Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80152 |
| ensemblid | ENSG00000102901.13 |
| hgncid | 25787 |
| symbol | CENPT |
| name | centromere protein T |
| refseq_nuc | NM_025082.4 |
| refseq_prot | NP_079358.3 |
| ensembl_nuc | ENST00000562787.6 |
| ensembl_prot | ENSP00000457810.1 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 67828157 |
| end | 67847693 |
| strand | - |
| ver | v1.2 |
| region | chr16:67828157-67847693 |
| region5000 | chr16:67823157-67852693 |
| regionname0 | CENPT_chr16_67828157_67847693 |
| regionname5000 | CENPT_chr16_67823157_67852693 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 561 | 224 | 79 | 50 | 62 | 3 | 28 | 37 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0002 | 0/0 | 561 | 19 | 0 | 1 | 18 | 0 | 0 | 12 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0003 | 0/0 | 561 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0004 | 0/0 | 561 | 5 | 0 | 4 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0005 | 0/0 | 561 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0006 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0007 | 0/0 | 561 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0008 | 0/0 | 561 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0009 | 0/0 | 561 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0010 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| a0011 | 0/0 | 561 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | MADHN others(556): Show |
chr16 | 67823157 | 67852693 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1683 | 218 | 74 | 50 | 62 | 3 | 27 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0001c0005 | 0/0 | 1683 | 5 | 5 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0001c0010 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0002c0002 | 0/0 | 1683 | 19 | 0 | 1 | 18 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0003c0003 | 0/0 | 1683 | 9 | 9 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0004c0004 | 0/0 | 1683 | 5 | 0 | 4 | 0 | 1 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0005c0006 | 0/0 | 1683 | 3 | 0 | 0 | 3 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0006c0013 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0007c0011 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0008c0007 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0009c0009 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0010c0008 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 | ||
| a0011c0012 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | ATGGC others(1678): Show |
chr16 | 67823157 | 67852693 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2580 | 206 | 68 | 49 | 58 | 3 | 26 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0001t0003 | 0/0 | 2580 | 3 | 0 | 0 | 3 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0001t0004 | 0/0 | 2580 | 3 | 3 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0001t0005 | 0/0 | 2580 | 2 | 2 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0001t0006 | 0/0 | 2580 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0001t0008 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0001t0009 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0001t0010 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0005t0001 | 0/0 | 2580 | 5 | 5 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0001c0010t0001 | 0/0 | 2580 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0002c0002t0001 | 0/0 | 2580 | 19 | 0 | 1 | 18 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0003c0003t0001 | 0/0 | 2580 | 8 | 8 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0003c0003t0007 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0004c0004t0002 | 0/0 | 2580 | 5 | 0 | 4 | 0 | 1 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0005c0006t0001 | 0/0 | 2580 | 3 | 0 | 0 | 3 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0006c0013t0001 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0007c0011t0001 | 0/0 | 2580 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0008c0007t0001 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0009c0009t0001 | 0/0 | 2580 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0010c0008t0001 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| a0011c0012t0001 | 0/0 | 2580 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | AGATC others(2575): Show |
chr16 | 67823157 | 67852693 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 11 | 1 | 5 | 4 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0002 | 0/0 | 7 | 4 | 0 | 2 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0003 | 0/0 | 5 | 1 | 1 | 0 | 1 | 2 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0004 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0008 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0009 | 0/0 | 4 | 3 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0023 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0005g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0006g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0008g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0009g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0001t0010g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0005t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0001c0010t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0003c0003t0007g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0004c0004t0002g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0004c0004t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0004c0004t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0004c0004t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0005c0006t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0005c0006t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0005c0006t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0006c0013t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0007c0011t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0008c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0009c0009t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0010c0008t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| a0011c0012t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00544 | hp2 | a0006 | c0013 | t0001 | g0157 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0084 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00741 | hp1 | a0004 | c0004 | t0002 | g0039 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01070 | hp2 | a0004 | c0004 | t0002 | g0038 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01071 | hp1 | a0004 | c0004 | t0002 | g0016 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01099 | hp1 | a0007 | c0011 | t0001 | g0085 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01346 | hp2 | a0004 | c0004 | t0002 | g0040 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01361 | hp2 | a0001 | c0001 | t0009 | g0104 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0154 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01891 | hp1 | a0001 | c0005 | t0001 | g0066 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02129 | hp1 | a0001 | c0001 | t0010 | g0197 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | CDX | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0015 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02886 | hp1 | a0003 | c0003 | t0001 | g0151 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0068 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02897 | hp1 | a0001 | c0005 | t0001 | g0011 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02965 | hp2 | a0009 | c0009 | t0001 | g0071 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0035 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03209 | hp2 | a0001 | c0005 | t0001 | g0011 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0067 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03486 | hp1 | a0003 | c0003 | t0001 | g0036 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0153 | AFR | ESN | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0065 | AFR | GWD | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0054 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03669 | hp2 | a0001 | c0010 | t0001 | g0155 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0032 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18522 | hp1 | a0003 | c0003 | t0007 | g0069 | AFR | YRI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CHB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | CHB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18945 | hp1 | a0005 | c0006 | t0001 | g0115 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18961 | hp2 | a0005 | c0006 | t0001 | g0177 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18991 | hp2 | a0010 | c0008 | t0001 | g0122 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19005 | hp1 | a0011 | c0012 | t0001 | g0182 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | LWK | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19065 | hp1 | a0005 | c0006 | t0001 | g0161 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | YRI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20752 | hp1 | a0004 | c0004 | t0002 | g0016 | EUR | TSI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | TSI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02486 | hp1 | a0008 | c0007 | t0001 | g0041 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | MSL | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0015 | AFR | USA | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | USA | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | USA | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0023 | REF | REF | CENPT_chr16_67823157_67852693 | CENPT | chr16 | 67823157 | 67852693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67828517 | G | A | 1 | a0007 | 1 | HG01099.hp1 | missense_variant | MODERATE | c.1519C>T | p.Arg507Cys | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 15/16 | 2303/2580 | 1519/1686 | 507/561 | chr16 | 67828517 | |||
| chr16:67828803 | G | C | 1 | a0011 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.1321C>G | p.Pro441Ala | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 14/16 | 2105/2580 | 1321/1686 | 441/561 | chr16 | 67828803 | |||
| chr16:67829438 | G | A | 1 | a0009 | 1 | HG02965.hp2 | missense_variant | MODERATE | c.1265C>T | p.Ala422Val | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 13/16 | 2049/2580 | 1265/1686 | 422/561 | chr16 | 67829438 | |||
| chr16:67830492 | C | T | 1 | a0006 | 1 | HG00544.hp2 | missense_variant | MODERATE | c.760G>A | p.Val254Met | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 11/16 | 1544/2580 | 760/1686 | 254/561 | chr16 | 67830492 | |||
| chr16:67832034 | T | C | 2 | a0002 a0006 |
20 | HG00408.hp1 HG00544.hp2 HG00673.hp1 others(17): Show |
missense_variant | MODERATE | c.364A>G | p.Arg122Gly | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 7/16 | 1148/2580 | 364/1686 | 122/561 | chr16 | 67832034 | |||
| chr16:67832037 | A | C | 1 | a0005 | 3 | NA18945.hp1 NA18961.hp2 NA19065.hp1 |
missense_variant | MODERATE | c.361T>G | p.Ser121Ala | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 7/16 | 1145/2580 | 361/1686 | 121/561 | chr16 | 67832037 | |||
| chr16:67832054 | G | A | 1 | a0003 | 9 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
missense_variant | MODERATE | c.344C>T | p.Pro115Leu | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 7/16 | 1128/2580 | 344/1686 | 115/561 | chr16 | 67832054 | |||
| chr16:67832299 | G | C | 1 | a0010 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.218C>G | p.Ala73Gly | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 6/16 | 1002/2580 | 218/1686 | 73/561 | chr16 | 67832299 | |||
| chr16:67832300 | C | G | 1 | a0010 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.217G>C | p.Ala73Pro | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 6/16 | 1001/2580 | 217/1686 | 73/561 | chr16 | 67832300 | |||
| chr16:67833793 | C | T | 1 | a0008 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.67G>A | p.Ala23Thr | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/16 | 851/2580 | 67/1686 | 23/561 | chr16 | 67833793 | |||
| chr16:67833836 | G | T | 1 | a0004 | 5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
missense_variant | MODERATE | c.24C>A | p.Ser8Arg | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/16 | 808/2580 | 24/1686 | 8/561 | chr16 | 67833836 | |||
| chr16:67847403 | A | G | 1 | a0001 | 1 | HG04199.hp2 | splice_region_variant | LOW | c.-494T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/16 | chr16 | 67847403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67828339 | G | A | 1 | a0001c0010 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.1614C>T | p.His538His | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 16/16 | 2398/2580 | 1614/1686 | 538/561 | chr16 | 67828339 | |||
| chr16:67831596 | A | G | 2 | a0001c0005 a0009c0009 |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.540T>C | p.Ala180Ala | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 9/16 | 1324/2580 | 540/1686 | 180/561 | chr16 | 67831596 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67828195 | G | A | 1 | a0001c0001t0008 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 16/16 | 72 | chr16 | 67828195 | ||||||
| chr16:67828197 | G | A | 1 | a0001c0001t0005 | 2 | HG01884.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*70C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 16/16 | 70 | chr16 | 67828197 | ||||||
| chr16:67828234 | G | C | 1 | a0001c0001t0003 | 3 | NA18952.hp2 NA18966.hp2 NA18995.hp2 |
3_prime_UTR_variant | MODIFIER | c.*33C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 16/16 | 33 | chr16 | 67828234 | ||||||
| chr16:67833865 | C | A | 1 | a0001c0001t0004 | 3 | HG02572.hp1 HG02717.hp1 HG02976.hp2 |
5_prime_UTR_variant | MODIFIER | c.-6G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/16 | 6 | chr16 | 67833865 | ||||||
| chr16:67833995 | G | A | 1 | a0001c0001t0009 | 1 | HG01361.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-136C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/16 | chr16 | 67833995 | |||||||
| chr16:67835628 | C | T | 1 | a0003c0003t0007 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-461G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 2/16 | 1769 | chr16 | 67835628 | ||||||
| chr16:67835638 | G | A | 1 | a0004c0004t0002 | 5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-471C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 2/16 | 1779 | chr16 | 67835638 | ||||||
| chr16:67847527 | G | A | 1 | a0001c0001t0010 | 1 | HG02129.hp1 | 5_prime_UTR_variant | MODIFIER | c.-618C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/16 | 13668 | chr16 | 67847527 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:67828893 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1281-50A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 13/15 | chr16 | 67828893 | |||||||
| chr16:67829072 | C | A | 1 | a0001c0001t0001g0047 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1281-229G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 13/15 | chr16 | 67829072 | |||||||
| chr16:67829083 | T | C | 1 | a0001c0001t0001g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1281-240A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 13/15 | chr16 | 67829083 | |||||||
| chr16:67829161 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG03041.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1280+262C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 13/15 | chr16 | 67829161 | |||||||
| chr16:67829400 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1280+23C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 13/15 | chr16 | 67829400 | |||||||
| chr16:67829548 | T | C | 123 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(120): Show |
157 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.1187-32A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 12/15 | chr16 | 67829548 | |||||||
| chr16:67829618 | C | G | 1 | a0008c0007t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1187-102G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 12/15 | chr16 | 67829618 | |||||||
| chr16:67830217 | C | T | 3 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0189 |
3 | HG01884.hp2 HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.863-129G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 11/15 | chr16 | 67830217 | |||||||
| chr16:67830266 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.862+124T>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 11/15 | chr16 | 67830266 | |||||||
| chr16:67830558 | G | A | 1 | a0010c0008t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.704-10C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67830558 | |||||||
| chr16:67830559 | A | G | 1 | a0010c0008t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.704-11T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67830559 | |||||||
| chr16:67830614 | G | C | 1 | a0010c0008t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.704-66C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67830614 | |||||||
| chr16:67830615 | C | G | 1 | a0010c0008t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.704-67G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67830615 | |||||||
| chr16:67830686 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
20 | HG01109.hp1 HG01884.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.704-138C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67830686 | |||||||
| chr16:67830703 | A | G | 1 | a0008c0007t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.704-155T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67830703 | |||||||
| chr16:67831162 | G | C | 1 | a0008c0007t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.703+54C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67831162 | |||||||
| chr16:67831170 | G | A | 15 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0152 others(12): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.703+46C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 10/15 | chr16 | 67831170 | |||||||
| chr16:67831384 | A | C | 14 | a0001c0001t0001g0072 a0001c0001t0001g0152 a0003c0003t0001g0015 others(11): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.561-26T>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 9/15 | chr16 | 67831384 | |||||||
| chr16:67831413 | C | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0189 |
3 | HG01884.hp2 HG02257.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.561-55G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 9/15 | chr16 | 67831413 | |||||||
| chr16:67831457 | G | A | 1 | a0010c0008t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.561-99C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 9/15 | chr16 | 67831457 | |||||||
| chr16:67831458 | A | G | 1 | a0010c0008t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.561-100T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 9/15 | chr16 | 67831458 | |||||||
| chr16:67831625 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.524-13C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 8/15 | chr16 | 67831625 | |||||||
| chr16:67831951 | C | A | 1 | a0010c0008t0001g0122 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.386+61G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 7/15 | chr16 | 67831951 | |||||||
| chr16:67831965 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0173 |
2 | HG02683.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.386+47C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 7/15 | chr16 | 67831965 | |||||||
| chr16:67831993 | G | A | 2 | a0001c0005t0001g0011 a0001c0005t0001g0066 |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.386+19C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 7/15 | chr16 | 67831993 | |||||||
| chr16:67832320 | C | T | 2 | a0001c0001t0005g0153 a0001c0001t0005g0154 |
2 | HG01884.hp1 HG03516.hp2 |
splice_region_variant&intron_variant | LOW | c.202-5G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 5/15 | chr16 | 67832320 | |||||||
| chr16:67832554 | A | T | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02622.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.111-9T>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832554 | |||||||
| chr16:67832571 | G | A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG03041.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.111-26C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832571 | |||||||
| chr16:67832596 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.111-51C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832596 | |||||||
| chr16:67832685 | C | T | 3 | a0001c0005t0001g0011 a0001c0005t0001g0065 a0001c0005t0001g0066 |
5 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.111-140G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832685 | |||||||
| chr16:67832754 | G | A | 1 | a0003c0003t0001g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.111-209C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832754 | |||||||
| chr16:67832778 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.111-233C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832778 | |||||||
| chr16:67832880 | C | T | 45 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(42): Show |
53 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.111-335G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832880 | |||||||
| chr16:67832927 | A | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
18 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.111-382T>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67832927 | |||||||
| chr16:67833192 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.110+558A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833192 | |||||||
| chr16:67833203 | C | A | 1 | a0008c0007t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.110+547G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833203 | |||||||
| chr16:67833216 | C | T | 4 | a0001c0005t0001g0011 a0001c0005t0001g0065 a0001c0005t0001g0066 others(1): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.110+534G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833216 | |||||||
| chr16:67833231 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.110+519G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833231 | |||||||
| chr16:67833364 | T | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0194 |
3 | HG02622.hp2 HG02723.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.110+386A>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833364 | |||||||
| chr16:67833397 | T | G | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.110+353A>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833397 | |||||||
| chr16:67833413 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.110+337A>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833413 | |||||||
| chr16:67833701 | T | A | 1 | a0002c0002t0001g0106 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.110+49A>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833701 | |||||||
| chr16:67833734 | G | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
18 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.110+16C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 4/15 | chr16 | 67833734 | |||||||
| chr16:67834104 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | splice_region_variant&intron_variant | LOW | c.-241-4A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834104 | |||||||
| chr16:67834249 | C | G | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-241-149G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834249 | |||||||
| chr16:67834378 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-241-278G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834378 | |||||||
| chr16:67834453 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-241-353G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834453 | |||||||
| chr16:67834491 | C | T | 4 | a0004c0004t0002g0016 a0004c0004t0002g0038 a0004c0004t0002g0039 others(1): Show |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-241-391G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834491 | |||||||
| chr16:67834510 | T | G | 1 | a0001c0001t0001g0105 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-241-410A>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834510 | |||||||
| chr16:67834767 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-242+405T>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834767 | |||||||
| chr16:67834850 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-242+322C>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834850 | |||||||
| chr16:67834851 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-242+321A>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 3/15 | chr16 | 67834851 | |||||||
| chr16:67835350 | T | C | 8 | a0003c0003t0001g0015 a0003c0003t0001g0035 a0003c0003t0001g0036 others(5): Show |
9 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-370-50A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 2/15 | chr16 | 67835350 | |||||||
| chr16:67835527 | G | C | 8 | a0002c0002t0001g0005 a0002c0002t0001g0007 a0002c0002t0001g0027 others(5): Show |
17 | HG00408.hp1 HG01943.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.-371+11C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 2/15 | chr16 | 67835527 | |||||||
| chr16:67835718 | T | C | 10 | a0001c0001t0001g0072 a0001c0001t0001g0152 a0003c0003t0001g0015 others(7): Show |
11 | HG01433.hp1 HG02622.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.-491-60A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67835718 | |||||||
| chr16:67835737 | A | G | 1 | a0005c0006t0001g0115 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-491-79T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67835737 | |||||||
| chr16:67835817 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-491-159T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67835817 | |||||||
| chr16:67835851 | T | G | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-491-193A>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67835851 | |||||||
| chr16:67836279 | C | A | 1 | a0001c0001t0001g0060 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-491-621G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836279 | |||||||
| chr16:67836376 | A | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0164 |
2 | HG01081.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-491-718T>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836376 | |||||||
| chr16:67836415 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-491-757T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836415 | |||||||
| chr16:67836439 | C | CT | 7 | a0001c0001t0001g0024 a0001c0001t0001g0086 a0001c0001t0001g0099 others(4): Show |
8 | HG00544.hp1 HG00544.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.-491-782dupA | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836439 | |||||||
| chr16:67836439 | CT | C | 33 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(30): Show |
45 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(42): Show |
intron_variant | MODIFIER | c.-491-782delA | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836439 | |||||||
| chr16:67836491 | T | G | 1 | a0003c0003t0001g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-491-833A>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836491 | |||||||
| chr16:67836514 | G | GCAACCTC others(3): Show |
1 | a0001c0001t0001g0082 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-491-866_-491-857d others(12): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836514 | |||||||
| chr16:67836623 | T | C | 1 | a0001c0001t0001g0189 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-491-965A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836623 | |||||||
| chr16:67836673 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0101 |
2 | HG01496.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.-491-1015G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836673 | |||||||
| chr16:67836731 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0136 |
2 | NA18962.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.-491-1073C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836731 | |||||||
| chr16:67836800 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-491-1142G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836800 | |||||||
| chr16:67836899 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0093 a0001c0001t0001g0120 others(2): Show |
6 | HG01346.hp1 HG01943.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-491-1241C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836899 | |||||||
| chr16:67836903 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0156 |
2 | NA20752.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-491-1245C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836903 | |||||||
| chr16:67836942 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-491-1284G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67836942 | |||||||
| chr16:67837134 | T | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
18 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-491-1476A>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67837134 | |||||||
| chr16:67837154 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0001g0189 others(1): Show |
4 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-491-1496C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67837154 | |||||||
| chr16:67837203 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-491-1545G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67837203 | |||||||
| chr16:67837598 | C | T | 45 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(42): Show |
53 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.-491-1940G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67837598 | |||||||
| chr16:67838035 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0152 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-491-2377A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838035 | |||||||
| chr16:67838327 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-491-2669G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838327 | |||||||
| chr16:67838348 | A | C | 14 | a0001c0001t0001g0072 a0001c0001t0001g0152 a0003c0003t0001g0015 others(11): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-491-2690T>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838348 | |||||||
| chr16:67838437 | C | T | 4 | a0004c0004t0002g0016 a0004c0004t0002g0038 a0004c0004t0002g0039 others(1): Show |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-491-2779G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838437 | |||||||
| chr16:67838474 | T | C | 2 | a0001c0001t0001g0091 a0001c0001t0001g0109 |
2 | HG02071.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.-491-2816A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838474 | |||||||
| chr16:67838591 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-491-2933G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838591 | |||||||
| chr16:67838677 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-491-3019G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838677 | |||||||
| chr16:67838693 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.-491-3035A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838693 | |||||||
| chr16:67838885 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-491-3227G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838885 | |||||||
| chr16:67838910 | GTGTGAGT others(9): Show |
G | 1 | a0001c0001t0001g0098 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-491-3268_-491-325 others(20): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838910 | |||||||
| chr16:67838932 | C | CA | 10 | a0001c0001t0001g0033 a0001c0001t0001g0042 a0001c0001t0001g0053 others(7): Show |
10 | HG01070.hp1 HG01192.hp2 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.-491-3275dupT | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838932 | |||||||
| chr16:67838932 | CA | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0062 a0001c0001t0001g0082 others(5): Show |
9 | HG01099.hp1 HG01099.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.-491-3275delT | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838932 | |||||||
| chr16:67838957 | G | T | 1 | a0008c0007t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-491-3299C>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67838957 | |||||||
| chr16:67839338 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-491-3680G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67839338 | |||||||
| chr16:67839381 | C | CA | 36 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0029 others(33): Show |
40 | HG00673.hp1 HG00673.hp2 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.-491-3724dupT | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67839381 | |||||||
| chr16:67839381 | CA | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0062 others(7): Show |
17 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-491-3724delT | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67839381 | |||||||
| chr16:67839448 | T | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG02056.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-491-3790A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67839448 | |||||||
| chr16:67839733 | T | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
20 | HG01109.hp1 HG01884.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-491-4075A>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67839733 | |||||||
| chr16:67839889 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-491-4231T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67839889 | |||||||
| chr16:67840096 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0152 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-491-4438G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840096 | |||||||
| chr16:67840175 | G | A | 14 | a0001c0001t0001g0072 a0001c0001t0001g0152 a0003c0003t0001g0015 others(11): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-491-4517C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840175 | |||||||
| chr16:67840236 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-491-4578A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840236 | |||||||
| chr16:67840242 | C | T | 2 | a0001c0005t0001g0011 a0001c0005t0001g0066 |
4 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-491-4584G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840242 | |||||||
| chr16:67840302 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-491-4644T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840302 | |||||||
| chr16:67840361 | T | C | 80 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(77): Show |
100 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(97): Show |
intron_variant | MODIFIER | c.-491-4703A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840361 | |||||||
| chr16:67840425 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-491-4767G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840425 | |||||||
| chr16:67840571 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-491-4913C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840571 | |||||||
| chr16:67840739 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-491-5081T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840739 | |||||||
| chr16:67840798 | A | G | 1 | a0001c0001t0001g0018 | 2 | HG00639.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.-491-5140T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840798 | |||||||
| chr16:67840920 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-491-5262C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840920 | |||||||
| chr16:67840977 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-491-5319A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67840977 | |||||||
| chr16:67841010 | C | CATACATA others(7): Show |
1 | a0003c0003t0001g0067 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-491-5353_-491-535 others(18): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | C | CATACATA others(15): Show |
2 | a0001c0005t0001g0065 a0009c0009t0001g0071 |
2 | HG02965.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-491-5353_-491-535 others(26): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | C | CATATATA others(3): Show |
2 | a0001c0001t0001g0128 a0003c0003t0007g0069 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-491-5362_-491-535 others(14): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | C | CATATATA others(5): Show |
2 | a0003c0003t0001g0035 a0003c0003t0001g0037 |
2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-491-5364_-491-535 others(16): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | C | CATATATA others(7): Show |
1 | a0003c0003t0001g0015 | 2 | HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-491-5366_-491-535 others(18): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | C | CATATATA others(9): Show |
2 | a0003c0003t0001g0151 a0004c0004t0002g0039 |
2 | HG00741.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-491-5368_-491-535 others(20): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | C | CATATATA others(13): Show |
2 | a0004c0004t0002g0016 a0004c0004t0002g0038 |
3 | HG01070.hp2 HG01071.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-491-5372_-491-535 others(24): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | C | CATATATA others(19): Show |
1 | a0001c0001t0001g0126 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-491-5378_-491-535 others(30): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | CAT | C | 6 | a0001c0001t0001g0072 a0001c0001t0001g0095 a0001c0001t0001g0152 others(3): Show |
6 | HG01433.hp1 HG01884.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.-491-5354_-491-535 others(6): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | CATAT | C | 15 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0076 others(12): Show |
20 | HG01081.hp1 HG01081.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.-491-5356_-491-535 others(8): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | CATATAT | C | 33 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(30): Show |
44 | HG00609.hp1 HG00609.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.-491-5358_-491-535 others(10): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | CATATATA others(1): Show |
C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(100): Show |
142 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.-491-5360_-491-535 others(12): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | CATATATA others(3): Show |
C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(10): Show |
23 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.-491-5362_-491-535 others(14): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | CATATATA others(5): Show |
C | 1 | a0008c0007t0001g0041 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-491-5364_-491-535 others(16): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841010 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0114 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-491-5376_-491-535 others(28): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841010 | |||||||
| chr16:67841016 | T | C | 4 | a0001c0001t0001g0072 a0001c0001t0001g0152 a0001c0001t0005g0153 others(1): Show |
4 | HG01433.hp1 HG01884.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-491-5358A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841016 | |||||||
| chr16:67841024 | T | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(7): Show |
18 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-491-5366A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841024 | |||||||
| chr16:67841048 | A | T | 1 | a0009c0009t0001g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-491-5390T>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841048 | |||||||
| chr16:67841123 | A | T | 14 | a0001c0001t0001g0072 a0001c0001t0001g0152 a0003c0003t0001g0015 others(11): Show |
16 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-491-5465T>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841123 | |||||||
| chr16:67841193 | C | CA | 38 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(35): Show |
50 | HG00673.hp2 HG00738.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.-491-5536dupT | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841193 | |||||||
| chr16:67841193 | C | CAA | 36 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(33): Show |
43 | HG00639.hp1 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.-491-5537_-491-553 others(6): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841193 | |||||||
| chr16:67841193 | C | CAAA | 16 | a0001c0001t0001g0021 a0001c0001t0001g0043 a0001c0001t0001g0052 others(13): Show |
17 | HG00438.hp1 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-491-5538_-491-553 others(7): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841193 | |||||||
| chr16:67841193 | CA | C | 9 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
9 | HG01070.hp2 HG01496.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.-491-5536delT | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841193 | |||||||
| chr16:67841193 | CAA | C | 9 | a0001c0005t0001g0011 a0001c0005t0001g0065 a0001c0005t0001g0066 others(6): Show |
12 | HG01891.hp1 HG02622.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-491-5537_-491-553 others(6): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841193 | |||||||
| chr16:67841253 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-491-5595C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841253 | |||||||
| chr16:67841362 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-491-5704G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841362 | |||||||
| chr16:67841608 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-492+5793A>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841608 | |||||||
| chr16:67841779 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-492+5622C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841779 | |||||||
| chr16:67841786 | A | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
4 | HG02132.hp2 NA18973.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-492+5615T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841786 | |||||||
| chr16:67841858 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-492+5543A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67841858 | |||||||
| chr16:67842066 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-492+5335G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842066 | |||||||
| chr16:67842118 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0080 a0001c0001t0001g0143 others(10): Show |
15 | HG01891.hp2 HG02109.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-492+5283C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842118 | |||||||
| chr16:67842406 | G | GGCGGGCC others(11): Show |
1 | a0001c0001t0001g0194 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-492+4977_-492+499 others(22): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842406 | |||||||
| chr16:67842450 | G | A | 8 | a0003c0003t0001g0015 a0003c0003t0001g0035 a0003c0003t0001g0036 others(5): Show |
9 | HG02622.hp1 HG02886.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-492+4951C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842450 | |||||||
| chr16:67842459 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-492+4942G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842459 | |||||||
| chr16:67842563 | C | G | 4 | a0001c0005t0001g0011 a0001c0005t0001g0065 a0001c0005t0001g0066 others(1): Show |
6 | HG01891.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-492+4838G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842563 | |||||||
| chr16:67842572 | C | T | 1 | a0007c0011t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-492+4829G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842572 | |||||||
| chr16:67842794 | C | T | 3 | a0002c0002t0001g0083 a0002c0002t0001g0084 a0006c0013t0001g0157 |
3 | HG00544.hp2 HG00673.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-492+4607G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842794 | |||||||
| chr16:67842862 | G | GGCAGCAG others(20): Show |
1 | a0001c0001t0003g0190 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-492+4512_-492+453 others(31): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842862 | |||||||
| chr16:67842875 | A | ACAGCAGC others(20): Show |
1 | a0001c0001t0001g0030 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-492+4525_-492+452 others(31): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842875 | |||||||
| chr16:67842875 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-492+4526T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842875 | |||||||
| chr16:67842881 | GCAGCAGC others(14): Show |
G | 1 | a0002c0002t0001g0083 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-492+4499_-492+451 others(25): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842881 | |||||||
| chr16:67842893 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-492+4508T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842893 | |||||||
| chr16:67842893 | ACAGCAGC others(11): Show |
A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0133 a0002c0002t0001g0007 |
3 | HG01071.hp2 NA18983.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-492+4490_-492+450 others(22): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842893 | |||||||
| chr16:67842893 | ACAGCAGC others(23): Show |
A | 1 | a0001c0001t0001g0020 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-492+4478_-492+450 others(34): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842893 | |||||||
| chr16:67842902 | A | ACAGCAGC others(20): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0173 a0002c0002t0001g0005 |
3 | HG04199.hp1 NA19085.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-492+4472_-492+449 others(31): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842902 | |||||||
| chr16:67842902 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0003g0190 |
2 | HG02486.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-492+4499T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842902 | |||||||
| chr16:67842902 | ACAGCAGC others(14): Show |
A | 3 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | HG03041.hp1 HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-492+4478_-492+449 others(25): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842902 | |||||||
| chr16:67842908 | GCAGCAGC others(5): Show |
G | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-492+4481_-492+449 others(16): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842908 | |||||||
| chr16:67842914 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-492+4487C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842914 | |||||||
| chr16:67842920 | A | ACAG | 3 | a0001c0001t0001g0004 a0001c0001t0001g0178 a0001c0001t0001g0189 |
3 | HG01993.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-492+4478_-492+448 others(7): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842920 | |||||||
| chr16:67842920 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0080 |
2 | HG03209.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-492+4481T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842920 | |||||||
| chr16:67842920 | ACAG | A | 58 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
75 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.-492+4478_-492+448 others(7): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842920 | |||||||
| chr16:67842923 | G | GCAGCAGC others(8): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02027.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-492+4477_-492+447 others(19): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842923 | |||||||
| chr16:67842951 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-492+4450A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67842951 | |||||||
| chr16:67843592 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-492+3809C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67843592 | |||||||
| chr16:67843621 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-492+3780C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67843621 | |||||||
| chr16:67843641 | G | C | 1 | a0001c0001t0001g0070 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-492+3760C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67843641 | |||||||
| chr16:67843647 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-492+3754G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67843647 | |||||||
| chr16:67843817 | A | T | 1 | a0001c0001t0001g0082 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-492+3584T>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67843817 | |||||||
| chr16:67844083 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-492+3318T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844083 | |||||||
| chr16:67844209 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-492+3192T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844209 | |||||||
| chr16:67844420 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-492+2981T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844420 | |||||||
| chr16:67844523 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-492+2878T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844523 | |||||||
| chr16:67844666 | T | C | 1 | a0009c0009t0001g0071 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-492+2735A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844666 | |||||||
| chr16:67844782 | AT | A | 6 | a0001c0001t0001g0022 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
7 | HG00438.hp1 HG01167.hp1 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.-492+2618delA | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844782 | |||||||
| chr16:67844782 | ATT | A | 32 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(29): Show |
44 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.-492+2617_-492+261 others(6): Show |
CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844782 | |||||||
| chr16:67844789 | T | A | 1 | a0001c0001t0001g0136 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-492+2612A>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844789 | |||||||
| chr16:67844830 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0152 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-492+2571G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844830 | |||||||
| chr16:67844888 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-492+2513T>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67844888 | |||||||
| chr16:67845009 | G | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0152 |
2 | HG01433.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-492+2392C>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845009 | |||||||
| chr16:67845031 | C | T | 1 | a0001c0010t0001g0155 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-492+2370G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845031 | |||||||
| chr16:67845032 | G | A | 12 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(9): Show |
20 | HG01109.hp1 HG01884.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.-492+2369C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845032 | |||||||
| chr16:67845382 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0137 a0001c0001t0001g0191 |
4 | HG02451.hp1 HG02486.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-492+2019C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845382 | |||||||
| chr16:67845408 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-492+1993A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845408 | |||||||
| chr16:67845497 | G | A | 44 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0018 others(41): Show |
52 | HG00438.hp1 HG00639.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.-492+1904C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845497 | |||||||
| chr16:67845572 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-492+1829G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845572 | |||||||
| chr16:67845633 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-492+1768A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845633 | |||||||
| chr16:67845670 | C | G | 1 | a0001c0001t0001g0079 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-492+1731G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845670 | |||||||
| chr16:67845924 | C | A | 4 | a0004c0004t0002g0016 a0004c0004t0002g0038 a0004c0004t0002g0039 others(1): Show |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-492+1477G>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67845924 | |||||||
| chr16:67846438 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-492+963G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67846438 | |||||||
| chr16:67846509 | G | A | 4 | a0004c0004t0002g0016 a0004c0004t0002g0038 a0004c0004t0002g0039 others(1): Show |
5 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.-492+892C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67846509 | |||||||
| chr16:67846554 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-492+847C>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67846554 | |||||||
| chr16:67846607 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(4): Show |
15 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.-492+794G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67846607 | |||||||
| chr16:67846713 | G | T | 1 | a0001c0001t0006g0032 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-492+688C>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67846713 | |||||||
| chr16:67846887 | G | T | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-492+514C>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67846887 | |||||||
| chr16:67846931 | C | T | 31 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(28): Show |
43 | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.-492+470G>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67846931 | |||||||
| chr16:67847088 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-492+313A>G | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67847088 | |||||||
| chr16:67847088 | T | TC | 50 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0031 others(47): Show |
62 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-492+312dupG | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67847088 | |||||||
| chr16:67847088 | TC | T | 34 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(31): Show |
42 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.-492+312delG | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67847088 | |||||||
| chr16:67847143 | G | T | 1 | a0001c0001t0001g0034 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-492+258C>A | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67847143 | |||||||
| chr16:67847176 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-492+225C>T | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67847176 | |||||||
| chr16:67847178 | C | G | 1 | a0001c0001t0001g0033 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-492+223G>C | CENPT | ENSG00000102901.13 | transcript | ENST00000562787.6 | protein_coding | 1/15 | chr16 | 67847178 |