Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10762 |
| ensemblid | ENSG00000093000.19 |
| hgncid | 8065 |
| symbol | NUP50 |
| name | nucleoporin 50 |
| refseq_nuc | NM_007172.4 |
| refseq_prot | NP_009103.2 |
| ensembl_nuc | ENST00000347635.9 |
| ensembl_prot | ENSP00000345895.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 45163925 |
| end | 45188017 |
| strand | + |
| ver | v1.2 |
| region | chr22:45163925-45188017 |
| region5000 | chr22:45158925-45193017 |
| regionname0 | NUP50_chr22_45163925_45188017 |
| regionname5000 | NUP50_chr22_45158925_45193017 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 468 | 429 | 97 | 80 | 191 | 16 | 43 | 160 | NUP50_chr22_45158925_45193017 | NUP50 | MAKRN others(463): Show |
chr22 | 45158925 | 45193017 |
| a0002 | 0/0 | 468 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | MAKRN others(463): Show |
chr22 | 45158925 | 45193017 |
| a0003 | 0/0 | 468 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | MAKRN others(463): Show |
chr22 | 45158925 | 45193017 |
| a0004 | 0/0 | 468 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | MAKRN others(463): Show |
chr22 | 45158925 | 45193017 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1404 | 263 | 69 | 60 | 88 | 10 | 34 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0001c0002 | 0/0 | 1404 | 156 | 23 | 16 | 103 | 5 | 9 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0001c0003 | 0/0 | 1404 | 5 | 4 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0001c0004 | 0/0 | 1404 | 3 | 0 | 2 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0001c0006 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0001c0008 | 0/0 | 1404 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0002c0007 | 0/0 | 1404 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0003c0005 | 0/0 | 1404 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 | ||
| a0004c0009 | 0/0 | 1404 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | ATGGC others(1399): Show |
chr22 | 45158925 | 45193017 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 5155 | 86 | 9 | 22 | 45 | 2 | 8 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0003 | 1/0 | 5151 | 50 | 10 | 19 | 0 | 6 | 14 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5146): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0004 | 0/0 | 5152 | 32 | 0 | 0 | 29 | 0 | 3 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0005 | 0/0 | 5153 | 23 | 5 | 11 | 0 | 2 | 5 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0007 | 0/0 | 5152 | 10 | 10 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0008 | 0/0 | 5153 | 9 | 9 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0009 | 0/0 | 5154 | 3 | 3 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0010 | 0/0 | 5150 | 5 | 3 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5145): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0011 | 0/0 | 5146 | 4 | 4 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0013 | 0/0 | 5152 | 4 | 4 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0014 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0015 | 0/0 | 5154 | 3 | 0 | 0 | 3 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0016 | 0/0 | 5155 | 3 | 0 | 0 | 3 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0018 | 0/0 | 5153 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0023 | 0/0 | 5156 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5151): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0025 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5145): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0026 | 0/0 | 5153 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0027 | 0/0 | 5153 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0028 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0029 | 0/0 | 5150 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5145): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0030 | 0/0 | 5153 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0032 | 0/0 | 5151 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5146): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0033 | 0/0 | 5152 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0034 | 0/0 | 5154 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0036 | 0/0 | 5153 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0037 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0038 | 0/0 | 5153 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0039 | 0/1 | 5151 | 1 | 0 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5146): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0040 | 0/0 | 5152 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0041 | 0/0 | 5153 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0042 | 0/0 | 5152 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0043 | 0/0 | 5153 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0045 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0055 | 0/0 | 5153 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5148): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0056 | 0/0 | 5156 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5151): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0057 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0058 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0059 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0060 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0001t0061 | 0/0 | 5149 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5144): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0001 | 0/0 | 5146 | 115 | 7 | 9 | 88 | 5 | 6 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0002 | 0/0 | 5155 | 3 | 0 | 0 | 3 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0006 | 0/0 | 5146 | 6 | 6 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0009 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0012 | 0/0 | 5147 | 5 | 1 | 2 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5142): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0014 | 0/0 | 5154 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0017 | 0/0 | 5146 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0019 | 0/0 | 5146 | 2 | 0 | 1 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0020 | 0/0 | 5146 | 2 | 0 | 0 | 1 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0021 | 0/0 | 5146 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0022 | 0/0 | 5146 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0024 | 0/0 | 5154 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5149): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0031 | 0/0 | 5146 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0035 | 0/0 | 5147 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5142): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0044 | 0/0 | 5152 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5147): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0046 | 0/0 | 5146 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0047 | 0/0 | 5146 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0048 | 0/0 | 5147 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5142): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0049 | 0/0 | 5146 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0050 | 0/0 | 5146 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0051 | 0/0 | 5146 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0052 | 0/0 | 5146 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0053 | 0/0 | 5146 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0002t0054 | 0/0 | 5146 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0003t0006 | 0/0 | 5146 | 5 | 4 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0004t0002 | 0/0 | 5155 | 3 | 0 | 2 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0001c0006t0001 | 0/0 | 5146 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0001c0008t0001 | 0/0 | 5146 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0002c0007t0002 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| a0003c0005t0011 | 0/0 | 5146 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5141): Show |
chr22 | 45158925 | 45193017 |
| a0004c0009t0002 | 0/0 | 5155 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | GCCGG others(5150): Show |
chr22 | 45158925 | 45193017 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 25 | 3 | 6 | 13 | 1 | 2 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0005 | 0/0 | 7 | 1 | 1 | 4 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0006 | 0/0 | 6 | 1 | 1 | 0 | 2 | 2 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0011 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0028 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0010 | 0/0 | 5 | 0 | 2 | 0 | 2 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0054 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0008g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0008g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0009g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0009g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0009g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0010g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0010g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0010g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0011g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0011g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0013g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0013g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0013g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0013g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0014g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0014g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0015g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0015g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0016g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0016g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0018g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0018g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0023g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0025g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0026g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0027g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0028g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0029g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0030g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0032g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0033g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0034g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0036g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0037g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0038g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0039g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0040g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0041g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0042g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0043g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0045g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0055g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0056g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0057g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0058g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0059g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0060g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0001t0061g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0002 | 0/0 | 17 | 0 | 0 | 16 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0020 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0031 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0006g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0006g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0012g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0012g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0012g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0012g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0017g0055 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0019g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0019g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0020g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0020g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0021g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0021g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0022g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0024g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0031g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0035g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0044g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0046g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0047g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0048g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0049g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0050g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0051g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0052g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0053g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0002t0054g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0003t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0003t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0003t0006g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0003t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0004t0002g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0004t0002g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0006t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0001c0008t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0002c0007t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0003c0005t0011g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| a0004c0009t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | GBR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0117 | EUR | GBR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0174 | EUR | GBR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00140 | hp2 | a0001 | c0004 | t0002 | g0001 | EUR | GBR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | FIN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0135 | EUR | FIN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0020 | EUR | FIN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00408 | hp2 | a0001 | c0002 | t0022 | g0002 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00423 | hp1 | a0001 | c0001 | t0038 | g0268 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0167 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00639 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00642 | hp1 | a0001 | c0001 | t0005 | g0256 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00642 | hp2 | a0001 | c0001 | t0028 | g0016 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0084 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00733 | hp2 | a0001 | c0002 | t0019 | g0043 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00735 | hp2 | a0001 | c0002 | t0017 | g0055 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0212 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0046 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01070 | hp2 | a0001 | c0002 | t0017 | g0055 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0042 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0046 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0124 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01099 | hp2 | a0001 | c0001 | t0005 | g0010 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01106 | hp1 | a0001 | c0002 | t0053 | g0161 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01109 | hp1 | a0001 | c0001 | t0010 | g0103 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01167 | hp1 | a0001 | c0002 | t0012 | g0032 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01168 | hp1 | a0001 | c0001 | t0005 | g0237 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01168 | hp2 | a0001 | c0001 | t0018 | g0114 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01169 | hp1 | a0001 | c0001 | t0018 | g0113 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01169 | hp2 | a0001 | c0002 | t0012 | g0032 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01243 | hp1 | a0001 | c0002 | t0054 | g0147 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01243 | hp2 | a0001 | c0003 | t0006 | g0169 | AMR | PUR | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01255 | hp2 | a0001 | c0008 | t0001 | g0007 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01256 | hp1 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0001 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0118 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0119 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0236 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0010 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01496 | hp1 | a0001 | c0001 | t0043 | g0009 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01496 | hp2 | a0001 | c0001 | t0042 | g0257 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0010 | EUR | IBS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0116 | EUR | IBS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0206 | EUR | IBS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01517 | hp2 | a0001 | c0001 | t0005 | g0010 | EUR | IBS | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01884 | hp2 | a0001 | c0001 | t0032 | g0127 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01891 | hp1 | a0001 | c0001 | t0026 | g0258 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0068 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01934 | hp1 | a0001 | c0001 | t0061 | g0001 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0176 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01943 | hp2 | a0001 | c0001 | t0005 | g0209 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0126 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0179 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02027 | hp1 | a0001 | c0002 | t0049 | g0150 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02040 | hp2 | a0001 | c0002 | t0020 | g0168 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02055 | hp1 | a0001 | c0002 | t0006 | g0157 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0250 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0166 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02071 | hp1 | a0001 | c0002 | t0046 | g0012 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02071 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02074 | hp2 | a0001 | c0001 | t0030 | g0121 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02145 | hp1 | a0001 | c0001 | t0007 | g0101 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0148 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0025 | EAS | CDX | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CDX | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0067 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02258 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0239 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0108 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02280 | hp2 | a0001 | c0002 | t0024 | g0041 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0177 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0017 | AMR | PEL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0066 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0194 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02523 | hp2 | a0002 | c0007 | t0002 | g0003 | EAS | KHV | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0251 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0142 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02622 | hp1 | a0001 | c0002 | t0044 | g0019 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02630 | hp1 | a0001 | c0002 | t0050 | g0172 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02630 | hp2 | a0001 | c0001 | t0009 | g0266 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02647 | hp1 | a0001 | c0001 | t0011 | g0061 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02647 | hp2 | a0001 | c0001 | t0007 | g0070 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0078 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02683 | hp2 | a0001 | c0001 | t0056 | g0224 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02698 | hp1 | a0001 | c0001 | t0055 | g0048 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02698 | hp2 | a0001 | c0002 | t0019 | g0271 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02717 | hp2 | a0001 | c0001 | t0036 | g0226 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02723 | hp1 | a0001 | c0002 | t0052 | g0208 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0018 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0132 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02738 | hp2 | a0001 | c0001 | t0005 | g0010 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0023 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02818 | hp1 | a0001 | c0001 | t0041 | g0231 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02886 | hp1 | a0001 | c0001 | t0059 | g0233 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0263 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02895 | hp1 | a0001 | c0001 | t0008 | g0253 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02895 | hp2 | a0001 | c0002 | t0009 | g0262 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02896 | hp1 | a0003 | c0005 | t0011 | g0098 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0071 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02897 | hp1 | a0001 | c0002 | t0009 | g0260 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02922 | hp1 | a0001 | c0001 | t0025 | g0104 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0173 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0216 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02970 | hp2 | a0001 | c0001 | t0013 | g0275 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0264 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02976 | hp2 | a0001 | c0003 | t0006 | g0018 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0171 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03098 | hp1 | a0001 | c0001 | t0009 | g0259 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0261 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03139 | hp1 | a0001 | c0001 | t0029 | g0102 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03139 | hp2 | a0001 | c0003 | t0006 | g0033 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03195 | hp2 | a0001 | c0002 | t0006 | g0156 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03209 | hp1 | a0001 | c0001 | t0010 | g0026 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03225 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0120 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0249 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0160 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03486 | hp1 | a0001 | c0002 | t0024 | g0041 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03486 | hp2 | a0001 | c0001 | t0008 | g0252 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03491 | hp1 | a0001 | c0002 | t0051 | g0155 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03516 | hp1 | a0001 | c0003 | t0006 | g0033 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0274 | AFR | ESN | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0106 | AFR | GWD | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03579 | hp2 | a0001 | c0003 | t0006 | g0170 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03654 | hp2 | a0001 | c0001 | t0005 | g0213 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0087 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0162 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0122 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0007 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03831 | hp2 | a0001 | c0001 | t0034 | g0092 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0217 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0130 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0085 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04115 | hp1 | a0004 | c0009 | t0002 | g0222 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0110 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04184 | hp2 | a0001 | c0001 | t0005 | g0210 | SAS | BEB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0211 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0229 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04228 | hp1 | a0001 | c0001 | t0057 | g0001 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG04228 | hp2 | a0001 | c0002 | t0020 | g0154 | SAS | STU | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18522 | hp1 | a0001 | c0001 | t0011 | g0023 | AFR | YRI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0273 | AFR | YRI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | CHB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0191 | EAS | CHB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0024 | EAS | CHB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | CHB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | YRI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | YRI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18942 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18943 | hp1 | a0001 | c0002 | t0047 | g0181 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18947 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18951 | hp1 | a0001 | c0001 | t0015 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18951 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18954 | hp1 | a0001 | c0002 | t0048 | g0004 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18956 | hp2 | a0001 | c0001 | t0016 | g0045 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18957 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18962 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18968 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0076 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0198 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18980 | hp2 | a0001 | c0001 | t0040 | g0267 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18983 | hp1 | a0001 | c0001 | t0060 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18985 | hp2 | a0001 | c0001 | t0016 | g0221 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18990 | hp1 | a0001 | c0001 | t0033 | g0081 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18991 | hp1 | a0001 | c0002 | t0012 | g0165 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18997 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18997 | hp2 | a0001 | c0002 | t0012 | g0202 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19001 | hp1 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19001 | hp2 | a0001 | c0002 | t0035 | g0099 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19002 | hp1 | a0001 | c0001 | t0023 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19004 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0182 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19007 | hp2 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0093 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19010 | hp2 | a0001 | c0001 | t0058 | g0244 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0025 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19030 | hp1 | a0001 | c0001 | t0027 | g0136 | AFR | LWK | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19030 | hp2 | a0001 | c0001 | t0045 | g0248 | AFR | LWK | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19043 | hp1 | a0001 | c0002 | t0031 | g0065 | AFR | LWK | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0022 | AFR | LWK | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0095 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19056 | hp1 | a0001 | c0002 | t0021 | g0199 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0163 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19068 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19074 | hp1 | a0001 | c0001 | t0016 | g0045 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19074 | hp2 | a0001 | c0002 | t0021 | g0178 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19081 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19081 | hp2 | a0001 | c0002 | t0022 | g0002 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19087 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19087 | hp2 | a0001 | c0001 | t0023 | g0001 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19088 | hp1 | a0001 | c0002 | t0002 | g0196 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19089 | hp2 | a0001 | c0002 | t0001 | g0187 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0022 | AFR | YRI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA19240 | hp2 | a0001 | c0002 | t0006 | g0018 | AFR | YRI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20129 | hp1 | a0001 | c0001 | t0013 | g0272 | AFR | ASW | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | ASW | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | TSI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0175 | EUR | TSI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0043 | EUR | TSI | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0111 | SAS | GIH | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02486 | hp1 | a0001 | c0001 | t0037 | g0137 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02486 | hp2 | a0001 | c0002 | t0014 | g0265 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG02559 | hp2 | a0001 | c0002 | t0006 | g0019 | AFR | ACB | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03471 | hp1 | a0001 | c0001 | t0007 | g0069 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0214 | AFR | MSL | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG06807 | hp1 | a0001 | c0002 | t0006 | g0019 | AFR | USA | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| HG06807 | hp2 | a0001 | c0002 | t0012 | g0151 | AFR | USA | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18955 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA18955 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | USA | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | USA | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0159 | AFR | LWK | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| NA21309 | hp2 | a0001 | c0001 | t0010 | g0105 | AFR | LWK | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0039 | g0276 | REF | REF | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0028 | REF | REF | NUP50_chr22_45158925_45193017 | NUP50 | chr22 | 45158925 | 45193017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45171664 | G | A | 1 | a0003 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.134G>A | p.Arg45His | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/8 | 516/5151 | 134/1407 | 45/468 | chr22 | 45171664 | |||
| chr22:45178721 | A | G | 1 | a0002 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.824A>G | p.Lys275Arg | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/8 | 1206/5151 | 824/1407 | 275/468 | chr22 | 45178721 | |||
| chr22:45181294 | G | A | 1 | a0004 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.1012G>A | p.Glu338Lys | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/8 | 1394/5151 | 1012/1407 | 338/468 | chr22 | 45181294 | |||
| chr22:45188017 | A | G | 4 | a0001 a0002 a0003 others(1): Show |
371 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(368): Show |
splice_region_variant | LOW | c.*3362A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | chr22 | 45188017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45178395 | C | T | 2 | a0001c0004 a0004c0009 |
4 | HG00140.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
synonymous_variant | LOW | c.498C>T | p.Ser166Ser | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/8 | 880/5151 | 498/1407 | 166/468 | chr22 | 45178395 | |||
| chr22:45178578 | A | G | 1 | a0001c0008 | 1 | HG01255.hp2 | synonymous_variant | LOW | c.681A>G | p.Ser227Ser | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/8 | 1063/5151 | 681/1407 | 227/468 | chr22 | 45178578 | |||
| chr22:45181350 | T | C | 4 | a0001c0002 a0001c0003 a0001c0006 others(1): Show |
163 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(160): Show |
synonymous_variant | LOW | c.1068T>C | p.Asp356Asp | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/8 | 1450/5151 | 1068/1407 | 356/468 | chr22 | 45181350 | |||
| chr22:45184514 | T | C | 1 | a0001c0006 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1266T>C | p.Asn422Asn | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1648/5151 | 1266/1407 | 422/468 | chr22 | 45184514 | |||
| chr22:45184553 | C | T | 1 | a0001c0003 | 5 | HG01243.hp2 HG02976.hp2 HG03139.hp2 others(2): Show |
synonymous_variant | LOW | c.1305C>T | p.Asp435Asp | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1687/5151 | 1305/1407 | 435/468 | chr22 | 45184553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45163977 | T | C | 1 | a0001c0001t0025 | 1 | HG02922.hp1 | 5_prime_UTR_variant | MODIFIER | c.-330T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | 4201 | chr22 | 45163977 | ||||||
| chr22:45164027 | C | T | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(43): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
5_prime_UTR_variant | MODIFIER | c.-280C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | 4151 | chr22 | 45164027 | ||||||
| chr22:45164049 | G | C | 1 | a0001c0001t0036 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-258G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | 4129 | chr22 | 45164049 | ||||||
| chr22:45164066 | C | G | 4 | a0001c0001t0004 a0001c0001t0033 a0001c0001t0034 others(1): Show |
35 | HG00673.hp1 HG02040.hp1 HG02165.hp1 others(32): Show |
5_prime_UTR_variant | MODIFIER | c.-241C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | 4112 | chr22 | 45164066 | ||||||
| chr22:45164116 | T | C | 53 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(50): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
5_prime_UTR_variant | MODIFIER | c.-191T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | 4062 | chr22 | 45164116 | ||||||
| chr22:45164221 | C | G | 1 | a0001c0001t0032 | 1 | HG01884.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | chr22 | 45164221 | |||||||
| chr22:45164255 | C | T | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-52C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | chr22 | 45164255 | |||||||
| chr22:45164259 | A | C | 1 | a0001c0001t0027 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/8 | 3919 | chr22 | 45164259 | ||||||
| chr22:45184688 | G | GTT | 15 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(12): Show |
110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*34_*35dupTT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 36 | INFO_REALIGN_3_PRIME | chr22 | 45184688 | |||||
| chr22:45184691 | G | T | 16 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(13): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*36G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 36 | chr22 | 45184691 | ||||||
| chr22:45184692 | C | T | 16 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0016 others(13): Show |
111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*37C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 37 | chr22 | 45184692 | ||||||
| chr22:45184710 | CTTAAAG | C | 25 | a0001c0001t0011 a0001c0001t0061 a0001c0002t0001 others(22): Show |
160 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
3_prime_UTR_variant | MODIFIER | c.*59_*64delAAGTTA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 59 | INFO_REALIGN_3_PRIME | chr22 | 45184710 | |||||
| chr22:45184795 | G | A | 1 | a0001c0002t0019 | 2 | HG00733.hp2 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*140G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 140 | chr22 | 45184795 | ||||||
| chr22:45184908 | C | A | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(6): Show |
55 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*253C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 253 | chr22 | 45184908 | ||||||
| chr22:45184955 | G | C | 24 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(21): Show |
149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*300G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 300 | chr22 | 45184955 | ||||||
| chr22:45185018 | G | C | 63 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(60): Show |
371 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*363G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 363 | chr22 | 45185018 | ||||||
| chr22:45185033 | A | T | 1 | a0001c0001t0043 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*378A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 378 | chr22 | 45185033 | ||||||
| chr22:45185139 | C | T | 6 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0026 others(3): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*484C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 484 | chr22 | 45185139 | ||||||
| chr22:45185141 | C | G | 1 | a0001c0002t0054 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*486C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 486 | chr22 | 45185141 | ||||||
| chr22:45185211 | C | T | 1 | a0001c0002t0053 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 556 | chr22 | 45185211 | ||||||
| chr22:45185473 | A | G | 1 | a0001c0001t0034 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*818A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 818 | chr22 | 45185473 | ||||||
| chr22:45185485 | C | T | 6 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0026 others(3): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*830C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 830 | chr22 | 45185485 | ||||||
| chr22:45185507 | A | T | 1 | a0001c0001t0013 | 4 | HG02970.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*852A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 852 | chr22 | 45185507 | ||||||
| chr22:45185547 | C | G | 2 | a0001c0002t0017 a0001c0002t0031 |
3 | HG00735.hp2 HG01070.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*892C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 892 | chr22 | 45185547 | ||||||
| chr22:45185582 | C | A | 1 | a0001c0001t0033 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*927C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 927 | chr22 | 45185582 | ||||||
| chr22:45185623 | A | G | 1 | a0001c0001t0060 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*968A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 968 | chr22 | 45185623 | ||||||
| chr22:45185640 | C | T | 63 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(60): Show |
370 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(367): Show |
3_prime_UTR_variant | MODIFIER | c.*985C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 985 | chr22 | 45185640 | ||||||
| chr22:45185655 | T | C | 1 | a0001c0001t0038 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1000T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1000 | chr22 | 45185655 | ||||||
| chr22:45185696 | C | T | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(6): Show |
55 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1041C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1041 | chr22 | 45185696 | ||||||
| chr22:45185864 | C | CTT | 64 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(61): Show |
372 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(369): Show |
3_prime_UTR_variant | MODIFIER | c.*1210_*1211insTT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1211 | INFO_REALIGN_3_PRIME | chr22 | 45185864 | |||||
| chr22:45185944 | G | T | 1 | a0001c0002t0022 | 2 | HG00408.hp2 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1289G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1289 | chr22 | 45185944 | ||||||
| chr22:45185958 | C | A | 1 | a0001c0001t0056 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1303C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1303 | chr22 | 45185958 | ||||||
| chr22:45185988 | A | G | 1 | a0001c0001t0025 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1333 | chr22 | 45185988 | ||||||
| chr22:45185989 | A | G | 3 | a0001c0001t0009 a0001c0001t0045 a0001c0002t0009 |
6 | HG02630.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1334A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1334 | chr22 | 45185989 | ||||||
| chr22:45186001 | A | C | 1 | a0001c0001t0042 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1346A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1346 | chr22 | 45186001 | ||||||
| chr22:45186004 | A | G | 1 | a0001c0001t0041 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1349A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1349 | chr22 | 45186004 | ||||||
| chr22:45186016 | T | C | 12 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(9): Show |
67 | HG00673.hp1 HG01243.hp2 HG01891.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1361T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1361 | chr22 | 45186016 | ||||||
| chr22:45186055 | T | C | 1 | a0001c0002t0046 | 1 | HG02071.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1400T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1400 | chr22 | 45186055 | ||||||
| chr22:45186132 | A | G | 1 | a0001c0001t0029 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1477A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1477 | chr22 | 45186132 | ||||||
| chr22:45186259 | A | G | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(6): Show |
55 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*1604A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1604 | chr22 | 45186259 | ||||||
| chr22:45186287 | G | A | 1 | a0001c0001t0037 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1632G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1632 | chr22 | 45186287 | ||||||
| chr22:45186326 | G | A | 1 | a0001c0001t0057 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1671G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1671 | chr22 | 45186326 | ||||||
| chr22:45186377 | A | G | 1 | a0001c0001t0016 | 3 | NA18956.hp2 NA18985.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1722A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1722 | chr22 | 45186377 | ||||||
| chr22:45186382 | G | A | 1 | a0001c0002t0047 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1727G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1727 | chr22 | 45186382 | ||||||
| chr22:45186385 | C | T | 1 | a0001c0002t0052 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1730C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1730 | chr22 | 45186385 | ||||||
| chr22:45186520 | A | G | 1 | a0001c0002t0021 | 2 | NA19056.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1865A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 1865 | chr22 | 45186520 | ||||||
| chr22:45186772 | C | T | 1 | a0001c0002t0051 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2117C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2117 | chr22 | 45186772 | ||||||
| chr22:45186814 | G | A | 1 | a0001c0001t0058 | 1 | NA19010.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2159G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2159 | chr22 | 45186814 | ||||||
| chr22:45186896 | C | G | 1 | a0001c0002t0050 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2241C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2241 | chr22 | 45186896 | ||||||
| chr22:45186979 | G | C | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0015 others(18): Show |
137 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*2324G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2324 | chr22 | 45186979 | ||||||
| chr22:45187137 | T | G | 1 | a0001c0001t0033 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2482T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2482 | chr22 | 45187137 | ||||||
| chr22:45187166 | C | CT | 3 | a0001c0001t0028 a0001c0002t0012 a0001c0002t0035 |
7 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2528dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2529 | INFO_REALIGN_3_PRIME | chr22 | 45187166 | |||||
| chr22:45187166 | CT | C | 3 | a0001c0001t0010 a0001c0001t0025 a0001c0001t0029 |
7 | HG01081.hp2 HG01109.hp1 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2528delT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2528 | INFO_REALIGN_3_PRIME | chr22 | 45187166 | |||||
| chr22:45187181 | TTTA | T | 5 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0008 others(2): Show |
16 | HG01496.hp1 HG02040.hp1 HG02258.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2527_*2529delTTA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2527 | chr22 | 45187181 | ||||||
| chr22:45187182 | TTA | T | 32 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(29): Show |
182 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*2528_*2529delTA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2528 | chr22 | 45187182 | ||||||
| chr22:45187183 | TA | T | 14 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(11): Show |
42 | HG00099.hp2 HG00280.hp2 HG00642.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2532delA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2532 | INFO_REALIGN_3_PRIME | chr22 | 45187183 | |||||
| chr22:45187184 | A | T | 27 | a0001c0001t0003 a0001c0001t0040 a0001c0002t0001 others(24): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*2529A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2529 | chr22 | 45187184 | ||||||
| chr22:45187201 | C | G | 1 | a0001c0001t0059 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2546C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2546 | chr22 | 45187201 | ||||||
| chr22:45187226 | A | C | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(6): Show |
55 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2571A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2571 | chr22 | 45187226 | ||||||
| chr22:45187260 | G | T | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(6): Show |
55 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*2605G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2605 | chr22 | 45187260 | ||||||
| chr22:45187370 | C | T | 1 | a0001c0001t0042 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2715C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2715 | chr22 | 45187370 | ||||||
| chr22:45187418 | C | CA | 8 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0023 others(5): Show |
13 | HG02486.hp2 HG02630.hp2 HG02683.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2777dupA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2778 | INFO_REALIGN_3_PRIME | chr22 | 45187418 | |||||
| chr22:45187418 | CA | C | 33 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(30): Show |
214 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*2777delA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2777 | INFO_REALIGN_3_PRIME | chr22 | 45187418 | |||||
| chr22:45187542 | A | G | 2 | a0001c0002t0020 a0001c0002t0048 |
3 | HG02040.hp2 HG04228.hp2 NA18954.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2887A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2887 | chr22 | 45187542 | ||||||
| chr22:45187633 | C | T | 1 | a0001c0002t0049 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2978C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 2978 | chr22 | 45187633 | ||||||
| chr22:45187725 | G | T | 38 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(35): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*3070G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 3070 | chr22 | 45187725 | ||||||
| chr22:45187761 | G | A | 8 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0011 others(5): Show |
54 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3106G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 3106 | chr22 | 45187761 | ||||||
| chr22:45187789 | G | C | 6 | a0001c0001t0009 a0001c0001t0014 a0001c0001t0026 others(3): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3134G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 3134 | chr22 | 45187789 | ||||||
| chr22:45187859 | G | C | 23 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(20): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
3_prime_UTR_variant | MODIFIER | c.*3204G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 3204 | chr22 | 45187859 | ||||||
| chr22:45187922 | A | G | 24 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0008 others(21): Show |
149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
3_prime_UTR_variant | MODIFIER | c.*3267A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 8/8 | 3267 | chr22 | 45187922 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:45164321 | A | G | 4 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(1): Show |
4 | HG02970.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+25A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164321 | |||||||
| chr22:45164344 | G | T | 1 | a0001c0001t0002g0056 | 2 | NA18943.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.-11+48G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164344 | |||||||
| chr22:45164430 | C | T | 1 | a0001c0002t0019g0271 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-11+134C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164430 | |||||||
| chr22:45164461 | G | C | 1 | a0001c0002t0001g0057 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-11+165G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164461 | |||||||
| chr22:45164504 | C | T | 1 | a0001c0001t0002g0270 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11+208C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164504 | |||||||
| chr22:45164520 | A | C | 199 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(196): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.-11+224A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164520 | |||||||
| chr22:45164566 | G | A | 1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+270G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164566 | |||||||
| chr22:45164675 | C | G | 1 | a0001c0001t0002g0269 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-11+379C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164675 | |||||||
| chr22:45164685 | T | G | 1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+389T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164685 | |||||||
| chr22:45164703 | C | T | 198 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(195): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.-11+407C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164703 | |||||||
| chr22:45164745 | C | T | 2 | a0001c0001t0038g0268 a0001c0001t0040g0267 |
2 | HG00423.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.-11+449C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164745 | |||||||
| chr22:45164747 | G | C | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-11+451G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164747 | |||||||
| chr22:45164760 | T | C | 102 | a0001c0001t0008g0171 a0001c0002t0001g0002 a0001c0002t0001g0004 others(99): Show |
156 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.-11+464T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164760 | |||||||
| chr22:45164826 | T | C | 200 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(197): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.-11+530T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164826 | |||||||
| chr22:45164850 | G | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(80): Show |
142 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.-11+554G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164850 | |||||||
| chr22:45164886 | G | A | 249 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(246): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-11+590G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164886 | |||||||
| chr22:45164906 | T | C | 259 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(256): Show |
380 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(377): Show |
intron_variant | MODIFIER | c.-11+610T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45164906 | |||||||
| chr22:45165008 | T | G | 1 | a0001c0001t0011g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+712T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165008 | |||||||
| chr22:45165041 | G | C | 1 | a0001c0001t0002g0207 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-11+745G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165041 | |||||||
| chr22:45165049 | G | C | 1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+753G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165049 | |||||||
| chr22:45165123 | C | G | 4 | a0001c0002t0001g0043 a0001c0002t0001g0206 a0001c0002t0019g0043 others(1): Show |
4 | HG00733.hp2 HG01517.hp1 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+827C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165123 | |||||||
| chr22:45165178 | C | A | 1 | a0001c0001t0004g0062 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-11+882C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165178 | |||||||
| chr22:45165185 | A | C | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-11+889A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165185 | |||||||
| chr22:45165196 | C | G | 1 | a0001c0001t0007g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-11+900C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165196 | |||||||
| chr22:45165239 | C | A | 1 | a0001c0002t0052g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-11+943C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165239 | |||||||
| chr22:45165310 | T | G | 1 | a0001c0002t0001g0138 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-11+1014T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165310 | |||||||
| chr22:45165363 | G | A | 1 | a0001c0001t0002g0269 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-11+1067G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165363 | |||||||
| chr22:45165488 | C | T | 2 | a0001c0002t0001g0042 a0001c0002t0001g0205 |
3 | HG00738.hp2 HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-11+1192C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165488 | |||||||
| chr22:45165511 | A | G | 57 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(54): Show |
94 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-11+1215A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165511 | |||||||
| chr22:45165511 | A | T | 1 | a0001c0001t0004g0100 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-11+1215A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165511 | |||||||
| chr22:45165587 | C | A | 1 | a0001c0002t0001g0139 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-11+1291C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165587 | |||||||
| chr22:45165587 | C | G | 1 | a0001c0001t0002g0255 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-11+1291C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165587 | |||||||
| chr22:45165611 | T | C | 3 | a0001c0002t0001g0034 a0001c0002t0001g0173 a0001c0002t0050g0172 |
4 | HG02630.hp1 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-11+1315T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165611 | |||||||
| chr22:45165669 | A | C | 1 | a0003c0005t0011g0098 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-11+1373A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165669 | |||||||
| chr22:45165779 | A | G | 49 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(46): Show |
54 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(51): Show |
intron_variant | MODIFIER | c.-11+1483A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165779 | |||||||
| chr22:45165932 | A | G | 1 | a0001c0001t0002g0254 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-11+1636A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45165932 | |||||||
| chr22:45166016 | C | T | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+1720C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166016 | |||||||
| chr22:45166090 | C | G | 1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-11+1794C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166090 | |||||||
| chr22:45166095 | G | T | 1 | a0001c0001t0037g0137 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-11+1799G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166095 | |||||||
| chr22:45166109 | C | T | 1 | a0001c0001t0011g0061 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-11+1813C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166109 | |||||||
| chr22:45166283 | C | CT | 15 | a0001c0001t0003g0133 a0001c0001t0003g0134 a0001c0001t0004g0060 others(12): Show |
17 | HG00544.hp2 HG00738.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-10-1863dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 45166283 | ||||||
| chr22:45166283 | C | T | 3 | a0001c0003t0006g0033 a0001c0003t0006g0169 a0001c0003t0006g0170 |
4 | HG01243.hp2 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-1885C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166283 | |||||||
| chr22:45166283 | CT | C | 58 | a0001c0001t0003g0027 a0001c0001t0003g0108 a0001c0001t0007g0063 others(55): Show |
97 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-10-1863delT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 45166283 | ||||||
| chr22:45166283 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0247 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-10-1873_-10-1863d others(13): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 45166283 | ||||||
| chr22:45166283 | CTTTTTTT others(5): Show |
C | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(73): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-10-1874_-10-1863d others(14): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 45166283 | ||||||
| chr22:45166288 | T | C | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-10-1880T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166288 | |||||||
| chr22:45166314 | G | A | 1 | a0001c0001t0005g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-10-1854G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166314 | |||||||
| chr22:45166337 | G | A | 1 | a0001c0002t0017g0055 | 2 | HG00735.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.-10-1831G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166337 | |||||||
| chr22:45166368 | A | G | 1 | a0001c0002t0014g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-10-1800A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166368 | |||||||
| chr22:45166374 | A | G | 1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-1794A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166374 | |||||||
| chr22:45166411 | C | T | 5 | a0001c0001t0002g0207 a0001c0001t0002g0243 a0001c0001t0002g0245 others(2): Show |
5 | NA18989.hp1 NA18998.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-1757C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166411 | |||||||
| chr22:45166467 | A | T | 30 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(27): Show |
34 | HG00673.hp1 HG02040.hp1 HG02165.hp1 others(31): Show |
intron_variant | MODIFIER | c.-10-1701A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166467 | |||||||
| chr22:45166587 | C | T | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(73): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-10-1581C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166587 | |||||||
| chr22:45166679 | G | A | 1 | a0001c0002t0001g0201 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-10-1489G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166679 | |||||||
| chr22:45166693 | G | A | 1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-10-1475G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166693 | |||||||
| chr22:45166705 | G | A | 1 | a0001c0002t0001g0012 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-10-1463G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166705 | |||||||
| chr22:45166718 | T | TAAAGAAT others(117): Show |
9 | a0001c0002t0001g0034 a0001c0002t0001g0138 a0001c0002t0001g0162 others(6): Show |
11 | HG02280.hp2 HG02630.hp1 HG02965.hp1 others(8): Show |
intron_variant | MODIFIER | c.-10-1437_-10-1436i others(126): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 45166718 | ||||||
| chr22:45166718 | T | TAAAGAAT others(118): Show |
91 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(88): Show |
144 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-10-1437_-10-1436i others(127): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 45166718 | ||||||
| chr22:45166718 | T | TAAAGAAT others(119): Show |
6 | a0001c0002t0001g0141 a0001c0002t0001g0142 a0001c0002t0001g0143 others(3): Show |
6 | HG01243.hp2 HG02572.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1437_-10-1436i others(128): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 45166718 | ||||||
| chr22:45166757 | A | T | 1 | a0001c0001t0007g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-10-1411A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166757 | |||||||
| chr22:45166785 | C | G | 84 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(81): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-10-1383C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166785 | |||||||
| chr22:45166785 | C | T | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-1383C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166785 | |||||||
| chr22:45166854 | C | T | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-10-1314C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166854 | |||||||
| chr22:45166966 | A | G | 1 | a0001c0002t0001g0198 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-10-1202A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45166966 | |||||||
| chr22:45167080 | G | C | 2 | a0001c0002t0001g0176 a0001c0002t0001g0177 |
2 | HG01934.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.-10-1088G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167080 | |||||||
| chr22:45167176 | A | T | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-992A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167176 | |||||||
| chr22:45167190 | G | A | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-10-978G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167190 | |||||||
| chr22:45167366 | T | C | 1 | a0001c0001t0008g0249 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-10-802T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167366 | |||||||
| chr22:45167413 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0242 |
3 | HG02615.hp2 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-10-755C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167413 | |||||||
| chr22:45167528 | G | T | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-10-640G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167528 | |||||||
| chr22:45167531 | A | G | 76 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(73): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-10-637A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167531 | |||||||
| chr22:45167679 | G | A | 2 | a0001c0002t0001g0174 a0001c0002t0001g0175 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-10-489G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167679 | |||||||
| chr22:45167680 | G | A | 249 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(246): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-10-488G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167680 | |||||||
| chr22:45167767 | T | G | 3 | a0001c0002t0001g0034 a0001c0002t0001g0173 a0001c0002t0050g0172 |
4 | HG02630.hp1 HG02965.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-401T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167767 | |||||||
| chr22:45167775 | T | C | 249 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(246): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.-10-393T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167775 | |||||||
| chr22:45167797 | G | A | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-10-371G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167797 | |||||||
| chr22:45167826 | T | C | 84 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(81): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.-10-342T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167826 | |||||||
| chr22:45167844 | C | G | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.-10-324C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167844 | |||||||
| chr22:45167888 | A | T | 1 | a0001c0001t0002g0241 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-10-280A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167888 | |||||||
| chr22:45167890 | T | A | 1 | a0001c0001t0002g0241 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-10-278T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167890 | |||||||
| chr22:45167894 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-10-274T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167894 | |||||||
| chr22:45167895 | C | T | 2 | a0001c0001t0002g0240 a0001c0001t0002g0241 |
2 | NA18986.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-10-273C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 1/7 | chr22 | 45167895 | |||||||
| chr22:45168356 | A | C | 1 | a0001c0001t0002g0239 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.69+110A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168356 | |||||||
| chr22:45168396 | T | G | 1 | a0001c0001t0005g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.69+150T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168396 | |||||||
| chr22:45168480 | C | T | 1 | a0001c0001t0002g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.69+234C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168480 | |||||||
| chr22:45168539 | A | G | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.69+293A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168539 | |||||||
| chr22:45168542 | C | T | 1 | a0001c0001t0002g0246 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.69+296C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168542 | |||||||
| chr22:45168546 | A | C | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.69+300A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168546 | |||||||
| chr22:45168706 | C | A | 1 | a0001c0002t0024g0041 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.69+460C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168706 | |||||||
| chr22:45168714 | A | G | 1 | a0001c0002t0053g0161 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.69+468A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168714 | |||||||
| chr22:45168757 | A | C | 1 | a0001c0001t0007g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.69+511A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168757 | |||||||
| chr22:45168894 | A | AC | 91 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(88): Show |
143 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.69+648_69+649insC | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168894 | |||||||
| chr22:45168895 | A | AG | 8 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0249 others(5): Show |
10 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.69+649_69+650insG | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168895 | |||||||
| chr22:45168895 | A | C | 15 | a0001c0001t0027g0136 a0001c0002t0001g0031 a0001c0002t0001g0035 others(12): Show |
18 | HG00735.hp2 HG01069.hp2 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.69+649A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168895 | |||||||
| chr22:45168896 | A | G | 85 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(82): Show |
143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.69+650A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168896 | |||||||
| chr22:45168898 | A | AAT | 40 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(37): Show |
45 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(42): Show |
intron_variant | MODIFIER | c.69+652_69+653insAT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168898 | |||||||
| chr22:45168898 | A | AT | 18 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(15): Show |
29 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.69+673dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 45168898 | ||||||
| chr22:45168898 | A | ATT | 17 | a0001c0001t0003g0131 a0001c0001t0003g0132 a0001c0001t0009g0259 others(14): Show |
18 | HG00735.hp2 HG01070.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.69+672_69+673dupTT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 45168898 | ||||||
| chr22:45168898 | A | T | 99 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0249 others(96): Show |
153 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.69+652A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168898 | |||||||
| chr22:45168898 | AT | A | 55 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(52): Show |
102 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.69+673delT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 45168898 | ||||||
| chr22:45168898 | ATT | A | 16 | a0001c0001t0002g0044 a0001c0001t0002g0241 a0001c0001t0002g0247 others(13): Show |
24 | HG00423.hp1 HG00639.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.69+672_69+673delTT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 45168898 | ||||||
| chr22:45168953 | G | C | 193 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(190): Show |
308 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.69+707G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45168953 | |||||||
| chr22:45169027 | G | A | 271 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(268): Show |
402 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(399): Show |
intron_variant | MODIFIER | c.69+781G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169027 | |||||||
| chr22:45169055 | C | T | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.69+809C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169055 | |||||||
| chr22:45169218 | T | C | 1 | a0001c0001t0011g0066 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.69+972T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169218 | |||||||
| chr22:45169225 | C | T | 6 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0069 others(3): Show |
6 | HG02647.hp2 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.69+979C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169225 | |||||||
| chr22:45169319 | G | A | 268 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(265): Show |
399 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(396): Show |
intron_variant | MODIFIER | c.69+1073G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169319 | |||||||
| chr22:45169369 | A | G | 3 | a0001c0001t0002g0049 a0001c0001t0002g0052 a0001c0001t0002g0235 |
5 | HG00280.hp1 HG00733.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.69+1123A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169369 | |||||||
| chr22:45169373 | A | G | 1 | a0001c0002t0002g0196 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.69+1127A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169373 | |||||||
| chr22:45169437 | A | C | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.69+1191A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169437 | |||||||
| chr22:45169450 | CACAAACT others(31): Show |
C | 1 | a0001c0001t0002g0218 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.69+1206_69+1243del others(38): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 45169450 | ||||||
| chr22:45169487 | A | G | 18 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(15): Show |
29 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.69+1241A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169487 | |||||||
| chr22:45169534 | T | G | 1 | a0001c0002t0001g0197 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.69+1288T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169534 | |||||||
| chr22:45169741 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.69+1495C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169741 | |||||||
| chr22:45169896 | C | T | 2 | a0001c0001t0003g0129 a0001c0001t0003g0134 |
2 | HG00738.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.69+1650C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169896 | |||||||
| chr22:45169944 | C | T | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-1656C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45169944 | |||||||
| chr22:45170034 | T | G | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-1566T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170034 | |||||||
| chr22:45170056 | G | A | 88 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(85): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.70-1544G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170056 | |||||||
| chr22:45170063 | G | A | 5 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(2): Show |
5 | HG01496.hp2 HG02970.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-1537G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170063 | |||||||
| chr22:45170065 | C | T | 88 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(85): Show |
148 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.70-1535C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170065 | |||||||
| chr22:45170206 | C | T | 45 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(42): Show |
50 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(47): Show |
intron_variant | MODIFIER | c.70-1394C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170206 | |||||||
| chr22:45170209 | C | T | 1 | a0001c0002t0052g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70-1391C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170209 | |||||||
| chr22:45170237 | C | T | 1 | a0001c0001t0059g0233 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.70-1363C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170237 | |||||||
| chr22:45170238 | G | A | 5 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(2): Show |
5 | HG01496.hp2 HG02970.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-1362G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170238 | |||||||
| chr22:45170246 | G | A | 45 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(42): Show |
50 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(47): Show |
intron_variant | MODIFIER | c.70-1354G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170246 | |||||||
| chr22:45170327 | C | G | 19 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(16): Show |
30 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.70-1273C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170327 | |||||||
| chr22:45170328 | C | T | 3 | a0001c0002t0001g0008 a0001c0002t0001g0195 a0001c0002t0001g0203 |
7 | HG02071.hp2 HG02080.hp1 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.70-1272C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170328 | |||||||
| chr22:45170341 | ACC | A | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-1257_70-1256del others(2): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 45170341 | ||||||
| chr22:45170479 | T | C | 44 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(41): Show |
61 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.70-1121T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170479 | |||||||
| chr22:45170532 | T | C | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-1068T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170532 | |||||||
| chr22:45170541 | T | G | 5 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(2): Show |
5 | HG01496.hp2 HG02970.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.70-1059T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170541 | |||||||
| chr22:45170576 | C | T | 45 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(42): Show |
50 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(47): Show |
intron_variant | MODIFIER | c.70-1024C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170576 | |||||||
| chr22:45170586 | A | G | 45 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(42): Show |
50 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(47): Show |
intron_variant | MODIFIER | c.70-1014A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170586 | |||||||
| chr22:45170619 | G | A | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-981G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170619 | |||||||
| chr22:45170681 | T | A | 45 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(42): Show |
50 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(47): Show |
intron_variant | MODIFIER | c.70-919T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170681 | |||||||
| chr22:45170737 | A | G | 9 | a0001c0001t0005g0054 a0001c0001t0005g0256 a0001c0001t0008g0022 others(6): Show |
12 | HG00642.hp1 HG02055.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.70-863A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170737 | |||||||
| chr22:45170821 | C | T | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-779C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170821 | |||||||
| chr22:45170878 | C | T | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.70-722C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170878 | |||||||
| chr22:45170962 | A | G | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-638A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170962 | |||||||
| chr22:45170977 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.70-623C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45170977 | |||||||
| chr22:45171031 | C | A | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-569C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171031 | |||||||
| chr22:45171154 | C | T | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-446C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171154 | |||||||
| chr22:45171173 | CAT | C | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-426_70-425delAT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171173 | |||||||
| chr22:45171186 | T | C | 57 | a0001c0002t0001g0002 a0001c0002t0001g0007 a0001c0002t0001g0008 others(54): Show |
94 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.70-414T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171186 | |||||||
| chr22:45171221 | C | CAG | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-378_70-377dupAG | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 45171221 | ||||||
| chr22:45171257 | T | C | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.70-343T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171257 | |||||||
| chr22:45171411 | C | T | 1 | a0001c0002t0001g0158 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.70-189C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171411 | |||||||
| chr22:45171463 | C | G | 1 | a0001c0001t0011g0023 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.70-137C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171463 | |||||||
| chr22:45171472 | G | T | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70-128G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171472 | |||||||
| chr22:45171473 | T | A | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70-127T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171473 | |||||||
| chr22:45171571 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.70-29A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171571 | |||||||
| chr22:45171596 | G | T | 4 | a0001c0002t0006g0019 a0001c0002t0006g0156 a0001c0002t0006g0157 others(1): Show |
5 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.70-4G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 2/7 | chr22 | 45171596 | |||||||
| chr22:45171699 | C | A | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.153+16C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45171699 | |||||||
| chr22:45171838 | G | A | 3 | a0001c0001t0003g0110 a0001c0001t0003g0111 a0001c0001t0003g0112 |
3 | HG03654.hp1 HG04115.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.153+155G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45171838 | |||||||
| chr22:45171971 | T | G | 1 | a0001c0002t0001g0180 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.153+288T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45171971 | |||||||
| chr22:45172102 | A | G | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.153+419A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172102 | |||||||
| chr22:45172223 | T | C | 49 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(46): Show |
54 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(51): Show |
intron_variant | MODIFIER | c.153+540T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172223 | |||||||
| chr22:45172429 | T | G | 19 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(16): Show |
30 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.153+746T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172429 | |||||||
| chr22:45172451 | C | A | 1 | a0001c0002t0047g0181 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.153+768C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172451 | |||||||
| chr22:45172458 | C | G | 1 | a0001c0002t0051g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.153+775C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172458 | |||||||
| chr22:45172486 | C | G | 1 | a0001c0002t0020g0168 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.153+803C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172486 | |||||||
| chr22:45172525 | T | C | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.153+842T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172525 | |||||||
| chr22:45172538 | G | A | 86 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(83): Show |
146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.153+855G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172538 | |||||||
| chr22:45172555 | T | C | 1 | a0001c0001t0005g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.153+872T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172555 | |||||||
| chr22:45172564 | C | A | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.153+881C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172564 | |||||||
| chr22:45172607 | C | CA | 50 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(47): Show |
55 | HG00673.hp1 HG01496.hp2 HG01891.hp2 others(52): Show |
intron_variant | MODIFIER | c.153+933dupA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45172607 | ||||||
| chr22:45172623 | G | A | 30 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(27): Show |
34 | HG00673.hp1 HG02040.hp1 HG02165.hp1 others(31): Show |
intron_variant | MODIFIER | c.153+940G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172623 | |||||||
| chr22:45172630 | G | T | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.153+947G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172630 | |||||||
| chr22:45172641 | A | T | 2 | a0001c0001t0005g0209 a0001c0001t0041g0231 |
2 | HG01943.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.153+958A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172641 | |||||||
| chr22:45172882 | C | T | 4 | a0001c0002t0001g0040 a0001c0002t0001g0176 a0001c0002t0001g0177 others(1): Show |
5 | HG01934.hp2 HG01952.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.153+1199C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172882 | |||||||
| chr22:45172940 | C | G | 1 | a0001c0001t0005g0209 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.153+1257C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172940 | |||||||
| chr22:45172983 | G | A | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.153+1300G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45172983 | |||||||
| chr22:45173105 | A | G | 106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.153+1422A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173105 | |||||||
| chr22:45173127 | A | G | 2 | a0001c0001t0003g0058 a0001c0001t0003g0059 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.153+1444A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173127 | |||||||
| chr22:45173182 | C | T | 1 | a0001c0001t0032g0127 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.153+1499C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173182 | |||||||
| chr22:45173258 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.153+1575G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173258 | |||||||
| chr22:45173338 | G | GT | 6 | a0001c0001t0002g0235 a0001c0001t0004g0097 a0001c0001t0005g0217 others(3): Show |
6 | HG01175.hp2 HG01496.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.153+1671dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45173338 | ||||||
| chr22:45173338 | G | GTT | 7 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(4): Show |
7 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.153+1670_153+1671d others(4): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45173338 | ||||||
| chr22:45173338 | GT | G | 7 | a0001c0001t0003g0026 a0001c0001t0010g0026 a0001c0002t0001g0193 others(4): Show |
8 | HG00735.hp2 HG01070.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.153+1671delT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45173338 | ||||||
| chr22:45173338 | GTT | G | 100 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(97): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.153+1670_153+1671d others(4): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45173338 | ||||||
| chr22:45173351 | T | G | 1 | a0001c0001t0005g0211 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.153+1668T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173351 | |||||||
| chr22:45173888 | A | G | 4 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(1): Show |
4 | HG02970.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-2006A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173888 | |||||||
| chr22:45173946 | C | T | 1 | a0001c0001t0005g0237 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.154-1948C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173946 | |||||||
| chr22:45173964 | C | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0021 others(68): Show |
116 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.154-1930C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45173964 | |||||||
| chr22:45174005 | C | T | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154-1889C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174005 | |||||||
| chr22:45174053 | G | T | 1 | a0001c0001t0003g0132 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.154-1841G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174053 | |||||||
| chr22:45174148 | C | T | 1 | a0001c0002t0001g0153 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.154-1746C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174148 | |||||||
| chr22:45174169 | C | T | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154-1725C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174169 | |||||||
| chr22:45174183 | C | CT | 50 | a0001c0001t0003g0126 a0001c0001t0003g0132 a0001c0001t0004g0014 others(47): Show |
55 | HG00673.hp1 HG01891.hp2 HG01981.hp1 others(52): Show |
intron_variant | MODIFIER | c.154-1695dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45174183 | ||||||
| chr22:45174183 | CT | C | 183 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(180): Show |
298 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.154-1695delT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45174183 | ||||||
| chr22:45174190 | T | C | 1 | a0001c0002t0051g0155 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.154-1704T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174190 | |||||||
| chr22:45174215 | T | A | 1 | a0001c0001t0007g0101 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.154-1679T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174215 | |||||||
| chr22:45174224 | G | C | 245 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(242): Show |
364 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.154-1670G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174224 | |||||||
| chr22:45174233 | G | A | 103 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(100): Show |
157 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.154-1661G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174233 | |||||||
| chr22:45174351 | C | T | 1 | a0001c0002t0017g0055 | 2 | HG00735.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.154-1543C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174351 | |||||||
| chr22:45174363 | C | G | 268 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(265): Show |
399 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(396): Show |
intron_variant | MODIFIER | c.154-1531C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174363 | |||||||
| chr22:45174425 | T | C | 1 | a0001c0001t0002g0223 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.154-1469T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174425 | |||||||
| chr22:45174428 | C | T | 1 | a0001c0002t0049g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.154-1466C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174428 | |||||||
| chr22:45174562 | G | A | 1 | a0001c0002t0001g0182 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.154-1332G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174562 | |||||||
| chr22:45174614 | C | G | 5 | a0001c0002t0006g0018 a0001c0003t0006g0018 a0001c0003t0006g0033 others(2): Show |
7 | HG01243.hp2 HG02723.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-1280C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174614 | |||||||
| chr22:45174675 | C | CATGAATC others(1): Show |
106 | a0001c0001t0027g0136 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.154-1218_154-1211d others(10): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45174675 | ||||||
| chr22:45174713 | C | T | 249 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(246): Show |
369 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(366): Show |
intron_variant | MODIFIER | c.154-1181C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174713 | |||||||
| chr22:45174795 | T | C | 7 | a0001c0001t0007g0063 a0001c0001t0007g0064 a0001c0001t0007g0069 others(4): Show |
7 | HG02145.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-1099T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174795 | |||||||
| chr22:45174804 | C | A | 49 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(46): Show |
54 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(51): Show |
intron_variant | MODIFIER | c.154-1090C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174804 | |||||||
| chr22:45174963 | A | AT | 52 | a0001c0001t0003g0027 a0001c0001t0003g0107 a0001c0001t0004g0014 others(49): Show |
58 | HG00673.hp1 HG01884.hp1 HG01891.hp2 others(55): Show |
intron_variant | MODIFIER | c.154-918dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 45174963 | ||||||
| chr22:45174987 | C | A | 3 | a0001c0002t0001g0036 a0001c0002t0001g0183 a0001c0002t0001g0184 |
4 | NA18968.hp2 NA18981.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-907C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174987 | |||||||
| chr22:45174995 | T | C | 3 | a0001c0001t0002g0053 a0001c0001t0002g0242 a0001c0004t0002g0046 |
5 | HG01070.hp1 HG01071.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-899T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45174995 | |||||||
| chr22:45175088 | C | T | 84 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(81): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.154-806C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175088 | |||||||
| chr22:45175111 | C | G | 1 | a0001c0002t0001g0140 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.154-783C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175111 | |||||||
| chr22:45175161 | T | G | 1 | a0001c0002t0014g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.154-733T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175161 | |||||||
| chr22:45175390 | C | T | 9 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(6): Show |
9 | HG01891.hp1 HG02630.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-504C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175390 | |||||||
| chr22:45175565 | C | T | 37 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0021 others(34): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.154-329C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175565 | |||||||
| chr22:45175626 | C | T | 4 | a0001c0001t0011g0023 a0001c0001t0011g0061 a0001c0001t0011g0066 others(1): Show |
5 | HG02451.hp1 HG02647.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-268C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175626 | |||||||
| chr22:45175669 | C | T | 9 | a0001c0002t0006g0018 a0001c0002t0006g0019 a0001c0002t0006g0156 others(6): Show |
12 | HG01243.hp2 HG02055.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-225C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175669 | |||||||
| chr22:45175776 | T | C | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154-118T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175776 | |||||||
| chr22:45175830 | C | T | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.154-64C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175830 | |||||||
| chr22:45175854 | A | C | 1 | a0001c0001t0003g0106 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.154-40A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 3/7 | chr22 | 45175854 | |||||||
| chr22:45176135 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.340+55C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45176135 | |||||||
| chr22:45176391 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.340+311G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45176391 | |||||||
| chr22:45176896 | C | T | 1 | a0001c0001t0002g0230 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.340+816C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45176896 | |||||||
| chr22:45176909 | T | A | 1 | a0001c0001t0008g0253 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.340+829T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45176909 | |||||||
| chr22:45176942 | A | G | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.340+862A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45176942 | |||||||
| chr22:45176983 | A | C | 19 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(16): Show |
30 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.340+903A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45176983 | |||||||
| chr22:45177022 | G | A | 1 | a0001c0002t0014g0265 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.340+942G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177022 | |||||||
| chr22:45177163 | G | C | 15 | a0001c0001t0002g0003 a0001c0001t0002g0050 a0001c0001t0002g0207 others(12): Show |
24 | HG00597.hp1 HG01069.hp1 HG02074.hp1 others(21): Show |
intron_variant | MODIFIER | c.341-1075G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177163 | |||||||
| chr22:45177204 | A | G | 1 | a0001c0001t0003g0123 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.341-1034A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177204 | |||||||
| chr22:45177211 | C | T | 3 | a0001c0001t0003g0106 a0001c0001t0010g0105 a0001c0001t0025g0104 |
3 | HG02922.hp1 HG03540.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.341-1027C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177211 | |||||||
| chr22:45177273 | C | T | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(80): Show |
143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.341-965C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177273 | |||||||
| chr22:45177347 | A | G | 1 | a0001c0001t0004g0091 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.341-891A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177347 | |||||||
| chr22:45177356 | T | C | 1 | a0001c0002t0001g0185 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.341-882T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177356 | |||||||
| chr22:45177517 | C | G | 1 | a0001c0002t0001g0191 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.341-721C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177517 | |||||||
| chr22:45177525 | C | A | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(80): Show |
143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.341-713C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177525 | |||||||
| chr22:45177569 | A | C | 19 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(16): Show |
30 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.341-669A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177569 | |||||||
| chr22:45177666 | G | C | 1 | a0001c0001t0002g0021 | 3 | NA18999.hp1 NA19066.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.341-572G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177666 | |||||||
| chr22:45177814 | CTT | C | 19 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(16): Show |
30 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.341-420_341-419del others(2): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 45177814 | ||||||
| chr22:45177866 | C | T | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.341-372C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45177866 | |||||||
| chr22:45178132 | G | T | 1 | a0001c0001t0004g0096 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.341-106G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 4/7 | chr22 | 45178132 | |||||||
| chr22:45178941 | A | C | 4 | a0001c0001t0002g0207 a0001c0001t0002g0243 a0001c0001t0002g0245 others(1): Show |
4 | NA18989.hp1 NA18998.hp1 NA19006.hp2 others(1): Show |
intron_variant | MODIFIER | c.1003+41A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45178941 | |||||||
| chr22:45179038 | C | A | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1003+138C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45179038 | |||||||
| chr22:45179105 | T | G | 78 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(75): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1003+205T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45179105 | |||||||
| chr22:45179457 | C | CCCCAGAC others(4): Show |
1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1003+559_1003+569d others(13): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45179457 | ||||||
| chr22:45179528 | A | C | 1 | a0001c0001t0002g0051 | 2 | HG01192.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1003+628A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45179528 | |||||||
| chr22:45179587 | A | G | 106 | a0001c0001t0040g0267 a0001c0002t0001g0002 a0001c0002t0001g0004 others(103): Show |
161 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1003+687A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45179587 | |||||||
| chr22:45179815 | T | G | 1 | a0001c0001t0002g0229 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1003+915T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45179815 | |||||||
| chr22:45179977 | C | T | 1 | a0001c0002t0024g0041 | 2 | HG02280.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1003+1077C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45179977 | |||||||
| chr22:45180128 | C | A | 1 | a0001c0002t0020g0168 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1004-1158C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180128 | |||||||
| chr22:45180259 | C | T | 15 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(12): Show |
26 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1004-1027C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180259 | |||||||
| chr22:45180383 | ATTTTTTT | A | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1004-902_1004-896d others(9): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180383 | |||||||
| chr22:45180395 | CAG | C | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1004-890_1004-889d others(4): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180395 | |||||||
| chr22:45180416 | A | G | 1 | a0001c0001t0002g0228 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1004-870A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180416 | |||||||
| chr22:45180520 | C | T | 83 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(80): Show |
143 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.1004-766C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180520 | |||||||
| chr22:45180641 | G | A | 1 | a0001c0001t0005g0237 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1004-645G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180641 | |||||||
| chr22:45180842 | T | TA | 124 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0016 others(121): Show |
191 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.1004-431dupA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45180842 | ||||||
| chr22:45180842 | TA | T | 51 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(48): Show |
57 | HG00642.hp1 HG00673.hp1 HG01891.hp2 others(54): Show |
intron_variant | MODIFIER | c.1004-431delA | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45180842 | ||||||
| chr22:45180842 | TAA | T | 11 | a0001c0001t0004g0095 a0001c0001t0009g0259 a0001c0001t0009g0261 others(8): Show |
11 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.1004-432_1004-431d others(4): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45180842 | ||||||
| chr22:45180856 | G | A | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1004-430G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45180856 | |||||||
| chr22:45180982 | A | AT | 104 | a0001c0001t0004g0090 a0001c0001t0007g0068 a0001c0002t0001g0002 others(101): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.1004-294dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45180982 | ||||||
| chr22:45181135 | T | TC | 56 | a0001c0001t0003g0016 a0001c0001t0003g0026 a0001c0001t0003g0029 others(53): Show |
67 | HG00323.hp1 HG00544.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1004-137dupC | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45181135 | ||||||
| chr22:45181135 | TC | T | 42 | a0001c0001t0003g0109 a0001c0001t0003g0116 a0001c0001t0003g0117 others(39): Show |
54 | HG00099.hp2 HG00673.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.1004-137delC | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45181135 | ||||||
| chr22:45181135 | TCCC | T | 77 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(74): Show |
133 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.1004-139_1004-137d others(5): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr22 | 45181135 | ||||||
| chr22:45181138 | C | T | 1 | a0001c0001t0007g0068 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1004-148C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45181138 | |||||||
| chr22:45181149 | C | A | 4 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(1): Show |
4 | HG02970.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1004-137C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45181149 | |||||||
| chr22:45181195 | T | C | 1 | a0001c0001t0004g0062 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1004-91T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45181195 | |||||||
| chr22:45181214 | G | A | 2 | a0001c0001t0038g0268 a0001c0001t0040g0267 |
2 | HG00423.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1004-72G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45181214 | |||||||
| chr22:45181229 | T | C | 105 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(102): Show |
160 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1004-57T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 5/7 | chr22 | 45181229 | |||||||
| chr22:45181467 | C | T | 4 | a0001c0001t0013g0272 a0001c0001t0013g0273 a0001c0001t0013g0274 others(1): Show |
4 | HG02970.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1085+100C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181467 | |||||||
| chr22:45181491 | TCAAGTGG others(31): Show |
T | 84 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(81): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1085+125_1085+162d others(40): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181491 | |||||||
| chr22:45181530 | A | T | 84 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(81): Show |
144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.1085+163A>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181530 | |||||||
| chr22:45181594 | T | C | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1085+227T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181594 | |||||||
| chr22:45181656 | C | A | 86 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(83): Show |
146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1085+289C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181656 | |||||||
| chr22:45181754 | A | G | 1 | a0001c0001t0004g0090 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1085+387A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181754 | |||||||
| chr22:45181859 | A | C | 1 | a0001c0002t0049g0150 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1085+492A>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181859 | |||||||
| chr22:45181923 | C | T | 268 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(265): Show |
399 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(396): Show |
intron_variant | MODIFIER | c.1085+556C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45181923 | |||||||
| chr22:45182128 | A | AT | 50 | a0001c0001t0002g0218 a0001c0001t0004g0014 a0001c0001t0004g0024 others(47): Show |
55 | HG00673.hp1 HG01891.hp1 HG01891.hp2 others(52): Show |
intron_variant | MODIFIER | c.1085+775dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182128 | ||||||
| chr22:45182129 | T | A | 1 | a0001c0001t0003g0110 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1085+762T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182129 | |||||||
| chr22:45182142 | T | A | 1 | a0001c0001t0025g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1085+775T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182142 | |||||||
| chr22:45182176 | C | T | 1 | a0001c0001t0008g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1085+809C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182176 | |||||||
| chr22:45182258 | T | C | 1 | a0001c0002t0001g0160 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1085+891T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182258 | |||||||
| chr22:45182319 | T | C | 2 | a0001c0002t0021g0178 a0001c0002t0021g0199 |
2 | NA19056.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1085+952T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182319 | |||||||
| chr22:45182374 | A | G | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1085+1007A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182374 | |||||||
| chr22:45182381 | G | C | 2 | a0001c0001t0016g0045 a0001c0001t0016g0221 |
3 | NA18956.hp2 NA18985.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1085+1014G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182381 | |||||||
| chr22:45182394 | A | G | 1 | a0001c0001t0042g0257 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1086-1008A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182394 | |||||||
| chr22:45182444 | G | T | 1 | a0001c0001t0005g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1086-958G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182444 | |||||||
| chr22:45182481 | TTAA | T | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1086-917_1086-915d others(5): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182481 | ||||||
| chr22:45182513 | G | A | 1 | a0001c0001t0041g0231 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1086-889G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182513 | |||||||
| chr22:45182608 | A | G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(93): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1086-794A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182608 | |||||||
| chr22:45182623 | G | GT | 21 | a0001c0001t0003g0006 a0001c0001t0003g0011 a0001c0001t0003g0015 others(18): Show |
32 | HG00099.hp1 HG00323.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.1086-760dupT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182623 | ||||||
| chr22:45182623 | G | GTT | 18 | a0001c0001t0002g0047 a0001c0001t0003g0030 a0001c0001t0003g0125 others(15): Show |
21 | HG01175.hp1 HG01192.hp1 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.1086-761_1086-760d others(4): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182623 | ||||||
| chr22:45182623 | G | GTTT | 63 | a0001c0001t0002g0001 a0001c0001t0002g0021 a0001c0001t0002g0044 others(60): Show |
101 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.1086-762_1086-760d others(5): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182623 | ||||||
| chr22:45182623 | G | GTTTT | 42 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0050 others(39): Show |
65 | HG00597.hp1 HG00639.hp1 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.1086-763_1086-760d others(6): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182623 | ||||||
| chr22:45182623 | G | GTTTTT | 14 | a0001c0001t0002g0207 a0001c0001t0002g0218 a0001c0001t0002g0220 others(11): Show |
14 | HG00741.hp1 HG02074.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1086-764_1086-760d others(7): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182623 | ||||||
| chr22:45182623 | G | GTTTTTT | 8 | a0001c0001t0004g0084 a0001c0001t0008g0022 a0001c0001t0008g0249 others(5): Show |
10 | HG00673.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.1086-765_1086-760d others(8): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182623 | ||||||
| chr22:45182623 | GT | G | 83 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(80): Show |
129 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1086-760delT | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182623 | ||||||
| chr22:45182629 | T | A | 1 | a0001c0002t0031g0065 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1086-773T>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182629 | |||||||
| chr22:45182629 | T | G | 1 | a0001c0001t0003g0116 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1086-773T>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182629 | |||||||
| chr22:45182653 | CTCTT | C | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1086-745_1086-742d others(6): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45182653 | ||||||
| chr22:45182665 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1086-737C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182665 | |||||||
| chr22:45182693 | C | T | 2 | a0001c0002t0001g0034 a0001c0002t0001g0173 |
3 | HG02965.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1086-709C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182693 | |||||||
| chr22:45182881 | C | T | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1086-521C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182881 | |||||||
| chr22:45182914 | C | T | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1086-488C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45182914 | |||||||
| chr22:45183035 | C | T | 48 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(45): Show |
53 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(50): Show |
intron_variant | MODIFIER | c.1086-367C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183035 | |||||||
| chr22:45183072 | C | T | 86 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(83): Show |
146 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1086-330C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183072 | |||||||
| chr22:45183084 | G | GC | 8 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086-317dupC | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45183084 | ||||||
| chr22:45183085 | C | CG | 14 | a0001c0001t0003g0006 a0001c0001t0003g0016 a0001c0001t0003g0107 others(11): Show |
20 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1086-302dupG | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45183085 | ||||||
| chr22:45183085 | C | G | 1 | a0001c0001t0027g0136 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1086-317C>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183085 | |||||||
| chr22:45183085 | CGG | C | 124 | a0001c0001t0004g0014 a0001c0001t0004g0074 a0001c0001t0004g0075 others(121): Show |
182 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1086-303_1086-302d others(4): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45183085 | ||||||
| chr22:45183085 | CGGG | C | 19 | a0001c0001t0002g0227 a0001c0001t0004g0024 a0001c0001t0004g0025 others(16): Show |
21 | HG01109.hp2 HG02040.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.1086-304_1086-302d others(5): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45183085 | ||||||
| chr22:45183085 | CGGGG | C | 91 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(88): Show |
151 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1086-305_1086-302d others(6): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 45183085 | ||||||
| chr22:45183086 | G | C | 2 | a0001c0001t0014g0264 a0001c0002t0009g0262 |
2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1086-316G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183086 | |||||||
| chr22:45183089 | G | C | 2 | a0001c0001t0004g0078 a0001c0001t0004g0085 |
2 | HG02683.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1086-313G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183089 | |||||||
| chr22:45183089 | G | T | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1086-313G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183089 | |||||||
| chr22:45183090 | G | T | 1 | a0001c0001t0003g0112 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1086-312G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183090 | |||||||
| chr22:45183091 | G | T | 8 | a0001c0001t0003g0110 a0001c0001t0003g0111 a0001c0002t0001g0146 others(5): Show |
8 | HG02027.hp1 HG02055.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086-311G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183091 | |||||||
| chr22:45183092 | G | T | 99 | a0001c0002t0001g0002 a0001c0002t0001g0004 a0001c0002t0001g0007 others(96): Show |
154 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1086-310G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183092 | |||||||
| chr22:45183093 | G | C | 1 | a0001c0001t0002g0227 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1086-309G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183093 | |||||||
| chr22:45183094 | G | C | 85 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(82): Show |
145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.1086-308G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183094 | |||||||
| chr22:45183095 | G | C | 8 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(5): Show |
8 | HG02630.hp2 HG02886.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086-307G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183095 | |||||||
| chr22:45183096 | G | A | 8 | a0001c0001t0004g0079 a0001c0001t0004g0080 a0001c0001t0004g0082 others(5): Show |
8 | NA18950.hp1 NA18955.hp2 NA18975.hp2 others(5): Show |
intron_variant | MODIFIER | c.1086-306G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183096 | |||||||
| chr22:45183098 | G | T | 4 | a0001c0001t0007g0064 a0001c0001t0007g0070 a0001c0001t0007g0071 others(1): Show |
4 | HG02647.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1086-304G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183098 | |||||||
| chr22:45183280 | T | C | 2 | a0001c0001t0008g0249 a0001c0001t0008g0250 |
2 | HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1086-122T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183280 | |||||||
| chr22:45183317 | A | G | 1 | a0001c0002t0001g0188 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1086-85A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183317 | |||||||
| chr22:45183346 | T | C | 10 | a0001c0001t0009g0259 a0001c0001t0009g0261 a0001c0001t0009g0266 others(7): Show |
10 | HG01891.hp1 HG02486.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1086-56T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 6/7 | chr22 | 45183346 | |||||||
| chr22:45183541 | A | G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(93): Show |
156 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.1204+21A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183541 | |||||||
| chr22:45183621 | G | T | 41 | a0001c0002t0001g0004 a0001c0002t0001g0012 a0001c0002t0001g0013 others(38): Show |
58 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.1204+101G>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183621 | |||||||
| chr22:45183657 | ATAGTTTT | A | 5 | a0001c0001t0008g0022 a0001c0001t0008g0171 a0001c0001t0008g0251 others(2): Show |
7 | HG02258.hp2 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1204+138_1204+144d others(9): Show |
NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183657 | |||||||
| chr22:45183849 | G | A | 1 | a0001c0001t0007g0069 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1204+329G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183849 | |||||||
| chr22:45183850 | C | A | 239 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(236): Show |
359 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1204+330C>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183850 | |||||||
| chr22:45183852 | T | C | 50 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(47): Show |
55 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(52): Show |
intron_variant | MODIFIER | c.1204+332T>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183852 | |||||||
| chr22:45183900 | C | T | 1 | a0001c0001t0011g0023 | 2 | HG02809.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1204+380C>T | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183900 | |||||||
| chr22:45183998 | A | G | 50 | a0001c0001t0004g0014 a0001c0001t0004g0024 a0001c0001t0004g0025 others(47): Show |
55 | HG00673.hp1 HG01891.hp2 HG02040.hp1 others(52): Show |
intron_variant | MODIFIER | c.1205-455A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45183998 | |||||||
| chr22:45184011 | G | A | 1 | a0001c0002t0001g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1205-442G>A | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45184011 | |||||||
| chr22:45184159 | A | G | 1 | a0001c0001t0008g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1205-294A>G | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45184159 | |||||||
| chr22:45184278 | G | C | 249 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0005 others(246): Show |
367 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(364): Show |
intron_variant | MODIFIER | c.1205-175G>C | NUP50 | ENSG00000093000.19 | transcript | ENST00000347635.9 | protein_coding | 7/7 | chr22 | 45184278 |