| geneid | 7077 |
|---|---|
| ensemblid | ENSG00000035862.13 |
| hgncid | 11821 |
| symbol | TIMP2 |
| name | TIMP metallopeptidase inhibitor 2 |
| refseq_nuc | NM_003255.5 |
| refseq_prot | NP_003246.1 |
| ensembl_nuc | ENST00000262768.11 |
| ensembl_prot | ENSP00000262768.6 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 78852977 |
| end | 78925387 |
| strand | - |
| ver | v1.2 |
| region | chr17:78852977-78925387 |
| region5000 | chr17:78847977-78930387 |
| regionname0 | TIMP2_chr17_78852977_78925387 |
| regionname5000 | TIMP2_chr17_78847977_78930387 |
| 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 | 220 | 315 | 90 | 50 | 123 | 10 | 40 | 86 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0002 | 0/0 | 220 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| 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 | 1/0 | 663 | 259 | 80 | 40 | 95 | 8 | 35 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| c0002 | 0/1 | 663 | 54 | 9 | 9 | 28 | 2 | 5 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| c0003 | 0/0 | 663 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| c0004 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| c0005 | 0/0 | 663 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 2989 | 55 | 15 | 10 | 19 | 3 | 8 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0002 | 0/0 | 2989 | 51 | 9 | 8 | 26 | 0 | 8 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0003 | 0/0 | 2990 | 43 | 18 | 11 | 9 | 0 | 5 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0004 | 1/0 | 2990 | 22 | 6 | 7 | 6 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0005 | 0/0 | 2988 | 21 | 3 | 4 | 8 | 3 | 3 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0006 | 0/0 | 2988 | 17 | 4 | 2 | 8 | 1 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0007 | 0/0 | 2989 | 15 | 0 | 0 | 14 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0008 | 0/0 | 2988 | 9 | 0 | 0 | 7 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0009 | 0/0 | 2990 | 7 | 1 | 0 | 6 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0010 | 0/0 | 2988 | 4 | 3 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0011 | 0/0 | 2988 | 4 | 4 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0012 | 0/1 | 2990 | 4 | 1 | 0 | 0 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0013 | 0/0 | 2991 | 3 | 1 | 1 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0014 | 0/0 | 2990 | 3 | 0 | 0 | 1 | 2 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0015 | 0/0 | 2990 | 3 | 3 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0016 | 0/0 | 2989 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0017 | 0/0 | 2990 | 2 | 1 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0018 | 0/0 | 2990 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0019 | 0/0 | 2990 | 2 | 0 | 0 | 1 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0020 | 0/0 | 2989 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0021 | 0/0 | 2990 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0022 | 0/0 | 2990 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0023 | 0/0 | 2989 | 2 | 0 | 0 | 0 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0024 | 0/0 | 2989 | 2 | 0 | 2 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0025 | 0/0 | 2988 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0026 | 0/0 | 2988 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0027 | 0/0 | 2990 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0028 | 0/0 | 2990 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0029 | 0/0 | 2990 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0030 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0031 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0032 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0033 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0034 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0035 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0036 | 0/0 | 2990 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0037 | 0/0 | 2990 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0038 | 0/0 | 2990 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0039 | 0/0 | 2990 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0040 | 0/0 | 2990 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0041 | 0/0 | 2990 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0042 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0043 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0044 | 0/0 | 2989 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0045 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0046 | 0/0 | 2988 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0047 | 0/0 | 2988 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0048 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0049 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0050 | 0/0 | 2990 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0051 | 0/0 | 2990 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0052 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0053 | 0/0 | 2990 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0054 | 0/0 | 2990 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0055 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0056 | 0/0 | 2989 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0057 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| t0058 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| 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 | 0 | 2 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| 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 | 1/0 | 663 | 259 | 80 | 40 | 95 | 8 | 35 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002 | 0/1 | 663 | 54 | 9 | 9 | 28 | 2 | 5 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0004 | 0/0 | 663 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0005 | 0/0 | 663 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0002c0003 | 0/0 | 663 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3651 | 48 | 14 | 10 | 13 | 3 | 8 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0002 | 0/0 | 3651 | 50 | 9 | 8 | 25 | 0 | 8 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0003 | 0/0 | 3652 | 31 | 14 | 6 | 8 | 0 | 3 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0004 | 1/0 | 3652 | 18 | 6 | 6 | 3 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0005 | 0/0 | 3650 | 18 | 3 | 4 | 5 | 3 | 3 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0006 | 0/0 | 3650 | 16 | 4 | 2 | 7 | 1 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0007 | 0/0 | 3651 | 15 | 0 | 0 | 14 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0008 | 0/0 | 3650 | 9 | 0 | 0 | 7 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0009 | 0/0 | 3652 | 6 | 0 | 0 | 6 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0010 | 0/0 | 3650 | 4 | 3 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0011 | 0/0 | 3650 | 3 | 3 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0012 | 0/0 | 3652 | 2 | 0 | 0 | 0 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0013 | 0/0 | 3653 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0015 | 0/0 | 3652 | 3 | 3 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0017 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0018 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0019 | 0/0 | 3652 | 2 | 0 | 0 | 1 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0020 | 0/0 | 3651 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0021 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0022 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0023 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0026 | 0/0 | 3650 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0027 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0029 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0031 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0032 | 0/0 | 3651 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0033 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0035 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0037 | 0/0 | 3652 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0038 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0041 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0042 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0045 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0046 | 0/0 | 3650 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0048 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0049 | 0/0 | 3651 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0050 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0051 | 0/0 | 3652 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0052 | 0/0 | 3651 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0055 | 0/0 | 3651 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0057 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0001t0058 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0001 | 0/0 | 3651 | 7 | 1 | 0 | 6 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0002 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0003 | 0/0 | 3652 | 11 | 4 | 4 | 1 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0004 | 0/0 | 3652 | 3 | 0 | 1 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0005 | 0/0 | 3650 | 3 | 0 | 0 | 3 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0006 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0009 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0012 | 0/1 | 3652 | 2 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0013 | 0/0 | 3653 | 2 | 1 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0014 | 0/0 | 3652 | 3 | 0 | 0 | 1 | 2 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0016 | 0/0 | 3651 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0017 | 0/0 | 3652 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0023 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0024 | 0/0 | 3651 | 2 | 0 | 2 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0025 | 0/0 | 3650 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0028 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0030 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0034 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0036 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0039 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0040 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0043 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0044 | 0/0 | 3651 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0047 | 0/0 | 3650 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0053 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0054 | 0/0 | 3652 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0002t0056 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0004t0011 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0001c0005t0003 | 0/0 | 3652 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| a0002c0003t0004 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | copy fasta | chr17 | 78847977 | 78930387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0012g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0012g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0013g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0015g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0015g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0017g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0018g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0019g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0019g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0020g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0020g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0021g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0021g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0022g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0022g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0023g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0026g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0026g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0027g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0027g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0029g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0031g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0032g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0033g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0035g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0037g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0038g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0041g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0042g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0045g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0046g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0048g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0049g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0050g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0051g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0052g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0055g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0057g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0058g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0005g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0006g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0012g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0012g0206 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0013g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0013g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0014g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0014g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0014g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0016g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0016g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0017g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0023g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0024g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0024g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0025g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0025g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0028g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0030g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0034g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0036g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0039g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0040g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0043g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0044g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0047g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0053g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0054g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0056g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0004t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0005t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0002c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0205 | EUR | GBR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0248 | EUR | GBR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00323 | hp1 | a0001 | c0001 | t0031 | g0024 | EUR | FIN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0296 | EUR | FIN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00438 | hp2 | a0001 | c0001 | t0007 | g0036 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00544 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00558 | hp1 | a0001 | c0002 | t0028 | g0035 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00558 | hp2 | a0001 | c0002 | t0034 | g0155 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00609 | hp2 | a0001 | c0002 | t0005 | g0176 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00621 | hp1 | a0001 | c0002 | t0013 | g0260 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00639 | hp1 | a0001 | c0001 | t0051 | g0162 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00673 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0243 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0179 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0123 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0301 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01070 | hp2 | a0001 | c0002 | t0047 | g0128 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01071 | hp1 | a0001 | c0002 | t0044 | g0068 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01074 | hp2 | a0001 | c0001 | t0046 | g0108 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01081 | hp1 | a0001 | c0002 | t0003 | g0262 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0247 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0244 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0131 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0060 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0039 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01361 | hp1 | a0001 | c0001 | t0013 | g0214 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01433 | hp1 | a0001 | c0002 | t0024 | g0193 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01496 | hp1 | a0001 | c0002 | t0004 | g0052 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01516 | hp1 | a0001 | c0002 | t0014 | g0274 | EUR | IBS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0311 | EUR | IBS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01517 | hp2 | a0001 | c0002 | t0014 | g0285 | EUR | IBS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0147 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01891 | hp1 | a0001 | c0001 | t0017 | g0133 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01928 | hp1 | a0001 | c0002 | t0024 | g0227 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0303 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02004 | hp1 | a0001 | c0005 | t0003 | g0315 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0102 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02055 | hp1 | a0001 | c0002 | t0013 | g0253 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02074 | hp2 | a0001 | c0002 | t0016 | g0159 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02080 | hp1 | a0001 | c0001 | t0019 | g0095 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02080 | hp2 | a0001 | c0002 | t0056 | g0252 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0215 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0221 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0098 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0027 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0104 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02155 | hp2 | a0001 | c0002 | t0005 | g0269 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02165 | hp2 | a0002 | c0003 | t0004 | g0084 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02258 | hp1 | a0001 | c0001 | t0055 | g0270 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0231 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02280 | hp2 | a0001 | c0001 | t0038 | g0124 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0070 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0135 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02451 | hp1 | a0001 | c0001 | t0015 | g0169 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02451 | hp2 | a0001 | c0001 | t0032 | g0016 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02523 | hp2 | a0001 | c0002 | t0006 | g0154 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0140 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0114 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02622 | hp1 | a0001 | c0001 | t0035 | g0067 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02630 | hp1 | a0001 | c0001 | t0027 | g0172 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02630 | hp2 | a0001 | c0001 | t0015 | g0185 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02647 | hp1 | a0001 | c0001 | t0022 | g0183 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0050 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0242 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0275 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0145 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0047 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0041 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0111 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02735 | hp2 | a0001 | c0001 | t0012 | g0297 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0313 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02738 | hp2 | a0001 | c0001 | t0019 | g0092 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0049 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0266 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02965 | hp1 | a0001 | c0001 | t0041 | g0046 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02965 | hp2 | a0001 | c0004 | t0011 | g0281 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02970 | hp1 | a0001 | c0001 | t0029 | g0033 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0078 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02976 | hp2 | a0001 | c0002 | t0003 | g0308 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03017 | hp1 | a0001 | c0001 | t0057 | g0204 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0010 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0289 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0283 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0195 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0037 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03225 | hp1 | a0001 | c0001 | t0052 | g0163 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03225 | hp2 | a0001 | c0001 | t0048 | g0043 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0265 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0312 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0257 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0165 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0170 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0017 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03491 | hp1 | a0001 | c0001 | t0037 | g0132 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0280 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0217 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03579 | hp1 | a0001 | c0001 | t0015 | g0168 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03654 | hp2 | a0001 | c0002 | t0023 | g0264 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0126 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0201 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03704 | hp2 | a0001 | c0001 | t0006 | g0110 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0038 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03834 | hp2 | a0001 | c0002 | t0017 | g0069 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0116 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0053 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04115 | hp2 | a0001 | c0001 | t0012 | g0295 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0294 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04228 | hp1 | a0001 | c0002 | t0054 | g0276 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18522 | hp2 | a0001 | c0001 | t0026 | g0290 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | CHB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0306 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0310 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0088 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18945 | hp2 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0175 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18947 | hp2 | a0001 | c0001 | t0009 | g0029 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18952 | hp1 | a0001 | c0001 | t0009 | g0008 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18952 | hp2 | a0001 | c0002 | t0003 | g0255 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0256 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0002 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18963 | hp2 | a0001 | c0002 | t0043 | g0117 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18964 | hp2 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18966 | hp2 | a0001 | c0002 | t0016 | g0157 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18968 | hp1 | a0001 | c0001 | t0009 | g0013 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18968 | hp2 | a0001 | c0002 | t0014 | g0189 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18970 | hp1 | a0001 | c0002 | t0053 | g0254 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18970 | hp2 | a0001 | c0001 | t0009 | g0030 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18971 | hp1 | a0001 | c0001 | t0033 | g0028 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18971 | hp2 | a0001 | c0001 | t0020 | g0142 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18973 | hp1 | a0001 | c0001 | t0042 | g0093 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0156 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0004 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0177 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18982 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18983 | hp2 | a0001 | c0001 | t0045 | g0064 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0021 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0014 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19000 | hp1 | a0001 | c0002 | t0030 | g0005 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19005 | hp1 | a0001 | c0001 | t0050 | g0091 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0032 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19011 | hp2 | a0001 | c0002 | t0025 | g0226 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0307 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0273 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19063 | hp2 | a0001 | c0001 | t0008 | g0025 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0250 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19066 | hp2 | a0001 | c0001 | t0020 | g0127 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0158 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19074 | hp1 | a0001 | c0002 | t0039 | g0144 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19077 | hp1 | a0001 | c0002 | t0005 | g0187 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19077 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19082 | hp1 | a0001 | c0002 | t0040 | g0160 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0066 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19083 | hp1 | a0001 | c0001 | t0007 | g0006 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19085 | hp1 | a0001 | c0002 | t0025 | g0167 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19088 | hp2 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19091 | hp1 | a0001 | c0001 | t0008 | g0018 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0040 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | ASW | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20129 | hp2 | a0001 | c0002 | t0012 | g0186 | AFR | ASW | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0220 | EUR | TSI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0087 | EUR | TSI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0249 | SAS | GIH | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | GIH | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0178 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0224 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0182 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02486 | hp1 | a0001 | c0001 | t0058 | g0292 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02486 | hp2 | a0001 | c0002 | t0036 | g0115 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0288 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02559 | hp2 | a0001 | c0001 | t0049 | g0146 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0251 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0048 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0012 | g0206 | REF | REF | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0153 | REF | REF | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78857596
|
C | T | 1 | a0002 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.391G>A | p.Val131Met | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/5 | 690/3652 | 391/663 | 131/220 | chr17 | 78857596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78857597
|
G | A | 1 | a0001c0004 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.390C>T | p.Ile130Ile | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/5 | 689/3652 | 390/663 | 130/220 | chr17 | 78857597 | ||
| chr17:78870935
|
C | T | 1 | a0001c0002 | 54 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(51): Show |
synonymous_variant | LOW | c.303G>A | p.Ser101Ser | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/5 | 602/3652 | 303/663 | 101/220 | chr17 | 78870935 | ||
| chr17:78925053
|
G | A | 1 | a0001c0005 | 1 | HG02004.hp1 | synonymous_variant | LOW | c.36C>T | p.Leu12Leu | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/5 | 335/3652 | 36/663 | 12/220 | chr17 | 78925053 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78853006
|
C | T | 1 | a0001c0001t0055 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2661G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2661 | chr17 | 78853006 | |||||
| chr17:78853016
|
G | A | 4 | a0001c0001t0010a0001c0001t0021a0001c0001t0051others(1): Show | 8 | HG00639.hp1 HG01243.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2651C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2651 | chr17 | 78853016 | |||||
| chr17:78853084
|
G | T | 1 | a0001c0002t0043 | 1 | NA18963.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2583C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2583 | chr17 | 78853084 | |||||
| chr17:78853304
|
G | T | 1 | a0001c0001t0031 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2363C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2363 | chr17 | 78853304 | |||||
| chr17:78853307
|
A | T | 1 | a0001c0001t0031 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2360 | chr17 | 78853307 | |||||
| chr17:78853308
|
G | T | 1 | a0001c0001t0031 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2359C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2359 | chr17 | 78853308 | |||||
| chr17:78853309
|
C | A | 1 | a0001c0001t0031 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2358G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2358 | chr17 | 78853309 | |||||
| chr17:78853369
|
T | C | 5 | a0001c0002t0024a0001c0002t0025a0001c0002t0030others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2298A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2298 | chr17 | 78853369 | |||||
| chr17:78853431
|
C | T | 1 | a0001c0002t0040 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2236G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2236 | chr17 | 78853431 | |||||
| chr17:78853570
|
A | G | 4 | a0001c0001t0011a0001c0001t0022a0001c0001t0046others(1): Show | 7 | HG01074.hp2 HG02647.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2097T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2097 | chr17 | 78853570 | |||||
| chr17:78853582
|
C | T | 1 | a0001c0002t0039 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2085G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2085 | chr17 | 78853582 | |||||
| chr17:78853650
|
C | T | 3 | a0001c0001t0023a0001c0001t0057a0001c0002t0023 | 3 | HG03017.hp1 HG03654.hp2 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2017G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 2017 | chr17 | 78853650 | |||||
| chr17:78853748
|
G | C | 2 | a0001c0001t0015a0001c0001t0018 | 5 | HG02451.hp1 HG02572.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1919C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 1919 | chr17 | 78853748 | |||||
| chr17:78853946
|
G | A | 1 | a0001c0001t0041 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1721C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 1721 | chr17 | 78853946 | |||||
| chr17:78853966
|
C | T | 1 | a0001c0001t0042 | 1 | NA18973.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1701G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 1701 | chr17 | 78853966 | |||||
| chr17:78854448
|
T | C | 2 | a0001c0001t0045a0001c0002t0056 | 2 | HG02080.hp2 NA18983.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1219A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 1219 | chr17 | 78854448 | |||||
| chr17:78854454
|
C | T | 1 | a0001c0001t0037 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1213G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 1213 | chr17 | 78854454 | |||||
| chr17:78854739
|
C | T | 2 | a0001c0001t0029a0001c0001t0038 | 2 | HG02280.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*928G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 928 | chr17 | 78854739 | |||||
| chr17:78854921
|
CG | C | 19 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(16): Show | 137 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*745delC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 745 | chr17 | 78854921 | |||||
| chr17:78854921
|
CGG | C | 18 | a0001c0001t0005a0001c0001t0006a0001c0001t0008others(15): Show | 67 | HG00323.hp1 HG00323.hp2 HG00558.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*744_*745delCC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 744 | chr17 | 78854921 | |||||
| chr17:78854922
|
G | T | 1 | a0001c0002t0054 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*745C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 745 | chr17 | 78854922 | |||||
| chr17:78854925
|
G | C | 3 | a0001c0001t0020a0001c0001t0033a0001c0001t0050 | 4 | NA18971.hp1 NA18971.hp2 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 742 | chr17 | 78854925 | |||||
| chr17:78854927
|
G | T | 1 | a0001c0001t0037 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*740C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 740 | chr17 | 78854927 | |||||
| chr17:78854929
|
G | T | 1 | a0001c0002t0053 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*738C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 738 | chr17 | 78854929 | |||||
| chr17:78854932
|
G | C | 3 | a0001c0001t0026a0001c0001t0048a0001c0001t0050 | 4 | HG02109.hp1 HG03225.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*735C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 735 | chr17 | 78854932 | |||||
| chr17:78854932
|
G | GT | 2 | a0001c0001t0013a0001c0002t0013 | 3 | HG00621.hp1 HG01361.hp1 HG02055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*734_*735insA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 734 | chr17 | 78854932 | |||||
| chr17:78854932
|
G | T | 7 | a0001c0001t0015a0001c0001t0017a0001c0001t0018others(4): Show | 12 | HG00558.hp1 HG01516.hp1 HG01517.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*735C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 735 | chr17 | 78854932 | |||||
| chr17:78854934
|
G | T | 1 | a0001c0001t0019 | 2 | HG02080.hp1 HG02738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*733C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 733 | chr17 | 78854934 | |||||
| chr17:78854935
|
T | C | 2 | a0001c0001t0027a0001c0001t0032 | 3 | HG02109.hp2 HG02451.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*732A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 732 | chr17 | 78854935 | |||||
| chr17:78854935
|
T | G | 4 | a0001c0001t0012a0001c0001t0019a0001c0002t0012others(1): Show | 7 | HG02080.hp1 HG02486.hp2 HG02735.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*732A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 732 | chr17 | 78854935 | |||||
| chr17:78854936
|
G | T | 2 | a0001c0001t0035a0001c0002t0036 | 2 | HG02486.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*731C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 731 | chr17 | 78854936 | |||||
| chr17:78854942
|
GT | G | 2 | a0001c0001t0020a0001c0001t0033 | 3 | NA18971.hp1 NA18971.hp2 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*724delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 724 | chr17 | 78854942 | |||||
| chr17:78854943
|
T | G | 2 | a0001c0001t0049a0001c0001t0050 | 2 | HG02559.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*724A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 724 | chr17 | 78854943 | |||||
| chr17:78855396
|
C | T | 2 | a0001c0002t0016a0001c0002t0034 | 3 | HG00558.hp2 HG02074.hp2 NA18966.hp2 |
3_prime_UTR_variant | MODIFIER | c.*271G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 271 | chr17 | 78855396 | |||||
| chr17:78855525
|
G | A | 4 | a0001c0001t0010a0001c0001t0021a0001c0001t0051others(1): Show | 8 | HG00639.hp1 HG01243.hp2 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*142C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 5/5 | 142 | chr17 | 78855525 | |||||
| chr17:78925158
|
T | G | 1 | a0001c0001t0051 | 1 | HG00639.hp1 | 5_prime_UTR_variant | MODIFIER | c.-70A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/5 | 70 | chr17 | 78925158 | |||||
| chr17:78925320
|
T | G | 1 | a0001c0001t0052 | 1 | HG03225.hp1 | 5_prime_UTR_variant | MODIFIER | c.-232A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/5 | 232 | chr17 | 78925320 | |||||
| chr17:78925349
|
T | C | 38 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(35): Show | 191 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(188): Show |
5_prime_UTR_variant | MODIFIER | c.-261A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/5 | 261 | chr17 | 78925349 | |||||
| chr17:78925357
|
G | T | 10 | a0001c0001t0007a0001c0001t0008a0001c0001t0009others(7): Show | 37 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(34): Show |
5_prime_UTR_variant | MODIFIER | c.-269C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/5 | 269 | chr17 | 78925357 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:78856015
|
G | A | 222 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(219): Show | 223 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.466-151C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856015 | ||||||
| chr17:78856116
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.466-252G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856116 | ||||||
| chr17:78856121
|
A | C | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.466-257T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856121 | ||||||
| chr17:78856157
|
C | T | 1 | a0001c0001t0008g0034 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.466-293G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856157 | ||||||
| chr17:78856527
|
C | G | 4 | a0001c0001t0020g0127a0001c0001t0020g0142a0001c0001t0033g0028others(1): Show | 4 | NA18971.hp1 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-663G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856527 | ||||||
| chr17:78856647
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0003g0249 | 2 | HG00140.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.466-783C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856647 | ||||||
| chr17:78856746
|
A | G | 290 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(287): Show | 291 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(288): Show |
intron_variant | MODIFIER | c.465+776T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856746 | ||||||
| chr17:78856811
|
C | A | 1 | a0001c0001t0008g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.465+711G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856811 | ||||||
| chr17:78856992
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.465+530G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78856992 | ||||||
| chr17:78857150
|
G | A | 1 | a0001c0001t0022g0183 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.465+372C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78857150 | ||||||
| chr17:78857255
|
C | T | 208 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(205): Show | 209 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.465+267G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78857255 | ||||||
| chr17:78857265
|
G | T | 8 | a0001c0001t0010g0039a0001c0001t0010g0040a0001c0001t0010g0048others(5): Show | 8 | HG00639.hp1 HG01243.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.465+257C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78857265 | ||||||
| chr17:78857268
|
G | A | 2 | a0001c0001t0029g0033a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.465+254C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78857268 | ||||||
| chr17:78857363
|
A | G | 1 | a0001c0001t0003g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.465+159T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78857363 | ||||||
| chr17:78857364
|
C | A | 1 | a0001c0001t0003g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.465+158G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 4/4 | chr17 | 78857364 | ||||||
| chr17:78857659
|
G | A | 1 | a0001c0001t0003g0309 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.341-13C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78857659 | ||||||
| chr17:78857746
|
C | A | 1 | a0001c0002t0056g0252 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.341-100G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78857746 | ||||||
| chr17:78857761
|
T | A | 1 | a0001c0001t0003g0293 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.341-115A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78857761 | ||||||
| chr17:78857873
|
C | A | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.341-227G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78857873 | ||||||
| chr17:78857937
|
T | G | 28 | a0001c0001t0001g0268a0001c0001t0003g0170a0001c0001t0003g0173others(25): Show | 28 | HG02109.hp1 HG02109.hp2 HG02280.hp2 others(25): Show |
intron_variant | MODIFIER | c.341-291A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78857937 | ||||||
| chr17:78858311
|
C | T | 2 | a0001c0001t0003g0300a0001c0001t0003g0301 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.341-665G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78858311 | ||||||
| chr17:78858508
|
T | G | 4 | a0001c0001t0020g0127a0001c0001t0020g0142a0001c0001t0033g0028others(1): Show | 4 | NA18971.hp1 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-862A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78858508 | ||||||
| chr17:78858534
|
T | G | 18 | a0001c0001t0001g0268a0001c0001t0003g0173a0001c0001t0003g0251others(15): Show | 18 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.341-888A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78858534 | ||||||
| chr17:78859123
|
A | G | 1 | a0001c0001t0002g0099 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.341-1477T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859123 | ||||||
| chr17:78859221
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.341-1575C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859221 | ||||||
| chr17:78859281
|
C | T | 1 | a0001c0002t0053g0254 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.341-1635G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859281 | ||||||
| chr17:78859287
|
A | C | 289 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(286): Show | 290 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.341-1641T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859287 | ||||||
| chr17:78859388
|
G | A | 2 | a0001c0001t0002g0151a0001c0001t0002g0152 | 2 | HG02083.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.341-1742C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859388 | ||||||
| chr17:78859421
|
A | G | 1 | a0001c0002t0001g0256 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.341-1775T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859421 | ||||||
| chr17:78859434
|
C | A | 15 | a0001c0001t0002g0045a0001c0001t0004g0141a0001c0001t0006g0078others(12): Show | 15 | HG01074.hp2 HG02451.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.341-1788G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859434 | ||||||
| chr17:78859540
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.341-1894C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859540 | ||||||
| chr17:78859606
|
T | C | 1 | a0001c0002t0024g0227 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.341-1960A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859606 | ||||||
| chr17:78859655
|
C | A | 1 | a0001c0001t0001g0232 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.341-2009G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78859655 | ||||||
| chr17:78860177
|
A | C | 260 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(257): Show | 261 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.341-2531T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78860177 | ||||||
| chr17:78860571
|
T | A | 43 | a0001c0001t0001g0208a0001c0001t0001g0263a0001c0001t0001g0277others(40): Show | 43 | HG00323.hp1 HG00673.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.341-2925A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78860571 | ||||||
| chr17:78860626
|
C | T | 1 | a0001c0001t0005g0250 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.341-2980G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78860626 | ||||||
| chr17:78860758
|
G | A | 1 | a0001c0001t0017g0133 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.341-3112C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78860758 | ||||||
| chr17:78860884
|
G | A | 289 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(286): Show | 290 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.341-3238C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78860884 | ||||||
| chr17:78860985
|
A | G | 1 | a0001c0001t0003g0235 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.341-3339T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78860985 | ||||||
| chr17:78861035
|
C | CA | 16 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(13): Show | 16 | HG00140.hp2 HG00558.hp1 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.341-3390dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861035 | ||||||
| chr17:78861035
|
C | CAA | 245 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(242): Show | 246 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(243): Show |
intron_variant | MODIFIER | c.341-3391_341-3390d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861035 | ||||||
| chr17:78861035
|
C | CAAA | 37 | a0001c0001t0001g0208a0001c0001t0001g0263a0001c0001t0001g0277others(34): Show | 37 | HG00323.hp1 HG00673.hp1 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.341-3392_341-3390d others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861035 | ||||||
| chr17:78861035
|
C | CAAAA | 9 | a0001c0001t0001g0314a0001c0001t0003g0272a0001c0001t0004g0141others(6): Show | 9 | HG01074.hp2 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-3393_341-3390d others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861035 | ||||||
| chr17:78861114
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.341-3468A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861114 | ||||||
| chr17:78861312
|
A | G | 1 | a0001c0001t0049g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.341-3666T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861312 | ||||||
| chr17:78861317
|
C | T | 9 | a0001c0001t0020g0127a0001c0001t0020g0142a0001c0001t0026g0224others(6): Show | 9 | HG02109.hp1 HG03209.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.341-3671G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861317 | ||||||
| chr17:78861487
|
T | C | 1 | a0001c0001t0008g0026 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.341-3841A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861487 | ||||||
| chr17:78861661
|
G | A | 29 | a0001c0001t0001g0208a0001c0001t0001g0263a0001c0001t0001g0277others(26): Show | 29 | HG00323.hp1 HG00673.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.341-4015C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861661 | ||||||
| chr17:78861951
|
G | A | 1 | a0001c0001t0007g0002 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.341-4305C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861951 | ||||||
| chr17:78861963
|
G | C | 2 | a0001c0001t0003g0170a0001c0001t0003g0225 | 2 | HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.341-4317C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861963 | ||||||
| chr17:78861979
|
G | A | 1 | a0001c0001t0031g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.341-4333C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78861979 | ||||||
| chr17:78862075
|
A | G | 1 | a0001c0002t0024g0193 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.341-4429T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862075 | ||||||
| chr17:78862141
|
T | C | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.341-4495A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862141 | ||||||
| chr17:78862146
|
G | A | 1 | a0001c0001t0003g0310 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.341-4500C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862146 | ||||||
| chr17:78862171
|
C | T | 2 | a0001c0001t0002g0103a0001c0001t0019g0095 | 2 | HG02080.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.341-4525G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862171 | ||||||
| chr17:78862271
|
G | A | 7 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(4): Show | 7 | HG00140.hp2 HG01358.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.341-4625C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862271 | ||||||
| chr17:78862280
|
G | A | 3 | a0001c0001t0026g0224a0001c0001t0026g0290a0001c0001t0048g0043 | 3 | HG02109.hp1 HG03225.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.341-4634C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862280 | ||||||
| chr17:78862457
|
T | C | 292 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(289): Show | 293 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(290): Show |
intron_variant | MODIFIER | c.341-4811A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862457 | ||||||
| chr17:78862500
|
G | A | 4 | a0001c0001t0015g0168a0001c0001t0015g0169a0001c0001t0015g0185others(1): Show | 4 | HG02451.hp1 HG02630.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.341-4854C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862500 | ||||||
| chr17:78862555
|
A | G | 2 | a0001c0001t0029g0033a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.341-4909T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862555 | ||||||
| chr17:78862613
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.341-4967A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862613 | ||||||
| chr17:78862656
|
A | G | 3 | a0001c0001t0001g0199a0001c0001t0005g0242a0001c0001t0037g0132 | 3 | HG02683.hp2 HG03491.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.341-5010T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862656 | ||||||
| chr17:78862777
|
T | C | 4 | a0001c0001t0026g0224a0001c0001t0026g0290a0001c0001t0048g0043others(1): Show | 4 | HG02109.hp1 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.341-5131A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862777 | ||||||
| chr17:78862911
|
C | T | 1 | a0001c0001t0018g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.341-5265G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862911 | ||||||
| chr17:78862937
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0017g0133 | 2 | HG01891.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.341-5291G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78862937 | ||||||
| chr17:78863155
|
G | T | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.341-5509C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863155 | ||||||
| chr17:78863432
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.341-5786G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863432 | ||||||
| chr17:78863438
|
T | C | 7 | a0001c0001t0001g0208a0001c0001t0001g0240a0001c0001t0001g0246others(4): Show | 7 | HG03831.hp1 NA18944.hp1 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.341-5792A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863438 | ||||||
| chr17:78863542
|
G | A | 5 | a0001c0001t0001g0233a0001c0001t0005g0250a0001c0001t0007g0012others(2): Show | 5 | HG00544.hp1 NA18947.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.341-5896C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863542 | ||||||
| chr17:78863713
|
C | A | 1 | a0001c0001t0001g0199 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.341-6067G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863713 | ||||||
| chr17:78863714
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.341-6068T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863714 | ||||||
| chr17:78863834
|
C | A | 69 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(66): Show | 70 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.341-6188G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863834 | ||||||
| chr17:78863914
|
T | C | 264 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(261): Show | 265 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.341-6268A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863914 | ||||||
| chr17:78864207
|
A | G | 81 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0212others(78): Show | 82 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.341-6561T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864207 | ||||||
| chr17:78864391
|
T | C | 258 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(255): Show | 259 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.340+6507A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864391 | ||||||
| chr17:78864518
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.340+6380G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864518 | ||||||
| chr17:78864621
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.340+6277G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864621 | ||||||
| chr17:78864773
|
CG | C | 7 | a0001c0001t0003g0171a0001c0001t0003g0267a0001c0001t0010g0114others(4): Show | 7 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+6124delC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864773 | ||||||
| chr17:78864900
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.340+5998T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864900 | ||||||
| chr17:78864968
|
T | C | 264 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(261): Show | 265 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(262): Show |
intron_variant | MODIFIER | c.340+5930A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864968 | ||||||
| chr17:78865055
|
TAAATA | T | 3 | a0001c0001t0001g0198a0001c0001t0001g0236a0001c0001t0006g0070 | 3 | HG01978.hp1 HG02300.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.340+5838_340+5842d others(7): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865055 | ||||||
| chr17:78865230
|
C | G | 178 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(175): Show | 178 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.340+5668G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865230 | ||||||
| chr17:78865343
|
G | A | 8 | a0001c0002t0001g0192a0001c0002t0024g0193a0001c0002t0024g0227others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+5555C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865343 | ||||||
| chr17:78865356
|
G | A | 17 | a0001c0001t0001g0248a0001c0001t0001g0261a0001c0001t0001g0284others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.340+5542C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865356 | ||||||
| chr17:78865399
|
C | T | 7 | a0001c0001t0001g0271a0001c0001t0001g0302a0001c0001t0002g0044others(4): Show | 7 | HG02572.hp1 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.340+5499G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865399 | ||||||
| chr17:78865400
|
G | A | 5 | a0001c0001t0001g0233a0001c0001t0005g0250a0001c0001t0007g0012others(2): Show | 5 | HG00544.hp1 NA18947.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+5498C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865400 | ||||||
| chr17:78865423
|
G | A | 1 | a0001c0001t0004g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.340+5475C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865423 | ||||||
| chr17:78865549
|
G | A | 1 | a0001c0001t0007g0019 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.340+5349C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865549 | ||||||
| chr17:78865581
|
G | A | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.340+5317C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865581 | ||||||
| chr17:78865624
|
C | CA | 203 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(200): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.340+5273dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865624 | ||||||
| chr17:78865624
|
C | CAA | 20 | a0001c0001t0001g0212a0001c0001t0002g0045a0001c0001t0002g0130others(17): Show | 20 | HG00609.hp1 HG00621.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.340+5272_340+5273d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865624 | ||||||
| chr17:78865758
|
C | T | 82 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(79): Show | 83 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.340+5140G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865758 | ||||||
| chr17:78865858
|
C | G | 106 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(103): Show | 107 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.340+5040G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865858 | ||||||
| chr17:78865906
|
G | A | 2 | a0001c0001t0003g0300a0001c0001t0003g0301 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.340+4992C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865906 | ||||||
| chr17:78865965
|
A | G | 3 | a0001c0001t0020g0127a0001c0001t0020g0142a0001c0001t0050g0091 | 3 | NA18971.hp2 NA19005.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.340+4933T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865965 | ||||||
| chr17:78866012
|
C | CAG | 75 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(72): Show | 76 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.340+4884_340+4885d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866012 | ||||||
| chr17:78866023
|
A | G | 75 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(72): Show | 76 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.340+4875T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866023 | ||||||
| chr17:78866172
|
G | A | 3 | a0001c0001t0003g0225a0001c0001t0003g0267a0001c0001t0041g0046 | 3 | HG02965.hp1 HG03098.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+4726C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866172 | ||||||
| chr17:78866252
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.340+4646G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866252 | ||||||
| chr17:78866263
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.340+4635C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866263 | ||||||
| chr17:78866273
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.340+4625C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866273 | ||||||
| chr17:78866361
|
GT | G | 5 | a0001c0001t0003g0225a0001c0001t0003g0267a0001c0001t0018g0140others(2): Show | 5 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+4536delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866361 | ||||||
| chr17:78866372
|
T | C | 10 | a0001c0001t0001g0271a0001c0001t0003g0225a0001c0001t0003g0267others(7): Show | 10 | HG02572.hp1 HG02622.hp1 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.340+4526A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866372 | ||||||
| chr17:78866432
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.340+4466C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866432 | ||||||
| chr17:78866513
|
A | AC | 10 | a0001c0001t0001g0261a0001c0001t0003g0249a0001c0001t0003g0267others(7): Show | 10 | HG01071.hp2 HG01993.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.340+4384dupG | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866513 | ||||||
| chr17:78866519
|
G | C | 27 | a0001c0001t0001g0248a0001c0001t0001g0261a0001c0001t0001g0284others(24): Show | 27 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.340+4379C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866519 | ||||||
| chr17:78866581
|
T | C | 12 | a0001c0001t0001g0166a0001c0001t0001g0229a0001c0001t0001g0258others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.340+4317A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866581 | ||||||
| chr17:78866708
|
T | C | 3 | a0001c0001t0001g0314a0001c0001t0029g0033a0001c0001t0038g0124 | 3 | HG02257.hp2 HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.340+4190A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866708 | ||||||
| chr17:78866757
|
A | C | 7 | a0001c0001t0002g0143a0001c0001t0003g0225a0001c0001t0018g0140others(4): Show | 7 | HG02572.hp1 HG02622.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.340+4141T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866757 | ||||||
| chr17:78866772
|
C | T | 1 | a0001c0001t0005g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.340+4126G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866772 | ||||||
| chr17:78866797
|
T | G | 1 | a0001c0001t0001g0194 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.340+4101A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866797 | ||||||
| chr17:78866895
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.340+4003C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866895 | ||||||
| chr17:78866945
|
G | C | 265 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(262): Show | 266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.340+3953C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866945 | ||||||
| chr17:78866974
|
T | C | 1 | a0001c0001t0020g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.340+3924A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866974 | ||||||
| chr17:78866987
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.340+3911C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78866987 | ||||||
| chr17:78867169
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.340+3729C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867169 | ||||||
| chr17:78867413
|
A | C | 1 | a0001c0001t0001g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.340+3485T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867413 | ||||||
| chr17:78867590
|
C | A | 4 | a0001c0001t0001g0212a0001c0001t0002g0149a0001c0001t0005g0257others(1): Show | 4 | HG01884.hp1 HG02055.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+3308G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867590 | ||||||
| chr17:78867594
|
C | CT | 9 | a0001c0001t0001g0222a0001c0001t0002g0053a0001c0001t0002g0113others(6): Show | 9 | HG03831.hp2 HG04115.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.340+3303dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867594 | ||||||
| chr17:78867594
|
CT | C | 32 | a0001c0001t0001g0210a0001c0001t0001g0271a0001c0001t0001g0302others(29): Show | 32 | HG00639.hp1 HG01069.hp1 HG02280.hp1 others(29): Show |
intron_variant | MODIFIER | c.340+3303delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867594 | ||||||
| chr17:78867594
|
CTT | C | 86 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0248others(83): Show | 87 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.340+3302_340+3303d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867594 | ||||||
| chr17:78867648
|
T | A | 95 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(92): Show | 96 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.340+3250A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867648 | ||||||
| chr17:78867671
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.340+3227G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867671 | ||||||
| chr17:78867780
|
C | T | 100 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(97): Show | 101 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.340+3118G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867780 | ||||||
| chr17:78867895
|
G | A | 3 | a0001c0001t0001g0305a0001c0001t0003g0267a0001c0001t0041g0046 | 3 | HG02809.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.340+3003C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867895 | ||||||
| chr17:78867952
|
A | ATCTG | 8 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0002g0143others(5): Show | 8 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.340+2945_340+2946i others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867952 | ||||||
| chr17:78867954
|
C | CTGT | 96 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(93): Show | 97 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.340+2943_340+2944i others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78867954 | ||||||
| chr17:78868056
|
C | T | 1 | a0001c0001t0006g0086 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.340+2842G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868056 | ||||||
| chr17:78868093
|
A | G | 168 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(165): Show | 168 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(165): Show |
intron_variant | MODIFIER | c.340+2805T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868093 | ||||||
| chr17:78868226
|
G | T | 1 | a0001c0001t0003g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.340+2672C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868226 | ||||||
| chr17:78868311
|
C | T | 3 | a0001c0001t0007g0012a0001c0001t0009g0029a0001c0001t0033g0028 | 3 | NA18947.hp2 NA18971.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.340+2587G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868311 | ||||||
| chr17:78868361
|
A | G | 104 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(101): Show | 105 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.340+2537T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868361 | ||||||
| chr17:78868455
|
T | C | 5 | a0001c0001t0008g0003a0001c0001t0008g0025a0001c0001t0009g0013others(2): Show | 5 | HG00609.hp1 NA18964.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+2443A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868455 | ||||||
| chr17:78868462
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.340+2436C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868462 | ||||||
| chr17:78868512
|
C | A | 166 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(163): Show | 166 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.340+2386G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868512 | ||||||
| chr17:78868529
|
C | G | 266 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.340+2369G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868529 | ||||||
| chr17:78868560
|
C | A | 1 | a0001c0001t0001g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.340+2338G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868560 | ||||||
| chr17:78868596
|
C | T | 1 | a0001c0001t0051g0162 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.340+2302G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868596 | ||||||
| chr17:78868733
|
G | A | 162 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(159): Show | 162 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.340+2165C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868733 | ||||||
| chr17:78868918
|
G | A | 9 | a0001c0001t0001g0166a0001c0001t0001g0258a0001c0001t0001g0282others(6): Show | 9 | HG01123.hp2 HG01884.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.340+1980C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868918 | ||||||
| chr17:78868939
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.340+1959C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868939 | ||||||
| chr17:78868941
|
G | A | 5 | a0001c0001t0003g0171a0001c0001t0010g0114a0001c0001t0021g0041others(2): Show | 5 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+1957C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78868941 | ||||||
| chr17:78869121
|
C | T | 96 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(93): Show | 96 | HG00544.hp1 HG00609.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.340+1777G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869121 | ||||||
| chr17:78869252
|
T | C | 1 | a0001c0001t0050g0091 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.340+1646A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869252 | ||||||
| chr17:78869278
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG00673.hp2 HG02074.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+1620C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869278 | ||||||
| chr17:78869300
|
T | C | 13 | a0001c0001t0001g0166a0001c0001t0001g0229a0001c0001t0001g0258others(10): Show | 13 | HG01123.hp2 HG01884.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.340+1598A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869300 | ||||||
| chr17:78869344
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.340+1554G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869344 | ||||||
| chr17:78869405
|
A | G | 52 | a0001c0001t0001g0212a0001c0001t0001g0305a0001c0001t0002g0149others(49): Show | 53 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.340+1493T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869405 | ||||||
| chr17:78869414
|
CA | C | 237 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(234): Show | 238 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(235): Show |
intron_variant | MODIFIER | c.340+1483delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869414 | ||||||
| chr17:78869425
|
A | C | 1 | a0001c0001t0001g0278 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.340+1473T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869425 | ||||||
| chr17:78869625
|
A | G | 2 | a0001c0001t0002g0109a0001c0001t0002g0112 | 2 | HG01433.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.340+1273T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869625 | ||||||
| chr17:78869684
|
G | A | 2 | a0001c0001t0018g0140a0001c0001t0035g0067 | 2 | HG02572.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.340+1214C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869684 | ||||||
| chr17:78869721
|
A | T | 1 | a0001c0001t0005g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.340+1177T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869721 | ||||||
| chr17:78869760
|
A | G | 2 | a0001c0001t0001g0229a0001c0001t0011g0195 | 2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.340+1138T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869760 | ||||||
| chr17:78869776
|
T | C | 8 | a0001c0001t0001g0212a0001c0001t0001g0271a0001c0001t0002g0125others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.340+1122A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869776 | ||||||
| chr17:78869989
|
G | C | 314 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(311): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.340+909C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869989 | ||||||
| chr17:78869991
|
C | A | 314 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(311): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.340+907G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869991 | ||||||
| chr17:78869993
|
A | G | 314 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(311): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.340+905T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869993 | ||||||
| chr17:78869999
|
A | AG | 314 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(311): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.340+898dupC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869999 | ||||||
| chr17:78870144
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.340+754C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870144 | ||||||
| chr17:78870154
|
G | A | 5 | a0001c0001t0003g0171a0001c0001t0010g0114a0001c0001t0021g0041others(2): Show | 5 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+744C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870154 | ||||||
| chr17:78870206
|
A | T | 1 | a0001c0001t0007g0006 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.340+692T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870206 | ||||||
| chr17:78870275
|
G | A | 34 | a0001c0001t0001g0166a0001c0001t0001g0229a0001c0001t0001g0248others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.340+623C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870275 | ||||||
| chr17:78870295
|
A | T | 1 | a0001c0001t0007g0006 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.340+603T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870295 | ||||||
| chr17:78870370
|
C | T | 1 | a0001c0002t0039g0144 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.340+528G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870370 | ||||||
| chr17:78870371
|
G | A | 3 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067 | 3 | HG02572.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+527C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870371 | ||||||
| chr17:78870403
|
G | A | 40 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0208others(37): Show | 40 | HG00609.hp1 HG00621.hp2 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.340+495C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870403 | ||||||
| chr17:78870421
|
A | AAAAG | 5 | a0001c0001t0049g0146a0001c0002t0001g0307a0001c0002t0003g0288others(2): Show | 5 | HG02559.hp1 HG02559.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.340+473_340+476dup others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870421 | ||||||
| chr17:78870421
|
AAAAG | A | 6 | a0001c0001t0001g0261a0001c0001t0002g0045a0001c0001t0003g0216others(3): Show | 6 | HG01346.hp1 HG01361.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.340+473_340+476del others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870421 | ||||||
| chr17:78870421
|
AAAAGAAA others(5): Show |
A | 3 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067 | 3 | HG02572.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.340+465_340+476del others(12): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870421 | ||||||
| chr17:78870423
|
AAGAAAG | A | 12 | a0001c0001t0001g0194a0001c0001t0003g0289a0001c0001t0003g0293others(9): Show | 12 | HG02109.hp2 HG02451.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.340+469_340+474del others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870423 | ||||||
| chr17:78870424
|
AGAAAG | A | 180 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(177): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.340+469_340+473del others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870424 | ||||||
| chr17:78870429
|
G | A | 5 | a0001c0001t0001g0261a0001c0001t0003g0216a0001c0001t0004g0073others(2): Show | 5 | HG01346.hp1 HG01361.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.340+469C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870429 | ||||||
| chr17:78870433
|
G | A | 183 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(180): Show | 183 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.340+465C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870433 | ||||||
| chr17:78870445
|
G | C | 156 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(153): Show | 156 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.340+453C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870445 | ||||||
| chr17:78870544
|
T | G | 1 | a0001c0001t0005g0220 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.340+354A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870544 | ||||||
| chr17:78870629
|
C | T | 197 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.340+269G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870629 | ||||||
| chr17:78870759
|
G | A | 2 | a0001c0001t0006g0147a0001c0001t0052g0163 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.340+139C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870759 | ||||||
| chr17:78870797
|
G | A | 1 | a0001c0002t0040g0160 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.340+101C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870797 | ||||||
| chr17:78870825
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.340+73C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78870825 | ||||||
| chr17:78871089
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.232-83G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871089 | ||||||
| chr17:78871103
|
G | T | 192 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(189): Show | 192 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.232-97C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871103 | ||||||
| chr17:78871184
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.232-178C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871184 | ||||||
| chr17:78871200
|
C | T | 3 | a0001c0001t0001g0291a0001c0001t0004g0050a0001c0001t0055g0270 | 3 | HG01261.hp1 HG02258.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.232-194G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871200 | ||||||
| chr17:78871244
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0005g0242 | 2 | HG01261.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.232-238C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871244 | ||||||
| chr17:78871267
|
C | T | 5 | a0001c0001t0001g0233a0001c0001t0005g0250a0001c0001t0007g0012others(2): Show | 5 | HG00544.hp1 NA18947.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.232-261G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871267 | ||||||
| chr17:78871449
|
C | CA | 56 | a0001c0001t0002g0082a0001c0001t0003g0171a0001c0001t0008g0018others(53): Show | 57 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.232-444dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871449 | ||||||
| chr17:78871466
|
A | AAAG | 6 | a0001c0001t0001g0222a0001c0001t0001g0230a0001c0001t0002g0063others(3): Show | 6 | HG01433.hp2 NA18974.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-461_232-460ins others(3): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871466 | ||||||
| chr17:78871466
|
A | AAG | 154 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(151): Show | 154 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(151): Show |
intron_variant | MODIFIER | c.232-461_232-460ins others(2): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871466 | ||||||
| chr17:78871466
|
A | AG | 35 | a0001c0001t0001g0212a0001c0001t0001g0229a0001c0001t0001g0248others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.232-461_232-460ins others(1): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871466 | ||||||
| chr17:78871466
|
A | G | 4 | a0001c0001t0003g0225a0001c0001t0012g0297a0001c0001t0018g0140others(1): Show | 4 | HG02572.hp1 HG02622.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.232-460T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871466 | ||||||
| chr17:78871472
|
A | C | 5 | a0001c0001t0003g0171a0001c0001t0010g0114a0001c0001t0021g0041others(2): Show | 5 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-466T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871472 | ||||||
| chr17:78871491
|
T | C | 3 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067 | 3 | HG02572.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.232-485A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871491 | ||||||
| chr17:78871527
|
T | C | 1 | a0001c0001t0002g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.232-521A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871527 | ||||||
| chr17:78871605
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.232-599C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871605 | ||||||
| chr17:78871628
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.232-622G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871628 | ||||||
| chr17:78871638
|
A | G | 5 | a0001c0001t0003g0171a0001c0001t0010g0114a0001c0001t0021g0041others(2): Show | 5 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-632T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871638 | ||||||
| chr17:78871671
|
C | T | 6 | a0001c0001t0001g0261a0001c0001t0003g0225a0001c0001t0018g0140others(3): Show | 6 | HG02109.hp1 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-665G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871671 | ||||||
| chr17:78871743
|
G | C | 40 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(37): Show | 40 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.232-737C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871743 | ||||||
| chr17:78871810
|
C | T | 193 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.232-804G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871810 | ||||||
| chr17:78871843
|
C | CA | 56 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0222others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.232-838dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871843 | ||||||
| chr17:78871914
|
A | G | 198 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.232-908T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871914 | ||||||
| chr17:78871956
|
G | C | 53 | a0001c0002t0001g0175a0001c0002t0001g0177a0001c0002t0001g0191others(50): Show | 54 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.232-950C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871956 | ||||||
| chr17:78872053
|
T | C | 199 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.232-1047A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872053 | ||||||
| chr17:78872059
|
T | C | 1 | a0001c0002t0039g0144 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.232-1053A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872059 | ||||||
| chr17:78872113
|
C | T | 1 | a0001c0001t0001g0194 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.232-1107G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872113 | ||||||
| chr17:78872152
|
C | CT | 6 | a0001c0001t0001g0302a0001c0001t0002g0063a0001c0001t0011g0283others(3): Show | 6 | HG00639.hp1 HG01074.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.232-1147dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872152 | ||||||
| chr17:78872208
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.232-1202G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872208 | ||||||
| chr17:78872271
|
A | G | 1 | a0001c0001t0007g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.232-1265T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872271 | ||||||
| chr17:78872478
|
G | A | 1 | a0001c0001t0002g0101 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.231+1341C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872478 | ||||||
| chr17:78872490
|
T | C | 2 | a0001c0001t0006g0147a0001c0001t0052g0163 | 2 | HG01884.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.231+1329A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872490 | ||||||
| chr17:78872532
|
A | G | 199 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.231+1287T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872532 | ||||||
| chr17:78872674
|
G | A | 2 | a0001c0001t0003g0309a0001c0001t0026g0290 | 2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.231+1145C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872674 | ||||||
| chr17:78872718
|
G | A | 7 | a0001c0002t0003g0313a0001c0002t0005g0269a0001c0002t0013g0253others(4): Show | 7 | HG00558.hp1 HG00621.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.231+1101C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872718 | ||||||
| chr17:78872836
|
T | C | 1 | a0001c0001t0002g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.231+983A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872836 | ||||||
| chr17:78872905
|
C | T | 1 | a0001c0001t0004g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.231+914G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78872905 | ||||||
| chr17:78873303
|
AT | A | 209 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(206): Show | 210 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.231+515delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873303 | ||||||
| chr17:78873303
|
ATT | A | 53 | a0001c0001t0001g0166a0001c0001t0001g0205a0001c0001t0001g0212others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.231+514_231+515del others(2): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873303 | ||||||
| chr17:78873305
|
T | A | 1 | a0001c0001t0004g0073 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.231+514A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873305 | ||||||
| chr17:78873306
|
T | A | 141 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(138): Show | 141 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.231+513A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873306 | ||||||
| chr17:78873307
|
T | A | 52 | a0001c0001t0001g0166a0001c0001t0001g0205a0001c0001t0001g0212others(49): Show | 52 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.231+512A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873307 | ||||||
| chr17:78873308
|
T | A | 10 | a0001c0001t0001g0208a0001c0001t0001g0287a0001c0001t0002g0063others(7): Show | 10 | HG02155.hp1 HG02683.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.231+511A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873308 | ||||||
| chr17:78873309
|
T | A | 42 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.231+510A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873309 | ||||||
| chr17:78873311
|
T | A | 17 | a0001c0001t0001g0248a0001c0001t0001g0305a0001c0001t0002g0134others(14): Show | 17 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.231+508A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873311 | ||||||
| chr17:78873313
|
T | A | 2 | a0001c0001t0003g0251a0001c0001t0003g0312 | 2 | HG03239.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.231+506A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873313 | ||||||
| chr17:78873331
|
TCTCA | T | 193 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.231+484_231+487del others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873331 | ||||||
| chr17:78873391
|
C | A | 148 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(145): Show | 148 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.231+428G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873391 | ||||||
| chr17:78873588
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.231+231G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873588 | ||||||
| chr17:78873657
|
A | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+162T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873657 | ||||||
| chr17:78873796
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.231+23C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873796 | ||||||
| chr17:78873811
|
A | G | 1 | a0001c0001t0001g0302 | 1 | HG03195.hp1 | splice_region_variant&intron_variant | LOW | c.231+8T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873811 | ||||||
| chr17:78873947
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.131-28C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78873947 | ||||||
| chr17:78873992
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-73G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78873992 | ||||||
| chr17:78874024
|
C | G | 56 | a0001c0001t0002g0112a0001c0001t0006g0110a0001c0001t0006g0135others(53): Show | 57 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.131-105G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874024 | ||||||
| chr17:78874038
|
G | A | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.131-119C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874038 | ||||||
| chr17:78874127
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-208G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874127 | ||||||
| chr17:78874211
|
A | G | 265 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(262): Show | 266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.131-292T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874211 | ||||||
| chr17:78874253
|
C | T | 1 | a0001c0001t0004g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.131-334G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874253 | ||||||
| chr17:78874287
|
CT | C | 262 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(259): Show | 263 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(260): Show |
intron_variant | MODIFIER | c.131-369delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874287 | ||||||
| chr17:78874377
|
C | T | 119 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(116): Show | 119 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.131-458G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874377 | ||||||
| chr17:78874410
|
C | A | 260 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(257): Show | 261 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.131-491G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874410 | ||||||
| chr17:78874432
|
T | C | 1 | a0001c0001t0049g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-513A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874432 | ||||||
| chr17:78874453
|
G | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0287 | 2 | HG01106.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.131-534C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874453 | ||||||
| chr17:78874499
|
C | G | 195 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.131-580G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874499 | ||||||
| chr17:78874536
|
C | A | 40 | a0001c0001t0001g0166a0001c0001t0001g0212a0001c0001t0001g0229others(37): Show | 40 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.131-617G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874536 | ||||||
| chr17:78874593
|
A | G | 214 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(211): Show | 215 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.131-674T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874593 | ||||||
| chr17:78874608
|
C | T | 1 | a0001c0001t0003g0298 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.131-689G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874608 | ||||||
| chr17:78874611
|
G | T | 201 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.131-692C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874611 | ||||||
| chr17:78874703
|
A | G | 65 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(62): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-784T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874703 | ||||||
| chr17:78874723
|
G | A | 1 | a0001c0001t0008g0026 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.131-804C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874723 | ||||||
| chr17:78874738
|
C | T | 1 | a0001c0001t0002g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.131-819G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874738 | ||||||
| chr17:78874739
|
G | A | 65 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(62): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-820C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874739 | ||||||
| chr17:78874744
|
A | ATTT | 59 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(56): Show | 60 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.131-828_131-826dup others(3): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874744 | ||||||
| chr17:78874763
|
C | T | 1 | a0001c0001t0002g0136 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.131-844G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874763 | ||||||
| chr17:78874780
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-861C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874780 | ||||||
| chr17:78874890
|
G | A | 65 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(62): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-971C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874890 | ||||||
| chr17:78875085
|
C | T | 2 | a0001c0001t0003g0225a0001c0001t0049g0146 | 2 | HG02559.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.131-1166G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875085 | ||||||
| chr17:78875098
|
G | A | 199 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.131-1179C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875098 | ||||||
| chr17:78875162
|
G | A | 1 | a0001c0001t0004g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.131-1243C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875162 | ||||||
| chr17:78875168
|
G | A | 1 | a0001c0001t0007g0036 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.131-1249C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875168 | ||||||
| chr17:78875293
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.131-1374C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875293 | ||||||
| chr17:78875432
|
G | T | 1 | a0001c0001t0005g0265 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.131-1513C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875432 | ||||||
| chr17:78875556
|
G | T | 26 | a0001c0001t0002g0112a0001c0001t0006g0110a0001c0001t0006g0135others(23): Show | 27 | HG00558.hp2 HG00609.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.131-1637C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875556 | ||||||
| chr17:78875652
|
C | T | 1 | a0001c0001t0008g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131-1733G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875652 | ||||||
| chr17:78875747
|
G | A | 2 | a0001c0001t0003g0300a0001c0001t0003g0301 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.131-1828C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875747 | ||||||
| chr17:78875968
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.131-2049G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875968 | ||||||
| chr17:78875969
|
A | G | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-2050T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875969 | ||||||
| chr17:78876003
|
T | G | 268 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.131-2084A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876003 | ||||||
| chr17:78876043
|
G | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-2124C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876043 | ||||||
| chr17:78876077
|
C | T | 70 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(67): Show | 71 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.131-2158G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876077 | ||||||
| chr17:78876121
|
C | T | 62 | a0001c0001t0002g0112a0001c0001t0003g0309a0001c0001t0006g0078others(59): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.131-2202G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876121 | ||||||
| chr17:78876141
|
T | A | 1 | a0001c0001t0004g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.131-2222A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876141 | ||||||
| chr17:78876256
|
C | G | 65 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(62): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-2337G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876256 | ||||||
| chr17:78876298
|
T | C | 266 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.131-2379A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876298 | ||||||
| chr17:78876313
|
C | T | 57 | a0001c0001t0002g0112a0001c0001t0003g0309a0001c0001t0006g0110others(54): Show | 58 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.131-2394G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876313 | ||||||
| chr17:78876314
|
G | A | 3 | a0001c0001t0010g0114a0001c0001t0021g0041a0001c0001t0051g0162 | 3 | HG00639.hp1 HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.131-2395C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876314 | ||||||
| chr17:78876400
|
T | C | 65 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(62): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-2481A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876400 | ||||||
| chr17:78876421
|
C | T | 65 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(62): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-2502G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876421 | ||||||
| chr17:78876492
|
T | C | 65 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(62): Show | 66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-2573A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876492 | ||||||
| chr17:78876648
|
C | A | 2 | a0001c0001t0029g0033a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.131-2729G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876648 | ||||||
| chr17:78876683
|
A | AT | 67 | a0001c0001t0001g0261a0001c0001t0001g0268a0001c0001t0001g0271others(64): Show | 68 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.131-2765dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876683 | ||||||
| chr17:78876683
|
A | ATT | 12 | a0001c0002t0001g0177a0001c0002t0001g0191a0001c0002t0001g0192others(9): Show | 12 | HG01070.hp2 HG01071.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-2766_131-2765d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876683 | ||||||
| chr17:78876683
|
A | T | 1 | a0001c0002t0016g0157 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.131-2764T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876683 | ||||||
| chr17:78876746
|
C | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-2827G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876746 | ||||||
| chr17:78876913
|
T | TA | 200 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.131-2995dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876913 | ||||||
| chr17:78876985
|
A | G | 10 | a0001c0001t0001g0305a0001c0001t0003g0267a0001c0001t0003g0289others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-3066T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876985 | ||||||
| chr17:78876997
|
G | A | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-3078C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876997 | ||||||
| chr17:78877071
|
T | C | 1 | a0001c0001t0005g0221 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.131-3152A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877071 | ||||||
| chr17:78877118
|
A | T | 6 | a0001c0002t0003g0001a0001c0002t0003g0217a0001c0002t0003g0244others(3): Show | 7 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-3199T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877118 | ||||||
| chr17:78877300
|
C | G | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.131-3381G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877300 | ||||||
| chr17:78877331
|
C | T | 1 | a0001c0001t0001g0212 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.131-3412G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877331 | ||||||
| chr17:78877388
|
A | T | 1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131-3469T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877388 | ||||||
| chr17:78877444
|
G | A | 66 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(63): Show | 67 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-3525C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877444 | ||||||
| chr17:78877546
|
CT | C | 66 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(63): Show | 67 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-3628delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877546 | ||||||
| chr17:78877554
|
AAAAGAAA others(2): Show |
A | 140 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(137): Show | 140 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.131-3644_131-3636d others(11): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877554 | ||||||
| chr17:78877555
|
A | T | 66 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(63): Show | 67 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-3636T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877555 | ||||||
| chr17:78877574
|
A | T | 1 | a0001c0001t0022g0266 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.131-3655T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877574 | ||||||
| chr17:78877615
|
C | T | 66 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(63): Show | 67 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-3696G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877615 | ||||||
| chr17:78877679
|
T | C | 66 | a0001c0001t0001g0271a0001c0001t0002g0112a0001c0001t0002g0125others(63): Show | 67 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-3760A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877679 | ||||||
| chr17:78877707
|
C | CT | 8 | a0001c0001t0003g0289a0001c0001t0005g0243a0001c0001t0007g0012others(5): Show | 8 | HG00609.hp2 HG00735.hp1 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-3789dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877707 | ||||||
| chr17:78877772
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.131-3853A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877772 | ||||||
| chr17:78877850
|
C | T | 1 | a0001c0001t0037g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.131-3931G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877850 | ||||||
| chr17:78877851
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.131-3932C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877851 | ||||||
| chr17:78877949
|
G | A | 1 | a0001c0001t0006g0104 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.131-4030C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877949 | ||||||
| chr17:78877958
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.131-4039C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877958 | ||||||
| chr17:78878063
|
C | G | 4 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-4144G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878063 | ||||||
| chr17:78878159
|
C | T | 268 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.131-4240G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878159 | ||||||
| chr17:78878176
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-4257G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878176 | ||||||
| chr17:78878177
|
G | C | 5 | a0001c0001t0003g0171a0001c0001t0010g0114a0001c0001t0021g0041others(2): Show | 5 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-4258C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878177 | ||||||
| chr17:78878262
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-4343G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878262 | ||||||
| chr17:78878302
|
T | C | 1 | a0001c0001t0001g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.131-4383A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878302 | ||||||
| chr17:78878338
|
T | C | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-4419A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878338 | ||||||
| chr17:78878340
|
G | C | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.131-4421C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878340 | ||||||
| chr17:78878379
|
T | C | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-4460A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878379 | ||||||
| chr17:78878410
|
G | C | 6 | a0001c0002t0003g0001a0001c0002t0003g0217a0001c0002t0003g0244others(3): Show | 7 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-4491C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878410 | ||||||
| chr17:78878430
|
A | C | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-4511T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878430 | ||||||
| chr17:78878452
|
C | T | 3 | a0001c0001t0001g0302a0001c0001t0018g0140a0001c0001t0035g0067 | 3 | HG02572.hp1 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.131-4533G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878452 | ||||||
| chr17:78878453
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-4534C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878453 | ||||||
| chr17:78878462
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-4543G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878462 | ||||||
| chr17:78878545
|
C | G | 3 | a0001c0001t0009g0013a0001c0001t0009g0030a0001c0001t0009g0031 | 3 | NA18964.hp2 NA18968.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.131-4626G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878545 | ||||||
| chr17:78878560
|
CTTCCCAG others(6): Show |
C | 1 | a0001c0002t0001g0175 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.131-4654_131-4642d others(15): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878560 | ||||||
| chr17:78878631
|
G | C | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-4712C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878631 | ||||||
| chr17:78878847
|
C | T | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-4928G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878847 | ||||||
| chr17:78878872
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-4953G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878872 | ||||||
| chr17:78878999
|
G | C | 1 | a0001c0001t0007g0009 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.131-5080C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878999 | ||||||
| chr17:78879024
|
C | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-5105G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879024 | ||||||
| chr17:78879104
|
T | C | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-5185A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879104 | ||||||
| chr17:78879146
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0287 | 2 | HG01106.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.131-5227T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879146 | ||||||
| chr17:78879182
|
A | G | 268 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.131-5263T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879182 | ||||||
| chr17:78879200
|
T | C | 1 | a0001c0001t0002g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.131-5281A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879200 | ||||||
| chr17:78879208
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-5289G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879208 | ||||||
| chr17:78879257
|
A | G | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-5338T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879257 | ||||||
| chr17:78879330
|
T | G | 268 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.131-5411A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879330 | ||||||
| chr17:78879331
|
T | A | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-5412A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879331 | ||||||
| chr17:78879375
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.131-5456G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879375 | ||||||
| chr17:78879511
|
T | A | 1 | a0001c0002t0001g0175 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.131-5592A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879511 | ||||||
| chr17:78879542
|
C | T | 3 | a0001c0001t0009g0013a0001c0001t0009g0030a0001c0001t0009g0031 | 3 | NA18964.hp2 NA18968.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.131-5623G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879542 | ||||||
| chr17:78879543
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-5624C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879543 | ||||||
| chr17:78879549
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-5630C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879549 | ||||||
| chr17:78879626
|
T | C | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-5707A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879626 | ||||||
| chr17:78879646
|
G | A | 268 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.131-5727C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879646 | ||||||
| chr17:78879653
|
C | T | 1 | a0002c0003t0004g0084 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.131-5734G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879653 | ||||||
| chr17:78879654
|
G | A | 57 | a0001c0001t0001g0212a0001c0001t0001g0271a0001c0001t0002g0125others(54): Show | 57 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.131-5735C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879654 | ||||||
| chr17:78879761
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.131-5842G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879761 | ||||||
| chr17:78879819
|
T | C | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-5900A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879819 | ||||||
| chr17:78879838
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-5919G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879838 | ||||||
| chr17:78879870
|
T | A | 3 | a0001c0001t0001g0305a0001c0001t0003g0267a0001c0001t0041g0046 | 3 | HG02809.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.131-5951A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879870 | ||||||
| chr17:78879902
|
C | A | 12 | a0001c0001t0001g0166a0001c0001t0001g0229a0001c0001t0001g0258others(9): Show | 12 | HG01123.hp2 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-5983G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879902 | ||||||
| chr17:78880015
|
A | T | 4 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-6096T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880015 | ||||||
| chr17:78880038
|
CT | C | 3 | a0001c0001t0001g0200a0001c0001t0001g0230a0001c0001t0005g0184 | 3 | NA18947.hp1 NA19063.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.131-6120delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880038 | ||||||
| chr17:78880102
|
T | C | 4 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-6183A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880102 | ||||||
| chr17:78880176
|
C | T | 2 | a0001c0001t0006g0094a0001c0001t0042g0093 | 2 | NA18945.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.131-6257G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880176 | ||||||
| chr17:78880177
|
G | A | 1 | a0001c0002t0004g0052 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.131-6258C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880177 | ||||||
| chr17:78880182
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131-6263C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880182 | ||||||
| chr17:78880217
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.131-6298G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880217 | ||||||
| chr17:78880219
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.131-6300G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880219 | ||||||
| chr17:78880336
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.131-6417C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880336 | ||||||
| chr17:78880374
|
G | C | 3 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067 | 3 | HG02572.hp1 HG02622.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.131-6455C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880374 | ||||||
| chr17:78880379
|
A | C | 1 | a0001c0002t0001g0175 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.131-6460T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880379 | ||||||
| chr17:78880382
|
C | T | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-6463G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880382 | ||||||
| chr17:78880410
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.131-6491C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880410 | ||||||
| chr17:78880411
|
G | A | 1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131-6492C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880411 | ||||||
| chr17:78880460
|
A | G | 208 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(205): Show | 208 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.131-6541T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880460 | ||||||
| chr17:78880521
|
T | C | 1 | a0001c0002t0004g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.131-6602A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880521 | ||||||
| chr17:78880535
|
C | CA | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-6617dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880535 | ||||||
| chr17:78880557
|
A | C | 1 | a0001c0001t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.131-6638T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880557 | ||||||
| chr17:78880574
|
G | A | 1 | a0001c0001t0005g0250 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.131-6655C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880574 | ||||||
| chr17:78880653
|
T | C | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-6734A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880653 | ||||||
| chr17:78880687
|
C | A | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-6768G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880687 | ||||||
| chr17:78880701
|
G | T | 2 | a0001c0001t0001g0282a0001c0001t0005g0178 | 2 | HG01123.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.131-6782C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880701 | ||||||
| chr17:78880722
|
G | A | 2 | a0001c0001t0027g0172a0001c0001t0032g0016 | 2 | HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.131-6803C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880722 | ||||||
| chr17:78880892
|
C | T | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-6973G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880892 | ||||||
| chr17:78880897
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-6978C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880897 | ||||||
| chr17:78880991
|
T | C | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-7072A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78880991 | ||||||
| chr17:78881249
|
T | C | 62 | a0001c0001t0001g0212a0001c0001t0001g0271a0001c0001t0002g0125others(59): Show | 63 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.131-7330A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881249 | ||||||
| chr17:78881280
|
T | C | 266 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(263): Show | 267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.131-7361A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881280 | ||||||
| chr17:78881281
|
T | C | 1 | a0001c0001t0002g0074 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.131-7362A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881281 | ||||||
| chr17:78881282
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.131-7363G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881282 | ||||||
| chr17:78881304
|
T | C | 1 | a0001c0001t0011g0195 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.131-7385A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881304 | ||||||
| chr17:78881319
|
C | T | 2 | a0001c0001t0029g0033a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.131-7400G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881319 | ||||||
| chr17:78881346
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0011g0195 | 2 | HG03041.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.131-7427A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881346 | ||||||
| chr17:78881413
|
T | C | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-7494A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881413 | ||||||
| chr17:78881418
|
G | C | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-7499C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881418 | ||||||
| chr17:78881545
|
G | A | 1 | a0001c0001t0003g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.131-7626C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881545 | ||||||
| chr17:78881573
|
G | A | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-7654C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881573 | ||||||
| chr17:78881589
|
C | A | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-7670G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881589 | ||||||
| chr17:78881590
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-7671C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881590 | ||||||
| chr17:78881597
|
G | T | 1 | a0001c0001t0008g0017 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.131-7678C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881597 | ||||||
| chr17:78881671
|
G | T | 1 | a0001c0001t0001g0302 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.131-7752C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881671 | ||||||
| chr17:78881742
|
T | A | 204 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(201): Show | 204 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.131-7823A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881742 | ||||||
| chr17:78881969
|
CTCTT | C | 203 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(200): Show | 203 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.131-8054_131-8051d others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881969 | ||||||
| chr17:78882028
|
G | A | 2 | a0001c0001t0003g0267a0001c0001t0041g0046 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.131-8109C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882028 | ||||||
| chr17:78882251
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.131-8332G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882251 | ||||||
| chr17:78882267
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.131-8348G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882267 | ||||||
| chr17:78882394
|
T | G | 4 | a0001c0001t0001g0271a0001c0001t0002g0125a0001c0001t0005g0165others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-8475A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882394 | ||||||
| chr17:78882447
|
C | T | 8 | a0001c0001t0001g0261a0001c0001t0003g0171a0001c0001t0010g0114others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-8528G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882447 | ||||||
| chr17:78882450
|
G | A | 144 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(141): Show | 144 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.131-8531C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882450 | ||||||
| chr17:78882536
|
G | A | 1 | a0001c0002t0023g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.131-8617C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882536 | ||||||
| chr17:78882547
|
G | A | 66 | a0001c0001t0001g0190a0001c0001t0001g0194a0001c0001t0001g0200others(63): Show | 66 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.131-8628C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882547 | ||||||
| chr17:78882624
|
C | T | 201 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.131-8705G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882624 | ||||||
| chr17:78882638
|
G | A | 5 | a0001c0001t0001g0190a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG00673.hp2 HG02074.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-8719C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882638 | ||||||
| chr17:78882642
|
C | A | 1 | a0001c0001t0002g0074 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.131-8723G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882642 | ||||||
| chr17:78882654
|
C | A | 4 | a0001c0001t0003g0225a0001c0001t0018g0140a0001c0001t0035g0067others(1): Show | 4 | HG02559.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-8735G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882654 | ||||||
| chr17:78882674
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.131-8755C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882674 | ||||||
| chr17:78882782
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.131-8863C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882782 | ||||||
| chr17:78882820
|
T | C | 267 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(264): Show | 268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-8901A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882820 | ||||||
| chr17:78882858
|
C | T | 1 | a0001c0001t0005g0311 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.131-8939G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882858 | ||||||
| chr17:78882859
|
A | G | 268 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(265): Show | 269 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.131-8940T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882859 | ||||||
| chr17:78882898
|
G | A | 54 | a0001c0001t0001g0212a0001c0001t0001g0305a0001c0001t0003g0309others(51): Show | 55 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.131-8979C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882898 | ||||||
| chr17:78883034
|
C | T | 49 | a0001c0001t0001g0212a0001c0001t0001g0305a0001c0001t0003g0309others(46): Show | 49 | HG00558.hp2 HG00609.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.131-9115G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883034 | ||||||
| chr17:78883307
|
T | G | 11 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0001t0001g0230others(8): Show | 11 | HG02027.hp1 HG02080.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-9388A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883307 | ||||||
| chr17:78883581
|
C | T | 5 | a0001c0001t0003g0171a0001c0001t0010g0114a0001c0001t0021g0041others(2): Show | 5 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-9662G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883581 | ||||||
| chr17:78883582
|
G | A | 35 | a0001c0001t0001g0166a0001c0001t0001g0229a0001c0001t0001g0248others(32): Show | 35 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.131-9663C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883582 | ||||||
| chr17:78883634
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.131-9715C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883634 | ||||||
| chr17:78883726
|
G | A | 1 | a0001c0001t0007g0019 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.131-9807C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883726 | ||||||
| chr17:78883743
|
G | GA | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-9825dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883743 | ||||||
| chr17:78883936
|
G | A | 22 | a0001c0001t0001g0284a0001c0001t0001g0287a0001c0001t0001g0314others(19): Show | 22 | HG01074.hp2 HG01106.hp1 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-10017C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78883936 | ||||||
| chr17:78884051
|
G | A | 1 | a0001c0001t0004g0131 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.131-10132C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884051 | ||||||
| chr17:78884107
|
G | A | 1 | a0001c0001t0010g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.131-10188C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884107 | ||||||
| chr17:78884236
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.131-10317G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884236 | ||||||
| chr17:78884358
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-10439C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884358 | ||||||
| chr17:78884562
|
C | T | 1 | a0001c0001t0005g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.131-10643G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884562 | ||||||
| chr17:78884613
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.131-10694G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884613 | ||||||
| chr17:78884616
|
C | T | 5 | a0001c0001t0001g0284a0001c0001t0001g0287a0001c0001t0001g0302others(2): Show | 5 | HG01106.hp1 HG01891.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-10697G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884616 | ||||||
| chr17:78884643
|
G | A | 11 | a0001c0001t0005g0221a0001c0002t0003g0313a0001c0002t0005g0269others(8): Show | 11 | HG00558.hp1 HG00621.hp1 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-10724C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884643 | ||||||
| chr17:78884737
|
G | A | 1 | a0001c0001t0041g0046 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.131-10818C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884737 | ||||||
| chr17:78884741
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-10822G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884741 | ||||||
| chr17:78884780
|
T | C | 1 | a0001c0001t0005g0179 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.131-10861A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884780 | ||||||
| chr17:78884871
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0001g0287 | 2 | HG01106.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.131-10952G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884871 | ||||||
| chr17:78884872
|
G | A | 1 | a0001c0001t0009g0029 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.131-10953C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884872 | ||||||
| chr17:78884975
|
A | G | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-11056T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78884975 | ||||||
| chr17:78885046
|
C | T | 10 | a0001c0001t0001g0194a0001c0001t0001g0200a0001c0001t0001g0230others(7): Show | 10 | HG02027.hp1 HG02080.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-11127G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885046 | ||||||
| chr17:78885106
|
C | T | 2 | a0001c0001t0003g0309a0001c0002t0003g0288 | 2 | HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.131-11187G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885106 | ||||||
| chr17:78885147
|
C | T | 1 | a0001c0001t0008g0018 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.131-11228G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885147 | ||||||
| chr17:78885164
|
C | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-11245G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885164 | ||||||
| chr17:78885346
|
A | G | 12 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-11427T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885346 | ||||||
| chr17:78885352
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.131-11433G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885352 | ||||||
| chr17:78885563
|
A | G | 1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131-11644T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885563 | ||||||
| chr17:78885621
|
T | C | 188 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(185): Show | 189 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.131-11702A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885621 | ||||||
| chr17:78885628
|
G | A | 1 | a0001c0002t0043g0117 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.131-11709C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885628 | ||||||
| chr17:78885669
|
T | TGGGTGTG others(2): Show |
5 | a0001c0001t0001g0190a0001c0001t0002g0089a0001c0001t0002g0090others(2): Show | 5 | HG00673.hp2 HG02074.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-11759_131-1175 others(13): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885669 | ||||||
| chr17:78885801
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.131-11882C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885801 | ||||||
| chr17:78885930
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-12011C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78885930 | ||||||
| chr17:78886174
|
G | A | 1 | a0001c0001t0005g0296 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.131-12255C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886174 | ||||||
| chr17:78886214
|
G | A | 1 | a0001c0002t0043g0117 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.131-12295C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886214 | ||||||
| chr17:78886270
|
G | T | 1 | a0001c0001t0020g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.131-12351C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886270 | ||||||
| chr17:78886373
|
G | A | 5 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(2): Show | 5 | NA18942.hp2 NA18989.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-12454C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886373 | ||||||
| chr17:78886382
|
AT | A | 21 | a0001c0001t0001g0248a0001c0001t0001g0268a0001c0001t0002g0149others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.131-12464delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886382 | ||||||
| chr17:78886433
|
C | A | 3 | a0001c0001t0001g0284a0001c0001t0001g0302a0001c0001t0017g0133 | 3 | HG01106.hp1 HG01891.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.131-12514G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886433 | ||||||
| chr17:78886573
|
T | C | 5 | a0001c0001t0003g0171a0001c0001t0010g0114a0001c0001t0021g0041others(2): Show | 5 | HG00639.hp1 HG02615.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-12654A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886573 | ||||||
| chr17:78886682
|
G | A | 12 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-12763C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886682 | ||||||
| chr17:78886740
|
T | C | 1 | a0001c0001t0026g0290 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.131-12821A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886740 | ||||||
| chr17:78886785
|
C | T | 1 | a0001c0001t0006g0087 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.131-12866G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886785 | ||||||
| chr17:78886828
|
G | C | 9 | a0001c0001t0001g0268a0001c0001t0002g0149a0001c0001t0003g0173others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-12909C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886828 | ||||||
| chr17:78886944
|
A | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13025T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78886944 | ||||||
| chr17:78887103
|
CA | C | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13185delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887103 | ||||||
| chr17:78887154
|
G | A | 9 | a0001c0001t0001g0268a0001c0001t0002g0149a0001c0001t0003g0173others(6): Show | 9 | HG01884.hp1 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-13235C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887154 | ||||||
| chr17:78887389
|
T | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13470A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887389 | ||||||
| chr17:78887498
|
C | T | 1 | a0001c0001t0037g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.131-13579G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887498 | ||||||
| chr17:78887508
|
C | T | 12 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-13589G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887508 | ||||||
| chr17:78887512
|
A | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13593T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887512 | ||||||
| chr17:78887531
|
C | T | 1 | a0001c0001t0020g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.131-13612G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887531 | ||||||
| chr17:78887574
|
G | A | 1 | a0001c0001t0004g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.131-13655C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887574 | ||||||
| chr17:78887665
|
A | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13746T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887665 | ||||||
| chr17:78887674
|
C | T | 2 | a0001c0001t0003g0309a0001c0002t0003g0288 | 2 | HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.131-13755G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887674 | ||||||
| chr17:78887736
|
GA | G | 102 | a0001c0001t0001g0166a0001c0001t0001g0181a0001c0001t0001g0198others(99): Show | 102 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.131-13818delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887736 | ||||||
| chr17:78887737
|
A | G | 1 | a0001c0001t0004g0054 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.131-13818T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887737 | ||||||
| chr17:78887742
|
A | AG | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13824_131-1382 others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887742 | ||||||
| chr17:78887743
|
A | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13824T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887743 | ||||||
| chr17:78887744
|
A | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13825T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887744 | ||||||
| chr17:78887827
|
C | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13908G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887827 | ||||||
| chr17:78887863
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-13944C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887863 | ||||||
| chr17:78887942
|
T | C | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-14023A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78887942 | ||||||
| chr17:78888144
|
T | A | 67 | a0001c0001t0001g0166a0001c0001t0001g0198a0001c0001t0001g0229others(64): Show | 67 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-14225A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888144 | ||||||
| chr17:78888155
|
C | CT | 88 | a0001c0001t0001g0166a0001c0001t0001g0198a0001c0001t0001g0229others(85): Show | 88 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.131-14237dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888155 | ||||||
| chr17:78888169
|
T | C | 2 | a0001c0001t0009g0029a0001c0001t0033g0028 | 2 | NA18947.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.131-14250A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888169 | ||||||
| chr17:78888315
|
C | A | 1 | a0001c0001t0002g0143 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.131-14396G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888315 | ||||||
| chr17:78888323
|
T | A | 1 | a0001c0001t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.131-14404A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888323 | ||||||
| chr17:78888342
|
T | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-14423A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888342 | ||||||
| chr17:78888362
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-14443C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888362 | ||||||
| chr17:78888398
|
A | G | 119 | a0001c0001t0001g0166a0001c0001t0001g0198a0001c0001t0001g0229others(116): Show | 119 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(116): Show |
intron_variant | MODIFIER | c.131-14479T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888398 | ||||||
| chr17:78888406
|
C | T | 5 | a0001c0001t0004g0060a0001c0001t0004g0071a0001c0001t0004g0126others(2): Show | 5 | HG01069.hp1 HG01175.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-14487G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888406 | ||||||
| chr17:78888458
|
T | C | 11 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0002g0143others(8): Show | 11 | HG02965.hp1 HG03098.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-14539A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888458 | ||||||
| chr17:78888575
|
C | T | 3 | a0001c0001t0003g0267a0001c0001t0005g0257a0001c0001t0041g0046 | 3 | HG02965.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-14656G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888575 | ||||||
| chr17:78888699
|
C | T | 2 | a0001c0001t0007g0011a0001c0001t0008g0026 | 2 | HG00544.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.131-14780G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888699 | ||||||
| chr17:78888870
|
A | G | 9 | a0001c0001t0001g0261a0001c0001t0002g0136a0001c0001t0002g0137others(6): Show | 9 | HG02109.hp1 HG02970.hp2 HG03225.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-14951T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78888870 | ||||||
| chr17:78889035
|
T | C | 113 | a0001c0001t0001g0166a0001c0001t0001g0198a0001c0001t0001g0229others(110): Show | 113 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.131-15116A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889035 | ||||||
| chr17:78889039
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.131-15120G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889039 | ||||||
| chr17:78889094
|
C | T | 1 | a0001c0001t0003g0203 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.131-15175G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889094 | ||||||
| chr17:78889136
|
T | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-15217A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889136 | ||||||
| chr17:78889148
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.131-15229G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889148 | ||||||
| chr17:78889230
|
A | C | 7 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0003g0267others(4): Show | 7 | HG02965.hp1 HG03098.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-15311T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889230 | ||||||
| chr17:78889278
|
C | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-15359G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889278 | ||||||
| chr17:78889310
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-15391C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889310 | ||||||
| chr17:78889450
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.131-15531G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889450 | ||||||
| chr17:78889475
|
T | G | 4 | a0001c0001t0010g0039a0001c0001t0010g0040a0001c0001t0010g0048others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-15556A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889475 | ||||||
| chr17:78889504
|
T | C | 12 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-15585A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889504 | ||||||
| chr17:78889580
|
T | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-15661A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889580 | ||||||
| chr17:78889636
|
G | A | 1 | a0001c0002t0028g0035 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.131-15717C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889636 | ||||||
| chr17:78889696
|
G | C | 2 | a0001c0001t0029g0033a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.131-15777C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889696 | ||||||
| chr17:78889697
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.131-15778C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889697 | ||||||
| chr17:78889750
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.131-15831G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889750 | ||||||
| chr17:78889754
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.131-15835T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889754 | ||||||
| chr17:78889847
|
C | T | 28 | a0001c0001t0001g0284a0001c0001t0001g0314a0001c0001t0002g0062others(25): Show | 28 | HG01074.hp2 HG01106.hp1 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.131-15928G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889847 | ||||||
| chr17:78889895
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-15976C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889895 | ||||||
| chr17:78889963
|
C | CA | 36 | a0001c0001t0001g0198a0001c0001t0001g0236a0001c0001t0001g0237others(33): Show | 36 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.131-16045dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78889963 | ||||||
| chr17:78890110
|
C | T | 5 | a0001c0001t0002g0137a0001c0001t0002g0138a0001c0001t0002g0139others(2): Show | 5 | HG03491.hp1 NA18942.hp2 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-16191G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890110 | ||||||
| chr17:78890113
|
CTCAA | C | 12 | a0001c0001t0002g0134a0001c0001t0002g0149a0001c0001t0003g0289others(9): Show | 12 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-16198_131-1619 others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890113 | ||||||
| chr17:78890125
|
A | G | 1 | a0001c0001t0005g0286 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.131-16206T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890125 | ||||||
| chr17:78890135
|
A | C | 2 | a0001c0001t0002g0075a0001c0001t0003g0267 | 2 | HG03098.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.131-16216T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890135 | ||||||
| chr17:78890203
|
C | CT | 49 | a0001c0001t0001g0284a0001c0001t0001g0287a0001c0001t0001g0302others(46): Show | 49 | HG00544.hp2 HG01074.hp2 HG01106.hp1 others(46): Show |
intron_variant | MODIFIER | c.131-16285dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890203 | ||||||
| chr17:78890203
|
CT | C | 7 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0002g0063others(4): Show | 7 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-16285delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890203 | ||||||
| chr17:78890225
|
C | T | 1 | a0001c0002t0004g0102 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.131-16306G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890225 | ||||||
| chr17:78890232
|
C | T | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-16313G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890232 | ||||||
| chr17:78890258
|
G | C | 1 | a0001c0001t0049g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-16339C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890258 | ||||||
| chr17:78890271
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.131-16352C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890271 | ||||||
| chr17:78890398
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.131-16479G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890398 | ||||||
| chr17:78890486
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-16567C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890486 | ||||||
| chr17:78890487
|
T | C | 36 | a0001c0001t0001g0271a0001c0001t0001g0284a0001c0001t0001g0302others(33): Show | 36 | HG01074.hp2 HG01106.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.131-16568A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890487 | ||||||
| chr17:78890488
|
G | A | 32 | a0001c0001t0001g0284a0001c0001t0001g0302a0001c0001t0001g0314others(29): Show | 32 | HG01074.hp2 HG01106.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.131-16569C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890488 | ||||||
| chr17:78890596
|
C | A | 2 | a0001c0001t0001g0291a0001c0001t0055g0270 | 2 | HG01261.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.131-16677G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890596 | ||||||
| chr17:78890661
|
G | A | 3 | a0001c0001t0003g0267a0001c0001t0005g0257a0001c0001t0041g0046 | 3 | HG02965.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-16742C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890661 | ||||||
| chr17:78890830
|
C | T | 1 | a0001c0001t0003g0170 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.131-16911G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890830 | ||||||
| chr17:78890921
|
A | G | 9 | a0001c0001t0003g0289a0001c0001t0003g0293a0001c0001t0003g0310others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-17002T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890921 | ||||||
| chr17:78890943
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.131-17024G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78890943 | ||||||
| chr17:78891023
|
T | C | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-17104A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891023 | ||||||
| chr17:78891170
|
T | C | 4 | a0001c0001t0010g0039a0001c0001t0010g0040a0001c0001t0010g0048others(1): Show | 4 | HG01243.hp2 HG02486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-17251A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891170 | ||||||
| chr17:78891191
|
G | A | 1 | a0001c0001t0002g0106 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.131-17272C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891191 | ||||||
| chr17:78891262
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0245 | 2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.131-17343G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891262 | ||||||
| chr17:78891278
|
G | C | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-17359C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891278 | ||||||
| chr17:78891345
|
C | T | 1 | a0001c0001t0049g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-17426G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891345 | ||||||
| chr17:78891350
|
C | A | 12 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(9): Show | 12 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-17431G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891350 | ||||||
| chr17:78891354
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.131-17435G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891354 | ||||||
| chr17:78891506
|
T | C | 1 | a0001c0002t0023g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.131-17587A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891506 | ||||||
| chr17:78891528
|
C | T | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-17609G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891528 | ||||||
| chr17:78891576
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-17657C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891576 | ||||||
| chr17:78891610
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-17691A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891610 | ||||||
| chr17:78891620
|
C | A | 1 | a0001c0001t0049g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-17701G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891620 | ||||||
| chr17:78891638
|
A | G | 1 | a0001c0001t0049g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-17719T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891638 | ||||||
| chr17:78891681
|
G | A | 4 | a0001c0001t0002g0057a0001c0001t0002g0079a0001c0001t0007g0023others(1): Show | 4 | HG00408.hp2 HG02027.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-17762C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891681 | ||||||
| chr17:78891772
|
C | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-17853G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891772 | ||||||
| chr17:78891794
|
C | T | 1 | a0001c0001t0007g0020 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.131-17875G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891794 | ||||||
| chr17:78891959
|
T | C | 31 | a0001c0001t0001g0284a0001c0001t0001g0302a0001c0001t0002g0062others(28): Show | 31 | HG01074.hp2 HG01106.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.131-18040A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78891959 | ||||||
| chr17:78892003
|
C | T | 1 | a0001c0001t0007g0010 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.131-18084G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892003 | ||||||
| chr17:78892009
|
C | T | 1 | a0001c0001t0002g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.131-18090G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892009 | ||||||
| chr17:78892129
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-18210C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892129 | ||||||
| chr17:78892141
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-18222A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892141 | ||||||
| chr17:78892278
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.131-18359T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892278 | ||||||
| chr17:78892293
|
T | C | 10 | a0001c0001t0002g0062a0001c0001t0002g0149a0001c0001t0003g0173others(7): Show | 10 | HG01884.hp1 HG02451.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-18374A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892293 | ||||||
| chr17:78892392
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-18473C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892392 | ||||||
| chr17:78892452
|
C | T | 1 | a0001c0001t0023g0294 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.131-18533G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892452 | ||||||
| chr17:78892537
|
G | A | 1 | a0001c0001t0010g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.131-18618C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892537 | ||||||
| chr17:78892593
|
C | A | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.131-18674G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892593 | ||||||
| chr17:78892594
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-18675C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892594 | ||||||
| chr17:78892666
|
C | T | 8 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0002g0143others(5): Show | 8 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-18747G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892666 | ||||||
| chr17:78892853
|
G | A | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-18934C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892853 | ||||||
| chr17:78892915
|
G | T | 13 | a0001c0001t0001g0190a0001c0001t0003g0225a0001c0001t0005g0221others(10): Show | 13 | HG00558.hp1 HG00621.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.131-18996C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78892915 | ||||||
| chr17:78893037
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.131-19118C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893037 | ||||||
| chr17:78893100
|
T | G | 1 | a0001c0002t0001g0191 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.131-19181A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893100 | ||||||
| chr17:78893113
|
A | G | 2 | a0001c0001t0002g0149a0001c0001t0006g0150 | 2 | HG01884.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.131-19194T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893113 | ||||||
| chr17:78893116
|
C | CACATGTG others(21): Show |
1 | a0001c0001t0003g0207 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.131-19225_131-1919 others(32): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893116 | ||||||
| chr17:78893116
|
CACATGTG others(21): Show |
C | 2 | a0001c0001t0011g0195a0001c0001t0019g0092 | 2 | HG02738.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.131-19225_131-1919 others(32): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893116 | ||||||
| chr17:78893129
|
A | G | 1 | a0001c0001t0009g0014 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.131-19210T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893129 | ||||||
| chr17:78893140
|
T | C | 2 | a0001c0002t0001g0213a0001c0002t0005g0187 | 2 | NA18612.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.131-19221A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893140 | ||||||
| chr17:78893140
|
TGC | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-19223_131-1922 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893140 | ||||||
| chr17:78893160
|
G | GGT | 3 | a0001c0002t0003g0262a0001c0002t0003g0275a0001c0002t0054g0276 | 3 | HG01081.hp1 HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.131-19243_131-1924 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893160 | ||||||
| chr17:78893198
|
A | G | 3 | a0001c0001t0003g0267a0001c0001t0005g0257a0001c0001t0041g0046 | 3 | HG02965.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-19279T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893198 | ||||||
| chr17:78893200
|
GATGTGTG others(3): Show |
G | 16 | a0001c0001t0001g0190a0001c0001t0001g0284a0001c0001t0002g0134others(13): Show | 16 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.131-19291_131-1928 others(14): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893200 | ||||||
| chr17:78893200
|
GATGTGTG others(7): Show |
G | 3 | a0001c0001t0003g0267a0001c0001t0005g0257a0001c0001t0041g0046 | 3 | HG02965.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-19295_131-1928 others(18): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893200 | ||||||
| chr17:78893212
|
T | TGTGTGTG others(15): Show |
4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19294_131-1929 others(26): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893212 | ||||||
| chr17:78893235
|
A | G | 3 | a0001c0001t0001g0200a0001c0001t0001g0230a0001c0001t0003g0211 | 3 | NA18947.hp1 NA19066.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.131-19316T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893235 | ||||||
| chr17:78893260
|
G | GGGGTGTG others(21): Show |
2 | a0001c0001t0029g0033a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.131-19369_131-1934 others(32): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893260 | ||||||
| chr17:78893285
|
G | T | 1 | a0001c0001t0007g0023 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.131-19366C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893285 | ||||||
| chr17:78893292
|
TG | T | 29 | a0001c0001t0001g0302a0001c0001t0002g0062a0001c0001t0002g0125others(26): Show | 29 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.131-19374delC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893292 | ||||||
| chr17:78893362
|
G | T | 128 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0198others(125): Show | 128 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.131-19443C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893362 | ||||||
| chr17:78893364
|
G | T | 128 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0198others(125): Show | 128 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.131-19445C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893364 | ||||||
| chr17:78893375
|
G | C | 29 | a0001c0001t0001g0302a0001c0001t0002g0062a0001c0001t0002g0125others(26): Show | 29 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.131-19456C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893375 | ||||||
| chr17:78893381
|
GTGCAGGG others(7): Show |
G | 3 | a0001c0002t0016g0157a0001c0002t0016g0159a0001c0002t0034g0155 | 3 | HG00558.hp2 HG02074.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.131-19476_131-1946 others(18): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893381 | ||||||
| chr17:78893405
|
G | GTGTGCGC others(9): Show |
123 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0198others(120): Show | 123 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.131-19487_131-1948 others(20): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893405 | ||||||
| chr17:78893405
|
G | GTGTGTGC others(9): Show |
1 | a0001c0001t0049g0146 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.131-19487_131-1948 others(20): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893405 | ||||||
| chr17:78893410
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19491A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893410 | ||||||
| chr17:78893413
|
A | G | 305 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(302): Show | 306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.131-19494T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893413 | ||||||
| chr17:78893417
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19498C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893417 | ||||||
| chr17:78893418
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19499C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893418 | ||||||
| chr17:78893421
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19502C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893421 | ||||||
| chr17:78893428
|
C | CGT | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19510_131-1950 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893428 | ||||||
| chr17:78893432
|
G | GGT | 128 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0198others(125): Show | 128 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.131-19515_131-1951 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893432 | ||||||
| chr17:78893461
|
G | C | 1 | a0001c0001t0035g0067 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.131-19542C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893461 | ||||||
| chr17:78893501
|
G | A | 12 | a0001c0001t0001g0190a0001c0001t0005g0221a0001c0002t0003g0313others(9): Show | 12 | HG00558.hp1 HG00621.hp1 HG01516.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-19582C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893501 | ||||||
| chr17:78893514
|
C | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19595G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893514 | ||||||
| chr17:78893527
|
GTTTA | G | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-19612_131-1960 others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893527 | ||||||
| chr17:78893529
|
TTA | T | 37 | a0001c0001t0001g0271a0001c0001t0001g0302a0001c0001t0002g0045others(34): Show | 37 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.131-19612_131-1961 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893529 | ||||||
| chr17:78893550
|
T | C | 1 | a0001c0001t0006g0088 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.131-19631A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893550 | ||||||
| chr17:78893617
|
G | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-19698C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893617 | ||||||
| chr17:78893649
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.131-19730C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893649 | ||||||
| chr17:78893718
|
A | C | 1 | a0001c0001t0003g0231 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.131-19799T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893718 | ||||||
| chr17:78893768
|
T | C | 3 | a0001c0002t0001g0307a0001c0002t0003g0306a0001c0002t0003g0308 | 3 | HG02976.hp2 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.131-19849A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893768 | ||||||
| chr17:78893814
|
A | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-19895T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893814 | ||||||
| chr17:78893856
|
A | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-19937T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893856 | ||||||
| chr17:78893888
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.131-19969A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78893888 | ||||||
| chr17:78894095
|
A | G | 37 | a0001c0001t0001g0271a0001c0001t0001g0302a0001c0001t0002g0045others(34): Show | 37 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.131-20176T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894095 | ||||||
| chr17:78894149
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131-20230G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894149 | ||||||
| chr17:78894193
|
A | AC | 18 | a0001c0001t0001g0190a0001c0001t0002g0109a0001c0001t0002g0161others(15): Show | 18 | HG00558.hp1 HG00621.hp1 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.131-20275dupG | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894193 | ||||||
| chr17:78894201
|
C | T | 38 | a0001c0001t0001g0271a0001c0001t0001g0302a0001c0001t0002g0045others(35): Show | 38 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.131-20282G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894201 | ||||||
| chr17:78894233
|
A | C | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-20314T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894233 | ||||||
| chr17:78894413
|
A | G | 28 | a0001c0001t0001g0302a0001c0001t0002g0062a0001c0001t0002g0125others(25): Show | 28 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-20494T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894413 | ||||||
| chr17:78894418
|
G | A | 1 | a0001c0002t0003g0217 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.131-20499C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894418 | ||||||
| chr17:78894425
|
A | G | 28 | a0001c0001t0001g0302a0001c0001t0002g0062a0001c0001t0002g0125others(25): Show | 28 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-20506T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894425 | ||||||
| chr17:78894456
|
G | A | 8 | a0001c0001t0003g0289a0001c0001t0003g0293a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-20537C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894456 | ||||||
| chr17:78894642
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-20723A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894642 | ||||||
| chr17:78894782
|
A | G | 128 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0198others(125): Show | 128 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.131-20863T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894782 | ||||||
| chr17:78894830
|
C | A | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-20911G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894830 | ||||||
| chr17:78894877
|
C | T | 29 | a0001c0001t0001g0302a0001c0001t0002g0062a0001c0001t0002g0125others(26): Show | 29 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.131-20958G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894877 | ||||||
| chr17:78894878
|
G | A | 3 | a0001c0001t0001g0282a0001c0001t0002g0042a0001c0001t0005g0178 | 3 | HG01123.hp2 HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.131-20959C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78894878 | ||||||
| chr17:78895056
|
G | A | 29 | a0001c0001t0001g0302a0001c0001t0002g0062a0001c0001t0002g0125others(26): Show | 29 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.131-21137C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895056 | ||||||
| chr17:78895065
|
G | A | 1 | a0001c0001t0008g0026 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.131-21146C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895065 | ||||||
| chr17:78895078
|
C | T | 8 | a0001c0001t0003g0289a0001c0001t0003g0293a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-21159G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895078 | ||||||
| chr17:78895097
|
A | G | 1 | a0001c0002t0053g0254 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.131-21178T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895097 | ||||||
| chr17:78895108
|
C | T | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-21189G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895108 | ||||||
| chr17:78895174
|
G | A | 8 | a0001c0001t0003g0289a0001c0001t0003g0293a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-21255C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895174 | ||||||
| chr17:78895383
|
C | T | 6 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(3): Show | 6 | HG03491.hp1 NA18942.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-21464G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895383 | ||||||
| chr17:78895507
|
T | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-21588A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895507 | ||||||
| chr17:78895717
|
T | C | 40 | a0001c0001t0001g0271a0001c0001t0001g0284a0001c0001t0001g0302others(37): Show | 40 | HG01074.hp2 HG01106.hp1 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.131-21798A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895717 | ||||||
| chr17:78895786
|
G | A | 3 | a0001c0001t0001g0284a0001c0001t0002g0134a0001c0001t0049g0146 | 3 | HG01106.hp1 HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.131-21867C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895786 | ||||||
| chr17:78895792
|
G | A | 1 | a0001c0001t0004g0098 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.131-21873C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895792 | ||||||
| chr17:78895920
|
C | G | 36 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0229others(33): Show | 36 | HG00558.hp1 HG00621.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.131-22001G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78895920 | ||||||
| chr17:78896147
|
T | C | 1 | a0001c0001t0020g0127 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.131-22228A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896147 | ||||||
| chr17:78896154
|
T | C | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-22235A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896154 | ||||||
| chr17:78896276
|
G | C | 3 | a0001c0001t0003g0267a0001c0001t0005g0257a0001c0001t0041g0046 | 3 | HG02965.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-22357C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896276 | ||||||
| chr17:78896335
|
G | T | 1 | a0001c0001t0002g0099 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.131-22416C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896335 | ||||||
| chr17:78896385
|
C | T | 1 | a0001c0002t0005g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.131-22466G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896385 | ||||||
| chr17:78896486
|
G | A | 30 | a0001c0001t0001g0302a0001c0001t0002g0062a0001c0001t0002g0125others(27): Show | 30 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.131-22567C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896486 | ||||||
| chr17:78896581
|
C | T | 88 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0229others(85): Show | 88 | HG00558.hp1 HG00621.hp1 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.131-22662G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896581 | ||||||
| chr17:78896610
|
T | C | 31 | a0001c0001t0001g0190a0001c0001t0001g0271a0001c0001t0001g0284others(28): Show | 31 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.131-22691A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896610 | ||||||
| chr17:78896630
|
A | C | 88 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0229others(85): Show | 88 | HG00558.hp1 HG00621.hp1 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.131-22711T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896630 | ||||||
| chr17:78896635
|
G | C | 1 | a0001c0002t0003g0255 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.131-22716C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896635 | ||||||
| chr17:78896636
|
A | C | 72 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0229others(69): Show | 72 | HG00558.hp1 HG00621.hp1 HG01074.hp2 others(69): Show |
intron_variant | MODIFIER | c.131-22717T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896636 | ||||||
| chr17:78896695
|
C | G | 2 | a0001c0001t0001g0212a0001c0002t0009g0037 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.131-22776G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896695 | ||||||
| chr17:78896715
|
C | T | 1 | a0001c0001t0021g0047 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.131-22796G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896715 | ||||||
| chr17:78896735
|
G | A | 3 | a0001c0001t0001g0261a0001c0001t0026g0224a0001c0001t0048g0043 | 3 | HG02109.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.131-22816C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896735 | ||||||
| chr17:78896856
|
A | G | 8 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0002g0143others(5): Show | 8 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-22937T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896856 | ||||||
| chr17:78896942
|
A | G | 8 | a0001c0001t0003g0289a0001c0001t0003g0293a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-23023T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78896942 | ||||||
| chr17:78897053
|
C | T | 30 | a0001c0001t0001g0190a0001c0001t0001g0248a0001c0001t0001g0284others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(27): Show |
intron_variant | MODIFIER | c.131-23134G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897053 | ||||||
| chr17:78897095
|
AC | A | 93 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0229others(90): Show | 93 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.131-23177delG | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897095 | ||||||
| chr17:78897113
|
G | A | 1 | a0001c0002t0012g0186 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.131-23194C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897113 | ||||||
| chr17:78897151
|
T | C | 4 | a0001c0001t0001g0271a0001c0001t0002g0045a0001c0001t0005g0165others(1): Show | 4 | HG03130.hp1 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-23232A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897151 | ||||||
| chr17:78897154
|
G | A | 17 | a0001c0001t0001g0166a0001c0001t0001g0229a0001c0001t0001g0258others(14): Show | 17 | HG01123.hp2 HG01884.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-23235C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897154 | ||||||
| chr17:78897174
|
G | A | 10 | a0001c0001t0001g0208a0001c0001t0001g0240a0001c0001t0001g0246others(7): Show | 10 | HG00621.hp2 HG03831.hp1 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-23255C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897174 | ||||||
| chr17:78897264
|
A | G | 4 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(1): Show | 4 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-23345T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897264 | ||||||
| chr17:78897312
|
G | T | 1 | a0001c0001t0003g0196 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.131-23393C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897312 | ||||||
| chr17:78897358
|
C | T | 1 | a0001c0002t0039g0144 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.131-23439G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897358 | ||||||
| chr17:78897445
|
C | T | 3 | a0001c0001t0003g0267a0001c0001t0005g0257a0001c0001t0041g0046 | 3 | HG02965.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.131-23526G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897445 | ||||||
| chr17:78897457
|
A | G | 46 | a0001c0001t0001g0271a0001c0001t0001g0302a0001c0001t0002g0045others(43): Show | 46 | HG01074.hp2 HG01243.hp2 HG01884.hp1 others(43): Show |
intron_variant | MODIFIER | c.131-23538T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897457 | ||||||
| chr17:78897479
|
C | T | 1 | a0001c0001t0002g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.131-23560G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897479 | ||||||
| chr17:78897580
|
G | A | 1 | a0001c0002t0003g0288 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-23661C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897580 | ||||||
| chr17:78897589
|
A | G | 99 | a0001c0001t0001g0166a0001c0001t0001g0190a0001c0001t0001g0229others(96): Show | 99 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.131-23670T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897589 | ||||||
| chr17:78897653
|
C | T | 6 | a0001c0001t0005g0286a0001c0001t0007g0011a0001c0001t0008g0026others(3): Show | 6 | HG00544.hp2 HG02135.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-23734G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897653 | ||||||
| chr17:78897849
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.131-23930T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897849 | ||||||
| chr17:78897956
|
T | C | 20 | a0001c0001t0001g0248a0001c0001t0001g0284a0001c0001t0001g0287others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.131-24037A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78897956 | ||||||
| chr17:78898026
|
G | A | 8 | a0001c0001t0003g0289a0001c0001t0003g0293a0001c0001t0003g0310others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-24107C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898026 | ||||||
| chr17:78898153
|
C | T | 1 | a0001c0001t0004g0077 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.131-24234G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898153 | ||||||
| chr17:78898183
|
C | G | 6 | a0001c0001t0001g0268a0001c0002t0003g0001a0001c0002t0003g0217others(3): Show | 7 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-24264G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898183 | ||||||
| chr17:78898211
|
A | C | 14 | a0001c0001t0001g0305a0001c0001t0002g0045a0001c0001t0003g0289others(11): Show | 14 | HG02109.hp2 HG02451.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-24292T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898211 | ||||||
| chr17:78898328
|
G | A | 279 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(276): Show | 279 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(276): Show |
intron_variant | MODIFIER | c.131-24409C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898328 | ||||||
| chr17:78898333
|
G | A | 92 | a0001c0001t0001g0166a0001c0001t0001g0194a0001c0001t0001g0200others(89): Show | 92 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.131-24414C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898333 | ||||||
| chr17:78898398
|
T | C | 122 | a0001c0001t0001g0166a0001c0001t0001g0194a0001c0001t0001g0200others(119): Show | 122 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.131-24479A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898398 | ||||||
| chr17:78898438
|
C | T | 5 | a0001c0001t0011g0283a0001c0001t0027g0172a0001c0001t0027g0182others(2): Show | 5 | HG02109.hp2 HG02280.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-24519G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898438 | ||||||
| chr17:78898443
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.131-24524C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898443 | ||||||
| chr17:78898598
|
A | G | 295 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(292): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.131-24679T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898598 | ||||||
| chr17:78898656
|
C | G | 1 | a0001c0001t0032g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.131-24737G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898656 | ||||||
| chr17:78898719
|
G | T | 9 | a0001c0001t0001g0287a0001c0001t0002g0143a0001c0001t0020g0127others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.131-24800C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898719 | ||||||
| chr17:78898749
|
CTTTT | C | 3 | a0001c0001t0027g0172a0001c0001t0032g0016a0001c0001t0038g0124 | 3 | HG02280.hp2 HG02451.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.131-24834_131-2483 others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898749 | ||||||
| chr17:78898765
|
T | G | 26 | a0001c0001t0001g0248a0001c0001t0001g0261a0001c0001t0001g0271others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.131-24846A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898765 | ||||||
| chr17:78898772
|
C | T | 4 | a0001c0001t0002g0045a0001c0001t0004g0050a0001c0001t0018g0049others(1): Show | 4 | HG02109.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-24853G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898772 | ||||||
| chr17:78898832
|
G | C | 6 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(3): Show | 6 | HG03491.hp1 NA18942.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-24913C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898832 | ||||||
| chr17:78898885
|
G | A | 1 | a0001c0001t0007g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.131-24966C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898885 | ||||||
| chr17:78898887
|
G | A | 1 | a0001c0002t0016g0159 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.131-24968C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898887 | ||||||
| chr17:78898958
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.131-25039T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78898958 | ||||||
| chr17:78899012
|
C | A | 1 | a0001c0001t0018g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.131-25093G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899012 | ||||||
| chr17:78899084
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0007g0032 | 2 | HG02809.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.131-25165C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899084 | ||||||
| chr17:78899147
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0011g0283 | 2 | HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.131-25228T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899147 | ||||||
| chr17:78899272
|
A | G | 9 | a0001c0001t0002g0042a0001c0001t0002g0045a0001c0001t0004g0050others(6): Show | 9 | HG01243.hp2 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.131-25353T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899272 | ||||||
| chr17:78899300
|
C | T | 1 | a0001c0001t0008g0017 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.131-25381G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899300 | ||||||
| chr17:78899309
|
C | G | 108 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(105): Show | 109 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.131-25390G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899309 | ||||||
| chr17:78899319
|
C | T | 10 | a0001c0001t0001g0263a0001c0001t0003g0216a0001c0001t0007g0023others(7): Show | 10 | HG00609.hp2 HG01346.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-25400G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899319 | ||||||
| chr17:78899349
|
A | C | 122 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(119): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.131-25430T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899349 | ||||||
| chr17:78899446
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0055g0270 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+25513G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899446 | ||||||
| chr17:78899473
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.130+25486G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899473 | ||||||
| chr17:78899604
|
C | T | 16 | a0001c0001t0001g0166a0001c0001t0001g0263a0001c0001t0001g0282others(13): Show | 16 | HG00609.hp2 HG01346.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.130+25355G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899604 | ||||||
| chr17:78899627
|
C | T | 1 | a0001c0001t0004g0141 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.130+25332G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899627 | ||||||
| chr17:78899704
|
G | A | 19 | a0001c0001t0001g0248a0001c0001t0002g0143a0001c0001t0003g0249others(16): Show | 19 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.130+25255C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899704 | ||||||
| chr17:78899731
|
C | T | 1 | a0001c0001t0005g0257 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130+25228G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899731 | ||||||
| chr17:78899738
|
T | C | 2 | a0001c0002t0001g0256a0001c0002t0056g0252 | 2 | HG02080.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.130+25221A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899738 | ||||||
| chr17:78899766
|
G | A | 289 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(286): Show | 290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.130+25193C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899766 | ||||||
| chr17:78899810
|
C | T | 20 | a0001c0001t0001g0248a0001c0001t0002g0143a0001c0001t0003g0249others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+25149G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899810 | ||||||
| chr17:78899994
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130+24965A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78899994 | ||||||
| chr17:78900022
|
G | A | 1 | a0001c0001t0003g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.130+24937C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900022 | ||||||
| chr17:78900052
|
G | A | 1 | a0001c0001t0007g0019 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.130+24907C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900052 | ||||||
| chr17:78900096
|
G | T | 1 | a0001c0001t0013g0214 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.130+24863C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900096 | ||||||
| chr17:78900200
|
T | G | 1 | a0001c0001t0001g0282 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.130+24759A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900200 | ||||||
| chr17:78900256
|
G | GT | 5 | a0001c0001t0002g0136a0001c0001t0007g0004a0001c0001t0007g0012others(2): Show | 5 | HG02109.hp2 NA18963.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+24702dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900256 | ||||||
| chr17:78900267
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130+24692G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900267 | ||||||
| chr17:78900333
|
G | A | 6 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0017g0133others(3): Show | 6 | HG01891.hp1 HG02258.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+24626C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900333 | ||||||
| chr17:78900483
|
T | G | 2 | a0001c0002t0025g0167a0001c0002t0025g0226 | 2 | NA19011.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.130+24476A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900483 | ||||||
| chr17:78900486
|
A | G | 96 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(93): Show | 97 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.130+24473T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900486 | ||||||
| chr17:78900544
|
C | CA | 96 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(93): Show | 96 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.130+24414dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900544 | ||||||
| chr17:78900544
|
CA | C | 147 | a0001c0001t0001g0164a0001c0001t0001g0194a0001c0001t0001g0198others(144): Show | 147 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.130+24414delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900544 | ||||||
| chr17:78900544
|
CAA | C | 24 | a0001c0001t0001g0248a0001c0001t0002g0063a0001c0001t0002g0103others(21): Show | 24 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.130+24413_130+2441 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900544 | ||||||
| chr17:78900570
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130+24389T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900570 | ||||||
| chr17:78900587
|
C | A | 1 | a0001c0001t0013g0214 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.130+24372G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900587 | ||||||
| chr17:78900626
|
A | T | 1 | a0001c0001t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+24333T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900626 | ||||||
| chr17:78900638
|
T | C | 13 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+24321A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900638 | ||||||
| chr17:78900761
|
C | G | 1 | a0001c0001t0005g0243 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.130+24198G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900761 | ||||||
| chr17:78900847
|
G | A | 2 | a0001c0001t0003g0251a0001c0001t0005g0257 | 2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130+24112C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900847 | ||||||
| chr17:78900870
|
C | T | 8 | a0001c0001t0001g0291a0001c0001t0003g0289a0001c0001t0003g0293others(5): Show | 8 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+24089G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900870 | ||||||
| chr17:78900955
|
C | T | 1 | a0001c0001t0004g0120 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+24004G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900955 | ||||||
| chr17:78900956
|
A | G | 290 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(287): Show | 291 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.130+24003T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900956 | ||||||
| chr17:78900961
|
G | A | 139 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.130+23998C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900961 | ||||||
| chr17:78901057
|
C | T | 126 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(123): Show | 127 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.130+23902G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901057 | ||||||
| chr17:78901110
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0003g0267 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130+23849C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901110 | ||||||
| chr17:78901137
|
G | A | 119 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(116): Show | 120 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.130+23822C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901137 | ||||||
| chr17:78901153
|
G | A | 1 | a0001c0001t0018g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130+23806C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901153 | ||||||
| chr17:78901192
|
C | T | 8 | a0001c0001t0001g0291a0001c0001t0003g0289a0001c0001t0003g0293others(5): Show | 8 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+23767G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901192 | ||||||
| chr17:78901205
|
G | C | 1 | a0001c0001t0002g0062 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.130+23754C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901205 | ||||||
| chr17:78901253
|
G | C | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+23706C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901253 | ||||||
| chr17:78901265
|
T | C | 294 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(291): Show | 295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.130+23694A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901265 | ||||||
| chr17:78901285
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0055g0270 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+23674G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901285 | ||||||
| chr17:78901340
|
G | A | 20 | a0001c0001t0001g0248a0001c0001t0002g0143a0001c0001t0003g0249others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+23619C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901340 | ||||||
| chr17:78901348
|
C | A | 20 | a0001c0001t0001g0248a0001c0001t0002g0143a0001c0001t0003g0249others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+23611G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901348 | ||||||
| chr17:78901372
|
A | T | 20 | a0001c0001t0001g0248a0001c0001t0002g0143a0001c0001t0003g0249others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+23587T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901372 | ||||||
| chr17:78901373
|
C | T | 21 | a0001c0001t0001g0166a0001c0001t0001g0263a0001c0001t0001g0282others(18): Show | 21 | HG00609.hp2 HG01346.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+23586G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901373 | ||||||
| chr17:78901374
|
G | A | 20 | a0001c0001t0001g0248a0001c0001t0002g0143a0001c0001t0003g0249others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+23585C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901374 | ||||||
| chr17:78901393
|
A | G | 119 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(116): Show | 120 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.130+23566T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901393 | ||||||
| chr17:78901458
|
A | G | 20 | a0001c0001t0001g0164a0001c0001t0001g0261a0001c0001t0001g0271others(17): Show | 20 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+23501T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901458 | ||||||
| chr17:78901460
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(9): Show | 12 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+23499C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901460 | ||||||
| chr17:78901511
|
G | A | 12 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(9): Show | 12 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+23448C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901511 | ||||||
| chr17:78901523
|
C | G | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.130+23436G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901523 | ||||||
| chr17:78901524
|
C | T | 1 | a0001c0001t0027g0172 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.130+23435G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901524 | ||||||
| chr17:78901526
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.130+23433G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901526 | ||||||
| chr17:78901606
|
T | C | 1 | a0001c0001t0027g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+23353A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901606 | ||||||
| chr17:78901636
|
T | C | 2 | a0001c0001t0002g0059a0001c0001t0004g0060 | 2 | HG01175.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.130+23323A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901636 | ||||||
| chr17:78901651
|
G | T | 119 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(116): Show | 120 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(117): Show |
intron_variant | MODIFIER | c.130+23308C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901651 | ||||||
| chr17:78901743
|
G | A | 16 | a0001c0001t0001g0263a0001c0001t0002g0136a0001c0001t0002g0137others(13): Show | 16 | HG00609.hp2 HG01346.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.130+23216C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901743 | ||||||
| chr17:78901819
|
C | A | 1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+23140G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901819 | ||||||
| chr17:78901831
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+23128G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901831 | ||||||
| chr17:78901892
|
C | T | 122 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(119): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.130+23067G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901892 | ||||||
| chr17:78901919
|
G | A | 3 | a0001c0002t0003g0262a0001c0002t0003g0275a0001c0002t0054g0276 | 3 | HG01081.hp1 HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.130+23040C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78901919 | ||||||
| chr17:78902053
|
C | T | 1 | a0001c0001t0004g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.130+22906G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902053 | ||||||
| chr17:78902075
|
A | C | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+22884T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902075 | ||||||
| chr17:78902080
|
C | T | 2 | a0001c0001t0002g0097a0001c0001t0004g0096 | 2 | NA18944.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.130+22879G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902080 | ||||||
| chr17:78902091
|
T | C | 139 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(136): Show | 140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.130+22868A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902091 | ||||||
| chr17:78902100
|
G | A | 117 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(114): Show | 118 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.130+22859C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902100 | ||||||
| chr17:78902178
|
C | T | 13 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+22781G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902178 | ||||||
| chr17:78902297
|
G | A | 1 | a0001c0001t0002g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.130+22662C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902297 | ||||||
| chr17:78902330
|
A | G | 22 | a0001c0001t0001g0248a0001c0001t0001g0282a0001c0001t0002g0143others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+22629T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902330 | ||||||
| chr17:78902353
|
T | C | 295 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(292): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.130+22606A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902353 | ||||||
| chr17:78902463
|
G | A | 21 | a0001c0001t0001g0248a0001c0001t0001g0282a0001c0001t0002g0143others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.130+22496C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902463 | ||||||
| chr17:78902477
|
T | C | 1 | a0001c0001t0002g0122 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.130+22482A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902477 | ||||||
| chr17:78902522
|
A | G | 13 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(10): Show | 13 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+22437T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902522 | ||||||
| chr17:78902526
|
C | T | 23 | a0001c0001t0001g0248a0001c0001t0001g0282a0001c0001t0002g0089others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+22433G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902526 | ||||||
| chr17:78902551
|
T | C | 88 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(85): Show | 89 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(86): Show |
intron_variant | MODIFIER | c.130+22408A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902551 | ||||||
| chr17:78902605
|
C | T | 6 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(3): Show | 6 | HG03491.hp1 NA18942.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+22354G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902605 | ||||||
| chr17:78902672
|
A | C | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22287T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902672 | ||||||
| chr17:78902737
|
C | T | 5 | a0001c0001t0001g0314a0001c0001t0002g0149a0001c0001t0003g0170others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+22222G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902737 | ||||||
| chr17:78902770
|
C | T | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+22189G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902770 | ||||||
| chr17:78902800
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0230a0001c0001t0005g0184 | 3 | NA18947.hp1 NA19063.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.130+22159C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902800 | ||||||
| chr17:78902830
|
G | C | 22 | a0001c0001t0001g0248a0001c0001t0001g0282a0001c0001t0001g0287others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+22129C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902830 | ||||||
| chr17:78902872
|
C | T | 116 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(113): Show | 117 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.130+22087G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902872 | ||||||
| chr17:78902929
|
C | T | 1 | a0001c0001t0005g0296 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.130+22030G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902929 | ||||||
| chr17:78902983
|
C | A | 196 | a0001c0001t0001g0164a0001c0001t0001g0190a0001c0001t0001g0194others(193): Show | 196 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.130+21976G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902983 | ||||||
| chr17:78903016
|
CG | C | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+21942delC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903016 | ||||||
| chr17:78903046
|
C | T | 6 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(3): Show | 6 | HG03491.hp1 NA18942.hp2 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+21913G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903046 | ||||||
| chr17:78903159
|
G | A | 1 | a0001c0001t0008g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.130+21800C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903159 | ||||||
| chr17:78903233
|
G | A | 2 | a0001c0001t0032g0016a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.130+21726C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903233 | ||||||
| chr17:78903281
|
C | G | 1 | a0001c0001t0003g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.130+21678G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903281 | ||||||
| chr17:78903397
|
C | T | 23 | a0001c0001t0001g0248a0001c0001t0002g0136a0001c0001t0002g0137others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+21562G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903397 | ||||||
| chr17:78903445
|
T | C | 58 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.130+21514A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903445 | ||||||
| chr17:78903548
|
C | T | 292 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(289): Show | 293 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.130+21411G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903548 | ||||||
| chr17:78903953
|
G | C | 1 | a0001c0001t0027g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.130+21006C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78903953 | ||||||
| chr17:78904089
|
T | TTGTGTGT others(19): Show |
2 | a0001c0001t0001g0287a0001c0001t0003g0267 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130+20869_130+2087 others(30): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904089 | ||||||
| chr17:78904091
|
A | ATATATAT others(27): Show |
3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056 | 3 | HG02886.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.130+20867_130+2086 others(38): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATATATAT others(31): Show |
7 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(4): Show | 7 | HG00140.hp2 HG01358.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(42): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATATATAT others(33): Show |
6 | a0001c0001t0003g0300a0001c0001t0003g0301a0001c0001t0005g0296others(3): Show | 6 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(44): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATG | 5 | a0001c0001t0001g0205a0001c0002t0003g0001a0001c0002t0003g0217others(2): Show | 6 | HG00140.hp1 HG01106.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+20866_130+2086 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(13): Show |
1 | a0001c0001t0003g0251 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+20867_130+2086 others(24): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(19): Show |
14 | a0001c0001t0001g0282a0001c0001t0001g0291a0001c0001t0002g0136others(11): Show | 14 | HG01261.hp1 HG02258.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(30): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(21): Show |
2 | a0001c0001t0002g0125a0001c0001t0003g0310 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.130+20867_130+2086 others(32): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(23): Show |
4 | a0001c0001t0001g0314a0001c0001t0003g0225a0001c0001t0005g0243others(1): Show | 4 | HG00735.hp1 HG02257.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(34): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(25): Show |
13 | a0001c0001t0001g0197a0001c0001t0001g0234a0001c0001t0001g0238others(10): Show | 13 | HG01261.hp2 HG01516.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(36): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(27): Show |
37 | a0001c0001t0001g0180a0001c0001t0001g0208a0001c0001t0001g0212others(34): Show | 37 | HG00544.hp1 HG00621.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(38): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(29): Show |
17 | a0001c0001t0001g0209a0001c0001t0001g0219a0001c0001t0001g0245others(14): Show | 17 | HG00621.hp1 HG00741.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(40): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(31): Show |
9 | a0001c0001t0001g0164a0001c0001t0001g0199a0001c0001t0001g0305others(6): Show | 9 | HG01884.hp1 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(42): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(33): Show |
7 | a0001c0001t0001g0181a0001c0001t0001g0210a0001c0001t0002g0044others(4): Show | 7 | HG01123.hp1 HG02572.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(44): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(35): Show |
7 | a0001c0001t0001g0232a0001c0001t0002g0143a0001c0001t0005g0165others(4): Show | 7 | HG00639.hp1 HG02040.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+20867_130+2086 others(46): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(37): Show |
3 | a0001c0001t0001g0302a0001c0001t0020g0142a0001c0002t0039g0144 | 3 | HG03195.hp1 NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.130+20867_130+2086 others(48): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(39): Show |
1 | a0001c0001t0010g0039 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.130+20867_130+2086 others(50): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | ATGTGTGT others(43): Show |
1 | a0001c0001t0003g0309 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+20867_130+2086 others(54): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904091
|
A | G | 2 | a0001c0001t0001g0287a0001c0001t0003g0267 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130+20868T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904091 | ||||||
| chr17:78904108
|
T | TGTGTGTG others(30): Show |
2 | a0001c0001t0003g0211a0001c0001t0022g0183 | 2 | HG02647.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.130+20850_130+2085 others(41): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904108 | ||||||
| chr17:78904108
|
T | TGTGTGTG others(32): Show |
2 | a0001c0001t0004g0050a0001c0002t0054g0276 | 2 | HG02647.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.130+20850_130+2085 others(43): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904108 | ||||||
| chr17:78904109
|
T | G | 1 | a0001c0001t0006g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.130+20850A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904109 | ||||||
| chr17:78904147
|
G | A | 16 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+20812C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904147 | ||||||
| chr17:78904221
|
CG | C | 16 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(13): Show | 16 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+20737delC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904221 | ||||||
| chr17:78904379
|
T | G | 141 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(138): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.130+20580A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904379 | ||||||
| chr17:78904503
|
C | T | 143 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.130+20456G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904503 | ||||||
| chr17:78904577
|
C | A | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056 | 3 | HG02886.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.130+20382G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904577 | ||||||
| chr17:78904590
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.130+20369G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904590 | ||||||
| chr17:78904657
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0055g0270 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+20302C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904657 | ||||||
| chr17:78904836
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.130+20123A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904836 | ||||||
| chr17:78904870
|
G | A | 1 | a0001c0001t0003g0225 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.130+20089C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904870 | ||||||
| chr17:78904886
|
G | A | 3 | a0001c0002t0003g0262a0001c0002t0003g0275a0001c0002t0054g0276 | 3 | HG01081.hp1 HG02698.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.130+20073C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904886 | ||||||
| chr17:78904941
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+20018A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904941 | ||||||
| chr17:78904976
|
C | T | 32 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(29): Show | 32 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.130+19983G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904976 | ||||||
| chr17:78904985
|
C | T | 1 | a0001c0001t0011g0283 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130+19974G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904985 | ||||||
| chr17:78905008
|
C | T | 137 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(134): Show | 138 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.130+19951G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905008 | ||||||
| chr17:78905025
|
A | G | 1 | a0001c0001t0002g0105 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.130+19934T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905025 | ||||||
| chr17:78905054
|
C | T | 23 | a0001c0001t0001g0248a0001c0001t0001g0287a0001c0001t0001g0291others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.130+19905G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905054 | ||||||
| chr17:78905096
|
C | T | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+19863G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905096 | ||||||
| chr17:78905139
|
C | CA | 171 | a0001c0001t0001g0190a0001c0001t0001g0194a0001c0001t0001g0198others(168): Show | 171 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.130+19819dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905139 | ||||||
| chr17:78905149
|
A | G | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+19810T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905149 | ||||||
| chr17:78905213
|
C | T | 13 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(10): Show | 13 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+19746G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905213 | ||||||
| chr17:78905228
|
A | G | 2 | a0001c0001t0032g0016a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.130+19731T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905228 | ||||||
| chr17:78905339
|
C | T | 2 | a0001c0002t0044g0068a0001c0002t0047g0128 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.130+19620G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905339 | ||||||
| chr17:78905383
|
G | A | 144 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(141): Show | 145 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.130+19576C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905383 | ||||||
| chr17:78905392
|
T | C | 1 | a0001c0001t0001g0263 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.130+19567A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905392 | ||||||
| chr17:78905429
|
T | C | 1 | a0001c0001t0006g0085 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.130+19530A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905429 | ||||||
| chr17:78905502
|
G | T | 1 | a0001c0001t0055g0270 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130+19457C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905502 | ||||||
| chr17:78905551
|
A | C | 105 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(102): Show | 106 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.130+19408T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905551 | ||||||
| chr17:78905583
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+19376C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905583 | ||||||
| chr17:78905674
|
T | C | 10 | a0001c0001t0001g0291a0001c0001t0003g0171a0001c0001t0003g0173others(7): Show | 10 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+19285A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905674 | ||||||
| chr17:78905904
|
G | C | 141 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(138): Show | 142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.130+19055C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905904 | ||||||
| chr17:78905927
|
A | G | 83 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(80): Show | 84 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.130+19032T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905927 | ||||||
| chr17:78906000
|
T | C | 145 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(142): Show | 146 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.130+18959A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906000 | ||||||
| chr17:78906148
|
A | G | 1 | a0001c0001t0003g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+18811T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906148 | ||||||
| chr17:78906167
|
T | C | 105 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(102): Show | 106 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.130+18792A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906167 | ||||||
| chr17:78906169
|
C | G | 145 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(142): Show | 146 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.130+18790G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906169 | ||||||
| chr17:78906332
|
C | A | 1 | a0001c0001t0005g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.130+18627G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906332 | ||||||
| chr17:78906576
|
C | T | 1 | a0001c0002t0005g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.130+18383G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906576 | ||||||
| chr17:78906732
|
G | A | 9 | a0001c0001t0002g0080a0001c0001t0002g0112a0001c0001t0002g0121others(6): Show | 9 | HG01109.hp1 HG01109.hp2 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+18227C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906732 | ||||||
| chr17:78906772
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+18187C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906772 | ||||||
| chr17:78906863
|
G | A | 1 | a0001c0001t0001g0210 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.130+18096C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906863 | ||||||
| chr17:78906873
|
G | A | 5 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(2): Show | 5 | HG03491.hp1 NA18942.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+18086C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906873 | ||||||
| chr17:78907070
|
G | C | 2 | a0001c0001t0001g0282a0001c0001t0055g0270 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+17889C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907070 | ||||||
| chr17:78907162
|
T | C | 8 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(5): Show | 8 | HG02258.hp1 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+17797A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907162 | ||||||
| chr17:78907175
|
A | C | 1 | a0001c0001t0006g0104 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.130+17784T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907175 | ||||||
| chr17:78907669
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+17290C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907669 | ||||||
| chr17:78907681
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+17278C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907681 | ||||||
| chr17:78907769
|
G | C | 1 | a0001c0001t0002g0125 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.130+17190C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907769 | ||||||
| chr17:78907847
|
G | A | 1 | a0001c0001t0003g0293 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.130+17112C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907847 | ||||||
| chr17:78907871
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.130+17088G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907871 | ||||||
| chr17:78907890
|
C | G | 32 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(29): Show | 32 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.130+17069G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78907890 | ||||||
| chr17:78908039
|
G | T | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+16920C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908039 | ||||||
| chr17:78908078
|
C | T | 136 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(133): Show | 136 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.130+16881G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908078 | ||||||
| chr17:78908196
|
GATTT | G | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+16759_130+1676 others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908196 | ||||||
| chr17:78908221
|
C | A | 1 | a0001c0001t0018g0049 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.130+16738G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908221 | ||||||
| chr17:78908314
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+16645A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908314 | ||||||
| chr17:78908404
|
C | G | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+16555G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908404 | ||||||
| chr17:78908432
|
C | CAAA | 15 | a0001c0001t0001g0200a0001c0001t0005g0250a0001c0001t0005g0286others(12): Show | 15 | HG00544.hp2 HG00609.hp1 HG02135.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+16524_130+1652 others(7): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908432 | ||||||
| chr17:78908448
|
C | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(5): Show | 8 | HG02258.hp1 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+16511G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908448 | ||||||
| chr17:78908533
|
C | T | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+16426G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908533 | ||||||
| chr17:78908555
|
T | A | 1 | a0001c0001t0005g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.130+16404A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908555 | ||||||
| chr17:78908700
|
G | A | 12 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0134others(9): Show | 12 | HG02258.hp1 HG02886.hp1 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+16259C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908700 | ||||||
| chr17:78908764
|
G | T | 1 | a0001c0001t0002g0103 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.130+16195C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908764 | ||||||
| chr17:78908793
|
C | T | 13 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(10): Show | 13 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+16166G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908793 | ||||||
| chr17:78908804
|
A | G | 122 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(119): Show | 123 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.130+16155T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908804 | ||||||
| chr17:78908841
|
G | A | 1 | a0001c0001t0019g0092 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.130+16118C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908841 | ||||||
| chr17:78908865
|
C | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(5): Show | 8 | HG02258.hp1 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+16094G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78908865 | ||||||
| chr17:78909067
|
G | A | 25 | a0001c0001t0001g0248a0001c0001t0001g0287a0001c0001t0001g0291others(22): Show | 25 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.130+15892C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909067 | ||||||
| chr17:78909132
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+15827C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909132 | ||||||
| chr17:78909169
|
A | G | 146 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(143): Show | 147 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(144): Show |
intron_variant | MODIFIER | c.130+15790T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909169 | ||||||
| chr17:78909269
|
T | C | 1 | a0001c0001t0004g0056 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+15690A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909269 | ||||||
| chr17:78909280
|
A | C | 11 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(8): Show | 11 | HG02258.hp1 HG02630.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+15679T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909280 | ||||||
| chr17:78909327
|
C | T | 1 | a0001c0002t0039g0144 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.130+15632G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909327 | ||||||
| chr17:78909358
|
T | TAAAAA | 6 | a0001c0001t0001g0166a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02886.hp2 HG03491.hp1 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+15596_130+1560 others(9): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909358 | ||||||
| chr17:78909382
|
G | A | 11 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(8): Show | 11 | HG02258.hp1 HG02630.hp1 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+15577C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909382 | ||||||
| chr17:78909390
|
C | G | 147 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(144): Show | 148 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.130+15569G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909390 | ||||||
| chr17:78909442
|
T | C | 1 | a0001c0001t0003g0216 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.130+15517A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909442 | ||||||
| chr17:78909533
|
C | T | 94 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(91): Show | 95 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.130+15426G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909533 | ||||||
| chr17:78909537
|
C | A | 43 | a0001c0001t0001g0164a0001c0001t0001g0248a0001c0001t0001g0287others(40): Show | 43 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.130+15422G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909537 | ||||||
| chr17:78909589
|
GC | G | 95 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(92): Show | 96 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.130+15369delG | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909589 | ||||||
| chr17:78909611
|
G | A | 14 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(11): Show | 14 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.130+15348C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909611 | ||||||
| chr17:78909721
|
C | T | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130+15238G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909721 | ||||||
| chr17:78909740
|
G | A | 11 | a0001c0001t0001g0263a0001c0001t0003g0216a0001c0001t0004g0116others(8): Show | 11 | HG00609.hp2 HG01346.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+15219C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909740 | ||||||
| chr17:78909805
|
C | A | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+15154G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909805 | ||||||
| chr17:78909945
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+15014G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909945 | ||||||
| chr17:78909974
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+14985G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909974 | ||||||
| chr17:78910003
|
A | C | 152 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(149): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.130+14956T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910003 | ||||||
| chr17:78910041
|
T | C | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130+14918A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910041 | ||||||
| chr17:78910066
|
T | C | 2 | a0001c0001t0004g0051a0001c0002t0004g0052 | 2 | HG01070.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.130+14893A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910066 | ||||||
| chr17:78910084
|
G | C | 1 | a0001c0002t0023g0264 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.130+14875C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910084 | ||||||
| chr17:78910194
|
C | CT | 14 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(11): Show | 14 | HG01928.hp1 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+14764dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910194 | ||||||
| chr17:78910261
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0055g0270 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+14698G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910261 | ||||||
| chr17:78910262
|
G | A | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056 | 3 | HG02886.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.130+14697C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910262 | ||||||
| chr17:78910266
|
C | T | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130+14693G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910266 | ||||||
| chr17:78910285
|
C | T | 85 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0197others(82): Show | 85 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(82): Show |
intron_variant | MODIFIER | c.130+14674G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910285 | ||||||
| chr17:78910295
|
C | T | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130+14664G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910295 | ||||||
| chr17:78910522
|
T | C | 306 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(303): Show | 307 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.130+14437A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910522 | ||||||
| chr17:78910529
|
C | T | 140 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(137): Show | 141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.130+14430G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910529 | ||||||
| chr17:78910752
|
G | A | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+14207C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910752 | ||||||
| chr17:78911008
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+13951C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911008 | ||||||
| chr17:78911021
|
T | C | 1 | a0001c0001t0003g0309 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+13938A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911021 | ||||||
| chr17:78911028
|
A | G | 1 | a0001c0001t0019g0095 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.130+13931T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911028 | ||||||
| chr17:78911075
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+13884C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911075 | ||||||
| chr17:78911083
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.130+13876C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911083 | ||||||
| chr17:78911239
|
C | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(5): Show | 8 | HG02258.hp1 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+13720G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911239 | ||||||
| chr17:78911271
|
T | C | 151 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(148): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.130+13688A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911271 | ||||||
| chr17:78911363
|
C | T | 105 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(102): Show | 106 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.130+13596G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911363 | ||||||
| chr17:78911379
|
A | G | 151 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(148): Show | 152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.130+13580T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911379 | ||||||
| chr17:78911422
|
GTTTTTGT | G | 26 | a0001c0001t0001g0248a0001c0001t0001g0287a0001c0001t0001g0291others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.130+13530_130+1353 others(11): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911422 | ||||||
| chr17:78911428
|
G | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0002g0136others(5): Show | 8 | HG02258.hp1 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+13531C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911428 | ||||||
| chr17:78911434
|
T | G | 2 | a0001c0001t0001g0282a0001c0001t0055g0270 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+13525A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911434 | ||||||
| chr17:78911516
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+13443G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911516 | ||||||
| chr17:78911584
|
T | C | 21 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(18): Show | 21 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.130+13375A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911584 | ||||||
| chr17:78911619
|
T | G | 4 | a0001c0001t0002g0134a0001c0001t0004g0054a0001c0001t0004g0055others(1): Show | 4 | HG02886.hp1 HG02896.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+13340A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911619 | ||||||
| chr17:78911736
|
T | C | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+13223A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911736 | ||||||
| chr17:78911771
|
T | C | 152 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(149): Show | 153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.130+13188A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911771 | ||||||
| chr17:78911772
|
G | A | 122 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(119): Show | 122 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(119): Show |
intron_variant | MODIFIER | c.130+13187C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911772 | ||||||
| chr17:78911817
|
G | A | 110 | a0001c0001t0001g0166a0001c0001t0001g0180a0001c0001t0001g0181others(107): Show | 111 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.130+13142C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911817 | ||||||
| chr17:78911869
|
A | T | 6 | a0001c0001t0001g0199a0001c0001t0005g0179a0001c0001t0019g0092others(3): Show | 6 | HG00735.hp2 HG01081.hp1 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+13090T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911869 | ||||||
| chr17:78911893
|
C | CA | 20 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.130+13065_130+1306 others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911893 | ||||||
| chr17:78911894
|
C | CA | 100 | a0001c0001t0001g0164a0001c0001t0001g0181a0001c0001t0001g0197others(97): Show | 101 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(98): Show |
intron_variant | MODIFIER | c.130+13064dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911894 | ||||||
| chr17:78911894
|
C | CAA | 8 | a0001c0001t0002g0125a0001c0001t0005g0165a0001c0001t0020g0127others(5): Show | 8 | HG02615.hp1 HG03209.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+13063_130+1306 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911894 | ||||||
| chr17:78911894
|
CA | C | 13 | a0001c0001t0001g0291a0001c0001t0003g0225a0001c0001t0003g0251others(10): Show | 13 | HG01261.hp1 HG01496.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+13064delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911894 | ||||||
| chr17:78911895
|
A | AC | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+13063_130+1306 others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911895 | ||||||
| chr17:78911897
|
A | C | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+13062T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911897 | ||||||
| chr17:78911899
|
A | C | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+13060T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911899 | ||||||
| chr17:78911901
|
A | C | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+13058T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911901 | ||||||
| chr17:78911903
|
A | C | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+13056T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911903 | ||||||
| chr17:78911905
|
A | C | 8 | a0001c0001t0001g0166a0001c0001t0002g0136a0001c0001t0002g0137others(5): Show | 8 | HG02735.hp2 HG02886.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+13054T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911905 | ||||||
| chr17:78911962
|
G | T | 1 | a0001c0001t0020g0142 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.130+12997C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911962 | ||||||
| chr17:78911972
|
G | A | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+12987C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911972 | ||||||
| chr17:78912135
|
A | G | 166 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(163): Show | 167 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.130+12824T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912135 | ||||||
| chr17:78912141
|
C | G | 2 | a0001c0001t0006g0094a0001c0001t0042g0093 | 2 | NA18945.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.130+12818G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912141 | ||||||
| chr17:78912212
|
C | T | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+12747G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912212 | ||||||
| chr17:78912295
|
T | A | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+12664A>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912295 | ||||||
| chr17:78912317
|
G | A | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+12642C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912317 | ||||||
| chr17:78912359
|
C | T | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+12600G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912359 | ||||||
| chr17:78912525
|
C | A | 8 | a0001c0001t0001g0291a0001c0001t0003g0225a0001c0001t0003g0251others(5): Show | 8 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+12434G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912525 | ||||||
| chr17:78912549
|
C | T | 2 | a0001c0001t0001g0282a0001c0001t0055g0270 | 2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.130+12410G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912549 | ||||||
| chr17:78912557
|
A | G | 1 | a0001c0002t0001g0175 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.130+12402T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912557 | ||||||
| chr17:78912614
|
C | A | 1 | a0001c0001t0002g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.130+12345G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912614 | ||||||
| chr17:78912679
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+12280C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912679 | ||||||
| chr17:78912760
|
G | A | 3 | a0001c0001t0010g0114a0001c0001t0015g0168a0001c0001t0035g0067 | 3 | HG02615.hp2 HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.130+12199C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912760 | ||||||
| chr17:78912830
|
G | A | 1 | a0001c0001t0011g0283 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.130+12129C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78912830 | ||||||
| chr17:78913042
|
T | C | 1 | a0001c0001t0003g0310 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.130+11917A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913042 | ||||||
| chr17:78913109
|
C | A | 38 | a0001c0001t0001g0164a0001c0001t0001g0287a0001c0001t0001g0291others(35): Show | 38 | HG00639.hp1 HG01243.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.130+11850G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913109 | ||||||
| chr17:78913153
|
A | G | 168 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(165): Show | 169 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.130+11806T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913153 | ||||||
| chr17:78913183
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+11776G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913183 | ||||||
| chr17:78913237
|
C | CA | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+11721dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913237 | ||||||
| chr17:78913357
|
G | A | 38 | a0001c0001t0001g0164a0001c0001t0001g0287a0001c0001t0001g0291others(35): Show | 38 | HG00639.hp1 HG01243.hp2 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.130+11602C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913357 | ||||||
| chr17:78913538
|
T | C | 30 | a0001c0001t0001g0164a0001c0001t0001g0287a0001c0001t0002g0042others(27): Show | 30 | HG00639.hp1 HG01243.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+11421A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913538 | ||||||
| chr17:78913595
|
C | A | 22 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0001g0282others(19): Show | 22 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+11364G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913595 | ||||||
| chr17:78913610
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0003g0267 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130+11349G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913610 | ||||||
| chr17:78913724
|
C | CA | 5 | a0001c0001t0001g0212a0001c0001t0052g0163a0001c0002t0013g0253others(2): Show | 5 | HG01433.hp1 HG02055.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+11234dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913724 | ||||||
| chr17:78913727
|
A | C | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+11232T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913727 | ||||||
| chr17:78913749
|
G | A | 1 | a0001c0001t0008g0017 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.130+11210C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913749 | ||||||
| chr17:78913835
|
C | T | 1 | a0001c0002t0025g0167 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.130+11124G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913835 | ||||||
| chr17:78913855
|
G | A | 1 | a0001c0001t0004g0116 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.130+11104C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913855 | ||||||
| chr17:78913859
|
T | G | 2 | a0001c0001t0007g0006a0001c0001t0008g0018 | 2 | NA19083.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.130+11100A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913859 | ||||||
| chr17:78913891
|
C | CG | 17 | a0001c0001t0001g0164a0001c0001t0001g0287a0001c0001t0001g0291others(14): Show | 17 | HG01261.hp1 HG01891.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+11067dupC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913891 | ||||||
| chr17:78913895
|
G | GA | 155 | a0001c0001t0001g0166a0001c0001t0001g0194a0001c0001t0001g0222others(152): Show | 155 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.130+11063dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913895 | ||||||
| chr17:78913895
|
G | GAA | 16 | a0001c0001t0001g0258a0001c0001t0002g0080a0001c0001t0002g0100others(13): Show | 16 | HG01175.hp1 HG01891.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+11062_130+1106 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913895 | ||||||
| chr17:78913895
|
G | GGA | 7 | a0001c0001t0001g0238a0001c0001t0001g0259a0001c0001t0003g0173others(4): Show | 7 | HG01516.hp2 HG02970.hp1 HG04204.hp2 others(4): Show |
intron_variant | MODIFIER | c.130+11063_130+1106 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913895 | ||||||
| chr17:78913895
|
G | GGAA | 84 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(81): Show | 85 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.130+11063_130+1106 others(7): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913895 | ||||||
| chr17:78913895
|
G | GGAAA | 14 | a0001c0001t0001g0212a0001c0001t0001g0219a0001c0001t0001g0230others(11): Show | 14 | HG00741.hp1 HG01243.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+11063_130+1106 others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913895 | ||||||
| chr17:78913895
|
GAA | G | 12 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0004g0050others(9): Show | 12 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+11062_130+1106 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913895 | ||||||
| chr17:78913896
|
A | G | 2 | a0001c0001t0001g0291a0001c0001t0027g0172 | 2 | HG01261.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.130+11063T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913896 | ||||||
| chr17:78913898
|
A | G | 12 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0004g0050others(9): Show | 12 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+11061T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913898 | ||||||
| chr17:78913899
|
A | G | 1 | a0001c0001t0002g0045 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.130+11060T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78913899 | ||||||
| chr17:78914099
|
G | T | 3 | a0001c0001t0001g0258a0001c0001t0005g0257a0001c0001t0026g0224 | 3 | HG02109.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.130+10860C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914099 | ||||||
| chr17:78914141
|
G | A | 1 | a0001c0001t0003g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.130+10818C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914141 | ||||||
| chr17:78914177
|
C | T | 105 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(102): Show | 106 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.130+10782G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914177 | ||||||
| chr17:78914204
|
T | C | 3 | a0001c0001t0003g0171a0001c0001t0003g0173a0001c0001t0027g0172 | 3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+10755A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914204 | ||||||
| chr17:78914255
|
CTATTCAT others(9): Show |
C | 17 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(14): Show | 17 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.130+10688_130+1070 others(20): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914255 | ||||||
| chr17:78914255
|
CTATTCAT others(13): Show |
C | 41 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0248others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.130+10684_130+1070 others(24): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914255 | ||||||
| chr17:78914256
|
TATTC | T | 3 | a0001c0001t0001g0282a0001c0001t0002g0090a0001c0001t0055g0270 | 3 | HG02258.hp1 HG03516.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.130+10699_130+1070 others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914256 | ||||||
| chr17:78914260
|
C | CATTT | 12 | a0001c0001t0001g0268a0001c0001t0002g0118a0001c0001t0002g0161others(9): Show | 12 | HG01070.hp1 HG01496.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+10695_130+1069 others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914260 | ||||||
| chr17:78914260
|
C | CATTTATT others(1): Show |
89 | a0001c0001t0001g0194a0001c0001t0001g0222a0001c0001t0001g0258others(86): Show | 89 | HG00323.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.130+10691_130+1069 others(12): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914260 | ||||||
| chr17:78914260
|
C | CATTTATT others(5): Show |
9 | a0001c0001t0001g0284a0001c0001t0002g0101a0001c0001t0004g0066others(6): Show | 9 | HG00558.hp1 HG01106.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+10687_130+1069 others(16): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914260 | ||||||
| chr17:78914260
|
C | CATTTATT others(9): Show |
2 | a0001c0001t0002g0089a0001c0001t0007g0015 | 2 | HG00408.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.130+10683_130+1069 others(20): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914260 | ||||||
| chr17:78914260
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.130+10699G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914260 | ||||||
| chr17:78914274
|
T | TTTATTTA others(1): Show |
106 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(103): Show | 107 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.130+10684_130+1068 others(12): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914274 | ||||||
| chr17:78914309
|
C | T | 108 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(105): Show | 109 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.130+10650G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914309 | ||||||
| chr17:78914311
|
C | T | 58 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0248others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.130+10648G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914311 | ||||||
| chr17:78914338
|
G | A | 58 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0248others(55): Show | 58 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.130+10621C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914338 | ||||||
| chr17:78914358
|
C | G | 11 | a0001c0001t0001g0194a0001c0001t0002g0097a0001c0001t0002g0099others(8): Show | 11 | HG02027.hp1 HG02080.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+10601G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914358 | ||||||
| chr17:78914462
|
T | C | 9 | a0001c0001t0002g0134a0001c0001t0002g0143a0001c0001t0004g0054others(6): Show | 9 | HG02886.hp1 HG02896.hp1 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+10497A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914462 | ||||||
| chr17:78914488
|
G | A | 4 | a0001c0001t0007g0015a0001c0001t0007g0021a0001c0001t0008g0034others(1): Show | 4 | HG00408.hp1 HG00558.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+10471C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914488 | ||||||
| chr17:78914490
|
C | T | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+10469G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914490 | ||||||
| chr17:78914576
|
C | T | 11 | a0001c0001t0001g0248a0001c0001t0003g0249a0001c0001t0003g0298others(8): Show | 11 | HG00140.hp2 HG00323.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+10383G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914576 | ||||||
| chr17:78914588
|
G | GT | 8 | a0001c0001t0002g0137a0001c0001t0002g0143a0001c0001t0003g0188others(5): Show | 8 | HG03130.hp2 NA18957.hp2 NA18971.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+10370dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914588 | ||||||
| chr17:78914714
|
T | G | 1 | a0001c0001t0015g0185 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.130+10245A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914714 | ||||||
| chr17:78914901
|
C | CT | 158 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(155): Show | 159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.130+10057dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914901 | ||||||
| chr17:78914901
|
C | CTT | 6 | a0001c0001t0002g0152a0001c0001t0003g0202a0001c0001t0004g0054others(3): Show | 6 | HG02630.hp1 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+10056_130+1005 others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914901 | ||||||
| chr17:78915161
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+9798A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915161 | ||||||
| chr17:78915177
|
G | A | 1 | a0001c0001t0003g0303 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.130+9782C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915177 | ||||||
| chr17:78915279
|
G | T | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+9680C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915279 | ||||||
| chr17:78915292
|
C | T | 13 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(10): Show | 13 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+9667G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915292 | ||||||
| chr17:78915454
|
G | A | 295 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(292): Show | 296 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.130+9505C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915454 | ||||||
| chr17:78915526
|
CT | C | 156 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(153): Show | 157 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.130+9432delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915526 | ||||||
| chr17:78915563
|
A | T | 12 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0003g0225others(9): Show | 12 | HG01261.hp1 HG01891.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+9396T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915563 | ||||||
| chr17:78915582
|
C | T | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+9377G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915582 | ||||||
| chr17:78915739
|
T | C | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+9220A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915739 | ||||||
| chr17:78915757
|
C | T | 1 | a0001c0001t0003g0310 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.130+9202G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915757 | ||||||
| chr17:78915899
|
C | T | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130+9060G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915899 | ||||||
| chr17:78916035
|
T | C | 6 | a0001c0001t0001g0291a0001c0001t0003g0289a0001c0001t0003g0293others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+8924A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916035 | ||||||
| chr17:78916155
|
G | A | 2 | a0001c0001t0002g0125a0001c0001t0006g0078 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.130+8804C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916155 | ||||||
| chr17:78916212
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0003g0267 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130+8747C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916212 | ||||||
| chr17:78916234
|
C | T | 1 | a0001c0001t0005g0201 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.130+8725G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916234 | ||||||
| chr17:78916314
|
G | A | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+8645C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916314 | ||||||
| chr17:78916327
|
C | G | 1 | a0001c0001t0007g0036 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.130+8632G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916327 | ||||||
| chr17:78916336
|
C | G | 20 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0002g0136others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+8623G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916336 | ||||||
| chr17:78916341
|
T | C | 153 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(150): Show | 154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.130+8618A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916341 | ||||||
| chr17:78916346
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.130+8613G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916346 | ||||||
| chr17:78916431
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+8528A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916431 | ||||||
| chr17:78916554
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0005g0165a0001c0001t0011g0283 | 3 | HG03098.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+8405C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916554 | ||||||
| chr17:78916608
|
G | A | 45 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0248others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.130+8351C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916608 | ||||||
| chr17:78916729
|
G | A | 6 | a0001c0001t0001g0291a0001c0001t0003g0289a0001c0001t0003g0293others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+8230C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916729 | ||||||
| chr17:78916750
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.130+8209G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916750 | ||||||
| chr17:78916755
|
G | A | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130+8204C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916755 | ||||||
| chr17:78916790
|
G | A | 8 | a0001c0001t0003g0216a0001c0001t0005g0215a0001c0001t0013g0214others(5): Show | 8 | HG00609.hp2 HG01346.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+8169C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916790 | ||||||
| chr17:78916928
|
C | T | 20 | a0001c0001t0001g0166a0001c0001t0001g0248a0001c0001t0002g0136others(17): Show | 20 | HG00140.hp2 HG00323.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+8031G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916928 | ||||||
| chr17:78916964
|
C | G | 10 | a0001c0001t0001g0291a0001c0001t0003g0225a0001c0001t0003g0251others(7): Show | 10 | HG01261.hp1 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+7995G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78916964 | ||||||
| chr17:78917120
|
C | T | 102 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(99): Show | 103 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.130+7839G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917120 | ||||||
| chr17:78917168
|
C | T | 8 | a0001c0001t0001g0291a0001c0001t0003g0225a0001c0001t0003g0251others(5): Show | 8 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+7791G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917168 | ||||||
| chr17:78917251
|
C | CA | 104 | a0001c0001t0001g0194a0001c0001t0001g0222a0001c0001t0001g0258others(101): Show | 104 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.130+7707dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917251 | ||||||
| chr17:78917251
|
C | CAA | 16 | a0001c0001t0002g0053a0001c0001t0002g0059a0001c0001t0002g0072others(13): Show | 16 | HG00609.hp1 HG00673.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.130+7706_130+7707d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917251 | ||||||
| chr17:78917251
|
C | CAAAAAAA | 18 | a0001c0001t0001g0229a0001c0001t0001g0248a0001c0001t0002g0148others(15): Show | 18 | HG00140.hp2 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.130+7701_130+7707d others(9): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917251 | ||||||
| chr17:78917251
|
C | CAAAAAAA others(1): Show |
11 | a0001c0001t0001g0166a0001c0001t0002g0136a0001c0001t0002g0137others(8): Show | 11 | HG00323.hp2 HG01358.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+7700_130+7707d others(10): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917251 | ||||||
| chr17:78917251
|
CA | C | 11 | a0001c0001t0001g0199a0001c0001t0001g0219a0001c0001t0001g0223others(8): Show | 11 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+7707delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917251 | ||||||
| chr17:78917251
|
CAA | C | 93 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(90): Show | 94 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.130+7706_130+7707d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917251 | ||||||
| chr17:78917276
|
A | G | 2 | a0001c0001t0002g0125a0001c0001t0006g0078 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.130+7683T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917276 | ||||||
| chr17:78917297
|
G | C | 102 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(99): Show | 103 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.130+7662C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917297 | ||||||
| chr17:78917302
|
C | T | 2 | a0001c0001t0032g0016a0001c0001t0038g0124 | 2 | HG02280.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.130+7657G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917302 | ||||||
| chr17:78917355
|
G | A | 2 | a0001c0001t0002g0061a0001c0002t0043g0117 | 2 | NA18963.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.130+7604C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917355 | ||||||
| chr17:78917384
|
C | A | 1 | a0001c0001t0005g0220 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.130+7575G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917384 | ||||||
| chr17:78917708
|
G | A | 11 | a0001c0001t0001g0229a0001c0001t0002g0148a0001c0001t0002g0149others(8): Show | 11 | HG01123.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+7251C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917708 | ||||||
| chr17:78917761
|
T | C | 91 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(88): Show | 92 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.130+7198A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917761 | ||||||
| chr17:78917847
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+7112G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78917847 | ||||||
| chr17:78918020
|
C | T | 11 | a0001c0001t0001g0302a0001c0001t0001g0305a0001c0001t0001g0314others(8): Show | 11 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+6939G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918020 | ||||||
| chr17:78918058
|
A | G | 20 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(17): Show | 20 | HG00544.hp1 HG00735.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.130+6901T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918058 | ||||||
| chr17:78918059
|
CACACAA | C | 3 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0003g0170 | 3 | HG02970.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.130+6894_130+6899d others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918059 | ||||||
| chr17:78918062
|
A | ACACACAC others(7): Show |
5 | a0001c0001t0001g0190a0001c0001t0001g0287a0001c0001t0003g0251others(2): Show | 5 | HG02129.hp2 HG02165.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+6896_130+6897i others(16): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918062 | ||||||
| chr17:78918062
|
A | ACACACAC others(5): Show |
8 | a0001c0001t0001g0291a0001c0001t0003g0289a0001c0001t0003g0293others(5): Show | 8 | HG01261.hp1 HG01891.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+6896_130+6897i others(14): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918062 | ||||||
| chr17:78918063
|
CAA | C | 3 | a0001c0001t0001g0258a0001c0001t0005g0257a0001c0001t0026g0224 | 3 | HG02109.hp1 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.130+6894_130+6895d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918063 | ||||||
| chr17:78918064
|
A | ACACACAC others(7): Show |
1 | a0001c0001t0029g0033 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+6894_130+6895i others(16): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918064 | ||||||
| chr17:78918064
|
A | ACACACAC others(5): Show |
87 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(84): Show | 88 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.130+6894_130+6895i others(14): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918064 | ||||||
| chr17:78918064
|
A | ACACACAC others(3): Show |
8 | a0001c0001t0001g0228a0001c0001t0002g0134a0001c0001t0003g0231others(5): Show | 8 | HG02080.hp2 HG02258.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+6894_130+6895i others(12): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918064 | ||||||
| chr17:78918064
|
A | ACACACAC others(5): Show |
2 | a0001c0001t0001g0248a0001c0001t0003g0249 | 2 | HG00140.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.130+6894_130+6895i others(14): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918064 | ||||||
| chr17:78918065
|
A | AAC | 8 | a0001c0001t0002g0138a0001c0001t0004g0131a0001c0001t0006g0094others(5): Show | 8 | HG01109.hp2 HG02523.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+6892_130+6893d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918065
|
A | AACAC | 3 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0032g0016 | 3 | HG02451.hp2 NA18989.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.130+6890_130+6893d others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918065
|
A | AACACACA others(3): Show |
8 | a0001c0001t0001g0302a0001c0001t0001g0305a0001c0001t0001g0314others(5): Show | 8 | HG02257.hp2 HG02451.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+6884_130+6893d others(12): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918065
|
A | AACACACA others(5): Show |
13 | a0001c0001t0002g0062a0001c0001t0003g0298a0001c0001t0003g0299others(10): Show | 13 | HG01069.hp2 HG01071.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+6882_130+6893d others(14): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918065
|
A | AACACACA others(11): Show |
1 | a0001c0001t0005g0296 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.130+6876_130+6893d others(20): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918065
|
A | C | 120 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(117): Show | 121 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.130+6894T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918065
|
AAC | A | 27 | a0001c0001t0001g0268a0001c0001t0001g0277a0001c0001t0001g0278others(24): Show | 27 | HG00609.hp1 HG00639.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.130+6892_130+6893d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918065
|
AACAC | A | 19 | a0001c0001t0002g0042a0001c0001t0002g0076a0001c0001t0002g0119others(16): Show | 19 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+6890_130+6893d others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918065 | ||||||
| chr17:78918066
|
A | ACACACAC others(5): Show |
5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+6892_130+6893i others(14): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918066 | ||||||
| chr17:78918066
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0006g0078 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.130+6892_130+6893i others(12): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918066 | ||||||
| chr17:78918072
|
A | ACGCGCAC others(9): Show |
1 | a0001c0001t0003g0267 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.130+6886_130+6887i others(18): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918072 | ||||||
| chr17:78918074
|
A | T | 13 | a0001c0001t0001g0190a0001c0001t0001g0287a0001c0001t0001g0291others(10): Show | 13 | HG01261.hp1 HG01891.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+6885T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918074 | ||||||
| chr17:78918076
|
A | T | 97 | a0001c0001t0001g0164a0001c0001t0001g0180a0001c0001t0001g0181others(94): Show | 98 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.130+6883T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918076 | ||||||
| chr17:78918078
|
A | ACACACAC others(7): Show |
10 | a0001c0001t0001g0229a0001c0001t0002g0148a0001c0001t0002g0149others(7): Show | 10 | HG01123.hp2 HG01884.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+6880_130+6881i others(16): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918078 | ||||||
| chr17:78918078
|
A | ACACACAC others(5): Show |
1 | a0001c0001t0018g0140 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.130+6880_130+6881i others(14): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918078 | ||||||
| chr17:78918078
|
A | T | 5 | a0001c0001t0002g0143a0001c0001t0020g0127a0001c0001t0020g0142others(2): Show | 5 | NA18957.hp2 NA18971.hp2 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+6881T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918078 | ||||||
| chr17:78918142
|
C | T | 2 | a0001c0001t0002g0123a0001c0001t0006g0087 | 2 | HG00741.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.130+6817G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918142 | ||||||
| chr17:78918200
|
A | G | 1 | a0001c0001t0003g0196 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.130+6759T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918200 | ||||||
| chr17:78918206
|
T | C | 1 | a0001c0001t0038g0124 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.130+6753A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918206 | ||||||
| chr17:78918206
|
T | G | 12 | a0001c0001t0001g0229a0001c0001t0002g0148a0001c0001t0002g0149others(9): Show | 12 | HG01123.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+6753A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918206 | ||||||
| chr17:78918210
|
C | T | 2 | a0001c0001t0001g0287a0001c0001t0003g0267 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130+6749G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918210 | ||||||
| chr17:78918301
|
T | C | 32 | a0001c0001t0001g0164a0001c0001t0001g0229a0001c0001t0001g0287others(29): Show | 32 | HG01123.hp2 HG01261.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.130+6658A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918301 | ||||||
| chr17:78918372
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.130+6587G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918372 | ||||||
| chr17:78918373
|
G | A | 20 | a0001c0001t0001g0164a0001c0001t0001g0287a0001c0001t0001g0291others(17): Show | 20 | HG01261.hp1 HG01891.hp1 HG02300.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+6586C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918373 | ||||||
| chr17:78918541
|
G | C | 4 | a0001c0001t0002g0080a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG01109.hp2 HG01928.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+6418C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918541 | ||||||
| chr17:78918602
|
C | T | 19 | a0001c0001t0001g0302a0001c0001t0001g0305a0001c0001t0001g0314others(16): Show | 19 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.130+6357G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918602 | ||||||
| chr17:78918606
|
C | T | 5 | a0001c0001t0001g0305a0001c0001t0003g0309a0001c0002t0001g0307others(2): Show | 5 | HG02809.hp2 HG02896.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+6353G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918606 | ||||||
| chr17:78918671
|
G | A | 1 | a0001c0001t0031g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.130+6288C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918671 | ||||||
| chr17:78918721
|
G | A | 2 | a0001c0001t0002g0125a0001c0001t0006g0078 | 2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.130+6238C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918721 | ||||||
| chr17:78918738
|
T | C | 314 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(311): Show | 315 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.130+6221A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918738 | ||||||
| chr17:78918836
|
A | C | 3 | a0001c0001t0002g0089a0001c0001t0002g0090a0001c0001t0006g0088 | 3 | HG00673.hp2 NA18942.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.130+6123T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918836 | ||||||
| chr17:78918849
|
A | C | 2 | a0001c0001t0001g0287a0001c0001t0003g0267 | 2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.130+6110T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918849 | ||||||
| chr17:78918878
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.130+6081C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918878 | ||||||
| chr17:78918906
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.130+6053C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918906 | ||||||
| chr17:78918979
|
CA | C | 162 | a0001c0001t0001g0194a0001c0001t0001g0229a0001c0001t0001g0258others(159): Show | 162 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.130+5979delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918979 | ||||||
| chr17:78918979
|
CAA | C | 118 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(115): Show | 119 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.130+5978_130+5979d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918979 | ||||||
| chr17:78918979
|
CAAA | C | 7 | a0001c0001t0002g0134a0001c0001t0004g0054a0001c0001t0004g0055others(4): Show | 7 | HG00323.hp1 HG02300.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+5977_130+5979d others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918979 | ||||||
| chr17:78918985
|
A | C | 3 | a0001c0001t0002g0143a0001c0001t0020g0142a0001c0002t0039g0144 | 3 | NA18957.hp2 NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.130+5974T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918985 | ||||||
| chr17:78918986
|
A | C | 97 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(94): Show | 98 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.130+5973T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918986 | ||||||
| chr17:78919042
|
A | G | 5 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138others(2): Show | 5 | HG03491.hp1 NA18942.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+5917T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919042 | ||||||
| chr17:78919181
|
G | A | 10 | a0001c0001t0001g0291a0001c0001t0003g0225a0001c0001t0003g0251others(7): Show | 10 | HG01261.hp1 HG01891.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+5778C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919181 | ||||||
| chr17:78919334
|
C | G | 36 | a0001c0001t0005g0250a0001c0001t0005g0286a0001c0001t0007g0002others(33): Show | 36 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.130+5625G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919334 | ||||||
| chr17:78919376
|
C | A | 185 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0229others(182): Show | 185 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.130+5583G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919376 | ||||||
| chr17:78919535
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.130+5424G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919535 | ||||||
| chr17:78919540
|
G | A | 5 | a0001c0001t0002g0134a0001c0001t0004g0054a0001c0001t0004g0055others(2): Show | 5 | HG02300.hp2 HG02886.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+5419C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919540 | ||||||
| chr17:78919628
|
A | C | 93 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(90): Show | 94 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.130+5331T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919628 | ||||||
| chr17:78919642
|
G | A | 10 | a0001c0001t0001g0261a0001c0001t0001g0271a0001c0001t0001g0291others(7): Show | 10 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+5317C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919642 | ||||||
| chr17:78919707
|
C | T | 1 | a0001c0001t0048g0043 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.130+5252G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919707 | ||||||
| chr17:78919708
|
A | G | 294 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(291): Show | 295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.130+5251T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919708 | ||||||
| chr17:78919710
|
C | T | 3 | a0001c0001t0002g0143a0001c0001t0020g0142a0001c0002t0039g0144 | 3 | NA18957.hp2 NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.130+5249G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919710 | ||||||
| chr17:78919722
|
C | G | 40 | a0001c0001t0001g0229a0001c0001t0001g0258a0001c0001t0001g0287others(37): Show | 40 | HG00639.hp1 HG01123.hp2 HG01243.hp2 others(37): Show |
intron_variant | MODIFIER | c.130+5237G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919722 | ||||||
| chr17:78919745
|
G | A | 5 | a0001c0001t0007g0015a0001c0001t0007g0021a0001c0001t0007g0036others(2): Show | 5 | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+5214C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919745 | ||||||
| chr17:78919791
|
C | A | 3 | a0001c0001t0002g0143a0001c0001t0020g0142a0001c0002t0039g0144 | 3 | NA18957.hp2 NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.130+5168G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919791 | ||||||
| chr17:78919812
|
A | T | 1 | a0001c0001t0002g0134 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.130+5147T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919812 | ||||||
| chr17:78919829
|
A | G | 15 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0287others(12): Show | 15 | HG01261.hp1 HG02300.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+5130T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919829 | ||||||
| chr17:78919834
|
G | GA | 34 | a0001c0001t0001g0258a0001c0001t0002g0042a0001c0001t0002g0044others(31): Show | 34 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.130+5124dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919834 | ||||||
| chr17:78919909
|
T | C | 31 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(28): Show | 31 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.130+5050A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78919909 | ||||||
| chr17:78920052
|
G | A | 15 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0287others(12): Show | 15 | HG01261.hp1 HG02300.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+4907C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920052 | ||||||
| chr17:78920270
|
C | T | 16 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0287others(13): Show | 16 | HG01261.hp1 HG02300.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.130+4689G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920270 | ||||||
| chr17:78920364
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.130+4595C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920364 | ||||||
| chr17:78920392
|
T | C | 282 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(279): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.130+4567A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920392 | ||||||
| chr17:78920542
|
C | T | 1 | a0001c0001t0007g0022 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.130+4417G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920542 | ||||||
| chr17:78920593
|
A | C | 1 | a0001c0001t0002g0083 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.130+4366T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920593 | ||||||
| chr17:78920952
|
A | G | 3 | a0001c0001t0002g0143a0001c0001t0020g0142a0001c0002t0039g0144 | 3 | NA18957.hp2 NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.130+4007T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920952 | ||||||
| chr17:78920990
|
A | G | 2 | a0001c0001t0002g0081a0001c0001t0002g0082 | 2 | HG03710.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.130+3969T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78920990 | ||||||
| chr17:78921031
|
T | C | 283 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(280): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.130+3928A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921031 | ||||||
| chr17:78921268
|
TC | T | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0003g0251others(1): Show | 4 | HG02886.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+3690delG | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921268 | ||||||
| chr17:78921295
|
TAGCTGG | T | 38 | a0001c0001t0005g0250a0001c0001t0005g0286a0001c0001t0007g0002others(35): Show | 38 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.130+3658_130+3663d others(8): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921295 | ||||||
| chr17:78921454
|
G | C | 13 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(10): Show | 13 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+3505C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921454 | ||||||
| chr17:78921511
|
T | C | 9 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0005g0257others(6): Show | 9 | HG00621.hp1 HG02055.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+3448A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921511 | ||||||
| chr17:78921574
|
T | G | 1 | a0001c0001t0001g0166 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.130+3385A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921574 | ||||||
| chr17:78921655
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0003g0251others(1): Show | 4 | HG02886.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+3304C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921655 | ||||||
| chr17:78921660
|
T | C | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0003g0251others(1): Show | 4 | HG02886.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+3299A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921660 | ||||||
| chr17:78921752
|
A | G | 1 | a0001c0001t0006g0058 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.130+3207T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921752 | ||||||
| chr17:78921960
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.130+2999T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921960 | ||||||
| chr17:78922044
|
AGCCCT | A | 8 | a0001c0001t0001g0194a0001c0002t0001g0177a0001c0002t0001g0191others(5): Show | 8 | HG01433.hp1 HG01928.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+2910_130+2914d others(7): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922044 | ||||||
| chr17:78922049
|
T | G | 77 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(74): Show | 78 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.130+2910A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922049 | ||||||
| chr17:78922051
|
G | A | 1 | a0001c0002t0024g0227 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.130+2908C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922051 | ||||||
| chr17:78922245
|
T | C | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.130+2714A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922245 | ||||||
| chr17:78922540
|
G | A | 3 | a0001c0001t0002g0143a0001c0001t0020g0142a0001c0002t0039g0144 | 3 | NA18957.hp2 NA18971.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.130+2419C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922540 | ||||||
| chr17:78922592
|
C | G | 1 | a0001c0001t0032g0016 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.130+2367G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922592 | ||||||
| chr17:78922763
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0003g0251others(1): Show | 4 | HG02886.hp2 HG03453.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+2196C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922763 | ||||||
| chr17:78922863
|
G | A | 1 | a0001c0001t0004g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.130+2096C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922863 | ||||||
| chr17:78922864
|
C | A | 1 | a0001c0001t0004g0126 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.130+2095G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922864 | ||||||
| chr17:78922890
|
A | G | 193 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(190): Show | 194 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.130+2069T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922890 | ||||||
| chr17:78922928
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.130+2031T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922928 | ||||||
| chr17:78922995
|
C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0079 | 2 | HG00408.hp2 HG02027.hp2 |
intron_variant | MODIFIER | c.130+1964G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78922995 | ||||||
| chr17:78923046
|
A | C | 200 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(197): Show | 201 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.130+1913T>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923046 | ||||||
| chr17:78923125
|
G | A | 2 | a0001c0002t0014g0274a0001c0002t0014g0285 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.130+1834C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923125 | ||||||
| chr17:78923232
|
C | T | 7 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0003g0289others(4): Show | 7 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+1727G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923232 | ||||||
| chr17:78923383
|
G | A | 11 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0287others(8): Show | 11 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+1576C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923383 | ||||||
| chr17:78923386
|
T | G | 11 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0287others(8): Show | 11 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+1573A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923386 | ||||||
| chr17:78923391
|
C | T | 1 | a0001c0001t0003g0304 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.130+1568G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923391 | ||||||
| chr17:78923396
|
T | G | 3 | a0001c0001t0007g0036a0001c0002t0013g0260a0001c0002t0025g0167 | 3 | HG00438.hp2 HG00621.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.130+1563A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923396 | ||||||
| chr17:78923396
|
T | TG | 57 | a0001c0001t0001g0180a0001c0001t0001g0181a0001c0001t0001g0190others(54): Show | 57 | HG00323.hp2 HG00639.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.130+1562dupC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923396 | ||||||
| chr17:78923396
|
T | TGG | 58 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199others(55): Show | 59 | HG00140.hp1 HG00621.hp2 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.130+1561_130+1562d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923396 | ||||||
| chr17:78923396
|
T | TGGG | 36 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(33): Show | 36 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.130+1560_130+1562d others(5): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923396 | ||||||
| chr17:78923396
|
T | TGGGG | 21 | a0001c0001t0001g0258a0001c0001t0005g0257a0001c0001t0007g0002others(18): Show | 21 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+1559_130+1562d others(6): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923396 | ||||||
| chr17:78923396
|
T | TGGGGGGG others(4): Show |
1 | a0001c0001t0001g0259 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.130+1552_130+1562d others(13): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923396 | ||||||
| chr17:78923396
|
TG | T | 28 | a0001c0001t0001g0164a0001c0001t0001g0261a0001c0001t0002g0057others(25): Show | 28 | HG00408.hp2 HG01069.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.130+1562delC | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923396 | ||||||
| chr17:78923425
|
C | T | 78 | a0001c0001t0002g0053a0001c0001t0002g0057a0001c0001t0002g0059others(75): Show | 78 | HG00408.hp2 HG00639.hp2 HG00673.hp2 others(75): Show |
intron_variant | MODIFIER | c.130+1534G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923425 | ||||||
| chr17:78923441
|
A | G | 3 | a0001c0001t0003g0170a0001c0001t0015g0168a0001c0001t0015g0169 | 3 | HG02451.hp1 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.130+1518T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923441 | ||||||
| chr17:78923444
|
A | T | 3 | a0001c0001t0004g0054a0001c0001t0004g0055a0001c0001t0004g0056 | 3 | HG02886.hp1 HG02896.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.130+1515T>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923444 | ||||||
| chr17:78923461
|
C | T | 1 | a0001c0002t0025g0167 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.130+1498G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923461 | ||||||
| chr17:78923563
|
G | A | 11 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0287others(8): Show | 11 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.130+1396C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923563 | ||||||
| chr17:78923566
|
A | G | 42 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0302others(39): Show | 42 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.130+1393T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923566 | ||||||
| chr17:78923583
|
C | T | 3 | a0001c0001t0002g0053a0001c0001t0004g0051a0001c0002t0004g0052 | 3 | HG01070.hp1 HG01496.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.130+1376G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923583 | ||||||
| chr17:78923684
|
C | CTG | 201 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0180others(198): Show | 202 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.130+1273_130+1274d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923684 | ||||||
| chr17:78923711
|
G | A | 7 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0003g0289others(4): Show | 7 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+1248C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923711 | ||||||
| chr17:78923754
|
T | C | 1 | a0001c0002t0009g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.130+1205A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923754 | ||||||
| chr17:78923944
|
G | A | 1 | a0001c0001t0007g0002 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.130+1015C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923944 | ||||||
| chr17:78923997
|
T | C | 7 | a0001c0001t0001g0287a0001c0001t0001g0291a0001c0001t0003g0289others(4): Show | 7 | HG01261.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+962A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78923997 | ||||||
| chr17:78924245
|
G | T | 1 | a0001c0001t0008g0003 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.130+714C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924245 | ||||||
| chr17:78924316
|
G | A | 1 | a0001c0001t0008g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.130+643C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924316 | ||||||
| chr17:78924361
|
G | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0005g0165 | 3 | HG02886.hp2 HG03453.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.130+598C>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924361 | ||||||
| chr17:78924366
|
G | A | 2 | a0001c0001t0004g0050a0001c0001t0018g0049 | 2 | HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.130+593C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924366 | ||||||
| chr17:78924511
|
G | A | 1 | a0001c0001t0023g0294 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.130+448C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924511 | ||||||
| chr17:78924586
|
C | T | 13 | a0001c0001t0002g0042a0001c0001t0002g0044a0001c0001t0002g0045others(10): Show | 13 | HG00639.hp1 HG01243.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.130+373G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924586 | ||||||
| chr17:78924626
|
G | A | 20 | a0001c0001t0001g0302a0001c0001t0001g0305a0001c0001t0001g0314others(17): Show | 20 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.130+333C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924626 | ||||||
| chr17:78924758
|
A | AGGGAAAG others(19): Show |
1 | a0001c0001t0007g0002 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.130+175_130+200dup others(26): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78924758 |