Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 221184 |
| ensemblid | ENSG00000140848.17 |
| hgncid | 2315 |
| symbol | CPNE2 |
| name | copine 2 |
| refseq_nuc | NM_152727.6 |
| refseq_prot | NP_689940.3 |
| ensembl_nuc | ENST00000290776.13 |
| ensembl_prot | ENSP00000290776.8 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 57092583 |
| end | 57148369 |
| strand | + |
| ver | v1.2 |
| region | chr16:57092583-57148369 |
| region5000 | chr16:57087583-57153369 |
| regionname0 | CPNE2_chr16_57092583_57148369 |
| regionname5000 | CPNE2_chr16_57087583_57153369 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 548 | 358 | 91 | 58 | 151 | 14 | 42 | 117 | CPNE2_chr16_57087583_57153369 | CPNE2 | MAHIP others(543): Show |
chr16 | 57087583 | 57153369 |
| a0002 | 0/0 | 548 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | MAHIP others(543): Show |
chr16 | 57087583 | 57153369 |
| a0003 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | MAHIP others(543): Show |
chr16 | 57087583 | 57153369 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1644 | 308 | 83 | 57 | 120 | 14 | 33 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 | ||
| a0001c0002 | 0/0 | 1644 | 38 | 0 | 1 | 28 | 0 | 9 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 | ||
| a0001c0003 | 0/1 | 1644 | 4 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 | ||
| a0001c0005 | 0/0 | 1644 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 | ||
| a0001c0006 | 0/0 | 1644 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 | ||
| a0001c0007 | 0/0 | 1644 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 | ||
| a0002c0004 | 0/0 | 1644 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 | ||
| a0003c0008 | 0/0 | 1644 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | ATGGC others(1639): Show |
chr16 | 57087583 | 57153369 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2601 | 286 | 70 | 56 | 117 | 12 | 30 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0001t0002 | 0/0 | 2601 | 11 | 10 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0001t0003 | 0/0 | 2601 | 6 | 2 | 1 | 0 | 2 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0001t0004 | 0/0 | 2602 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2597): Show |
chr16 | 57087583 | 57153369 |
| a0001c0001t0005 | 0/0 | 2601 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0001t0006 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0001t0007 | 0/0 | 2601 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0001t0008 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0002t0001 | 0/0 | 2601 | 35 | 0 | 1 | 25 | 0 | 9 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0002t0004 | 0/0 | 2602 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2597): Show |
chr16 | 57087583 | 57153369 |
| a0001c0003t0001 | 0/0 | 2601 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0003t0003 | 0/1 | 2601 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0005t0001 | 0/0 | 2601 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0006t0001 | 0/0 | 2601 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0001c0007t0001 | 0/0 | 2601 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0002c0004t0001 | 0/0 | 2601 | 3 | 3 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| a0003c0008t0001 | 0/0 | 2601 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | GCCCG others(2596): Show |
chr16 | 57087583 | 57153369 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0283 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0007g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0001t0008g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0002t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0003t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0003t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0003t0003g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0005t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0005t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0006t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0006t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0007t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0001c0007t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0002c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0002c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| a0003c0008t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0306 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0291 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0222 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0164 | EUR | IBS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0298 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02071 | hp1 | a0001 | c0001 | t0006 | g0315 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CDX | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | KHV | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02572 | hp1 | a0001 | c0007 | t0001 | g0302 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0104 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02622 | hp1 | a0002 | c0004 | t0001 | g0040 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0102 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0311 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0294 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0309 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02717 | hp2 | a0002 | c0004 | t0001 | g0162 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0038 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0097 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02886 | hp2 | a0001 | c0007 | t0001 | g0090 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0191 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0060 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0310 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0333 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0340 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0206 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0323 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0293 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | BEB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0332 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0336 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0278 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18942 | hp1 | a0001 | c0002 | t0004 | g0173 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18961 | hp1 | a0003 | c0008 | t0001 | g0056 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18965 | hp2 | a0001 | c0006 | t0001 | g0199 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18967 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0263 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18998 | hp2 | a0001 | c0002 | t0004 | g0058 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19000 | hp1 | a0001 | c0006 | t0001 | g0190 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19043 | hp2 | a0002 | c0004 | t0001 | g0039 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19060 | hp1 | a0001 | c0001 | t0008 | g0106 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19062 | hp2 | a0001 | c0006 | t0001 | g0184 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19083 | hp2 | a0001 | c0002 | t0004 | g0188 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | YRI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ASW | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ASW | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0287 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0289 | EUR | TSI | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0194 | SAS | GIH | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | CLM | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| HG06807 | hp2 | a0001 | c0005 | t0001 | g0007 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0321 | AFR | LWK | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| homoSapiens | chm13v2 | a0001 | c0003 | t0003 | g0276 | REF | REF | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0283 | REF | REF | CPNE2_chr16_57087583_57153369 | CPNE2 | chr16 | 57087583 | 57153369 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57110901 | G | C | 1 | a0002 | 3 | HG02622.hp1 HG02717.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.159G>C | p.Glu53Asp | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/16 | 402/2601 | 159/1647 | 53/548 | chr16 | 57110901 | |||
| chr16:57119209 | G | T | 1 | a0003 | 1 | NA18961.hp1 | missense_variant | MODERATE | c.522G>T | p.Lys174Asn | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 6/16 | 765/2601 | 522/1647 | 174/548 | chr16 | 57119209 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57113362 | C | T | 1 | a0001c0003 | 3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.255C>T | p.Phe85Phe | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/16 | 498/2601 | 255/1647 | 85/548 | chr16 | 57113362 | |||
| chr16:57117546 | G | A | 1 | a0001c0007 | 2 | HG02572.hp1 HG02886.hp2 |
synonymous_variant | LOW | c.486G>A | p.Ala162Ala | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/16 | 729/2601 | 486/1647 | 162/548 | chr16 | 57117546 | |||
| chr16:57146165 | C | A | 1 | a0001c0005 | 3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.1383C>A | p.Ser461Ser | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/16 | 1626/2601 | 1383/1647 | 461/548 | chr16 | 57146165 | |||
| chr16:57146246 | C | A | 1 | a0001c0002 | 38 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(35): Show |
synonymous_variant | LOW | c.1464C>A | p.Arg488Arg | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/16 | 1707/2601 | 1464/1647 | 488/548 | chr16 | 57146246 | |||
| chr16:57146288 | T | C | 1 | a0001c0006 | 3 | NA18965.hp2 NA19000.hp1 NA19062.hp2 |
synonymous_variant | LOW | c.1506T>C | p.Ile502Ile | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/16 | 1749/2601 | 1506/1647 | 502/548 | chr16 | 57146288 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57092592 | C | G | 1 | a0001c0001t0008 | 1 | NA19060.hp1 | 5_prime_UTR_variant | MODIFIER | c.-234C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/16 | 18151 | chr16 | 57092592 | ||||||
| chr16:57110736 | G | A | 1 | a0001c0001t0005 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-7G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/16 | 7 | chr16 | 57110736 | ||||||
| chr16:57147771 | T | A | 1 | a0001c0001t0006 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 113 | chr16 | 57147771 | ||||||
| chr16:57147964 | T | C | 1 | a0001c0001t0003 | 6 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*306T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 306 | chr16 | 57147964 | ||||||
| chr16:57147970 | G | A | 1 | a0001c0001t0007 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 312 | chr16 | 57147970 | ||||||
| chr16:57148026 | T | TA | 2 | a0001c0001t0004 a0001c0002t0004 |
4 | NA18942.hp1 NA18970.hp1 NA18998.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*369dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 370 | INFO_REALIGN_3_PRIME | chr16 | 57148026 | |||||
| chr16:57148265 | T | C | 1 | a0001c0001t0002 | 11 | HG01884.hp2 HG02145.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*607T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 607 | chr16 | 57148265 | ||||||
| chr16:57148356 | A | G | 1 | a0001c0001t0003 | 6 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*698A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 16/16 | 698 | chr16 | 57148356 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57093349 | T | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-36+559T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093349 | |||||||
| chr16:57093441 | C | G | 1 | a0001c0001t0001g0342 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-36+651C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093441 | |||||||
| chr16:57093453 | C | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(18): Show |
22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36+663C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093453 | |||||||
| chr16:57093522 | C | T | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG01243.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.-36+732C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093522 | |||||||
| chr16:57093538 | G | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(126): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.-36+748G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093538 | |||||||
| chr16:57093596 | C | T | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0334 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36+806C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093596 | |||||||
| chr16:57093723 | C | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+933C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093723 | |||||||
| chr16:57093800 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0005g0038 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-36+1010C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093800 | |||||||
| chr16:57093841 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(62): Show |
70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.-36+1051G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093841 | |||||||
| chr16:57093895 | G | A | 1 | a0001c0007t0001g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36+1105G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093895 | |||||||
| chr16:57093971 | C | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-36+1181C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57093971 | |||||||
| chr16:57094095 | AGCTCCAG others(4): Show |
A | 2 | a0002c0004t0001g0039 a0002c0004t0001g0040 |
2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-36+1308_-36+1318d others(13): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57094095 | ||||||
| chr16:57094184 | G | A | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+1394G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094184 | |||||||
| chr16:57094187 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
119 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.-36+1397T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094187 | |||||||
| chr16:57094220 | C | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
58 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-36+1430C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094220 | |||||||
| chr16:57094400 | C | T | 1 | a0001c0001t0007g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36+1610C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094400 | |||||||
| chr16:57094443 | A | T | 2 | a0001c0002t0001g0198 a0001c0006t0001g0199 |
2 | NA18964.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-36+1653A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094443 | |||||||
| chr16:57094476 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
69 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.-36+1686G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094476 | |||||||
| chr16:57094478 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+1688T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094478 | |||||||
| chr16:57094489 | G | A | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-36+1699G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094489 | |||||||
| chr16:57094529 | A | G | 2 | a0001c0003t0001g0014 a0001c0003t0001g0333 |
3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-36+1739A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094529 | |||||||
| chr16:57094543 | A | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+1753A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094543 | |||||||
| chr16:57094579 | T | C | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-36+1789T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094579 | |||||||
| chr16:57094833 | G | A | 19 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(16): Show |
19 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.-36+2043G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094833 | |||||||
| chr16:57094959 | G | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(45): Show |
53 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.-36+2169G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094959 | |||||||
| chr16:57094968 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-36+2178G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094968 | |||||||
| chr16:57094971 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | NA19060.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-36+2181C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094971 | |||||||
| chr16:57094974 | G | A | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+2184G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094974 | |||||||
| chr16:57094976 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-36+2186T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57094976 | |||||||
| chr16:57095072 | G | C | 3 | a0001c0001t0001g0219 a0001c0001t0001g0221 a0001c0001t0003g0220 |
3 | HG03688.hp1 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-36+2282G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095072 | |||||||
| chr16:57095178 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-36+2388C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095178 | |||||||
| chr16:57095619 | C | T | 1 | a0001c0001t0001g0331 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-36+2829C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095619 | |||||||
| chr16:57095653 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0324 a0001c0001t0001g0325 others(5): Show |
10 | NA18944.hp2 NA18952.hp2 NA18974.hp1 others(7): Show |
intron_variant | MODIFIER | c.-36+2863C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095653 | |||||||
| chr16:57095712 | A | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
108 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.-36+2922A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095712 | |||||||
| chr16:57095745 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-36+2955A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095745 | |||||||
| chr16:57095768 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-36+2978G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57095768 | |||||||
| chr16:57096042 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-36+3252T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096042 | |||||||
| chr16:57096105 | G | GTTTAAAT others(4): Show |
1 | a0001c0001t0001g0083 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-36+3317_-36+3318i others(13): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57096105 | ||||||
| chr16:57096119 | T | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-36+3329T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096119 | |||||||
| chr16:57096549 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-36+3759A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096549 | |||||||
| chr16:57096573 | C | T | 7 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(4): Show |
8 | HG01884.hp2 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-36+3783C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096573 | |||||||
| chr16:57096698 | C | CA | 67 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(64): Show |
70 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.-36+3927dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57096698 | ||||||
| chr16:57096698 | CA | C | 15 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(12): Show |
15 | HG00673.hp2 HG02015.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-36+3927delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57096698 | ||||||
| chr16:57096725 | G | T | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-36+3935G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57096725 | |||||||
| chr16:57097087 | C | G | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36+4297C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097087 | |||||||
| chr16:57097121 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp1 HG01496.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+4331G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097121 | |||||||
| chr16:57097169 | A | T | 1 | a0001c0001t0006g0315 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-36+4379A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097169 | |||||||
| chr16:57097285 | A | T | 1 | a0001c0001t0001g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-36+4495A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097285 | |||||||
| chr16:57097388 | A | G | 244 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(241): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.-36+4598A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097388 | |||||||
| chr16:57097416 | A | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+4626A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097416 | |||||||
| chr16:57097490 | G | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(51): Show |
55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+4700G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097490 | |||||||
| chr16:57097622 | T | C | 38 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0168 others(35): Show |
39 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.-36+4832T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097622 | |||||||
| chr16:57097865 | C | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(51): Show |
55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+5075C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097865 | |||||||
| chr16:57097917 | C | T | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+5127C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097917 | |||||||
| chr16:57097958 | G | C | 2 | a0001c0003t0001g0014 a0001c0003t0001g0333 |
3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-36+5168G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57097958 | |||||||
| chr16:57098032 | C | T | 1 | a0001c0007t0001g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36+5242C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098032 | |||||||
| chr16:57098034 | A | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+5244A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098034 | |||||||
| chr16:57098151 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-36+5361G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098151 | |||||||
| chr16:57098273 | C | T | 1 | a0001c0001t0001g0299 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-36+5483C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098273 | |||||||
| chr16:57098277 | G | A | 50 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(47): Show |
51 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(48): Show |
intron_variant | MODIFIER | c.-36+5487G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098277 | |||||||
| chr16:57098333 | C | T | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+5543C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098333 | |||||||
| chr16:57098342 | G | A | 54 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(51): Show |
55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+5552G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098342 | |||||||
| chr16:57098351 | A | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
171 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(168): Show |
intron_variant | MODIFIER | c.-36+5561A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098351 | |||||||
| chr16:57098406 | G | A | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | NA18946.hp1 NA19062.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-36+5616G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098406 | |||||||
| chr16:57098419 | C | T | 1 | a0001c0001t0007g0332 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-36+5629C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098419 | |||||||
| chr16:57098452 | C | T | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+5662C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098452 | |||||||
| chr16:57098668 | C | T | 1 | a0001c0001t0001g0298 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-36+5878C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098668 | |||||||
| chr16:57098785 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-36+5995C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098785 | |||||||
| chr16:57098873 | G | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(47): Show |
56 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.-36+6083G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098873 | |||||||
| chr16:57098937 | T | C | 1 | a0001c0001t0002g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-36+6147T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57098937 | |||||||
| chr16:57099092 | C | A | 48 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0085 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.-36+6302C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099092 | |||||||
| chr16:57099157 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(232): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.-36+6367A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099157 | |||||||
| chr16:57099261 | C | T | 21 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(18): Show |
22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36+6471C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099261 | |||||||
| chr16:57099291 | A | G | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-36+6501A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099291 | |||||||
| chr16:57099349 | A | G | 38 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0168 others(35): Show |
39 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.-36+6559A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099349 | |||||||
| chr16:57099439 | C | T | 38 | a0001c0001t0001g0163 a0001c0001t0001g0166 a0001c0001t0001g0168 others(35): Show |
39 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(36): Show |
intron_variant | MODIFIER | c.-36+6649C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099439 | |||||||
| chr16:57099459 | A | G | 1 | a0001c0001t0001g0312 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-36+6669A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099459 | |||||||
| chr16:57099607 | C | CT | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+6827dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099607 | ||||||
| chr16:57099660 | C | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+6870C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099660 | |||||||
| chr16:57099748 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
170 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.-36+6958T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099748 | |||||||
| chr16:57099775 | A | AT | 43 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0018 others(40): Show |
45 | HG00140.hp1 HG00621.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.-36+7006dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099775 | ||||||
| chr16:57099775 | AT | A | 19 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0001t0001g0047 others(16): Show |
20 | HG01069.hp1 HG01884.hp2 HG02622.hp1 others(17): Show |
intron_variant | MODIFIER | c.-36+7006delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099775 | ||||||
| chr16:57099775 | ATT | A | 7 | a0001c0001t0001g0037 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.-36+7005_-36+7006d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57099775 | ||||||
| chr16:57099838 | C | T | 2 | a0001c0002t0001g0293 a0001c0002t0001g0294 |
2 | HG02683.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-36+7048C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099838 | |||||||
| chr16:57099971 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-36+7181C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099971 | |||||||
| chr16:57099995 | G | A | 25 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0107 others(22): Show |
26 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-36+7205G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57099995 | |||||||
| chr16:57100024 | C | T | 54 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(51): Show |
55 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(52): Show |
intron_variant | MODIFIER | c.-36+7234C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100024 | |||||||
| chr16:57100372 | A | G | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-36+7582A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100372 | |||||||
| chr16:57100426 | A | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+7636A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100426 | |||||||
| chr16:57100526 | A | G | 2 | a0001c0003t0001g0014 a0001c0003t0001g0333 |
3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-36+7736A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100526 | |||||||
| chr16:57100822 | G | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8032G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100822 | |||||||
| chr16:57100826 | G | A | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-36+8036G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57100826 | |||||||
| chr16:57100922 | AT | A | 21 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(18): Show |
22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-36+8134delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57100922 | ||||||
| chr16:57101009 | G | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8219G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101009 | |||||||
| chr16:57101065 | G | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8275G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101065 | |||||||
| chr16:57101140 | G | A | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8350G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101140 | |||||||
| chr16:57101394 | A | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+8604A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101394 | |||||||
| chr16:57101419 | G | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-36+8629G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101419 | |||||||
| chr16:57101535 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-36+8745A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101535 | |||||||
| chr16:57101592 | CATT | C | 48 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0085 others(45): Show |
49 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.-36+8805_-36+8807d others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57101592 | ||||||
| chr16:57101680 | C | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8890C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101680 | |||||||
| chr16:57101681 | G | C | 1 | a0001c0007t0001g0090 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-36+8891G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101681 | |||||||
| chr16:57101684 | T | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8894T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101684 | |||||||
| chr16:57101708 | C | A | 39 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0166 others(36): Show |
40 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-36+8918C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101708 | |||||||
| chr16:57101708 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01891.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-36+8918C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101708 | |||||||
| chr16:57101722 | G | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-36+8932G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101722 | |||||||
| chr16:57101724 | T | A | 4 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(1): Show |
4 | HG02723.hp2 HG03471.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+8934T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101724 | |||||||
| chr16:57101736 | G | C | 1 | a0001c0001t0008g0106 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-36+8946G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101736 | |||||||
| chr16:57101889 | A | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8819A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101889 | |||||||
| chr16:57101892 | A | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8816A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101892 | |||||||
| chr16:57101950 | C | CT | 60 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0094 others(57): Show |
61 | HG00323.hp1 HG00597.hp2 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.-35-8744dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57101950 | ||||||
| chr16:57101950 | C | CTT | 39 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0166 others(36): Show |
40 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-35-8745_-35-8744d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57101950 | ||||||
| chr16:57101971 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-35-8737G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57101971 | |||||||
| chr16:57102040 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-35-8668G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102040 | |||||||
| chr16:57102060 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-35-8648A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102060 | |||||||
| chr16:57102079 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0002g0153 |
3 | HG01891.hp1 HG02055.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.-35-8629C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102079 | |||||||
| chr16:57102114 | A | AT | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8585dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57102114 | ||||||
| chr16:57102171 | T | C | 234 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.-35-8537T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102171 | |||||||
| chr16:57102196 | T | C | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8512T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102196 | |||||||
| chr16:57102246 | G | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0226 a0001c0001t0001g0227 |
4 | HG01433.hp1 HG01496.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-8462G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102246 | |||||||
| chr16:57102274 | G | A | 13 | a0001c0001t0001g0011 a0001c0001t0001g0231 a0001c0001t0001g0232 others(10): Show |
14 | HG00639.hp1 HG01074.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-35-8434G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102274 | |||||||
| chr16:57102284 | G | A | 3 | a0001c0001t0002g0098 a0001c0005t0001g0007 a0001c0005t0001g0097 |
4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-8424G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102284 | |||||||
| chr16:57102295 | A | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0095 a0001c0001t0001g0096 others(53): Show |
57 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(54): Show |
intron_variant | MODIFIER | c.-35-8413A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102295 | |||||||
| chr16:57102497 | C | T | 11 | a0001c0001t0001g0105 a0001c0001t0001g0133 a0001c0001t0001g0135 others(8): Show |
11 | NA18951.hp1 NA18955.hp1 NA18963.hp2 others(8): Show |
intron_variant | MODIFIER | c.-35-8211C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102497 | |||||||
| chr16:57102500 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-35-8208G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102500 | |||||||
| chr16:57102502 | C | T | 2 | a0001c0003t0001g0014 a0001c0003t0001g0333 |
3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-35-8206C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102502 | |||||||
| chr16:57102605 | CT | C | 6 | a0001c0001t0001g0043 a0001c0001t0001g0050 a0001c0001t0001g0192 others(3): Show |
6 | HG00741.hp1 HG01074.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-35-8089delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57102605 | ||||||
| chr16:57102684 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-35-8024C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102684 | |||||||
| chr16:57102703 | G | C | 25 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0107 others(22): Show |
26 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-35-8005G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57102703 | |||||||
| chr16:57103030 | G | A | 3 | a0001c0001t0002g0098 a0001c0005t0001g0007 a0001c0005t0001g0097 |
4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-7678G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103030 | |||||||
| chr16:57103097 | C | T | 1 | a0001c0001t0003g0306 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-35-7611C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103097 | |||||||
| chr16:57103175 | C | G | 3 | a0001c0001t0002g0098 a0001c0005t0001g0007 a0001c0005t0001g0097 |
4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-7533C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103175 | |||||||
| chr16:57103356 | T | TCA | 70 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(67): Show |
72 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.-35-7351_-35-7350d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57103356 | ||||||
| chr16:57103543 | C | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0099 a0001c0001t0001g0100 others(52): Show |
56 | HG00597.hp2 HG00621.hp2 HG01099.hp2 others(53): Show |
intron_variant | MODIFIER | c.-35-7165C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103543 | |||||||
| chr16:57103573 | C | G | 12 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(9): Show |
12 | HG01891.hp1 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.-35-7135C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103573 | |||||||
| chr16:57103621 | C | G | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
48 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.-35-7087C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103621 | |||||||
| chr16:57103733 | C | G | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-6975C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57103733 | |||||||
| chr16:57104057 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-35-6651A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104057 | |||||||
| chr16:57104162 | G | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(239): Show |
255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.-35-6546G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104162 | |||||||
| chr16:57104213 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-35-6495C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104213 | |||||||
| chr16:57104217 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0149 |
2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-35-6491C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104217 | |||||||
| chr16:57104218 | G | A | 2 | a0001c0001t0001g0055 a0003c0008t0001g0056 |
2 | NA18961.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-35-6490G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104218 | |||||||
| chr16:57104295 | G | C | 43 | a0001c0001t0001g0049 a0001c0001t0001g0095 a0001c0001t0001g0096 others(40): Show |
44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-35-6413G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104295 | |||||||
| chr16:57104352 | T | G | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-35-6356T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104352 | |||||||
| chr16:57104470 | G | T | 50 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0085 others(47): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-35-6238G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104470 | |||||||
| chr16:57104512 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-35-6196G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104512 | |||||||
| chr16:57104555 | C | T | 1 | a0001c0002t0001g0196 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-35-6153C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104555 | |||||||
| chr16:57104567 | C | T | 38 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0166 others(35): Show |
39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-6141C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104567 | |||||||
| chr16:57104985 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-5723G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57104985 | |||||||
| chr16:57105073 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-35-5635C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105073 | |||||||
| chr16:57105157 | C | T | 2 | a0001c0001t0001g0310 a0001c0001t0001g0312 |
2 | HG03490.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-35-5551C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105157 | |||||||
| chr16:57105176 | C | G | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-35-5532C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105176 | |||||||
| chr16:57105430 | G | GT | 15 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0091 others(12): Show |
15 | HG00741.hp1 HG00741.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.-35-5262dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57105430 | ||||||
| chr16:57105430 | GT | G | 16 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0034 others(13): Show |
20 | HG01884.hp2 HG02258.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35-5262delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57105430 | ||||||
| chr16:57105435 | T | G | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-35-5273T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105435 | |||||||
| chr16:57105491 | A | C | 1 | a0001c0001t0001g0243 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-35-5217A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105491 | |||||||
| chr16:57105579 | G | C | 10 | a0001c0001t0001g0166 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
11 | HG00673.hp1 HG02056.hp2 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.-35-5129G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105579 | |||||||
| chr16:57105627 | G | A | 38 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0166 others(35): Show |
39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-5081G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105627 | |||||||
| chr16:57105692 | T | G | 28 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0125 others(25): Show |
28 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(25): Show |
intron_variant | MODIFIER | c.-35-5016T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105692 | |||||||
| chr16:57105722 | A | G | 50 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0085 others(47): Show |
51 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-35-4986A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105722 | |||||||
| chr16:57105735 | A | G | 46 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(43): Show |
48 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(45): Show |
intron_variant | MODIFIER | c.-35-4973A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105735 | |||||||
| chr16:57105766 | C | T | 3 | a0001c0001t0002g0098 a0001c0005t0001g0007 a0001c0005t0001g0097 |
4 | HG01884.hp2 HG02818.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-4942C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105766 | |||||||
| chr16:57105773 | G | A | 1 | a0001c0001t0001g0313 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-35-4935G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105773 | |||||||
| chr16:57105851 | C | A | 20 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0200 others(17): Show |
20 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.-35-4857C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105851 | |||||||
| chr16:57105928 | C | T | 1 | a0001c0001t0002g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-35-4780C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105928 | |||||||
| chr16:57105944 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-35-4764C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57105944 | |||||||
| chr16:57106180 | T | C | 1 | a0001c0001t0001g0334 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-35-4528T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106180 | |||||||
| chr16:57106230 | C | G | 100 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0019 others(97): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.-35-4478C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106230 | |||||||
| chr16:57106270 | G | A | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(16): Show |
20 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35-4438G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106270 | |||||||
| chr16:57106277 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-35-4431T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106277 | |||||||
| chr16:57106345 | C | T | 10 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-4363C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106345 | |||||||
| chr16:57106526 | G | T | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0091 others(54): Show |
61 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(58): Show |
intron_variant | MODIFIER | c.-35-4182G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106526 | |||||||
| chr16:57106550 | G | A | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02630.hp1 HG02965.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-4158G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106550 | |||||||
| chr16:57106611 | AGAAGAGA others(81): Show |
A | 1 | a0001c0001t0001g0296 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-35-4095_-35-4008d others(90): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57106611 | ||||||
| chr16:57106858 | C | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0018 |
2 | HG01891.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-35-3850C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106858 | |||||||
| chr16:57106864 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-35-3844C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106864 | |||||||
| chr16:57106872 | C | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0334 others(11): Show |
18 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.-35-3836C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57106872 | |||||||
| chr16:57107155 | C | T | 3 | a0002c0004t0001g0039 a0002c0004t0001g0040 a0002c0004t0001g0162 |
3 | HG02622.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-35-3553C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107155 | |||||||
| chr16:57107207 | A | G | 19 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(16): Show |
20 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(17): Show |
intron_variant | MODIFIER | c.-35-3501A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107207 | |||||||
| chr16:57107310 | A | G | 38 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0166 others(35): Show |
39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-3398A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107310 | |||||||
| chr16:57107341 | G | A | 20 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0200 others(17): Show |
20 | HG00099.hp2 HG00323.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.-35-3367G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107341 | |||||||
| chr16:57107399 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(167): Show |
181 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.-35-3309A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107399 | |||||||
| chr16:57107754 | A | C | 71 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(68): Show |
73 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.-35-2954A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107754 | |||||||
| chr16:57107847 | G | A | 1 | a0001c0001t0001g0019 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-35-2861G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107847 | |||||||
| chr16:57107865 | C | CT | 35 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0122 others(32): Show |
35 | HG00597.hp2 HG01884.hp1 HG02071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-35-2820dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57107865 | ||||||
| chr16:57107865 | CT | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(129): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-35-2820delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57107865 | ||||||
| chr16:57107914 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-35-2794A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107914 | |||||||
| chr16:57107948 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0103 others(1): Show |
4 | HG02257.hp2 HG02647.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-35-2760G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107948 | |||||||
| chr16:57107961 | C | G | 10 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
10 | HG02145.hp1 HG02258.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-2747C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107961 | |||||||
| chr16:57107964 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0003g0102 |
2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-35-2744G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57107964 | |||||||
| chr16:57108241 | A | C | 3 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0336 |
3 | HG02055.hp1 HG02280.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-35-2467A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108241 | |||||||
| chr16:57108337 | C | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-35-2371C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108337 | |||||||
| chr16:57108405 | C | A | 1 | a0001c0001t0001g0289 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-35-2303C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108405 | |||||||
| chr16:57108991 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-35-1717T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57108991 | |||||||
| chr16:57109041 | T | C | 2 | a0001c0001t0001g0037 a0001c0001t0005g0038 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-35-1667T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109041 | |||||||
| chr16:57109115 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
2 | HG02257.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-35-1593G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109115 | |||||||
| chr16:57109201 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-35-1507G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109201 | |||||||
| chr16:57109265 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-35-1443C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109265 | |||||||
| chr16:57109310 | T | TA | 21 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(18): Show |
22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35-1397dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57109310 | ||||||
| chr16:57109312 | C | G | 21 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(18): Show |
22 | HG00408.hp1 HG02015.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.-35-1396C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109312 | |||||||
| chr16:57109470 | T | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(234): Show |
249 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.-35-1238T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109470 | |||||||
| chr16:57109475 | C | CA | 49 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0042 others(46): Show |
50 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(47): Show |
intron_variant | MODIFIER | c.-35-1217dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57109475 | ||||||
| chr16:57109475 | C | CAA | 14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0047 others(11): Show |
18 | HG00438.hp1 HG02738.hp1 NA18945.hp2 others(15): Show |
intron_variant | MODIFIER | c.-35-1218_-35-1217d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57109475 | ||||||
| chr16:57109505 | T | C | 15 | a0001c0001t0001g0099 a0001c0001t0001g0107 a0001c0001t0001g0108 others(12): Show |
15 | HG00621.hp2 HG01123.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.-35-1203T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109505 | |||||||
| chr16:57109518 | A | G | 38 | a0001c0001t0001g0049 a0001c0001t0001g0163 a0001c0001t0001g0166 others(35): Show |
39 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.-35-1190A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109518 | |||||||
| chr16:57109703 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-35-1005C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109703 | |||||||
| chr16:57109868 | G | A | 2 | a0001c0003t0001g0014 a0001c0003t0001g0333 |
3 | HG02886.hp1 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-35-840G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109868 | |||||||
| chr16:57109983 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-35-725T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57109983 | |||||||
| chr16:57110224 | C | CTTT | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0334 others(5): Show |
10 | HG02055.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.-35-468_-35-466dup others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57110224 | ||||||
| chr16:57110224 | CT | C | 36 | a0001c0001t0001g0071 a0001c0001t0001g0075 a0001c0001t0001g0091 others(33): Show |
36 | HG01123.hp1 HG01175.hp2 HG01255.hp1 others(33): Show |
intron_variant | MODIFIER | c.-35-466delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57110224 | ||||||
| chr16:57110224 | CTT | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.-35-467_-35-466del others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr16 | 57110224 | ||||||
| chr16:57110274 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-35-434G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110274 | |||||||
| chr16:57110492 | A | C | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-35-216A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110492 | |||||||
| chr16:57110508 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-35-200G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110508 | |||||||
| chr16:57110569 | T | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-35-139T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 1/15 | chr16 | 57110569 | |||||||
| chr16:57110945 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.180+23C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57110945 | |||||||
| chr16:57111008 | T | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+86T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111008 | |||||||
| chr16:57111009 | G | C | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+87G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111009 | |||||||
| chr16:57111113 | TG | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+192delG | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111113 | |||||||
| chr16:57111139 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.180+217C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111139 | |||||||
| chr16:57111182 | C | CT | 48 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(45): Show |
53 | HG00323.hp2 HG00597.hp2 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.180+274dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 57111182 | ||||||
| chr16:57111182 | CT | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.180+274delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr16 | 57111182 | ||||||
| chr16:57111228 | G | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0103 others(4): Show |
7 | HG01891.hp1 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+306G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111228 | |||||||
| chr16:57111304 | T | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(221): Show |
233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.180+382T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111304 | |||||||
| chr16:57111419 | C | A | 21 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0085 others(18): Show |
22 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.180+497C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111419 | |||||||
| chr16:57111428 | T | G | 2 | a0001c0001t0001g0074 a0001c0001t0001g0193 |
2 | NA19057.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.180+506T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111428 | |||||||
| chr16:57111439 | A | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(11): Show |
14 | HG00408.hp1 HG02056.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.180+517A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111439 | |||||||
| chr16:57111464 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.180+542C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111464 | |||||||
| chr16:57111526 | G | A | 2 | a0001c0005t0001g0007 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.180+604G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111526 | |||||||
| chr16:57111590 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.180+668G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111590 | |||||||
| chr16:57111992 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0003g0102 |
2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.180+1070G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57111992 | |||||||
| chr16:57112113 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.181-1175A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112113 | |||||||
| chr16:57112377 | C | A | 43 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0049 others(40): Show |
44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.181-911C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112377 | |||||||
| chr16:57112379 | G | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
191 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.181-909G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112379 | |||||||
| chr16:57112490 | C | T | 104 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0049 others(101): Show |
105 | HG00099.hp2 HG00544.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.181-798C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112490 | |||||||
| chr16:57112692 | A | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.181-596A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112692 | |||||||
| chr16:57112744 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
236 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.181-544T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112744 | |||||||
| chr16:57112768 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
194 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.181-520G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112768 | |||||||
| chr16:57112789 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
170 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.181-499G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112789 | |||||||
| chr16:57112879 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0101 a0001c0001t0001g0201 |
3 | HG02895.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.181-409C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112879 | |||||||
| chr16:57112942 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.181-346C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112942 | |||||||
| chr16:57112965 | G | C | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.181-323G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112965 | |||||||
| chr16:57112985 | C | T | 43 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0049 others(40): Show |
44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.181-303C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57112985 | |||||||
| chr16:57113225 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.181-63A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 2/15 | chr16 | 57113225 | |||||||
| chr16:57113476 | G | T | 80 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(77): Show |
84 | HG00408.hp1 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.360+9G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113476 | |||||||
| chr16:57113479 | C | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.360+12C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113479 | |||||||
| chr16:57113536 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.360+69C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113536 | |||||||
| chr16:57113580 | G | A | 1 | a0001c0002t0001g0060 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.360+113G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113580 | |||||||
| chr16:57113610 | C | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
56 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.360+143C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113610 | |||||||
| chr16:57113714 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(174): Show |
186 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.360+247A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113714 | |||||||
| chr16:57113735 | C | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.360+268C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113735 | |||||||
| chr16:57113776 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+309C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113776 | |||||||
| chr16:57113862 | G | T | 9 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0243 others(6): Show |
9 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.360+395G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113862 | |||||||
| chr16:57113940 | T | G | 40 | a0001c0001t0001g0071 a0001c0001t0001g0091 a0001c0001t0001g0092 others(37): Show |
40 | HG00099.hp2 HG01123.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.360+473T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57113940 | |||||||
| chr16:57114019 | C | CT | 3 | a0001c0001t0001g0305 a0001c0001t0001g0339 a0001c0001t0003g0320 |
3 | HG03195.hp2 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.360+553dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114019 | ||||||
| chr16:57114033 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+566T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114033 | |||||||
| chr16:57114041 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+574A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114041 | |||||||
| chr16:57114143 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.360+676G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114143 | |||||||
| chr16:57114182 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.360+715G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114182 | |||||||
| chr16:57114393 | G | C | 1 | a0001c0001t0002g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.360+926G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114393 | |||||||
| chr16:57114437 | CG | C | 15 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0161 others(12): Show |
15 | HG00099.hp2 HG02055.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.360+975delG | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114437 | ||||||
| chr16:57114444 | C | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0002t0001g0069 |
3 | HG00609.hp1 NA19088.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.360+977C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114444 | |||||||
| chr16:57114457 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.360+990G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114457 | |||||||
| chr16:57114536 | C | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.361-940C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114536 | |||||||
| chr16:57114538 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-938C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114538 | |||||||
| chr16:57114570 | C | T | 43 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0049 others(40): Show |
44 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.361-906C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114570 | |||||||
| chr16:57114573 | C | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-903C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114573 | |||||||
| chr16:57114641 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.361-835G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114641 | |||||||
| chr16:57114661 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.361-815G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114661 | |||||||
| chr16:57114775 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-701A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114775 | |||||||
| chr16:57114789 | T | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-687T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114789 | |||||||
| chr16:57114803 | A | AATAG | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-671_361-668dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114803 | ||||||
| chr16:57114878 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.361-598G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114878 | |||||||
| chr16:57114907 | A | G | 107 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.361-569A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114907 | |||||||
| chr16:57114934 | C | CA | 61 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0024 others(58): Show |
64 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.361-516dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114934 | C | CAA | 18 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0049 others(15): Show |
18 | HG00544.hp2 HG01891.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.361-517_361-516dup others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114934 | C | CAAA | 11 | a0001c0001t0001g0037 a0001c0001t0001g0059 a0001c0001t0001g0105 others(8): Show |
11 | HG02559.hp2 HG02895.hp2 HG03486.hp1 others(8): Show |
intron_variant | MODIFIER | c.361-518_361-516dup others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114934 | C | CAAAA | 35 | a0001c0001t0001g0013 a0001c0001t0001g0084 a0001c0001t0001g0085 others(32): Show |
36 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.361-519_361-516dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114934 | C | CAAAAA | 17 | a0001c0001t0001g0071 a0001c0001t0001g0092 a0001c0001t0001g0094 others(14): Show |
17 | HG00280.hp2 HG00735.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.361-520_361-516dup others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114934 | C | CAAAAAA | 38 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0041 others(35): Show |
40 | HG00408.hp2 HG00544.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.361-521_361-516dup others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114934 | C | CAAAAAAA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0055 others(16): Show |
22 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.361-522_361-516dup others(7): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114934 | C | CCAA | 19 | a0001c0001t0001g0099 a0001c0001t0001g0110 a0001c0001t0001g0111 others(16): Show |
19 | HG00099.hp2 HG01255.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.361-542_361-541ins others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114934 | |||||||
| chr16:57114934 | C | CCAAA | 7 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0143 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.361-542_361-541ins others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114934 | |||||||
| chr16:57114934 | CA | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0118 a0001c0001t0001g0119 others(7): Show |
11 | HG00597.hp2 HG01070.hp2 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-516delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr16 | 57114934 | ||||||
| chr16:57114935 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.361-541A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114935 | |||||||
| chr16:57114968 | G | A | 11 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0024 others(8): Show |
11 | HG00408.hp1 HG02056.hp1 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.361-508G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57114968 | |||||||
| chr16:57115002 | G | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.361-474G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115002 | |||||||
| chr16:57115005 | G | T | 1 | a0001c0001t0001g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.361-471G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115005 | |||||||
| chr16:57115015 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.361-461G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115015 | |||||||
| chr16:57115046 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.361-430G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115046 | |||||||
| chr16:57115115 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.361-361A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115115 | |||||||
| chr16:57115262 | C | T | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(103): Show |
112 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.361-214C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115262 | |||||||
| chr16:57115335 | G | A | 5 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(2): Show |
5 | HG02723.hp2 HG03471.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.361-141G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115335 | |||||||
| chr16:57115370 | G | A | 3 | a0002c0004t0001g0039 a0002c0004t0001g0040 a0002c0004t0001g0162 |
3 | HG02622.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.361-106G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115370 | |||||||
| chr16:57115406 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01069.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.361-70G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 3/15 | chr16 | 57115406 | |||||||
| chr16:57115729 | G | A | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 |
3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.435+179G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57115729 | |||||||
| chr16:57115733 | C | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
57 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.435+183C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57115733 | |||||||
| chr16:57115802 | C | T | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.435+252C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57115802 | |||||||
| chr16:57116066 | C | T | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.435+516C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116066 | |||||||
| chr16:57116108 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.435+558C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116108 | |||||||
| chr16:57116279 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0334 a0001c0001t0001g0335 others(2): Show |
6 | HG02055.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.435+729C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116279 | |||||||
| chr16:57116337 | G | A | 41 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0049 others(38): Show |
42 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.435+787G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116337 | |||||||
| chr16:57116498 | G | A | 2 | a0002c0004t0001g0039 a0002c0004t0001g0040 |
2 | HG02622.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.435+948G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116498 | |||||||
| chr16:57116501 | A | G | 1 | a0001c0002t0001g0186 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.435+951A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116501 | |||||||
| chr16:57116580 | C | T | 1 | a0001c0002t0001g0138 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.436-916C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116580 | |||||||
| chr16:57116594 | C | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(98): Show |
110 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.436-902C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116594 | |||||||
| chr16:57116661 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.436-835C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116661 | |||||||
| chr16:57116765 | G | A | 2 | a0001c0002t0001g0172 a0001c0002t0001g0180 |
2 | HG00558.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.436-731G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116765 | |||||||
| chr16:57116852 | G | GAGGCCCC others(6): Show |
1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.436-633_436-621dup others(13): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr16 | 57116852 | ||||||
| chr16:57116897 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.436-599G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116897 | |||||||
| chr16:57116935 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0160 a0001c0001t0001g0334 others(2): Show |
6 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.436-561T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116935 | |||||||
| chr16:57116975 | G | A | 2 | a0001c0001t0001g0303 a0001c0001t0002g0098 |
2 | HG01884.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.436-521G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57116975 | |||||||
| chr16:57117031 | T | G | 5 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG00639.hp1 HG01074.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.436-465T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117031 | |||||||
| chr16:57117194 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0001g0270 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.436-302G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117194 | |||||||
| chr16:57117263 | A | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
63 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.436-233A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117263 | |||||||
| chr16:57117314 | G | C | 4 | a0001c0001t0001g0037 a0001c0001t0001g0150 a0001c0001t0005g0038 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.436-182G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117314 | |||||||
| chr16:57117472 | G | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0071 a0001c0001t0001g0232 others(4): Show |
8 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.436-24G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 4/15 | chr16 | 57117472 | |||||||
| chr16:57117630 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.507+63G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117630 | |||||||
| chr16:57117647 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.507+80C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117647 | |||||||
| chr16:57117704 | G | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0201 a0001c0001t0002g0321 others(2): Show |
5 | HG02647.hp1 HG02717.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.507+137G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117704 | |||||||
| chr16:57117884 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(200): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.507+317C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117884 | |||||||
| chr16:57117885 | G | A | 13 | a0001c0001t0001g0037 a0001c0001t0001g0103 a0001c0001t0001g0150 others(10): Show |
14 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.507+318G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117885 | |||||||
| chr16:57117942 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.507+375C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57117942 | |||||||
| chr16:57118082 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0150 a0001c0001t0005g0038 others(3): Show |
7 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+515G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118082 | |||||||
| chr16:57118129 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.507+562G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118129 | |||||||
| chr16:57118142 | T | C | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.507+575T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118142 | |||||||
| chr16:57118167 | C | CT | 15 | a0001c0001t0001g0059 a0001c0001t0001g0074 a0001c0001t0001g0105 others(12): Show |
15 | NA18944.hp1 NA18955.hp1 NA18969.hp2 others(12): Show |
intron_variant | MODIFIER | c.507+616dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118167 | ||||||
| chr16:57118167 | CT | C | 59 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(56): Show |
61 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.507+616delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118167 | ||||||
| chr16:57118250 | C | G | 28 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0166 others(25): Show |
29 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(26): Show |
intron_variant | MODIFIER | c.507+683C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118250 | |||||||
| chr16:57118311 | G | A | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
223 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.507+744G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118311 | |||||||
| chr16:57118322 | C | T | 6 | a0001c0001t0001g0290 a0001c0001t0001g0305 a0001c0001t0001g0339 others(3): Show |
6 | HG02647.hp1 HG02717.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+755C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118322 | |||||||
| chr16:57118332 | A | ATT | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
61 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.507+778_507+779dup others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | ||||||
| chr16:57118332 | A | ATTT | 7 | a0001c0001t0001g0095 a0001c0001t0001g0125 a0001c0001t0001g0247 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+777_507+779dup others(3): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | ||||||
| chr16:57118332 | A | ATTTT | 133 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(130): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.507+776_507+779dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | ||||||
| chr16:57118332 | A | ATTTTT | 6 | a0001c0001t0001g0011 a0001c0001t0001g0121 a0001c0001t0001g0182 others(3): Show |
7 | HG01099.hp1 HG01109.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.507+775_507+779dup others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | ||||||
| chr16:57118332 | AT | A | 55 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(52): Show |
57 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.507+779delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118332 | ||||||
| chr16:57118524 | A | C | 10 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0243 others(7): Show |
10 | HG00280.hp2 HG00735.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.508-671A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118524 | |||||||
| chr16:57118564 | C | A | 7 | a0001c0001t0001g0095 a0001c0001t0001g0205 a0001c0001t0001g0247 others(4): Show |
7 | HG02109.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-631C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118564 | |||||||
| chr16:57118648 | A | AGATG | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.508-507_508-504dup others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | ||||||
| chr16:57118648 | A | AGATGGAT others(1): Show |
24 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0068 others(21): Show |
26 | HG00280.hp2 HG00544.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.508-511_508-504dup others(8): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | ||||||
| chr16:57118648 | A | AGATGGAT others(5): Show |
1 | a0001c0001t0001g0308 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.508-515_508-504dup others(12): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | ||||||
| chr16:57118648 | AGATGGAT others(5): Show |
A | 2 | a0001c0001t0001g0127 a0001c0001t0001g0157 |
2 | HG02723.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.508-515_508-504del others(12): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118648 | ||||||
| chr16:57118668 | GGATGGAT others(17): Show |
G | 1 | a0001c0002t0001g0021 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.508-523_508-500del others(24): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118668 | ||||||
| chr16:57118688 | G | GGATGGAT others(1): Show |
3 | a0001c0001t0001g0206 a0001c0001t0001g0218 a0001c0001t0001g0291 |
3 | HG00323.hp1 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.508-504_508-503ins others(8): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118688 | ||||||
| chr16:57118688 | GGATA | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0150 a0001c0001t0005g0038 others(1): Show |
4 | HG02559.hp2 HG02809.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.508-488_508-485del others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr16 | 57118688 | ||||||
| chr16:57118692 | A | G | 51 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0023 others(48): Show |
53 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.508-503A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118692 | |||||||
| chr16:57118696 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0150 a0001c0001t0005g0038 others(3): Show |
7 | HG02559.hp2 HG02572.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.508-499A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118696 | |||||||
| chr16:57118720 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.508-475A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118720 | |||||||
| chr16:57118894 | C | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
62 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.508-301C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118894 | |||||||
| chr16:57118900 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0218 |
2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.508-295A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118900 | |||||||
| chr16:57118958 | G | T | 2 | a0001c0001t0001g0096 a0001c0001t0002g0153 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.508-237G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57118958 | |||||||
| chr16:57119020 | A | G | 2 | a0001c0001t0001g0096 a0001c0001t0002g0153 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.508-175A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57119020 | |||||||
| chr16:57119107 | G | A | 34 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0166 others(31): Show |
35 | HG00558.hp2 HG00673.hp1 HG01515.hp1 others(32): Show |
intron_variant | MODIFIER | c.508-88G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 5/15 | chr16 | 57119107 | |||||||
| chr16:57119491 | T | C | 1 | a0001c0001t0002g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.592-70T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 6/15 | chr16 | 57119491 | |||||||
| chr16:57119529 | C | G | 57 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
62 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.592-32C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 6/15 | chr16 | 57119529 | |||||||
| chr16:57119655 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG01099.hp1 | splice_region_variant&intron_variant | LOW | c.681+5G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57119655 | |||||||
| chr16:57119952 | A | T | 4 | a0001c0001t0001g0155 a0001c0001t0001g0201 a0001c0001t0002g0123 others(1): Show |
4 | HG02895.hp1 HG03041.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+302A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57119952 | |||||||
| chr16:57120005 | TCTCATGC others(295): Show |
T | 1 | a0001c0001t0001g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.681+388_681+689del | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120005 | ||||||
| chr16:57120195 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.681+545T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120195 | |||||||
| chr16:57120244 | A | C | 1 | a0001c0002t0001g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.681+594A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120244 | |||||||
| chr16:57120270 | C | CA | 48 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0094 others(45): Show |
49 | HG00558.hp2 HG00673.hp1 HG01175.hp2 others(46): Show |
intron_variant | MODIFIER | c.681+636dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120270 | ||||||
| chr16:57120286 | A | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
89 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.681+636A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120286 | |||||||
| chr16:57120297 | G | T | 139 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(136): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.681+647G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120297 | |||||||
| chr16:57120378 | C | T | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.682-715C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120378 | |||||||
| chr16:57120439 | CA | C | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(198): Show |
215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.682-639delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120439 | ||||||
| chr16:57120439 | CAA | C | 7 | a0001c0001t0001g0066 a0001c0001t0001g0091 a0001c0001t0001g0092 others(4): Show |
7 | HG00408.hp2 HG01243.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-640_682-639del others(2): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr16 | 57120439 | ||||||
| chr16:57120635 | A | C | 307 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(304): Show |
325 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.682-458A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120635 | |||||||
| chr16:57120635 | A | T | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.682-458A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120635 | |||||||
| chr16:57120774 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.682-319G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57120774 | |||||||
| chr16:57121075 | G | C | 2 | a0001c0001t0003g0102 a0002c0004t0001g0162 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.682-18G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 7/15 | chr16 | 57121075 | |||||||
| chr16:57121286 | C | T | 4 | a0001c0001t0001g0290 a0001c0001t0001g0305 a0001c0001t0001g0339 others(1): Show |
4 | HG03139.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.780+95C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121286 | |||||||
| chr16:57121484 | G | A | 137 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(134): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.781-190G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121484 | |||||||
| chr16:57121545 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(199): Show |
214 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.781-129T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121545 | |||||||
| chr16:57121566 | C | T | 1 | a0001c0001t0001g0016 | 2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.781-108C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121566 | |||||||
| chr16:57121649 | T | C | 1 | a0001c0001t0001g0323 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.781-25T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 8/15 | chr16 | 57121649 | |||||||
| chr16:57121770 | C | G | 1 | a0001c0001t0001g0282 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.867+10C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121770 | |||||||
| chr16:57121782 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.867+22C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121782 | |||||||
| chr16:57121783 | G | A | 4 | a0001c0001t0001g0290 a0001c0001t0001g0305 a0001c0001t0001g0339 others(1): Show |
4 | HG03139.hp1 HG03195.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.867+23G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121783 | |||||||
| chr16:57121888 | T | A | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.867+128T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57121888 | |||||||
| chr16:57122023 | C | T | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.867+263C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122023 | |||||||
| chr16:57122056 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.867+296A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122056 | |||||||
| chr16:57122083 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(194): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.867+323G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122083 | |||||||
| chr16:57122165 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.867+405G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122165 | |||||||
| chr16:57122417 | A | G | 2 | a0001c0001t0001g0246 a0001c0001t0001g0250 |
2 | HG03209.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.867+657A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122417 | |||||||
| chr16:57122454 | A | G | 9 | a0001c0001t0001g0103 a0001c0001t0001g0290 a0001c0001t0001g0305 others(6): Show |
9 | HG02647.hp1 HG02717.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.867+694A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122454 | |||||||
| chr16:57122546 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.867+786C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122546 | |||||||
| chr16:57122593 | T | C | 3 | a0001c0001t0001g0103 a0001c0001t0001g0313 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.868-821T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122593 | |||||||
| chr16:57122797 | C | T | 4 | a0001c0001t0001g0200 a0001c0001t0001g0214 a0001c0001t0001g0215 others(1): Show |
4 | HG00323.hp2 HG00738.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-617C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122797 | |||||||
| chr16:57122887 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.868-527C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57122887 | |||||||
| chr16:57122905 | CT | C | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(197): Show |
212 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.868-494delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr16 | 57122905 | ||||||
| chr16:57123119 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.868-295T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123119 | |||||||
| chr16:57123123 | G | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(189): Show |
203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.868-291G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123123 | |||||||
| chr16:57123133 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.868-281G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123133 | |||||||
| chr16:57123137 | G | T | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.868-277G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123137 | |||||||
| chr16:57123258 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.868-156A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123258 | |||||||
| chr16:57123294 | C | T | 132 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(129): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.868-120C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123294 | |||||||
| chr16:57123297 | A | G | 3 | a0001c0005t0001g0007 a0001c0007t0001g0090 a0001c0007t0001g0302 |
4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.868-117A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123297 | |||||||
| chr16:57123346 | G | A | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.868-68G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 9/15 | chr16 | 57123346 | |||||||
| chr16:57123488 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.927+15G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123488 | |||||||
| chr16:57123524 | C | G | 3 | a0001c0001t0001g0103 a0001c0001t0001g0313 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.927+51C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123524 | |||||||
| chr16:57123529 | T | G | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.927+56T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123529 | |||||||
| chr16:57123592 | G | T | 1 | a0001c0001t0001g0016 | 2 | HG02258.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.927+119G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123592 | |||||||
| chr16:57123674 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.927+201A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57123674 | |||||||
| chr16:57123917 | TC | T | 53 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0023 others(50): Show |
55 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.927+447delC | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57123917 | ||||||
| chr16:57124063 | CTTTCT | C | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0103 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.927+614_927+618del others(5): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124063 | ||||||
| chr16:57124063 | CTTTCTTT others(8): Show |
C | 1 | a0001c0001t0001g0262 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.927+604_927+618del others(15): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124063 | ||||||
| chr16:57124082 | CTTTTCTT others(3): Show |
C | 34 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(31): Show |
36 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.927+614_927+623del others(10): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124082 | ||||||
| chr16:57124087 | C | CT | 11 | a0001c0001t0001g0075 a0001c0001t0001g0146 a0001c0001t0001g0147 others(8): Show |
11 | HG02451.hp2 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.927+626dupT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr16 | 57124087 | ||||||
| chr16:57124108 | G | T | 2 | a0001c0001t0001g0037 a0001c0001t0005g0038 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.927+635G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124108 | |||||||
| chr16:57124122 | C | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(31): Show |
36 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.927+649C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124122 | |||||||
| chr16:57124200 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.927+727G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124200 | |||||||
| chr16:57124438 | C | T | 1 | a0001c0001t0001g0314 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.927+965C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124438 | |||||||
| chr16:57124440 | C | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0200 a0001c0001t0001g0214 others(11): Show |
16 | HG00323.hp2 HG01515.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.927+967C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124440 | |||||||
| chr16:57124552 | A | C | 1 | a0001c0001t0002g0322 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.927+1079A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124552 | |||||||
| chr16:57124716 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.928-1144A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124716 | |||||||
| chr16:57124767 | G | A | 224 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(221): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.928-1093G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124767 | |||||||
| chr16:57124935 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.928-925C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124935 | |||||||
| chr16:57124960 | C | T | 17 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0094 others(14): Show |
17 | HG00280.hp1 HG00280.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.928-900C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124960 | |||||||
| chr16:57124995 | C | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(175): Show |
187 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.928-865C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57124995 | |||||||
| chr16:57125055 | C | G | 1 | a0001c0002t0001g0191 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.928-805C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125055 | |||||||
| chr16:57125321 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.928-539A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125321 | |||||||
| chr16:57125336 | C | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.928-524C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125336 | |||||||
| chr16:57125490 | A | G | 226 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(223): Show |
238 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.928-370A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125490 | |||||||
| chr16:57125613 | G | T | 3 | a0001c0005t0001g0007 a0001c0007t0001g0090 a0001c0007t0001g0302 |
4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.928-247G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125613 | |||||||
| chr16:57125633 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0002g0153 |
2 | HG02258.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.928-227C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125633 | |||||||
| chr16:57125663 | A | C | 1 | a0001c0001t0001g0237 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.928-197A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125663 | |||||||
| chr16:57125777 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0307 |
3 | HG03490.hp2 HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.928-83A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 10/15 | chr16 | 57125777 | |||||||
| chr16:57126114 | T | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(39): Show |
44 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.1061+121T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126114 | |||||||
| chr16:57126180 | C | G | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1061+187C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126180 | |||||||
| chr16:57126205 | A | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0200 a0001c0001t0001g0214 others(10): Show |
15 | HG00323.hp2 HG01515.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1061+212A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126205 | |||||||
| chr16:57126277 | A | G | 1 | a0002c0004t0001g0162 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1061+284A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126277 | |||||||
| chr16:57126326 | G | A | 10 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0111 others(7): Show |
10 | HG01123.hp1 HG01175.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.1061+333G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126326 | |||||||
| chr16:57126340 | G | T | 1 | a0001c0001t0001g0193 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1061+347G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126340 | |||||||
| chr16:57126427 | T | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(32): Show |
37 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1061+434T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126427 | |||||||
| chr16:57126502 | G | A | 8 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(5): Show |
8 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1061+509G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126502 | |||||||
| chr16:57126526 | T | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(162): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1061+533T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126526 | |||||||
| chr16:57126526 | T | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0200 a0001c0001t0001g0214 others(10): Show |
15 | HG00323.hp2 HG01515.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1061+533T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126526 | |||||||
| chr16:57126560 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0111 |
2 | HG01123.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.1061+567G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126560 | |||||||
| chr16:57126931 | C | G | 2 | a0001c0001t0001g0091 a0002c0004t0001g0040 |
2 | HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1062-918C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126931 | |||||||
| chr16:57126957 | C | G | 21 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0030 others(18): Show |
21 | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1062-892C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126957 | |||||||
| chr16:57126995 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1062-854C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57126995 | |||||||
| chr16:57127108 | C | T | 3 | a0001c0001t0001g0037 a0001c0001t0001g0088 a0001c0001t0005g0038 |
3 | HG02559.hp2 HG02809.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1062-741C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127108 | |||||||
| chr16:57127131 | C | T | 34 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(31): Show |
36 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.1062-718C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127131 | |||||||
| chr16:57127200 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1062-649G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127200 | |||||||
| chr16:57127348 | G | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0192 |
2 | NA18950.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.1062-501G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127348 | |||||||
| chr16:57127544 | G | C | 1 | a0001c0001t0001g0157 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1062-305G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127544 | |||||||
| chr16:57127592 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0143 a0001c0001t0001g0215 others(1): Show |
5 | HG00738.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062-257T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127592 | |||||||
| chr16:57127771 | G | C | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1062-78G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127771 | |||||||
| chr16:57127785 | G | GGTTCCTG others(35): Show |
2 | a0001c0001t0001g0037 a0001c0001t0005g0038 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1062-63_1062-62ins others(42): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr16 | 57127785 | ||||||
| chr16:57127796 | C | T | 2 | a0001c0001t0001g0290 a0001c0001t0002g0104 |
2 | HG02615.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1062-53C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 11/15 | chr16 | 57127796 | |||||||
| chr16:57127916 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0292 |
2 | HG00735.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1116+13G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57127916 | |||||||
| chr16:57128070 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1116+167C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128070 | |||||||
| chr16:57128341 | T | C | 2 | a0001c0002t0001g0198 a0001c0006t0001g0199 |
2 | NA18964.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1116+438T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128341 | |||||||
| chr16:57128378 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1116+475C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128378 | |||||||
| chr16:57128520 | A | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(240): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1116+617A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128520 | |||||||
| chr16:57128659 | G | A | 1 | a0001c0005t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1116+756G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128659 | |||||||
| chr16:57128744 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0008 others(195): Show |
208 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1116+841G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128744 | |||||||
| chr16:57128752 | T | C | 2 | a0001c0002t0001g0194 a0001c0002t0001g0293 |
2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1116+849T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128752 | |||||||
| chr16:57128769 | T | C | 43 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(40): Show |
45 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1116+866T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57128769 | |||||||
| chr16:57129005 | A | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0158 others(3): Show |
6 | HG02145.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+1102A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129005 | |||||||
| chr16:57129119 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0005g0038 |
2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1116+1216G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129119 | |||||||
| chr16:57129216 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1116+1313G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129216 | |||||||
| chr16:57129218 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1116+1315G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129218 | |||||||
| chr16:57129237 | A | C | 1 | a0001c0002t0001g0170 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1116+1334A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129237 | |||||||
| chr16:57129295 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0266 |
2 | HG01496.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.1116+1392C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129295 | |||||||
| chr16:57129306 | C | T | 2 | a0001c0002t0001g0228 a0001c0002t0001g0229 |
2 | NA18977.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1116+1403C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129306 | |||||||
| chr16:57129471 | G | A | 16 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0030 others(13): Show |
16 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1116+1568G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129471 | |||||||
| chr16:57129635 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(33): Show |
38 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1116+1732A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129635 | |||||||
| chr16:57129789 | A | G | 7 | a0001c0001t0001g0200 a0001c0001t0001g0214 a0001c0001t0001g0339 others(4): Show |
7 | HG00323.hp2 HG01515.hp1 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.1116+1886A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129789 | |||||||
| chr16:57129869 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1116+1966A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57129869 | |||||||
| chr16:57130127 | T | C | 35 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(32): Show |
37 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.1116+2224T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130127 | |||||||
| chr16:57130176 | C | T | 2 | a0001c0001t0003g0102 a0002c0004t0001g0162 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1116+2273C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130176 | |||||||
| chr16:57130269 | C | T | 16 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0030 others(13): Show |
16 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1116+2366C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130269 | |||||||
| chr16:57130342 | A | G | 9 | a0001c0001t0001g0070 a0001c0001t0001g0241 a0001c0001t0001g0256 others(6): Show |
9 | HG00438.hp2 HG00741.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1116+2439A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130342 | |||||||
| chr16:57130400 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0274 a0001c0001t0001g0275 |
3 | HG03017.hp1 HG03688.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1116+2497A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130400 | |||||||
| chr16:57130431 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1116+2528C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130431 | |||||||
| chr16:57130432 | G | A | 1 | a0001c0001t0002g0321 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1116+2529G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130432 | |||||||
| chr16:57130445 | G | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0284 others(5): Show |
9 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1116+2542G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130445 | |||||||
| chr16:57130566 | A | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0158 others(3): Show |
6 | HG02145.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+2663A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130566 | |||||||
| chr16:57130616 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0002t0001g0198 others(1): Show |
4 | HG00673.hp1 HG02056.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+2713C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130616 | |||||||
| chr16:57130699 | G | A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0254 a0001c0001t0001g0255 |
3 | NA18949.hp2 NA18979.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1116+2796G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130699 | |||||||
| chr16:57130967 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1116+3064C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130967 | |||||||
| chr16:57130968 | G | A | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0303 |
3 | HG01123.hp2 HG02280.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1116+3065G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57130968 | |||||||
| chr16:57131051 | A | G | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(250): Show |
265 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.1116+3148A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131051 | |||||||
| chr16:57131089 | A | C | 3 | a0001c0005t0001g0007 a0001c0007t0001g0090 a0001c0007t0001g0302 |
4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1116+3186A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131089 | |||||||
| chr16:57131148 | T | A | 252 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(249): Show |
264 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1116+3245T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131148 | |||||||
| chr16:57131151 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1116+3248G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131151 | |||||||
| chr16:57131257 | C | A | 6 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0158 others(3): Show |
6 | HG02145.hp1 HG02630.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1116+3354C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131257 | |||||||
| chr16:57131469 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1117-3306G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131469 | |||||||
| chr16:57131470 | G | T | 1 | a0001c0002t0001g0263 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1117-3305G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131470 | |||||||
| chr16:57131617 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1117-3158G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131617 | |||||||
| chr16:57131633 | C | T | 15 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0030 others(12): Show |
15 | HG02109.hp2 HG02257.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1117-3142C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131633 | |||||||
| chr16:57131711 | C | T | 16 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0030 others(13): Show |
16 | HG02109.hp2 HG02257.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.1117-3064C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131711 | |||||||
| chr16:57131725 | C | T | 2 | a0001c0001t0001g0339 a0001c0001t0002g0286 |
2 | HG02572.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1117-3050C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131725 | |||||||
| chr16:57131836 | G | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0023 others(50): Show |
55 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1117-2939G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57131836 | |||||||
| chr16:57132066 | G | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0023 others(50): Show |
55 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1117-2709G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132066 | |||||||
| chr16:57132275 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1117-2500G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132275 | |||||||
| chr16:57132306 | C | G | 1 | a0001c0002t0001g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1117-2469C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132306 | |||||||
| chr16:57132315 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1117-2460G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132315 | |||||||
| chr16:57132317 | G | C | 39 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(36): Show |
42 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1117-2458G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132317 | |||||||
| chr16:57132334 | T | A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(36): Show |
42 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.1117-2441T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132334 | |||||||
| chr16:57132626 | A | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(40): Show |
45 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1117-2149A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132626 | |||||||
| chr16:57132864 | C | T | 1 | a0001c0002t0001g0288 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1117-1911C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132864 | |||||||
| chr16:57132869 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1117-1906G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132869 | |||||||
| chr16:57132869 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1117-1906G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132869 | |||||||
| chr16:57132991 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1117-1784A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132991 | |||||||
| chr16:57132992 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1117-1783T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132992 | |||||||
| chr16:57132993 | C | A | 1 | a0001c0001t0001g0100 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1117-1782C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57132993 | |||||||
| chr16:57133000 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1117-1775G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133000 | |||||||
| chr16:57133073 | T | C | 7 | a0001c0001t0001g0200 a0001c0001t0001g0214 a0001c0001t0001g0339 others(4): Show |
7 | HG00280.hp2 HG00323.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1117-1702T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133073 | |||||||
| chr16:57133104 | C | A | 1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1117-1671C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133104 | |||||||
| chr16:57133268 | C | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(33): Show |
38 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.1117-1507C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133268 | |||||||
| chr16:57133318 | G | A | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.1117-1457G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133318 | |||||||
| chr16:57133465 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0214 |
2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1117-1310C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133465 | |||||||
| chr16:57133567 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1117-1208C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133567 | |||||||
| chr16:57133706 | C | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0029 others(41): Show |
47 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1117-1069C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133706 | |||||||
| chr16:57133755 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1117-1020G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133755 | |||||||
| chr16:57133889 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1117-886C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133889 | |||||||
| chr16:57133890 | G | A | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1117-885G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133890 | |||||||
| chr16:57133992 | G | A | 1 | a0001c0002t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1117-783G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57133992 | |||||||
| chr16:57134047 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1117-728G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134047 | |||||||
| chr16:57134102 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1117-673A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134102 | |||||||
| chr16:57134125 | C | G | 1 | a0001c0001t0001g0169 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1117-650C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134125 | |||||||
| chr16:57134260 | C | G | 3 | a0001c0001t0001g0305 a0001c0001t0002g0123 a0001c0001t0002g0271 |
3 | HG02145.hp2 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1117-515C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134260 | |||||||
| chr16:57134320 | A | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(165): Show |
180 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.1117-455A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134320 | |||||||
| chr16:57134385 | G | A | 1 | a0001c0002t0004g0058 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1117-390G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134385 | |||||||
| chr16:57134422 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1117-353G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134422 | |||||||
| chr16:57134523 | A | G | 43 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0029 others(40): Show |
46 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.1117-252A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134523 | |||||||
| chr16:57134544 | G | A | 3 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0265 |
3 | HG00438.hp2 NA19067.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1117-231G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134544 | |||||||
| chr16:57134629 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1117-146G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134629 | |||||||
| chr16:57134654 | G | A | 1 | a0001c0005t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1117-121G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134654 | |||||||
| chr16:57134710 | G | A | 1 | a0001c0001t0001g0304 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1117-65G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134710 | |||||||
| chr16:57134739 | G | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0029 others(41): Show |
47 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.1117-36G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 12/15 | chr16 | 57134739 | |||||||
| chr16:57134945 | T | C | 4 | a0001c0001t0001g0305 a0001c0001t0002g0123 a0001c0001t0002g0271 others(1): Show |
4 | HG02145.hp2 HG02572.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168+119T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57134945 | |||||||
| chr16:57134951 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1168+125T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57134951 | |||||||
| chr16:57135239 | T | C | 1 | a0001c0001t0001g0325 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1168+413T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135239 | |||||||
| chr16:57135280 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
158 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1168+455delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135280 | |||||||
| chr16:57135373 | A | G | 1 | a0001c0002t0001g0222 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1168+547A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135373 | |||||||
| chr16:57135395 | G | A | 2 | a0001c0002t0001g0196 a0001c0002t0001g0293 |
2 | HG03831.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1168+569G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135395 | |||||||
| chr16:57135574 | G | A | 1 | a0001c0003t0001g0333 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1168+748G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135574 | |||||||
| chr16:57135646 | G | A | 2 | a0001c0001t0001g0101 a0001c0001t0001g0335 |
2 | HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1168+820G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135646 | |||||||
| chr16:57135661 | G | A | 3 | a0001c0005t0001g0007 a0001c0007t0001g0090 a0001c0007t0001g0302 |
4 | HG02572.hp1 HG02886.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1168+835G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135661 | |||||||
| chr16:57135851 | G | A | 3 | a0001c0001t0002g0123 a0001c0001t0002g0271 a0001c0001t0002g0286 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1168+1025G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135851 | |||||||
| chr16:57135873 | CA | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.1168+1065delA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57135873 | ||||||
| chr16:57135873 | CAA | C | 7 | a0001c0001t0001g0083 a0001c0001t0001g0148 a0001c0001t0001g0235 others(4): Show |
7 | HG01169.hp2 HG01515.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1168+1064_1168+106 others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57135873 | ||||||
| chr16:57135962 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1168+1136G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135962 | |||||||
| chr16:57135978 | G | A | 6 | a0001c0001t0001g0339 a0001c0001t0003g0164 a0001c0001t0003g0220 others(3): Show |
6 | HG00280.hp2 HG01515.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1168+1152G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57135978 | |||||||
| chr16:57136047 | GAAGA | G | 3 | a0001c0001t0002g0123 a0001c0001t0002g0271 a0001c0001t0002g0286 |
3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1169-1091_1169-108 others(8): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57136047 | ||||||
| chr16:57136057 | A | C | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1169-1092A>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136057 | |||||||
| chr16:57136110 | ACT | A | 44 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0029 others(41): Show |
47 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.1169-1036_1169-103 others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr16 | 57136110 | ||||||
| chr16:57136277 | T | C | 5 | a0001c0001t0001g0339 a0001c0001t0003g0164 a0001c0001t0003g0220 others(2): Show |
5 | HG00280.hp2 HG01515.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169-872T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136277 | |||||||
| chr16:57136842 | G | A | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(323): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1169-307G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136842 | |||||||
| chr16:57136946 | G | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0044 others(40): Show |
46 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(43): Show |
intron_variant | MODIFIER | c.1169-203G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57136946 | |||||||
| chr16:57137024 | G | C | 10 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0087 others(7): Show |
10 | HG00099.hp2 HG00140.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1169-125G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 13/15 | chr16 | 57137024 | |||||||
| chr16:57137321 | C | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(318): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1302+39C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137321 | |||||||
| chr16:57137325 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1302+43C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137325 | |||||||
| chr16:57137485 | C | T | 258 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(255): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.1302+203C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137485 | |||||||
| chr16:57137553 | A | T | 1 | a0001c0001t0001g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1302+271A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137553 | |||||||
| chr16:57137591 | T | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0073 a0001c0001t0001g0082 others(1): Show |
4 | HG02071.hp2 HG02155.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+309T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137591 | |||||||
| chr16:57137645 | C | G | 2 | a0001c0001t0002g0124 a0001c0001t0002g0322 |
2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1302+363C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137645 | |||||||
| chr16:57137653 | G | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0318 |
2 | HG02015.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1302+371G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137653 | |||||||
| chr16:57137728 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(107): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1302+446G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137728 | |||||||
| chr16:57137924 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1302+642A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57137924 | |||||||
| chr16:57138095 | C | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0292 |
2 | HG00735.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1302+813C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138095 | |||||||
| chr16:57138107 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(107): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1302+825G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138107 | |||||||
| chr16:57138120 | C | T | 1 | a0001c0001t0001g0337 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1302+838C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138120 | |||||||
| chr16:57138195 | C | T | 13 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(10): Show |
14 | HG00280.hp2 HG01123.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1302+913C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138195 | |||||||
| chr16:57138273 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1302+991T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138273 | |||||||
| chr16:57138343 | C | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(2): Show |
5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+1061C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138343 | |||||||
| chr16:57138421 | G | A | 261 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(258): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.1302+1139G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138421 | |||||||
| chr16:57138492 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0318 |
2 | HG02015.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1302+1210C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138492 | |||||||
| chr16:57138632 | C | A | 1 | a0001c0002t0004g0188 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1302+1350C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138632 | |||||||
| chr16:57138652 | A | AC | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(327): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1302+1371dupC | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57138652 | ||||||
| chr16:57138717 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1302+1435T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138717 | |||||||
| chr16:57138946 | C | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+1664C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138946 | |||||||
| chr16:57138947 | G | A | 4 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0281 others(1): Show |
4 | HG02145.hp1 HG02451.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1302+1665G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138947 | |||||||
| chr16:57138979 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1302+1697A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138979 | |||||||
| chr16:57138996 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1302+1714T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57138996 | |||||||
| chr16:57139059 | G | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1302+1777G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139059 | |||||||
| chr16:57139066 | G | A | 1 | a0001c0002t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1302+1784G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139066 | |||||||
| chr16:57139096 | T | A | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1302+1814T>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139096 | |||||||
| chr16:57139099 | C | G | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.1302+1817C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139099 | |||||||
| chr16:57139168 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1302+1886A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139168 | |||||||
| chr16:57139358 | A | T | 2 | a0001c0005t0001g0007 a0001c0005t0001g0097 |
3 | HG02818.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1302+2076A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139358 | |||||||
| chr16:57139616 | C | T | 1 | a0001c0001t0001g0244 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1302+2334C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139616 | |||||||
| chr16:57139717 | T | C | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1302+2435T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139717 | |||||||
| chr16:57139735 | C | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1302+2453C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139735 | |||||||
| chr16:57139762 | A | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1302+2480A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139762 | |||||||
| chr16:57139855 | C | T | 5 | a0001c0001t0001g0339 a0001c0001t0003g0164 a0001c0001t0003g0220 others(2): Show |
5 | HG00280.hp2 HG01515.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+2573C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57139855 | |||||||
| chr16:57140042 | G | A | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(2): Show |
5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+2760G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140042 | |||||||
| chr16:57140050 | A | G | 1 | a0001c0002t0001g0294 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1302+2768A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140050 | |||||||
| chr16:57140093 | C | T | 2 | a0001c0001t0002g0271 a0001c0001t0002g0286 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1302+2811C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140093 | |||||||
| chr16:57140223 | TGCAATGG others(3): Show |
T | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(66): Show |
76 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.1302+2942_1302+295 others(14): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140223 | |||||||
| chr16:57140254 | T | G | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1302+2972T>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140254 | |||||||
| chr16:57140284 | T | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1302+3002T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140284 | |||||||
| chr16:57140296 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1302+3014A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140296 | |||||||
| chr16:57140415 | G | A | 1 | a0001c0001t0001g0029 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1302+3133G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140415 | |||||||
| chr16:57140589 | A | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0214 |
2 | HG00323.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1302+3307A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140589 | |||||||
| chr16:57140775 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1302+3493C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140775 | |||||||
| chr16:57140785 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1302+3503G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140785 | |||||||
| chr16:57140798 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0032 a0001c0001t0001g0061 |
3 | HG00408.hp1 HG00609.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1302+3516C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140798 | |||||||
| chr16:57140810 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1302+3528C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140810 | |||||||
| chr16:57140820 | C | T | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(2): Show |
5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1302+3538C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140820 | |||||||
| chr16:57140868 | AT | A | 28 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0062 others(25): Show |
28 | HG01952.hp1 HG02280.hp2 HG02572.hp2 others(25): Show |
intron_variant | MODIFIER | c.1302+3613delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57140868 | ||||||
| chr16:57140868 | ATT | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(222): Show |
239 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.1302+3612_1302+361 others(6): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57140868 | ||||||
| chr16:57140868 | ATTT | A | 68 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(65): Show |
73 | HG00099.hp2 HG00280.hp2 HG00558.hp2 others(70): Show |
intron_variant | MODIFIER | c.1302+3611_1302+361 others(7): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57140868 | ||||||
| chr16:57140871 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0053 |
2 | NA18993.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1302+3589T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140871 | |||||||
| chr16:57140985 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1302+3703G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57140985 | |||||||
| chr16:57141079 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0029 others(42): Show |
48 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(45): Show |
intron_variant | MODIFIER | c.1302+3797G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141079 | |||||||
| chr16:57141193 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.1302+3911G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141193 | |||||||
| chr16:57141315 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1302+4033C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141315 | |||||||
| chr16:57141837 | T | C | 5 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(2): Show |
5 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-4248T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57141837 | |||||||
| chr16:57142376 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0248 a0001c0001t0001g0250 |
4 | HG02258.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-3709G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142376 | |||||||
| chr16:57142389 | C | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0149 |
2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1303-3696C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142389 | |||||||
| chr16:57142390 | G | A | 1 | a0001c0001t0001g0305 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1303-3695G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142390 | |||||||
| chr16:57142495 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1303-3590C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142495 | |||||||
| chr16:57142670 | G | C | 1 | a0001c0001t0002g0123 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1303-3415G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142670 | |||||||
| chr16:57142737 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(319): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1303-3348A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142737 | |||||||
| chr16:57142751 | C | A | 1 | a0001c0001t0002g0210 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1303-3334C>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142751 | |||||||
| chr16:57142756 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0160 others(2): Show |
6 | HG01891.hp1 HG02055.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-3329C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57142756 | |||||||
| chr16:57143055 | C | G | 9 | a0001c0001t0001g0339 a0001c0001t0003g0102 a0001c0001t0003g0164 others(6): Show |
10 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.1303-3030C>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143055 | |||||||
| chr16:57143082 | CT | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(1): Show |
4 | HG01123.hp2 HG01884.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-3001delT | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57143082 | ||||||
| chr16:57143107 | C | T | 1 | a0001c0005t0001g0097 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1303-2978C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143107 | |||||||
| chr16:57143202 | G | C | 1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1303-2883G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143202 | |||||||
| chr16:57143343 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1303-2742C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57143343 | |||||||
| chr16:57144135 | C | T | 2 | a0001c0001t0001g0029 a0001c0001t0001g0318 |
2 | HG02015.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1303-1950C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144135 | |||||||
| chr16:57144501 | G | C | 6 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(3): Show |
6 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-1584G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144501 | |||||||
| chr16:57144591 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1303-1494G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144591 | |||||||
| chr16:57144762 | A | T | 6 | a0001c0001t0001g0125 a0001c0001t0001g0128 a0001c0001t0001g0284 others(3): Show |
6 | HG01123.hp2 HG01884.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.1303-1323A>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144762 | |||||||
| chr16:57144763 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1303-1322C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144763 | |||||||
| chr16:57144954 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1303-1131G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57144954 | |||||||
| chr16:57145028 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1303-1057G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145028 | |||||||
| chr16:57145298 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1303-787G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145298 | |||||||
| chr16:57145348 | T | C | 1 | a0001c0001t0003g0102 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1303-737T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145348 | |||||||
| chr16:57145383 | C | T | 5 | a0001c0001t0001g0231 a0001c0001t0001g0233 a0001c0001t0001g0234 others(2): Show |
5 | HG00639.hp1 HG01074.hp1 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.1303-702C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145383 | |||||||
| chr16:57145490 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1303-595G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145490 | |||||||
| chr16:57145491 | A | ACCTGCTT others(5): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0248 a0001c0001t0001g0250 |
4 | HG02258.hp2 HG02717.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1303-591_1303-580d others(14): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr16 | 57145491 | ||||||
| chr16:57145701 | A | G | 9 | a0001c0001t0001g0096 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
10 | HG01496.hp2 HG02818.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.1303-384A>G | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145701 | |||||||
| chr16:57145764 | C | T | 6 | a0001c0001t0003g0102 a0001c0001t0003g0164 a0001c0001t0003g0213 others(3): Show |
6 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1303-321C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145764 | |||||||
| chr16:57145921 | G | T | 1 | a0001c0001t0001g0137 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1303-164G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145921 | |||||||
| chr16:57145998 | C | T | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0155 others(2): Show |
5 | HG03471.hp1 HG03486.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1303-87C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57145998 | |||||||
| chr16:57146014 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0152 a0001c0001t0001g0245 others(5): Show |
10 | NA18952.hp2 NA18963.hp1 NA18993.hp1 others(7): Show |
intron_variant | MODIFIER | c.1303-71T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 14/15 | chr16 | 57146014 | |||||||
| chr16:57146351 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0247 a0001c0001t0001g0304 others(2): Show |
5 | HG02109.hp2 HG02257.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1539+30G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146351 | |||||||
| chr16:57146352 | G | A | 1 | a0001c0001t0001g0284 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1539+31G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146352 | |||||||
| chr16:57146555 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1539+234G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146555 | |||||||
| chr16:57146580 | G | A | 1 | a0001c0001t0001g0193 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1539+259G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146580 | |||||||
| chr16:57146624 | G | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0253 |
2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1539+303G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146624 | |||||||
| chr16:57146660 | G | C | 6 | a0001c0001t0003g0102 a0001c0001t0003g0164 a0001c0001t0003g0213 others(3): Show |
6 | HG00280.hp2 HG01070.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1539+339G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146660 | |||||||
| chr16:57146805 | G | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(249): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.1539+484G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146805 | |||||||
| chr16:57146862 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1539+541G>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146862 | |||||||
| chr16:57146922 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1539+601T>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146922 | |||||||
| chr16:57146972 | G | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 |
3 | NA18946.hp1 NA19062.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1540-579G>C | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57146972 | |||||||
| chr16:57147222 | C | T | 39 | a0001c0001t0001g0020 a0001c0001t0001g0029 a0001c0001t0001g0318 others(36): Show |
41 | HG00558.hp2 HG00621.hp1 HG01255.hp2 others(38): Show |
intron_variant | MODIFIER | c.1540-329C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147222 | |||||||
| chr16:57147239 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1540-312G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147239 | |||||||
| chr16:57147251 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1540-300C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147251 | |||||||
| chr16:57147330 | T | TA | 3 | a0001c0001t0001g0075 a0001c0001t0001g0246 a0001c0001t0001g0249 |
3 | HG02630.hp2 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1540-220dupA | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr16 | 57147330 | ||||||
| chr16:57147360 | CAG | C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0077 a0001c0001t0001g0109 others(13): Show |
17 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1540-190_1540-189d others(4): Show |
CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147360 | |||||||
| chr16:57147366 | G | A | 3 | a0001c0001t0001g0206 a0001c0001t0001g0218 a0001c0001t0001g0341 |
3 | HG01243.hp1 HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1540-185G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147366 | |||||||
| chr16:57147456 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1540-95G>A | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147456 | |||||||
| chr16:57147483 | C | T | 1 | a0001c0002t0001g0288 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1540-68C>T | CPNE2 | ENSG00000140848.17 | transcript | ENST00000290776.13 | protein_coding | 15/15 | chr16 | 57147483 |