256
|
AT | A | 99 | a0001c0001t0001g0044a0001c0001t0001g0106a0001c0001t0001g0107others(96): Show | 99 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.94+13602delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501256 | ||||||
| chr2:70501256
|
ATT | A | 20 | a0001c0001t0001g0118a0001c0001t0005g0338a0001c0001t0006g0047others(17): Show | 21 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+13601_94+13602d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501256 | ||||||
| chr2:70501745
|
G | A | 58 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(55): Show | 58 | HG00735.hp2 HG01099.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.94+13114C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501745 | ||||||
| chr2:70501799
|
A | T | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+13060T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501799 | ||||||
| chr2:70501818
|
C | T | 1 | a0001c0002t0003g0220 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.94+13041G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501818 | ||||||
| chr2:70501947
|
T | C | 3 | a0001c0001t0002g0201a0001c0001t0019g0139a0001c0001t0019g0140 | 3 | HG03041.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.94+12912A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501947 | ||||||
| chr2:70501963
|
A | G | 3 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+12896T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70501963 | ||||||
| chr2:70502121
|
A | C | 97 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(94): Show | 98 | HG00621.hp2 HG00735.hp2 HG01070.hp2 others(95): Show |
intron_variant | MODIFIER | c.94+12738T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502121 | ||||||
| chr2:70502179
|
T | C | 1 | a0001c0001t0001g0315 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.94+12680A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502179 | ||||||
| chr2:70502182
|
G | A | 88 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(85): Show | 90 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.94+12677C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502182 | ||||||
| chr2:70502245
|
G | T | 26 | a0001c0001t0001g0118a0001c0001t0005g0072a0001c0001t0005g0239others(23): Show | 27 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.94+12614C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502245 | ||||||
| chr2:70502294
|
C | A | 1 | a0001c0002t0003g0085 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.94+12565G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502294 | ||||||
| chr2:70502376
|
A | G | 90 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(87): Show | 91 | HG00621.hp2 HG00735.hp2 HG01070.hp2 others(88): Show |
intron_variant | MODIFIER | c.94+12483T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502376 | ||||||
| chr2:70502433
|
G | A | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+12426C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502433 | ||||||
| chr2:70502493
|
C | T | 1 | a0001c0002t0003g0129 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.94+12366G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502493 | ||||||
| chr2:70502511
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.94+12348C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70502511 | ||||||
| chr2:70503071
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.94+11788A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503071 | ||||||
| chr2:70503138
|
A | G | 32 | a0001c0001t0001g0118a0001c0001t0005g0035a0001c0001t0005g0036others(29): Show | 33 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+11721T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503138 | ||||||
| chr2:70503207
|
G | A | 6 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(3): Show | 6 | HG01433.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+11652C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503207 | ||||||
| chr2:70503228
|
G | A | 6 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(3): Show | 6 | HG01433.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+11631C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503228 | ||||||
| chr2:70503273
|
A | G | 1 | a0001c0001t0008g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.94+11586T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503273 | ||||||
| chr2:70503318
|
A | G | 32 | a0001c0001t0001g0118a0001c0001t0005g0035a0001c0001t0005g0036others(29): Show | 33 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.94+11541T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503318 | ||||||
| chr2:70503319
|
C | T | 43 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(40): Show | 43 | HG00735.hp2 HG01099.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.94+11540G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503319 | ||||||
| chr2:70503374
|
T | C | 1 | a0001c0001t0005g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.94+11485A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503374 | ||||||
| chr2:70503523
|
T | C | 43 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(40): Show | 43 | HG00735.hp2 HG01099.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.94+11336A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503523 | ||||||
| chr2:70503538
|
C | T | 20 | a0001c0001t0001g0118a0001c0001t0006g0026a0001c0001t0006g0047others(17): Show | 21 | HG00621.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+11321G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503538 | ||||||
| chr2:70503578
|
A | AT | 3 | a0001c0001t0004g0155a0001c0002t0003g0152a0001c0002t0003g0153 | 3 | NA18941.hp2 NA19010.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.94+11280dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503578 | ||||||
| chr2:70503579
|
T | TA | 106 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0125others(103): Show | 108 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.94+11279dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503579 | ||||||
| chr2:70503581
|
AT | A | 7 | a0001c0001t0005g0035a0001c0001t0005g0108a0001c0001t0005g0278others(4): Show | 7 | HG01167.hp1 HG01433.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+11277delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503581 | ||||||
| chr2:70503582
|
T | A | 225 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(222): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.94+11277A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503582 | ||||||
| chr2:70503582
|
T | TA | 6 | a0001c0001t0008g0098a0001c0001t0013g0260a0001c0001t0013g0261others(3): Show | 6 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+11276dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503582 | ||||||
| chr2:70503582
|
T | TGA | 5 | a0001c0001t0001g0043a0001c0001t0001g0147a0001c0001t0001g0149others(2): Show | 5 | NA18950.hp2 NA18955.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+11276_94+11277i others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503582 | ||||||
| chr2:70503583
|
A | T | 5 | a0001c0001t0001g0043a0001c0001t0001g0147a0001c0001t0001g0149others(2): Show | 5 | NA18950.hp2 NA18955.hp1 NA18967.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+11276T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503583 | ||||||
| chr2:70503585
|
A | T | 3 | a0001c0001t0002g0083a0001c0001t0004g0184a0001c0001t0004g0185 | 3 | HG03491.hp2 HG03492.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.94+11274T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503585 | ||||||
| chr2:70503630
|
C | G | 2 | a0001c0001t0004g0310a0001c0001t0004g0319 | 2 | HG00099.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.94+11229G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503630 | ||||||
| chr2:70503732
|
T | G | 3 | a0001c0001t0002g0332a0001c0001t0004g0017a0001c0001t0004g0258 | 3 | HG00558.hp1 HG02080.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.94+11127A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503732 | ||||||
| chr2:70503816
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0014g0175a0001c0001t0033g0103others(2): Show | 5 | HG01884.hp1 HG02572.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+11043C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503816 | ||||||
| chr2:70503887
|
A | T | 1 | a0002c0003t0012g0105 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.94+10972T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503887 | ||||||
| chr2:70503944
|
C | T | 2 | a0001c0001t0005g0200a0001c0001t0005g0273 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.94+10915G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70503944 | ||||||
| chr2:70504068
|
C | G | 5 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291others(2): Show | 5 | HG03130.hp2 HG03225.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10791G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504068 | ||||||
| chr2:70504224
|
C | A | 7 | a0001c0001t0004g0077a0001c0001t0008g0249a0001c0001t0021g0271others(4): Show | 7 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+10635G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504224 | ||||||
| chr2:70504346
|
G | T | 5 | a0003c0004t0010g0178a0003c0004t0010g0205a0003c0004t0010g0252others(2): Show | 5 | NA18969.hp2 NA18973.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+10513C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504346 | ||||||
| chr2:70504404
|
T | C | 2 | a0001c0001t0001g0277a0001c0001t0002g0084 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.94+10455A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504404 | ||||||
| chr2:70504420
|
A | C | 8 | a0001c0001t0004g0011a0001c0001t0004g0286a0001c0001t0004g0287others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+10439T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504420 | ||||||
| chr2:70504433
|
A | AAT | 10 | a0001c0001t0002g0203a0001c0001t0005g0036a0001c0001t0005g0108others(7): Show | 10 | HG00639.hp2 HG01884.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+10424_94+10425d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATAT | 4 | a0001c0001t0001g0118a0001c0001t0002g0208a0001c0001t0005g0035others(1): Show | 4 | HG01433.hp2 HG02071.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+10420_94+10425d others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(1): Show |
4 | a0001c0001t0002g0063a0001c0001t0002g0064a0001c0001t0002g0067others(1): Show | 4 | HG00558.hp1 HG00642.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+10418_94+10425d others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(3): Show |
6 | a0001c0001t0001g0044a0001c0001t0002g0120a0001c0001t0002g0270others(3): Show | 6 | HG01109.hp1 HG03834.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+10416_94+10425d others(12): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(5): Show |
13 | a0001c0001t0002g0053a0001c0001t0002g0230a0001c0001t0002g0323others(10): Show | 14 | HG00099.hp1 HG01167.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+10414_94+10425d others(14): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(7): Show |
21 | a0001c0001t0002g0007a0001c0001t0002g0041a0001c0001t0002g0054others(18): Show | 21 | HG00140.hp1 HG00323.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+10412_94+10425d others(16): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(9): Show |
12 | a0001c0001t0001g0171a0001c0001t0002g0014a0001c0001t0002g0023others(9): Show | 12 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+10410_94+10425d others(18): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(11): Show |
4 | a0001c0001t0001g0174a0001c0001t0002g0028a0001c0001t0004g0287others(1): Show | 4 | HG00609.hp2 HG00733.hp1 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+10408_94+10425d others(20): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(13): Show |
2 | a0001c0001t0002g0022a0001c0001t0004g0286 | 2 | NA18991.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.94+10406_94+10425d others(22): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(15): Show |
1 | a0001c0001t0001g0172 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.94+10404_94+10425d others(24): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | AATATATA others(19): Show |
1 | a0001c0001t0004g0288 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.94+10400_94+10425d others(28): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0002g0256a0002c0003t0001g0114 | 2 | HG02293.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.94+10425_94+10426i others(17): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
AAT | A | 17 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0089others(14): Show | 17 | HG01081.hp1 HG01169.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+10424_94+10425d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
AATAT | A | 54 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0032others(51): Show | 55 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.94+10422_94+10425d others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504433
|
AATATATA others(5): Show |
A | 1 | a0001c0001t0001g0325 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.94+10414_94+10425d others(14): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504433 | ||||||
| chr2:70504443
|
T | TATATATA others(31): Show |
1 | a0001c0002t0003g0006 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.94+10415_94+10416i others(40): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504443 | ||||||
| chr2:70504445
|
T | TATATATA others(29): Show |
1 | a0001c0002t0003g0110 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.94+10413_94+10414i others(38): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504445 | ||||||
| chr2:70504447
|
T | TATATATA others(21): Show |
2 | a0001c0002t0035g0154a0001c0002t0039g0206 | 2 | HG00642.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.94+10411_94+10412i others(30): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504447 | ||||||
| chr2:70504447
|
T | TATATATA others(27): Show |
1 | a0001c0002t0003g0037 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.94+10411_94+10412i others(36): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504447 | ||||||
| chr2:70504447
|
TATATATA others(11): Show |
T | 8 | a0001c0001t0002g0117a0001c0001t0005g0336a0001c0001t0007g0013others(5): Show | 8 | HG02257.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+10394_94+10411d others(20): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504447 | ||||||
| chr2:70504447
|
TATATATA others(13): Show |
T | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+10392_94+10411d others(22): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504447 | ||||||
| chr2:70504447
|
TATATATA others(15): Show |
T | 32 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(29): Show | 32 | HG00735.hp2 HG01099.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.94+10390_94+10411d others(24): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504447 | ||||||
| chr2:70504447
|
TATATATA others(19): Show |
T | 2 | a0001c0005t0002g0176a0001c0005t0002g0274 | 2 | HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.94+10386_94+10411d others(28): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504447 | ||||||
| chr2:70504449
|
T | C | 1 | a0001c0001t0005g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+10410A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504449
|
T | TATATATA others(19): Show |
11 | a0001c0001t0002g0335a0001c0001t0004g0155a0001c0001t0004g0283others(8): Show | 11 | HG00558.hp2 HG01074.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+10409_94+10410i others(28): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504449
|
T | TATATATA others(49): Show |
1 | a0001c0002t0003g0034 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.94+10409_94+10410i others(58): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504449
|
T | TATATATA others(21): Show |
6 | a0001c0001t0001g0236a0001c0002t0003g0148a0001c0002t0003g0182others(3): Show | 6 | HG00423.hp1 HG01433.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+10409_94+10410i others(30): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504449
|
T | TATATATA others(23): Show |
3 | a0001c0001t0001g0218a0001c0002t0003g0012a0001c0002t0038g0284 | 3 | HG00621.hp1 HG01981.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.94+10409_94+10410i others(32): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504449
|
T | TATATATA others(25): Show |
3 | a0001c0001t0001g0125a0001c0002t0003g0129a0001c0002t0003g0213 | 3 | HG00323.hp2 HG01192.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.94+10409_94+10410i others(34): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504449
|
T | TATATATA others(27): Show |
5 | a0001c0001t0018g0021a0001c0002t0003g0005a0001c0002t0003g0128others(2): Show | 6 | HG02015.hp1 HG02165.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+10409_94+10410i others(36): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504449
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0151 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.94+10409_94+10410i others(44): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504449 | ||||||
| chr2:70504451
|
T | C | 1 | a0001c0001t0005g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+10408A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504451 | ||||||
| chr2:70504451
|
T | TATATATA others(17): Show |
1 | a0001c0001t0002g0327 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.94+10407_94+10408i others(26): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504451 | ||||||
| chr2:70504451
|
T | TATATATA others(21): Show |
3 | a0001c0002t0003g0027a0001c0002t0003g0328a0001c0002t0009g0237 | 3 | HG00544.hp2 HG01106.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.94+10407_94+10408i others(30): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504451 | ||||||
| chr2:70504451
|
T | TATATATA others(25): Show |
1 | a0001c0002t0003g0145 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.94+10407_94+10408i others(34): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504451 | ||||||
| chr2:70504451
|
T | TATATATA others(31): Show |
1 | a0001c0001t0030g0266 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.94+10407_94+10408i others(40): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504451 | ||||||
| chr2:70504453
|
T | TATATATA others(19): Show |
1 | a0001c0001t0024g0289 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.94+10405_94+10406i others(28): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504453 | ||||||
| chr2:70504453
|
TATATATA others(5): Show |
T | 5 | a0001c0001t0004g0142a0001c0001t0005g0280a0001c0001t0006g0259others(2): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+10394_94+10405d others(14): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504453 | ||||||
| chr2:70504453
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0017g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94+10392_94+10405d others(16): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504453 | ||||||
| chr2:70504455
|
T | C | 1 | a0001c0001t0006g0326 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.94+10404A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504455 | ||||||
| chr2:70504455
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0337 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.94+10403_94+10404i others(26): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504455 | ||||||
| chr2:70504459
|
T | C | 1 | a0001c0001t0006g0326 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.94+10400A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504459 | ||||||
| chr2:70504461
|
T | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0196 | 3 | HG00438.hp1 NA19063.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.94+10398A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504461 | ||||||
| chr2:70504463
|
T | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0147others(2): Show | 5 | HG00438.hp1 HG03516.hp1 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+10396A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATAC | 3 | a0001c0001t0006g0026a0001c0001t0006g0243a0001c0002t0003g0242 | 3 | HG00621.hp2 NA18966.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.94+10395_94+10396i others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(3): Show |
5 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0049others(2): Show | 6 | HG01167.hp1 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+10395_94+10396i others(12): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(5): Show |
2 | a0001c0001t0001g0160a0001c0002t0011g0115 | 2 | HG02055.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.94+10395_94+10396i others(14): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(7): Show |
1 | a0001c0001t0022g0082 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.94+10395_94+10396i others(16): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0293 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.94+10395_94+10396i others(16): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(9): Show |
1 | a0001c0001t0016g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.94+10395_94+10396i others(18): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(9): Show |
2 | a0001c0001t0024g0081a0002c0003t0001g0102 | 2 | HG02145.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.94+10395_94+10396i others(18): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(11): Show |
1 | a0001c0001t0016g0100 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.94+10395_94+10396i others(20): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(11): Show |
1 | a0001c0001t0008g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.94+10395_94+10396i others(20): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(17): Show |
1 | a0001c0001t0016g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.94+10395_94+10396i others(26): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
T | TATATATA others(13): Show |
1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+10395_94+10396i others(22): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504463
|
TAC | T | 3 | a0001c0001t0006g0326a0001c0001t0033g0103a0001c0002t0011g0290 | 3 | HG02572.hp1 HG02818.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.94+10394_94+10395d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504463 | ||||||
| chr2:70504465
|
C | T | 158 | a0001c0001t0001g0044a0001c0001t0001g0068a0001c0001t0001g0090others(155): Show | 160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.94+10394G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504465 | ||||||
| chr2:70504467
|
C | T | 116 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0068others(113): Show | 118 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.94+10392G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504467 | ||||||
| chr2:70504469
|
C | CATACATA others(15): Show |
1 | a0001c0002t0003g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.94+10389_94+10390i others(24): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | CATACATA others(17): Show |
17 | a0001c0001t0001g0068a0001c0001t0001g0159a0001c0001t0001g0221others(14): Show | 17 | HG00099.hp2 HG01081.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+10389_94+10390i others(26): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | CATACATA others(19): Show |
5 | a0001c0001t0001g0090a0001c0002t0003g0071a0001c0002t0003g0181others(2): Show | 5 | HG01256.hp1 HG01258.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+10389_94+10390i others(28): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | CATACATA others(21): Show |
1 | a0001c0002t0003g0042 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.94+10389_94+10390i others(30): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | CATATATA others(1): Show |
3 | a0001c0001t0002g0120a0001c0002t0003g0161a0001c0002t0003g0263 | 3 | HG02071.hp2 NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.94+10389_94+10390i others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | CATATATA others(5): Show |
1 | a0001c0001t0002g0208 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.94+10389_94+10390i others(14): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | CATATATA others(13): Show |
2 | a0001c0001t0014g0124a0001c0001t0029g0296 | 2 | HG03540.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.94+10389_94+10390i others(22): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | CATATATA others(15): Show |
1 | a0001c0002t0009g0311 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.94+10389_94+10390i others(24): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504469
|
C | T | 72 | a0001c0001t0001g0125a0001c0001t0001g0137a0001c0001t0001g0151others(69): Show | 73 | HG00323.hp2 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.94+10390G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504469 | ||||||
| chr2:70504471
|
T | C | 46 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(43): Show | 46 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.94+10388A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504471 | ||||||
| chr2:70504473
|
C | CATATATA others(5): Show |
1 | a0001c0002t0003g0300 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.94+10385_94+10386i others(14): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504473
|
C | CATATATA others(9): Show |
4 | a0001c0001t0002g0207a0001c0001t0002g0209a0001c0001t0002g0224others(1): Show | 4 | HG00673.hp2 NA18956.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+10385_94+10386i others(18): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504473
|
C | CATATATA others(13): Show |
1 | a0001c0002t0003g0029 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.94+10385_94+10386i others(22): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504473
|
C | CATATATA others(15): Show |
1 | a0001c0002t0003g0330 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.94+10385_94+10386i others(24): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504473
|
C | CATATATA others(17): Show |
1 | a0001c0002t0037g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.94+10385_94+10386i others(26): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504473
|
C | T | 26 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0001g0337others(23): Show | 26 | HG01884.hp1 HG02071.hp2 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.94+10386G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504473
|
CAT | C | 6 | a0001c0001t0005g0278a0001c0001t0005g0336a0001c0002t0003g0111others(3): Show | 6 | HG02257.hp2 HG02451.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+10384_94+10385d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504473
|
CATACAT | C | 4 | a0001c0001t0002g0117a0001c0001t0007g0013a0001c0001t0013g0095others(1): Show | 4 | HG02630.hp2 HG02717.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+10380_94+10385d others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504473 | ||||||
| chr2:70504475
|
T | C | 4 | a0001c0001t0005g0280a0001c0001t0008g0249a0001c0005t0002g0176others(1): Show | 4 | HG02258.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+10384A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504475 | ||||||
| chr2:70504475
|
T | TAC | 5 | a0001c0001t0002g0308a0001c0001t0002g0333a0001c0001t0004g0077others(2): Show | 5 | HG02055.hp2 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+10382_94+10383d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504475 | ||||||
| chr2:70504477
|
C | CATATATA others(7): Show |
1 | a0001c0002t0003g0019 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.94+10381_94+10382i others(16): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504477 | ||||||
| chr2:70504477
|
C | CATATATA others(9): Show |
1 | a0001c0001t0002g0301 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.94+10381_94+10382i others(18): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504477 | ||||||
| chr2:70504477
|
C | CATATATA others(11): Show |
1 | a0001c0002t0003g0018 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.94+10381_94+10382i others(20): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504477 | ||||||
| chr2:70504477
|
C | T | 16 | a0001c0001t0001g0137a0001c0001t0001g0168a0001c0001t0002g0120others(13): Show | 16 | HG00673.hp2 HG02071.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+10382G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504477 | ||||||
| chr2:70504479
|
T | C | 47 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(44): Show | 48 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(45): Show |
intron_variant | MODIFIER | c.94+10380A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504479 | ||||||
| chr2:70504479
|
T | TAC | 3 | a0001c0001t0005g0035a0001c0001t0014g0096a0001c0001t0022g0082 | 3 | HG01433.hp2 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.94+10378_94+10379d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504479 | ||||||
| chr2:70504479
|
T | TACAC | 8 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0049others(5): Show | 9 | HG01167.hp1 HG01192.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+10379_94+10380i others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504479 | ||||||
| chr2:70504481
|
C | CATATATA others(17): Show |
1 | a0001c0001t0002g0203 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.94+10377_94+10378i others(26): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504481 | ||||||
| chr2:70504481
|
C | T | 9 | a0001c0001t0002g0120a0001c0001t0002g0301a0001c0001t0006g0326others(6): Show | 9 | HG00597.hp1 HG01256.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+10378G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504481 | ||||||
| chr2:70504481
|
CAT | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0196others(7): Show | 10 | HG00438.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+10376_94+10377d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504481 | ||||||
| chr2:70504483
|
T | C | 71 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(68): Show | 73 | HG00621.hp2 HG00735.hp2 HG01069.hp1 others(70): Show |
intron_variant | MODIFIER | c.94+10376A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504483
|
T | TAC | 13 | a0001c0001t0001g0089a0001c0001t0002g0270a0001c0001t0004g0299others(10): Show | 13 | HG00609.hp2 HG01074.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.94+10374_94+10375d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504483
|
T | TACACACA others(1): Show |
3 | a0001c0001t0006g0165a0001c0001t0006g0166a0001c0001t0006g0210 | 3 | HG01070.hp2 HG01071.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.94+10368_94+10375d others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504483
|
T | TATATATA others(19): Show |
1 | a0001c0002t0009g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.94+10375_94+10376i others(28): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504483
|
T | TATATATA others(23): Show |
1 | a0001c0001t0006g0279 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.94+10375_94+10376i others(32): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504483
|
T | TATATATA others(25): Show |
1 | a0001c0001t0005g0217 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.94+10375_94+10376i others(34): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504483
|
TAC | T | 23 | a0001c0001t0001g0160a0001c0001t0001g0295a0001c0001t0002g0053others(20): Show | 23 | HG00099.hp1 HG00639.hp1 HG01074.hp2 others(20): Show |
intron_variant | MODIFIER | c.94+10374_94+10375d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504483
|
TACAC | T | 3 | a0001c0001t0001g0325a0001c0001t0005g0200a0001c0001t0006g0248 | 3 | HG01243.hp2 HG03195.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.94+10372_94+10375d others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504483 | ||||||
| chr2:70504485
|
C | CAT | 14 | a0001c0001t0001g0337a0001c0001t0002g0207a0001c0001t0002g0208others(11): Show | 14 | HG00673.hp2 HG02056.hp1 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+10373_94+10374i others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504485 | ||||||
| chr2:70504485
|
C | T | 2 | a0001c0001t0005g0217a0001c0001t0006g0279 | 2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.94+10374G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504485 | ||||||
| chr2:70504487
|
C | T | 13 | a0001c0001t0002g0060a0001c0001t0002g0120a0001c0001t0002g0203others(10): Show | 13 | HG00597.hp1 HG01106.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.94+10372G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504487 | ||||||
| chr2:70504489
|
C | T | 6 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(3): Show | 6 | HG00673.hp2 NA18940.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+10370G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504489 | ||||||
| chr2:70504491
|
C | T | 9 | a0001c0001t0002g0120a0001c0001t0002g0203a0001c0001t0002g0301others(6): Show | 9 | HG00597.hp1 HG02071.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+10368G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504491 | ||||||
| chr2:70504495
|
C | T | 9 | a0001c0001t0002g0120a0001c0001t0002g0203a0001c0001t0002g0301others(6): Show | 9 | HG00597.hp1 HG02071.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+10364G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504495 | ||||||
| chr2:70504572
|
A | G | 6 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(3): Show | 6 | HG01433.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+10287T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504572 | ||||||
| chr2:70504727
|
G | A | 36 | a0001c0001t0001g0118a0001c0001t0001g0172a0001c0001t0001g0174others(33): Show | 37 | HG00621.hp2 HG00733.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.94+10132C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504727 | ||||||
| chr2:70504858
|
G | A | 1 | a0001c0001t0006g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.94+10001C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504858 | ||||||
| chr2:70504926
|
G | T | 1 | a0001c0001t0005g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.94+9933C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70504926 | ||||||
| chr2:70505063
|
T | C | 59 | a0001c0001t0001g0010a0001c0001t0001g0044a0001c0001t0001g0070others(56): Show | 59 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.94+9796A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505063 | ||||||
| chr2:70505098
|
T | C | 1 | a0001c0001t0004g0077 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.94+9761A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505098 | ||||||
| chr2:70505130
|
T | G | 45 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0116others(42): Show | 45 | HG00735.hp2 HG01099.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.94+9729A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505130 | ||||||
| chr2:70505144
|
A | G | 3 | a0001c0001t0002g0332a0001c0001t0004g0017a0001c0001t0004g0258 | 3 | HG00558.hp1 HG02080.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.94+9715T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505144 | ||||||
| chr2:70505217
|
A | C | 6 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(3): Show | 6 | HG01433.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+9642T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505217 | ||||||
| chr2:70505457
|
C | T | 3 | a0001c0001t0005g0072a0001c0001t0005g0239a0001c0001t0005g0291 | 3 | HG03471.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.94+9402G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505457 | ||||||
| chr2:70505525
|
C | T | 6 | a0001c0001t0001g0337a0001c0001t0006g0279a0001c0001t0014g0124others(3): Show | 6 | HG00735.hp1 HG02895.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+9334G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505525 | ||||||
| chr2:70505612
|
C | A | 1 | a0001c0001t0024g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.94+9247G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505612 | ||||||
| chr2:70505699
|
A | T | 2 | a0001c0001t0014g0124a0001c0002t0003g0094 | 2 | HG03540.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.94+9160T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505699 | ||||||
| chr2:70505706
|
C | A | 1 | a0001c0001t0002g0207 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.94+9153G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505706 | ||||||
| chr2:70505720
|
A | G | 193 | a0001c0001t0001g0068a0001c0001t0001g0090a0001c0001t0001g0106others(190): Show | 197 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.94+9139T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505720 | ||||||
| chr2:70505800
|
A | G | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.94+9059T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505800 | ||||||
| chr2:70505872
|
C | T | 1 | a0001c0001t0025g0292 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.94+8987G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505872 | ||||||
| chr2:70505883
|
C | T | 1 | a0001c0002t0003g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.94+8976G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70505883 | ||||||
| chr2:70506029
|
C | CA | 6 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(3): Show | 6 | HG01433.hp2 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8829dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70506029 | ||||||
| chr2:70506036
|
A | G | 1 | a0001c0001t0017g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.94+8823T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70506036 | ||||||
| chr2:70506154
|
C | T | 3 | a0001c0001t0001g0127a0001c0001t0001g0268a0001c0001t0001g0315 | 3 | NA18945.hp1 NA18973.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.94+8705G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70506154 | ||||||
| chr2:70506281
|
C | T | 1 | a0001c0001t0002g0083 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.94+8578G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70506281 | ||||||
| chr2:70506348
|
C | G | 3 | a0001c0001t0013g0260a0001c0001t0013g0261a0001c0001t0017g0078 | 3 | HG03130.hp2 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.94+8511G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70506348 | ||||||
| chr2:70506394
|
T | C | 268 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(265): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.94+8465A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70506394 | ||||||
| chr2:70506656
|
A | C | 11 | a0001c0001t0001g0116a0001c0001t0001g0246a0001c0001t0002g0083others(8): Show | 11 | HG00735.hp1 HG02055.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+8203T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70506656 | ||||||
| chr2:70507054
|
G | A | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.94+7805C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507054 | ||||||
| chr2:70507105
|
G | A | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.94+7754C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507105 | ||||||
| chr2:70507156
|
G | A | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.94+7703C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507156 | ||||||
| chr2:70507174
|
A | C | 1 | a0001c0001t0005g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.94+7685T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507174 | ||||||
| chr2:70507208
|
C | T | 1 | a0001c0002t0003g0033 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.94+7651G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507208 | ||||||
| chr2:70507523
|
C | T | 1 | a0001c0001t0006g0243 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.94+7336G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507523 | ||||||
| chr2:70507555
|
T | C | 46 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0118others(43): Show | 47 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.94+7304A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507555 | ||||||
| chr2:70507614
|
T | A | 1 | a0001c0002t0003g0313 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.94+7245A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507614 | ||||||
| chr2:70507843
|
C | T | 6 | a0001c0001t0005g0280a0001c0001t0006g0097a0001c0001t0006g0248others(3): Show | 6 | HG02572.hp2 HG02647.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+7016G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507843 | ||||||
| chr2:70507919
|
T | C | 1 | a0001c0002t0003g0006 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.94+6940A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507919 | ||||||
| chr2:70507960
|
G | A | 24 | a0001c0001t0002g0163a0001c0001t0002g0201a0001c0001t0002g0321others(21): Show | 25 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.94+6899C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70507960 | ||||||
| chr2:70508113
|
C | T | 6 | a0001c0001t0001g0246a0001c0001t0005g0336a0001c0002t0003g0202others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+6746G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508113 | ||||||
| chr2:70508265
|
C | T | 1 | a0001c0001t0007g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.94+6594G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508265 | ||||||
| chr2:70508303
|
G | A | 6 | a0001c0001t0001g0179a0001c0001t0001g0186a0001c0001t0001g0189others(3): Show | 6 | HG00140.hp2 HG00738.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+6556C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508303 | ||||||
| chr2:70508405
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0013g0260a0001c0001t0013g0261 | 3 | HG03130.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.94+6454T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508405 | ||||||
| chr2:70508639
|
A | G | 1 | a0002c0003t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.94+6220T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508639 | ||||||
| chr2:70508642
|
A | G | 3 | a0001c0001t0002g0083a0001c0001t0013g0260a0001c0001t0013g0261 | 3 | HG03130.hp2 HG03225.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.94+6217T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508642 | ||||||
| chr2:70508908
|
G | C | 3 | a0001c0001t0004g0142a0001c0001t0013g0141a0001c0001t0014g0138 | 3 | HG01884.hp2 HG02976.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.94+5951C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508908 | ||||||
| chr2:70508944
|
T | C | 4 | a0001c0001t0001g0125a0001c0001t0030g0266a0001c0002t0003g0006others(1): Show | 5 | HG00735.hp1 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+5915A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508944 | ||||||
| chr2:70508944
|
T | G | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.94+5915A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70508944 | ||||||
| chr2:70509053
|
C | T | 11 | a0001c0001t0001g0068a0001c0001t0001g0127a0001c0001t0002g0022others(8): Show | 11 | HG01257.hp1 HG01258.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+5806G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509053 | ||||||
| chr2:70509087
|
A | G | 143 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0044others(140): Show | 146 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.94+5772T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509087 | ||||||
| chr2:70509287
|
G | A | 1 | a0001c0001t0024g0081 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.94+5572C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509287 | ||||||
| chr2:70509396
|
T | C | 17 | a0001c0001t0001g0246a0001c0001t0002g0117a0001c0001t0002g0121others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.94+5463A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509396 | ||||||
| chr2:70509488
|
A | C | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.94+5371T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509488 | ||||||
| chr2:70509494
|
G | A | 5 | a0001c0001t0001g0137a0001c0001t0008g0134a0001c0001t0014g0175others(2): Show | 5 | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+5365C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509494 | ||||||
| chr2:70509623
|
C | A | 1 | a0002c0003t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.94+5236G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509623 | ||||||
| chr2:70509667
|
G | A | 1 | a0001c0005t0021g0136 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.94+5192C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509667 | ||||||
| chr2:70509727
|
G | A | 1 | a0002c0003t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.94+5132C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509727 | ||||||
| chr2:70509761
|
G | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0211 | 2 | HG01069.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.94+5098C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509761 | ||||||
| chr2:70509823
|
C | G | 2 | a0001c0001t0001g0168a0001c0001t0005g0338 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.94+5036G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509823 | ||||||
| chr2:70509875
|
A | G | 1 | a0001c0001t0017g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.94+4984T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70509875 | ||||||
| chr2:70510051
|
G | A | 5 | a0001c0001t0002g0163a0001c0001t0002g0335a0001c0001t0006g0047others(2): Show | 5 | HG03017.hp1 HG03669.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+4808C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510051 | ||||||
| chr2:70510147
|
T | G | 11 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+4712A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510147 | ||||||
| chr2:70510155
|
C | T | 3 | a0001c0001t0005g0035a0001c0001t0005g0108a0001c0001t0014g0096 | 3 | HG01433.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.94+4704G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510155 | ||||||
| chr2:70510182
|
T | C | 1 | a0001c0001t0004g0191 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.94+4677A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510182 | ||||||
| chr2:70510184
|
C | T | 5 | a0001c0001t0004g0283a0001c0001t0004g0297a0001c0001t0004g0298others(2): Show | 5 | HG00673.hp2 NA18946.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+4675G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510184 | ||||||
| chr2:70510191
|
G | C | 1 | a0001c0001t0002g0327 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.94+4668C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510191 | ||||||
| chr2:70510203
|
A | G | 11 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+4656T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510203 | ||||||
| chr2:70510235
|
T | A | 1 | a0001c0001t0005g0239 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.94+4624A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510235 | ||||||
| chr2:70510300
|
G | T | 11 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+4559C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510300 | ||||||
| chr2:70510667
|
A | T | 2 | a0001c0001t0001g0125a0001c0002t0009g0173 | 2 | HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.94+4192T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510667 | ||||||
| chr2:70510713
|
C | T | 11 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+4146G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510713 | ||||||
| chr2:70510756
|
T | G | 114 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(111): Show | 116 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.94+4103A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510756 | ||||||
| chr2:70510825
|
C | T | 11 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+4034G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510825 | ||||||
| chr2:70510945
|
A | G | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.94+3914T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510945 | ||||||
| chr2:70510950
|
G | A | 6 | a0001c0001t0002g0201a0001c0001t0004g0142a0001c0001t0013g0141others(3): Show | 6 | HG01884.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+3909C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510950 | ||||||
| chr2:70510972
|
T | C | 8 | a0001c0001t0002g0117a0001c0001t0002g0121a0001c0001t0002g0123others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+3887A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510972 | ||||||
| chr2:70510986
|
GA | G | 65 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(62): Show | 66 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.94+3872delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70510986 | ||||||
| chr2:70511020
|
G | A | 17 | a0001c0001t0001g0137a0001c0001t0002g0083a0001c0001t0002g0084others(14): Show | 18 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.94+3839C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511020 | ||||||
| chr2:70511173
|
C | T | 1 | a0001c0001t0005g0036 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.94+3686G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511173 | ||||||
| chr2:70511240
|
C | T | 8 | a0001c0001t0001g0137a0001c0001t0008g0134a0001c0001t0014g0175others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+3619G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511240 | ||||||
| chr2:70511360
|
G | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0211 | 2 | HG01069.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.94+3499C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511360 | ||||||
| chr2:70511418
|
G | C | 68 | a0001c0001t0001g0039a0001c0001t0001g0090a0001c0001t0001g0125others(65): Show | 69 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.94+3441C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511418 | ||||||
| chr2:70511602
|
A | G | 15 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(12): Show | 16 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.94+3257T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511602 | ||||||
| chr2:70511610
|
T | TG | 12 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+3248_94+3249ins others(1): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511610 | ||||||
| chr2:70511890
|
T | TAC | 57 | a0001c0001t0001g0010a0001c0001t0001g0043a0001c0001t0001g0106others(54): Show | 60 | HG00140.hp1 HG00544.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.94+2967_94+2968dup others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
T | TACAC | 20 | a0001c0001t0001g0107a0001c0001t0001g0116a0001c0001t0001g0118others(17): Show | 20 | HG00597.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.94+2965_94+2968dup others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
T | TACACAC | 8 | a0001c0001t0001g0016a0001c0001t0001g0169a0001c0001t0001g0211others(5): Show | 8 | HG00438.hp1 HG01069.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+2963_94+2968dup others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
T | TACACACA others(5): Show |
1 | a0001c0001t0005g0280 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.94+2957_94+2968dup others(12): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
TAC | T | 52 | a0001c0001t0001g0137a0001c0001t0001g0160a0001c0001t0001g0293others(49): Show | 53 | HG00099.hp1 HG00408.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.94+2967_94+2968del others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
TACAC | T | 14 | a0001c0001t0001g0090a0001c0001t0001g0167a0001c0001t0001g0186others(11): Show | 14 | HG00733.hp2 HG01243.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.94+2965_94+2968del others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
TACACACA others(1): Show |
T | 3 | a0001c0001t0001g0337a0001c0001t0002g0083a0001c0001t0002g0084 | 3 | HG01109.hp2 HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.94+2961_94+2968del others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
TACACACA others(3): Show |
T | 11 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(8): Show | 11 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+2959_94+2968del others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511890
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0017g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.94+2957_94+2968del others(12): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511890 | ||||||
| chr2:70511933
|
G | A | 3 | a0001c0001t0005g0239a0001c0002t0003g0073a0001c0002t0011g0257 | 3 | HG02970.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.94+2926C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511933 | ||||||
| chr2:70511998
|
C | G | 1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+2861G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70511998 | ||||||
| chr2:70512000
|
G | A | 1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+2859C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512000 | ||||||
| chr2:70512002
|
A | G | 1 | a0001c0001t0004g0055 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.94+2857T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512002 | ||||||
| chr2:70512022
|
T | A | 7 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0193others(4): Show | 8 | HG00544.hp1 HG02080.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+2837A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512022 | ||||||
| chr2:70512036
|
G | A | 8 | a0001c0001t0001g0137a0001c0001t0008g0134a0001c0001t0014g0175others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+2823C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512036 | ||||||
| chr2:70512081
|
G | T | 3 | a0001c0001t0002g0201a0001c0001t0019g0139a0001c0001t0019g0140 | 3 | HG03041.hp1 HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.94+2778C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512081 | ||||||
| chr2:70512095
|
C | G | 12 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+2764G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512095 | ||||||
| chr2:70512102
|
G | A | 1 | a0002c0003t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.94+2757C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512102 | ||||||
| chr2:70512170
|
G | A | 8 | a0001c0001t0002g0117a0001c0001t0002g0121a0001c0001t0002g0123others(5): Show | 8 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.94+2689C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512170 | ||||||
| chr2:70512359
|
C | T | 2 | a0001c0001t0001g0337a0001c0002t0015g0075 | 2 | HG02723.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.94+2500G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512359 | ||||||
| chr2:70512465
|
C | T | 7 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0028g0122others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+2394G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512465 | ||||||
| chr2:70512502
|
G | A | 12 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+2357C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512502 | ||||||
| chr2:70512920
|
G | A | 1 | a0001c0001t0002g0322 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.94+1939C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512920 | ||||||
| chr2:70512944
|
G | T | 1 | a0001c0001t0013g0095 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.94+1915C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70512944 | ||||||
| chr2:70513102
|
C | A | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.94+1757G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513102 | ||||||
| chr2:70513115
|
G | A | 7 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0028g0122others(4): Show | 7 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+1744C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513115 | ||||||
| chr2:70513317
|
G | A | 2 | a0001c0001t0017g0078a0001c0001t0020g0002 | 3 | HG01167.hp2 HG01169.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.94+1542C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513317 | ||||||
| chr2:70513596
|
G | A | 12 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1263C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513596 | ||||||
| chr2:70513690
|
A | T | 1 | a0002c0003t0001g0114 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.94+1169T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513690 | ||||||
| chr2:70513738
|
G | A | 12 | a0001c0001t0001g0246a0001c0001t0001g0337a0001c0001t0005g0278others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+1121C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513738 | ||||||
| chr2:70513814
|
C | G | 1 | a0001c0001t0014g0138 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.94+1045G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513814 | ||||||
| chr2:70513890
|
T | C | 9 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0005g0200others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+969A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513890 | ||||||
| chr2:70513907
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.94+952C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513907 | ||||||
| chr2:70513924
|
C | T | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+935G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513924 | ||||||
| chr2:70513946
|
G | A | 3 | a0002c0003t0012g0104a0002c0003t0012g0133a0002c0003t0012g0250 | 3 | HG02109.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+913C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70513946 | ||||||
| chr2:70514002
|
G | T | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+857C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514002 | ||||||
| chr2:70514051
|
T | G | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+808A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514051 | ||||||
| chr2:70514117
|
C | A | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+742G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514117 | ||||||
| chr2:70514197
|
G | A | 1 | a0001c0002t0003g0029 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.94+662C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514197 | ||||||
| chr2:70514233
|
T | C | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+626A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514233 | ||||||
| chr2:70514253
|
C | A | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+606G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514253 | ||||||
| chr2:70514328
|
A | G | 1 | a0002c0003t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.94+531T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514328 | ||||||
| chr2:70514374
|
C | T | 7 | a0001c0001t0002g0201a0001c0001t0004g0142a0001c0001t0013g0141others(4): Show | 8 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+485G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514374 | ||||||
| chr2:70514408
|
TA | T | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.94+450delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514408 | ||||||
| chr2:70514423
|
A | AT | 7 | a0001c0001t0001g0156a0001c0001t0001g0169a0001c0001t0001g0211others(4): Show | 7 | HG00423.hp2 HG01069.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.94+435dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514423 | ||||||
| chr2:70514423
|
AT | A | 78 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(75): Show | 78 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.94+435delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514423 | ||||||
| chr2:70514423
|
ATT | A | 14 | a0001c0001t0001g0137a0001c0001t0002g0083a0001c0001t0002g0084others(11): Show | 15 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+434_94+435delAA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514423 | ||||||
| chr2:70514548
|
C | CAT | 113 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(110): Show | 115 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.94+310_94+311insAT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514548 | ||||||
| chr2:70514613
|
T | C | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+246A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514613 | ||||||
| chr2:70514723
|
G | A | 1 | a0001c0001t0006g0324 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.94+136C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514723 | ||||||
| chr2:70514757
|
C | T | 1 | a0001c0002t0009g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.94+102G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 2/5 | chr2 | 70514757 | ||||||
| chr2:70514962
|
G | A | 9 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0005g0200others(6): Show | 9 | HG01243.hp2 HG02145.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-50C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70514962 | ||||||
| chr2:70514983
|
G | A | 1 | a0001c0001t0031g0170 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.41-71C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70514983 | ||||||
| chr2:70515041
|
T | G | 24 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0083others(21): Show | 25 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.41-129A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515041 | ||||||
| chr2:70515189
|
G | A | 1 | a0001c0001t0001g0183 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.41-277C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515189 | ||||||
| chr2:70515423
|
A | G | 1 | a0001c0002t0003g0073 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.41-511T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515423 | ||||||
| chr2:70515481
|
C | T | 5 | a0001c0001t0001g0246a0001c0001t0021g0271a0001c0002t0015g0076others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-569G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515481 | ||||||
| chr2:70515607
|
C | T | 4 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209others(1): Show | 4 | NA18940.hp2 NA18956.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-695G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515607 | ||||||
| chr2:70515612
|
T | A | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-700A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515612 | ||||||
| chr2:70515721
|
C | T | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.41-809G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515721 | ||||||
| chr2:70515828
|
G | A | 24 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0083others(21): Show | 25 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.41-916C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515828 | ||||||
| chr2:70515830
|
G | A | 24 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0083others(21): Show | 25 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.41-918C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515830 | ||||||
| chr2:70515885
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0211 | 2 | HG01069.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.41-973T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515885 | ||||||
| chr2:70515932
|
A | G | 50 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(47): Show | 51 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.41-1020T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70515932 | ||||||
| chr2:70516018
|
G | T | 13 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(10): Show | 14 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-1106C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516018 | ||||||
| chr2:70516166
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.41-1254C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516166 | ||||||
| chr2:70516180
|
C | G | 76 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(73): Show | 77 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.41-1268G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516180 | ||||||
| chr2:70516192
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.41-1280G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516192 | ||||||
| chr2:70516193
|
G | A | 1 | a0001c0001t0005g0200 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.41-1281C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516193 | ||||||
| chr2:70516320
|
G | GC | 7 | a0001c0001t0002g0201a0001c0001t0004g0142a0001c0001t0013g0141others(4): Show | 8 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-1409dupG | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516320 | ||||||
| chr2:70516409
|
T | C | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1497A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516409 | ||||||
| chr2:70516410
|
G | A | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1498C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516410 | ||||||
| chr2:70516462
|
T | C | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1550A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516462 | ||||||
| chr2:70516534
|
C | CA | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1623dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516534 | ||||||
| chr2:70516708
|
A | G | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1796T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516708 | ||||||
| chr2:70516754
|
G | A | 10 | a0001c0001t0001g0246a0001c0001t0005g0278a0001c0001t0005g0336others(7): Show | 10 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-1842C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516754 | ||||||
| chr2:70516769
|
A | G | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1857T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516769 | ||||||
| chr2:70516779
|
A | G | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1867T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516779 | ||||||
| chr2:70516803
|
G | C | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-1891C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516803 | ||||||
| chr2:70516807
|
T | C | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-1895A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516807 | ||||||
| chr2:70516820
|
C | T | 1 | a0001c0001t0004g0011 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.41-1908G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516820 | ||||||
| chr2:70516874
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(4): Show | 7 | HG00735.hp1 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-1962G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516874 | ||||||
| chr2:70516876
|
C | CT | 101 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(98): Show | 103 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.41-1965_41-1964ins others(1): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516876 | ||||||
| chr2:70516876
|
C | T | 1 | a0001c0001t0008g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-1964G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516876 | ||||||
| chr2:70516975
|
T | C | 155 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0044others(152): Show | 158 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.41-2063A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516975 | ||||||
| chr2:70516990
|
G | T | 5 | a0001c0001t0005g0278a0001c0001t0005g0336a0001c0001t0013g0095others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-2078C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70516990 | ||||||
| chr2:70517191
|
C | T | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-2279G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517191 | ||||||
| chr2:70517228
|
A | G | 1 | a0001c0001t0002g0333 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.41-2316T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517228 | ||||||
| chr2:70517327
|
T | C | 52 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0121others(49): Show | 53 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.41-2415A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517327 | ||||||
| chr2:70517354
|
C | T | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-2442G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517354 | ||||||
| chr2:70517378
|
A | G | 2 | a0001c0002t0003g0005a0001c0002t0003g0110 | 3 | NA18946.hp2 NA18963.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.41-2466T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517378 | ||||||
| chr2:70517380
|
C | T | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-2468G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517380 | ||||||
| chr2:70517485
|
C | T | 50 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(47): Show | 51 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.41-2573G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517485 | ||||||
| chr2:70517494
|
T | G | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-2582A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517494 | ||||||
| chr2:70517504
|
G | A | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41-2592C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517504 | ||||||
| chr2:70517517
|
T | A | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-2605A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517517 | ||||||
| chr2:70517521
|
C | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0211 | 2 | HG01069.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.41-2609G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517521 | ||||||
| chr2:70517775
|
T | G | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-2863A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517775 | ||||||
| chr2:70517852
|
T | C | 2 | a0001c0002t0003g0008a0001c0002t0003g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.41-2940A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517852 | ||||||
| chr2:70517957
|
C | T | 25 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0002g0163others(22): Show | 25 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-3045G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70517957 | ||||||
| chr2:70518014
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.41-3102G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518014 | ||||||
| chr2:70518041
|
G | A | 1 | a0001c0005t0002g0176 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.41-3129C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518041 | ||||||
| chr2:70518151
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.41-3239C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518151 | ||||||
| chr2:70518155
|
C | A | 1 | a0001c0001t0005g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.41-3243G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518155 | ||||||
| chr2:70518175
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.41-3263G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518175 | ||||||
| chr2:70518314
|
G | A | 23 | a0001c0001t0001g0137a0001c0001t0001g0246a0001c0001t0002g0201others(20): Show | 24 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.41-3402C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518314 | ||||||
| chr2:70518413
|
A | T | 48 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(45): Show | 48 | HG00323.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.41-3501T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518413 | ||||||
| chr2:70518437
|
G | A | 3 | a0001c0001t0005g0239a0001c0002t0003g0073a0001c0002t0011g0257 | 3 | HG02970.hp2 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.41-3525C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518437 | ||||||
| chr2:70518653
|
T | A | 1 | a0001c0001t0007g0254 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.41-3741A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518653 | ||||||
| chr2:70518708
|
A | C | 22 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(19): Show | 23 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.41-3796T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518708 | ||||||
| chr2:70518763
|
C | T | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-3851G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518763 | ||||||
| chr2:70518852
|
G | T | 7 | a0001c0001t0002g0201a0001c0001t0004g0142a0001c0001t0013g0141others(4): Show | 8 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-3940C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518852 | ||||||
| chr2:70518866
|
A | G | 25 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0002g0163others(22): Show | 25 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.41-3954T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518866 | ||||||
| chr2:70518896
|
C | T | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-3984G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518896 | ||||||
| chr2:70518997
|
G | A | 4 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(1): Show | 4 | HG01433.hp2 HG02486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-4085C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70518997 | ||||||
| chr2:70519023
|
G | T | 8 | a0001c0001t0005g0280a0001c0001t0006g0097a0001c0001t0006g0248others(5): Show | 8 | HG02572.hp2 HG02647.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.41-4111C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519023 | ||||||
| chr2:70519101
|
G | A | 2 | a0001c0001t0001g0043a0001c0002t0003g0263 | 2 | NA18967.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.41-4189C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519101 | ||||||
| chr2:70519194
|
G | C | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-4282C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519194 | ||||||
| chr2:70519538
|
C | T | 1 | a0001c0001t0017g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.41-4626G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519538 | ||||||
| chr2:70519594
|
T | C | 107 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(104): Show | 109 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.41-4682A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519594 | ||||||
| chr2:70519836
|
G | A | 1 | a0001c0001t0001g0320 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.41-4924C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519836 | ||||||
| chr2:70519861
|
C | T | 7 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(4): Show | 7 | HG00735.hp1 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-4949G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519861 | ||||||
| chr2:70519879
|
A | G | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-4967T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519879 | ||||||
| chr2:70519911
|
T | C | 2 | a0001c0001t0023g0045a0001c0001t0023g0065 | 2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.41-4999A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519911 | ||||||
| chr2:70519951
|
T | A | 3 | a0001c0002t0003g0111a0001c0002t0003g0143a0001c0002t0003g0144 | 3 | NA18964.hp2 NA18992.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.41-5039A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70519951 | ||||||
| chr2:70520237
|
C | T | 2 | a0001c0001t0002g0332a0001c0001t0004g0017 | 2 | HG02080.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.41-5325G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520237 | ||||||
| chr2:70520247
|
G | A | 1 | a0001c0002t0003g0303 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.41-5335C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520247 | ||||||
| chr2:70520305
|
G | A | 2 | a0001c0001t0002g0208a0001c0001t0002g0209 | 2 | NA18940.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.41-5393C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520305 | ||||||
| chr2:70520330
|
A | C | 22 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(19): Show | 23 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.41-5418T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520330 | ||||||
| chr2:70520340
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.41-5428G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520340 | ||||||
| chr2:70520419
|
G | GC | 337 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0016others(334): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.41-5508_41-5507ins others(1): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520419 | ||||||
| chr2:70520513
|
C | A | 1 | a0001c0001t0025g0215 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.41-5601G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520513 | ||||||
| chr2:70520577
|
C | T | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-5665G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520577 | ||||||
| chr2:70520866
|
G | A | 1 | a0001c0001t0017g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.41-5954C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520866 | ||||||
| chr2:70520945
|
T | TATCCAAG others(28): Show |
1 | a0001c0001t0025g0215 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.41-6034_41-6033ins others(35): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520945 | ||||||
| chr2:70520975
|
C | T | 18 | a0001c0001t0002g0163a0001c0001t0002g0321a0001c0001t0002g0335others(15): Show | 18 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-6063G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520975 | ||||||
| chr2:70520985
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.41-6073C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70520985 | ||||||
| chr2:70521009
|
T | A | 13 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(10): Show | 14 | HG01884.hp1 HG01884.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.41-6097A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521009 | ||||||
| chr2:70521042
|
C | T | 6 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-6130G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521042 | ||||||
| chr2:70521097
|
T | TA | 19 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(16): Show | 20 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.41-6186dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521097 | ||||||
| chr2:70521107
|
A | T | 1 | a0001c0002t0003g0148 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.41-6195T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521107 | ||||||
| chr2:70521192
|
A | G | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-6280T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521192 | ||||||
| chr2:70521201
|
C | T | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.41-6289G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521201 | ||||||
| chr2:70521202
|
G | A | 64 | a0001c0001t0001g0090a0001c0001t0001g0125a0001c0001t0001g0151others(61): Show | 65 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.41-6290C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521202 | ||||||
| chr2:70521267
|
T | C | 17 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(14): Show | 18 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.41-6355A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521267 | ||||||
| chr2:70521435
|
T | C | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-6523A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521435 | ||||||
| chr2:70521449
|
G | A | 4 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(1): Show | 4 | HG01433.hp2 HG02486.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-6537C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521449 | ||||||
| chr2:70521507
|
G | T | 1 | a0001c0001t0001g0043 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.41-6595C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521507 | ||||||
| chr2:70521518
|
A | G | 107 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(104): Show | 109 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.41-6606T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521518 | ||||||
| chr2:70521609
|
G | GTTGGT | 3 | a0001c0005t0002g0176a0001c0005t0002g0274a0001c0005t0021g0136 | 3 | HG01243.hp1 HG02258.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.41-6698_41-6697ins others(5): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521609 | ||||||
| chr2:70521609
|
G | GTTGGTTT others(1): Show |
17 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(14): Show | 18 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.41-6698_41-6697ins others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521609 | ||||||
| chr2:70521609
|
G | GTTTTTTT others(1): Show |
11 | a0001c0001t0001g0066a0001c0001t0001g0267a0001c0001t0002g0046others(8): Show | 11 | HG00558.hp1 HG00609.hp2 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-6698_41-6697ins others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521609 | ||||||
| chr2:70521609
|
G | GTTTTTTT others(2): Show |
16 | a0001c0001t0001g0059a0001c0001t0001g0171a0001c0001t0002g0007others(13): Show | 16 | HG01106.hp1 HG01358.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.41-6698_41-6697ins others(9): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521609 | ||||||
| chr2:70521609
|
G | GTTTTTTT others(3): Show |
6 | a0001c0001t0001g0044a0001c0001t0001g0236a0001c0001t0002g0067others(3): Show | 6 | HG00544.hp2 HG01109.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-6698_41-6697ins others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521609 | ||||||
| chr2:70521609
|
G | GTTTTTTT others(4): Show |
3 | a0001c0001t0001g0246a0001c0001t0002g0135a0001c0001t0021g0271 | 3 | HG02280.hp2 HG02615.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.41-6698_41-6697ins others(11): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521609 | ||||||
| chr2:70521609
|
G | GTTTTTTT others(8): Show |
2 | a0001c0002t0015g0076a0001c0002t0015g0113 | 2 | HG02257.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.41-6698_41-6697ins others(15): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521609 | ||||||
| chr2:70521612
|
T | G | 1 | a0001c0002t0003g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.41-6700A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521612 | ||||||
| chr2:70521613
|
G | GTTTTT | 6 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0006g0279others(3): Show | 6 | HG02809.hp2 HG02896.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-6702_41-6701ins others(5): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521613
|
G | GTTTTTT | 5 | a0001c0001t0001g0118a0001c0001t0005g0200a0001c0001t0016g0099others(2): Show | 5 | HG01243.hp2 HG02280.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-6702_41-6701ins others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521613
|
G | GTTTTTTT | 7 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0005g0108others(4): Show | 7 | HG01433.hp2 HG02486.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-6702_41-6701ins others(7): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521613
|
G | GTTTTTTT others(1): Show |
6 | a0001c0001t0002g0321a0001c0001t0006g0166a0001c0001t0006g0210others(3): Show | 6 | HG00140.hp1 HG01070.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-6702_41-6701ins others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521613
|
G | GTTTTTTT others(2): Show |
7 | a0001c0001t0005g0280a0001c0001t0006g0165a0001c0001t0006g0248others(4): Show | 7 | HG01071.hp1 HG01192.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.41-6702_41-6701ins others(9): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521613
|
G | GTTTTTTT others(3): Show |
6 | a0001c0001t0002g0163a0001c0001t0006g0097a0001c0001t0006g0162others(3): Show | 6 | HG02809.hp1 HG02970.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-6702_41-6701ins others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521613
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0006g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.41-6702_41-6701ins others(11): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521613
|
G | T | 49 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(46): Show | 49 | HG00323.hp1 HG00544.hp2 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.41-6701C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521613 | ||||||
| chr2:70521617
|
G | GT | 109 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0039others(106): Show | 111 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.41-6706dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521617 | ||||||
| chr2:70521617
|
G | GTT | 91 | a0001c0001t0001g0003a0001c0001t0001g0032a0001c0001t0001g0051others(88): Show | 93 | HG00099.hp2 HG00408.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.41-6707_41-6706dup others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521617 | ||||||
| chr2:70521617
|
G | GTTT | 16 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0304others(13): Show | 16 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.41-6708_41-6706dup others(3): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521617 | ||||||
| chr2:70521617
|
G | T | 106 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(103): Show | 108 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.41-6705C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521617 | ||||||
| chr2:70521618
|
T | G | 17 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(14): Show | 18 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.41-6706A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521618 | ||||||
| chr2:70521622
|
T | G | 1 | a0001c0002t0003g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.41-6710A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521622 | ||||||
| chr2:70521623
|
T | G | 17 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(14): Show | 18 | HG01884.hp1 HG01884.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.41-6711A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521623 | ||||||
| chr2:70521732
|
C | T | 1 | a0001c0002t0003g0303 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.41-6820G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521732 | ||||||
| chr2:70521739
|
C | T | 5 | a0001c0001t0005g0278a0001c0001t0005g0336a0001c0001t0013g0095others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-6827G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521739 | ||||||
| chr2:70521747
|
T | C | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-6835A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521747 | ||||||
| chr2:70521764
|
G | A | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-6852C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521764 | ||||||
| chr2:70521830
|
G | T | 1 | a0001c0001t0001g0302 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.41-6918C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521830 | ||||||
| chr2:70521905
|
A | G | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-6993T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521905 | ||||||
| chr2:70521908
|
G | C | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-6996C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70521908 | ||||||
| chr2:70522109
|
C | T | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-7197G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522109 | ||||||
| chr2:70522266
|
G | A | 4 | a0001c0001t0005g0072a0001c0001t0006g0279a0001c0001t0033g0103others(1): Show | 4 | HG02572.hp1 HG02723.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-7354C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522266 | ||||||
| chr2:70522400
|
G | T | 1 | a0001c0001t0002g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.41-7488C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522400 | ||||||
| chr2:70522544
|
C | T | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-7632G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522544 | ||||||
| chr2:70522575
|
A | G | 6 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(3): Show | 6 | HG02055.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-7663T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522575 | ||||||
| chr2:70522597
|
C | G | 85 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(82): Show | 86 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.41-7685G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522597 | ||||||
| chr2:70522664
|
A | G | 1 | a0001c0001t0002g0235 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.41-7752T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522664 | ||||||
| chr2:70522696
|
A | G | 7 | a0001c0001t0002g0201a0001c0001t0004g0142a0001c0001t0013g0141others(4): Show | 8 | HG01884.hp2 HG02895.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-7784T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522696 | ||||||
| chr2:70522777
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.41-7865C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522777 | ||||||
| chr2:70522860
|
C | A | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-7948G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522860 | ||||||
| chr2:70522867
|
C | T | 1 | a0001c0001t0008g0048 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.41-7955G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522867 | ||||||
| chr2:70522980
|
A | T | 1 | a0001c0001t0001g0211 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.41-8068T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522980 | ||||||
| chr2:70522981
|
T | C | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.41-8069A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522981 | ||||||
| chr2:70522991
|
G | C | 5 | a0001c0001t0005g0278a0001c0001t0005g0336a0001c0001t0013g0095others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-8079C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70522991 | ||||||
| chr2:70523025
|
A | G | 11 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-8113T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523025 | ||||||
| chr2:70523031
|
T | C | 1 | a0001c0001t0002g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.41-8119A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523031 | ||||||
| chr2:70523101
|
G | A | 1 | a0001c0002t0003g0161 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.41-8189C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523101 | ||||||
| chr2:70523153
|
A | G | 5 | a0001c0001t0001g0246a0001c0001t0021g0271a0001c0002t0015g0076others(2): Show | 5 | HG02257.hp1 HG02280.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-8241T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523153 | ||||||
| chr2:70523157
|
G | A | 1 | a0001c0002t0015g0272 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.41-8245C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523157 | ||||||
| chr2:70523250
|
C | T | 1 | a0001c0001t0004g0212 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.41-8338G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523250 | ||||||
| chr2:70523307
|
C | T | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.41-8395G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523307 | ||||||
| chr2:70523324
|
C | G | 11 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(8): Show | 11 | HG00735.hp1 HG01243.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-8412G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523324 | ||||||
| chr2:70523399
|
T | C | 108 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(105): Show | 110 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.41-8487A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523399 | ||||||
| chr2:70523400
|
G | A | 1 | a0002c0003t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.41-8488C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523400 | ||||||
| chr2:70523486
|
G | A | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-8574C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523486 | ||||||
| chr2:70523517
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0001g0211 | 2 | HG01069.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.41-8605G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523517 | ||||||
| chr2:70523521
|
G | A | 10 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-8609C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523521 | ||||||
| chr2:70523642
|
C | G | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-8730G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523642 | ||||||
| chr2:70523822
|
T | C | 1 | a0001c0002t0015g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.41-8910A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523822 | ||||||
| chr2:70523871
|
G | A | 18 | a0001c0001t0001g0137a0001c0001t0002g0201a0001c0001t0004g0142others(15): Show | 19 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-8959C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70523871 | ||||||
| chr2:70524064
|
G | C | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41-9152C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524064 | ||||||
| chr2:70524070
|
G | C | 1 | a0001c0001t0007g0234 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.41-9158C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524070 | ||||||
| chr2:70524234
|
C | T | 1 | a0001c0001t0017g0004 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.41-9322G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524234 | ||||||
| chr2:70524261
|
G | A | 10 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-9349C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524261 | ||||||
| chr2:70524299
|
T | C | 10 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-9387A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524299 | ||||||
| chr2:70524357
|
C | T | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-9445G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524357 | ||||||
| chr2:70524386
|
G | A | 4 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0022g0082others(1): Show | 4 | HG01109.hp2 HG02145.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-9474C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524386 | ||||||
| chr2:70524445
|
T | A | 10 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-9533A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524445 | ||||||
| chr2:70524466
|
AT | A | 4 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0022g0082others(1): Show | 4 | HG01109.hp2 HG02145.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-9555delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524466 | ||||||
| chr2:70524528
|
C | T | 5 | a0001c0001t0005g0278a0001c0001t0005g0336a0001c0001t0013g0095others(2): Show | 5 | HG02257.hp2 HG02451.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-9616G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524528 | ||||||
| chr2:70524718
|
C | T | 5 | a0001c0001t0008g0001a0001c0001t0008g0048a0001c0001t0008g0049others(2): Show | 6 | HG01167.hp1 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-9806G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524718 | ||||||
| chr2:70524843
|
A | G | 1 | a0001c0002t0009g0087 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.41-9931T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524843 | ||||||
| chr2:70524876
|
G | T | 10 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-9964C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524876 | ||||||
| chr2:70524910
|
T | TGGCCCCA others(2): Show |
4 | a0001c0001t0005g0072a0001c0001t0006g0279a0001c0001t0033g0103others(1): Show | 4 | HG02572.hp1 HG02723.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-10007_41-9999du others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70524910 | ||||||
| chr2:70525063
|
A | C | 36 | a0001c0001t0001g0137a0001c0001t0002g0163a0001c0001t0002g0201others(33): Show | 37 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.41-10151T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70525063 | ||||||
| chr2:70525211
|
A | G | 115 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(112): Show | 117 | HG00140.hp1 HG00323.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.41-10299T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70525211 | ||||||
| chr2:70525379
|
C | CTG | 4 | a0001c0001t0002g0120a0001c0001t0002g0197a0001c0002t0003g0018others(1): Show | 4 | HG00597.hp1 HG02132.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-10469_41-10468d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70525379 | ||||||
| chr2:70525566
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.41-10654C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70525566 | ||||||
| chr2:70525573
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0005g0291a0001c0001t0008g0134others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-10661C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70525573 | ||||||
| chr2:70525742
|
G | C | 36 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0002g0163others(33): Show | 36 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.41-10830C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70525742 | ||||||
| chr2:70526064
|
G | A | 3 | a0001c0001t0005g0072a0001c0001t0006g0279a0001c0001t0033g0103 | 3 | HG02572.hp1 NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.41-11152C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526064 | ||||||
| chr2:70526135
|
A | C | 1 | a0001c0002t0003g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.41-11223T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526135 | ||||||
| chr2:70526140
|
C | A | 1 | a0001c0001t0007g0109 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.41-11228G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526140 | ||||||
| chr2:70526369
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.41-11457G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526369 | ||||||
| chr2:70526463
|
C | T | 3 | a0001c0001t0005g0035a0001c0001t0005g0108a0001c0001t0014g0096 | 3 | HG01433.hp2 HG03516.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.41-11551G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526463 | ||||||
| chr2:70526464
|
G | A | 10 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-11552C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526464 | ||||||
| chr2:70526528
|
T | C | 10 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0004g0077others(7): Show | 10 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.41-11616A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526528 | ||||||
| chr2:70526621
|
G | A | 124 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(121): Show | 126 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.41-11709C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526621 | ||||||
| chr2:70526750
|
T | C | 124 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(121): Show | 126 | HG00140.hp1 HG00323.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.41-11838A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526750 | ||||||
| chr2:70526788
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.41-11876C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526788 | ||||||
| chr2:70526832
|
C | T | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-11920G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526832 | ||||||
| chr2:70526846
|
C | T | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.41-11934G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526846 | ||||||
| chr2:70526973
|
C | T | 6 | a0001c0001t0001g0137a0001c0001t0005g0291a0001c0001t0008g0134others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-12061G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70526973 | ||||||
| chr2:70527085
|
A | C | 1 | a0001c0002t0003g0037 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.41-12173T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70527085 | ||||||
| chr2:70527333
|
C | T | 6 | a0001c0001t0002g0201a0001c0001t0004g0142a0001c0001t0013g0141others(3): Show | 6 | HG01884.hp2 HG02976.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-12421G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70527333 | ||||||
| chr2:70527371
|
T | G | 1 | a0001c0002t0003g0037 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.41-12459A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70527371 | ||||||
| chr2:70527402
|
G | C | 9 | a0001c0001t0001g0337a0001c0001t0005g0072a0001c0001t0006g0279others(6): Show | 10 | HG01167.hp1 HG01891.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.41-12490C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70527402 | ||||||
| chr2:70527476
|
T | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0051a0001c0001t0001g0193others(4): Show | 8 | HG00544.hp1 HG02080.hp2 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.41-12564A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70527476 | ||||||
| chr2:70527564
|
T | C | 3 | a0001c0002t0003g0027a0001c0002t0003g0037a0001c0002t0003g0328 | 3 | HG00544.hp2 NA18955.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.41-12652A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70527564 | ||||||
| chr2:70527711
|
G | A | 6 | a0001c0001t0001g0137a0001c0001t0005g0291a0001c0001t0008g0134others(3): Show | 6 | HG01884.hp1 HG02559.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-12799C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70527711 | ||||||
| chr2:70528096
|
T | C | 4 | a0001c0005t0001g0177a0001c0005t0002g0176a0001c0005t0002g0274others(1): Show | 4 | HG01243.hp1 HG02055.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-13184A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528096 | ||||||
| chr2:70528137
|
T | A | 2 | a0001c0001t0005g0072a0001c0001t0006g0279 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.41-13225A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528137 | ||||||
| chr2:70528379
|
C | T | 3 | a0002c0003t0012g0104a0002c0003t0012g0133a0002c0003t0012g0250 | 3 | HG02109.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.41-13467G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528379 | ||||||
| chr2:70528386
|
G | A | 4 | a0001c0001t0014g0175a0001c0005t0001g0177a0001c0005t0002g0176others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.41-13474C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528386 | ||||||
| chr2:70528442
|
A | G | 1 | a0001c0005t0002g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.41-13530T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528442 | ||||||
| chr2:70528718
|
T | C | 3 | a0002c0003t0012g0104a0002c0003t0012g0133a0002c0003t0012g0250 | 3 | HG02109.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.41-13806A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528718 | ||||||
| chr2:70528800
|
C | A | 3 | a0001c0001t0001g0246a0001c0001t0021g0271a0001c0002t0015g0272 | 3 | HG02280.hp2 HG02615.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.41-13888G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528800 | ||||||
| chr2:70528863
|
A | G | 1 | a0001c0002t0015g0076 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.41-13951T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528863 | ||||||
| chr2:70528895
|
C | A | 1 | a0001c0001t0005g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.41-13983G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528895 | ||||||
| chr2:70528925
|
C | A | 91 | a0001c0001t0001g0010a0001c0001t0001g0106a0001c0001t0001g0107others(88): Show | 92 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.41-14013G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70528925 | ||||||
| chr2:70529159
|
C | G | 89 | a0001c0001t0001g0010a0001c0001t0001g0106a0001c0001t0001g0107others(86): Show | 90 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.41-14247G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529159 | ||||||
| chr2:70529204
|
A | C | 164 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(161): Show | 167 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.41-14292T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529204 | ||||||
| chr2:70529329
|
C | T | 5 | a0001c0001t0002g0201a0001c0001t0014g0175a0001c0005t0001g0177others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-14417G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529329 | ||||||
| chr2:70529466
|
A | G | 1 | a0001c0002t0003g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.41-14554T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529466 | ||||||
| chr2:70529549
|
T | C | 21 | a0001c0001t0001g0167a0001c0001t0001g0267a0001c0001t0002g0163others(18): Show | 21 | HG00558.hp1 HG00642.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.41-14637A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529549 | ||||||
| chr2:70529564
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.41-14652G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529564 | ||||||
| chr2:70529565
|
G | A | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0008g0079others(4): Show | 8 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-14653C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529565 | ||||||
| chr2:70529588
|
T | TC | 18 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0004g0077others(15): Show | 18 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-14677dupG | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529588 | ||||||
| chr2:70529593
|
C | CG | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0008g0079others(4): Show | 8 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-14682_41-14681i others(3): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529593 | ||||||
| chr2:70529593
|
CCG | C | 19 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.41-14683_41-14682d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529593 | ||||||
| chr2:70529595
|
G | C | 122 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0044others(119): Show | 125 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.41-14683C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529595 | ||||||
| chr2:70529595
|
G | T | 10 | a0001c0001t0004g0077a0001c0001t0004g0142a0001c0001t0013g0141others(7): Show | 10 | HG01884.hp2 HG02040.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.41-14683C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529595 | ||||||
| chr2:70529597
|
C | A | 4 | a0001c0001t0008g0098a0001c0001t0016g0099a0001c0001t0016g0100others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-14685G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529597 | ||||||
| chr2:70529598
|
C | A | 49 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0044others(46): Show | 51 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.41-14686G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529598 | ||||||
| chr2:70529619
|
T | C | 81 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0106others(78): Show | 82 | HG00558.hp1 HG00609.hp2 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.41-14707A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529619 | ||||||
| chr2:70529627
|
G | A | 4 | a0001c0001t0008g0098a0001c0001t0016g0099a0001c0001t0016g0100others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-14715C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529627 | ||||||
| chr2:70529644
|
C | T | 2 | a0001c0001t0005g0336a0001c0001t0017g0078 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.41-14732G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529644 | ||||||
| chr2:70529680
|
C | T | 1 | a0001c0002t0003g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.41-14768G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529680 | ||||||
| chr2:70529753
|
G | A | 2 | a0001c0001t0001g0337a0001c0001t0005g0278 | 2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.41-14841C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529753 | ||||||
| chr2:70529890
|
G | C | 1 | a0001c0002t0003g0037 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.41-14978C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529890 | ||||||
| chr2:70529943
|
C | A | 5 | a0001c0001t0002g0201a0001c0001t0014g0175a0001c0005t0001g0177others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-15031G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70529943 | ||||||
| chr2:70530226
|
A | G | 48 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0044others(45): Show | 50 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.41-15314T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530226 | ||||||
| chr2:70530302
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02165.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.41-15390G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530302 | ||||||
| chr2:70530308
|
C | G | 1 | a0001c0001t0002g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.41-15396G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530308 | ||||||
| chr2:70530309
|
C | T | 6 | a0001c0001t0001g0169a0001c0001t0001g0171a0001c0001t0001g0172others(3): Show | 6 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.41-15397G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530309 | ||||||
| chr2:70530414
|
A | G | 8 | a0001c0001t0004g0077a0001c0001t0004g0142a0001c0001t0013g0141others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.41-15502T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530414 | ||||||
| chr2:70530530
|
GA | G | 3 | a0001c0001t0004g0077a0001c0002t0015g0076a0001c0002t0015g0113 | 3 | HG02257.hp1 HG02451.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.41-15619delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530530 | ||||||
| chr2:70530550
|
T | C | 21 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(18): Show | 21 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.41-15638A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530550 | ||||||
| chr2:70530571
|
C | CTGGGCCA others(11): Show |
1 | a0002c0003t0012g0250 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.41-15677_41-15660d others(20): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530571 | ||||||
| chr2:70530571
|
CTGGGCCA others(11): Show |
C | 8 | a0001c0001t0004g0077a0001c0001t0004g0142a0001c0001t0013g0141others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.41-15677_41-15660d others(20): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530571 | ||||||
| chr2:70530713
|
C | G | 5 | a0001c0001t0001g0246a0001c0001t0005g0108a0001c0001t0005g0273others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-15801G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530713 | ||||||
| chr2:70530895
|
T | C | 1 | a0001c0001t0002g0007 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.41-15983A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530895 | ||||||
| chr2:70530968
|
C | G | 2 | a0001c0001t0005g0336a0001c0001t0017g0078 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.41-16056G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530968 | ||||||
| chr2:70530980
|
C | T | 5 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0030g0266others(2): Show | 5 | HG00735.hp1 HG02055.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-16068G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530980 | ||||||
| chr2:70530991
|
A | G | 67 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0106others(64): Show | 68 | HG00544.hp2 HG00558.hp1 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.41-16079T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70530991 | ||||||
| chr2:70531077
|
A | G | 2 | a0001c0001t0005g0336a0001c0001t0017g0078 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.41-16165T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531077 | ||||||
| chr2:70531123
|
G | A | 1 | a0001c0002t0003g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.41-16211C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531123 | ||||||
| chr2:70531128
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0004g0011a0001c0001t0004g0286others(3): Show | 6 | NA18747.hp2 NA18943.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.41-16216C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531128 | ||||||
| chr2:70531430
|
G | A | 20 | a0001c0001t0001g0167a0001c0001t0001g0267a0001c0001t0002g0163others(17): Show | 20 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.41-16518C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531430 | ||||||
| chr2:70531444
|
A | G | 3 | a0001c0001t0002g0207a0001c0001t0002g0208a0001c0001t0002g0209 | 3 | NA18940.hp2 NA18956.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.41-16532T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531444 | ||||||
| chr2:70531511
|
C | T | 5 | a0001c0001t0002g0201a0001c0001t0014g0175a0001c0005t0001g0177others(2): Show | 5 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.41-16599G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531511 | ||||||
| chr2:70531545
|
C | T | 8 | a0001c0001t0004g0077a0001c0001t0004g0142a0001c0001t0013g0141others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.41-16633G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531545 | ||||||
| chr2:70531720
|
G | A | 11 | a0001c0001t0001g0167a0001c0001t0001g0267a0001c0001t0002g0163others(8): Show | 11 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-16808C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531720 | ||||||
| chr2:70531812
|
T | C | 49 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0044others(46): Show | 51 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.41-16900A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531812 | ||||||
| chr2:70531832
|
C | A | 11 | a0001c0001t0001g0167a0001c0001t0001g0267a0001c0001t0002g0163others(8): Show | 11 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.41-16920G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531832 | ||||||
| chr2:70531935
|
C | A | 1 | a0001c0001t0004g0011 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.41-17023G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70531935 | ||||||
| chr2:70532013
|
T | C | 9 | a0001c0001t0004g0077a0001c0001t0004g0142a0001c0001t0013g0141others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-17101A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532013 | ||||||
| chr2:70532029
|
T | C | 139 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(136): Show | 142 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.41-17117A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532029 | ||||||
| chr2:70532078
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0006g0243a0001c0002t0003g0242 | 3 | HG00621.hp2 NA18950.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.41-17166A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532078 | ||||||
| chr2:70532170
|
T | G | 30 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(27): Show | 30 | HG00544.hp2 HG01243.hp1 HG01358.hp2 others(27): Show |
intron_variant | MODIFIER | c.41-17258A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532170 | ||||||
| chr2:70532295
|
C | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.41-17383G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532295 | ||||||
| chr2:70532310
|
A | T | 3 | a0001c0001t0006g0262a0001c0002t0003g0033a0001c0002t0003g0034 | 3 | HG03688.hp2 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.41-17398T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532310 | ||||||
| chr2:70532359
|
C | A | 62 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0106others(59): Show | 63 | HG00544.hp2 HG00558.hp1 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.41-17447G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532359 | ||||||
| chr2:70532365
|
A | G | 24 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(21): Show | 24 | HG00544.hp2 HG01891.hp2 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-17453T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532365 | ||||||
| chr2:70532368
|
A | T | 9 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337others(6): Show | 9 | HG02451.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-17456T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532368 | ||||||
| chr2:70532429
|
A | G | 1 | a0001c0002t0003g0181 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.41-17517T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532429 | ||||||
| chr2:70532529
|
C | T | 17 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(14): Show | 17 | HG00544.hp2 HG02559.hp2 HG03017.hp2 others(14): Show |
intron_variant | MODIFIER | c.41-17617G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532529 | ||||||
| chr2:70532550
|
G | A | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.41-17638C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532550 | ||||||
| chr2:70532640
|
C | T | 1 | a0001c0005t0002g0274 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.41-17728G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532640 | ||||||
| chr2:70532684
|
C | T | 19 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337others(16): Show | 20 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.41-17772G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532684 | ||||||
| chr2:70532689
|
C | T | 20 | a0001c0001t0001g0167a0001c0001t0001g0267a0001c0001t0002g0163others(17): Show | 20 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.41-17777G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532689 | ||||||
| chr2:70532753
|
G | A | 19 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337others(16): Show | 20 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.41-17841C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532753 | ||||||
| chr2:70532758
|
A | G | 4 | a0001c0001t0008g0098a0001c0001t0016g0099a0001c0001t0016g0100others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-17846T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532758 | ||||||
| chr2:70532774
|
A | G | 24 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(21): Show | 24 | HG00544.hp2 HG01891.hp2 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-17862T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532774 | ||||||
| chr2:70532865
|
C | CT | 18 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337others(15): Show | 18 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.41-17954dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532865 | ||||||
| chr2:70532865
|
CT | C | 173 | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0068others(170): Show | 176 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.41-17954delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532865 | ||||||
| chr2:70532865
|
CTT | C | 53 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0174others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.41-17955_41-17954d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532865 | ||||||
| chr2:70532868
|
T | TTC | 24 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(21): Show | 24 | HG00544.hp2 HG01891.hp2 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.41-17957_41-17956i others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532868 | ||||||
| chr2:70532931
|
G | A | 13 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.41-18019C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70532931 | ||||||
| chr2:70533036
|
A | AT | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(22): Show | 25 | HG00544.hp2 HG01891.hp2 HG02559.hp2 others(22): Show |
intron_variant | MODIFIER | c.41-18125dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533036 | ||||||
| chr2:70533072
|
T | G | 25 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(22): Show | 25 | HG00544.hp2 HG01358.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.41-18160A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533072 | ||||||
| chr2:70533156
|
C | T | 9 | a0001c0001t0004g0077a0001c0001t0004g0142a0001c0001t0013g0141others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-18244G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533156 | ||||||
| chr2:70533160
|
C | T | 5 | a0001c0001t0001g0246a0001c0001t0005g0108a0001c0001t0005g0273others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-18248G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533160 | ||||||
| chr2:70533235
|
C | G | 5 | a0001c0001t0001g0246a0001c0001t0005g0108a0001c0001t0005g0273others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-18323G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533235 | ||||||
| chr2:70533236
|
C | T | 1 | a0001c0001t0008g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.41-18324G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533236 | ||||||
| chr2:70533293
|
T | C | 1 | a0001c0001t0001g0040 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.41-18381A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533293 | ||||||
| chr2:70533335
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.41-18423G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533335 | ||||||
| chr2:70533359
|
G | T | 20 | a0001c0001t0001g0167a0001c0001t0001g0267a0001c0001t0002g0163others(17): Show | 20 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.41-18447C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533359 | ||||||
| chr2:70533527
|
T | C | 4 | a0001c0001t0008g0098a0001c0001t0016g0099a0001c0001t0016g0100others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.41-18615A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533527 | ||||||
| chr2:70533606
|
AGGATAGG others(5): Show |
A | 34 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(31): Show | 34 | HG00544.hp2 HG00558.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.41-18706_41-18695d others(14): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533606 | ||||||
| chr2:70533612
|
G | A | 47 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0044others(44): Show | 49 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.41-18700C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533612 | ||||||
| chr2:70533719
|
G | A | 2 | a0001c0001t0005g0336a0001c0001t0017g0078 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.41-18807C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533719 | ||||||
| chr2:70533840
|
T | G | 5 | a0001c0001t0001g0246a0001c0001t0005g0108a0001c0001t0005g0273others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.41-18928A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533840 | ||||||
| chr2:70533847
|
A | G | 9 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337others(6): Show | 9 | HG02451.hp2 HG02572.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.41-18935T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533847 | ||||||
| chr2:70533870
|
A | AT | 37 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(34): Show | 37 | HG00544.hp2 HG00558.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.41-18959dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533870 | ||||||
| chr2:70533942
|
A | G | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0008g0079others(4): Show | 8 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.41-19030T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533942 | ||||||
| chr2:70533979
|
GA | G | 14 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337others(11): Show | 15 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.41-19068delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533979 | ||||||
| chr2:70533981
|
A | G | 2 | a0001c0001t0006g0097a0001c0002t0003g0094 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.41-19069T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70533981 | ||||||
| chr2:70534139
|
A | G | 46 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0137others(43): Show | 47 | HG00544.hp2 HG00558.hp1 HG01070.hp2 others(44): Show |
intron_variant | MODIFIER | c.41-19227T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534139 | ||||||
| chr2:70534396
|
G | A | 2 | a0001c0001t0018g0329a0001c0002t0003g0330 | 2 | HG02040.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.40+19332C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534396 | ||||||
| chr2:70534421
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.40+19307C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534421 | ||||||
| chr2:70534472
|
G | A | 1 | a0001c0001t0007g0331 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.40+19256C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534472 | ||||||
| chr2:70534472
|
G | T | 13 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+19256C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534472 | ||||||
| chr2:70534566
|
C | A | 1 | a0001c0001t0014g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.40+19162G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534566 | ||||||
| chr2:70534673
|
GA | G | 4 | a0001c0001t0008g0098a0001c0001t0016g0099a0001c0001t0016g0100others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+19054delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534673 | ||||||
| chr2:70534703
|
T | TATG | 79 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(76): Show | 80 | HG00544.hp2 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.40+19024_40+19025i others(5): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534703 | ||||||
| chr2:70534880
|
C | T | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02165.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.40+18848G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534880 | ||||||
| chr2:70534894
|
C | G | 4 | a0001c0001t0005g0108a0001c0001t0005g0273a0001c0001t0021g0271others(1): Show | 4 | HG02280.hp2 HG03139.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+18834G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534894 | ||||||
| chr2:70534927
|
A | C | 1 | a0001c0002t0003g0202 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.40+18801T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534927 | ||||||
| chr2:70534951
|
C | T | 3 | a0001c0001t0013g0260a0001c0001t0013g0261a0001c0001t0017g0004 | 4 | HG02895.hp2 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+18777G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70534951 | ||||||
| chr2:70535039
|
G | GT | 114 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(111): Show | 115 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.40+18688dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70535039 | ||||||
| chr2:70535218
|
A | G | 26 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(23): Show | 27 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.40+18510T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70535218 | ||||||
| chr2:70535219
|
AG | A | 91 | a0001c0001t0001g0010a0001c0001t0001g0106a0001c0001t0001g0107others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.40+18508delC | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70535219 | ||||||
| chr2:70535369
|
C | T | 117 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(114): Show | 118 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.40+18359G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70535369 | ||||||
| chr2:70535478
|
C | A | 32 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0137others(29): Show | 32 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.40+18250G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70535478 | ||||||
| chr2:70535614
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0002g0180 | 2 | HG00140.hp2 HG00323.hp1 |
intron_variant | MODIFIER | c.40+18114T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70535614 | ||||||
| chr2:70535773
|
G | A | 13 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+17955C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70535773 | ||||||
| chr2:70536018
|
A | G | 1 | a0001c0001t0005g0278 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.40+17710T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536018 | ||||||
| chr2:70536075
|
T | C | 4 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0002t0003g0145others(1): Show | 4 | HG02165.hp2 NA18967.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+17653A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536075 | ||||||
| chr2:70536473
|
T | A | 1 | a0001c0001t0001g0337 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.40+17255A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536473 | ||||||
| chr2:70536750
|
T | C | 116 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.40+16978A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536750 | ||||||
| chr2:70536760
|
C | A | 2 | a0001c0001t0002g0323a0001c0001t0006g0324 | 2 | HG00639.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.40+16968G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536760 | ||||||
| chr2:70536922
|
T | G | 1 | a0001c0001t0017g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40+16806A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536922 | ||||||
| chr2:70536980
|
TTTTTTC | T | 23 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0002g0201others(20): Show | 23 | HG00609.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+16742_40+16747d others(8): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536980 | ||||||
| chr2:70536998
|
C | CT | 6 | a0001c0001t0001g0293a0001c0001t0007g0294a0001c0001t0033g0103others(3): Show | 6 | HG00408.hp2 HG02572.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+16729dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536998 | ||||||
| chr2:70536998
|
C | CTT | 67 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(64): Show | 69 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.40+16728_40+16729d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536998 | ||||||
| chr2:70536998
|
CT | C | 63 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(60): Show | 64 | HG00558.hp1 HG00733.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.40+16729delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70536998 | ||||||
| chr2:70537050
|
C | T | 1 | a0001c0001t0022g0074 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.40+16678G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537050 | ||||||
| chr2:70537119
|
TG | T | 17 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(14): Show | 17 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.40+16608delC | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537119 | ||||||
| chr2:70537262
|
C | T | 1 | a0001c0001t0027g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.40+16466G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537262 | ||||||
| chr2:70537456
|
T | C | 1 | a0001c0001t0017g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40+16272A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537456 | ||||||
| chr2:70537479
|
C | G | 116 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.40+16249G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537479 | ||||||
| chr2:70537489
|
C | T | 1 | a0001c0002t0003g0145 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.40+16239G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537489 | ||||||
| chr2:70537556
|
C | A | 173 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(170): Show | 176 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.40+16172G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537556 | ||||||
| chr2:70537644
|
C | A | 17 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0066others(14): Show | 17 | HG00642.hp1 HG00738.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.40+16084G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537644 | ||||||
| chr2:70537681
|
G | C | 2 | a0001c0001t0033g0103a0002c0003t0001g0102 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.40+16047C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537681 | ||||||
| chr2:70537853
|
C | T | 18 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(15): Show | 18 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.40+15875G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537853 | ||||||
| chr2:70537924
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.40+15804A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70537924 | ||||||
| chr2:70538185
|
C | A | 4 | a0001c0001t0006g0248a0001c0001t0008g0249a0001c0002t0003g0247others(1): Show | 4 | HG02622.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+15543G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538185 | ||||||
| chr2:70538230
|
G | A | 2 | a0001c0001t0005g0336a0001c0001t0017g0078 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.40+15498C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538230 | ||||||
| chr2:70538243
|
G | C | 67 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(64): Show | 69 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.40+15485C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538243 | ||||||
| chr2:70538436
|
G | A | 51 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0293others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.40+15292C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538436 | ||||||
| chr2:70538479
|
G | A | 3 | a0001c0001t0002g0121a0001c0001t0002g0123a0001c0001t0028g0122 | 3 | HG02809.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.40+15249C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538479 | ||||||
| chr2:70538498
|
A | G | 36 | a0001c0001t0001g0003a0001c0001t0001g0069a0001c0001t0001g0070others(33): Show | 37 | HG00140.hp2 HG00323.hp1 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.40+15230T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538498 | ||||||
| chr2:70538581
|
T | C | 51 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0293others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.40+15147A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538581 | ||||||
| chr2:70538766
|
A | C | 1 | a0002c0003t0012g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.40+14962T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538766 | ||||||
| chr2:70538931
|
T | G | 1 | a0001c0002t0003g0251 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.40+14797A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538931 | ||||||
| chr2:70538950
|
C | G | 13 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(10): Show | 13 | HG00733.hp1 HG01069.hp2 HG01070.hp1 others(10): Show |
intron_variant | MODIFIER | c.40+14778G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70538950 | ||||||
| chr2:70539023
|
A | G | 31 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0137others(28): Show | 31 | HG00558.hp1 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.40+14705T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539023 | ||||||
| chr2:70539033
|
T | G | 186 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(183): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.40+14695A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539033 | ||||||
| chr2:70539121
|
T | C | 1 | a0001c0001t0017g0078 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.40+14607A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539121 | ||||||
| chr2:70539149
|
C | T | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.40+14579G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539149 | ||||||
| chr2:70539174
|
A | C | 1 | a0001c0001t0008g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.40+14554T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539174 | ||||||
| chr2:70539256
|
C | A | 65 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(62): Show | 67 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.40+14472G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539256 | ||||||
| chr2:70539261
|
C | G | 1 | a0003c0004t0010g0178 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.40+14467G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539261 | ||||||
| chr2:70539272
|
G | A | 114 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(111): Show | 115 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.40+14456C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539272 | ||||||
| chr2:70539321
|
C | G | 1 | a0001c0001t0001g0044 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.40+14407G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539321 | ||||||
| chr2:70539330
|
G | A | 5 | a0001c0001t0004g0142a0001c0001t0013g0141a0001c0001t0014g0138others(2): Show | 5 | HG01884.hp2 HG02976.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+14398C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539330 | ||||||
| chr2:70539350
|
C | T | 1 | a0001c0001t0025g0292 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.40+14378G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539350 | ||||||
| chr2:70539396
|
G | GA | 182 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(179): Show | 185 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.40+14331dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539396 | ||||||
| chr2:70539507
|
T | G | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.40+14221A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539507 | ||||||
| chr2:70539580
|
A | G | 186 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(183): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.40+14148T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539580 | ||||||
| chr2:70539605
|
C | T | 2 | a0001c0001t0033g0103a0002c0003t0001g0102 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.40+14123G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539605 | ||||||
| chr2:70539608
|
T | C | 186 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(183): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.40+14120A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539608 | ||||||
| chr2:70539871
|
G | A | 3 | a0001c0001t0001g0325a0001c0001t0004g0282a0001c0002t0038g0284 | 3 | HG00621.hp1 NA18963.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.40+13857C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539871 | ||||||
| chr2:70539893
|
C | T | 186 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(183): Show | 189 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.40+13835G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539893 | ||||||
| chr2:70539919
|
C | A | 1 | a0001c0001t0016g0101 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.40+13809G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70539919 | ||||||
| chr2:70540034
|
C | T | 4 | a0001c0001t0014g0175a0001c0005t0001g0177a0001c0005t0002g0176others(1): Show | 4 | HG01243.hp1 HG01884.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+13694G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540034 | ||||||
| chr2:70540043
|
T | C | 1 | a0001c0001t0002g0270 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.40+13685A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540043 | ||||||
| chr2:70540148
|
C | T | 5 | a0001c0001t0001g0337a0001c0001t0008g0098a0001c0001t0016g0099others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.40+13580G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540148 | ||||||
| chr2:70540285
|
C | G | 1 | a0001c0001t0005g0291 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.40+13443G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540285 | ||||||
| chr2:70540316
|
G | C | 1 | a0001c0001t0023g0065 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.40+13412C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540316 | ||||||
| chr2:70540482
|
T | C | 2 | a0003c0004t0010g0252a0003c0004t0010g0253 | 2 | NA18969.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.40+13246A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540482 | ||||||
| chr2:70540721
|
A | G | 68 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(65): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.40+13007T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540721 | ||||||
| chr2:70540724
|
C | A | 2 | a0001c0001t0001g0043a0001c0002t0003g0042 | 2 | NA18967.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.40+13004G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70540724 | ||||||
| chr2:70541030
|
C | T | 114 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(111): Show | 115 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.40+12698G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541030 | ||||||
| chr2:70541031
|
A | G | 50 | a0001c0001t0001g0010a0001c0001t0001g0160a0001c0001t0001g0293others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.40+12697T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541031 | ||||||
| chr2:70541048
|
A | C | 68 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(65): Show | 70 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.40+12680T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541048 | ||||||
| chr2:70541059
|
A | G | 14 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0043others(11): Show | 14 | HG00544.hp2 HG01358.hp2 HG03017.hp2 others(11): Show |
intron_variant | MODIFIER | c.40+12669T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541059 | ||||||
| chr2:70541607
|
T | C | 1 | a0001c0001t0001g0066 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.40+12121A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541607 | ||||||
| chr2:70541625
|
G | A | 1 | a0001c0001t0007g0254 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.40+12103C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541625 | ||||||
| chr2:70541648
|
C | T | 1 | a0001c0001t0026g0126 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.40+12080G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541648 | ||||||
| chr2:70541651
|
T | C | 183 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(180): Show | 186 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.40+12077A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541651 | ||||||
| chr2:70541790
|
A | C | 183 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(180): Show | 186 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.40+11938T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541790 | ||||||
| chr2:70541808
|
A | G | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40+11920T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70541808 | ||||||
| chr2:70542111
|
C | T | 1 | a0001c0001t0014g0124 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.40+11617G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542111 | ||||||
| chr2:70542184
|
G | A | 1 | a0003c0004t0010g0255 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.40+11544C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542184 | ||||||
| chr2:70542196
|
T | C | 71 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(68): Show | 73 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.40+11532A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542196 | ||||||
| chr2:70542233
|
A | C | 113 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(110): Show | 114 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.40+11495T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542233 | ||||||
| chr2:70542331
|
G | C | 1 | a0001c0001t0005g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.40+11397C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542331 | ||||||
| chr2:70542463
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.40+11265A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542463 | ||||||
| chr2:70542465
|
C | T | 109 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0088others(106): Show | 110 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.40+11263G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542465 | ||||||
| chr2:70542596
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40+11132G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542596 | ||||||
| chr2:70542868
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.40+10860G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542868 | ||||||
| chr2:70542959
|
C | T | 14 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0150others(11): Show | 14 | HG00423.hp1 HG02132.hp1 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.40+10769G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542959 | ||||||
| chr2:70542964
|
G | A | 1 | a0001c0002t0011g0257 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.40+10764C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542964 | ||||||
| chr2:70542976
|
G | A | 1 | a0001c0001t0013g0095 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.40+10752C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70542976 | ||||||
| chr2:70543027
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02818.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40+10701G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543027 | ||||||
| chr2:70543133
|
A | G | 1 | a0001c0001t0002g0007 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.40+10595T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543133 | ||||||
| chr2:70543194
|
T | C | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0008g0079others(4): Show | 8 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.40+10534A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543194 | ||||||
| chr2:70543207
|
T | C | 1 | a0001c0001t0004g0258 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.40+10521A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543207 | ||||||
| chr2:70543267
|
C | G | 3 | a0001c0001t0005g0035a0001c0001t0005g0036a0001c0001t0014g0096 | 3 | HG01433.hp2 HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.40+10461G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543267 | ||||||
| chr2:70543353
|
C | T | 2 | a0001c0002t0003g0008a0001c0002t0003g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.40+10375G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543353 | ||||||
| chr2:70543374
|
C | T | 171 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(168): Show | 174 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.40+10354G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543374 | ||||||
| chr2:70543513
|
G | A | 1 | a0001c0005t0021g0136 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.40+10215C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543513 | ||||||
| chr2:70543525
|
C | CA | 6 | a0001c0001t0001g0277a0001c0001t0006g0259a0001c0001t0006g0262others(3): Show | 6 | HG00735.hp1 HG03579.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+10202dupT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543525 | ||||||
| chr2:70543525
|
CAA | C | 154 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(151): Show | 156 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.40+10201_40+10202d others(4): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543525 | ||||||
| chr2:70543758
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.40+9970G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70543758 | ||||||
| chr2:70544070
|
A | T | 3 | a0001c0001t0005g0291a0001c0001t0024g0289a0001c0002t0011g0290 | 3 | HG02818.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.40+9658T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544070 | ||||||
| chr2:70544088
|
T | C | 1 | a0001c0001t0027g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.40+9640A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544088 | ||||||
| chr2:70544120
|
T | A | 3 | a0001c0001t0005g0273a0001c0001t0021g0271a0001c0002t0015g0272 | 3 | HG02280.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.40+9608A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544120 | ||||||
| chr2:70544130
|
T | C | 1 | a0002c0003t0012g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.40+9598A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544130 | ||||||
| chr2:70544170
|
G | A | 146 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(143): Show | 149 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.40+9558C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544170 | ||||||
| chr2:70544188
|
C | T | 3 | a0001c0001t0001g0337a0001c0001t0033g0103a0002c0003t0001g0102 | 3 | HG02572.hp1 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.40+9540G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544188 | ||||||
| chr2:70544189
|
G | A | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.40+9539C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544189 | ||||||
| chr2:70544319
|
A | C | 1 | a0001c0005t0021g0136 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.40+9409T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544319 | ||||||
| chr2:70544373
|
A | C | 12 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0005g0072others(9): Show | 13 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.40+9355T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544373 | ||||||
| chr2:70544376
|
GTTA | G | 3 | a0001c0001t0005g0278a0001c0001t0005g0280a0001c0001t0006g0279 | 3 | HG02451.hp2 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+9349_40+9351del others(3): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544376 | ||||||
| chr2:70544389
|
A | T | 126 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(123): Show | 128 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.40+9339T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544389 | ||||||
| chr2:70544543
|
A | G | 1 | a0001c0001t0027g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.40+9185T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544543 | ||||||
| chr2:70544937
|
G | A | 6 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0002g0014others(3): Show | 6 | HG02165.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+8791C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70544937 | ||||||
| chr2:70545050
|
T | C | 2 | a0001c0001t0013g0260a0001c0001t0013g0261 | 2 | HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.40+8678A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545050 | ||||||
| chr2:70545213
|
G | A | 1 | a0001c0001t0005g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.40+8515C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545213 | ||||||
| chr2:70545248
|
C | A | 9 | a0001c0001t0004g0077a0001c0001t0005g0278a0001c0001t0005g0280others(6): Show | 9 | HG02451.hp1 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+8480G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545248 | ||||||
| chr2:70545267
|
AAAGAAG | A | 7 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337others(4): Show | 7 | HG02572.hp1 HG02622.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.40+8455_40+8460del others(6): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545267 | ||||||
| chr2:70545323
|
C | T | 15 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(12): Show | 15 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.40+8405G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545323 | ||||||
| chr2:70545408
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0281a0001c0001t0004g0017others(6): Show | 9 | HG00438.hp1 HG00597.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.40+8320G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545408 | ||||||
| chr2:70545571
|
G | T | 2 | a0001c0001t0013g0095a0001c0002t0003g0094 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.40+8157C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545571 | ||||||
| chr2:70545588
|
A | G | 59 | a0001c0001t0001g0010a0001c0001t0001g0293a0001c0001t0001g0295others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.40+8140T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545588 | ||||||
| chr2:70545756
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.40+7972G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545756 | ||||||
| chr2:70545947
|
G | A | 1 | a0001c0001t0005g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.40+7781C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70545947 | ||||||
| chr2:70546023
|
G | T | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337 | 3 | HG02818.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40+7705C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546023 | ||||||
| chr2:70546248
|
C | CACTGTAC others(12): Show |
160 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(157): Show | 163 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.40+7479_40+7480ins others(19): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546248 | ||||||
| chr2:70546397
|
C | A | 3 | a0001c0001t0005g0278a0001c0001t0005g0280a0001c0001t0006g0279 | 3 | HG02451.hp2 HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.40+7331G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546397 | ||||||
| chr2:70546397
|
C | T | 1 | a0001c0001t0008g0134 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.40+7331G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546397 | ||||||
| chr2:70546415
|
A | G | 3 | a0001c0001t0005g0273a0001c0001t0021g0271a0001c0002t0015g0272 | 3 | HG02280.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.40+7313T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546415 | ||||||
| chr2:70546439
|
C | T | 22 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 23 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+7289G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546439 | ||||||
| chr2:70546459
|
C | A | 3 | a0001c0001t0005g0273a0001c0001t0021g0271a0001c0002t0015g0272 | 3 | HG02280.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.40+7269G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546459 | ||||||
| chr2:70546459
|
C | T | 9 | a0001c0001t0004g0077a0001c0001t0005g0278a0001c0001t0005g0280others(6): Show | 9 | HG02451.hp1 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+7269G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546459 | ||||||
| chr2:70546483
|
C | A | 59 | a0001c0001t0001g0010a0001c0001t0001g0293a0001c0001t0001g0295others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.40+7245G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546483 | ||||||
| chr2:70546561
|
C | T | 1 | a0001c0001t0027g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.40+7167G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546561 | ||||||
| chr2:70546653
|
CT | C | 24 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(21): Show | 25 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.40+7074delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546653 | ||||||
| chr2:70546662
|
T | C | 4 | a0001c0001t0008g0098a0001c0001t0016g0099a0001c0001t0016g0100others(1): Show | 4 | HG02572.hp2 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.40+7066A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546662 | ||||||
| chr2:70546772
|
C | G | 22 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 23 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+6956G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546772 | ||||||
| chr2:70546786
|
C | T | 3 | a0001c0001t0005g0273a0001c0001t0021g0271a0001c0002t0015g0272 | 3 | HG02280.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.40+6942G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70546786 | ||||||
| chr2:70547069
|
T | C | 1 | a0001c0001t0006g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.40+6659A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547069 | ||||||
| chr2:70547103
|
G | T | 2 | a0001c0001t0001g0132a0002c0003t0012g0133 | 2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.40+6625C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547103 | ||||||
| chr2:70547106
|
G | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337 | 3 | HG02818.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40+6622C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547106 | ||||||
| chr2:70547110
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.40+6618A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547110 | ||||||
| chr2:70547116
|
C | T | 23 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(20): Show | 24 | HG00609.hp2 HG01081.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+6612G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547116 | ||||||
| chr2:70547135
|
G | A | 2 | a0001c0001t0033g0103a0002c0003t0001g0102 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.40+6593C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547135 | ||||||
| chr2:70547163
|
T | A | 22 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 23 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+6565A>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547163 | ||||||
| chr2:70547322
|
C | T | 22 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 23 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+6406G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547322 | ||||||
| chr2:70547432
|
A | G | 6 | a0001c0001t0001g0127a0001c0001t0001g0275a0001c0001t0004g0130others(3): Show | 6 | HG02040.hp2 NA18948.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+6296T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547432 | ||||||
| chr2:70547498
|
G | A | 22 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(19): Show | 23 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+6230C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547498 | ||||||
| chr2:70547545
|
GA | G | 234 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0116others(231): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.40+6182delT | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547545 | ||||||
| chr2:70547545
|
GAA | G | 20 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(17): Show | 21 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.40+6181_40+6182del others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547545 | ||||||
| chr2:70547563
|
T | C | 169 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(166): Show | 172 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.40+6165A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547563 | ||||||
| chr2:70547564
|
G | A | 1 | a0001c0001t0027g0112 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.40+6164C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547564 | ||||||
| chr2:70547662
|
G | C | 4 | a0001c0001t0005g0072a0001c0001t0005g0336a0001c0001t0033g0103others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.40+6066C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547662 | ||||||
| chr2:70547753
|
T | C | 8 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+5975A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547753 | ||||||
| chr2:70547759
|
ACTATATA others(2): Show |
A | 136 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(133): Show | 138 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.40+5960_40+5968del others(9): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547759 | ||||||
| chr2:70547785
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.40+5943C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547785 | ||||||
| chr2:70547787
|
A | G | 24 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0281others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.40+5941T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547787 | ||||||
| chr2:70547844
|
G | GAT | 23 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0281others(20): Show | 23 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.40+5882_40+5883dup others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547844 | ||||||
| chr2:70547862
|
T | G | 142 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(139): Show | 144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.40+5866A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547862 | ||||||
| chr2:70547896
|
A | G | 138 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(135): Show | 140 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.40+5832T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547896 | ||||||
| chr2:70547952
|
C | A | 15 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(12): Show | 16 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.40+5776G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547952 | ||||||
| chr2:70547953
|
A | G | 153 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(150): Show | 156 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.40+5775T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70547953 | ||||||
| chr2:70548048
|
T | C | 1 | a0001c0002t0003g0071 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.40+5680A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548048 | ||||||
| chr2:70548062
|
A | AT | 15 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(12): Show | 16 | HG01081.hp1 HG01109.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.40+5665dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548062 | ||||||
| chr2:70548094
|
A | C | 3 | a0001c0001t0005g0273a0001c0001t0021g0271a0001c0002t0015g0272 | 3 | HG02280.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.40+5634T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548094 | ||||||
| chr2:70548105
|
T | C | 6 | a0001c0001t0005g0072a0001c0001t0005g0336a0001c0001t0013g0095others(3): Show | 6 | HG02572.hp1 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.40+5623A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548105 | ||||||
| chr2:70548211
|
T | C | 1 | a0001c0001t0001g0267 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.40+5517A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548211 | ||||||
| chr2:70548234
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.40+5494C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548234 | ||||||
| chr2:70548371
|
A | G | 1 | a0001c0001t0002g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.40+5357T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548371 | ||||||
| chr2:70548393
|
C | T | 3 | a0001c0001t0005g0273a0001c0001t0021g0271a0001c0002t0015g0272 | 3 | HG02280.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.40+5335G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548393 | ||||||
| chr2:70548565
|
A | C | 1 | a0001c0001t0005g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40+5163T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548565 | ||||||
| chr2:70548568
|
GAAC | G | 9 | a0001c0001t0004g0077a0001c0001t0005g0278a0001c0001t0005g0280others(6): Show | 9 | HG02451.hp1 HG02451.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.40+5157_40+5159del others(3): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548568 | ||||||
| chr2:70548780
|
C | T | 8 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+4948G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548780 | ||||||
| chr2:70548870
|
G | GT | 14 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(11): Show | 14 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.40+4857dupA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70548870 | ||||||
| chr2:70549080
|
C | T | 1 | a0001c0001t0007g0119 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.40+4648G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549080 | ||||||
| chr2:70549138
|
A | C | 2 | a0001c0001t0033g0103a0002c0003t0001g0102 | 2 | HG02572.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.40+4590T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549138 | ||||||
| chr2:70549149
|
T | C | 8 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+4579A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549149 | ||||||
| chr2:70549252
|
T | C | 166 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(163): Show | 169 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.40+4476A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549252 | ||||||
| chr2:70549416
|
C | G | 6 | a0001c0001t0001g0116a0001c0001t0001g0118a0001c0001t0002g0117others(3): Show | 6 | HG02055.hp2 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.40+4312G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549416 | ||||||
| chr2:70549453
|
C | G | 9 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0005g0108others(6): Show | 10 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.40+4275G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549453 | ||||||
| chr2:70549545
|
G | A | 1 | a0001c0001t0001g0269 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.40+4183C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549545 | ||||||
| chr2:70549602
|
A | T | 1 | a0001c0001t0007g0015 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.40+4126T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549602 | ||||||
| chr2:70549655
|
G | A | 1 | a0001c0001t0005g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40+4073C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70549655 | ||||||
| chr2:70550121
|
C | T | 2 | a0001c0001t0021g0271a0001c0002t0015g0272 | 2 | HG02280.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.40+3607G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550121 | ||||||
| chr2:70550235
|
A | G | 1 | a0001c0002t0003g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.40+3493T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550235 | ||||||
| chr2:70550418
|
G | A | 85 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(82): Show | 87 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.40+3310C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550418 | ||||||
| chr2:70550427
|
TAA | T | 11 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(8): Show | 11 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+3299_40+3300del others(2): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550427 | ||||||
| chr2:70550430
|
A | T | 11 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(8): Show | 11 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+3298T>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550430 | ||||||
| chr2:70550564
|
T | C | 2 | a0001c0001t0013g0095a0001c0002t0003g0094 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.40+3164A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550564 | ||||||
| chr2:70550574
|
C | A | 148 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.40+3154G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550574 | ||||||
| chr2:70550663
|
A | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+3065T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550663 | ||||||
| chr2:70550698
|
C | T | 84 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(81): Show | 86 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.40+3030G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550698 | ||||||
| chr2:70550704
|
G | A | 1 | a0001c0001t0002g0270 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.40+3024C>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550704 | ||||||
| chr2:70550737
|
C | T | 1 | a0001c0001t0002g0014 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.40+2991G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550737 | ||||||
| chr2:70550745
|
C | T | 1 | a0001c0002t0038g0284 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.40+2983G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550745 | ||||||
| chr2:70550757
|
C | G | 148 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.40+2971G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550757 | ||||||
| chr2:70550882
|
G | C | 2 | a0001c0001t0013g0095a0001c0002t0003g0094 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.40+2846C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550882 | ||||||
| chr2:70550921
|
C | G | 1 | a0001c0002t0003g0111 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.40+2807G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550921 | ||||||
| chr2:70550954
|
G | T | 148 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.40+2774C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550954 | ||||||
| chr2:70550995
|
C | G | 1 | a0001c0002t0003g0110 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.40+2733G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70550995 | ||||||
| chr2:70551058
|
C | T | 148 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.40+2670G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551058 | ||||||
| chr2:70551071
|
A | AATG | 148 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(145): Show | 150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.40+2656_40+2657ins others(3): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551071 | ||||||
| chr2:70551073
|
C | T | 150 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(147): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.40+2655G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551073 | ||||||
| chr2:70551074
|
A | G | 150 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(147): Show | 152 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.40+2654T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551074 | ||||||
| chr2:70551098
|
A | C | 165 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0032others(162): Show | 168 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.40+2630T>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551098 | ||||||
| chr2:70551101
|
T | C | 7 | a0001c0001t0002g0083a0001c0001t0002g0084a0001c0001t0008g0079others(4): Show | 8 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.40+2627A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551101 | ||||||
| chr2:70551306
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337 | 3 | HG02818.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40+2422A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551306 | ||||||
| chr2:70551312
|
G | T | 1 | a0001c0001t0007g0013 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.40+2416C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551312 | ||||||
| chr2:70551384
|
C | T | 1 | a0001c0001t0005g0108 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.40+2344G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551384 | ||||||
| chr2:70551458
|
T | G | 11 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(8): Show | 11 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.40+2270A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551458 | ||||||
| chr2:70551478
|
A | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0088a0001c0001t0001g0089others(5): Show | 8 | HG01081.hp1 HG01175.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.40+2250T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551478 | ||||||
| chr2:70551495
|
G | C | 83 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(80): Show | 85 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.40+2233C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551495 | ||||||
| chr2:70551497
|
T | G | 83 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(80): Show | 85 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.40+2231A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551497 | ||||||
| chr2:70551517
|
A | G | 3 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0337 | 3 | HG02818.hp1 HG02895.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.40+2211T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551517 | ||||||
| chr2:70551615
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.40+2113A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551615 | ||||||
| chr2:70551645
|
G | C | 1 | a0001c0001t0014g0096 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.40+2083C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551645 | ||||||
| chr2:70551706
|
CT | C | 61 | a0001c0001t0001g0010a0001c0001t0001g0293a0001c0001t0001g0295others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.40+2021delA | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551706 | ||||||
| chr2:70551716
|
T | C | 2 | a0001c0001t0001g0277a0002c0003t0012g0105 | 2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.40+2012A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551716 | ||||||
| chr2:70551762
|
T | C | 83 | a0001c0001t0001g0010a0001c0001t0001g0277a0001c0001t0001g0293others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.40+1966A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551762 | ||||||
| chr2:70551796
|
C | T | 83 | a0001c0001t0001g0010a0001c0001t0001g0277a0001c0001t0001g0293others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.40+1932G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551796 | ||||||
| chr2:70551888
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.40+1840A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551888 | ||||||
| chr2:70551892
|
C | T | 1 | a0001c0001t0004g0283 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.40+1836G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551892 | ||||||
| chr2:70551923
|
G | C | 1 | a0001c0001t0001g0277 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.40+1805C>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70551923 | ||||||
| chr2:70552088
|
A | G | 1 | a0001c0001t0004g0282 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.40+1640T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552088 | ||||||
| chr2:70552194
|
T | TCCACAGG others(3): Show |
92 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(89): Show | 95 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.40+1533_40+1534ins others(10): Show |
TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552194 | ||||||
| chr2:70552390
|
T | C | 61 | a0001c0001t0001g0010a0001c0001t0001g0293a0001c0001t0001g0295others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.40+1338A>G | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552390 | ||||||
| chr2:70552463
|
C | A | 1 | a0001c0001t0002g0335 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.40+1265G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552463 | ||||||
| chr2:70552548
|
G | T | 5 | a0001c0001t0006g0097a0001c0001t0008g0098a0001c0001t0016g0099others(2): Show | 5 | HG02572.hp2 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.40+1180C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552548 | ||||||
| chr2:70552659
|
G | T | 66 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(63): Show | 67 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.40+1069C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552659 | ||||||
| chr2:70552663
|
C | T | 2 | a0001c0001t0013g0095a0001c0002t0003g0094 | 2 | HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.40+1065G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552663 | ||||||
| chr2:70552949
|
C | G | 87 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0039others(84): Show | 89 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.40+779G>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552949 | ||||||
| chr2:70552960
|
A | G | 1 | a0001c0002t0003g0012 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.40+768T>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552960 | ||||||
| chr2:70552967
|
C | A | 1 | a0001c0001t0005g0336 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.40+761G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70552967 | ||||||
| chr2:70553040
|
C | A | 1 | a0001c0001t0001g0337 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.40+688G>T | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70553040 | ||||||
| chr2:70553215
|
G | T | 2 | a0001c0001t0001g0010a0001c0001t0004g0011 | 2 | NA18747.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.40+513C>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70553215 | ||||||
| chr2:70553325
|
C | T | 2 | a0001c0002t0003g0008a0001c0002t0003g0009 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.40+403G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70553325 | ||||||
| chr2:70553468
|
T | G | 1 | a0001c0001t0005g0338 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.40+260A>C | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70553468 | ||||||
| chr2:70553541
|
C | T | 1 | a0001c0001t0002g0007 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.40+187G>A | TGFA | ENSG00000163235.16 | transcript | ENST00000295400.11 | protein_coding | 1/5 | chr2 | 70553541 |