Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51138 |
| ensemblid | ENSG00000138663.9 |
| hgncid | 16702 |
| symbol | COPS4 |
| name | COP9 signalosome subunit 4 |
| refseq_nuc | NM_016129.3 |
| refseq_prot | NP_057213.2 |
| ensembl_nuc | ENST00000264389.7 |
| ensembl_prot | ENSP00000264389.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 83035183 |
| end | 83075818 |
| strand | + |
| ver | v1.2 |
| region | chr4:83035183-83075818 |
| region5000 | chr4:83030183-83080818 |
| regionname0 | COPS4_chr4_83035183_83075818 |
| regionname5000 | COPS4_chr4_83030183_83080818 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 406 | 371 | 90 | 48 | 181 | 8 | 42 | 145 | COPS4_chr4_83030183_83080818 | COPS4 | MAAAV others(401): Show |
chr4 | 83030183 | 83080818 |
| a0002 | 0/0 | 406 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | MAAAV others(401): Show |
chr4 | 83030183 | 83080818 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1218 | 369 | 88 | 48 | 181 | 8 | 42 | COPS4_chr4_83030183_83080818 | COPS4 | ATGGC others(1213): Show |
chr4 | 83030183 | 83080818 | ||
| a0001c0002 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | ATGGC others(1213): Show |
chr4 | 83030183 | 83080818 | ||
| a0001c0003 | 0/0 | 1218 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | ATGGC others(1213): Show |
chr4 | 83030183 | 83080818 | ||
| a0002c0004 | 0/0 | 1218 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | ATGGC others(1213): Show |
chr4 | 83030183 | 83080818 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1651 | 368 | 87 | 48 | 181 | 8 | 42 | COPS4_chr4_83030183_83080818 | COPS4 | GCTGC others(1646): Show |
chr4 | 83030183 | 83080818 |
| a0001c0001t0002 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | GCTGC others(1646): Show |
chr4 | 83030183 | 83080818 |
| a0001c0002t0001 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | GCTGC others(1646): Show |
chr4 | 83030183 | 83080818 |
| a0001c0003t0001 | 0/0 | 1651 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | GCTGC others(1646): Show |
chr4 | 83030183 | 83080818 |
| a0002c0004t0001 | 0/0 | 1651 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | GCTGC others(1646): Show |
chr4 | 83030183 | 83080818 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 2 | 2 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0005 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0006 | 0/0 | 3 | 1 | 0 | 1 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0326 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0001c0003t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| a0002c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | GBR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | FIN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01884 | hp1 | a0001 | c0003 | t0001 | g0328 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CDX | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | CDX | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0263 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0302 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | BEB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | BEB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | STU | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | YRI | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | YRI | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | YRI | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19056 | hp2 | a0002 | c0004 | t0001 | g0304 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | YRI | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ASW | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ASW | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | GIH | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | USA | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | USA | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | USA | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0326 | REF | REF | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0029 | REF | REF | COPS4_chr4_83030183_83080818 | COPS4 | chr4 | 83030183 | 83080818 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83035292 | C | T | 1 | a0002 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.68C>T | p.Ala23Val | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/10 | 110/1651 | 68/1221 | 23/406 | chr4 | 83035292 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83049230 | T | C | 1 | a0001c0002 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.219T>C | p.Leu73Leu | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 3/10 | 261/1651 | 219/1221 | 73/406 | chr4 | 83049230 | |||
| chr4:83056998 | A | G | 1 | a0001c0003 | 1 | HG01884.hp1 | synonymous_variant | LOW | c.483A>G | p.Pro161Pro | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 5/10 | 525/1651 | 483/1221 | 161/406 | chr4 | 83056998 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83075493 | T | A | 1 | a0001c0001t0002 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 10/10 | 63 | chr4 | 83075493 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:83035328 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.74+30A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035328 | |||||||
| chr4:83035335 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0027 |
3 | HG03486.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.74+37G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035335 | |||||||
| chr4:83035512 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(320): Show |
365 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(362): Show |
intron_variant | MODIFIER | c.74+214A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035512 | |||||||
| chr4:83035547 | T | C | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(321): Show |
366 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.74+249T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035547 | |||||||
| chr4:83035556 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.74+258C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035556 | |||||||
| chr4:83035916 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG02258.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.74+618G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035916 | |||||||
| chr4:83035970 | C | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.74+672C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035970 | |||||||
| chr4:83035975 | A | T | 1 | a0001c0001t0001g0327 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.74+677A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83035975 | |||||||
| chr4:83036258 | ACC | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(236): Show |
277 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.74+970_74+971delCC | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83036258 | ||||||
| chr4:83036414 | G | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG02258.hp1 HG02895.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+1116G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83036414 | |||||||
| chr4:83036465 | T | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
102 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.74+1167T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83036465 | |||||||
| chr4:83036531 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(85): Show |
102 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.74+1233G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83036531 | |||||||
| chr4:83036672 | G | A | 8 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.74+1374G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83036672 | |||||||
| chr4:83036691 | T | A | 6 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(3): Show |
6 | HG02818.hp2 HG03041.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.74+1393T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83036691 | |||||||
| chr4:83036918 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.74+1620C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83036918 | |||||||
| chr4:83036984 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.74+1686A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83036984 | |||||||
| chr4:83037228 | G | C | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG01261.hp1 HG01928.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.74+1930G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83037228 | |||||||
| chr4:83037581 | T | G | 1 | a0001c0001t0001g0329 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.74+2283T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83037581 | |||||||
| chr4:83037646 | T | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA18989.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.74+2348T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83037646 | |||||||
| chr4:83037910 | C | G | 1 | a0001c0001t0001g0200 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.74+2612C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83037910 | |||||||
| chr4:83038021 | G | T | 1 | a0001c0001t0001g0323 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.74+2723G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038021 | |||||||
| chr4:83038281 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0120 |
3 | HG02257.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.74+2983C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038281 | |||||||
| chr4:83038310 | T | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.74+3012T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038310 | |||||||
| chr4:83038361 | C | A | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
5 | HG02027.hp1 HG02080.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.74+3063C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038361 | |||||||
| chr4:83038461 | G | A | 8 | a0001c0001t0001g0017 a0001c0001t0001g0051 a0001c0001t0001g0052 others(5): Show |
9 | HG00597.hp1 HG02015.hp2 NA18978.hp1 others(6): Show |
intron_variant | MODIFIER | c.74+3163G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038461 | |||||||
| chr4:83038506 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.74+3208T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038506 | |||||||
| chr4:83038608 | T | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.74+3310T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038608 | |||||||
| chr4:83038628 | TTTTG | T | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
368 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(365): Show |
intron_variant | MODIFIER | c.74+3346_74+3349del others(4): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83038628 | ||||||
| chr4:83038718 | T | A | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.74+3420T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038718 | |||||||
| chr4:83038802 | C | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.74+3504C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038802 | |||||||
| chr4:83038921 | G | A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(27): Show |
32 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.74+3623G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83038921 | |||||||
| chr4:83039508 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.74+4210A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83039508 | |||||||
| chr4:83039708 | T | G | 1 | a0001c0001t0001g0128 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.74+4410T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83039708 | |||||||
| chr4:83040024 | C | G | 1 | a0001c0001t0001g0322 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.74+4726C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040024 | |||||||
| chr4:83040201 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.74+4903A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040201 | |||||||
| chr4:83040217 | C | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.74+4919C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040217 | |||||||
| chr4:83040444 | A | T | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
138 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.74+5146A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040444 | |||||||
| chr4:83040476 | G | T | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG02258.hp1 HG02895.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.75-5150G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040476 | |||||||
| chr4:83040527 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.75-5099A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040527 | |||||||
| chr4:83040561 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.75-5065T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040561 | |||||||
| chr4:83040592 | TCTC | T | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-5029_75-5027del others(3): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83040592 | ||||||
| chr4:83040724 | AT | A | 23 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.75-4892delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83040724 | ||||||
| chr4:83040760 | CT | C | 12 | a0001c0001t0001g0039 a0001c0001t0001g0112 a0001c0001t0001g0113 others(9): Show |
12 | HG01175.hp2 HG01361.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.75-4848delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83040760 | ||||||
| chr4:83040760 | CTT | C | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(303): Show |
348 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(345): Show |
intron_variant | MODIFIER | c.75-4849_75-4848del others(2): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83040760 | ||||||
| chr4:83040760 | CTTT | C | 9 | a0001c0001t0001g0055 a0001c0001t0001g0129 a0001c0001t0001g0130 others(6): Show |
9 | HG01496.hp2 HG01884.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.75-4850_75-4848del others(3): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83040760 | ||||||
| chr4:83040989 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.75-4637G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83040989 | |||||||
| chr4:83041068 | G | GT | 7 | a0001c0001t0001g0028 a0001c0001t0001g0127 a0001c0001t0001g0197 others(4): Show |
7 | HG01981.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.75-4546dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83041068 | ||||||
| chr4:83041278 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.75-4348G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041278 | |||||||
| chr4:83041308 | C | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.75-4318C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041308 | |||||||
| chr4:83041343 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.75-4283G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041343 | |||||||
| chr4:83041355 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.75-4271G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041355 | |||||||
| chr4:83041538 | C | T | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(27): Show |
32 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.75-4088C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041538 | |||||||
| chr4:83041612 | T | C | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(321): Show |
366 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.75-4014T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041612 | |||||||
| chr4:83041616 | C | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.75-4010C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041616 | |||||||
| chr4:83041629 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.75-3997G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041629 | |||||||
| chr4:83041703 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75-3923A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041703 | |||||||
| chr4:83041765 | C | A | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.75-3861C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041765 | |||||||
| chr4:83041834 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.75-3792A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041834 | |||||||
| chr4:83041975 | G | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.75-3651G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83041975 | |||||||
| chr4:83042012 | G | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.75-3614G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042012 | |||||||
| chr4:83042116 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0199 |
2 | HG02738.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.75-3510C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042116 | |||||||
| chr4:83042315 | A | T | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.75-3311A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042315 | |||||||
| chr4:83042320 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.75-3306A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042320 | |||||||
| chr4:83042517 | A | AT | 90 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(87): Show |
104 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.75-3094dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83042517 | ||||||
| chr4:83042704 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.75-2922G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042704 | |||||||
| chr4:83042717 | C | G | 4 | a0001c0001t0001g0107 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
4 | HG01081.hp1 HG01261.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.75-2909C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042717 | |||||||
| chr4:83042753 | C | G | 1 | a0001c0001t0001g0318 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.75-2873C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042753 | |||||||
| chr4:83042914 | A | AT | 11 | a0001c0001t0001g0050 a0001c0001t0001g0105 a0001c0001t0001g0106 others(8): Show |
11 | HG02027.hp1 HG02738.hp1 HG03098.hp2 others(8): Show |
intron_variant | MODIFIER | c.75-2696dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83042914 | ||||||
| chr4:83042939 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.75-2687G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042939 | |||||||
| chr4:83042977 | T | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75-2649T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83042977 | |||||||
| chr4:83043034 | GC | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.75-2590delC | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83043034 | ||||||
| chr4:83043042 | G | A | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.75-2584G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83043042 | |||||||
| chr4:83043121 | T | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.75-2505T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83043121 | |||||||
| chr4:83043307 | A | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0192 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.75-2319A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83043307 | |||||||
| chr4:83043404 | A | G | 1 | a0001c0001t0001g0317 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.75-2222A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83043404 | |||||||
| chr4:83043485 | C | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75-2141C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83043485 | |||||||
| chr4:83043518 | C | CA | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(149): Show |
167 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.75-2080dupA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83043518 | ||||||
| chr4:83043518 | C | CAA | 44 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0046 others(41): Show |
45 | HG00140.hp1 HG00438.hp2 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.75-2081_75-2080dup others(2): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83043518 | ||||||
| chr4:83043518 | CA | C | 8 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0189 others(5): Show |
8 | HG01891.hp2 HG02040.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.75-2080delA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83043518 | ||||||
| chr4:83043537 | A | C | 1 | a0001c0001t0001g0016 | 2 | NA18954.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.75-2089A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83043537 | |||||||
| chr4:83043795 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.75-1831G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83043795 | |||||||
| chr4:83044075 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0101 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.75-1551G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044075 | |||||||
| chr4:83044170 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.75-1456C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044170 | |||||||
| chr4:83044265 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.75-1361G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044265 | |||||||
| chr4:83044321 | T | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.75-1305T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044321 | |||||||
| chr4:83044334 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.75-1292A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044334 | |||||||
| chr4:83044401 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.75-1225C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044401 | |||||||
| chr4:83044444 | C | CA | 10 | a0001c0001t0001g0012 a0001c0001t0001g0120 a0001c0001t0001g0129 others(7): Show |
11 | HG01884.hp1 HG02055.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.75-1163dupA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83044444 | ||||||
| chr4:83044444 | CA | C | 76 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0040 others(73): Show |
79 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.75-1163delA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | 83044444 | ||||||
| chr4:83044505 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.75-1121C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044505 | |||||||
| chr4:83044508 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.75-1118T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044508 | |||||||
| chr4:83044636 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.75-990G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044636 | |||||||
| chr4:83044761 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0049 |
2 | NA19065.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.75-865C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044761 | |||||||
| chr4:83044970 | T | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0272 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.75-656T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83044970 | |||||||
| chr4:83045166 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.75-460G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83045166 | |||||||
| chr4:83045222 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.75-404A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83045222 | |||||||
| chr4:83045281 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75-345T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83045281 | |||||||
| chr4:83045424 | T | C | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0200 |
3 | HG00558.hp2 HG02015.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.75-202T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83045424 | |||||||
| chr4:83045496 | A | G | 9 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 others(6): Show |
9 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.75-130A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83045496 | |||||||
| chr4:83045586 | A | G | 1 | a0001c0001t0001g0312 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.75-40A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 1/9 | chr4 | 83045586 | |||||||
| chr4:83045797 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0159 |
2 | HG01109.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.154+92A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83045797 | |||||||
| chr4:83045974 | C | G | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+269C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83045974 | |||||||
| chr4:83046385 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+680A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83046385 | |||||||
| chr4:83046529 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG00323.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.154+824C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83046529 | |||||||
| chr4:83046534 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.154+829C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83046534 | |||||||
| chr4:83046558 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0187 |
2 | HG00673.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.154+853A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83046558 | |||||||
| chr4:83046561 | G | T | 5 | a0001c0001t0001g0053 a0001c0001t0001g0077 a0001c0001t0001g0078 others(2): Show |
5 | HG00438.hp2 HG00558.hp1 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+856G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83046561 | |||||||
| chr4:83046617 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.154+912A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83046617 | |||||||
| chr4:83046699 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.154+994A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83046699 | |||||||
| chr4:83047036 | A | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG02258.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+1331A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047036 | |||||||
| chr4:83047050 | G | A | 1 | a0001c0001t0001g0273 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.154+1345G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047050 | |||||||
| chr4:83047066 | AACTGCCT others(9): Show |
A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0187 |
2 | HG00673.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.154+1375_154+1390d others(18): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 83047066 | ||||||
| chr4:83047333 | C | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.154+1628C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047333 | |||||||
| chr4:83047382 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154+1677C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047382 | |||||||
| chr4:83047391 | A | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+1686A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047391 | |||||||
| chr4:83047479 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.155-1687C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047479 | |||||||
| chr4:83047480 | G | A | 13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0237 others(10): Show |
15 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.155-1686G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047480 | |||||||
| chr4:83047572 | T | C | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0163 |
3 | HG00597.hp2 NA18973.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.155-1594T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047572 | |||||||
| chr4:83047573 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.155-1593A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047573 | |||||||
| chr4:83047583 | T | A | 76 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.155-1583T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047583 | |||||||
| chr4:83047739 | G | A | 6 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0081 others(3): Show |
6 | NA18947.hp2 NA18954.hp1 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.155-1427G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047739 | |||||||
| chr4:83047767 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.155-1399G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047767 | |||||||
| chr4:83047844 | C | CA | 9 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
9 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.155-1315dupA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 83047844 | ||||||
| chr4:83047881 | G | A | 5 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG02258.hp1 HG02895.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-1285G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047881 | |||||||
| chr4:83047963 | T | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.155-1203T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83047963 | |||||||
| chr4:83048012 | AT | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
106 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.155-1153delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048012 | |||||||
| chr4:83048013 | T | A | 231 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(228): Show |
256 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(253): Show |
intron_variant | MODIFIER | c.155-1153T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048013 | |||||||
| chr4:83048016 | T | A | 1 | a0001c0001t0001g0164 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.155-1150T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048016 | |||||||
| chr4:83048025 | A | T | 5 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0226 others(2): Show |
6 | HG02572.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-1141A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048025 | |||||||
| chr4:83048245 | G | A | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(27): Show |
32 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.155-921G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048245 | |||||||
| chr4:83048312 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.155-854C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048312 | |||||||
| chr4:83048336 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.155-830A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048336 | |||||||
| chr4:83048510 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18967.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.155-656T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048510 | |||||||
| chr4:83048597 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.155-569A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048597 | |||||||
| chr4:83048603 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0229 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.155-563G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048603 | |||||||
| chr4:83048697 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG02258.hp1 HG02895.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.155-469G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048697 | |||||||
| chr4:83048888 | G | A | 5 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(2): Show |
5 | HG02145.hp1 HG03195.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-278G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048888 | |||||||
| chr4:83048935 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.155-231G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | chr4 | 83048935 | |||||||
| chr4:83049144 | CT | C | 11 | a0001c0001t0001g0085 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG01516.hp1 HG02004.hp1 HG02280.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.155-8delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | 83049144 | ||||||
| chr4:83049366 | T | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0165 |
2 | HG02165.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.306+49T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 3/9 | chr4 | 83049366 | |||||||
| chr4:83049871 | A | G | 3 | a0001c0001t0001g0311 a0001c0001t0001g0316 a0001c0001t0001g0318 |
3 | HG02523.hp1 NA18955.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.307-10A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 3/9 | chr4 | 83049871 | |||||||
| chr4:83050045 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.410+61A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050045 | |||||||
| chr4:83050140 | A | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410+156A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050140 | |||||||
| chr4:83050165 | A | G | 25 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(22): Show |
26 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.410+181A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050165 | |||||||
| chr4:83050186 | T | C | 23 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.410+202T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050186 | |||||||
| chr4:83050294 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.410+310G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050294 | |||||||
| chr4:83050510 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
83 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.410+526A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050510 | |||||||
| chr4:83050565 | C | G | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.410+581C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050565 | |||||||
| chr4:83050630 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.410+646C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050630 | |||||||
| chr4:83050847 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.410+863A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83050847 | |||||||
| chr4:83051058 | C | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410+1074C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83051058 | |||||||
| chr4:83051098 | C | CA | 41 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(38): Show |
43 | HG00733.hp1 HG00735.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.410+1132dupA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83051098 | ||||||
| chr4:83051098 | C | CAA | 7 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG02258.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+1131_410+1132d others(4): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83051098 | ||||||
| chr4:83051247 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.410+1263A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83051247 | |||||||
| chr4:83051473 | A | G | 1 | a0001c0001t0001g0321 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.410+1489A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83051473 | |||||||
| chr4:83051726 | T | A | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.410+1742T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83051726 | |||||||
| chr4:83051786 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.410+1802G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83051786 | |||||||
| chr4:83051802 | G | A | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+1818G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83051802 | |||||||
| chr4:83051859 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.410+1875T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83051859 | |||||||
| chr4:83052164 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.410+2180C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052164 | |||||||
| chr4:83052185 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.410+2201A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052185 | |||||||
| chr4:83052289 | T | C | 2 | a0001c0001t0001g0280 a0001c0001t0001g0323 |
2 | HG03017.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.410+2305T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052289 | |||||||
| chr4:83052312 | G | C | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410+2328G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052312 | |||||||
| chr4:83052335 | A | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410+2351A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052335 | |||||||
| chr4:83052436 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.410+2452G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052436 | |||||||
| chr4:83052511 | T | G | 1 | a0001c0001t0001g0281 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.410+2527T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052511 | |||||||
| chr4:83052541 | A | C | 1 | a0001c0001t0001g0281 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.410+2557A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052541 | |||||||
| chr4:83052583 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.410+2599T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052583 | |||||||
| chr4:83052776 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.410+2792G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052776 | |||||||
| chr4:83052804 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(167): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.410+2820C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83052804 | |||||||
| chr4:83053132 | C | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+3148C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053132 | |||||||
| chr4:83053265 | G | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410+3281G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053265 | |||||||
| chr4:83053372 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.410+3388G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053372 | |||||||
| chr4:83053567 | G | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411-3359G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053567 | |||||||
| chr4:83053578 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.411-3348C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053578 | |||||||
| chr4:83053630 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0027 |
3 | HG03486.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.411-3296C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053630 | |||||||
| chr4:83053635 | G | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(112): Show |
137 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(134): Show |
intron_variant | MODIFIER | c.411-3291G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053635 | |||||||
| chr4:83053677 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.411-3249C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053677 | |||||||
| chr4:83053713 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.411-3213G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053713 | |||||||
| chr4:83053762 | C | G | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(27): Show |
32 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.411-3164C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053762 | |||||||
| chr4:83053795 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.411-3131G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053795 | |||||||
| chr4:83053834 | T | G | 76 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
80 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.411-3092T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053834 | |||||||
| chr4:83053839 | C | CAAAAAAA others(1): Show |
14 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0049 others(11): Show |
15 | HG01109.hp2 HG02055.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.411-3081_411-3074d others(10): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83053839 | ||||||
| chr4:83053839 | C | CAAAAAAA others(3): Show |
117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
138 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.411-3083_411-3074d others(12): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83053839 | ||||||
| chr4:83053839 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0238 a0001c0001t0001g0251 a0001c0001t0001g0320 |
3 | HG02074.hp1 HG03516.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.411-3084_411-3074d others(13): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83053839 | ||||||
| chr4:83053839 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0282 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.411-3085_411-3074d others(14): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83053839 | ||||||
| chr4:83053881 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-3045C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83053881 | |||||||
| chr4:83054027 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.411-2899C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054027 | |||||||
| chr4:83054144 | C | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411-2782C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054144 | |||||||
| chr4:83054176 | A | C | 1 | a0001c0001t0001g0185 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.411-2750A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054176 | |||||||
| chr4:83054342 | A | AAAAAC | 3 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0208 |
3 | HG02886.hp1 HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.411-2559_411-2555d others(7): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83054342 | ||||||
| chr4:83054342 | A | AAAAACAA others(3): Show |
6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-2564_411-2555d others(12): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83054342 | ||||||
| chr4:83054394 | C | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(3): Show |
6 | HG02818.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-2532C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054394 | |||||||
| chr4:83054397 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0226 others(2): Show |
6 | HG02572.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.411-2529G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054397 | |||||||
| chr4:83054445 | G | A | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-2481G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054445 | |||||||
| chr4:83054709 | C | G | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.411-2217C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054709 | |||||||
| chr4:83054833 | A | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411-2093A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054833 | |||||||
| chr4:83054890 | C | T | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-2036C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83054890 | |||||||
| chr4:83055054 | C | T | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-1872C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055054 | |||||||
| chr4:83055056 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0101 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.411-1870C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055056 | |||||||
| chr4:83055062 | C | T | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(321): Show |
366 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.411-1864C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055062 | |||||||
| chr4:83055063 | T | C | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(321): Show |
366 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.411-1863T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055063 | |||||||
| chr4:83055063 | TC | T | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0167 |
3 | NA18962.hp1 NA18963.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.411-1861delC | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83055063 | ||||||
| chr4:83055064 | C | T | 324 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(321): Show |
366 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.411-1862C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055064 | |||||||
| chr4:83055284 | A | G | 1 | a0001c0001t0001g0016 | 2 | NA18954.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.411-1642A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055284 | |||||||
| chr4:83055339 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.411-1587A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055339 | |||||||
| chr4:83055390 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.411-1536G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055390 | |||||||
| chr4:83055447 | CT | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
367 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.411-1465delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83055447 | ||||||
| chr4:83055497 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.411-1429G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055497 | |||||||
| chr4:83055512 | C | T | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-1414C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055512 | |||||||
| chr4:83055557 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.411-1369C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055557 | |||||||
| chr4:83055731 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0227 |
4 | HG02630.hp2 HG03486.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-1195G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055731 | |||||||
| chr4:83055824 | A | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411-1102A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83055824 | |||||||
| chr4:83055932 | CT | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
367 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.411-980delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | 83055932 | ||||||
| chr4:83056083 | A | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(108): Show |
133 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(130): Show |
intron_variant | MODIFIER | c.411-843A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056083 | |||||||
| chr4:83056091 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.411-835C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056091 | |||||||
| chr4:83056138 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG02258.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-788G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056138 | |||||||
| chr4:83056228 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-698G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056228 | |||||||
| chr4:83056292 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.411-634A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056292 | |||||||
| chr4:83056354 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0272 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.411-572C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056354 | |||||||
| chr4:83056525 | G | A | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-401G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056525 | |||||||
| chr4:83056536 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.411-390C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056536 | |||||||
| chr4:83056583 | G | C | 2 | a0001c0001t0001g0253 a0001c0001t0001g0281 |
2 | NA18993.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.411-343G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056583 | |||||||
| chr4:83056595 | G | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411-331G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056595 | |||||||
| chr4:83056660 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
134 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.411-266G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056660 | |||||||
| chr4:83056681 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.411-245C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056681 | |||||||
| chr4:83056794 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.411-132A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056794 | |||||||
| chr4:83056822 | C | T | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
368 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(365): Show |
intron_variant | MODIFIER | c.411-104C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056822 | |||||||
| chr4:83056823 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.411-103G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056823 | |||||||
| chr4:83056857 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.411-69T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056857 | |||||||
| chr4:83056863 | A | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.411-63A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 4/9 | chr4 | 83056863 | |||||||
| chr4:83057622 | G | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.715+214G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83057622 | |||||||
| chr4:83057648 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.715+240C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83057648 | |||||||
| chr4:83057794 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.715+386C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83057794 | |||||||
| chr4:83057919 | C | CA | 23 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
23 | HG00323.hp2 HG00423.hp1 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.715+531dupA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83057919 | ||||||
| chr4:83057919 | CA | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(4): Show |
7 | HG00609.hp2 HG01516.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.715+531delA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83057919 | ||||||
| chr4:83057993 | A | G | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.715+585A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83057993 | |||||||
| chr4:83058052 | ATAAT | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0027 |
3 | HG03486.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.715+649_715+652del others(4): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83058052 | ||||||
| chr4:83058074 | G | GT | 80 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(77): Show |
84 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.715+677dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83058074 | ||||||
| chr4:83058136 | G | A | 13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0237 others(10): Show |
15 | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.715+728G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058136 | |||||||
| chr4:83058165 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.715+757T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058165 | |||||||
| chr4:83058202 | G | T | 1 | a0001c0001t0001g0053 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.715+794G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058202 | |||||||
| chr4:83058304 | A | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.715+896A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058304 | |||||||
| chr4:83058318 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.715+910A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058318 | |||||||
| chr4:83058409 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0226 others(2): Show |
6 | HG02572.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.715+1001G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058409 | |||||||
| chr4:83058575 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.715+1167C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058575 | |||||||
| chr4:83058697 | A | C | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.715+1289A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83058697 | |||||||
| chr4:83058795 | C | CT | 8 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(5): Show |
8 | HG02818.hp2 HG02886.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.715+1388dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83058795 | ||||||
| chr4:83059410 | C | G | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.715+2002C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83059410 | |||||||
| chr4:83059519 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.715+2111T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83059519 | |||||||
| chr4:83059549 | A | G | 116 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
138 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(135): Show |
intron_variant | MODIFIER | c.715+2141A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83059549 | |||||||
| chr4:83059674 | T | G | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.715+2266T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83059674 | |||||||
| chr4:83059697 | T | G | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.715+2289T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83059697 | |||||||
| chr4:83059720 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.715+2312G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83059720 | |||||||
| chr4:83059934 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG02258.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.715+2526C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83059934 | |||||||
| chr4:83060133 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.715+2725T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060133 | |||||||
| chr4:83060180 | A | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
83 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.715+2772A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060180 | |||||||
| chr4:83060186 | C | CT | 201 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(198): Show |
228 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(225): Show |
intron_variant | MODIFIER | c.715+2793dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83060186 | ||||||
| chr4:83060231 | T | G | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.715+2823T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060231 | |||||||
| chr4:83060239 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.715+2831A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060239 | |||||||
| chr4:83060350 | AT | A | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.716-2710delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83060350 | ||||||
| chr4:83060596 | G | C | 16 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0119 others(13): Show |
18 | HG00438.hp1 HG00673.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.716-2480G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060596 | |||||||
| chr4:83060632 | T | G | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.716-2444T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060632 | |||||||
| chr4:83060688 | G | A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
218 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(215): Show |
intron_variant | MODIFIER | c.716-2388G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060688 | |||||||
| chr4:83060988 | C | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
83 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.716-2088C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060988 | |||||||
| chr4:83060991 | G | A | 23 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.716-2085G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83060991 | |||||||
| chr4:83061029 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0272 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.716-2047T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061029 | |||||||
| chr4:83061034 | C | CA | 9 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
9 | HG02486.hp1 HG02818.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.716-2032dupA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83061034 | ||||||
| chr4:83061045 | T | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(319): Show |
364 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(361): Show |
intron_variant | MODIFIER | c.716-2031T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061045 | |||||||
| chr4:83061048 | T | A | 24 | a0001c0001t0001g0013 a0001c0001t0001g0056 a0001c0001t0001g0065 others(21): Show |
25 | HG01243.hp2 HG01884.hp2 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.716-2028T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061048 | |||||||
| chr4:83061051 | T | A | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0217 others(3): Show |
6 | HG01243.hp2 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.716-2025T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061051 | |||||||
| chr4:83061089 | C | T | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG03654.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.716-1987C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061089 | |||||||
| chr4:83061097 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.716-1979C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061097 | |||||||
| chr4:83061711 | C | CT | 5 | a0001c0001t0001g0015 a0001c0001t0001g0075 a0001c0001t0001g0201 others(2): Show |
6 | HG00323.hp1 HG01255.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.716-1351dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83061711 | ||||||
| chr4:83061887 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.716-1189G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061887 | |||||||
| chr4:83061887 | G | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-1189G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061887 | |||||||
| chr4:83061995 | A | G | 23 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.716-1081A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83061995 | |||||||
| chr4:83062086 | G | A | 2 | a0001c0001t0001g0260 a0001c0001t0001g0292 |
2 | HG00733.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.716-990G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83062086 | |||||||
| chr4:83062096 | G | C | 30 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(27): Show |
32 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.716-980G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83062096 | |||||||
| chr4:83062158 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0030 a0001c0001t0001g0031 others(1): Show |
4 | HG01891.hp2 HG02109.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.716-918T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83062158 | |||||||
| chr4:83062201 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.716-875A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83062201 | |||||||
| chr4:83062547 | T | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.716-529T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83062547 | |||||||
| chr4:83062575 | CTGTT | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.716-499_716-496del others(4): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | 83062575 | ||||||
| chr4:83063073 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18952.hp2 | splice_region_variant&intron_variant | LOW | c.716-3T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 6/9 | chr4 | 83063073 | |||||||
| chr4:83063272 | TGGTAGTC others(524): Show |
T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0102 |
3 | HG02647.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.886+30_886+560del | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83063272 | ||||||
| chr4:83063280 | A | G | 84 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(81): Show |
88 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.886+34A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063280 | |||||||
| chr4:83063389 | T | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.886+143T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063389 | |||||||
| chr4:83063394 | T | G | 1 | a0001c0001t0001g0245 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.886+148T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063394 | |||||||
| chr4:83063409 | A | AT | 94 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(91): Show |
108 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.886+171dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83063409 | ||||||
| chr4:83063462 | CA | C | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
135 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.886+218delA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83063462 | ||||||
| chr4:83063493 | T | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(322): Show |
367 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(364): Show |
intron_variant | MODIFIER | c.886+247T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063493 | |||||||
| chr4:83063534 | A | C | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.886+288A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063534 | |||||||
| chr4:83063659 | G | A | 113 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(110): Show |
135 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(132): Show |
intron_variant | MODIFIER | c.886+413G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063659 | |||||||
| chr4:83063858 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0252 |
2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.886+612C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063858 | |||||||
| chr4:83063923 | C | A | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.886+677C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063923 | |||||||
| chr4:83063957 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0102 |
3 | HG02647.hp1 HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.886+711C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063957 | |||||||
| chr4:83063975 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.886+729C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83063975 | |||||||
| chr4:83064024 | C | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0044 |
2 | HG02080.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.886+778C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064024 | |||||||
| chr4:83064046 | T | C | 2 | a0001c0001t0001g0222 a0001c0001t0001g0225 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.886+800T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064046 | |||||||
| chr4:83064213 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.886+967T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064213 | |||||||
| chr4:83064227 | C | G | 3 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG02258.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+981C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064227 | |||||||
| chr4:83064236 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.886+990C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064236 | |||||||
| chr4:83064334 | TA | T | 84 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(81): Show |
88 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.886+1097delA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064334 | ||||||
| chr4:83064448 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.886+1202A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064448 | |||||||
| chr4:83064672 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG00323.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.886+1426G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064672 | |||||||
| chr4:83064760 | G | C | 3 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | NA18991.hp2 NA18999.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.886+1514G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064760 | |||||||
| chr4:83064869 | C | CT | 16 | a0001c0001t0001g0035 a0001c0001t0001g0112 a0001c0001t0001g0114 others(13): Show |
16 | HG01109.hp2 HG01258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.887-1538dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | C | CTT | 50 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(47): Show |
66 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.887-1539_887-1538d others(4): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | C | CTTT | 49 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0022 others(46): Show |
55 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.887-1540_887-1538d others(5): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | C | CTTTT | 11 | a0001c0001t0001g0028 a0001c0001t0001g0212 a0001c0001t0001g0239 others(8): Show |
11 | HG01346.hp2 HG02145.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.887-1541_887-1538d others(6): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | CT | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(81): Show |
98 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.887-1538delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | CTT | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(64): Show |
71 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.887-1539_887-1538d others(4): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.887-1550_887-1538d others(15): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.887-1551_887-1538d others(16): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064869 | CTTTTTTT others(10): Show |
C | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.887-1554_887-1538d others(19): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83064869 | ||||||
| chr4:83064899 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.887-1539T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064899 | |||||||
| chr4:83064900 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.887-1538T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83064900 | |||||||
| chr4:83065006 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0252 |
2 | HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.887-1432C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83065006 | |||||||
| chr4:83065227 | TATTTA | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(109): Show |
134 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.887-1205_887-1201d others(7): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | 83065227 | ||||||
| chr4:83065511 | C | G | 83 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(80): Show |
87 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.887-927C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83065511 | |||||||
| chr4:83065809 | G | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0203 |
3 | HG03130.hp2 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.887-629G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83065809 | |||||||
| chr4:83065850 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.887-588T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83065850 | |||||||
| chr4:83065893 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.887-545G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83065893 | |||||||
| chr4:83066096 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0174 a0001c0001t0001g0182 |
3 | HG00741.hp2 NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.887-342G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83066096 | |||||||
| chr4:83066351 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.887-87G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83066351 | |||||||
| chr4:83066366 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.887-72C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83066366 | |||||||
| chr4:83066400 | C | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.887-38C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 7/9 | chr4 | 83066400 | |||||||
| chr4:83066707 | A | G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0093 others(2): Show |
5 | NA18943.hp1 NA18948.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.1002+154A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83066707 | |||||||
| chr4:83066872 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1002+319G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83066872 | |||||||
| chr4:83066909 | C | T | 10 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0063 others(7): Show |
10 | HG02074.hp2 NA18940.hp1 NA18961.hp1 others(7): Show |
intron_variant | MODIFIER | c.1002+356C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83066909 | |||||||
| chr4:83067005 | G | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+452G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067005 | |||||||
| chr4:83067064 | A | T | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+511A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067064 | |||||||
| chr4:83067104 | G | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1002+551G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067104 | |||||||
| chr4:83067104 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1002+551G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067104 | |||||||
| chr4:83067157 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1002+604T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067157 | |||||||
| chr4:83067159 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1002+606G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067159 | |||||||
| chr4:83067160 | T | C | 1 | a0001c0001t0001g0040 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1002+607T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067160 | |||||||
| chr4:83067460 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1002+907A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067460 | |||||||
| chr4:83067500 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0101 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1003-938A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067500 | |||||||
| chr4:83067524 | C | CT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0074 a0001c0001t0001g0128 others(4): Show |
7 | HG00609.hp1 HG01891.hp2 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.1003-894dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 83067524 | ||||||
| chr4:83067524 | CT | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(213): Show |
242 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(239): Show |
intron_variant | MODIFIER | c.1003-894delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 83067524 | ||||||
| chr4:83067524 | CTTT | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0226 others(2): Show |
6 | HG02572.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-896_1003-894d others(5): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 83067524 | ||||||
| chr4:83067528 | T | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0226 others(2): Show |
6 | HG02572.hp2 HG02630.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1003-910T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067528 | |||||||
| chr4:83067549 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1003-889A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067549 | |||||||
| chr4:83067616 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1003-822G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067616 | |||||||
| chr4:83067707 | T | G | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG01243.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003-731T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067707 | |||||||
| chr4:83067997 | T | C | 31 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0027 others(28): Show |
33 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.1003-441T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83067997 | |||||||
| chr4:83068084 | T | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0226 others(1): Show |
5 | HG02572.hp2 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003-354T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83068084 | |||||||
| chr4:83068142 | A | G | 1 | a0001c0001t0001g0079 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1003-296A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83068142 | |||||||
| chr4:83068257 | C | T | 23 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
24 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1003-181C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83068257 | |||||||
| chr4:83068363 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.1003-75T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83068363 | |||||||
| chr4:83068416 | G | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1003-22G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | chr4 | 83068416 | |||||||
| chr4:83068418 | G | GT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
139 | HG00423.hp2 HG00438.hp1 HG00597.hp1 others(136): Show |
intron_variant | MODIFIER | c.1003-11dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | 83068418 | ||||||
| chr4:83068813 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG01109.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1087+291T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83068813 | |||||||
| chr4:83068832 | T | A | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(324): Show |
369 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(366): Show |
intron_variant | MODIFIER | c.1087+310T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83068832 | |||||||
| chr4:83068969 | CA | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(316): Show |
361 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(358): Show |
intron_variant | MODIFIER | c.1087+464delA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 83068969 | ||||||
| chr4:83069352 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1087+830C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83069352 | |||||||
| chr4:83069457 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1087+935C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83069457 | |||||||
| chr4:83069490 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0260 a0001c0001t0001g0291 others(2): Show |
6 | HG00733.hp2 HG00735.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.1087+968C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83069490 | |||||||
| chr4:83069582 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 |
4 | HG02258.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+1060G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83069582 | |||||||
| chr4:83069730 | C | G | 1 | a0001c0001t0001g0307 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1087+1208C>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83069730 | |||||||
| chr4:83070076 | T | G | 6 | a0001c0001t0001g0009 a0001c0001t0001g0027 a0001c0001t0001g0226 others(3): Show |
7 | HG02451.hp1 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1087+1554T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83070076 | |||||||
| chr4:83070376 | A | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(174): Show |
207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.1087+1854A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83070376 | |||||||
| chr4:83070397 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1087+1875T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83070397 | |||||||
| chr4:83070400 | T | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0079 |
2 | HG02647.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1087+1878T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83070400 | |||||||
| chr4:83070498 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1087+1976T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83070498 | |||||||
| chr4:83070526 | T | A | 87 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(84): Show |
104 | HG00423.hp2 HG00597.hp1 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.1087+2004T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83070526 | |||||||
| chr4:83070580 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1087+2058G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83070580 | |||||||
| chr4:83071048 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1087+2526T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071048 | |||||||
| chr4:83071057 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1087+2535T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071057 | |||||||
| chr4:83071060 | C | A | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1087+2538C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071060 | |||||||
| chr4:83071062 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1087+2540T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071062 | |||||||
| chr4:83071076 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1087+2554T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071076 | |||||||
| chr4:83071079 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1087+2557C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071079 | |||||||
| chr4:83071082 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1087+2560T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071082 | |||||||
| chr4:83071263 | T | C | 4 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0174 others(1): Show |
4 | HG00741.hp2 HG03669.hp1 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.1087+2741T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071263 | |||||||
| chr4:83071277 | T | C | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1087+2755T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071277 | |||||||
| chr4:83071283 | TTGAATAA others(17): Show |
T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1087+2765_1087+278 others(28): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 83071283 | ||||||
| chr4:83071302 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1087+2780A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071302 | |||||||
| chr4:83071315 | T | C | 5 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(2): Show |
5 | HG02280.hp1 HG02486.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1087+2793T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071315 | |||||||
| chr4:83071382 | T | C | 200 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(197): Show |
219 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1087+2860T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071382 | |||||||
| chr4:83071450 | G | T | 3 | a0001c0001t0001g0201 a0001c0001t0001g0203 a0001c0001t0001g0245 |
3 | HG02630.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1087+2928G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071450 | |||||||
| chr4:83071822 | C | T | 2 | a0001c0001t0001g0278 a0001c0001t0001g0301 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1087+3300C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071822 | |||||||
| chr4:83071861 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1087+3339G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83071861 | |||||||
| chr4:83072427 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1088-2870G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072427 | |||||||
| chr4:83072465 | T | TTATGCTT others(7): Show |
1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2831_1088-283 others(18): Show |
COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 83072465 | ||||||
| chr4:83072473 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2824C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072473 | |||||||
| chr4:83072474 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2823A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072474 | |||||||
| chr4:83072475 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 |
3 | HG01891.hp2 HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1088-2822A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072475 | |||||||
| chr4:83072477 | T | A | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2820T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072477 | |||||||
| chr4:83072478 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2819A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072478 | |||||||
| chr4:83072479 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2818G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072479 | |||||||
| chr4:83072480 | G | C | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2817G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072480 | |||||||
| chr4:83072483 | A | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2814A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072483 | |||||||
| chr4:83072484 | A | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2813A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072484 | |||||||
| chr4:83072485 | T | A | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2812T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072485 | |||||||
| chr4:83072491 | A | C | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2806A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072491 | |||||||
| chr4:83072496 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2801A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072496 | |||||||
| chr4:83072498 | G | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2799G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072498 | |||||||
| chr4:83072499 | G | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2798G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072499 | |||||||
| chr4:83072500 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2797C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072500 | |||||||
| chr4:83072505 | G | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2792G>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072505 | |||||||
| chr4:83072506 | A | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2791A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072506 | |||||||
| chr4:83072523 | A | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2774A>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072523 | |||||||
| chr4:83072531 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2766C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072531 | |||||||
| chr4:83072533 | C | T | 1 | a0001c0001t0001g0259 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1088-2764C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072533 | |||||||
| chr4:83072754 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1088-2543A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072754 | |||||||
| chr4:83072837 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1088-2460T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072837 | |||||||
| chr4:83072838 | T | G | 104 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(101): Show |
112 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1088-2459T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072838 | |||||||
| chr4:83072928 | A | G | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(100): Show |
111 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1088-2369A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072928 | |||||||
| chr4:83072967 | A | C | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1088-2330A>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83072967 | |||||||
| chr4:83073008 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1088-2289T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83073008 | |||||||
| chr4:83073303 | G | C | 1 | a0001c0001t0001g0272 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1088-1994G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83073303 | |||||||
| chr4:83073320 | A | G | 1 | a0001c0001t0001g0303 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1088-1977A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83073320 | |||||||
| chr4:83073405 | A | G | 16 | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0119 others(13): Show |
18 | HG00438.hp1 HG00673.hp2 NA18945.hp1 others(15): Show |
intron_variant | MODIFIER | c.1088-1892A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83073405 | |||||||
| chr4:83073421 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1088-1876C>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83073421 | |||||||
| chr4:83073563 | A | G | 103 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(100): Show |
111 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1088-1734A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83073563 | |||||||
| chr4:83073854 | G | A | 1 | a0001c0001t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1088-1443G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83073854 | |||||||
| chr4:83073956 | C | CA | 210 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(207): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.1088-1328dupA | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 83073956 | ||||||
| chr4:83074389 | T | A | 1 | a0001c0003t0001g0328 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1088-908T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074389 | |||||||
| chr4:83074461 | G | GT | 34 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0039 others(31): Show |
34 | HG00423.hp2 HG00438.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1088-819dupT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 83074461 | ||||||
| chr4:83074461 | GT | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(90): Show |
97 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.1088-819delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 83074461 | ||||||
| chr4:83074475 | T | G | 3 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 |
3 | HG03098.hp2 HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1088-822T>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074475 | |||||||
| chr4:83074607 | C | T | 2 | a0001c0001t0001g0184 a0001c0001t0001g0321 |
2 | HG03579.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1088-690C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074607 | |||||||
| chr4:83074612 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0302 |
2 | HG02738.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1088-685G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074612 | |||||||
| chr4:83074625 | G | C | 2 | a0001c0001t0001g0261 a0001c0001t0001g0319 |
2 | NA18979.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1088-672G>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074625 | |||||||
| chr4:83074649 | CT | C | 6 | a0001c0001t0001g0151 a0001c0001t0001g0167 a0001c0001t0001g0221 others(3): Show |
6 | HG01109.hp2 HG02896.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088-635delT | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | 83074649 | ||||||
| chr4:83074697 | G | A | 3 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 |
3 | HG01109.hp2 HG06807.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1088-600G>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074697 | |||||||
| chr4:83074704 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1088-593C>T | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074704 | |||||||
| chr4:83074978 | A | G | 5 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
6 | HG01891.hp2 HG02109.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1088-319A>G | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83074978 | |||||||
| chr4:83075135 | T | A | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1088-162T>A | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83075135 | |||||||
| chr4:83075192 | T | C | 1 | a0001c0001t0001g0298 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1088-105T>C | COPS4 | ENSG00000138663.9 | transcript | ENST00000264389.7 | protein_coding | 9/9 | chr4 | 83075192 |