Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MGAAA others(215): Show |
chr17 | 78847977 | 78930387 |
| a0002 | 0/0 | 220 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | MGAAA others(215): Show |
chr17 | 78847977 | 78930387 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 660 | 259 | 80 | 40 | 95 | 8 | 35 | TIMP2_chr17_78847977_78930387 | TIMP2 | ATGGG others(655): Show |
chr17 | 78847977 | 78930387 | ||
| a0001c0002 | 0/1 | 660 | 54 | 9 | 9 | 28 | 2 | 5 | TIMP2_chr17_78847977_78930387 | TIMP2 | ATGGG others(655): Show |
chr17 | 78847977 | 78930387 | ||
| a0001c0004 | 0/0 | 660 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | ATGGG others(655): Show |
chr17 | 78847977 | 78930387 | ||
| a0001c0005 | 0/0 | 660 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | ATGGG others(655): Show |
chr17 | 78847977 | 78930387 | ||
| a0002c0003 | 0/0 | 660 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | ATGGG others(655): Show |
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 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0002 | 0/0 | 3651 | 51 | 10 | 8 | 25 | 0 | 8 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0003 | 0/0 | 3652 | 31 | 14 | 6 | 8 | 0 | 3 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0004 | 1/0 | 3652 | 18 | 6 | 6 | 3 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0005 | 0/0 | 3650 | 18 | 3 | 4 | 5 | 3 | 3 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0006 | 0/0 | 3650 | 16 | 4 | 2 | 7 | 1 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0007 | 0/0 | 3651 | 15 | 0 | 0 | 14 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0008 | 0/0 | 3650 | 9 | 0 | 0 | 7 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0009 | 0/0 | 3652 | 6 | 0 | 0 | 6 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0010 | 0/0 | 3650 | 4 | 3 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0011 | 0/0 | 3650 | 3 | 3 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0012 | 0/0 | 3653 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3648): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0014 | 0/0 | 3652 | 3 | 3 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0015 | 0/0 | 3652 | 2 | 0 | 0 | 0 | 0 | 2 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0017 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0018 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0019 | 0/0 | 3652 | 2 | 0 | 0 | 1 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0020 | 0/0 | 3651 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0021 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0022 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0023 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0026 | 0/0 | 3650 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0027 | 0/0 | 3652 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0029 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0031 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0032 | 0/0 | 3651 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0033 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0035 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0037 | 0/0 | 3652 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0038 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0041 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0042 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0045 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0046 | 0/0 | 3650 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0048 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0049 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0050 | 0/0 | 3652 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0051 | 0/0 | 3651 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0054 | 0/0 | 3651 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0056 | 0/0 | 3650 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0001t0057 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0001 | 0/0 | 3651 | 7 | 1 | 0 | 6 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0002 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0003 | 0/0 | 3652 | 12 | 4 | 4 | 1 | 0 | 3 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0004 | 0/0 | 3652 | 3 | 0 | 1 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0005 | 0/0 | 3650 | 3 | 0 | 0 | 3 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0006 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0009 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0012 | 0/0 | 3653 | 2 | 1 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3648): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0013 | 0/0 | 3652 | 3 | 0 | 0 | 1 | 2 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0015 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0016 | 0/0 | 3651 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0017 | 0/0 | 3652 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0023 | 0/0 | 3651 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0024 | 0/0 | 3651 | 2 | 0 | 2 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0025 | 0/0 | 3650 | 2 | 0 | 0 | 2 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0028 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0030 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0034 | 0/0 | 3650 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0036 | 0/0 | 3652 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0039 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0040 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0043 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0044 | 0/0 | 3651 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0047 | 0/0 | 3650 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0052 | 0/1 | 3653 | 1 | 0 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3648): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0053 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0001c0002t0055 | 0/0 | 3651 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3646): Show |
chr17 | 78847977 | 78930387 |
| a0001c0004t0011 | 0/0 | 3650 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3645): Show |
chr17 | 78847977 | 78930387 |
| a0001c0005t0003 | 0/0 | 3652 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| a0002c0003t0004 | 0/0 | 3652 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | AGCAA others(3647): Show |
chr17 | 78847977 | 78930387 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0231 | 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 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0260 | 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 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0043 | 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 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0056 | 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 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0073 | 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 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0088 | 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 |
| a0001c0001t0002g0095 | 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 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0146 | 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 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0201 | 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 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0003g0302 | 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 |
| a0001c0001t0003g0307 | 0/0 | 1 | 1 | 0 | 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 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0004g0152 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0177 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0005g0301 | 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 |
| a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0102 | 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 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0006g0144 | 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 |
| a0001c0001t0007g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0005 | 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 |
| a0001c0001t0007g0016 | 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 |
| a0001c0001t0007g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0004 | 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 |
| a0001c0001t0008g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0019 | 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 |
| a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0008g0039 | 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 |
| a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0011g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0012g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0014g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0014g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0014g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0015g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0015g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0017g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0019g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0019g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0020g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0020g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0021g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0021g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0022g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0022g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0023g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0026g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0026g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0027g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0027g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0029g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0031g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0032g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0033g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0035g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0037g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0038g0123 | 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 |
| a0001c0001t0042g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0045g0063 | 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 |
| a0001c0001t0048g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0049g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0050g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0051g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0054g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0056g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0001t0057g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0190 | 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 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0002t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0003g0305 | 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 |
| a0001c0002t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0005g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0009g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0012g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0012g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0013g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0013g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0013g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0015g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0016g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0016g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0017g0066 | 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 |
| a0001c0002t0024g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0024g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0025g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0025g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0028g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0030g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0034g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0036g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0039g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0040g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0043g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0044g0065 | 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 |
| a0001c0002t0052g0224 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0053g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0002t0055g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0004t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0001c0005t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| a0002c0003t0004g0083 | 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 | g0204 | EUR | GBR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0247 | EUR | GBR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00323 | hp1 | a0001 | c0001 | t0031 | g0025 | EUR | FIN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00323 | hp2 | a0001 | c0001 | t0005 | g0301 | EUR | FIN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00408 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0056 | 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 | g0037 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00544 | hp2 | a0001 | c0001 | t0007 | g0012 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00558 | hp1 | a0001 | c0002 | t0028 | g0036 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00558 | hp2 | a0001 | c0002 | t0034 | g0154 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00609 | hp1 | a0001 | c0001 | t0008 | g0004 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00609 | hp2 | a0001 | c0002 | t0005 | g0172 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00621 | hp1 | a0001 | c0002 | t0012 | g0259 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00639 | hp1 | a0001 | c0001 | t0050 | g0161 | 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 | g0021 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00735 | hp1 | a0001 | c0001 | t0005 | g0242 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00735 | hp2 | a0001 | c0001 | t0005 | g0178 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0068 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0052 | 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 | g0065 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0299 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0179 | 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 | g0261 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0246 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01106 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01109 | hp1 | a0001 | c0002 | t0003 | g0243 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0115 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01243 | hp2 | a0001 | c0001 | t0010 | g0040 | AMR | PUR | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0002 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01361 | hp1 | a0001 | c0001 | t0012 | g0212 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01361 | hp2 | a0001 | c0001 | t0004 | g0075 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01433 | hp1 | a0001 | c0002 | t0024 | g0192 | 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 | g0053 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01516 | hp1 | a0001 | c0002 | t0013 | g0273 | EUR | IBS | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0236 | 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 | t0013 | g0284 | 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 | g0132 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01928 | hp1 | a0001 | c0002 | t0024 | g0226 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0235 | 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 | g0234 | 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 | g0120 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0302 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02004 | hp1 | a0001 | c0005 | t0003 | g0314 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0121 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02040 | hp1 | a0001 | c0002 | t0004 | g0099 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02055 | hp1 | a0001 | c0002 | t0012 | g0252 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02074 | hp2 | a0001 | c0002 | t0016 | g0158 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02080 | hp1 | a0001 | c0001 | t0019 | g0093 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02080 | hp2 | a0001 | c0002 | t0055 | g0251 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0213 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02129 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02135 | hp1 | a0001 | c0001 | t0008 | g0029 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0102 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02155 | hp2 | a0001 | c0002 | t0005 | g0268 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02165 | hp2 | a0002 | c0003 | t0004 | g0083 | EAS | CDX | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02258 | hp1 | a0001 | c0001 | t0054 | g0269 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02280 | hp2 | a0001 | c0001 | t0038 | g0123 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0067 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02300 | hp2 | a0001 | c0001 | t0006 | g0134 | AMR | PEL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02451 | hp1 | a0001 | c0001 | t0014 | g0168 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02451 | hp2 | a0001 | c0001 | t0032 | g0017 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02523 | hp2 | a0001 | c0002 | t0006 | g0153 | EAS | KHV | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02572 | hp1 | a0001 | c0001 | t0018 | g0139 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02615 | hp2 | a0001 | c0001 | t0010 | g0113 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02622 | hp1 | a0001 | c0001 | t0035 | g0071 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02630 | hp1 | a0001 | c0001 | t0027 | g0174 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02630 | hp2 | a0001 | c0001 | t0014 | g0184 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02647 | hp1 | a0001 | c0001 | t0022 | g0182 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0240 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0297 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02698 | hp2 | a0001 | c0002 | t0003 | g0274 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02717 | hp2 | a0001 | c0001 | t0021 | g0048 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02723 | hp1 | a0001 | c0001 | t0021 | g0042 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02723 | hp2 | a0001 | c0001 | t0003 | g0271 | 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 | t0015 | g0296 | 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 | g0091 | 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 | g0304 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0050 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0061 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0307 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02922 | hp1 | a0001 | c0001 | t0022 | g0265 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0173 | 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 | g0280 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02970 | hp1 | a0001 | c0001 | t0029 | g0034 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0077 | 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 | t0056 | g0203 | 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 | g0288 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0266 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0282 | 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 | g0194 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03209 | hp2 | a0001 | c0002 | t0009 | g0038 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03225 | hp1 | a0001 | c0001 | t0051 | g0162 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03225 | hp2 | a0001 | c0001 | t0048 | g0044 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03239 | hp1 | a0001 | c0001 | t0005 | g0262 | 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 | g0256 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0164 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0018 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03491 | hp1 | a0001 | c0001 | t0037 | g0131 | 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 | g0281 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03516 | hp2 | a0001 | c0001 | t0011 | g0279 | AFR | ESN | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0001 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03540 | hp2 | a0001 | c0002 | t0003 | g0215 | AFR | GWD | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03579 | hp1 | a0001 | c0001 | t0014 | g0167 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0227 | 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 | g0125 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0200 | 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 | g0105 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0114 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03834 | hp1 | a0001 | c0001 | t0008 | g0039 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03834 | hp2 | a0001 | c0002 | t0017 | g0066 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0118 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04115 | hp2 | a0001 | c0001 | t0015 | g0294 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04204 | hp2 | a0001 | c0001 | t0023 | g0293 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04228 | hp1 | a0001 | c0002 | t0003 | g0275 | SAS | STU | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0151 | 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 | g0289 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | CHB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18906 | hp1 | a0001 | c0002 | t0003 | g0305 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18942 | hp1 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18945 | hp1 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18945 | hp2 | a0001 | c0001 | t0008 | g0028 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18947 | hp2 | a0001 | c0001 | t0009 | g0033 | 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 | g0254 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0003 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18963 | hp2 | a0001 | c0002 | t0043 | g0119 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18964 | hp2 | a0001 | c0001 | t0009 | g0032 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18966 | hp2 | a0001 | c0002 | t0016 | g0156 | 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 | t0013 | g0188 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18970 | hp1 | a0001 | c0002 | t0053 | g0253 | 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 | g0031 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18971 | hp2 | a0001 | c0001 | t0020 | g0141 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18973 | hp1 | a0001 | c0001 | t0042 | g0092 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18973 | hp2 | a0001 | c0002 | t0002 | g0155 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18974 | hp1 | a0001 | c0001 | t0005 | g0285 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0024 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0011 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0176 | 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 | g0232 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18983 | hp2 | a0001 | c0001 | t0045 | g0063 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18984 | hp1 | a0001 | c0001 | t0007 | g0022 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0095 | 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 | g0237 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19000 | hp1 | a0001 | c0002 | t0030 | g0006 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19005 | hp1 | a0001 | c0001 | t0049 | g0090 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19009 | hp2 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19011 | hp2 | a0001 | c0002 | t0025 | g0225 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0306 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0272 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19063 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19063 | hp2 | a0001 | c0001 | t0008 | g0026 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19065 | hp1 | a0001 | c0001 | t0006 | g0084 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0249 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19066 | hp2 | a0001 | c0001 | t0020 | g0126 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19068 | hp1 | a0001 | c0002 | t0004 | g0157 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0064 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19074 | hp1 | a0001 | c0002 | t0039 | g0143 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19077 | hp1 | a0001 | c0002 | t0005 | g0186 | 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 | g0073 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19082 | hp1 | a0001 | c0002 | t0040 | g0159 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19083 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0187 | 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 | g0060 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19085 | hp1 | a0001 | c0002 | t0025 | g0166 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19085 | hp2 | a0001 | c0001 | t0008 | g0035 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19088 | hp2 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19091 | hp1 | a0001 | c0001 | t0008 | g0019 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19091 | hp2 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0041 | AFR | YRI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | ASW | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20129 | hp2 | a0001 | c0002 | t0015 | g0185 | AFR | ASW | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0218 | EUR | TSI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0086 | EUR | TSI | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0248 | 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 | g0180 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG01123 | hp2 | a0001 | c0001 | t0005 | g0177 | AMR | CLM | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02109 | hp1 | a0001 | c0001 | t0026 | g0222 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02109 | hp2 | a0001 | c0001 | t0027 | g0181 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02486 | hp1 | a0001 | c0001 | t0057 | g0291 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02486 | hp2 | a0001 | c0002 | t0036 | g0116 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02559 | hp1 | a0001 | c0002 | t0003 | g0287 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0145 | AFR | ACB | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| HG06807 | hp2 | a0001 | c0001 | t0010 | g0049 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | USA | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0052 | g0224 | REF | REF | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0152 | REF | REF | TIMP2_chr17_78847977_78930387 | TIMP2 | chr17 | 78847977 | 78930387 |
| view | 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 |
| view | 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 | 53 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(50): 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 |
| view | 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 | a0001c0001t0054 | 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 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0050 others(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 | a0001c0002t0024 a0001c0002t0025 a0001c0002t0030 others(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 | a0001c0001t0011 a0001c0001t0022 a0001c0001t0046 others(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 | a0001c0001t0023 a0001c0001t0056 a0001c0002t0023 |
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 | a0001c0001t0014 a0001c0001t0018 |
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 | a0001c0001t0045 a0001c0002t0055 |
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 | a0001c0001t0029 a0001c0001t0038 |
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 | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(15): 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 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0008 others(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 | a0001c0002t0003 | 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 | a0001c0001t0020 a0001c0001t0033 a0001c0001t0049 |
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 | a0001c0001t0026 a0001c0001t0048 a0001c0001t0049 |
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 | a0001c0001t0012 a0001c0002t0012 |
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 | a0001c0001t0014 a0001c0001t0017 a0001c0001t0018 others(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 | a0001c0001t0027 a0001c0001t0032 |
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 | a0001c0001t0015 a0001c0001t0019 a0001c0002t0015 others(1): Show |
6 | HG02080.hp1 HG02486.hp2 HG02735.hp2 others(3): 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 | a0001c0001t0035 a0001c0002t0036 |
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 | a0001c0001t0020 a0001c0001t0033 |
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 | a0001c0001t0002 a0001c0001t0049 |
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 | a0001c0002t0016 a0001c0002t0034 |
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 | a0001c0001t0010 a0001c0001t0021 a0001c0001t0050 others(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 | a0001c0001t0050 | 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 | a0001c0001t0051 | 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 | 37 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(34): Show |
190 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(187): 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 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0009 others(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 |
| view | 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 | 221 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(218): Show |
222 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(219): 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 | a0001c0001t0002g0073 | 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 | a0001c0001t0002g0073 | 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 | a0001c0001t0008g0035 | 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 | a0001c0001t0020g0126 a0001c0001t0020g0141 a0001c0001t0033g0031 others(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 | a0001c0001t0001g0247 a0001c0001t0003g0248 |
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 | 288 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(285): Show |
290 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(287): 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 | a0001c0001t0008g0039 | 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 | a0001c0001t0022g0182 | 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 | 207 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(204): Show |
208 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(205): 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 | a0001c0001t0010g0040 a0001c0001t0010g0041 a0001c0001t0010g0049 others(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 | a0001c0001t0029g0034 a0001c0001t0038g0123 |
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 | a0001c0001t0003g0303 | 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 | a0001c0001t0003g0303 | 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 | a0001c0001t0003g0307 | 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 | a0001c0002t0055g0251 | 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 | a0001c0001t0003g0292 | 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 | a0001c0001t0001g0283 | 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 | 27 | a0001c0001t0001g0267 a0001c0001t0003g0169 a0001c0001t0003g0175 others(24): 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 | a0001c0001t0003g0299 a0001c0001t0003g0300 |
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 | a0001c0001t0020g0126 a0001c0001t0020g0141 a0001c0001t0033g0031 others(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 | 17 | a0001c0001t0001g0267 a0001c0001t0003g0175 a0001c0001t0003g0250 others(14): 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 | a0001c0001t0002g0097 | 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 | a0001c0001t0001g0193 | 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 | a0001c0002t0053g0253 | 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 | 287 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(284): Show |
289 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(286): 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 | a0001c0001t0002g0146 a0001c0001t0002g0151 |
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 | a0001c0002t0001g0255 | 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 | a0001c0001t0002g0045 a0001c0001t0004g0140 a0001c0001t0006g0077 others(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 | a0001c0002t0024g0226 | 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 | a0001c0001t0001g0230 | 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 | 259 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(256): Show |
260 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(257): 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 | a0001c0001t0001g0206 a0001c0001t0001g0263 a0001c0001t0001g0276 others(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 | a0001c0001t0005g0249 | 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 | a0001c0001t0017g0132 | 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 | 287 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(284): Show |
289 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(286): 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 | a0001c0001t0003g0233 | 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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | 243 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(240): Show |
245 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(242): 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 | a0001c0001t0001g0206 a0001c0001t0001g0263 a0001c0001t0001g0276 others(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 | a0001c0001t0001g0310 a0001c0001t0003g0271 a0001c0001t0004g0140 others(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 | a0001c0001t0001g0230 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0020g0126 a0001c0001t0020g0141 a0001c0001t0026g0222 others(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 | a0001c0001t0008g0028 | 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 | a0001c0001t0001g0206 a0001c0001t0001g0263 a0001c0001t0001g0276 others(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 | a0001c0001t0007g0003 | 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 | a0001c0001t0003g0169 a0001c0001t0003g0223 |
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 | a0001c0001t0031g0025 | 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 | a0001c0002t0024g0192 | 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 | a0001c0002t0009g0038 | 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 | a0001c0001t0003g0309 | 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 | a0001c0001t0002g0101 a0001c0001t0019g0093 |
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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0026g0222 a0001c0001t0026g0289 a0001c0001t0048g0044 |
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 | 290 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(287): Show |
292 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(289): 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 | a0001c0001t0014g0167 a0001c0001t0014g0168 a0001c0001t0014g0184 others(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 | a0001c0001t0029g0034 a0001c0001t0038g0123 |
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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0198 a0001c0001t0005g0240 a0001c0001t0037g0131 |
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 | a0001c0001t0002g0145 a0001c0001t0026g0222 a0001c0001t0026g0289 others(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 | a0001c0001t0018g0139 | 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 | a0001c0001t0001g0267 a0001c0001t0017g0132 |
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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0001g0206 a0001c0001t0001g0238 a0001c0001t0001g0245 others(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 | a0001c0001t0001g0231 a0001c0001t0005g0249 a0001c0001t0007g0011 others(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 | a0001c0001t0001g0198 | 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 | a0001c0001t0002g0103 | 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 | 68 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(65): Show |
69 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.341-6188G>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863834 | |||||||
| chr17:78863914 | T | C | 262 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(259): Show |
264 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(261): Show |
intron_variant | MODIFIER | c.341-6268A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78863914 | |||||||
| chr17:78864207 | A | G | 80 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0210 others(77): Show |
81 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.341-6561T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78864207 | |||||||
| chr17:78864391 | T | C | 256 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(253): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(255): 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0003g0173 a0001c0001t0003g0266 a0001c0001t0010g0113 others(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 | a0001c0001t0002g0133 | 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 | 262 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(259): Show |
264 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(261): 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 | a0001c0001t0001g0197 a0001c0001t0001g0234 a0001c0001t0006g0067 |
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 | 177 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(174): 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 | a0001c0002t0001g0191 a0001c0002t0024g0192 a0001c0002t0024g0226 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0260 a0001c0001t0001g0283 others(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 | a0001c0001t0001g0270 a0001c0001t0001g0295 a0001c0001t0002g0047 others(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 | a0001c0001t0001g0231 a0001c0001t0005g0249 a0001c0001t0007g0011 others(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 | a0001c0001t0004g0115 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0002g0133 | 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 | 201 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(198): Show |
203 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.340+5273dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865624 | |||||||
| chr17:78865624 | C | CAA | 20 | a0001c0001t0001g0210 a0001c0001t0002g0045 a0001c0001t0002g0127 others(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 | 81 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(78): Show |
82 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.340+5140G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78865758 | |||||||
| chr17:78865858 | C | G | 105 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(102): Show |
106 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(103): 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 | a0001c0001t0003g0299 a0001c0001t0003g0300 |
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 | a0001c0001t0020g0126 a0001c0001t0020g0141 a0001c0001t0049g0090 |
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 | 74 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(71): Show |
75 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(72): 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 | 74 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(71): Show |
75 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(72): 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 | a0001c0001t0003g0223 a0001c0001t0003g0266 a0001c0001t0041g0046 |
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 | a0001c0001t0002g0097 | 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 | a0001c0001t0003g0233 | 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 | a0001c0001t0003g0223 a0001c0001t0003g0266 a0001c0001t0018g0139 others(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 | a0001c0001t0001g0270 a0001c0001t0003g0223 a0001c0001t0003g0266 others(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 | a0001c0001t0003g0170 | 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 | a0001c0001t0001g0260 a0001c0001t0003g0248 a0001c0001t0003g0266 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0260 a0001c0001t0001g0283 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0228 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0310 a0001c0001t0029g0034 a0001c0001t0038g0123 |
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 | a0001c0001t0002g0142 a0001c0001t0003g0223 a0001c0001t0018g0139 others(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 | a0001c0001t0005g0219 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0002g0081 | 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 | 263 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(260): Show |
265 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(262): 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 | a0001c0001t0020g0126 | 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 | a0001c0001t0003g0223 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0210 a0001c0001t0002g0149 a0001c0001t0005g0256 others(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 | a0001c0001t0001g0220 a0001c0001t0002g0054 a0001c0001t0002g0114 others(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 | a0001c0001t0001g0208 a0001c0001t0001g0270 a0001c0001t0001g0295 others(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 | 85 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0247 others(82): Show |
86 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(83): 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 | 94 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(91): Show |
95 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(92): 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 | a0001c0001t0002g0081 | 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 | 99 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(96): Show |
100 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(97): 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 | a0001c0001t0001g0304 a0001c0001t0003g0266 a0001c0001t0041g0046 |
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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0002g0142 others(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 | 95 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(92): Show |
96 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(93): 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 | a0001c0001t0006g0085 | 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 | 167 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(164): 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 | a0001c0001t0003g0302 | 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 | a0001c0001t0007g0011 a0001c0001t0009g0033 a0001c0001t0033g0031 |
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 | 103 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(100): Show |
104 | HG00140.hp2 HG00323.hp2 HG00558.hp1 others(101): 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 | a0001c0001t0008g0004 a0001c0001t0008g0026 a0001c0001t0009g0013 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | 165 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(162): 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 | 264 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(261): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0050g0161 | 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 | 161 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(158): 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 | a0001c0001t0001g0165 a0001c0001t0001g0257 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0207 | 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 | a0001c0001t0003g0173 a0001c0001t0010g0113 a0001c0001t0021g0042 others(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 | 95 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(92): 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 | a0001c0001t0049g0090 | 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 | a0001c0001t0001g0189 a0001c0001t0002g0088 a0001c0001t0002g0089 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0228 a0001c0001t0001g0257 others(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 | a0001c0001t0002g0062 | 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 | 51 | a0001c0001t0001g0210 a0001c0001t0001g0304 a0001c0001t0002g0149 others(48): Show |
52 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.340+1493T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869405 | |||||||
| chr17:78869414 | CA | C | 235 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(232): Show |
237 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(234): Show |
intron_variant | MODIFIER | c.340+1483delT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 3/4 | chr17 | 78869414 | |||||||
| chr17:78869425 | A | C | 1 | a0001c0001t0001g0277 | 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 | a0001c0001t0002g0109 a0001c0001t0002g0112 |
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 | a0001c0001t0018g0139 a0001c0001t0035g0071 |
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 | a0001c0001t0005g0240 | 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 | a0001c0001t0001g0228 a0001c0001t0011g0194 |
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 | a0001c0001t0001g0210 a0001c0001t0001g0270 a0001c0001t0002g0124 others(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 | |||||||
| chr17:78870144 | G | A | 4 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0003g0173 a0001c0001t0010g0113 a0001c0001t0021g0042 others(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 | a0001c0001t0007g0015 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0228 a0001c0001t0001g0247 others(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 | a0001c0001t0007g0015 | 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 | a0001c0002t0039g0143 | 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 | a0001c0001t0003g0223 a0001c0001t0018g0139 a0001c0001t0035g0071 |
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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0206 others(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 | a0001c0001t0002g0145 a0001c0002t0001g0306 a0001c0002t0003g0287 others(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 | a0001c0001t0001g0260 a0001c0001t0002g0045 a0001c0001t0003g0214 others(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 | a0001c0001t0003g0223 a0001c0001t0018g0139 a0001c0001t0035g0071 |
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 | 11 | a0001c0001t0001g0193 a0001c0001t0003g0288 a0001c0001t0003g0292 others(8): 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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(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 | a0001c0001t0001g0260 a0001c0001t0003g0214 a0001c0001t0004g0075 others(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 | 182 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(179): 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 | 155 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(152): 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 | a0001c0001t0005g0218 | 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 | 196 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(193): 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 | a0001c0001t0006g0147 a0001c0001t0051g0162 |
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 | a0001c0002t0040g0159 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0004g0051 | 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 | 191 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(188): 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0290 a0001c0001t0004g0051 a0001c0001t0054g0269 |
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 | a0001c0001t0001g0239 a0001c0001t0005g0240 |
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 | a0001c0001t0001g0231 a0001c0001t0005g0249 a0001c0001t0007g0011 others(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 | 55 | a0001c0001t0002g0081 a0001c0001t0003g0173 a0001c0001t0008g0019 others(52): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.232-444dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871449 | |||||||
| chr17:78871466 | A | AAAG | 6 | a0001c0001t0001g0220 a0001c0001t0001g0229 a0001c0001t0002g0062 others(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 | 153 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(150): 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 | a0001c0001t0001g0210 a0001c0001t0001g0228 a0001c0001t0001g0247 others(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 | a0001c0001t0003g0223 a0001c0001t0015g0296 a0001c0001t0018g0139 others(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 | a0001c0001t0003g0173 a0001c0001t0010g0113 a0001c0001t0021g0042 others(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 | a0001c0001t0003g0223 a0001c0001t0018g0139 a0001c0001t0035g0071 |
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 | a0001c0001t0002g0098 | 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 | a0001c0001t0003g0205 | 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 | a0001c0001t0003g0250 | 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 | a0001c0001t0003g0173 a0001c0001t0010g0113 a0001c0001t0021g0042 others(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 | a0001c0001t0001g0260 a0001c0001t0003g0223 a0001c0001t0018g0139 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(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 | 192 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(189): 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 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0220 others(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 | 197 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(194): 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 | 52 | a0001c0002t0001g0171 a0001c0002t0001g0176 a0001c0002t0001g0190 others(49): Show |
53 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.232-950C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78871956 | |||||||
| chr17:78872053 | T | C | 198 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(195): 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 | a0001c0002t0039g0143 | 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0001g0295 a0001c0001t0002g0062 a0001c0001t0011g0282 others(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 | a0001c0001t0003g0223 | 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 | a0001c0001t0007g0011 | 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0006g0147 a0001c0001t0051g0162 |
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 | 198 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(195): 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 | a0001c0001t0003g0307 a0001c0001t0026g0289 |
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 | a0001c0002t0003g0313 a0001c0002t0005g0268 a0001c0002t0012g0252 others(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 | a0001c0001t0002g0082 | 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 | a0001c0001t0004g0140 | 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 | 207 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(204): Show |
209 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.231+515delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 2/4 | chr17 | 78873303 | |||||||
| chr17:78873303 | ATT | A | 53 | a0001c0001t0001g0165 a0001c0001t0001g0204 a0001c0001t0001g0210 others(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 | a0001c0001t0004g0075 | 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 | 140 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(137): 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 | a0001c0001t0001g0165 a0001c0001t0001g0204 a0001c0001t0001g0210 others(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 | a0001c0001t0001g0206 a0001c0001t0001g0286 a0001c0001t0002g0062 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0304 a0001c0001t0002g0133 others(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 | a0001c0001t0003g0250 a0001c0001t0003g0312 |
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 | 192 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(189): 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 | 147 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(144): 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 | a0001c0001t0002g0088 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0295 | 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | 55 | a0001c0001t0002g0112 a0001c0001t0006g0110 a0001c0001t0006g0134 others(52): Show |
56 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(53): 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 | a0001c0001t0002g0081 | 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 | a0001c0001t0003g0223 | 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 | 263 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(260): Show |
265 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(262): 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 | a0001c0001t0004g0140 | 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 | 260 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(257): Show |
262 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.131-369delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874287 | |||||||
| chr17:78874377 | C | T | 119 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(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 | 258 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(255): Show |
260 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(257): 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0283 a0001c0001t0001g0286 |
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 | 194 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(191): 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 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0228 others(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 | 212 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(209): Show |
214 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(211): 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 | a0001c0001t0003g0297 | 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 | 200 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(197): 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 | 64 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(61): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): 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 | a0001c0001t0008g0028 | 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 | 64 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(61): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.131-820C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78874739 | |||||||
| chr17:78874744 | A | ATTT | 58 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(55): Show |
59 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(56): 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 | a0001c0001t0002g0135 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 64 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(61): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): 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 | a0001c0001t0002g0145 a0001c0001t0003g0223 |
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 | 198 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(195): 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 | a0001c0001t0004g0096 | 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 | a0001c0001t0007g0037 | 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 | a0001c0001t0002g0070 | 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 | a0001c0001t0005g0262 | 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 | 25 | a0001c0001t0002g0112 a0001c0001t0006g0110 a0001c0001t0006g0134 others(22): Show |
26 | HG00558.hp2 HG00609.hp2 HG01081.hp1 others(23): 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 | a0001c0001t0008g0039 | 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 | a0001c0001t0003g0299 a0001c0001t0003g0300 |
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 | a0001c0001t0001g0295 | 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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.131-2050T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78875969 | |||||||
| chr17:78876003 | T | G | 266 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): 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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | 69 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(66): Show |
70 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.131-2158G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876077 | |||||||
| chr17:78876121 | C | T | 61 | a0001c0001t0002g0112 a0001c0001t0003g0307 a0001c0001t0006g0077 others(58): Show |
62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): 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 | a0001c0001t0004g0052 | 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 | 64 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(61): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.131-2337G>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876256 | |||||||
| chr17:78876298 | T | C | 264 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(261): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): Show |
intron_variant | MODIFIER | c.131-2379A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876298 | |||||||
| chr17:78876313 | C | T | 56 | a0001c0001t0002g0112 a0001c0001t0003g0307 a0001c0001t0006g0110 others(53): Show |
57 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(54): 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 | a0001c0001t0010g0113 a0001c0001t0021g0042 a0001c0001t0050g0161 |
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 | 64 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(61): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.131-2481A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876400 | |||||||
| chr17:78876421 | C | T | 64 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(61): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.131-2502G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876421 | |||||||
| chr17:78876492 | T | C | 64 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(61): Show |
65 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(62): 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 | a0001c0001t0029g0034 a0001c0001t0038g0123 |
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 | 66 | a0001c0001t0001g0260 a0001c0001t0001g0267 a0001c0001t0001g0270 others(63): Show |
67 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-2765dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78876683 | |||||||
| chr17:78876683 | A | ATT | 12 | a0001c0002t0001g0176 a0001c0002t0001g0190 a0001c0002t0001g0191 others(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 | a0001c0002t0016g0156 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 199 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(196): 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 | a0001c0001t0001g0304 a0001c0001t0003g0266 a0001c0001t0003g0288 others(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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | a0001c0001t0005g0219 | 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 | 5 | a0001c0002t0003g0002 a0001c0002t0003g0215 a0001c0002t0003g0243 others(2): Show |
6 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(3): 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 | a0001c0001t0002g0081 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0003g0250 | 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 | 65 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(62): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-3525C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877444 | |||||||
| chr17:78877546 | CT | C | 65 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(62): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): 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 | 139 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(136): 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 | 65 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(62): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): 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 | a0001c0001t0022g0265 | 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 | 65 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(62): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.131-3696G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78877615 | |||||||
| chr17:78877679 | T | C | 65 | a0001c0001t0001g0270 a0001c0001t0002g0112 a0001c0001t0002g0124 others(62): Show |
66 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(63): 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 | a0001c0001t0002g0145 a0001c0001t0003g0288 a0001c0001t0005g0242 others(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 | a0001c0001t0002g0061 | 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 | a0001c0001t0037g0131 | 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 | a0001c0001t0002g0073 | 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 | a0001c0001t0006g0102 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0002g0145 a0001c0001t0003g0223 a0001c0001t0018g0139 others(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 | 266 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): 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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | a0001c0001t0003g0173 a0001c0001t0010g0113 a0001c0001t0021g0042 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0295 | 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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | a0001c0001t0002g0133 | 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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.131-4460A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878379 | |||||||
| chr17:78878410 | G | C | 5 | a0001c0002t0003g0002 a0001c0002t0003g0215 a0001c0002t0003g0243 others(2): Show |
6 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-4491C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78878410 | |||||||
| chr17:78878430 | A | C | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | a0001c0001t0001g0295 a0001c0001t0018g0139 a0001c0001t0035g0071 |
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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | a0001c0001t0009g0013 a0001c0001t0009g0030 a0001c0001t0009g0032 |
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 | a0001c0002t0001g0171 | 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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | a0001c0001t0001g0283 a0001c0001t0001g0286 |
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 | 266 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0003g0223 | 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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.131-5338T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879257 | |||||||
| chr17:78879330 | T | G | 266 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-5411A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78879330 | |||||||
| chr17:78879331 | T | A | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | a0001c0001t0002g0081 | 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 | a0001c0002t0001g0171 | 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 | a0001c0001t0009g0013 a0001c0001t0009g0030 a0001c0001t0009g0032 |
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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | 266 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): 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 | a0002c0003t0004g0083 | 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 | a0001c0001t0001g0210 a0001c0001t0001g0270 a0001c0001t0002g0124 others(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 | a0001c0001t0001g0267 | 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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0304 a0001c0001t0003g0266 a0001c0001t0041g0046 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0228 a0001c0001t0001g0257 others(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 | a0001c0001t0002g0145 a0001c0001t0003g0223 a0001c0001t0018g0139 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0229 a0001c0001t0005g0183 |
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 | a0001c0001t0002g0145 a0001c0001t0003g0223 a0001c0001t0018g0139 others(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 | a0001c0001t0006g0100 a0001c0001t0042g0092 |
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 | a0001c0002t0004g0053 | 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 | a0001c0001t0003g0250 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0208 | 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 | a0001c0001t0003g0223 a0001c0001t0018g0139 a0001c0001t0035g0071 |
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 | a0001c0002t0001g0171 | 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | a0001c0001t0001g0221 | 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 | a0001c0001t0003g0250 | 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 | 207 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(204): 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 | a0001c0002t0004g0157 | 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0005g0249 | 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | a0001c0001t0001g0281 a0001c0001t0005g0177 |
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 | a0001c0001t0027g0174 a0001c0001t0032g0017 |
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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | 61 | a0001c0001t0001g0210 a0001c0001t0001g0270 a0001c0001t0002g0124 others(58): Show |
62 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.131-7330A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78881249 | |||||||
| chr17:78881280 | T | C | 264 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(261): Show |
266 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(263): 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0002g0076 | 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 | a0001c0001t0011g0194 | 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 | a0001c0001t0029g0034 a0001c0001t0038g0123 |
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 | a0001c0001t0001g0228 a0001c0001t0011g0194 |
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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | a0001c0001t0003g0266 | 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0008g0018 | 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 | a0001c0001t0001g0295 | 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 | 203 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(200): 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 | 202 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(199): 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 | a0001c0001t0003g0266 a0001c0001t0041g0046 |
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 | a0001c0001t0001g0276 | 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 | a0001c0001t0003g0214 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0124 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0260 a0001c0001t0003g0173 a0001c0001t0010g0113 others(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 | 143 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(140): 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 | a0001c0001t0001g0189 a0001c0001t0001g0193 a0001c0001t0001g0199 others(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 | 200 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(197): 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 | a0001c0001t0001g0189 a0001c0001t0002g0088 a0001c0001t0002g0089 others(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 | a0001c0001t0002g0076 | 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 | a0001c0001t0002g0145 a0001c0001t0003g0223 a0001c0001t0018g0139 others(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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0258 | 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 | 265 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(262): Show |
267 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(264): 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 | 266 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(263): Show |
268 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.131-8940T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78882859 | |||||||
| chr17:78882898 | G | A | 53 | a0001c0001t0001g0210 a0001c0001t0001g0304 a0001c0001t0003g0307 others(50): Show |
54 | HG00558.hp1 HG00558.hp2 HG00609.hp2 others(51): 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 | a0001c0001t0001g0210 a0001c0001t0001g0304 a0001c0001t0003g0307 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0001g0229 others(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 | a0001c0001t0003g0173 a0001c0001t0010g0113 a0001c0001t0021g0042 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0228 a0001c0001t0001g0247 others(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 | a0001c0001t0004g0130 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | 21 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0310 others(18): 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 | a0001c0001t0004g0130 | 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 | a0001c0001t0010g0041 | 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0003g0223 | 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 | a0001c0001t0005g0246 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0295 others(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 | a0001c0001t0005g0219 a0001c0002t0003g0313 a0001c0002t0005g0268 others(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 | a0001c0001t0003g0223 | 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 | a0001c0001t0005g0178 | 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 | a0001c0001t0001g0283 a0001c0001t0001g0286 |
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 | a0001c0001t0009g0033 | 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 | a0001c0001t0003g0223 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0199 a0001c0001t0001g0229 others(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 | a0001c0001t0003g0307 a0001c0002t0003g0287 |
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 | a0001c0001t0008g0019 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0002g0117 | 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 | a0001c0001t0003g0250 | 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 | 187 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(184): Show |
188 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(185): 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 | a0001c0002t0043g0119 | 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 | a0001c0001t0001g0189 a0001c0001t0002g0088 a0001c0001t0002g0089 others(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 | a0001c0001t0004g0118 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0005g0301 | 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 | a0001c0002t0043g0119 | 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 | a0001c0001t0020g0126 | 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 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0267 a0001c0001t0002g0149 others(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 | a0001c0001t0001g0283 a0001c0001t0001g0295 a0001c0001t0017g0132 |
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 | a0001c0001t0003g0173 a0001c0001t0010g0113 a0001c0001t0021g0042 others(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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0026g0289 | 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 | a0001c0001t0006g0086 | 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 | a0001c0001t0001g0267 a0001c0001t0002g0149 a0001c0001t0003g0175 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0267 a0001c0001t0002g0149 a0001c0001t0003g0175 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0037g0131 | 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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0020g0141 | 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 | a0001c0001t0004g0140 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0003g0307 a0001c0002t0003g0287 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0180 a0001c0001t0001g0197 others(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 | a0001c0001t0004g0001 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0197 a0001c0001t0001g0228 others(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 | 87 | a0001c0001t0001g0165 a0001c0001t0001g0197 a0001c0001t0001g0228 others(84): 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 | a0001c0001t0009g0033 a0001c0001t0033g0031 |
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 | a0001c0001t0002g0142 | 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 118 | a0001c0001t0001g0165 a0001c0001t0001g0197 a0001c0001t0001g0228 others(115): 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 | a0001c0001t0004g0058 a0001c0001t0004g0068 a0001c0001t0004g0125 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0002g0142 others(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 | a0001c0001t0003g0266 a0001c0001t0005g0256 a0001c0001t0041g0046 |
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 | a0001c0001t0007g0012 a0001c0001t0008g0028 |
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 | a0001c0001t0001g0260 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | 112 | a0001c0001t0001g0165 a0001c0001t0001g0197 a0001c0001t0001g0228 others(109): 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 | a0001c0001t0002g0124 | 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 | a0001c0001t0003g0202 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0003g0266 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0010g0040 a0001c0001t0010g0041 a0001c0001t0010g0049 others(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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0002t0028g0036 | 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 | a0001c0001t0029g0034 a0001c0001t0038g0123 |
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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0286 | 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 | 27 | a0001c0001t0001g0283 a0001c0001t0001g0310 a0001c0001t0002g0061 others(24): 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0197 a0001c0001t0001g0234 a0001c0001t0001g0235 others(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 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 others(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 | a0001c0001t0002g0133 a0001c0001t0002g0149 a0001c0001t0003g0288 others(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 | a0001c0001t0005g0285 | 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 | a0001c0001t0002g0073 a0001c0001t0003g0266 |
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 | 48 | a0001c0001t0001g0283 a0001c0001t0001g0286 a0001c0001t0001g0295 others(45): 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0002g0062 others(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 | a0001c0002t0004g0099 | 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 | a0001c0001t0003g0223 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 35 | a0001c0001t0001g0270 a0001c0001t0001g0283 a0001c0001t0001g0295 others(32): 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 | 31 | a0001c0001t0001g0283 a0001c0001t0001g0295 a0001c0001t0001g0310 others(28): 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 | a0001c0001t0001g0290 a0001c0001t0054g0269 |
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 | a0001c0001t0003g0266 a0001c0001t0005g0256 a0001c0001t0041g0046 |
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 | a0001c0001t0003g0169 | 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 | a0001c0001t0003g0288 a0001c0001t0003g0292 a0001c0001t0003g0309 others(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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | a0001c0001t0010g0040 a0001c0001t0010g0041 a0001c0001t0010g0049 others(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 | a0001c0001t0002g0105 | 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 | a0001c0001t0001g0217 a0001c0001t0001g0244 |
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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0002g0124 | 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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0002g0145 | 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0002g0056 a0001c0001t0002g0078 a0001c0001t0007g0024 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 30 | a0001c0001t0001g0283 a0001c0001t0001g0295 a0001c0001t0002g0061 others(27): 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 | a0001c0001t0002g0098 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0002g0061 a0001c0001t0002g0149 a0001c0001t0003g0175 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0023g0293 | 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 | a0001c0001t0010g0041 | 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 | a0001c0001t0002g0133 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0002g0142 others(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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | a0001c0001t0001g0189 a0001c0001t0003g0223 a0001c0001t0005g0219 others(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 | a0001c0001t0002g0056 | 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 | a0001c0002t0001g0190 | 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 | a0001c0001t0002g0149 a0001c0001t0006g0150 |
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 | a0001c0001t0003g0205 | 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 | a0001c0001t0011g0194 a0001c0001t0019g0091 |
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 | a0001c0002t0001g0211 a0001c0002t0005g0186 |
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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0002t0003g0261 a0001c0002t0003g0274 a0001c0002t0003g0275 |
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 | a0001c0001t0003g0266 a0001c0001t0005g0256 a0001c0001t0041g0046 |
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 | a0001c0001t0001g0189 a0001c0001t0001g0283 a0001c0001t0002g0133 others(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 | a0001c0001t0003g0266 a0001c0001t0005g0256 a0001c0001t0041g0046 |
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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0229 a0001c0001t0003g0209 |
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 | a0001c0001t0029g0034 a0001c0001t0038g0123 |
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 | a0001c0001t0007g0024 | 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 | 28 | a0001c0001t0001g0295 a0001c0001t0002g0061 a0001c0001t0002g0124 others(25): 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 | 127 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0197 others(124): 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 | 127 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0197 others(124): 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 | 28 | a0001c0001t0001g0295 a0001c0001t0002g0061 a0001c0001t0002g0124 others(25): 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 | a0001c0002t0016g0156 a0001c0002t0016g0158 a0001c0002t0034g0154 |
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 |
122 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0197 others(119): 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 | a0001c0001t0002g0145 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | 303 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(300): Show |
305 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(302): 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | 127 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0197 others(124): 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 | a0001c0001t0035g0071 | 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 | a0001c0001t0001g0189 a0001c0001t0005g0219 a0001c0002t0003g0313 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | 36 | a0001c0001t0001g0270 a0001c0001t0001g0295 a0001c0001t0002g0045 others(33): 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 | a0001c0001t0006g0087 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0236 | 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 | a0001c0001t0003g0241 | 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 | a0001c0002t0001g0306 a0001c0002t0003g0305 a0001c0002t0003g0308 |
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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0286 | 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 | 36 | a0001c0001t0001g0270 a0001c0001t0001g0295 a0001c0001t0002g0045 others(33): 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 | a0001c0001t0003g0250 | 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 | a0001c0001t0001g0189 a0001c0001t0002g0109 a0001c0001t0002g0160 others(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 | 37 | a0001c0001t0001g0270 a0001c0001t0001g0295 a0001c0001t0002g0045 others(34): 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | 27 | a0001c0001t0001g0295 a0001c0001t0002g0061 a0001c0001t0002g0124 others(24): 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 | a0001c0002t0003g0215 | 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 | 27 | a0001c0001t0001g0295 a0001c0001t0002g0061 a0001c0001t0002g0124 others(24): 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 | a0001c0001t0003g0288 a0001c0001t0003g0292 a0001c0001t0003g0309 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | 127 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0197 others(124): 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 28 | a0001c0001t0001g0295 a0001c0001t0002g0061 a0001c0001t0002g0124 others(25): 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 | a0001c0001t0001g0281 a0001c0001t0002g0043 a0001c0001t0005g0177 |
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 | 28 | a0001c0001t0001g0295 a0001c0001t0002g0061 a0001c0001t0002g0124 others(25): 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 | a0001c0001t0008g0028 | 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 | a0001c0001t0003g0288 a0001c0001t0003g0292 a0001c0001t0003g0309 others(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 | a0001c0002t0053g0253 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0003g0288 a0001c0001t0003g0292 a0001c0001t0003g0309 others(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 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | 39 | a0001c0001t0001g0270 a0001c0001t0001g0283 a0001c0001t0001g0295 others(36): 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 | a0001c0001t0001g0283 a0001c0001t0002g0133 a0001c0001t0002g0145 |
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 | a0001c0001t0004g0096 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0228 others(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 | a0001c0001t0020g0126 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0003g0266 a0001c0001t0005g0256 a0001c0001t0041g0046 |
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 | a0001c0001t0002g0097 | 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 | a0001c0002t0005g0172 | 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 | 29 | a0001c0001t0001g0295 a0001c0001t0002g0061 a0001c0001t0002g0124 others(26): 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 | 87 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0228 others(84): 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 | a0001c0001t0001g0189 a0001c0001t0001g0270 a0001c0001t0001g0283 others(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 | 87 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0228 others(84): 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 | a0001c0002t0003g0254 | 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 | 71 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0228 others(68): 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 | a0001c0001t0001g0210 a0001c0002t0009g0038 |
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 | a0001c0001t0021g0048 | 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 | a0001c0001t0001g0260 a0001c0001t0026g0222 a0001c0001t0048g0044 |
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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0002g0142 others(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 | a0001c0001t0003g0288 a0001c0001t0003g0292 a0001c0001t0003g0309 others(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 | a0001c0001t0001g0189 a0001c0001t0001g0247 a0001c0001t0001g0283 others(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 | 92 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0228 others(89): 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 | a0001c0002t0015g0185 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0045 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0228 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0206 a0001c0001t0001g0238 a0001c0001t0001g0245 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0003g0195 | 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 | a0001c0002t0039g0143 | 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 | a0001c0001t0003g0266 a0001c0001t0005g0256 a0001c0001t0041g0046 |
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 | 45 | a0001c0001t0001g0270 a0001c0001t0001g0295 a0001c0001t0002g0045 others(42): 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 | a0001c0001t0002g0082 | 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 | a0001c0002t0003g0287 | 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 | 98 | a0001c0001t0001g0165 a0001c0001t0001g0189 a0001c0001t0001g0228 others(95): 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 | a0001c0001t0002g0145 a0001c0001t0005g0285 a0001c0001t0007g0012 others(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 | a0001c0001t0001g0286 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0283 a0001c0001t0001g0286 others(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 | a0001c0001t0003g0288 a0001c0001t0003g0292 a0001c0001t0003g0309 others(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 | a0001c0001t0004g0072 | 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 | 5 | a0001c0001t0001g0267 a0001c0002t0003g0002 a0001c0002t0003g0215 others(2): Show |
6 | HG01106.hp2 HG01109.hp1 HG01346.hp2 others(3): 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 | a0001c0001t0001g0304 a0001c0001t0002g0045 a0001c0001t0003g0288 others(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 | 278 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(275): 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 | a0001c0001t0001g0165 a0001c0001t0001g0193 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0193 a0001c0001t0001g0199 others(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 | a0001c0001t0011g0282 a0001c0001t0027g0174 a0001c0001t0027g0181 others(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 | a0001c0001t0001g0197 | 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 | 293 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(290): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): 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 | a0001c0001t0032g0017 | 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 | a0001c0001t0001g0286 a0001c0001t0002g0142 a0001c0001t0020g0126 others(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 | a0001c0001t0027g0174 a0001c0001t0032g0017 a0001c0001t0038g0123 |
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 | a0001c0001t0001g0247 a0001c0001t0001g0260 a0001c0001t0001g0270 others(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 | a0001c0001t0002g0045 a0001c0001t0004g0051 a0001c0001t0018g0050 others(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 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(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 | a0001c0001t0007g0023 | 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 | a0001c0002t0016g0158 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0018g0139 | 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 | a0001c0001t0002g0148 a0001c0001t0007g0027 |
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 | a0001c0001t0001g0163 a0001c0001t0011g0282 |
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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0004g0051 others(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 | a0001c0001t0008g0018 | 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 | 106 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(103): Show |
108 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(105): 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 | a0001c0001t0001g0263 a0001c0001t0003g0214 a0001c0001t0007g0024 others(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 | 120 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(117): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): 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 | a0001c0001t0001g0281 a0001c0001t0054g0269 |
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 | a0001c0001t0001g0179 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0263 a0001c0001t0001g0281 others(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 | a0001c0001t0004g0140 | 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 | a0001c0001t0001g0247 a0001c0001t0002g0142 a0001c0001t0003g0248 others(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 | a0001c0001t0005g0256 | 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 | a0001c0002t0001g0255 a0001c0002t0055g0251 |
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 | 287 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(284): Show |
289 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(286): 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 | a0001c0001t0001g0247 a0001c0001t0002g0142 a0001c0001t0003g0248 others(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 | a0001c0001t0002g0133 | 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 | a0001c0001t0003g0266 | 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 | a0001c0001t0007g0021 | 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 | a0001c0001t0012g0212 | 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 | a0001c0001t0001g0281 | 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 | a0001c0001t0002g0135 a0001c0001t0007g0005 a0001c0001t0007g0011 others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0017g0132 others(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 | a0001c0002t0025g0166 a0001c0002t0025g0225 |
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 | 94 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(91): Show |
96 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.130+24473T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900486 | |||||||
| chr17:78900544 | C | CA | 95 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(92): 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 | a0001c0001t0001g0163 a0001c0001t0001g0193 a0001c0001t0001g0197 others(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 | a0001c0001t0001g0247 a0001c0001t0002g0062 a0001c0001t0002g0101 others(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 | a0001c0001t0002g0054 | 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 | a0001c0001t0012g0212 | 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0005g0242 | 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 | a0001c0001t0003g0250 a0001c0001t0005g0256 |
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 | a0001c0001t0001g0290 a0001c0001t0003g0288 a0001c0001t0003g0292 others(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 | a0001c0001t0004g0115 | 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 | 288 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(285): Show |
290 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.130+24003T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900956 | |||||||
| chr17:78900961 | G | A | 137 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(134): Show |
139 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.130+23998C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78900961 | |||||||
| chr17:78901057 | C | T | 124 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(121): Show |
126 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(123): 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 | a0001c0001t0001g0286 a0001c0001t0003g0266 |
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 | 117 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(114): Show |
119 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(116): 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 | a0001c0001t0018g0050 | 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 | a0001c0001t0001g0290 a0001c0001t0003g0288 a0001c0001t0003g0292 others(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 | a0001c0001t0002g0061 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | 292 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(289): Show |
294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): 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 | a0001c0001t0001g0281 a0001c0001t0054g0269 |
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 | a0001c0001t0001g0247 a0001c0001t0002g0142 a0001c0001t0003g0248 others(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 | a0001c0001t0001g0247 a0001c0001t0002g0142 a0001c0001t0003g0248 others(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 | a0001c0001t0001g0247 a0001c0001t0002g0142 a0001c0001t0003g0248 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0263 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0247 a0001c0001t0002g0142 a0001c0001t0003g0248 others(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 | 117 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(114): Show |
119 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(116): 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 | a0001c0001t0001g0163 a0001c0001t0001g0260 a0001c0001t0001g0270 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | a0001c0001t0001g0283 | 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 | a0001c0001t0027g0174 | 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 | a0001c0001t0001g0230 | 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 | a0001c0001t0027g0181 | 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 | a0001c0001t0002g0059 a0001c0001t0004g0058 |
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 | 117 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(114): Show |
119 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(116): 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 | a0001c0001t0001g0263 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0003g0250 | 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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | 121 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(118): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): 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 | a0001c0002t0003g0261 a0001c0002t0003g0274 a0001c0002t0003g0275 |
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 | a0001c0001t0004g0118 | 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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0002g0095 a0001c0001t0004g0094 |
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 | 137 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(134): Show |
139 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.130+22868A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78902091 | |||||||
| chr17:78902100 | G | A | 115 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(112): Show |
117 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(114): 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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0281 a0001c0001t0002g0142 others(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 | 293 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(290): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): 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 | a0001c0001t0001g0247 a0001c0001t0001g0281 a0001c0001t0002g0142 others(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 | a0001c0001t0002g0121 | 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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0281 a0001c0001t0002g0088 others(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 | 87 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(84): Show |
88 | HG00140.hp1 HG00544.hp1 HG00621.hp2 others(85): 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 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0310 a0001c0001t0002g0149 a0001c0001t0003g0169 others(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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0229 a0001c0001t0005g0183 |
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 | a0001c0001t0001g0247 a0001c0001t0001g0281 a0001c0001t0001g0286 others(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 | 114 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(111): Show |
116 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(113): 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 | a0001c0001t0005g0301 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0189 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(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 | a0001c0001t0008g0039 | 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 | a0001c0001t0032g0017 a0001c0001t0038g0123 |
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 | a0001c0001t0003g0214 | 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 | 22 | a0001c0001t0001g0247 a0001c0001t0002g0135 a0001c0001t0002g0136 others(19): 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 | 57 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(54): 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 | 290 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(287): Show |
292 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(289): 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 | a0001c0001t0027g0181 | 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 | a0001c0001t0001g0286 a0001c0001t0003g0266 |
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 |
2 | a0001c0001t0004g0001 a0001c0001t0004g0055 |
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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0003g0299 a0001c0001t0003g0300 a0001c0001t0005g0301 others(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 | 4 | a0001c0001t0001g0204 a0001c0002t0003g0002 a0001c0002t0003g0215 others(1): Show |
5 | HG00140.hp1 HG01106.hp2 HG01346.hp2 others(2): 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 | a0001c0001t0003g0250 | 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 | a0001c0001t0001g0281 a0001c0001t0001g0290 a0001c0001t0002g0135 others(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 | a0001c0001t0002g0124 a0001c0001t0003g0309 |
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 | a0001c0001t0001g0310 a0001c0001t0003g0223 a0001c0001t0005g0242 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0232 a0001c0001t0001g0236 others(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 | a0001c0001t0001g0179 a0001c0001t0001g0206 a0001c0001t0001g0210 others(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 | a0001c0001t0001g0207 a0001c0001t0001g0217 a0001c0001t0001g0244 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0198 a0001c0001t0001g0304 others(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 | a0001c0001t0001g0180 a0001c0001t0001g0208 a0001c0001t0002g0047 others(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 | a0001c0001t0001g0230 a0001c0001t0002g0142 a0001c0001t0005g0164 others(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 | a0001c0001t0001g0295 a0001c0001t0020g0141 a0001c0002t0039g0143 |
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 | a0001c0001t0010g0040 | 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 | a0001c0001t0003g0307 | 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 | a0001c0001t0001g0286 a0001c0001t0003g0266 |
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 | a0001c0001t0003g0209 a0001c0001t0022g0182 |
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 | a0001c0001t0004g0051 a0001c0002t0003g0275 |
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 | a0001c0001t0006g0077 | 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 | 15 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(12): 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 | 15 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(12): 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 | 139 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(136): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.130+20580A>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904379 | |||||||
| chr17:78904503 | C | T | 141 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(138): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.130+20456G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78904503 | |||||||
| chr17:78904577 | C | A | 2 | a0001c0001t0004g0001 a0001c0001t0004g0055 |
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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0281 a0001c0001t0054g0269 |
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 | a0001c0001t0001g0207 | 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 | a0001c0001t0003g0223 | 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 | a0001c0002t0003g0261 a0001c0002t0003g0274 a0001c0002t0003g0275 |
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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0011g0282 | 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 | 136 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(133): Show |
137 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(134): 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0001g0247 a0001c0001t0001g0286 a0001c0001t0001g0290 others(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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0001g0189 a0001c0001t0001g0193 a0001c0001t0001g0197 others(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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | a0001c0001t0032g0017 a0001c0001t0038g0123 |
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 | a0001c0002t0044g0065 a0001c0002t0047g0128 |
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 | 142 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(139): Show |
144 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(141): 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 | a0001c0001t0006g0084 | 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 | a0001c0001t0054g0269 | 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 | 104 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(101): Show |
105 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(102): 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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0001g0290 a0001c0001t0003g0173 a0001c0001t0003g0175 others(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 | 140 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(137): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.130+19055C>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905904 | |||||||
| chr17:78905927 | A | G | 82 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(79): Show |
83 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(80): Show |
intron_variant | MODIFIER | c.130+19032T>C | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78905927 | |||||||
| chr17:78906000 | T | C | 143 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(140): Show |
145 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(142): 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 | a0001c0001t0003g0271 | 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 | 104 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(101): Show |
105 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.130+18792A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78906167 | |||||||
| chr17:78906169 | C | G | 143 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(140): Show |
145 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(142): 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 | a0001c0001t0005g0246 | 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 | a0001c0002t0005g0172 | 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 | a0001c0001t0002g0079 a0001c0001t0002g0112 a0001c0001t0002g0120 others(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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0001g0208 | 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 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(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 | a0001c0001t0001g0281 a0001c0001t0054g0269 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | a0001c0001t0006g0102 | 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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0002g0124 | 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 | a0001c0001t0003g0292 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0018g0050 | 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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0001g0199 a0001c0001t0005g0249 a0001c0001t0005g0285 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0005g0246 | 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 | 11 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0133 others(8): 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | 120 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(117): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(119): 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 | a0001c0001t0019g0091 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | a0001c0001t0001g0247 a0001c0001t0001g0286 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0165 | 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 | 144 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(141): Show |
146 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(143): 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 | a0001c0001t0004g0055 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | a0001c0002t0039g0143 | 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 | a0001c0001t0001g0165 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | 145 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(144): 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 | a0001c0001t0003g0214 | 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 | 93 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(90): Show |
94 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(91): 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 | a0001c0001t0001g0163 a0001c0001t0001g0247 a0001c0001t0001g0286 others(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 | 94 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(91): Show |
95 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.130+15369delG | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78909589 | |||||||
| chr17:78909611 | G | A | 14 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0002t0009g0038 | 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 | a0001c0001t0001g0263 a0001c0001t0003g0214 a0001c0001t0004g0118 others(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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | 150 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): 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 | a0001c0002t0009g0038 | 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 | a0001c0001t0004g0052 a0001c0002t0004g0053 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | a0001c0001t0001g0281 a0001c0001t0054g0269 |
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 | 2 | a0001c0001t0004g0001 a0001c0001t0004g0055 |
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 | a0001c0002t0009g0038 | 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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0196 others(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 | a0001c0002t0009g0038 | 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 | 304 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(301): Show |
306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.130+14437A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78910522 | |||||||
| chr17:78910529 | C | T | 138 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(135): Show |
140 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(137): 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0003g0307 | 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 | a0001c0001t0019g0093 | 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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0002g0062 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | 149 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(146): Show |
151 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.130+13688A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911271 | |||||||
| chr17:78911363 | C | T | 104 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(101): Show |
105 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.130+13596G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911363 | |||||||
| chr17:78911379 | A | G | 149 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(146): Show |
151 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0001g0247 a0001c0001t0001g0286 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0281 a0001c0001t0002g0135 others(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 | a0001c0001t0001g0281 a0001c0001t0054g0269 |
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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | 3 | a0001c0001t0002g0133 a0001c0001t0004g0001 a0001c0001t0004g0055 |
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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | 150 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(147): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.130+13188A>G | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911771 | |||||||
| chr17:78911772 | G | A | 121 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(118): 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 | 109 | a0001c0001t0001g0165 a0001c0001t0001g0179 a0001c0001t0001g0180 others(106): Show |
110 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(107): 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 | a0001c0001t0001g0198 a0001c0001t0005g0178 a0001c0001t0019g0091 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | 99 | a0001c0001t0001g0163 a0001c0001t0001g0180 a0001c0001t0001g0196 others(96): Show |
100 | HG00140.hp1 HG00544.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.130+13064dupT | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78911894 | |||||||
| chr17:78911894 | C | CAA | 8 | a0001c0001t0002g0124 a0001c0001t0005g0164 a0001c0001t0020g0126 others(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 | a0001c0001t0001g0290 a0001c0001t0003g0223 a0001c0001t0003g0250 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0002g0135 a0001c0001t0002g0136 others(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 | a0001c0001t0020g0141 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | 164 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(161): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): 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 | a0001c0001t0006g0100 a0001c0001t0042g0092 |
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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0290 a0001c0001t0003g0223 a0001c0001t0003g0250 others(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 | a0001c0001t0001g0281 a0001c0001t0054g0269 |
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 | a0001c0002t0001g0171 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | a0001c0001t0010g0113 a0001c0001t0014g0167 a0001c0001t0035g0071 |
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 | a0001c0001t0011g0282 | 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 | a0001c0001t0003g0309 | 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 | 37 | a0001c0001t0001g0163 a0001c0001t0001g0286 a0001c0001t0001g0290 others(34): 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 | 166 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(163): Show |
168 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(165): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | 37 | a0001c0001t0001g0163 a0001c0001t0001g0286 a0001c0001t0001g0290 others(34): 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 | 29 | a0001c0001t0001g0163 a0001c0001t0001g0286 a0001c0001t0002g0043 others(26): 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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0001g0281 others(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 | a0001c0001t0001g0286 a0001c0001t0003g0266 |
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 | a0001c0001t0001g0210 a0001c0001t0051g0162 a0001c0002t0012g0252 others(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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0008g0018 | 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 | a0001c0002t0025g0166 | 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 | a0001c0001t0004g0118 | 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 | a0001c0001t0007g0015 a0001c0001t0008g0019 |
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 | a0001c0001t0001g0163 a0001c0001t0001g0286 a0001c0001t0001g0290 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0193 a0001c0001t0001g0220 others(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 | a0001c0001t0001g0257 a0001c0001t0002g0079 a0001c0001t0002g0098 others(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 | a0001c0001t0001g0236 a0001c0001t0001g0258 a0001c0001t0003g0175 others(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 | 83 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(80): Show |
84 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(81): 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 | a0001c0001t0001g0210 a0001c0001t0001g0217 a0001c0001t0001g0229 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0004g0051 others(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 | a0001c0001t0001g0290 a0001c0001t0027g0174 |
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 | a0001c0001t0002g0043 a0001c0001t0002g0047 a0001c0001t0004g0051 others(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 | a0001c0001t0001g0257 a0001c0001t0005g0256 a0001c0001t0026g0222 |
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 | a0001c0001t0003g0187 | 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 | 104 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(101): Show |
105 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(102): 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 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
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 | 16 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(13): 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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0247 others(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 | a0001c0001t0001g0281 a0001c0001t0002g0089 a0001c0001t0054g0269 |
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 | a0001c0001t0001g0267 a0001c0001t0002g0106 a0001c0001t0002g0160 others(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 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0001g0257 others(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 | a0001c0001t0001g0283 a0001c0001t0002g0104 a0001c0001t0004g0069 others(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 | a0001c0001t0002g0088 a0001c0001t0007g0016 |
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 | a0001c0001t0002g0073 | 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 |
105 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(102): Show |
106 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(103): 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 | 107 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(104): Show |
108 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.130+10650G>A | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914309 | |||||||
| chr17:78914311 | C | T | 57 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0247 others(54): 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 | 57 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0247 others(54): 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 | a0001c0001t0001g0193 a0001c0001t0002g0095 a0001c0001t0002g0097 others(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 | 8 | a0001c0001t0002g0133 a0001c0001t0002g0142 a0001c0001t0004g0001 others(5): 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 | a0001c0001t0007g0016 a0001c0001t0007g0022 a0001c0001t0008g0035 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0247 a0001c0001t0003g0248 a0001c0001t0003g0297 others(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 | a0001c0001t0002g0137 a0001c0001t0002g0142 a0001c0001t0003g0187 others(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 | a0001c0001t0014g0184 | 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 | 157 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(154): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.130+10057dupA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78914901 | |||||||
| chr17:78914901 | C | CTT | 5 | a0001c0001t0002g0151 a0001c0001t0003g0201 a0001c0001t0004g0001 others(2): 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 | a0001c0001t0001g0286 | 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 | a0001c0001t0003g0302 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | 293 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(290): Show |
295 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.130+9505C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915454 | |||||||
| chr17:78915526 | CT | C | 154 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(151): Show |
156 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.130+9432delA | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78915526 | |||||||
| chr17:78915563 | A | T | 12 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0003g0223 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | a0001c0001t0003g0309 | 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 | a0001c0002t0009g0038 | 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 | a0001c0001t0001g0290 a0001c0001t0003g0288 a0001c0001t0003g0292 others(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 | a0001c0001t0002g0124 a0001c0001t0006g0077 |
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 | a0001c0001t0001g0286 a0001c0001t0003g0266 |
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 | a0001c0001t0005g0200 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0007g0037 | 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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0002g0135 others(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 | 151 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(148): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(150): 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0163 a0001c0001t0005g0164 a0001c0001t0011g0282 |
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 | 44 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0247 others(41): 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 | a0001c0001t0001g0290 a0001c0001t0003g0288 a0001c0001t0003g0292 others(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 | a0001c0002t0009g0038 | 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 | a0001c0001t0003g0214 a0001c0001t0005g0213 a0001c0001t0012g0212 others(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 | a0001c0001t0001g0165 a0001c0001t0001g0247 a0001c0001t0002g0135 others(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 | a0001c0001t0001g0290 a0001c0001t0003g0223 a0001c0001t0003g0250 others(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 | 101 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(98): Show |
102 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(99): 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 | a0001c0001t0001g0290 a0001c0001t0003g0223 a0001c0001t0003g0250 others(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 | 103 | a0001c0001t0001g0193 a0001c0001t0001g0220 a0001c0001t0001g0257 others(100): 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 | a0001c0001t0002g0054 a0001c0001t0002g0059 a0001c0001t0002g0073 others(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 | a0001c0001t0001g0228 a0001c0001t0001g0247 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0165 a0001c0001t0002g0135 a0001c0001t0002g0137 others(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 | a0001c0001t0001g0198 a0001c0001t0001g0217 a0001c0001t0001g0221 others(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 | 92 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(89): Show |
93 | HG00140.hp1 HG00544.hp1 HG00735.hp1 others(90): 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 | a0001c0001t0002g0124 a0001c0001t0006g0077 |
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 | 101 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(98): Show |
102 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(99): 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 | a0001c0001t0032g0017 a0001c0001t0038g0123 |
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 | a0001c0001t0002g0060 a0001c0002t0043g0119 |
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 | a0001c0001t0005g0218 | 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 | a0001c0001t0001g0228 a0001c0001t0002g0145 a0001c0001t0002g0148 others(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 | 90 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(87): Show |
91 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(88): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0295 a0001c0001t0001g0304 a0001c0001t0001g0310 others(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 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(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 | a0001c0001t0001g0260 a0001c0001t0001g0270 a0001c0001t0003g0169 |
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 | a0001c0001t0001g0189 a0001c0001t0001g0286 a0001c0001t0003g0250 others(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 | a0001c0001t0001g0290 a0001c0001t0003g0288 a0001c0001t0003g0292 others(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 | a0001c0001t0001g0257 a0001c0001t0005g0256 a0001c0001t0026g0222 |
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 | a0001c0001t0029g0034 | 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 |
86 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(83): Show |
87 | HG00140.hp1 HG00323.hp1 HG00544.hp1 others(84): 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 |
7 | a0001c0001t0001g0227 a0001c0001t0002g0133 a0001c0001t0003g0241 others(4): 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 | a0001c0001t0001g0247 a0001c0001t0003g0248 |
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 | a0001c0001t0002g0136 a0001c0001t0004g0130 a0001c0001t0006g0100 others(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 | a0001c0001t0002g0135 a0001c0001t0002g0137 a0001c0001t0032g0017 |
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 | a0001c0001t0001g0295 a0001c0001t0001g0304 a0001c0001t0001g0310 others(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 | a0001c0001t0002g0061 a0001c0001t0003g0297 a0001c0001t0003g0298 others(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 | a0001c0001t0005g0301 | 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 | 118 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(115): Show |
120 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(117): 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 | a0001c0001t0001g0267 a0001c0001t0001g0276 a0001c0001t0001g0277 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0070 a0001c0001t0002g0117 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0006g0077 | 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 | a0001c0001t0003g0266 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0286 a0001c0001t0001g0290 others(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 | 95 | a0001c0001t0001g0163 a0001c0001t0001g0179 a0001c0001t0001g0180 others(92): Show |
97 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(94): 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 | a0001c0001t0001g0228 a0001c0001t0002g0145 a0001c0001t0002g0148 others(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 | a0001c0001t0018g0139 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0126 a0001c0001t0020g0141 others(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 | a0001c0001t0002g0122 a0001c0001t0006g0086 |
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 | a0001c0001t0003g0195 | 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 | a0001c0001t0038g0123 | 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 | a0001c0001t0001g0228 a0001c0001t0002g0145 a0001c0001t0002g0148 others(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 | a0001c0001t0001g0286 a0001c0001t0003g0266 |
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 | 31 | a0001c0001t0001g0163 a0001c0001t0001g0228 a0001c0001t0001g0286 others(28): 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 | a0001c0001t0001g0229 | 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 | 19 | a0001c0001t0001g0163 a0001c0001t0001g0286 a0001c0001t0001g0290 others(16): 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 | a0001c0001t0002g0079 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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 | a0001c0001t0001g0295 a0001c0001t0001g0304 a0001c0001t0001g0310 others(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 | a0001c0001t0001g0304 a0001c0001t0003g0307 a0001c0002t0001g0306 others(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 | a0001c0001t0031g0025 | 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 | a0001c0001t0002g0124 a0001c0001t0006g0077 |
2 | HG02615.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.130+6238C>T | TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78918721 | |||||||
| chr17:78918836 | A | C | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0006g0087 |
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 | a0001c0001t0001g0286 a0001c0001t0003g0266 |
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 | a0001c0001t0001g0221 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0001g0193 a0001c0001t0001g0228 a0001c0001t0001g0257 others(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 | 117 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(114): Show |
118 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(115): 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 | 6 | a0001c0001t0002g0133 a0001c0001t0004g0001 a0001c0001t0004g0055 others(3): 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 | a0001c0001t0002g0142 a0001c0001t0020g0141 a0001c0002t0039g0143 |
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 | 96 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(93): Show |
97 | HG00140.hp1 HG00544.hp1 HG00609.hp2 others(94): 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 | a0001c0001t0002g0135 a0001c0001t0002g0136 a0001c0001t0002g0137 others(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 | a0001c0001t0001g0290 a0001c0001t0003g0223 a0001c0001t0003g0250 others(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 | a0001c0001t0005g0249 a0001c0001t0005g0285 a0001c0001t0007g0003 others(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 | 184 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0228 others(181): 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 | a0001c0001t0003g0173 | 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 | 4 | a0001c0001t0002g0133 a0001c0001t0004g0001 a0001c0001t0004g0055 others(1): 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 | 92 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(89): Show |
93 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(90): 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 | a0001c0001t0001g0260 a0001c0001t0001g0270 a0001c0001t0001g0290 others(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 | a0001c0001t0048g0044 | 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 | 292 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(289): Show |
294 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(291): 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 | a0001c0001t0002g0142 a0001c0001t0020g0141 a0001c0002t0039g0143 |
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 | a0001c0001t0001g0228 a0001c0001t0001g0257 a0001c0001t0001g0286 others(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 | a0001c0001t0007g0016 a0001c0001t0007g0022 a0001c0001t0007g0037 others(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 | a0001c0001t0002g0142 a0001c0001t0020g0141 a0001c0002t0039g0143 |
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 | a0001c0001t0002g0133 | 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 | 14 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0286 others(11): 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 | a0001c0001t0001g0257 a0001c0001t0002g0043 a0001c0001t0002g0045 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | 14 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0286 others(11): 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 | 15 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0286 others(12): 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 | a0001c0001t0001g0283 | 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 | 280 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(277): Show |
282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): 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 | a0001c0001t0007g0023 | 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 | a0001c0001t0002g0082 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0141 a0001c0002t0039g0143 |
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 | a0001c0001t0002g0080 a0001c0001t0002g0081 |
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 | 281 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(278): Show |
283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): 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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0003g0250 others(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 | |||||||
| chr17:78921289 | CCT | C | 3 | a0001c0001t0003g0173 a0001c0001t0003g0175 a0001c0001t0027g0174 |
3 | HG02630.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.130+3668_130+3669d others(4): Show |
TIMP2 | ENSG00000035862.13 | transcript | ENST00000262768.11 | protein_coding | 1/4 | chr17 | 78921289 | |||||||
| chr17:78921295 | TAGCTGG | T | 38 | a0001c0001t0005g0249 a0001c0001t0005g0285 a0001c0001t0007g0003 others(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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0005g0256 others(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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0003g0250 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0003g0250 others(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 | a0001c0001t0006g0057 | 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 | a0001c0001t0002g0079 | 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 | a0001c0001t0001g0193 a0001c0002t0001g0176 a0001c0002t0001g0190 others(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 | 76 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(73): Show |
77 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(74): 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 | a0001c0002t0024g0226 | 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0002g0142 a0001c0001t0020g0141 a0001c0002t0039g0143 |
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 | a0001c0001t0032g0017 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0003g0250 others(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 | a0001c0001t0004g0125 | 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 | a0001c0001t0004g0125 | 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 | 191 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(188): Show |
193 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(190): 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0002g0056 a0001c0001t0002g0078 |
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 | 198 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(195): Show |
200 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(197): 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 | a0001c0002t0013g0273 a0001c0002t0013g0284 |
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 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0003g0288 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0286 others(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 | a0001c0001t0003g0303 | 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 | a0001c0001t0007g0037 a0001c0002t0012g0259 a0001c0002t0025g0166 |
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 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0189 others(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 | 57 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 others(54): Show |
58 | HG00140.hp1 HG00621.hp2 HG00741.hp1 others(55): 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 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(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 | a0001c0001t0001g0257 a0001c0001t0005g0256 a0001c0001t0007g0003 others(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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0260 a0001c0001t0002g0056 others(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 | a0001c0001t0002g0054 a0001c0001t0002g0056 a0001c0001t0002g0059 others(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 | a0001c0001t0003g0169 a0001c0001t0014g0167 a0001c0001t0014g0168 |
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 | 2 | a0001c0001t0004g0001 a0001c0001t0004g0055 |
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 | a0001c0002t0025g0166 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0286 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0295 others(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 | a0001c0001t0002g0054 a0001c0001t0004g0052 a0001c0002t0004g0053 |
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 | 199 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0001g0179 others(196): Show |
201 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(198): 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 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0003g0288 others(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 | a0001c0002t0009g0038 | 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 | a0001c0001t0007g0003 | 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 | a0001c0001t0001g0286 a0001c0001t0001g0290 a0001c0001t0003g0288 others(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 | a0001c0001t0008g0004 | 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 | a0001c0001t0008g0039 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0165 a0001c0001t0005g0164 |
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 | a0001c0001t0004g0051 a0001c0001t0018g0050 |
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 | a0001c0001t0023g0293 | 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 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0047 others(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 | a0001c0001t0001g0295 a0001c0001t0001g0304 a0001c0001t0001g0310 others(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 | a0001c0001t0007g0003 | 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 |