Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4869 |
| ensemblid | ENSG00000181163.14 |
| hgncid | 7910 |
| symbol | NPM1 |
| name | nucleophosmin 1 |
| refseq_nuc | NM_002520.7 |
| refseq_prot | NP_002511.1 |
| ensembl_nuc | ENST00000296930.10 |
| ensembl_prot | ENSP00000296930.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 171387849 |
| end | 171410900 |
| strand | + |
| ver | v1.2 |
| region | chr5:171387849-171410900 |
| region5000 | chr5:171382849-171415900 |
| regionname0 | NPM1_chr5_171387849_171410900 |
| regionname5000 | NPM1_chr5_171382849_171415900 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 294 | 400 | 91 | 74 | 181 | 14 | 38 | 140 | NPM1_chr5_171382849_171415900 | NPM1 | MEDSM others(289): Show |
chr5 | 171382849 | 171415900 |
| a0002 | 0/0 | 294 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | MEDSM others(289): Show |
chr5 | 171382849 | 171415900 |
| a0003 | 0/0 | 294 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | MEDSM others(289): Show |
chr5 | 171382849 | 171415900 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 882 | 398 | 90 | 73 | 181 | 14 | 38 | NPM1_chr5_171382849_171415900 | NPM1 | ATGGA others(877): Show |
chr5 | 171382849 | 171415900 | ||
| a0001c0002 | 0/0 | 882 | 2 | 1 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | ATGGA others(877): Show |
chr5 | 171382849 | 171415900 | ||
| a0002c0004 | 0/0 | 882 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | ATGGA others(877): Show |
chr5 | 171382849 | 171415900 | ||
| a0003c0003 | 0/0 | 882 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | ATGGA others(877): Show |
chr5 | 171382849 | 171415900 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1320 | 271 | 79 | 56 | 99 | 9 | 26 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0002 | 0/0 | 1319 | 99 | 8 | 17 | 57 | 5 | 12 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1314): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0003 | 0/0 | 1319 | 22 | 0 | 0 | 22 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1314): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0004 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0005 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0006 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0007 | 0/0 | 1319 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1314): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0008 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| a0001c0001t0009 | 0/0 | 1319 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1314): Show |
chr5 | 171382849 | 171415900 |
| a0001c0002t0001 | 0/0 | 1320 | 2 | 1 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| a0002c0004t0001 | 0/0 | 1320 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| a0003c0003t0001 | 0/0 | 1320 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | CTTTC others(1315): Show |
chr5 | 171382849 | 171415900 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 29 | 1 | 9 | 10 | 0 | 9 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 3 | 5 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0009 | 0/0 | 6 | 0 | 3 | 0 | 2 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0011 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0012 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0016 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0017 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0021 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0119 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0002 | 0/0 | 23 | 2 | 5 | 11 | 1 | 4 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0003 | 0/0 | 10 | 0 | 0 | 10 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0007 | 0/0 | 7 | 1 | 3 | 1 | 1 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0014 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0015 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0048 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0053 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0008g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0001t0009g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0001c0002t0001g0033 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0002c0004t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | GBR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0046 | EUR | IBS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | IBS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0041 | EUR | IBS | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CDX | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | KHV | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0197 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0079 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0178 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0142 | AFR | ESN | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0015 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0183 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | YRI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | YRI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18747 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | CHB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | YRI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18941 | hp2 | a0001 | c0001 | t0005 | g0043 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18965 | hp2 | a0001 | c0001 | t0007 | g0020 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18971 | hp2 | a0001 | c0001 | t0009 | g0192 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ASW | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0007 | EUR | TSI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0157 | EUR | TSI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | TSI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | TSI | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | USA | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | USA | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | LWK | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0119 | REF | REF | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0017 | REF | REF | NPM1_chr5_171382849_171415900 | NPM1 | chr5 | 171382849 | 171415900 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171392815 | A | G | 1 | a0002 | 1 | HG02922.hp2 | missense_variant&splice_region_variant | MODERATE | c.458A>G | p.Gln153Arg | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 5/11 | 558/1320 | 458/885 | 153/294 | chr5 | 171392815 | |||
| chr5:171400206 | A | G | 1 | a0003 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.578A>G | p.Lys193Arg | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/11 | 678/1320 | 578/885 | 193/294 | chr5 | 171400206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171400171 | T | C | 1 | a0001c0002 | 2 | HG01243.hp2 HG03471.hp2 |
synonymous_variant | LOW | c.543T>C | p.Phe181Phe | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/11 | 643/1320 | 543/885 | 181/294 | chr5 | 171400171 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171387873 | G | T | 1 | a0001c0001t0009 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-76G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/11 | 76 | chr5 | 171387873 | ||||||
| chr5:171387885 | T | C | 1 | a0001c0001t0004 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-64T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/11 | 64 | chr5 | 171387885 | ||||||
| chr5:171387895 | C | T | 1 | a0001c0001t0008 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/11 | 54 | chr5 | 171387895 | ||||||
| chr5:171387921 | C | T | 1 | a0001c0001t0007 | 1 | NA18965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-28C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/11 | 28 | chr5 | 171387921 | ||||||
| chr5:171410699 | C | G | 1 | a0001c0001t0006 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*134C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 11/11 | 134 | chr5 | 171410699 | ||||||
| chr5:171410729 | CT | C | 4 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(1): Show |
123 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*165delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 11/11 | 165 | chr5 | 171410729 | ||||||
| chr5:171410888 | C | T | 1 | a0001c0001t0005 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*323C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 11/11 | 323 | chr5 | 171410888 | ||||||
| chr5:171410896 | A | G | 2 | a0001c0001t0003 a0001c0001t0007 |
23 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*331A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 11/11 | 331 | chr5 | 171410896 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:171388098 | C | G | 1 | a0001c0001t0003g0209 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.58+92C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388098 | |||||||
| chr5:171388121 | G | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
208 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.58+115G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388121 | |||||||
| chr5:171388141 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58+135A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388141 | |||||||
| chr5:171388475 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.58+469G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388475 | |||||||
| chr5:171388517 | C | T | 8 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(5): Show |
15 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.58+511C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388517 | |||||||
| chr5:171388518 | A | G | 1 | a0001c0001t0001g0042 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.58+512A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388518 | |||||||
| chr5:171388557 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58+551G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388557 | |||||||
| chr5:171388760 | GCT | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
6 | NA18971.hp1 NA18983.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.58+758_58+759delTC | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 171388760 | ||||||
| chr5:171388869 | G | C | 1 | a0001c0001t0008g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.58+863G>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388869 | |||||||
| chr5:171388888 | A | G | 1 | a0001c0001t0003g0209 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.58+882A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388888 | |||||||
| chr5:171388947 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.58+941G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171388947 | |||||||
| chr5:171389197 | CT | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(10): Show |
23 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-851delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 171389197 | ||||||
| chr5:171389231 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-820A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389231 | |||||||
| chr5:171389238 | T | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(21): Show |
49 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.59-813T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389238 | |||||||
| chr5:171389322 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-729A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389322 | |||||||
| chr5:171389397 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.59-654T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389397 | |||||||
| chr5:171389399 | T | G | 13 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0058 others(10): Show |
22 | HG00323.hp1 HG00558.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.59-652T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389399 | |||||||
| chr5:171389488 | C | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-563C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389488 | |||||||
| chr5:171389494 | G | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.59-557G>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389494 | |||||||
| chr5:171389537 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(12): Show |
26 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.59-514G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389537 | |||||||
| chr5:171389739 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.59-312T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389739 | |||||||
| chr5:171389977 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0203 |
3 | HG02630.hp2 HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.59-74C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 1/10 | chr5 | 171389977 | |||||||
| chr5:171390411 | A | G | 19 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0038 others(16): Show |
30 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.138+281A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171390411 | |||||||
| chr5:171390551 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.138+421C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171390551 | |||||||
| chr5:171390616 | A | T | 1 | a0001c0001t0002g0202 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.138+486A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171390616 | |||||||
| chr5:171390678 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0136 |
3 | HG01070.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.138+548A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171390678 | |||||||
| chr5:171390696 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.138+566T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171390696 | |||||||
| chr5:171390727 | GT | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
198 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.139-567delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 171390727 | ||||||
| chr5:171390864 | A | G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0120 others(3): Show |
10 | NA18747.hp2 NA18954.hp1 NA18973.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-441A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171390864 | |||||||
| chr5:171390943 | C | CA | 86 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
178 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.139-359dupA | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 171390943 | ||||||
| chr5:171391095 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0001c0001t0001g0078 others(1): Show |
5 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-210T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171391095 | |||||||
| chr5:171391159 | T | G | 1 | a0001c0001t0001g0123 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.139-146T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171391159 | |||||||
| chr5:171391248 | G | A | 1 | a0001c0001t0002g0046 | 2 | HG00140.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.139-57G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171391248 | |||||||
| chr5:171391284 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.139-21G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 2/10 | chr5 | 171391284 | |||||||
| chr5:171391429 | G | A | 2 | a0001c0001t0001g0043 a0001c0001t0005g0043 |
2 | NA18941.hp2 NA18942.hp2 |
splice_region_variant&intron_variant | LOW | c.258+5G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 3/10 | chr5 | 171391429 | |||||||
| chr5:171391893 | A | G | 58 | a0001c0001t0001g0164 a0001c0001t0002g0002 a0001c0001t0002g0003 others(55): Show |
124 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.352+94A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171391893 | |||||||
| chr5:171391902 | T | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.352+103T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171391902 | |||||||
| chr5:171391904 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.352+105A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171391904 | |||||||
| chr5:171391917 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0151 |
3 | HG03130.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.352+118G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171391917 | |||||||
| chr5:171391957 | C | CG | 23 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0025 others(20): Show |
38 | HG00609.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
intron_variant | MODIFIER | c.352+165dupG | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171391957 | ||||||
| chr5:171391960 | G | GGT | 62 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(59): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.352+162_352+163ins others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171391960 | ||||||
| chr5:171391965 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.352+166A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171391965 | |||||||
| chr5:171392043 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.352+244G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392043 | |||||||
| chr5:171392087 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.352+288G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392087 | |||||||
| chr5:171392106 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.352+307C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392106 | |||||||
| chr5:171392118 | A | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.352+319A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392118 | |||||||
| chr5:171392209 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.352+410A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392209 | |||||||
| chr5:171392285 | A | T | 1 | a0001c0001t0008g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.353-425A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392285 | |||||||
| chr5:171392303 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(8): Show |
18 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.353-407T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392303 | |||||||
| chr5:171392440 | TCTTGGCC others(13): Show |
T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0077 a0002c0004t0001g0079 |
4 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.353-260_353-241del others(20): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171392440 | ||||||
| chr5:171392459 | G | A | 1 | a0001c0001t0002g0002 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.353-251G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392459 | |||||||
| chr5:171392488 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.353-222G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392488 | |||||||
| chr5:171392502 | C | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.353-208C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392502 | |||||||
| chr5:171392586 | C | CT | 17 | a0001c0001t0001g0009 a0001c0001t0001g0030 a0001c0001t0001g0041 others(14): Show |
25 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.353-107dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171392586 | ||||||
| chr5:171392586 | C | CTTTT | 5 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0121 others(2): Show |
9 | NA18747.hp2 NA18954.hp1 NA18973.hp2 others(6): Show |
intron_variant | MODIFIER | c.353-110_353-107dup others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171392586 | ||||||
| chr5:171392586 | CT | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0060 a0001c0001t0001g0063 others(4): Show |
8 | HG01070.hp1 HG01256.hp2 HG01516.hp1 others(5): Show |
intron_variant | MODIFIER | c.353-107delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171392586 | ||||||
| chr5:171392586 | CTT | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(8): Show |
18 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.353-108_353-107del others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171392586 | ||||||
| chr5:171392586 | CTTT | C | 85 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
177 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.353-109_353-107del others(3): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171392586 | ||||||
| chr5:171392586 | CTTTT | C | 5 | a0001c0001t0001g0057 a0001c0001t0001g0143 a0001c0001t0001g0205 others(2): Show |
6 | HG01070.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.353-110_353-107del others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 171392586 | ||||||
| chr5:171392602 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.353-108T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392602 | |||||||
| chr5:171392603 | T | A | 78 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(75): Show |
162 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.353-107T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 4/10 | chr5 | 171392603 | |||||||
| chr5:171392883 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.460-31G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 5/10 | chr5 | 171392883 | |||||||
| chr5:171393020 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.524+42G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393020 | |||||||
| chr5:171393106 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.524+128A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393106 | |||||||
| chr5:171393281 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.524+303T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393281 | |||||||
| chr5:171393312 | G | A | 132 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(129): Show |
246 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(243): Show |
intron_variant | MODIFIER | c.524+334G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393312 | |||||||
| chr5:171393315 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.524+337G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393315 | |||||||
| chr5:171393559 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.524+581C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393559 | |||||||
| chr5:171393626 | ACTT | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(53): Show |
122 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.524+649_524+651del others(3): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393626 | |||||||
| chr5:171393751 | G | A | 1 | a0001c0001t0002g0165 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.524+773G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393751 | |||||||
| chr5:171393791 | G | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+813G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393791 | |||||||
| chr5:171393859 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0001g0151 |
3 | HG03130.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.524+881G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393859 | |||||||
| chr5:171393876 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0093 |
2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.524+898T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393876 | |||||||
| chr5:171393943 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.524+965A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393943 | |||||||
| chr5:171393958 | T | G | 1 | a0001c0001t0002g0166 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.524+980T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393958 | |||||||
| chr5:171393980 | G | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0151 |
3 | HG03130.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.524+1002G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393980 | |||||||
| chr5:171393998 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.524+1020C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171393998 | |||||||
| chr5:171394041 | C | CT | 26 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0024 others(23): Show |
40 | HG00140.hp2 HG00733.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.524+1084dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171394041 | ||||||
| chr5:171394041 | CT | C | 5 | a0001c0001t0001g0031 a0001c0001t0001g0064 a0001c0001t0001g0082 others(2): Show |
7 | HG01243.hp2 HG02717.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.524+1084delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171394041 | ||||||
| chr5:171394043 | T | TTTC | 13 | a0001c0001t0002g0003 a0001c0001t0002g0028 a0001c0001t0002g0053 others(10): Show |
25 | HG00423.hp1 HG00438.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.524+1067_524+1068i others(5): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171394043 | ||||||
| chr5:171394044 | T | TTC | 48 | a0001c0001t0001g0025 a0001c0001t0001g0047 a0001c0001t0001g0149 others(45): Show |
105 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.524+1067_524+1068i others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171394044 | ||||||
| chr5:171394045 | T | TC | 39 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(36): Show |
70 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.524+1067_524+1068i others(3): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394045 | |||||||
| chr5:171394046 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.524+1068T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394046 | |||||||
| chr5:171394048 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18970.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.524+1070T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394048 | |||||||
| chr5:171394096 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.524+1118C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394096 | |||||||
| chr5:171394103 | G | A | 1 | a0001c0001t0008g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.524+1125G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394103 | |||||||
| chr5:171394135 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.524+1157G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394135 | |||||||
| chr5:171394203 | T | A | 1 | a0001c0001t0002g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.524+1225T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394203 | |||||||
| chr5:171394408 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.524+1430G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394408 | |||||||
| chr5:171394543 | C | T | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(8): Show |
18 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.524+1565C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394543 | |||||||
| chr5:171394559 | A | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0132 a0001c0001t0001g0134 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01099.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+1581A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394559 | |||||||
| chr5:171394601 | G | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+1623G>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394601 | |||||||
| chr5:171394750 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+1772A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394750 | |||||||
| chr5:171394778 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(8): Show |
26 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.524+1800T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394778 | |||||||
| chr5:171394891 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+1913T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394891 | |||||||
| chr5:171394895 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.524+1917T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171394895 | |||||||
| chr5:171395016 | TAA | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(8): Show |
26 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.524+2042_524+2043d others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171395016 | ||||||
| chr5:171395144 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.524+2166T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395144 | |||||||
| chr5:171395188 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+2210T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395188 | |||||||
| chr5:171395251 | G | T | 1 | a0001c0001t0002g0194 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.524+2273G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395251 | |||||||
| chr5:171395258 | A | C | 1 | a0001c0001t0001g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.524+2280A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395258 | |||||||
| chr5:171395281 | A | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+2303A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395281 | |||||||
| chr5:171395330 | G | A | 3 | a0001c0001t0002g0014 a0001c0001t0002g0168 a0001c0001t0002g0202 |
7 | NA18954.hp2 NA19011.hp2 NA19012.hp2 others(4): Show |
intron_variant | MODIFIER | c.524+2352G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395330 | |||||||
| chr5:171395571 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.524+2593G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395571 | |||||||
| chr5:171395670 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(8): Show |
26 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.524+2692C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395670 | |||||||
| chr5:171395760 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.524+2782C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395760 | |||||||
| chr5:171395871 | G | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.524+2893G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395871 | |||||||
| chr5:171395924 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.524+2946T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395924 | |||||||
| chr5:171395962 | A | AT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.524+2984_524+2985i others(3): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395962 | |||||||
| chr5:171395963 | A | AT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0062 a0001c0001t0001g0089 others(2): Show |
9 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.524+3002dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171395963 | ||||||
| chr5:171395963 | A | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
21 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.524+2985A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171395963 | |||||||
| chr5:171395963 | AT | A | 85 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(82): Show |
177 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.524+3002delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171395963 | ||||||
| chr5:171395963 | ATTT | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(8): Show |
18 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.524+3000_524+3002d others(5): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171395963 | ||||||
| chr5:171396002 | G | A | 13 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(10): Show |
23 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.524+3024G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396002 | |||||||
| chr5:171396406 | C | T | 1 | a0001c0001t0002g0052 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.524+3428C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396406 | |||||||
| chr5:171396533 | T | A | 1 | a0001c0001t0001g0196 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.524+3555T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396533 | |||||||
| chr5:171396573 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.525-3580T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396573 | |||||||
| chr5:171396597 | C | T | 56 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(53): Show |
122 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.525-3556C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396597 | |||||||
| chr5:171396725 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.525-3428A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396725 | |||||||
| chr5:171396745 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-3408T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396745 | |||||||
| chr5:171396751 | C | T | 4 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0092 others(1): Show |
12 | HG01884.hp1 HG02055.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.525-3402C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396751 | |||||||
| chr5:171396808 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0093 |
2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.525-3345C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396808 | |||||||
| chr5:171396909 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-3244G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396909 | |||||||
| chr5:171396921 | C | T | 1 | a0001c0001t0003g0182 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.525-3232C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396921 | |||||||
| chr5:171396960 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-3193T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171396960 | |||||||
| chr5:171397057 | A | G | 1 | a0001c0001t0002g0055 | 2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.525-3096A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397057 | |||||||
| chr5:171397122 | CT | C | 7 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
14 | HG02129.hp2 HG02148.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.525-3028delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397122 | ||||||
| chr5:171397130 | A | G | 1 | a0001c0001t0003g0051 | 2 | NA19003.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.525-3023A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397130 | |||||||
| chr5:171397149 | T | TA | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.525-3003dupA | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397149 | ||||||
| chr5:171397194 | T | A | 3 | a0001c0001t0003g0020 a0001c0001t0003g0169 a0001c0001t0007g0020 |
5 | NA18955.hp1 NA18965.hp2 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.525-2959T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397194 | |||||||
| chr5:171397317 | G | A | 1 | a0001c0001t0002g0170 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.525-2836G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397317 | |||||||
| chr5:171397329 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.525-2824C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397329 | |||||||
| chr5:171397343 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.525-2810T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397343 | |||||||
| chr5:171397590 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-2563A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397590 | |||||||
| chr5:171397601 | TTTAC | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-2549_525-2546d others(6): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397601 | ||||||
| chr5:171397634 | ATTCTTTT | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.525-2503_525-2497d others(9): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397634 | ||||||
| chr5:171397661 | T | C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(8): Show |
18 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.525-2492T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397661 | |||||||
| chr5:171397712 | T | TTCTTAAA others(289): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0091 |
2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.525-2436_525-2141d others(298): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397712 | ||||||
| chr5:171397757 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.525-2396A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397757 | |||||||
| chr5:171397802 | C | CT | 44 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0016 others(41): Show |
75 | HG00544.hp2 HG00735.hp1 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.525-2335dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397802 | ||||||
| chr5:171397802 | C | CTT | 50 | a0001c0001t0001g0047 a0001c0001t0001g0148 a0001c0001t0001g0158 others(47): Show |
110 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.525-2336_525-2335d others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397802 | ||||||
| chr5:171397935 | AC | A | 90 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(87): Show |
183 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.525-2210delC | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171397935 | ||||||
| chr5:171397982 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.525-2171C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171397982 | |||||||
| chr5:171398172 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-1981C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398172 | |||||||
| chr5:171398268 | T | G | 1 | a0001c0001t0002g0052 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.525-1885T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398268 | |||||||
| chr5:171398269 | C | T | 1 | a0001c0001t0002g0052 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.525-1884C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398269 | |||||||
| chr5:171398472 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.525-1681A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398472 | |||||||
| chr5:171398645 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.525-1508C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398645 | |||||||
| chr5:171398800 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.525-1353T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398800 | |||||||
| chr5:171398851 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02145.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.525-1302C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398851 | |||||||
| chr5:171398909 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-1244T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171398909 | |||||||
| chr5:171399113 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.525-1040A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399113 | |||||||
| chr5:171399118 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.525-1035C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399118 | |||||||
| chr5:171399320 | T | C | 61 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(58): Show |
128 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.525-833T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399320 | |||||||
| chr5:171399330 | C | G | 1 | a0001c0001t0008g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.525-823C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399330 | |||||||
| chr5:171399337 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(8): Show |
21 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.525-816C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399337 | |||||||
| chr5:171399373 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-780A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399373 | |||||||
| chr5:171399417 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-736A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399417 | |||||||
| chr5:171399511 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.525-642A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171399511 | |||||||
| chr5:171399683 | A | AT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0082 others(6): Show |
15 | HG00741.hp1 HG01109.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.525-459dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171399683 | ||||||
| chr5:171399683 | A | ATT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
200 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.525-460_525-459dup others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171399683 | ||||||
| chr5:171399683 | A | ATTT | 13 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
20 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.525-461_525-459dup others(3): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 171399683 | ||||||
| chr5:171400021 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.525-132A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171400021 | |||||||
| chr5:171400080 | A | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.525-73A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171400080 | |||||||
| chr5:171400111 | C | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-42C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171400111 | |||||||
| chr5:171400114 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.525-39A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 6/10 | chr5 | 171400114 | |||||||
| chr5:171400307 | T | TGGGAGAT others(13): Show |
101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.582+98_582+117dupG others(19): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 171400307 | ||||||
| chr5:171400446 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.582+236C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400446 | |||||||
| chr5:171400457 | T | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.582+247T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400457 | |||||||
| chr5:171400460 | C | CT | 11 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0067 others(8): Show |
15 | HG00741.hp1 HG01109.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.582+266dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 171400460 | ||||||
| chr5:171400460 | CT | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(9): Show |
19 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.582+266delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 171400460 | ||||||
| chr5:171400460 | CTT | C | 86 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
178 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.582+265_582+266del others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 171400460 | ||||||
| chr5:171400502 | G | A | 3 | a0001c0001t0002g0014 a0001c0001t0002g0168 a0001c0001t0002g0202 |
7 | NA18954.hp2 NA19011.hp2 NA19012.hp2 others(4): Show |
intron_variant | MODIFIER | c.582+292G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400502 | |||||||
| chr5:171400517 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.582+307C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400517 | |||||||
| chr5:171400549 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.583-290C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400549 | |||||||
| chr5:171400650 | G | A | 1 | a0001c0001t0006g0197 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.583-189G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400650 | |||||||
| chr5:171400652 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.583-187C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400652 | |||||||
| chr5:171400659 | G | T | 1 | a0001c0001t0002g0180 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.583-180G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400659 | |||||||
| chr5:171400675 | T | A | 1 | a0001c0001t0001g0126 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.583-164T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400675 | |||||||
| chr5:171400800 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.583-39G>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400800 | |||||||
| chr5:171400807 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.583-32G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400807 | |||||||
| chr5:171400815 | A | C | 1 | a0001c0001t0001g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.583-24A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 7/10 | chr5 | 171400815 | |||||||
| chr5:171400936 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.669+11A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171400936 | |||||||
| chr5:171400980 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.669+55C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171400980 | |||||||
| chr5:171401144 | G | T | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.669+219G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171401144 | |||||||
| chr5:171401166 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.669+241C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171401166 | |||||||
| chr5:171401255 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(8): Show |
26 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.669+330G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171401255 | |||||||
| chr5:171401265 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0136 |
3 | HG01070.hp1 HG01071.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.669+340G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171401265 | |||||||
| chr5:171401375 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.669+450G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171401375 | |||||||
| chr5:171401385 | TAC | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0099 |
3 | HG03579.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.669+474_669+475del others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171401385 | ||||||
| chr5:171401428 | G | A | 1 | a0001c0001t0002g0028 | 3 | HG00438.hp1 NA18945.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.669+503G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171401428 | |||||||
| chr5:171401990 | G | T | 1 | a0001c0001t0002g0186 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.669+1065G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171401990 | |||||||
| chr5:171402053 | C | CTTT | 9 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0153 others(6): Show |
12 | HG01081.hp1 HG01255.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.669+1142_669+1144d others(5): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402053 | ||||||
| chr5:171402053 | C | CTTTT | 35 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(32): Show |
61 | HG00140.hp1 HG00735.hp1 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.669+1141_669+1144d others(6): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402053 | ||||||
| chr5:171402053 | C | CTTTTT | 46 | a0001c0001t0001g0004 a0001c0001t0001g0057 a0001c0001t0001g0143 others(43): Show |
108 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.669+1140_669+1144d others(7): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402053 | ||||||
| chr5:171402053 | C | CTTTTTT | 6 | a0001c0001t0001g0054 a0001c0001t0001g0196 a0001c0001t0001g0205 others(3): Show |
9 | HG00544.hp2 HG01069.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.669+1139_669+1144d others(8): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402053 | ||||||
| chr5:171402053 | C | CTTTTTTT | 4 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0208 others(1): Show |
10 | HG01243.hp1 HG02055.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.669+1138_669+1144d others(9): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402053 | ||||||
| chr5:171402053 | CT | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0065 a0001c0001t0001g0071 others(8): Show |
12 | HG01069.hp2 HG01109.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.669+1144delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402053 | ||||||
| chr5:171402299 | A | G | 1 | a0001c0001t0001g0019 | 4 | HG02040.hp1 HG02074.hp1 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+1374A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402299 | |||||||
| chr5:171402344 | T | A | 62 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(59): Show |
129 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.669+1419T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402344 | |||||||
| chr5:171402523 | T | G | 4 | a0001c0001t0003g0027 a0001c0001t0003g0050 a0001c0001t0003g0181 others(1): Show |
7 | NA18940.hp1 NA18953.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.669+1598T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402523 | |||||||
| chr5:171402591 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.669+1666T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402591 | |||||||
| chr5:171402682 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.669+1757G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402682 | |||||||
| chr5:171402712 | C | G | 1 | a0001c0001t0002g0171 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.669+1787C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402712 | |||||||
| chr5:171402790 | C | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.669+1865C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402790 | |||||||
| chr5:171402798 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.669+1873T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402798 | |||||||
| chr5:171402930 | A | C | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.669+2005A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402930 | |||||||
| chr5:171402952 | C | CT | 26 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0030 others(23): Show |
39 | HG00639.hp1 HG00642.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.669+2041dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402952 | ||||||
| chr5:171402966 | TCA | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0029 others(17): Show |
35 | HG00609.hp1 HG01069.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.669+2042_669+2043d others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402966 | |||||||
| chr5:171402967 | C | T | 76 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(73): Show |
160 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.669+2042C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402967 | |||||||
| chr5:171402968 | A | T | 76 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(73): Show |
160 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.669+2043A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402968 | |||||||
| chr5:171402969 | TTTTA | T | 7 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0076 others(4): Show |
9 | HG02071.hp2 HG02135.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.669+2064_669+2067d others(6): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402969 | ||||||
| chr5:171402971 | T | C | 16 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0025 others(13): Show |
23 | HG00741.hp2 HG01070.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.669+2046T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402971 | |||||||
| chr5:171402972 | T | A | 16 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0025 others(13): Show |
23 | HG00741.hp2 HG01070.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.669+2047T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402972 | |||||||
| chr5:171402972 | T | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0029 others(22): Show |
38 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.669+2047T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402972 | |||||||
| chr5:171402972 | T | TCA | 50 | a0001c0001t0001g0158 a0001c0001t0002g0002 a0001c0001t0002g0003 others(47): Show |
93 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.669+2047_669+2048i others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402972 | |||||||
| chr5:171402972 | T | TTCA | 15 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(12): Show |
34 | HG00735.hp1 HG01081.hp1 HG01346.hp2 others(31): Show |
intron_variant | MODIFIER | c.669+2047_669+2048i others(5): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402972 | |||||||
| chr5:171402972 | T | TTTCA | 3 | a0001c0001t0001g0047 a0001c0001t0001g0152 a0001c0001t0003g0002 |
4 | HG00738.hp2 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+2047_669+2048i others(6): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402972 | |||||||
| chr5:171402973 | A | AT | 24 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0029 others(21): Show |
37 | HG00609.hp1 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.669+2051dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171402973 | ||||||
| chr5:171402973 | A | T | 79 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(76): Show |
157 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.669+2048A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402973 | |||||||
| chr5:171402975 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.669+2050T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402975 | |||||||
| chr5:171402976 | T | A | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.669+2051T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402976 | |||||||
| chr5:171402977 | A | T | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.669+2052A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402977 | |||||||
| chr5:171402989 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.669+2064A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171402989 | |||||||
| chr5:171403012 | T | A | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
388 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(385): Show |
intron_variant | MODIFIER | c.669+2087T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403012 | |||||||
| chr5:171403017 | T | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(9): Show |
22 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.669+2092T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403017 | |||||||
| chr5:171403104 | T | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(7): Show |
20 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.669+2179T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403104 | |||||||
| chr5:171403146 | C | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(7): Show |
20 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.670-2156C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403146 | |||||||
| chr5:171403151 | C | T | 1 | a0001c0001t0002g0175 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.670-2151C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403151 | |||||||
| chr5:171403152 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.670-2150G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403152 | |||||||
| chr5:171403159 | C | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0093 |
2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.670-2143C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403159 | |||||||
| chr5:171403172 | TA | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(7): Show |
20 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.670-2129delA | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403172 | |||||||
| chr5:171403173 | A | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(109): Show |
213 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(210): Show |
intron_variant | MODIFIER | c.670-2129A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403173 | |||||||
| chr5:171403205 | ACT | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(54): Show |
123 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.670-2094_670-2093d others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171403205 | ||||||
| chr5:171403260 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0089 a0001c0001t0001g0090 |
7 | HG00741.hp1 HG01109.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-2042C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403260 | |||||||
| chr5:171403444 | C | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0106 |
2 | HG01928.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.670-1858C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403444 | |||||||
| chr5:171403461 | T | C | 18 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
26 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.670-1841T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403461 | |||||||
| chr5:171403482 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1820T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403482 | |||||||
| chr5:171403535 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1767C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403535 | |||||||
| chr5:171403584 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
222 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.670-1718T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403584 | |||||||
| chr5:171403630 | AGGGGGGC others(43): Show |
A | 1 | a0001c0001t0002g0161 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.670-1654_670-1605d others(52): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171403630 | ||||||
| chr5:171403640 | A | AC | 17 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(14): Show |
24 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.670-1654dupC | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171403640 | ||||||
| chr5:171403641 | CCCCCCCC others(42): Show |
C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(7): Show |
24 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.670-1638_670-1590d others(51): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171403641 | ||||||
| chr5:171403652 | T | C | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-1650T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403652 | |||||||
| chr5:171403653 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-1649C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403653 | |||||||
| chr5:171403660 | G | T | 4 | a0001c0001t0001g0057 a0001c0001t0001g0205 a0001c0001t0001g0206 others(1): Show |
5 | HG02257.hp2 HG02970.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-1642G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403660 | |||||||
| chr5:171403664 | G | A | 90 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0025 others(87): Show |
176 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.670-1638G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403664 | |||||||
| chr5:171403672 | T | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0025 others(87): Show |
176 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.670-1630T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403672 | |||||||
| chr5:171403677 | A | G | 1 | a0001c0001t0003g0209 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.670-1625A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403677 | |||||||
| chr5:171403708 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.670-1594C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403708 | |||||||
| chr5:171403721 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.670-1581C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403721 | |||||||
| chr5:171403724 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.670-1578C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403724 | |||||||
| chr5:171403726 | G | A | 1 | a0001c0001t0002g0188 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.670-1576G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403726 | |||||||
| chr5:171403782 | G | T | 58 | a0001c0001t0001g0164 a0001c0001t0002g0002 a0001c0001t0002g0003 others(55): Show |
124 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.670-1520G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403782 | |||||||
| chr5:171403796 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0081 |
4 | HG00140.hp2 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-1506C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403796 | |||||||
| chr5:171403830 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-1472C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403830 | |||||||
| chr5:171403836 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.670-1466A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403836 | |||||||
| chr5:171403856 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.670-1446C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403856 | |||||||
| chr5:171403884 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.670-1418C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403884 | |||||||
| chr5:171403885 | G | C | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.670-1417G>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403885 | |||||||
| chr5:171403888 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.670-1414C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403888 | |||||||
| chr5:171403891 | G | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1411G>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403891 | |||||||
| chr5:171403892 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1410G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403892 | |||||||
| chr5:171403897 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(201): Show |
388 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(385): Show |
intron_variant | MODIFIER | c.670-1405C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403897 | |||||||
| chr5:171403905 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1397C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403905 | |||||||
| chr5:171403914 | T | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1388T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403914 | |||||||
| chr5:171403917 | C | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(8): Show |
26 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.670-1385C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403917 | |||||||
| chr5:171403952 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.670-1350G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403952 | |||||||
| chr5:171403977 | CCCGGACG others(67): Show |
C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1322_670-1249d others(76): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171403977 | ||||||
| chr5:171403983 | C | T | 1 | a0001c0002t0001g0033 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.670-1319C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171403983 | |||||||
| chr5:171404045 | A | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0031 others(18): Show |
34 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.670-1257A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404045 | |||||||
| chr5:171404061 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0155 |
7 | HG00735.hp1 HG01346.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-1241C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404061 | |||||||
| chr5:171404072 | GCCGGGCG others(174): Show |
G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1225_670-1045d others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171404072 | ||||||
| chr5:171404075 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0137 |
6 | HG01069.hp2 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-1227G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404075 | |||||||
| chr5:171404078 | CGGGGGGC others(42): Show |
C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0071 others(3): Show |
8 | HG00639.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.670-1192_670-1144d others(51): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171404078 | ||||||
| chr5:171404095 | C | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0032 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.670-1207C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404095 | |||||||
| chr5:171404110 | CGGCACGG others(42): Show |
C | 1 | a0001c0001t0001g0021 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.670-1178_670-1130d others(51): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171404110 | ||||||
| chr5:171404111 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.670-1191G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404111 | |||||||
| chr5:171404176 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.670-1126C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404176 | |||||||
| chr5:171404235 | A | AC | 14 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0017 others(11): Show |
17 | HG00544.hp1 HG02027.hp1 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.670-1058dupC | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr5 | 171404235 | ||||||
| chr5:171404267 | C | A | 1 | a0001c0001t0002g0176 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.670-1035C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404267 | |||||||
| chr5:171404268 | T | C | 2 | a0001c0001t0001g0037 a0003c0003t0001g0037 |
2 | NA18747.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.670-1034T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404268 | |||||||
| chr5:171404271 | T | C | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-1031T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404271 | |||||||
| chr5:171404276 | G | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.670-1026G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404276 | |||||||
| chr5:171404315 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-987C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404315 | |||||||
| chr5:171404356 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-946G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404356 | |||||||
| chr5:171404412 | T | A | 1 | a0001c0001t0003g0209 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.670-890T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404412 | |||||||
| chr5:171404413 | C | T | 1 | a0001c0001t0003g0209 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.670-889C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404413 | |||||||
| chr5:171404471 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.670-831G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404471 | |||||||
| chr5:171404500 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(54): Show |
123 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.670-802G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404500 | |||||||
| chr5:171404505 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.670-797G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404505 | |||||||
| chr5:171404534 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(8): Show |
26 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.670-768G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404534 | |||||||
| chr5:171404595 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.670-707G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404595 | |||||||
| chr5:171404621 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.670-681G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404621 | |||||||
| chr5:171404625 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
21 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.670-677G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404625 | |||||||
| chr5:171404729 | G | A | 19 | a0001c0001t0001g0008 a0001c0001t0001g0018 a0001c0001t0001g0038 others(16): Show |
30 | HG00423.hp2 HG00558.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.670-573G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404729 | |||||||
| chr5:171404830 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0151 |
3 | HG03130.hp1 HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.670-472C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404830 | |||||||
| chr5:171404871 | T | C | 115 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
222 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.670-431T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404871 | |||||||
| chr5:171404880 | T | C | 1 | a0001c0001t0008g0142 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.670-422T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404880 | |||||||
| chr5:171404908 | C | T | 115 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
222 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.670-394C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404908 | |||||||
| chr5:171404919 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.670-383A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171404919 | |||||||
| chr5:171405080 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.670-222G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171405080 | |||||||
| chr5:171405088 | C | A | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.670-214C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171405088 | |||||||
| chr5:171405115 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.670-187C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171405115 | |||||||
| chr5:171405183 | G | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
21 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.670-119G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171405183 | |||||||
| chr5:171405216 | A | C | 1 | a0001c0001t0009g0192 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.670-86A>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171405216 | |||||||
| chr5:171405239 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.670-63A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171405239 | |||||||
| chr5:171405288 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.670-14C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 8/10 | chr5 | 171405288 | |||||||
| chr5:171405604 | A | G | 1 | a0001c0001t0001g0031 | 2 | HG03540.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.771+201A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171405604 | |||||||
| chr5:171405633 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.771+230C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171405633 | |||||||
| chr5:171405635 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.771+232T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171405635 | |||||||
| chr5:171405763 | TACAA | T | 61 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(58): Show |
128 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.771+364_771+367del others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 171405763 | ||||||
| chr5:171405912 | T | C | 4 | a0001c0001t0003g0027 a0001c0001t0003g0050 a0001c0001t0003g0181 others(1): Show |
7 | NA18940.hp1 NA18953.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.771+509T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171405912 | |||||||
| chr5:171405923 | C | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(17): Show |
32 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.771+520C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171405923 | |||||||
| chr5:171406001 | A | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.771+598A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171406001 | |||||||
| chr5:171406333 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0129 |
2 | NA19086.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.771+930G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171406333 | |||||||
| chr5:171406340 | T | G | 1 | a0001c0001t0001g0101 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.771+937T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171406340 | |||||||
| chr5:171406854 | C | A | 14 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
21 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.772-846C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171406854 | |||||||
| chr5:171407080 | G | A | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.772-620G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171407080 | |||||||
| chr5:171407287 | T | C | 1 | a0001c0001t0004g0195 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.772-413T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171407287 | |||||||
| chr5:171407367 | T | C | 1 | a0001c0001t0001g0023 | 3 | HG00639.hp2 HG00733.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.772-333T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171407367 | |||||||
| chr5:171407453 | T | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
10 | HG00423.hp2 HG00558.hp2 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.772-247T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171407453 | |||||||
| chr5:171407488 | C | G | 1 | a0001c0001t0001g0199 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.772-212C>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171407488 | |||||||
| chr5:171407532 | A | T | 1 | a0001c0002t0001g0033 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.772-168A>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171407532 | |||||||
| chr5:171407654 | C | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.772-46C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 9/10 | chr5 | 171407654 | |||||||
| chr5:171407912 | T | A | 1 | a0001c0001t0002g0168 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.846+138T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171407912 | |||||||
| chr5:171408017 | C | A | 1 | a0001c0001t0001g0138 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.846+243C>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408017 | |||||||
| chr5:171408030 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.846+256T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408030 | |||||||
| chr5:171408074 | G | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(8): Show |
18 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.846+300G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408074 | |||||||
| chr5:171408147 | C | CT | 79 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0044 others(76): Show |
155 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.846+387dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 171408147 | ||||||
| chr5:171408147 | C | CTT | 22 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(19): Show |
46 | HG00609.hp1 HG00735.hp1 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.846+386_846+387dup others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 171408147 | ||||||
| chr5:171408425 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.846+651T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408425 | |||||||
| chr5:171408496 | T | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0054 others(8): Show |
18 | HG01069.hp1 HG01071.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.846+722T>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408496 | |||||||
| chr5:171408497 | T | C | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.846+723T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408497 | |||||||
| chr5:171408609 | T | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
21 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.846+835T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408609 | |||||||
| chr5:171408650 | C | T | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.846+876C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408650 | |||||||
| chr5:171408749 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.846+975G>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408749 | |||||||
| chr5:171408759 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.846+985G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408759 | |||||||
| chr5:171408862 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(98): Show |
201 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(198): Show |
intron_variant | MODIFIER | c.846+1088C>T | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171408862 | |||||||
| chr5:171408918 | T | TTATAACA others(21): Show |
1 | a0001c0001t0001g0130 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.846+1146_846+1173d others(30): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 171408918 | ||||||
| chr5:171409215 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.847-1312T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171409215 | |||||||
| chr5:171409376 | ACT | A | 2 | a0001c0001t0001g0082 a0001c0002t0001g0033 |
3 | HG01243.hp2 HG02717.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.847-1148_847-1147d others(4): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 171409376 | ||||||
| chr5:171409811 | G | GT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0011 others(97): Show |
200 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.847-708dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 171409811 | ||||||
| chr5:171409827 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.847-700T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171409827 | |||||||
| chr5:171410034 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.847-493G>A | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171410034 | |||||||
| chr5:171410218 | C | CAG | 115 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(112): Show |
222 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.847-309_847-308ins others(2): Show |
NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171410218 | |||||||
| chr5:171410275 | T | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0019 others(6): Show |
23 | HG00735.hp1 HG00738.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.847-252T>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171410275 | |||||||
| chr5:171410453 | A | G | 14 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
21 | HG00642.hp1 HG00733.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.847-74A>G | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171410453 | |||||||
| chr5:171410509 | C | CT | 6 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0076 others(3): Show |
6 | HG02647.hp2 HG02965.hp2 HG03098.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.847-5dupT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 171410509 | ||||||
| chr5:171410509 | CT | C | 20 | a0001c0001t0001g0004 a0001c0001t0001g0025 a0001c0001t0001g0043 others(17): Show |
31 | HG00609.hp1 HG01070.hp2 HG01257.hp1 others(28): Show |
splice_region_variant&intron_variant | LOW | c.847-5delT | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 171410509 | ||||||
| chr5:171410522 | T | C | 4 | a0001c0001t0001g0047 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
5 | HG02145.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.847-5T>C | NPM1 | ENSG00000181163.14 | transcript | ENST00000296930.10 | protein_coding | 10/10 | chr5 | 171410522 |