Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55839 |
| ensemblid | ENSG00000166451.14 |
| hgncid | 30873 |
| symbol | CENPN |
| name | centromere protein N |
| refseq_nuc | NM_001100624.3 |
| refseq_prot | NP_001094094.2 |
| ensembl_nuc | ENST00000305850.10 |
| ensembl_prot | ENSP00000305608.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 81007214 |
| end | 81031485 |
| strand | + |
| ver | v1.2 |
| region | chr16:81007214-81031485 |
| region5000 | chr16:81002214-81036485 |
| regionname0 | CENPN_chr16_81007214_81031485 |
| regionname5000 | CENPN_chr16_81002214_81036485 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 339 | 190 | 33 | 43 | 82 | 7 | 24 | 62 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0002 | 0/0 | 339 | 188 | 48 | 20 | 110 | 2 | 8 | 92 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0003 | 1/0 | 339 | 5 | 3 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0004 | 0/0 | 339 | 5 | 0 | 2 | 0 | 1 | 2 | 0 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0005 | 0/0 | 339 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0006 | 0/0 | 339 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0007 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0008 | 0/0 | 339 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0009 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| a0010 | 0/0 | 339 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | MDETV others(334): Show |
chr16 | 81002214 | 81036485 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/1 | 1017 | 175 | 33 | 43 | 68 | 7 | 23 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0001c0003 | 0/0 | 1017 | 14 | 0 | 0 | 13 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0001c0010 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0002c0001 | 0/0 | 1017 | 183 | 44 | 20 | 110 | 1 | 8 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0002c0006 | 0/0 | 1017 | 4 | 4 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0002c0011 | 0/0 | 1017 | 1 | 0 | 0 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0003c0004 | 1/0 | 1017 | 5 | 3 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0004c0005 | 0/0 | 1017 | 5 | 0 | 2 | 0 | 1 | 2 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0005c0007 | 0/0 | 1017 | 4 | 0 | 0 | 4 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0006c0008 | 0/0 | 1017 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0007c0014 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0008c0012 | 0/0 | 1017 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0009c0013 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 | ||
| a0010c0009 | 0/0 | 1017 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | ATGGA others(1012): Show |
chr16 | 81002214 | 81036485 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/1 | 3928 | 91 | 9 | 26 | 31 | 5 | 19 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0004 | 0/0 | 3928 | 29 | 5 | 13 | 7 | 2 | 2 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0005 | 0/0 | 3928 | 19 | 0 | 0 | 19 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0011 | 0/0 | 3928 | 6 | 6 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0012 | 0/0 | 3928 | 5 | 4 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0014 | 0/0 | 3928 | 4 | 3 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0015 | 0/0 | 3928 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0016 | 0/0 | 3929 | 3 | 3 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3924): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0017 | 0/0 | 3928 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0026 | 0/0 | 3928 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0031 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0048 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0049 | 0/0 | 3928 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0050 | 0/0 | 3929 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3924): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0051 | 0/0 | 3928 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0052 | 0/0 | 3928 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0053 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0054 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0056 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0002t0058 | 0/0 | 3928 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0003t0001 | 0/0 | 3928 | 9 | 0 | 0 | 9 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0003t0010 | 0/0 | 3928 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0001c0003t0025 | 0/0 | 3927 | 2 | 0 | 0 | 1 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0001c0010t0001 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0002 | 0/0 | 3927 | 60 | 5 | 8 | 43 | 1 | 3 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0003 | 0/0 | 3927 | 46 | 1 | 3 | 39 | 0 | 3 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0006 | 0/0 | 3927 | 14 | 1 | 0 | 13 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0007 | 0/0 | 3928 | 5 | 2 | 3 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0008 | 0/0 | 3928 | 10 | 2 | 1 | 7 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0009 | 0/0 | 3927 | 9 | 8 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0013 | 0/0 | 3929 | 5 | 5 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3924): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0018 | 0/0 | 3927 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0019 | 0/0 | 3927 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0020 | 0/0 | 3927 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0021 | 0/0 | 3927 | 2 | 0 | 1 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0022 | 0/0 | 3927 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0023 | 0/0 | 3928 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0024 | 0/0 | 3929 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3924): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0027 | 0/0 | 3928 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0028 | 0/0 | 3927 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0029 | 0/0 | 3927 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0032 | 0/0 | 3929 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3924): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0033 | 0/0 | 3927 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0034 | 0/0 | 3927 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0035 | 0/0 | 3927 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0036 | 0/0 | 3928 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0037 | 0/0 | 3927 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0038 | 0/0 | 3927 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0039 | 0/0 | 3927 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0040 | 0/0 | 3927 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0041 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0042 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0043 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0044 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0045 | 0/0 | 3928 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0046 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0047 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0001t0057 | 0/0 | 3927 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| a0002c0006t0007 | 0/0 | 3928 | 4 | 4 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0002c0011t0007 | 0/0 | 3928 | 1 | 0 | 0 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0003c0004t0010 | 1/0 | 3928 | 4 | 2 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0003c0004t0030 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0004c0005t0001 | 0/0 | 3928 | 5 | 0 | 2 | 0 | 1 | 2 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0005c0007t0001 | 0/0 | 3928 | 4 | 0 | 0 | 4 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0006c0008t0004 | 0/0 | 3928 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0007c0014t0011 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0008c0012t0055 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0009c0013t0015 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3923): Show |
chr16 | 81002214 | 81036485 |
| a0010c0009t0020 | 0/0 | 3927 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | GGCTT others(3922): Show |
chr16 | 81002214 | 81036485 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0001 | 0/1 | 34 | 3 | 11 | 12 | 2 | 5 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0006 | 0/0 | 7 | 0 | 5 | 0 | 2 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0005g0001 | 0/0 | 18 | 0 | 0 | 18 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0011g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0012g0008 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0014g0004 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0015g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0015g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0016g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0016g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0017g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0026g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0026g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0048g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0049g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0050g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0051g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0052g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0053g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0054g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0056g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0002t0058g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0010g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0010g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0025g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0003t0025g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0001c0010t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0003 | 0/0 | 20 | 0 | 6 | 14 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0009 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0002 | 0/0 | 19 | 0 | 0 | 18 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0007 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0007g0005 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0007g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0008g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0009g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0009g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0009g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0009g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0013g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0013g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0013g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0013g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0018g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0019g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0020g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0021g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0021g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0022g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0022g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0023g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0023g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0024g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0027g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0027g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0028g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0029g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0032g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0033g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0034g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0035g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0036g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0037g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0038g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0039g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0040g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0041g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0042g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0043g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0044g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0045g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0046g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0047g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0001t0057g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0006t0007g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0002c0011t0007g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0003c0004t0010g0016 | 1/0 | 4 | 2 | 1 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0003c0004t0030g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0004c0005t0001g0015 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0004c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0005c0007t0001g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0006c0008t0004g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0007c0014t0011g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0008c0012t0055g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0009c0013t0015g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| a0010c0009t0020g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0021 | EUR | GBR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0136 | EUR | GBR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0101 | EUR | FIN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00323 | hp2 | a0002 | c0011 | t0007 | g0005 | EUR | FIN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00408 | hp1 | a0002 | c0001 | t0003 | g0124 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00408 | hp2 | a0002 | c0001 | t0006 | g0007 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00423 | hp1 | a0002 | c0001 | t0003 | g0056 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00438 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00438 | hp2 | a0002 | c0001 | t0003 | g0025 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00558 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0140 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00597 | hp2 | a0002 | c0001 | t0002 | g0147 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00609 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00609 | hp2 | a0001 | c0002 | t0004 | g0138 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00621 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00621 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00639 | hp1 | a0003 | c0004 | t0010 | g0016 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00639 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00673 | hp1 | a0001 | c0002 | t0031 | g0001 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00673 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | CHS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0037 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00735 | hp2 | a0002 | c0001 | t0007 | g0170 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00741 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01069 | hp1 | a0001 | c0002 | t0004 | g0029 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01070 | hp2 | a0002 | c0001 | t0007 | g0005 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0033 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01071 | hp2 | a0001 | c0002 | t0004 | g0029 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01074 | hp2 | a0002 | c0001 | t0002 | g0003 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01081 | hp1 | a0001 | c0002 | t0012 | g0008 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01081 | hp2 | a0002 | c0001 | t0036 | g0005 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01099 | hp1 | a0001 | c0002 | t0004 | g0126 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01099 | hp2 | a0002 | c0001 | t0002 | g0003 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01106 | hp2 | a0001 | c0002 | t0014 | g0004 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01109 | hp1 | a0002 | c0001 | t0008 | g0017 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01109 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01168 | hp1 | a0002 | c0001 | t0009 | g0022 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0041 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01175 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01175 | hp2 | a0002 | c0001 | t0021 | g0151 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0004 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01255 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0027 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01258 | hp1 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01258 | hp2 | a0001 | c0002 | t0004 | g0027 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01346 | hp1 | a0002 | c0001 | t0007 | g0005 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01346 | hp2 | a0004 | c0005 | t0001 | g0015 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01358 | hp2 | a0001 | c0002 | t0004 | g0030 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01361 | hp2 | a0006 | c0008 | t0004 | g0040 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01433 | hp1 | a0002 | c0001 | t0045 | g0173 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01433 | hp2 | a0001 | c0002 | t0004 | g0006 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01496 | hp2 | a0002 | c0001 | t0002 | g0003 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01515 | hp1 | a0004 | c0005 | t0001 | g0137 | EUR | IBS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01515 | hp2 | a0001 | c0002 | t0004 | g0006 | EUR | IBS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01516 | hp1 | a0002 | c0001 | t0002 | g0164 | EUR | IBS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01516 | hp2 | a0001 | c0002 | t0004 | g0006 | EUR | IBS | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01884 | hp1 | a0002 | c0001 | t0009 | g0049 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01884 | hp2 | a0002 | c0001 | t0002 | g0112 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01928 | hp1 | a0001 | c0002 | t0004 | g0030 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01928 | hp2 | a0004 | c0005 | t0001 | g0015 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01934 | hp1 | a0006 | c0008 | t0004 | g0040 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01952 | hp1 | a0002 | c0001 | t0003 | g0024 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01952 | hp2 | a0002 | c0001 | t0035 | g0069 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01975 | hp2 | a0001 | c0002 | t0058 | g0083 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01978 | hp1 | a0001 | c0002 | t0052 | g0004 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01981 | hp1 | a0001 | c0002 | t0004 | g0028 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01981 | hp2 | a0002 | c0001 | t0003 | g0061 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01993 | hp1 | a0002 | c0001 | t0003 | g0024 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02015 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02015 | hp2 | a0002 | c0001 | t0003 | g0055 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02027 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02027 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02055 | hp1 | a0002 | c0001 | t0002 | g0162 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02055 | hp2 | a0002 | c0001 | t0009 | g0011 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02056 | hp2 | a0002 | c0001 | t0002 | g0042 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02071 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02074 | hp1 | a0002 | c0001 | t0003 | g0064 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02074 | hp2 | a0002 | c0001 | t0006 | g0179 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02080 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02083 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02083 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02129 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02145 | hp1 | a0003 | c0004 | t0030 | g0142 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02145 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0129 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02257 | hp2 | a0002 | c0001 | t0023 | g0017 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0004 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02258 | hp2 | a0002 | c0006 | t0007 | g0005 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02273 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02280 | hp1 | a0001 | c0002 | t0004 | g0128 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02280 | hp2 | a0002 | c0001 | t0009 | g0046 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02293 | hp1 | a0002 | c0001 | t0002 | g0003 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02300 | hp1 | a0002 | c0001 | t0002 | g0009 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PEL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02523 | hp1 | a0001 | c0003 | t0025 | g0109 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02523 | hp2 | a0002 | c0001 | t0008 | g0092 | EAS | KHV | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02572 | hp1 | a0002 | c0001 | t0006 | g0155 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02572 | hp2 | a0002 | c0006 | t0007 | g0005 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02602 | hp1 | a0002 | c0001 | t0003 | g0002 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02615 | hp1 | a0002 | c0001 | t0013 | g0172 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02615 | hp2 | a0002 | c0006 | t0007 | g0005 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02622 | hp2 | a0002 | c0001 | t0040 | g0005 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02630 | hp1 | a0007 | c0014 | t0011 | g0117 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02630 | hp2 | a0002 | c0001 | t0057 | g0054 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02647 | hp2 | a0001 | c0002 | t0014 | g0004 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02683 | hp2 | a0001 | c0002 | t0004 | g0041 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02698 | hp1 | a0001 | c0002 | t0004 | g0131 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02717 | hp1 | a0002 | c0001 | t0039 | g0043 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02717 | hp2 | a0002 | c0001 | t0024 | g0032 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02723 | hp2 | a0002 | c0001 | t0013 | g0052 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0116 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02735 | hp2 | a0002 | c0001 | t0002 | g0159 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02738 | hp2 | a0002 | c0001 | t0002 | g0161 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0008 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02809 | hp2 | a0002 | c0001 | t0007 | g0005 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02818 | hp1 | a0001 | c0002 | t0016 | g0026 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02818 | hp2 | a0002 | c0001 | t0002 | g0114 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02886 | hp1 | a0002 | c0001 | t0009 | g0011 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02886 | hp2 | a0002 | c0001 | t0043 | g0150 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02896 | hp1 | a0001 | c0002 | t0016 | g0026 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02896 | hp2 | a0002 | c0001 | t0009 | g0011 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02897 | hp1 | a0001 | c0002 | t0014 | g0004 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02897 | hp2 | a0001 | c0002 | t0016 | g0077 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02970 | hp1 | a0002 | c0001 | t0009 | g0011 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0008 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02976 | hp1 | a0002 | c0001 | t0023 | g0051 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02976 | hp2 | a0002 | c0001 | t0002 | g0100 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03041 | hp1 | a0002 | c0001 | t0047 | g0044 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03041 | hp2 | a0001 | c0002 | t0011 | g0004 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03098 | hp1 | a0001 | c0002 | t0011 | g0004 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03098 | hp2 | a0002 | c0001 | t0018 | g0099 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03130 | hp1 | a0001 | c0002 | t0056 | g0177 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03130 | hp2 | a0001 | c0002 | t0011 | g0004 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03139 | hp1 | a0002 | c0001 | t0013 | g0183 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03139 | hp2 | a0002 | c0001 | t0024 | g0032 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03195 | hp1 | a0002 | c0001 | t0046 | g0044 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03195 | hp2 | a0002 | c0001 | t0032 | g0184 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03225 | hp1 | a0001 | c0002 | t0011 | g0004 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03225 | hp2 | a0002 | c0001 | t0009 | g0046 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03453 | hp1 | a0001 | c0002 | t0011 | g0004 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03453 | hp2 | a0002 | c0001 | t0029 | g0154 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03486 | hp1 | a0002 | c0001 | t0009 | g0023 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03486 | hp2 | a0002 | c0001 | t0038 | g0153 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03490 | hp2 | a0004 | c0005 | t0001 | g0015 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03491 | hp2 | a0001 | c0002 | t0049 | g0001 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0038 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03492 | hp2 | a0004 | c0005 | t0001 | g0015 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03516 | hp1 | a0001 | c0002 | t0012 | g0008 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03516 | hp2 | a0008 | c0012 | t0055 | g0178 | AFR | ESN | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0001 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0012 | AFR | GWD | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03579 | hp1 | a0001 | c0002 | t0026 | g0176 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03579 | hp2 | a0003 | c0004 | t0010 | g0016 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0139 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03688 | hp1 | a0002 | c0001 | t0037 | g0073 | SAS | STU | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | STU | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0103 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03831 | hp2 | a0001 | c0003 | t0025 | g0108 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03834 | hp1 | a0001 | c0002 | t0051 | g0001 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0115 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03927 | hp2 | a0002 | c0001 | t0003 | g0072 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0125 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03942 | hp2 | a0002 | c0001 | t0002 | g0002 | SAS | BEB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG04115 | hp1 | a0001 | c0002 | t0001 | g0001 | SAS | STU | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG04115 | hp2 | a0001 | c0002 | t0001 | g0110 | SAS | STU | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG04228 | hp1 | a0002 | c0001 | t0003 | g0071 | SAS | STU | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG04228 | hp2 | a0002 | c0001 | t0021 | g0074 | SAS | STU | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18522 | hp1 | a0002 | c0001 | t0018 | g0098 | AFR | YRI | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18522 | hp2 | a0001 | c0002 | t0011 | g0004 | AFR | YRI | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18747 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | CHB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18747 | hp2 | a0002 | c0001 | t0002 | g0148 | EAS | CHB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18906 | hp1 | a0002 | c0001 | t0008 | g0017 | AFR | YRI | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | YRI | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18939 | hp1 | a0001 | c0002 | t0015 | g0035 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18939 | hp2 | a0002 | c0001 | t0003 | g0066 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18940 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18940 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18941 | hp1 | a0002 | c0001 | t0002 | g0047 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18941 | hp2 | a0002 | c0001 | t0003 | g0068 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18944 | hp1 | a0001 | c0003 | t0010 | g0123 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18944 | hp2 | a0005 | c0007 | t0001 | g0010 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18945 | hp1 | a0001 | c0002 | t0017 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18945 | hp2 | a0002 | c0001 | t0006 | g0180 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18946 | hp2 | a0002 | c0001 | t0002 | g0022 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18947 | hp1 | a0001 | c0002 | t0004 | g0084 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18947 | hp2 | a0002 | c0001 | t0003 | g0065 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18948 | hp1 | a0002 | c0001 | t0008 | g0031 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18948 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18949 | hp1 | a0002 | c0001 | t0008 | g0090 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18949 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18950 | hp1 | a0002 | c0001 | t0006 | g0007 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18950 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18951 | hp1 | a0005 | c0007 | t0001 | g0010 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18951 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18952 | hp1 | a0001 | c0002 | t0005 | g0134 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18954 | hp1 | a0002 | c0001 | t0003 | g0018 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18954 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18956 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18959 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18959 | hp2 | a0002 | c0001 | t0003 | g0135 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18960 | hp1 | a0002 | c0001 | t0006 | g0096 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18960 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18961 | hp2 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18962 | hp1 | a0002 | c0001 | t0003 | g0018 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18962 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18964 | hp1 | a0002 | c0001 | t0002 | g0022 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18964 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18965 | hp1 | a0002 | c0001 | t0008 | g0031 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18965 | hp2 | a0002 | c0001 | t0003 | g0057 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18967 | hp1 | a0009 | c0013 | t0015 | g0021 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18967 | hp2 | a0002 | c0001 | t0003 | g0166 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18968 | hp1 | a0002 | c0001 | t0019 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18968 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18969 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18969 | hp2 | a0002 | c0001 | t0034 | g0067 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18970 | hp1 | a0002 | c0001 | t0003 | g0019 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18971 | hp1 | a0001 | c0002 | t0004 | g0082 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18971 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18972 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18972 | hp2 | a0002 | c0001 | t0002 | g0149 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18973 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18973 | hp2 | a0001 | c0003 | t0010 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18974 | hp2 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18975 | hp2 | a0002 | c0001 | t0003 | g0019 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18977 | hp1 | a0001 | c0002 | t0048 | g0080 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18977 | hp2 | a0002 | c0001 | t0008 | g0156 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18978 | hp1 | a0002 | c0001 | t0003 | g0059 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18978 | hp2 | a0002 | c0001 | t0006 | g0095 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18979 | hp1 | a0010 | c0009 | t0020 | g0152 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18979 | hp2 | a0002 | c0001 | t0006 | g0007 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18980 | hp1 | a0002 | c0001 | t0002 | g0146 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18980 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18981 | hp1 | a0002 | c0001 | t0006 | g0097 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18981 | hp2 | a0001 | c0002 | t0015 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18983 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18983 | hp2 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18985 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18986 | hp2 | a0002 | c0001 | t0002 | g0070 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18987 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18987 | hp2 | a0002 | c0001 | t0008 | g0091 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18988 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18988 | hp2 | a0002 | c0001 | t0003 | g0062 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18989 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18989 | hp2 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18990 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18990 | hp2 | a0002 | c0001 | t0002 | g0160 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18991 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18991 | hp2 | a0001 | c0002 | t0017 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18993 | hp2 | a0002 | c0001 | t0006 | g0007 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18994 | hp1 | a0002 | c0001 | t0033 | g0019 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18994 | hp2 | a0002 | c0001 | t0002 | g0167 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18995 | hp1 | a0001 | c0002 | t0017 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18995 | hp2 | a0002 | c0001 | t0003 | g0018 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18997 | hp1 | a0002 | c0001 | t0003 | g0063 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18997 | hp2 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18998 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA18998 | hp2 | a0002 | c0001 | t0002 | g0042 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19000 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19003 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19004 | hp1 | a0001 | c0002 | t0015 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19004 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19005 | hp1 | a0002 | c0001 | t0006 | g0007 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19005 | hp2 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19009 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19009 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19010 | hp1 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19010 | hp2 | a0002 | c0001 | t0002 | g0169 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19012 | hp1 | a0001 | c0010 | t0001 | g0104 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19012 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19043 | hp1 | a0002 | c0001 | t0022 | g0043 | AFR | LWK | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19043 | hp2 | a0002 | c0001 | t0042 | g0157 | AFR | LWK | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19054 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19054 | hp2 | a0002 | c0001 | t0041 | g0081 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19056 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19057 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19057 | hp2 | a0002 | c0001 | t0028 | g0007 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19058 | hp1 | a0001 | c0002 | t0053 | g0079 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19058 | hp2 | a0002 | c0001 | t0002 | g0145 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19060 | hp1 | a0002 | c0001 | t0002 | g0168 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19062 | hp1 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19062 | hp2 | a0002 | c0001 | t0027 | g0181 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19063 | hp1 | a0005 | c0007 | t0001 | g0010 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19063 | hp2 | a0002 | c0001 | t0027 | g0045 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19065 | hp1 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19065 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19067 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19068 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19070 | hp1 | a0005 | c0007 | t0001 | g0010 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19070 | hp2 | a0002 | c0001 | t0006 | g0007 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19074 | hp1 | a0002 | c0001 | t0002 | g0009 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19074 | hp2 | a0002 | c0001 | t0003 | g0075 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19075 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19075 | hp2 | a0002 | c0001 | t0002 | g0165 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19076 | hp1 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19076 | hp2 | a0001 | c0002 | t0050 | g0013 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19077 | hp1 | a0002 | c0001 | t0002 | g0163 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0085 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19078 | hp1 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19078 | hp2 | a0001 | c0003 | t0010 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19079 | hp1 | a0002 | c0001 | t0006 | g0045 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19079 | hp2 | a0002 | c0001 | t0002 | g0003 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19080 | hp2 | a0002 | c0001 | t0006 | g0007 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19082 | hp1 | a0002 | c0001 | t0002 | g0144 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19082 | hp2 | a0002 | c0001 | t0019 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19084 | hp1 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19084 | hp2 | a0002 | c0001 | t0002 | g0143 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19085 | hp2 | a0002 | c0001 | t0003 | g0002 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19086 | hp1 | a0001 | c0002 | t0005 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19086 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19087 | hp1 | a0002 | c0001 | t0002 | g0058 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19090 | hp1 | a0001 | c0002 | t0054 | g0122 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19090 | hp2 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19091 | hp1 | a0002 | c0001 | t0003 | g0025 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19091 | hp2 | a0002 | c0001 | t0008 | g0093 | EAS | JPT | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19240 | hp1 | a0001 | c0002 | t0012 | g0008 | AFR | YRI | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA19240 | hp2 | a0002 | c0001 | t0013 | g0053 | AFR | YRI | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA20129 | hp1 | a0002 | c0001 | t0008 | g0050 | AFR | ASW | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA20129 | hp2 | a0001 | c0002 | t0014 | g0004 | AFR | ASW | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01123 | hp1 | a0002 | c0001 | t0002 | g0009 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02109 | hp1 | a0001 | c0002 | t0012 | g0008 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02109 | hp2 | a0002 | c0006 | t0007 | g0005 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0118 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02486 | hp2 | a0003 | c0004 | t0010 | g0016 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02559 | hp1 | a0001 | c0002 | t0026 | g0175 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG02559 | hp2 | a0002 | c0001 | t0002 | g0023 | AFR | ACB | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03471 | hp1 | a0002 | c0001 | t0007 | g0005 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| HG03471 | hp2 | a0002 | c0001 | t0022 | g0158 | AFR | MSL | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA20300 | hp1 | a0002 | c0001 | t0003 | g0060 | AFR | USA | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA20300 | hp2 | a0002 | c0001 | t0020 | g0171 | AFR | USA | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA21309 | hp1 | a0002 | c0001 | t0013 | g0182 | AFR | LWK | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| NA21309 | hp2 | a0002 | c0001 | t0044 | g0174 | AFR | LWK | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0001 | REF | REF | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| homoSapiens | grch38p0 | a0003 | c0004 | t0010 | g0016 | REF | REF | CENPN_chr16_81002214_81036485 | CENPN | chr16 | 81002214 | 81036485 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81012044 | A | C | 1 | a0005 | 4 | NA18944.hp2 NA18951.hp1 NA19063.hp1 others(1): Show |
missense_variant | MODERATE | c.105A>C | p.Gln35His | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/11 | 179/3928 | 105/1020 | 35/339 | chr16 | 81012044 | |||
| chr16:81017360 | A | T | 9 | a0001 a0002 a0004 others(6): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
missense_variant | MODERATE | c.252A>T | p.Glu84Asp | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/11 | 326/3928 | 252/1020 | 84/339 | chr16 | 81017360 | |||
| chr16:81017800 | C | T | 1 | a0007 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.320C>T | p.Ser107Leu | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/11 | 394/3928 | 320/1020 | 107/339 | chr16 | 81017800 | |||
| chr16:81020136 | G | C | 1 | a0010 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.391G>C | p.Val131Leu | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/11 | 465/3928 | 391/1020 | 131/339 | chr16 | 81020136 | |||
| chr16:81024731 | A | T | 1 | a0009 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.650A>T | p.Asn217Ile | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/11 | 724/3928 | 650/1020 | 217/339 | chr16 | 81024731 | |||
| chr16:81024749 | A | G | 1 | a0004 | 5 | HG01346.hp2 HG01515.hp1 HG01928.hp2 others(2): Show |
missense_variant | MODERATE | c.668A>G | p.Gln223Arg | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/11 | 742/3928 | 668/1020 | 223/339 | chr16 | 81024749 | |||
| chr16:81026555 | G | A | 1 | a0008 | 1 | HG03516.hp2 | missense_variant | MODERATE | c.727G>A | p.Val243Ile | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/11 | 801/3928 | 727/1020 | 243/339 | chr16 | 81026555 | |||
| chr16:81026592 | C | T | 1 | a0006 | 2 | HG01361.hp2 HG01934.hp1 |
missense_variant | MODERATE | c.764C>T | p.Thr255Ile | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/11 | 838/3928 | 764/1020 | 255/339 | chr16 | 81026592 | |||
| chr16:81028222 | G | A | 7 | a0001 a0004 a0005 others(4): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
missense_variant | MODERATE | c.862G>A | p.Glu288Lys | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 10/11 | 936/3928 | 862/1020 | 288/339 | chr16 | 81028222 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81017333 | A | G | 1 | a0001c0003 | 14 | HG02523.hp1 HG03831.hp2 NA18940.hp2 others(11): Show |
synonymous_variant | LOW | c.225A>G | p.Gln75Gln | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/11 | 299/3928 | 225/1020 | 75/339 | chr16 | 81017333 | |||
| chr16:81020237 | C | A | 1 | a0002c0006 | 4 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(1): Show |
synonymous_variant | LOW | c.492C>A | p.Ser164Ser | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/11 | 566/3928 | 492/1020 | 164/339 | chr16 | 81020237 | |||
| chr16:81022602 | G | A | 1 | a0001c0010 | 1 | NA19012.hp1 | synonymous_variant | LOW | c.537G>A | p.Leu179Leu | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/11 | 611/3928 | 537/1020 | 179/339 | chr16 | 81022602 | |||
| chr16:81022608 | T | C | 1 | a0002c0011 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.543T>C | p.Ile181Ile | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/11 | 617/3928 | 543/1020 | 181/339 | chr16 | 81022608 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81028659 | G | A | 4 | a0002c0001t0006 a0002c0001t0018 a0002c0001t0028 others(1): Show |
18 | HG00408.hp2 HG02074.hp2 HG02572.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*8G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 8 | chr16 | 81028659 | ||||||
| chr16:81028757 | A | T | 5 | a0002c0001t0006 a0002c0001t0018 a0002c0001t0027 others(2): Show |
20 | HG00408.hp2 HG02074.hp2 HG02572.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*106A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 106 | chr16 | 81028757 | ||||||
| chr16:81028914 | G | C | 1 | a0003c0004t0030 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 263 | chr16 | 81028914 | ||||||
| chr16:81028964 | T | C | 1 | a0001c0002t0031 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*313T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 313 | chr16 | 81028964 | ||||||
| chr16:81028968 | G | A | 1 | a0001c0002t0012 | 5 | HG01081.hp1 HG02109.hp1 HG02809.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*317G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 317 | chr16 | 81028968 | ||||||
| chr16:81029186 | G | T | 1 | a0001c0002t0017 | 3 | NA18945.hp1 NA18991.hp2 NA18995.hp1 |
3_prime_UTR_variant | MODIFIER | c.*535G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 535 | chr16 | 81029186 | ||||||
| chr16:81029235 | C | T | 1 | a0001c0002t0058 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*584C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 584 | chr16 | 81029235 | ||||||
| chr16:81029241 | C | T | 1 | a0002c0001t0057 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*590C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 590 | chr16 | 81029241 | ||||||
| chr16:81029544 | C | T | 29 | a0001c0002t0001 a0001c0002t0004 a0001c0002t0005 others(26): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*893C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 893 | chr16 | 81029544 | ||||||
| chr16:81029560 | C | G | 2 | a0002c0001t0046 a0002c0001t0047 |
2 | HG03041.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*909C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 909 | chr16 | 81029560 | ||||||
| chr16:81029566 | AT | A | 25 | a0001c0003t0025 a0002c0001t0002 a0002c0001t0003 others(22): Show |
162 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*925delT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 925 | INFO_REALIGN_3_PRIME | chr16 | 81029566 | |||||
| chr16:81029573 | T | TG | 2 | a0002c0001t0013 a0002c0001t0032 |
6 | HG02615.hp1 HG02723.hp2 HG03139.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*922_*923insG | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 923 | chr16 | 81029573 | ||||||
| chr16:81029612 | A | G | 2 | a0002c0001t0044 a0002c0001t0045 |
2 | HG01433.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*961A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 961 | chr16 | 81029612 | ||||||
| chr16:81029722 | G | C | 1 | a0001c0002t0005 | 19 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1071G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1071 | chr16 | 81029722 | ||||||
| chr16:81029731 | T | A | 2 | a0001c0002t0048 a0002c0001t0041 |
2 | NA18977.hp1 NA19054.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1080T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1080 | chr16 | 81029731 | ||||||
| chr16:81029932 | C | T | 18 | a0001c0002t0004 a0001c0002t0011 a0001c0002t0012 others(15): Show |
76 | HG00323.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*1281C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1281 | chr16 | 81029932 | ||||||
| chr16:81029998 | T | C | 1 | a0002c0001t0019 | 2 | NA18968.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1347T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1347 | chr16 | 81029998 | ||||||
| chr16:81030000 | T | C | 1 | a0002c0001t0019 | 2 | NA18968.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1349T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1349 | chr16 | 81030000 | ||||||
| chr16:81030001 | C | T | 1 | a0002c0001t0019 | 2 | NA18968.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1350C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1350 | chr16 | 81030001 | ||||||
| chr16:81030003 | T | A | 1 | a0002c0001t0019 | 2 | NA18968.hp1 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1352T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1352 | chr16 | 81030003 | ||||||
| chr16:81030044 | A | C | 1 | a0002c0001t0045 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1393A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1393 | chr16 | 81030044 | ||||||
| chr16:81030107 | C | T | 1 | a0001c0002t0026 | 2 | HG02559.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1456C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1456 | chr16 | 81030107 | ||||||
| chr16:81030130 | C | G | 4 | a0002c0001t0006 a0002c0001t0027 a0002c0001t0029 others(1): Show |
18 | HG00408.hp2 HG02074.hp2 HG02572.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1479C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1479 | chr16 | 81030130 | ||||||
| chr16:81030132 | C | T | 11 | a0001c0002t0011 a0001c0002t0016 a0001c0002t0056 others(8): Show |
20 | HG01433.hp1 HG02630.hp1 HG02717.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1481C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1481 | chr16 | 81030132 | ||||||
| chr16:81030170 | C | A | 1 | a0001c0002t0049 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1519C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1519 | chr16 | 81030170 | ||||||
| chr16:81030227 | G | A | 1 | a0002c0001t0033 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1576G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1576 | chr16 | 81030227 | ||||||
| chr16:81030232 | C | T | 1 | a0002c0001t0024 | 2 | HG02717.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1581C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1581 | chr16 | 81030232 | ||||||
| chr16:81030362 | T | G | 1 | a0002c0001t0034 | 1 | NA18969.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1711T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1711 | chr16 | 81030362 | ||||||
| chr16:81030430 | A | G | 1 | a0002c0001t0018 | 2 | HG03098.hp2 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1779A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1779 | chr16 | 81030430 | ||||||
| chr16:81030473 | G | T | 10 | a0002c0001t0006 a0002c0001t0009 a0002c0001t0018 others(7): Show |
33 | HG00408.hp2 HG01168.hp1 HG01884.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1822G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1822 | chr16 | 81030473 | ||||||
| chr16:81030511 | A | G | 2 | a0001c0002t0015 a0009c0013t0015 |
4 | NA18939.hp1 NA18967.hp1 NA18981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1860A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1860 | chr16 | 81030511 | ||||||
| chr16:81030580 | C | G | 2 | a0001c0002t0016 a0002c0001t0024 |
5 | HG02717.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1929C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1929 | chr16 | 81030580 | ||||||
| chr16:81030621 | C | T | 5 | a0002c0001t0020 a0002c0001t0021 a0002c0001t0032 others(2): Show |
6 | HG01175.hp2 HG02886.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1970C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1970 | chr16 | 81030621 | ||||||
| chr16:81030649 | T | C | 1 | a0001c0002t0014 | 4 | HG01106.hp2 HG02647.hp2 HG02897.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1998T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 1998 | chr16 | 81030649 | ||||||
| chr16:81030782 | A | G | 12 | a0001c0002t0054 a0002c0001t0003 a0002c0001t0007 others(9): Show |
66 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2131A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2131 | chr16 | 81030782 | ||||||
| chr16:81030973 | C | T | 1 | a0001c0002t0053 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2322C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2322 | chr16 | 81030973 | ||||||
| chr16:81031003 | T | G | 1 | a0002c0001t0035 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2352T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2352 | chr16 | 81031003 | ||||||
| chr16:81031097 | G | A | 9 | a0001c0002t0016 a0002c0001t0007 a0002c0001t0024 others(6): Show |
19 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2446G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2446 | chr16 | 81031097 | ||||||
| chr16:81031175 | C | CA | 7 | a0001c0002t0016 a0001c0002t0050 a0002c0001t0007 others(4): Show |
17 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2534dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2535 | INFO_REALIGN_3_PRIME | chr16 | 81031175 | |||||
| chr16:81031208 | C | T | 1 | a0001c0002t0052 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2557C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2557 | chr16 | 81031208 | ||||||
| chr16:81031216 | T | C | 2 | a0002c0001t0044 a0002c0001t0045 |
2 | HG01433.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2565T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2565 | chr16 | 81031216 | ||||||
| chr16:81031222 | C | G | 1 | a0001c0002t0051 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2571C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2571 | chr16 | 81031222 | ||||||
| chr16:81031343 | T | C | 1 | a0002c0001t0037 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2692T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2692 | chr16 | 81031343 | ||||||
| chr16:81031421 | C | T | 1 | a0001c0002t0052 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2770C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2770 | chr16 | 81031421 | ||||||
| chr16:81031454 | A | G | 8 | a0001c0002t0016 a0002c0001t0007 a0002c0001t0008 others(5): Show |
28 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2803A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 11/11 | 2803 | chr16 | 81031454 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:81007318 | G | A | 1 | a0002c0001t0002g0047 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-11+41G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007318 | |||||||
| chr16:81007356 | G | A | 1 | a0001c0002t0001g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-11+79G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007356 | |||||||
| chr16:81007357 | G | A | 4 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(1): Show |
7 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-11+80G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007357 | |||||||
| chr16:81007497 | G | C | 4 | a0002c0001t0008g0017 a0002c0001t0008g0050 a0002c0001t0023g0017 others(1): Show |
5 | HG01109.hp1 HG02257.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11+220G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007497 | |||||||
| chr16:81007523 | G | C | 7 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(4): Show |
10 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11+246G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007523 | |||||||
| chr16:81007536 | G | C | 30 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(27): Show |
57 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11+259G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007536 | |||||||
| chr16:81007575 | A | G | 3 | a0002c0001t0013g0182 a0002c0001t0013g0183 a0002c0001t0032g0184 |
3 | HG03139.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+298A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007575 | |||||||
| chr16:81007600 | C | G | 1 | a0002c0001t0009g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-11+323C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007600 | |||||||
| chr16:81007601 | A | G | 7 | a0002c0001t0006g0007 a0002c0001t0006g0045 a0002c0001t0006g0179 others(4): Show |
13 | HG00408.hp2 HG02074.hp2 NA18945.hp2 others(10): Show |
intron_variant | MODIFIER | c.-11+324A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007601 | |||||||
| chr16:81007652 | C | G | 100 | a0001c0002t0026g0175 a0001c0002t0026g0176 a0001c0002t0056g0177 others(97): Show |
171 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.-11+375C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007652 | |||||||
| chr16:81007656 | A | G | 30 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(27): Show |
57 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11+379A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007656 | |||||||
| chr16:81007709 | G | C | 1 | a0002c0001t0002g0143 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-11+432G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007709 | |||||||
| chr16:81007741 | T | C | 217 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(214): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.-11+464T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007741 | |||||||
| chr16:81007778 | T | C | 1 | a0001c0002t0001g0076 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-11+501T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007778 | |||||||
| chr16:81007787 | C | A | 1 | a0002c0001t0003g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-11+510C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007787 | |||||||
| chr16:81007817 | T | C | 2 | a0001c0002t0016g0026 a0001c0002t0016g0077 |
3 | HG02818.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-11+540T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007817 | |||||||
| chr16:81007934 | C | A | 1 | a0002c0001t0003g0056 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-11+657C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007934 | |||||||
| chr16:81007938 | C | T | 1 | a0002c0001t0003g0075 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-11+661C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81007938 | |||||||
| chr16:81008088 | C | G | 3 | a0002c0001t0013g0182 a0002c0001t0013g0183 a0002c0001t0032g0184 |
3 | HG03139.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-11+811C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008088 | |||||||
| chr16:81008178 | A | G | 1 | a0001c0003t0001g0141 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-11+901A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008178 | |||||||
| chr16:81008206 | AT | A | 10 | a0002c0001t0002g0003 a0002c0001t0002g0042 a0002c0001t0002g0047 others(7): Show |
30 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.-11+932delT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81008206 | ||||||
| chr16:81008308 | G | C | 1 | a0001c0002t0001g0012 | 4 | HG01243.hp2 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-11+1031G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008308 | |||||||
| chr16:81008323 | G | A | 24 | a0001c0002t0001g0028 a0001c0002t0001g0086 a0001c0002t0001g0087 others(21): Show |
32 | HG01069.hp1 HG01071.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.-11+1046G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008323 | |||||||
| chr16:81008345 | G | A | 52 | a0001c0003t0001g0094 a0002c0001t0002g0002 a0002c0001t0002g0020 others(49): Show |
86 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-11+1068G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008345 | |||||||
| chr16:81008399 | T | A | 35 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(32): Show |
69 | HG00323.hp2 HG00597.hp2 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.-11+1122T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008399 | |||||||
| chr16:81008423 | G | T | 109 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(106): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-11+1146G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008423 | |||||||
| chr16:81008485 | C | T | 3 | a0002c0001t0006g0045 a0002c0001t0027g0045 a0002c0001t0027g0181 |
3 | NA19062.hp2 NA19063.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-11+1208C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008485 | |||||||
| chr16:81008511 | A | G | 9 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(6): Show |
12 | HG01433.hp1 HG01884.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11+1234A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008511 | |||||||
| chr16:81008633 | C | G | 1 | a0002c0001t0013g0172 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-11+1356C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008633 | |||||||
| chr16:81008718 | C | T | 1 | a0002c0001t0021g0074 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-11+1441C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008718 | |||||||
| chr16:81008876 | G | T | 84 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(81): Show |
151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-11+1599G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008876 | |||||||
| chr16:81008937 | A | T | 105 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(102): Show |
177 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.-11+1660A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008937 | |||||||
| chr16:81008954 | C | G | 106 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(103): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-11+1677C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008954 | |||||||
| chr16:81008994 | C | A | 217 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(214): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.-11+1717C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81008994 | |||||||
| chr16:81009099 | C | T | 1 | a0001c0002t0001g0140 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-11+1822C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009099 | |||||||
| chr16:81009153 | G | A | 9 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(6): Show |
11 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11+1876G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009153 | |||||||
| chr16:81009193 | G | C | 1 | a0002c0001t0003g0075 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-11+1916G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009193 | |||||||
| chr16:81009208 | T | C | 1 | a0002c0001t0009g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-11+1931T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009208 | |||||||
| chr16:81009239 | G | A | 5 | a0002c0001t0013g0052 a0002c0001t0013g0053 a0002c0001t0013g0182 others(2): Show |
5 | HG02723.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+1962G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009239 | |||||||
| chr16:81009240 | C | G | 1 | a0001c0002t0001g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-11+1963C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009240 | |||||||
| chr16:81009316 | GAA | G | 5 | a0002c0001t0013g0052 a0002c0001t0013g0053 a0002c0001t0013g0182 others(2): Show |
5 | HG02723.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-11+2040_-11+2041d others(4): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009316 | |||||||
| chr16:81009369 | T | C | 89 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(86): Show |
156 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.-11+2092T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009369 | |||||||
| chr16:81009427 | G | A | 2 | a0002c0001t0018g0098 a0002c0001t0018g0099 |
2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-11+2150G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009427 | |||||||
| chr16:81009600 | A | G | 106 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(103): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.-11+2323A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009600 | |||||||
| chr16:81009636 | T | C | 1 | a0001c0002t0001g0033 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.-10-2294T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009636 | |||||||
| chr16:81009652 | T | C | 1 | a0001c0002t0001g0101 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-10-2278T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009652 | |||||||
| chr16:81009666 | T | C | 1 | a0002c0001t0022g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-2264T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009666 | |||||||
| chr16:81009769 | T | C | 1 | a0002c0001t0002g0159 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-10-2161T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009769 | |||||||
| chr16:81009828 | G | T | 5 | a0002c0001t0013g0052 a0002c0001t0013g0053 a0002c0001t0013g0182 others(2): Show |
5 | HG02723.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-2102G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009828 | |||||||
| chr16:81009858 | G | C | 2 | a0002c0001t0018g0098 a0002c0001t0018g0099 |
2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-10-2072G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009858 | |||||||
| chr16:81009880 | G | A | 217 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(214): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.-10-2050G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009880 | |||||||
| chr16:81009918 | A | G | 1 | a0002c0001t0009g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-10-2012A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009918 | |||||||
| chr16:81009926 | C | T | 3 | a0002c0001t0022g0043 a0002c0001t0039g0043 a0002c0001t0042g0157 |
3 | HG02717.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-10-2004C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009926 | |||||||
| chr16:81009957 | A | G | 84 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(81): Show |
151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-10-1973A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009957 | |||||||
| chr16:81009965 | G | A | 2 | a0001c0002t0016g0026 a0001c0002t0016g0077 |
3 | HG02818.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-10-1965G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81009965 | |||||||
| chr16:81010034 | A | C | 1 | a0002c0001t0013g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-10-1896A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010034 | |||||||
| chr16:81010055 | C | T | 2 | a0002c0001t0046g0044 a0002c0001t0047g0044 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10-1875C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010055 | |||||||
| chr16:81010059 | C | T | 1 | a0002c0001t0002g0149 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-10-1871C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010059 | |||||||
| chr16:81010060 | G | A | 105 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(102): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-10-1870G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010060 | |||||||
| chr16:81010063 | G | C | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-10-1867G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010063 | |||||||
| chr16:81010139 | A | G | 84 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(81): Show |
151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-10-1791A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010139 | |||||||
| chr16:81010224 | G | A | 2 | a0002c0001t0022g0043 a0002c0001t0039g0043 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-10-1706G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010224 | |||||||
| chr16:81010441 | A | T | 1 | a0002c0001t0006g0180 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-10-1489A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010441 | |||||||
| chr16:81010537 | C | T | 2 | a0002c0001t0002g0100 a0002c0001t0024g0032 |
3 | HG02717.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-10-1393C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010537 | |||||||
| chr16:81010542 | G | A | 2 | a0002c0001t0003g0018 a0002c0001t0003g0057 |
4 | NA18954.hp1 NA18962.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10-1388G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010542 | |||||||
| chr16:81010671 | G | GA | 84 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(81): Show |
151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.-10-1258dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr16 | 81010671 | ||||||
| chr16:81010731 | G | A | 27 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(24): Show |
55 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.-10-1199G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81010731 | |||||||
| chr16:81011025 | A | C | 28 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(25): Show |
56 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(53): Show |
intron_variant | MODIFIER | c.-10-905A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011025 | |||||||
| chr16:81011031 | G | T | 5 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(2): Show |
8 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.-10-899G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011031 | |||||||
| chr16:81011083 | C | T | 2 | a0002c0001t0046g0044 a0002c0001t0047g0044 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-10-847C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011083 | |||||||
| chr16:81011227 | A | G | 1 | a0002c0001t0009g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-10-703A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011227 | |||||||
| chr16:81011342 | T | C | 40 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(37): Show |
73 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-10-588T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011342 | |||||||
| chr16:81011381 | A | T | 2 | a0004c0005t0001g0015 a0004c0005t0001g0137 |
5 | HG01346.hp2 HG01515.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-549A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011381 | |||||||
| chr16:81011439 | C | T | 1 | a0002c0001t0037g0073 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10-491C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011439 | |||||||
| chr16:81011547 | C | T | 1 | a0001c0002t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-10-383C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011547 | |||||||
| chr16:81011571 | C | T | 73 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(70): Show |
134 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.-10-359C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011571 | |||||||
| chr16:81011623 | T | G | 90 | a0001c0002t0001g0102 a0002c0001t0002g0002 a0002c0001t0002g0003 others(87): Show |
157 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.-10-307T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011623 | |||||||
| chr16:81011657 | A | G | 85 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(82): Show |
152 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.-10-273A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011657 | |||||||
| chr16:81011664 | G | C | 1 | a0002c0001t0003g0055 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-10-266G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011664 | |||||||
| chr16:81011717 | C | T | 215 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(212): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.-10-213C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011717 | |||||||
| chr16:81011774 | G | A | 1 | a0002c0001t0018g0098 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-10-156G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011774 | |||||||
| chr16:81011869 | A | G | 1 | a0002c0001t0037g0073 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-10-61A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011869 | |||||||
| chr16:81011926 | A | G | 1 | a0002c0001t0002g0148 | 1 | NA18747.hp2 | splice_region_variant&intron_variant | LOW | c.-10-4A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 1/10 | chr16 | 81011926 | |||||||
| chr16:81012119 | G | A | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.171+9G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012119 | |||||||
| chr16:81012496 | A | G | 105 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(102): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.171+386A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012496 | |||||||
| chr16:81012559 | T | C | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.171+449T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012559 | |||||||
| chr16:81012672 | T | C | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.171+562T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012672 | |||||||
| chr16:81012730 | C | G | 90 | a0001c0002t0001g0102 a0002c0001t0002g0002 a0002c0001t0002g0003 others(87): Show |
157 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.171+620C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012730 | |||||||
| chr16:81012742 | C | T | 2 | a0002c0001t0018g0098 a0002c0001t0018g0099 |
2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.171+632C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012742 | |||||||
| chr16:81012776 | G | A | 1 | a0002c0001t0021g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.171+666G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012776 | |||||||
| chr16:81012784 | G | A | 2 | a0002c0001t0018g0098 a0002c0001t0018g0099 |
2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.171+674G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012784 | |||||||
| chr16:81012800 | G | C | 27 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(24): Show |
55 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.171+690G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81012800 | |||||||
| chr16:81013018 | G | C | 215 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(212): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.171+908G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013018 | |||||||
| chr16:81013124 | C | G | 1 | a0001c0002t0001g0136 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.172-1012C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013124 | |||||||
| chr16:81013128 | A | G | 12 | a0002c0001t0006g0007 a0002c0001t0006g0045 a0002c0001t0006g0095 others(9): Show |
18 | HG00408.hp2 HG02074.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.172-1008A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013128 | |||||||
| chr16:81013183 | T | C | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.172-953T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013183 | |||||||
| chr16:81013246 | T | C | 2 | a0002c0001t0046g0044 a0002c0001t0047g0044 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.172-890T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013246 | |||||||
| chr16:81013424 | C | T | 1 | a0002c0001t0002g0147 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.172-712C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013424 | |||||||
| chr16:81013491 | G | C | 2 | a0002c0001t0002g0100 a0002c0001t0024g0032 |
3 | HG02717.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.172-645G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013491 | |||||||
| chr16:81013573 | C | T | 89 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(86): Show |
156 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-563C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013573 | |||||||
| chr16:81013589 | T | C | 89 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(86): Show |
156 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-547T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013589 | |||||||
| chr16:81013677 | C | T | 1 | a0001c0002t0005g0134 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.172-459C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013677 | |||||||
| chr16:81013679 | C | T | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.172-457C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013679 | |||||||
| chr16:81013733 | G | A | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.172-403G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013733 | |||||||
| chr16:81013814 | A | G | 89 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(86): Show |
156 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.172-322A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013814 | |||||||
| chr16:81013864 | G | A | 1 | a0002c0001t0006g0095 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.172-272G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81013864 | |||||||
| chr16:81014063 | C | G | 1 | a0002c0001t0009g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.172-73C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81014063 | |||||||
| chr16:81014092 | A | C | 1 | a0002c0001t0002g0169 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.172-44A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 2/10 | chr16 | 81014092 | |||||||
| chr16:81014228 | G | C | 2 | a0002c0001t0002g0100 a0002c0001t0024g0032 |
3 | HG02717.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.217+47G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014228 | |||||||
| chr16:81014273 | C | T | 1 | a0008c0012t0055g0178 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.217+92C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014273 | |||||||
| chr16:81014329 | G | A | 2 | a0002c0001t0002g0144 a0002c0001t0002g0147 |
2 | HG00597.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.217+148G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014329 | |||||||
| chr16:81014430 | G | A | 1 | a0002c0001t0003g0057 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.217+249G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014430 | |||||||
| chr16:81014457 | T | C | 3 | a0002c0001t0021g0074 a0002c0001t0021g0151 a0010c0009t0020g0152 |
3 | HG01175.hp2 HG04228.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.217+276T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014457 | |||||||
| chr16:81014549 | CAG | C | 34 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(31): Show |
61 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.217+371_217+372del others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81014549 | ||||||
| chr16:81014554 | T | A | 7 | a0002c0001t0007g0005 a0002c0001t0007g0170 a0002c0001t0020g0171 others(4): Show |
13 | HG00323.hp2 HG00735.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.217+373T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014554 | |||||||
| chr16:81014766 | G | GGCTTTGT others(4): Show |
4 | a0001c0002t0001g0087 a0001c0002t0001g0088 a0001c0002t0001g0089 others(1): Show |
4 | HG02027.hp2 NA18961.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+586_217+596dup others(11): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81014766 | ||||||
| chr16:81014820 | A | G | 72 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(69): Show |
133 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.217+639A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014820 | |||||||
| chr16:81014950 | T | C | 29 | a0002c0001t0002g0023 a0002c0001t0006g0007 a0002c0001t0006g0045 others(26): Show |
40 | HG00408.hp2 HG01109.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.217+769T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014950 | |||||||
| chr16:81014959 | A | C | 105 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(102): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.217+778A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81014959 | |||||||
| chr16:81015029 | T | C | 1 | a0001c0002t0001g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.217+848T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015029 | |||||||
| chr16:81015133 | T | C | 1 | a0001c0003t0001g0094 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.217+952T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015133 | |||||||
| chr16:81015606 | G | A | 1 | a0002c0001t0009g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.217+1425G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015606 | |||||||
| chr16:81015677 | A | G | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.217+1496A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015677 | |||||||
| chr16:81015700 | G | A | 1 | a0002c0001t0009g0049 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.217+1519G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015700 | |||||||
| chr16:81015773 | A | G | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.218-1553A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015773 | |||||||
| chr16:81015782 | G | C | 3 | a0002c0001t0002g0058 a0002c0001t0003g0059 a0002c0001t0003g0135 |
3 | NA18959.hp2 NA18978.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.218-1544G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015782 | |||||||
| chr16:81015879 | T | G | 1 | a0002c0001t0003g0060 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218-1447T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015879 | |||||||
| chr16:81015949 | C | G | 215 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(212): Show |
389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.218-1377C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015949 | |||||||
| chr16:81015951 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218-1375G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015951 | |||||||
| chr16:81015982 | C | T | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.218-1344C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015982 | |||||||
| chr16:81015989 | G | A | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.218-1337G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81015989 | |||||||
| chr16:81016003 | C | CA | 86 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(83): Show |
153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.218-1312dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81016003 | ||||||
| chr16:81016021 | A | G | 86 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(83): Show |
153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.218-1305A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016021 | |||||||
| chr16:81016078 | A | G | 86 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(83): Show |
153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.218-1248A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016078 | |||||||
| chr16:81016160 | G | A | 2 | a0001c0002t0016g0026 a0001c0002t0016g0077 |
3 | HG02818.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.218-1166G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016160 | |||||||
| chr16:81016195 | T | C | 58 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(55): Show |
97 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.218-1131T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016195 | |||||||
| chr16:81016273 | T | C | 5 | a0002c0001t0022g0043 a0002c0001t0039g0043 a0002c0001t0042g0157 others(2): Show |
5 | HG02717.hp1 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-1053T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016273 | |||||||
| chr16:81016371 | G | A | 67 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(64): Show |
108 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.218-955G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016371 | |||||||
| chr16:81016376 | T | G | 68 | a0001c0002t0001g0102 a0002c0001t0002g0002 a0002c0001t0002g0020 others(65): Show |
109 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.218-950T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016376 | |||||||
| chr16:81016546 | G | A | 7 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(4): Show |
10 | HG01433.hp1 HG01884.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-780G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016546 | |||||||
| chr16:81016567 | A | G | 108 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(105): Show |
180 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(177): Show |
intron_variant | MODIFIER | c.218-759A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016567 | |||||||
| chr16:81016613 | A | C | 86 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(83): Show |
153 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.218-713A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016613 | |||||||
| chr16:81016719 | A | G | 4 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(1): Show |
7 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-607A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016719 | |||||||
| chr16:81016786 | C | CACAT | 17 | a0002c0001t0006g0007 a0002c0001t0006g0045 a0002c0001t0006g0095 others(14): Show |
23 | HG00408.hp2 HG02074.hp2 HG02572.hp1 others(20): Show |
intron_variant | MODIFIER | c.218-522_218-519dup others(4): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81016786 | ||||||
| chr16:81016841 | G | C | 1 | a0002c0001t0009g0046 | 2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218-485G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016841 | |||||||
| chr16:81016857 | G | A | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-469G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016857 | |||||||
| chr16:81016862 | G | T | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-464G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81016862 | |||||||
| chr16:81017041 | G | A | 1 | a0002c0001t0021g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.218-285G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81017041 | |||||||
| chr16:81017162 | A | G | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.218-164A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81017162 | |||||||
| chr16:81017164 | T | TA | 216 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(213): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.218-161dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr16 | 81017164 | ||||||
| chr16:81017212 | T | C | 91 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(88): Show |
161 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.218-114T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81017212 | |||||||
| chr16:81017288 | A | G | 1 | a0001c0002t0001g0132 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.218-38A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 3/10 | chr16 | 81017288 | |||||||
| chr16:81017431 | A | G | 1 | a0002c0001t0021g0151 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.277+46A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/10 | chr16 | 81017431 | |||||||
| chr16:81017496 | C | T | 91 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(88): Show |
161 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.277+111C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/10 | chr16 | 81017496 | |||||||
| chr16:81017520 | A | G | 103 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(100): Show |
175 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.277+135A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/10 | chr16 | 81017520 | |||||||
| chr16:81017572 | C | T | 1 | a0002c0001t0022g0158 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.278-186C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/10 | chr16 | 81017572 | |||||||
| chr16:81017598 | T | G | 96 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(93): Show |
166 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.278-160T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/10 | chr16 | 81017598 | |||||||
| chr16:81017722 | C | T | 217 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(214): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.278-36C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 4/10 | chr16 | 81017722 | |||||||
| chr16:81017873 | C | T | 3 | a0001c0003t0001g0014 a0001c0003t0001g0094 a0001c0003t0001g0141 |
6 | NA18940.hp2 NA18954.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+39C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81017873 | |||||||
| chr16:81017971 | A | G | 1 | a0001c0002t0004g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.354+137A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81017971 | |||||||
| chr16:81018071 | T | C | 214 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(211): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.354+237T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018071 | |||||||
| chr16:81018140 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.354+306C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018140 | |||||||
| chr16:81018201 | G | A | 67 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(64): Show |
128 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.354+367G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018201 | |||||||
| chr16:81018203 | G | C | 1 | a0001c0010t0001g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.354+369G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018203 | |||||||
| chr16:81018292 | G | T | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.354+458G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018292 | |||||||
| chr16:81018325 | C | A | 12 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(9): Show |
14 | HG01109.hp1 HG01433.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+491C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018325 | |||||||
| chr16:81018364 | G | C | 31 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(28): Show |
64 | HG00323.hp2 HG00597.hp2 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.354+530G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018364 | |||||||
| chr16:81018394 | G | A | 2 | a0002c0001t0018g0098 a0002c0001t0018g0099 |
2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.354+560G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018394 | |||||||
| chr16:81018398 | T | G | 2 | a0002c0001t0022g0043 a0002c0001t0039g0043 |
2 | HG02717.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.354+564T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018398 | |||||||
| chr16:81018645 | A | C | 1 | a0001c0002t0001g0129 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.354+811A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018645 | |||||||
| chr16:81018734 | C | G | 3 | a0001c0003t0001g0014 a0001c0003t0001g0094 a0001c0003t0001g0141 |
6 | NA18940.hp2 NA18954.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.354+900C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018734 | |||||||
| chr16:81018735 | T | C | 12 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(9): Show |
14 | HG01109.hp1 HG01433.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.354+901T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018735 | |||||||
| chr16:81018807 | G | T | 2 | a0002c0001t0046g0044 a0002c0001t0047g0044 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.354+973G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018807 | |||||||
| chr16:81018987 | A | G | 1 | a0002c0001t0013g0053 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.355-1113A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81018987 | |||||||
| chr16:81019009 | T | C | 2 | a0002c0001t0003g0024 a0002c0001t0003g0061 |
3 | HG01952.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.355-1091T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019009 | |||||||
| chr16:81019128 | A | T | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.355-972A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019128 | |||||||
| chr16:81019155 | A | G | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-945A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019155 | |||||||
| chr16:81019218 | G | C | 1 | a0001c0002t0001g0034 | 2 | HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.355-882G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019218 | |||||||
| chr16:81019234 | G | A | 2 | a0002c0001t0046g0044 a0002c0001t0047g0044 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.355-866G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019234 | |||||||
| chr16:81019240 | G | A | 102 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(99): Show |
174 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.355-860G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019240 | |||||||
| chr16:81019380 | C | CT | 6 | a0001c0002t0001g0086 a0002c0001t0002g0167 a0002c0001t0003g0059 others(3): Show |
6 | HG01175.hp1 HG01981.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.355-706dupT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81019380 | ||||||
| chr16:81019503 | C | T | 1 | a0002c0001t0003g0071 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.355-597C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019503 | |||||||
| chr16:81019654 | C | T | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-446C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019654 | |||||||
| chr16:81019703 | C | CA | 5 | a0001c0002t0001g0035 a0001c0002t0001g0105 a0001c0002t0015g0035 others(2): Show |
5 | HG02056.hp1 HG02074.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.355-388dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81019703 | ||||||
| chr16:81019814 | C | T | 30 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(27): Show |
58 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.355-286C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019814 | |||||||
| chr16:81019845 | C | G | 1 | a0002c0001t0038g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.355-255C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019845 | |||||||
| chr16:81019876 | C | CA | 94 | a0001c0002t0004g0078 a0002c0001t0002g0002 a0002c0001t0002g0003 others(91): Show |
163 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.355-211dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81019876 | ||||||
| chr16:81019912 | T | A | 2 | a0002c0001t0018g0098 a0002c0001t0018g0099 |
2 | HG03098.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.355-188T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019912 | |||||||
| chr16:81019913 | T | A | 95 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(92): Show |
165 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.355-187T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019913 | |||||||
| chr16:81019914 | T | A | 105 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(102): Show |
177 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.355-186T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019914 | |||||||
| chr16:81019915 | A | T | 7 | a0001c0002t0001g0130 a0001c0002t0004g0008 a0001c0002t0004g0030 others(4): Show |
13 | HG01081.hp1 HG01358.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.355-185A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019915 | |||||||
| chr16:81019927 | T | C | 1 | a0001c0010t0001g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.355-173T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | chr16 | 81019927 | |||||||
| chr16:81020077 | CT | C | 201 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(198): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(370): Show |
intron_variant | MODIFIER | c.355-11delT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81020077 | ||||||
| chr16:81020077 | CTT | C | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.355-12_355-11delTT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr16 | 81020077 | ||||||
| chr16:81020330 | C | G | 1 | a0002c0001t0002g0165 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.531+54C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020330 | |||||||
| chr16:81020441 | C | T | 2 | a0001c0002t0004g0084 a0001c0002t0004g0085 |
2 | NA18947.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.531+165C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020441 | |||||||
| chr16:81020464 | C | T | 1 | a0002c0001t0002g0165 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.531+188C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020464 | |||||||
| chr16:81020571 | G | A | 1 | a0001c0002t0004g0027 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.531+295G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020571 | |||||||
| chr16:81020675 | C | T | 1 | a0002c0001t0002g0164 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.531+399C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020675 | |||||||
| chr16:81020692 | A | G | 9 | a0001c0002t0001g0006 a0001c0002t0001g0041 a0001c0002t0001g0125 others(6): Show |
16 | HG00639.hp2 HG00741.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.531+416A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020692 | |||||||
| chr16:81020869 | C | G | 1 | a0002c0001t0032g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.531+593C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020869 | |||||||
| chr16:81020890 | G | A | 90 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(87): Show |
160 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.531+614G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81020890 | |||||||
| chr16:81021087 | C | T | 2 | a0002c0001t0046g0044 a0002c0001t0047g0044 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.531+811C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021087 | |||||||
| chr16:81021092 | T | TA | 31 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0042 others(28): Show |
63 | HG00323.hp2 HG00597.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.531+831dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81021092 | ||||||
| chr16:81021335 | G | A | 1 | a0001c0002t0001g0106 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.531+1059G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021335 | |||||||
| chr16:81021507 | G | A | 17 | a0002c0001t0002g0023 a0002c0001t0006g0007 a0002c0001t0006g0045 others(14): Show |
26 | HG00408.hp2 HG01884.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.532-1090G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021507 | |||||||
| chr16:81021519 | A | G | 17 | a0002c0001t0002g0023 a0002c0001t0006g0007 a0002c0001t0006g0045 others(14): Show |
26 | HG00408.hp2 HG01884.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.532-1078A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021519 | |||||||
| chr16:81021598 | A | G | 5 | a0002c0001t0013g0052 a0002c0001t0013g0053 a0002c0001t0013g0182 others(2): Show |
5 | HG02723.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.532-999A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021598 | |||||||
| chr16:81021738 | A | G | 1 | a0002c0001t0008g0093 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.532-859A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021738 | |||||||
| chr16:81021739 | T | C | 1 | a0002c0001t0003g0063 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.532-858T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021739 | |||||||
| chr16:81021759 | CT | C | 12 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(9): Show |
14 | HG01109.hp1 HG01433.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.532-825delT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr16 | 81021759 | ||||||
| chr16:81021847 | A | C | 217 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(214): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.532-750A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021847 | |||||||
| chr16:81021903 | C | A | 3 | a0001c0003t0001g0014 a0001c0003t0001g0094 a0001c0003t0001g0141 |
6 | NA18940.hp2 NA18954.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-694C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021903 | |||||||
| chr16:81021903 | C | G | 30 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(27): Show |
63 | HG00323.hp2 HG00597.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.532-694C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81021903 | |||||||
| chr16:81022024 | G | A | 2 | a0001c0002t0001g0107 a0001c0002t0001g0132 |
2 | NA18993.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.532-573G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81022024 | |||||||
| chr16:81022242 | G | A | 216 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(213): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.532-355G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81022242 | |||||||
| chr16:81022273 | G | A | 106 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(103): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.532-324G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81022273 | |||||||
| chr16:81022480 | T | G | 3 | a0001c0003t0001g0014 a0001c0003t0001g0094 a0001c0003t0001g0141 |
6 | NA18940.hp2 NA18954.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.532-117T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81022480 | |||||||
| chr16:81022488 | C | T | 1 | a0001c0002t0004g0085 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.532-109C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81022488 | |||||||
| chr16:81022506 | C | A | 108 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(105): Show |
180 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.532-91C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 6/10 | chr16 | 81022506 | |||||||
| chr16:81022765 | C | G | 1 | a0002c0001t0024g0032 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.633+67C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81022765 | |||||||
| chr16:81022788 | C | CAAGAGGA others(7): Show |
1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.633+91_633+104dupA others(13): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81022788 | ||||||
| chr16:81022790 | A | C | 2 | a0002c0001t0002g0020 a0002c0001t0002g0070 |
4 | NA18986.hp2 NA19005.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.633+92A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81022790 | |||||||
| chr16:81022836 | T | G | 42 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(39): Show |
75 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.633+138T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81022836 | |||||||
| chr16:81022966 | G | C | 2 | a0001c0003t0025g0108 a0001c0003t0025g0109 |
2 | HG02523.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.633+268G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81022966 | |||||||
| chr16:81023075 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.633+377G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023075 | |||||||
| chr16:81023132 | C | T | 1 | a0003c0004t0030g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.633+434C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023132 | |||||||
| chr16:81023220 | A | G | 3 | a0002c0001t0003g0018 a0002c0001t0003g0057 a0002c0001t0035g0069 |
5 | HG01952.hp2 NA18954.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.633+522A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023220 | |||||||
| chr16:81023230 | G | A | 106 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(103): Show |
178 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.633+532G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023230 | |||||||
| chr16:81023328 | G | T | 13 | a0001c0002t0056g0177 a0002c0001t0008g0017 a0002c0001t0008g0031 others(10): Show |
15 | HG01109.hp1 HG01433.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.633+630G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023328 | |||||||
| chr16:81023367 | C | T | 1 | a0001c0002t0004g0029 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.633+669C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023367 | |||||||
| chr16:81023464 | G | C | 13 | a0001c0002t0056g0177 a0002c0001t0008g0017 a0002c0001t0008g0031 others(10): Show |
15 | HG01109.hp1 HG01433.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.633+766G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023464 | |||||||
| chr16:81023508 | T | C | 1 | a0001c0002t0001g0111 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.633+810T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023508 | |||||||
| chr16:81023571 | G | A | 10 | a0001c0002t0004g0010 a0001c0002t0004g0078 a0001c0002t0004g0082 others(7): Show |
14 | HG02080.hp1 NA18944.hp2 NA18947.hp1 others(11): Show |
intron_variant | MODIFIER | c.633+873G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023571 | |||||||
| chr16:81023600 | C | T | 1 | a0001c0002t0001g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.633+902C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023600 | |||||||
| chr16:81023766 | G | A | 2 | a0002c0001t0046g0044 a0002c0001t0047g0044 |
2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.634-949G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023766 | |||||||
| chr16:81023793 | C | G | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.634-922C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023793 | |||||||
| chr16:81023803 | G | A | 2 | a0002c0001t0002g0159 a0002c0001t0002g0161 |
2 | HG02735.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.634-912G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023803 | |||||||
| chr16:81023805 | G | A | 1 | a0002c0001t0002g0160 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.634-910G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023805 | |||||||
| chr16:81023808 | C | T | 1 | a0001c0002t0001g0089 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.634-907C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023808 | |||||||
| chr16:81023817 | A | C | 1 | a0002c0001t0003g0068 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.634-898A>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023817 | |||||||
| chr16:81023819 | A | G | 1 | a0002c0001t0003g0068 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.634-896A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023819 | |||||||
| chr16:81023844 | T | G | 217 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(214): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.634-871T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023844 | |||||||
| chr16:81023888 | T | G | 34 | a0001c0002t0001g0113 a0001c0002t0016g0026 a0001c0002t0016g0077 others(31): Show |
46 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.634-827T>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81023888 | |||||||
| chr16:81024013 | A | G | 1 | a0002c0001t0034g0067 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.634-702A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81024013 | |||||||
| chr16:81024060 | G | A | 19 | a0002c0001t0002g0023 a0002c0001t0006g0007 a0002c0001t0006g0045 others(16): Show |
28 | HG00408.hp2 HG01884.hp1 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.634-655G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81024060 | |||||||
| chr16:81024244 | A | G | 1 | a0001c0003t0010g0123 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.634-471A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81024244 | |||||||
| chr16:81024376 | T | C | 1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.634-339T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81024376 | |||||||
| chr16:81024386 | G | A | 5 | a0002c0001t0013g0052 a0002c0001t0013g0053 a0002c0001t0013g0182 others(2): Show |
5 | HG02723.hp2 HG03139.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-329G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81024386 | |||||||
| chr16:81024422 | G | A | 2 | a0001c0003t0025g0108 a0001c0003t0025g0109 |
2 | HG02523.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.634-293G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | chr16 | 81024422 | |||||||
| chr16:81024565 | T | TCAACTCA others(2): Show |
90 | a0002c0001t0002g0002 a0002c0001t0002g0003 a0002c0001t0002g0009 others(87): Show |
160 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.634-138_634-130dup others(9): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81024565 | ||||||
| chr16:81024646 | T | TA | 5 | a0001c0002t0001g0028 a0001c0002t0004g0027 a0001c0002t0004g0028 others(2): Show |
8 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.634-59dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr16 | 81024646 | ||||||
| chr16:81024859 | T | C | 2 | a0001c0002t0001g0125 a0001c0002t0004g0126 |
2 | HG01099.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.697+81T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81024859 | |||||||
| chr16:81024864 | G | T | 1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.697+86G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81024864 | |||||||
| chr16:81024938 | C | T | 1 | a0002c0001t0002g0161 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.697+160C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81024938 | |||||||
| chr16:81025148 | ACT | A | 197 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(194): Show |
369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.697+375_697+376del others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025148 | ||||||
| chr16:81025295 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.697+517T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025295 | |||||||
| chr16:81025382 | A | T | 1 | a0001c0002t0054g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.697+604A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025382 | |||||||
| chr16:81025478 | G | C | 1 | a0002c0001t0057g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.697+700G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025478 | |||||||
| chr16:81025654 | C | T | 47 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0023 others(44): Show |
83 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.698-872C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025654 | |||||||
| chr16:81025663 | C | A | 1 | a0001c0002t0001g0036 | 2 | HG00544.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.698-863C>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025663 | |||||||
| chr16:81025689 | C | CTTTTTTT others(1): Show |
6 | a0002c0001t0008g0031 a0002c0001t0008g0050 a0002c0001t0008g0091 others(3): Show |
7 | HG02976.hp1 NA18948.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.698-836_698-835ins others(8): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025689 | ||||||
| chr16:81025689 | CTCTTTTT others(3): Show |
C | 41 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(38): Show |
73 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(70): Show |
intron_variant | MODIFIER | c.698-835_698-826del others(10): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025689 | ||||||
| chr16:81025689 | CTCTTTTT others(4): Show |
C | 56 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(53): Show |
94 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.698-835_698-825del others(11): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025689 | ||||||
| chr16:81025689 | CTCTTTTT others(5): Show |
C | 5 | a0001c0002t0001g0107 a0001c0002t0001g0113 a0001c0002t0001g0121 others(2): Show |
5 | HG00423.hp2 HG02602.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-835_698-824del others(12): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025689 | ||||||
| chr16:81025689 | CTCTTTTT others(6): Show |
C | 90 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(87): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.698-835_698-823del others(13): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025689 | ||||||
| chr16:81025689 | CTCTTTTT others(7): Show |
C | 8 | a0001c0002t0001g0021 a0001c0002t0001g0101 a0001c0002t0001g0116 others(5): Show |
9 | HG00099.hp1 HG00323.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.698-835_698-822del others(14): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025689 | ||||||
| chr16:81025691 | C | T | 13 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(10): Show |
15 | HG01109.hp1 HG01433.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.698-835C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025691 | |||||||
| chr16:81025721 | A | T | 1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.698-805A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025721 | |||||||
| chr16:81025725 | C | CA | 12 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(9): Show |
14 | HG01109.hp1 HG01433.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.698-800dupA | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81025725 | ||||||
| chr16:81025779 | T | A | 1 | a0002c0001t0038g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.698-747T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025779 | |||||||
| chr16:81025962 | T | C | 213 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(210): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.698-564T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025962 | |||||||
| chr16:81025963 | G | A | 1 | a0002c0001t0024g0032 | 2 | HG02717.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.698-563G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81025963 | |||||||
| chr16:81026015 | C | T | 1 | a0001c0002t0001g0120 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.698-511C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026015 | |||||||
| chr16:81026052 | G | GAT | 2 | a0002c0001t0003g0019 a0002c0001t0033g0019 |
3 | NA18970.hp1 NA18975.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.698-457_698-456dup others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026052 | ||||||
| chr16:81026052 | GAT | G | 6 | a0002c0001t0002g0023 a0002c0001t0002g0058 a0002c0001t0009g0011 others(3): Show |
9 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.698-457_698-456del others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026052 | ||||||
| chr16:81026063 | A | G | 1 | a0002c0001t0045g0173 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.698-463A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026063 | |||||||
| chr16:81026065 | A | ATG | 5 | a0002c0001t0002g0162 a0002c0001t0002g0163 a0002c0001t0002g0165 others(2): Show |
5 | HG02055.hp1 NA18967.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.698-460_698-459ins others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026065 | ||||||
| chr16:81026065 | A | ATGTG | 11 | a0001c0002t0001g0012 a0001c0002t0001g0028 a0001c0002t0001g0118 others(8): Show |
17 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.698-460_698-459ins others(4): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026065 | ||||||
| chr16:81026065 | A | ATGTGTGT others(1): Show |
8 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0090 others(5): Show |
10 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.698-460_698-459ins others(8): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026065 | ||||||
| chr16:81026065 | A | ATGTGTGT others(5): Show |
1 | a0002c0001t0008g0091 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.698-460_698-459ins others(12): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026065 | ||||||
| chr16:81026065 | A | G | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.698-461A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026065 | |||||||
| chr16:81026067 | A | ATG | 30 | a0001c0002t0004g0128 a0002c0001t0002g0003 a0002c0001t0002g0009 others(27): Show |
58 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.698-458_698-457ins others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026067 | ||||||
| chr16:81026067 | A | ATGTG | 73 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0021 others(70): Show |
158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.698-458_698-457ins others(4): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026067 | ||||||
| chr16:81026067 | A | ATGTGTG | 14 | a0001c0002t0001g0004 a0001c0002t0001g0041 a0001c0002t0001g0110 others(11): Show |
23 | HG00099.hp2 HG01106.hp2 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.698-458_698-457ins others(6): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026067 | ||||||
| chr16:81026067 | A | ATGTGTGT others(1): Show |
4 | a0001c0002t0001g0013 a0001c0002t0001g0106 a0001c0002t0001g0133 others(1): Show |
6 | NA18946.hp1 NA18961.hp2 NA18985.hp1 others(3): Show |
intron_variant | MODIFIER | c.698-458_698-457ins others(8): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026067 | ||||||
| chr16:81026067 | A | G | 27 | a0001c0002t0001g0012 a0001c0002t0001g0028 a0001c0002t0001g0118 others(24): Show |
35 | HG00741.hp2 HG01069.hp1 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.698-459A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026067 | |||||||
| chr16:81026069 | A | ATATG | 12 | a0002c0001t0006g0007 a0002c0001t0006g0045 a0002c0001t0006g0095 others(9): Show |
18 | HG00408.hp2 HG02074.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.698-456_698-455ins others(4): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026069 | ||||||
| chr16:81026069 | A | ATGTG | 3 | a0002c0001t0022g0043 a0002c0001t0039g0043 a0002c0001t0042g0157 |
3 | HG02717.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.698-439_698-436dup others(4): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026069 | ||||||
| chr16:81026069 | A | G | 154 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(151): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.698-457A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026069 | |||||||
| chr16:81026089 | G | GTGTGTGT others(31): Show |
1 | a0002c0001t0045g0173 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.698-436_698-435ins others(38): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026089 | ||||||
| chr16:81026089 | G | GTGTGTGT others(33): Show |
1 | a0002c0001t0044g0174 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.698-436_698-435ins others(40): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026089 | ||||||
| chr16:81026091 | A | G | 112 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(109): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.698-435A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026091 | |||||||
| chr16:81026099 | G | A | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.698-427G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026099 | |||||||
| chr16:81026105 | G | GTA | 6 | a0002c0001t0008g0031 a0002c0001t0008g0090 a0002c0001t0008g0091 others(3): Show |
7 | HG02523.hp2 NA18948.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.698-411_698-410dup others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026105 | ||||||
| chr16:81026115 | A | ATATGTAT others(9): Show |
1 | a0001c0002t0026g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.698-410_698-409ins others(16): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026115 | ||||||
| chr16:81026127 | G | GTGTGTAT others(5): Show |
10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.698-397_698-386dup others(12): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026127 | ||||||
| chr16:81026131 | G | A | 1 | a0001c0002t0026g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.698-395G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026131 | |||||||
| chr16:81026131 | G | GTATATAT others(7): Show |
3 | a0001c0002t0026g0176 a0001c0002t0056g0177 a0008c0012t0055g0178 |
3 | HG03130.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.698-386_698-385ins others(14): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026131 | ||||||
| chr16:81026139 | A | ATGTG | 2 | a0002c0001t0003g0018 a0002c0001t0003g0057 |
4 | NA18954.hp1 NA18962.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-386_698-385ins others(4): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026139 | ||||||
| chr16:81026141 | A | G | 205 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(202): Show |
378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.698-385A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026141 | |||||||
| chr16:81026143 | G | A | 2 | a0002c0001t0003g0018 a0002c0001t0003g0057 |
4 | NA18954.hp1 NA18962.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.698-383G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026143 | |||||||
| chr16:81026143 | G | GTA | 127 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(124): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.698-373_698-372dup others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026143 | ||||||
| chr16:81026145 | A | G | 6 | a0001c0002t0026g0175 a0001c0002t0026g0176 a0001c0002t0056g0177 others(3): Show |
6 | HG02559.hp1 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.698-381A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026145 | |||||||
| chr16:81026145 | ATATATAT others(5): Show |
A | 4 | a0002c0001t0006g0096 a0002c0001t0022g0043 a0002c0001t0039g0043 others(1): Show |
4 | HG02717.hp1 NA18960.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.698-355_698-344del others(12): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026145 | ||||||
| chr16:81026147 | A | T | 1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.698-379A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026147 | |||||||
| chr16:81026147 | ATATATAT others(3): Show |
A | 1 | a0001c0002t0001g0120 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.698-371_698-362del others(10): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026147 | ||||||
| chr16:81026153 | A | G | 2 | a0002c0001t0044g0174 a0002c0001t0045g0173 |
2 | HG01433.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.698-373A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026153 | |||||||
| chr16:81026179 | G | A | 1 | a0002c0001t0038g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.698-347G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026179 | |||||||
| chr16:81026185 | G | A | 1 | a0002c0001t0038g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.698-341G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026185 | |||||||
| chr16:81026193 | A | G | 1 | a0002c0001t0038g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.698-333A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026193 | |||||||
| chr16:81026211 | G | A | 1 | a0002c0001t0002g0162 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.698-315G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026211 | |||||||
| chr16:81026211 | G | GTA | 33 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(30): Show |
61 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(58): Show |
intron_variant | MODIFIER | c.698-304_698-303dup others(2): Show |
CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr16 | 81026211 | ||||||
| chr16:81026226 | C | T | 4 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(1): Show |
7 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.698-300C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026226 | |||||||
| chr16:81026246 | T | A | 1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.698-280T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026246 | |||||||
| chr16:81026293 | G | A | 1 | a0001c0002t0001g0105 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.698-233G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026293 | |||||||
| chr16:81026312 | A | G | 1 | a0002c0001t0043g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.698-214A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026312 | |||||||
| chr16:81026519 | C | T | 34 | a0002c0001t0002g0003 a0002c0001t0002g0009 a0002c0001t0002g0022 others(31): Show |
62 | HG00597.hp2 HG00673.hp2 HG01074.hp2 others(59): Show |
splice_region_variant&intron_variant | LOW | c.698-7C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 8/10 | chr16 | 81026519 | |||||||
| chr16:81026702 | T | A | 1 | a0002c0001t0003g0057 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.810+64T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81026702 | |||||||
| chr16:81026946 | T | A | 116 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(113): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.810+308T>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81026946 | |||||||
| chr16:81026957 | A | AT | 5 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(2): Show |
8 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.810+330dupT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr16 | 81026957 | ||||||
| chr16:81027047 | C | T | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.810+409C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027047 | |||||||
| chr16:81027156 | T | C | 101 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(98): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.810+518T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027156 | |||||||
| chr16:81027243 | C | T | 31 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(28): Show |
58 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.810+605C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027243 | |||||||
| chr16:81027349 | G | A | 1 | a0002c0001t0038g0153 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.810+711G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027349 | |||||||
| chr16:81027362 | G | C | 1 | a0001c0002t0001g0036 | 2 | HG00544.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.810+724G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027362 | |||||||
| chr16:81027440 | G | A | 4 | a0002c0001t0002g0058 a0002c0001t0003g0059 a0002c0001t0003g0124 others(1): Show |
4 | HG00408.hp1 NA18959.hp2 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.811-731G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027440 | |||||||
| chr16:81027497 | A | G | 1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.811-674A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027497 | |||||||
| chr16:81027498 | G | A | 1 | a0002c0001t0002g0145 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.811-673G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027498 | |||||||
| chr16:81027627 | T | C | 117 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(114): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.811-544T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027627 | |||||||
| chr16:81027632 | C | T | 101 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(98): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.811-539C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027632 | |||||||
| chr16:81027642 | A | G | 1 | a0001c0002t0001g0037 | 2 | HG00735.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.811-529A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027642 | |||||||
| chr16:81027669 | T | C | 11 | a0001c0002t0001g0120 a0002c0001t0008g0017 a0002c0001t0008g0031 others(8): Show |
13 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.811-502T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027669 | |||||||
| chr16:81027731 | G | A | 1 | a0001c0003t0025g0108 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.811-440G>A | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027731 | |||||||
| chr16:81027754 | G | C | 2 | a0001c0002t0026g0175 a0001c0002t0026g0176 |
2 | HG02559.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.811-417G>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027754 | |||||||
| chr16:81027951 | C | T | 1 | a0001c0002t0001g0088 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.811-220C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81027951 | |||||||
| chr16:81028013 | A | T | 10 | a0002c0001t0008g0017 a0002c0001t0008g0031 a0002c0001t0008g0050 others(7): Show |
12 | HG01109.hp1 HG02257.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.811-158A>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81028013 | |||||||
| chr16:81028130 | T | C | 1 | a0001c0010t0001g0104 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.811-41T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81028130 | |||||||
| chr16:81028136 | A | G | 1 | a0002c0001t0023g0051 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.811-35A>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 9/10 | chr16 | 81028136 | |||||||
| chr16:81028425 | G | T | 101 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(98): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.937+128G>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 10/10 | chr16 | 81028425 | |||||||
| chr16:81028503 | C | G | 5 | a0002c0001t0002g0023 a0002c0001t0009g0011 a0002c0001t0009g0023 others(2): Show |
8 | HG01884.hp1 HG02055.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.938-66C>G | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 10/10 | chr16 | 81028503 | |||||||
| chr16:81028546 | CT | C | 47 | a0002c0001t0002g0002 a0002c0001t0002g0020 a0002c0001t0002g0058 others(44): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.938-9delT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 81028546 | ||||||
| chr16:81028546 | CTT | C | 104 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(101): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.938-10_938-9delTT | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr16 | 81028546 | ||||||
| chr16:81028552 | T | C | 102 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(99): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.938-17T>C | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 10/10 | chr16 | 81028552 | |||||||
| chr16:81028566 | C | T | 116 | a0001c0002t0001g0001 a0001c0002t0001g0004 a0001c0002t0001g0006 others(113): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
splice_region_variant&intron_variant | LOW | c.938-3C>T | CENPN | ENSG00000166451.14 | transcript | ENST00000305850.10 | protein_coding | 10/10 | chr16 | 81028566 |