Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55166 |
| ensemblid | ENSG00000031691.7 |
| hgncid | 21347 |
| symbol | CENPQ |
| name | centromere protein Q |
| refseq_nuc | NM_018132.4 |
| refseq_prot | NP_060602.2 |
| ensembl_nuc | ENST00000335783.4 |
| ensembl_prot | ENSP00000337289.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 49463370 |
| end | 49493107 |
| strand | + |
| ver | v1.2 |
| region | chr6:49463370-49493107 |
| region5000 | chr6:49458370-49498107 |
| regionname0 | CENPQ_chr6_49463370_49493107 |
| regionname5000 | CENPQ_chr6_49458370_49498107 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 268 | 138 | 26 | 30 | 63 | 7 | 11 | 46 | CENPQ_chr6_49458370_49498107 | CENPQ | MSGKA others(263): Show |
chr6 | 49458370 | 49498107 |
| a0002 | 0/0 | 268 | 100 | 38 | 10 | 36 | 6 | 10 | 26 | CENPQ_chr6_49458370_49498107 | CENPQ | MSGKA others(263): Show |
chr6 | 49458370 | 49498107 |
| a0003 | 1/0 | 268 | 97 | 18 | 14 | 49 | 1 | 14 | 38 | CENPQ_chr6_49458370_49498107 | CENPQ | MSGKA others(263): Show |
chr6 | 49458370 | 49498107 |
| a0004 | 0/0 | 268 | 18 | 2 | 1 | 12 | 0 | 3 | 10 | CENPQ_chr6_49458370_49498107 | CENPQ | MSGKA others(263): Show |
chr6 | 49458370 | 49498107 |
| a0005 | 0/0 | 268 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | MSGKA others(263): Show |
chr6 | 49458370 | 49498107 |
| a0006 | 0/0 | 268 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | MSGKA others(263): Show |
chr6 | 49458370 | 49498107 |
| a0007 | 0/0 | 268 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | MSGKA others(263): Show |
chr6 | 49458370 | 49498107 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 804 | 138 | 26 | 30 | 63 | 7 | 11 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 | ||
| a0002c0002 | 0/0 | 804 | 100 | 38 | 10 | 36 | 6 | 10 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 | ||
| a0003c0003 | 1/0 | 804 | 96 | 18 | 14 | 49 | 1 | 13 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 | ||
| a0003c0008 | 0/0 | 804 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 | ||
| a0004c0004 | 0/0 | 804 | 18 | 2 | 1 | 12 | 0 | 3 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 | ||
| a0005c0005 | 0/0 | 804 | 5 | 3 | 2 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 | ||
| a0006c0006 | 0/0 | 804 | 3 | 0 | 3 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 | ||
| a0007c0007 | 0/0 | 804 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ATGTC others(799): Show |
chr6 | 49458370 | 49498107 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1740 | 105 | 0 | 26 | 63 | 7 | 8 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0001c0001t0004 | 0/0 | 1740 | 31 | 25 | 4 | 0 | 0 | 2 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0001c0001t0010 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0001c0001t0011 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0002c0002t0002 | 0/0 | 1741 | 90 | 29 | 10 | 36 | 5 | 10 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0002c0002t0003 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0002c0002t0005 | 0/0 | 1741 | 7 | 7 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0002c0002t0007 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0002c0002t0008 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0003c0003t0002 | 0/0 | 1741 | 8 | 5 | 1 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0003c0003t0003 | 0/0 | 1740 | 84 | 11 | 12 | 47 | 1 | 13 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0003c0003t0005 | 1/0 | 1741 | 1 | 0 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0003c0003t0006 | 0/0 | 1740 | 2 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0003c0003t0009 | 0/0 | 1741 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| a0003c0008t0003 | 0/0 | 1740 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0004c0004t0004 | 0/0 | 1740 | 18 | 2 | 1 | 12 | 0 | 3 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0005c0005t0004 | 0/0 | 1740 | 5 | 3 | 2 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0006c0006t0004 | 0/0 | 1740 | 3 | 0 | 3 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1735): Show |
chr6 | 49458370 | 49498107 |
| a0007c0007t0007 | 0/0 | 1741 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | ACTTC others(1736): Show |
chr6 | 49458370 | 49498107 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 5 | 7 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0006 | 0/0 | 8 | 0 | 3 | 4 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0024 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0010g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0001c0001t0011g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0002 | 0/0 | 20 | 3 | 2 | 12 | 1 | 2 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0004 | 0/0 | 10 | 3 | 1 | 4 | 0 | 2 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0012 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0015 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0005g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0002c0002t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0001 | 0/0 | 21 | 0 | 1 | 15 | 0 | 5 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0007 | 0/0 | 6 | 0 | 3 | 0 | 0 | 3 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0008 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0005g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0003t0009g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0003c0008t0003g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0005 | 0/0 | 9 | 0 | 0 | 8 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0004c0004t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0005c0005t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0005c0005t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0005c0005t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0005c0005t0004g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0005c0005t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0006c0006t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0006c0006t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0006c0006t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| a0007c0007t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0194 | EUR | GBR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00323 | hp2 | a0003 | c0003 | t0003 | g0055 | EUR | FIN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00408 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00423 | hp1 | a0003 | c0003 | t0003 | g0057 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00438 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00558 | hp1 | a0003 | c0003 | t0003 | g0079 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0211 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00621 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00642 | hp1 | a0003 | c0003 | t0003 | g0007 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00642 | hp2 | a0001 | c0001 | t0004 | g0024 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0176 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01081 | hp2 | a0003 | c0003 | t0003 | g0066 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0197 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0205 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01109 | hp1 | a0003 | c0003 | t0003 | g0075 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01168 | hp2 | a0003 | c0003 | t0003 | g0077 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01192 | hp1 | a0002 | c0002 | t0002 | g0204 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01243 | hp1 | a0003 | c0003 | t0003 | g0173 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01255 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01256 | hp1 | a0003 | c0003 | t0003 | g0022 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01256 | hp2 | a0005 | c0005 | t0004 | g0161 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01257 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01258 | hp1 | a0005 | c0005 | t0004 | g0155 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0034 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01346 | hp2 | a0003 | c0003 | t0003 | g0170 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01361 | hp1 | a0003 | c0003 | t0002 | g0226 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01361 | hp2 | a0003 | c0003 | t0003 | g0001 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01433 | hp2 | a0003 | c0003 | t0003 | g0007 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0229 | EUR | IBS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0195 | EUR | IBS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01517 | hp1 | a0002 | c0002 | t0002 | g0215 | EUR | IBS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0133 | EUR | IBS | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01884 | hp1 | a0003 | c0003 | t0002 | g0227 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01884 | hp2 | a0003 | c0003 | t0003 | g0082 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01891 | hp1 | a0003 | c0003 | t0003 | g0085 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0187 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01928 | hp1 | a0003 | c0003 | t0003 | g0008 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01934 | hp1 | a0003 | c0003 | t0003 | g0007 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01934 | hp2 | a0004 | c0004 | t0004 | g0185 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01952 | hp2 | a0006 | c0006 | t0004 | g0207 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01978 | hp1 | a0006 | c0006 | t0004 | g0039 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01993 | hp1 | a0006 | c0006 | t0004 | g0210 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02040 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02056 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02071 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02071 | hp2 | a0003 | c0003 | t0003 | g0047 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0188 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02080 | hp2 | a0003 | c0003 | t0003 | g0064 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02083 | hp2 | a0003 | c0003 | t0003 | g0063 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02132 | hp2 | a0002 | c0002 | t0002 | g0203 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02135 | hp1 | a0003 | c0003 | t0003 | g0065 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0169 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02145 | hp2 | a0002 | c0002 | t0002 | g0224 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CDX | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | CDX | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CDX | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CDX | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02257 | hp1 | a0002 | c0002 | t0005 | g0183 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02257 | hp2 | a0001 | c0001 | t0011 | g0111 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02258 | hp1 | a0003 | c0003 | t0002 | g0041 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0004 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02280 | hp1 | a0005 | c0005 | t0004 | g0158 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02300 | hp2 | a0003 | c0003 | t0003 | g0068 | AMR | PEL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02451 | hp1 | a0005 | c0005 | t0004 | g0157 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02451 | hp2 | a0003 | c0003 | t0006 | g0172 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02523 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | KHV | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02572 | hp1 | a0005 | c0005 | t0004 | g0156 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02572 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02602 | hp2 | a0002 | c0002 | t0002 | g0222 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0083 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02622 | hp1 | a0003 | c0003 | t0003 | g0081 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02630 | hp1 | a0002 | c0002 | t0005 | g0009 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0015 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0220 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0167 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02717 | hp2 | a0002 | c0002 | t0007 | g0178 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02723 | hp1 | a0002 | c0002 | t0005 | g0009 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0181 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02886 | hp1 | a0002 | c0002 | t0005 | g0009 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02886 | hp2 | a0002 | c0002 | t0008 | g0199 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0218 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02896 | hp1 | a0002 | c0002 | t0002 | g0219 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0033 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02922 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0033 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0089 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0225 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03017 | hp1 | a0004 | c0004 | t0004 | g0209 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03017 | hp2 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0084 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0200 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03130 | hp2 | a0003 | c0003 | t0006 | g0171 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03139 | hp2 | a0003 | c0003 | t0003 | g0044 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0018 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0002 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03209 | hp2 | a0002 | c0002 | t0005 | g0009 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03225 | hp1 | a0002 | c0002 | t0005 | g0009 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03239 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03453 | hp2 | a0003 | c0003 | t0002 | g0228 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03486 | hp1 | a0003 | c0003 | t0003 | g0049 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | MSL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03491 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03491 | hp2 | a0001 | c0001 | t0010 | g0014 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03492 | hp1 | a0003 | c0003 | t0003 | g0007 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03492 | hp2 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03516 | hp2 | a0003 | c0003 | t0003 | g0018 | AFR | ESN | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0012 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03540 | hp2 | a0002 | c0002 | t0005 | g0182 | AFR | GWD | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03669 | hp1 | a0003 | c0003 | t0003 | g0050 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03669 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0198 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03710 | hp1 | a0003 | c0003 | t0003 | g0001 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03834 | hp1 | a0003 | c0003 | t0003 | g0073 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03834 | hp2 | a0003 | c0003 | t0003 | g0056 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03927 | hp1 | a0003 | c0008 | t0003 | g0022 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03927 | hp2 | a0002 | c0002 | t0002 | g0202 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG03942 | hp2 | a0004 | c0004 | t0004 | g0186 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04115 | hp1 | a0003 | c0003 | t0003 | g0061 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04184 | hp1 | a0003 | c0003 | t0003 | g0007 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0004 | SAS | BEB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0017 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04204 | hp2 | a0003 | c0003 | t0003 | g0074 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04228 | hp1 | a0003 | c0003 | t0003 | g0007 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0201 | SAS | STU | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | YRI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | YRI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | CHB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0180 | AFR | YRI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0221 | AFR | YRI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18939 | hp1 | a0003 | c0003 | t0003 | g0071 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18939 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18940 | hp2 | a0003 | c0003 | t0003 | g0046 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18941 | hp2 | a0003 | c0003 | t0003 | g0070 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18943 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18947 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18948 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18948 | hp2 | a0003 | c0003 | t0003 | g0019 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18949 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18957 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18960 | hp1 | a0004 | c0004 | t0004 | g0039 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18960 | hp2 | a0003 | c0003 | t0003 | g0023 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18964 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18966 | hp2 | a0003 | c0003 | t0003 | g0020 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18968 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18969 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18971 | hp1 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18974 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18977 | hp2 | a0003 | c0003 | t0003 | g0060 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18979 | hp1 | a0003 | c0003 | t0003 | g0019 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18980 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18987 | hp2 | a0003 | c0003 | t0002 | g0052 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18988 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18989 | hp1 | a0003 | c0003 | t0003 | g0051 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18989 | hp2 | a0004 | c0004 | t0004 | g0189 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18990 | hp2 | a0004 | c0004 | t0004 | g0208 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18991 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18994 | hp1 | a0003 | c0003 | t0003 | g0048 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18994 | hp2 | a0003 | c0003 | t0003 | g0058 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18995 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18997 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18997 | hp2 | a0004 | c0004 | t0004 | g0206 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18998 | hp1 | a0003 | c0003 | t0003 | g0076 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18999 | hp1 | a0003 | c0003 | t0003 | g0054 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19004 | hp1 | a0003 | c0003 | t0003 | g0020 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19009 | hp1 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19010 | hp1 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19011 | hp2 | a0003 | c0003 | t0003 | g0001 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19012 | hp1 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | LWK | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0080 | AFR | LWK | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | LWK | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19043 | hp2 | a0007 | c0007 | t0007 | g0177 | AFR | LWK | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19054 | hp2 | a0003 | c0003 | t0003 | g0008 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19056 | hp2 | a0003 | c0003 | t0003 | g0023 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0213 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19067 | hp1 | a0003 | c0003 | t0003 | g0053 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19067 | hp2 | a0004 | c0004 | t0004 | g0005 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19072 | hp1 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19072 | hp2 | a0003 | c0003 | t0003 | g0072 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19076 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19081 | hp2 | a0003 | c0003 | t0003 | g0021 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19082 | hp1 | a0003 | c0003 | t0003 | g0059 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19083 | hp1 | a0003 | c0003 | t0003 | g0067 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19090 | hp1 | a0003 | c0003 | t0003 | g0062 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0002 | AFR | YRI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0179 | AFR | YRI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | ASW | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20129 | hp2 | a0004 | c0004 | t0004 | g0038 | AFR | ASW | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0196 | EUR | TSI | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0037 | SAS | GIH | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20905 | hp2 | a0004 | c0004 | t0004 | g0005 | SAS | GIH | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG01123 | hp2 | a0003 | c0003 | t0009 | g0232 | AMR | CLM | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02109 | hp1 | a0003 | c0003 | t0003 | g0231 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02109 | hp2 | a0002 | c0002 | t0002 | g0012 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0174 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02559 | hp1 | a0003 | c0003 | t0002 | g0223 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG02559 | hp2 | a0003 | c0003 | t0003 | g0045 | AFR | ACB | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG06807 | hp1 | a0003 | c0003 | t0003 | g0078 | AFR | USA | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| HG06807 | hp2 | a0003 | c0003 | t0002 | g0041 | AFR | USA | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20300 | hp1 | a0004 | c0004 | t0004 | g0038 | AFR | USA | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0040 | AFR | USA | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0130 | REF | REF | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| homoSapiens | grch38p0 | a0003 | c0003 | t0005 | g0142 | REF | REF | CENPQ_chr6_49458370_49498107 | CENPQ | chr6 | 49458370 | 49498107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49472092 | G | A | 4 | a0002 a0004 a0006 others(1): Show |
122 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
missense_variant | MODERATE | c.187G>A | p.Gly63Arg | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 4/9 | 289/1741 | 187/807 | 63/268 | chr6 | 49472092 | |||
| chr6:49488358 | A | G | 1 | a0007 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.484A>G | p.Ile162Val | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 7/9 | 586/1741 | 484/807 | 162/268 | chr6 | 49488358 | |||
| chr6:49492157 | C | T | 1 | a0005 | 5 | HG01256.hp2 HG01258.hp1 HG02280.hp1 others(2): Show |
missense_variant | MODERATE | c.689C>T | p.Ala230Val | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 791/1741 | 689/807 | 230/268 | chr6 | 49492157 | |||
| chr6:49492253 | A | G | 1 | a0006 | 3 | HG01952.hp2 HG01978.hp1 HG01993.hp1 |
missense_variant | MODERATE | c.785A>G | p.Tyr262Cys | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 887/1741 | 785/807 | 262/268 | chr6 | 49492253 | |||
| chr6:49492265 | A | G | 4 | a0001 a0004 a0005 others(1): Show |
163 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
missense_variant | MODERATE | c.797A>G | p.Asp266Gly | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 899/1741 | 797/807 | 266/268 | chr6 | 49492265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49488450 | A | G | 1 | a0003c0008 | 1 | HG03927.hp1 | synonymous_variant | LOW | c.576A>G | p.Glu192Glu | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 7/9 | 678/1741 | 576/807 | 192/268 | chr6 | 49488450 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49463407 | G | C | 1 | a0002c0002t0008 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/9 | 6770 | chr6 | 49463407 | ||||||
| chr6:49463415 | C | G | 2 | a0002c0002t0007 a0007c0007t0007 |
2 | HG02717.hp2 NA19043.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/9 | chr6 | 49463415 | |||||||
| chr6:49463416 | T | A | 2 | a0002c0002t0007 a0007c0007t0007 |
2 | HG02717.hp2 NA19043.hp2 |
5_prime_UTR_variant | MODIFIER | c.-56T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/9 | 6761 | chr6 | 49463416 | ||||||
| chr6:49463434 | G | A | 1 | a0003c0003t0006 | 2 | HG02451.hp2 HG03130.hp2 |
5_prime_UTR_variant | MODIFIER | c.-38G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/9 | 6743 | chr6 | 49463434 | ||||||
| chr6:49492439 | A | G | 7 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(4): Show |
163 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 164 | chr6 | 49492439 | ||||||
| chr6:49492555 | G | A | 17 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(14): Show |
353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
3_prime_UTR_variant | MODIFIER | c.*280G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 280 | chr6 | 49492555 | ||||||
| chr6:49492744 | A | G | 1 | a0003c0003t0006 | 2 | HG02451.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*469A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 469 | chr6 | 49492744 | ||||||
| chr6:49493029 | C | G | 1 | a0003c0003t0009 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*754C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 754 | chr6 | 49493029 | ||||||
| chr6:49493054 | G | C | 1 | a0001c0001t0010 | 1 | HG03491.hp2 | 3_prime_UTR_variant | MODIFIER | c.*779G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 779 | chr6 | 49493054 | ||||||
| chr6:49493056 | GT | G | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(7): Show |
250 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(247): Show |
3_prime_UTR_variant | MODIFIER | c.*798delT | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 798 | INFO_REALIGN_3_PRIME | chr6 | 49493056 | |||||
| chr6:49493060 | T | G | 2 | a0001c0001t0001 a0001c0001t0010 |
105 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*785T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 9/9 | 785 | chr6 | 49493060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:49463647 | G | T | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-19+194G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49463647 | |||||||
| chr6:49463671 | A | G | 1 | a0003c0003t0003g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+218A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49463671 | |||||||
| chr6:49463679 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-19+226C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49463679 | |||||||
| chr6:49463856 | A | G | 73 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(70): Show |
128 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.-19+403A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49463856 | |||||||
| chr6:49463900 | T | C | 2 | a0002c0002t0002g0174 a0002c0002t0002g0175 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-19+447T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49463900 | |||||||
| chr6:49464007 | G | T | 76 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(73): Show |
131 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.-19+554G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464007 | |||||||
| chr6:49464096 | T | A | 2 | a0001c0001t0004g0017 a0001c0001t0004g0042 |
3 | HG01257.hp1 HG02683.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-19+643T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464096 | |||||||
| chr6:49464131 | A | C | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+678A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464131 | |||||||
| chr6:49464164 | C | T | 1 | a0002c0002t0002g0229 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-19+711C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464164 | |||||||
| chr6:49464423 | T | C | 1 | a0001c0001t0001g0043 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19+970T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464423 | |||||||
| chr6:49464532 | G | A | 2 | a0002c0002t0002g0033 a0002c0002t0002g0176 |
3 | HG00741.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-19+1079G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464532 | |||||||
| chr6:49464603 | A | G | 1 | a0003c0003t0003g0170 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-19+1150A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464603 | |||||||
| chr6:49464786 | C | A | 2 | a0002c0002t0002g0033 a0002c0002t0002g0176 |
3 | HG00741.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-19+1333C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49464786 | |||||||
| chr6:49465114 | T | A | 2 | a0003c0003t0006g0171 a0003c0003t0006g0172 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-19+1661T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465114 | |||||||
| chr6:49465141 | T | G | 1 | a0007c0007t0007g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+1688T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465141 | |||||||
| chr6:49465181 | C | T | 3 | a0001c0001t0004g0167 a0001c0001t0004g0168 a0001c0001t0004g0169 |
3 | HG02145.hp1 HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-19+1728C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465181 | |||||||
| chr6:49465227 | T | A | 1 | a0003c0003t0003g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-19+1774T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465227 | |||||||
| chr6:49465292 | C | A | 2 | a0002c0002t0007g0178 a0007c0007t0007g0177 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-19+1839C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465292 | |||||||
| chr6:49465303 | C | T | 1 | a0007c0007t0007g0177 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+1850C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465303 | |||||||
| chr6:49465485 | T | C | 133 | a0001c0001t0001g0069 a0001c0001t0004g0013 a0001c0001t0004g0080 others(130): Show |
224 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.-19+2032T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465485 | |||||||
| chr6:49465621 | C | G | 8 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 others(5): Show |
12 | HG01361.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+2168C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465621 | |||||||
| chr6:49465660 | G | A | 50 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0052 others(47): Show |
84 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.-19+2207G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465660 | |||||||
| chr6:49465842 | G | A | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+2389G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49465842 | |||||||
| chr6:49466024 | G | A | 10 | a0001c0001t0004g0017 a0001c0001t0004g0042 a0001c0001t0004g0086 others(7): Show |
11 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+2571G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466024 | |||||||
| chr6:49466396 | A | G | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+2943A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466396 | |||||||
| chr6:49466432 | C | G | 1 | a0002c0002t0002g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-19+2979C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466432 | |||||||
| chr6:49466440 | A | C | 2 | a0003c0003t0006g0171 a0003c0003t0006g0172 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-19+2987A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466440 | |||||||
| chr6:49466569 | T | A | 3 | a0003c0003t0003g0018 a0003c0003t0003g0044 a0003c0003t0003g0045 |
4 | HG02559.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+3116T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466569 | |||||||
| chr6:49466644 | A | G | 2 | a0002c0002t0002g0174 a0002c0002t0002g0175 |
2 | HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-19+3191A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466644 | |||||||
| chr6:49466665 | A | T | 3 | a0003c0003t0002g0226 a0003c0003t0002g0227 a0003c0003t0002g0228 |
3 | HG01361.hp1 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-19+3212A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466665 | |||||||
| chr6:49466952 | T | G | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-18-3207T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49466952 | |||||||
| chr6:49467008 | A | G | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-18-3151A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467008 | |||||||
| chr6:49467043 | G | A | 1 | a0002c0002t0002g0034 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-18-3116G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467043 | |||||||
| chr6:49467096 | A | G | 1 | a0002c0002t0002g0176 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18-3063A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467096 | |||||||
| chr6:49467218 | G | T | 53 | a0001c0001t0001g0032 a0001c0001t0001g0069 a0001c0001t0001g0164 others(50): Show |
88 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.-18-2941G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467218 | |||||||
| chr6:49467298 | G | A | 1 | a0001c0001t0004g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18-2861G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467298 | |||||||
| chr6:49467300 | A | G | 1 | a0003c0003t0003g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-2859A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467300 | |||||||
| chr6:49467502 | T | C | 1 | a0001c0001t0004g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18-2657T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467502 | |||||||
| chr6:49467981 | G | A | 49 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0052 others(46): Show |
83 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.-18-2178G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49467981 | |||||||
| chr6:49468130 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18-2029C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468130 | |||||||
| chr6:49468234 | G | C | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-18-1925G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468234 | |||||||
| chr6:49468314 | C | T | 2 | a0002c0002t0002g0220 a0002c0002t0002g0221 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18-1845C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468314 | |||||||
| chr6:49468486 | T | C | 130 | a0001c0001t0001g0069 a0002c0002t0002g0002 a0002c0002t0002g0004 others(127): Show |
219 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.-18-1673T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468486 | |||||||
| chr6:49468673 | G | T | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-18-1486G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468673 | |||||||
| chr6:49468813 | C | A | 1 | a0003c0003t0003g0044 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18-1346C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468813 | |||||||
| chr6:49468874 | C | T | 2 | a0002c0002t0002g0220 a0002c0002t0002g0221 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18-1285C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468874 | |||||||
| chr6:49468950 | T | C | 2 | a0002c0002t0002g0220 a0002c0002t0002g0221 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18-1209T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49468950 | |||||||
| chr6:49469239 | C | G | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-18-920C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469239 | |||||||
| chr6:49469288 | T | C | 2 | a0002c0002t0002g0033 a0002c0002t0002g0176 |
3 | HG00741.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-18-871T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469288 | |||||||
| chr6:49469382 | C | T | 2 | a0002c0002t0002g0040 a0002c0002t0002g0219 |
3 | HG02896.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-18-777C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469382 | |||||||
| chr6:49469411 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18-748C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469411 | |||||||
| chr6:49469572 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18-587T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469572 | |||||||
| chr6:49469643 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-18-516G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469643 | |||||||
| chr6:49469687 | A | C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-472A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469687 | |||||||
| chr6:49469954 | TAA | T | 51 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(48): Show |
97 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.-18-204_-18-203del others(2): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | chr6 | 49469954 | |||||||
| chr6:49470037 | T | TA | 6 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0004g0024 others(3): Show |
7 | HG00642.hp2 HG01934.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-107dupA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 49470037 | ||||||
| chr6:49470037 | TA | T | 14 | a0001c0001t0001g0166 a0002c0002t0002g0214 a0002c0002t0002g0215 others(11): Show |
16 | HG00558.hp1 HG01243.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18-107delA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 49470037 | ||||||
| chr6:49470140 | A | AT | 29 | a0001c0001t0001g0069 a0001c0001t0001g0160 a0003c0003t0002g0001 others(26): Show |
50 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
splice_region_variant&intron_variant | LOW | c.-18-6dupT | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 49470140 | ||||||
| chr6:49470140 | AT | A | 50 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(47): Show |
96 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
splice_region_variant&intron_variant | LOW | c.-18-6delT | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr6 | 49470140 | ||||||
| chr6:49470320 | G | T | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.102+42G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470320 | |||||||
| chr6:49470376 | G | C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+98G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470376 | |||||||
| chr6:49470449 | C | CA | 7 | a0001c0001t0001g0032 a0001c0001t0001g0164 a0001c0001t0001g0165 others(4): Show |
8 | HG01123.hp2 HG02486.hp1 NA18522.hp1 others(5): Show |
intron_variant | MODIFIER | c.102+182dupA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 49470449 | ||||||
| chr6:49470474 | C | G | 1 | a0003c0003t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.102+196C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470474 | |||||||
| chr6:49470512 | G | A | 7 | a0001c0001t0004g0017 a0001c0001t0004g0042 a0001c0001t0004g0086 others(4): Show |
8 | HG01257.hp1 HG02486.hp2 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.102+234G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470512 | |||||||
| chr6:49470566 | G | T | 1 | a0001c0001t0004g0090 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.102+288G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470566 | |||||||
| chr6:49470618 | G | A | 1 | a0001c0001t0004g0042 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.102+340G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470618 | |||||||
| chr6:49470622 | C | CA | 33 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0093 others(30): Show |
36 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.103-328dupA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 49470622 | ||||||
| chr6:49470622 | CA | C | 63 | a0001c0001t0001g0159 a0001c0001t0004g0031 a0002c0002t0002g0002 others(60): Show |
109 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.103-328delA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 49470622 | ||||||
| chr6:49470622 | CAAAAAAA others(4): Show |
C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.103-338_103-328del others(11): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 49470622 | ||||||
| chr6:49470758 | TTC | T | 2 | a0002c0002t0002g0033 a0002c0002t0002g0176 |
3 | HG00741.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.103-214_103-213del others(2): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr6 | 49470758 | ||||||
| chr6:49470799 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.103-175C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470799 | |||||||
| chr6:49470855 | C | T | 1 | a0003c0003t0003g0019 | 2 | NA18948.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.103-119C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 2/8 | chr6 | 49470855 | |||||||
| chr6:49471177 | G | A | 1 | a0003c0003t0003g0047 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.157+149G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 3/8 | chr6 | 49471177 | |||||||
| chr6:49471193 | C | T | 5 | a0005c0005t0004g0155 a0005c0005t0004g0156 a0005c0005t0004g0157 others(2): Show |
5 | HG01256.hp2 HG01258.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.157+165C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 3/8 | chr6 | 49471193 | |||||||
| chr6:49471321 | A | C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.157+293A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 3/8 | chr6 | 49471321 | |||||||
| chr6:49471855 | T | C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.158-208T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 3/8 | chr6 | 49471855 | |||||||
| chr6:49472323 | C | T | 1 | a0002c0002t0002g0212 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.278+140C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 4/8 | chr6 | 49472323 | |||||||
| chr6:49472507 | G | A | 1 | a0003c0003t0003g0048 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.279-283G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 4/8 | chr6 | 49472507 | |||||||
| chr6:49472565 | A | T | 2 | a0003c0003t0006g0171 a0003c0003t0006g0172 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.279-225A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 4/8 | chr6 | 49472565 | |||||||
| chr6:49472573 | A | G | 8 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 others(5): Show |
12 | HG01361.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.279-217A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 4/8 | chr6 | 49472573 | |||||||
| chr6:49472650 | C | A | 65 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(62): Show |
116 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.279-140C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 4/8 | chr6 | 49472650 | |||||||
| chr6:49472690 | G | C | 2 | a0003c0003t0006g0171 a0003c0003t0006g0172 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.279-100G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 4/8 | chr6 | 49472690 | |||||||
| chr6:49472886 | T | A | 54 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0041 others(51): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.347+28T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49472886 | |||||||
| chr6:49472901 | A | T | 68 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(65): Show |
122 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.347+43A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49472901 | |||||||
| chr6:49473023 | CAT | C | 10 | a0001c0001t0004g0017 a0001c0001t0004g0042 a0001c0001t0004g0086 others(7): Show |
11 | HG01257.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.347+166_347+167del others(2): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473023 | |||||||
| chr6:49473242 | T | C | 4 | a0002c0002t0002g0035 a0002c0002t0002g0190 a0002c0002t0002g0191 others(1): Show |
5 | HG00544.hp2 NA18941.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+384T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473242 | |||||||
| chr6:49473393 | C | T | 1 | a0004c0004t0004g0038 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.347+535C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473393 | |||||||
| chr6:49473655 | A | C | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.347+797A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473655 | |||||||
| chr6:49473664 | A | G | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.347+806A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473664 | |||||||
| chr6:49473767 | G | C | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.347+909G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473767 | |||||||
| chr6:49473940 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.347+1082A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473940 | |||||||
| chr6:49473941 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.347+1083A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473941 | |||||||
| chr6:49473942 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.347+1084G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473942 | |||||||
| chr6:49473943 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.347+1085G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473943 | |||||||
| chr6:49473944 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.347+1086G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473944 | |||||||
| chr6:49473988 | C | T | 3 | a0002c0002t0005g0009 a0002c0002t0005g0182 a0002c0002t0005g0183 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.347+1130C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49473988 | |||||||
| chr6:49474132 | A | G | 1 | a0001c0001t0004g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347+1274A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474132 | |||||||
| chr6:49474134 | A | C | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.347+1276A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474134 | |||||||
| chr6:49474138 | T | G | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.347+1280T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474138 | |||||||
| chr6:49474203 | A | C | 1 | a0002c0002t0002g0211 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.347+1345A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474203 | |||||||
| chr6:49474366 | C | T | 1 | a0006c0006t0004g0210 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.347+1508C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474366 | |||||||
| chr6:49474383 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.347+1525A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474383 | |||||||
| chr6:49474385 | A | G | 1 | a0003c0003t0003g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.347+1527A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474385 | |||||||
| chr6:49474469 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.347+1611C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474469 | |||||||
| chr6:49474470 | G | A | 2 | a0003c0003t0006g0171 a0003c0003t0006g0172 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.347+1612G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474470 | |||||||
| chr6:49474483 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.347+1625C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474483 | |||||||
| chr6:49474491 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.347+1633C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474491 | |||||||
| chr6:49474502 | C | G | 1 | a0003c0003t0003g0054 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.347+1644C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474502 | |||||||
| chr6:49474578 | C | A | 1 | a0004c0004t0004g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.347+1720C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474578 | |||||||
| chr6:49474725 | G | A | 1 | a0003c0003t0006g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.347+1867G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474725 | |||||||
| chr6:49474812 | C | A | 73 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(70): Show |
128 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.347+1954C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474812 | |||||||
| chr6:49474981 | C | T | 51 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(48): Show |
97 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.347+2123C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49474981 | |||||||
| chr6:49475049 | C | A | 1 | a0002c0002t0005g0182 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.347+2191C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475049 | |||||||
| chr6:49475076 | A | G | 12 | a0004c0004t0004g0005 a0004c0004t0004g0038 a0004c0004t0004g0039 others(9): Show |
21 | HG00438.hp2 HG01934.hp2 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.347+2218A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475076 | |||||||
| chr6:49475131 | G | C | 4 | a0002c0002t0002g0033 a0002c0002t0002g0176 a0002c0002t0007g0178 others(1): Show |
5 | HG00741.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.347+2273G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475131 | |||||||
| chr6:49475192 | G | C | 1 | a0001c0001t0001g0096 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.347+2334G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475192 | |||||||
| chr6:49475212 | A | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG01074.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.347+2354A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475212 | |||||||
| chr6:49475227 | T | C | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.347+2369T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475227 | |||||||
| chr6:49475309 | C | A | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.347+2451C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475309 | |||||||
| chr6:49475314 | A | G | 76 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(73): Show |
131 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(128): Show |
intron_variant | MODIFIER | c.347+2456A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475314 | |||||||
| chr6:49475334 | C | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0117 |
2 | NA18978.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.347+2476C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475334 | |||||||
| chr6:49475375 | C | T | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.347+2517C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475375 | |||||||
| chr6:49475422 | C | T | 4 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0220 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.347+2564C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475422 | |||||||
| chr6:49475456 | C | T | 1 | a0002c0002t0002g0218 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.347+2598C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475456 | |||||||
| chr6:49475467 | A | G | 2 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
2 | HG00609.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.347+2609A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475467 | |||||||
| chr6:49475737 | A | G | 2 | a0001c0001t0004g0147 a0001c0001t0004g0148 |
2 | HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.347+2879A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475737 | |||||||
| chr6:49475759 | A | C | 3 | a0003c0003t0003g0173 a0003c0003t0006g0171 a0003c0003t0006g0172 |
3 | HG01243.hp1 HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.347+2901A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475759 | |||||||
| chr6:49475778 | T | C | 1 | a0002c0002t0002g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.347+2920T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475778 | |||||||
| chr6:49475872 | G | A | 2 | a0002c0002t0002g0192 a0002c0002t0002g0193 |
2 | NA19012.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.347+3014G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475872 | |||||||
| chr6:49475877 | G | C | 1 | a0003c0003t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.347+3019G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49475877 | |||||||
| chr6:49475887 | AAGG | A | 68 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(65): Show |
122 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.347+3032_347+3034d others(5): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 49475887 | ||||||
| chr6:49476064 | G | GA | 6 | a0002c0002t0002g0012 a0002c0002t0002g0033 a0002c0002t0002g0176 others(3): Show |
10 | HG00741.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.347+3216dupA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 49476064 | ||||||
| chr6:49476092 | C | G | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.347+3234C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476092 | |||||||
| chr6:49476127 | G | C | 1 | a0003c0003t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.347+3269G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476127 | |||||||
| chr6:49476199 | C | A | 1 | a0001c0001t0004g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.347+3341C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476199 | |||||||
| chr6:49476229 | G | T | 1 | a0003c0003t0003g0079 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.347+3371G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476229 | |||||||
| chr6:49476271 | A | G | 68 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(65): Show |
122 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.347+3413A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476271 | |||||||
| chr6:49476360 | G | T | 1 | a0004c0004t0004g0209 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.347+3502G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476360 | |||||||
| chr6:49476427 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.347+3569G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476427 | |||||||
| chr6:49476483 | T | C | 1 | a0002c0002t0002g0220 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.347+3625T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476483 | |||||||
| chr6:49476530 | G | A | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.347+3672G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476530 | |||||||
| chr6:49476581 | A | G | 1 | a0003c0003t0003g0075 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.347+3723A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476581 | |||||||
| chr6:49476838 | A | G | 1 | a0003c0003t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.347+3980A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476838 | |||||||
| chr6:49476918 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.348-4033C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476918 | |||||||
| chr6:49476949 | G | A | 1 | a0002c0002t0002g0194 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.348-4002G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49476949 | |||||||
| chr6:49477134 | G | A | 2 | a0002c0002t0002g0215 a0002c0002t0003g0195 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.348-3817G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477134 | |||||||
| chr6:49477144 | A | G | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.348-3807A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477144 | |||||||
| chr6:49477147 | A | G | 1 | a0003c0003t0003g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.348-3804A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477147 | |||||||
| chr6:49477183 | A | G | 5 | a0003c0003t0002g0041 a0003c0003t0002g0223 a0003c0003t0002g0226 others(2): Show |
6 | HG01361.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.348-3768A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477183 | |||||||
| chr6:49477238 | C | T | 27 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0003g0001 others(24): Show |
48 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.348-3713C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477238 | |||||||
| chr6:49477275 | A | G | 3 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0181 |
3 | HG02809.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.348-3676A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477275 | |||||||
| chr6:49477307 | A | G | 21 | a0003c0003t0002g0052 a0003c0003t0003g0007 a0003c0003t0003g0008 others(18): Show |
34 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.348-3644A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477307 | |||||||
| chr6:49477408 | C | T | 3 | a0002c0002t0005g0009 a0002c0002t0005g0182 a0002c0002t0005g0183 |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.348-3543C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477408 | |||||||
| chr6:49477425 | T | TG | 17 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0116 others(14): Show |
17 | HG01255.hp2 HG02683.hp1 HG02809.hp2 others(14): Show |
intron_variant | MODIFIER | c.348-3520dupG | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 49477425 | ||||||
| chr6:49477432 | A | G | 1 | a0004c0004t0004g0186 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.348-3519A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477432 | |||||||
| chr6:49477566 | TA | T | 7 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0004g0086 others(4): Show |
7 | HG00323.hp1 HG02486.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.348-3371delA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 49477566 | ||||||
| chr6:49477593 | T | C | 68 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0012 others(65): Show |
122 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.348-3358T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477593 | |||||||
| chr6:49477607 | G | A | 4 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0220 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-3344G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477607 | |||||||
| chr6:49477728 | G | T | 1 | a0003c0003t0003g0077 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.348-3223G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49477728 | |||||||
| chr6:49478062 | G | A | 1 | a0002c0002t0002g0036 | 2 | NA18975.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.348-2889G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49478062 | |||||||
| chr6:49478388 | T | C | 5 | a0003c0003t0002g0041 a0003c0003t0002g0223 a0003c0003t0002g0226 others(2): Show |
6 | HG01361.hp1 HG01884.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.348-2563T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49478388 | |||||||
| chr6:49478449 | G | C | 4 | a0003c0003t0003g0081 a0003c0003t0003g0082 a0003c0003t0003g0083 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-2502G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49478449 | |||||||
| chr6:49478520 | T | G | 27 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0003g0001 others(24): Show |
48 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.348-2431T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49478520 | |||||||
| chr6:49478683 | T | C | 1 | a0001c0001t0004g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.348-2268T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49478683 | |||||||
| chr6:49478743 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0112 a0001c0001t0001g0143 |
4 | HG02155.hp1 NA18950.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-2208A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49478743 | |||||||
| chr6:49478796 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(101): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.348-2155G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49478796 | |||||||
| chr6:49479194 | T | C | 2 | a0002c0002t0007g0178 a0007c0007t0007g0177 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.348-1757T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49479194 | |||||||
| chr6:49479237 | C | T | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.348-1714C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49479237 | |||||||
| chr6:49479238 | A | G | 166 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(163): Show |
238 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.348-1713A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49479238 | |||||||
| chr6:49479282 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(101): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.348-1669A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49479282 | |||||||
| chr6:49479429 | G | A | 2 | a0002c0002t0002g0033 a0002c0002t0002g0176 |
3 | HG00741.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.348-1522G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49479429 | |||||||
| chr6:49479676 | T | C | 1 | a0001c0001t0001g0118 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.348-1275T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49479676 | |||||||
| chr6:49479731 | A | AT | 2 | a0001c0001t0004g0029 a0001c0001t0011g0111 |
3 | HG02257.hp2 HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.348-1219dupT | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr6 | 49479731 | ||||||
| chr6:49479967 | G | A | 1 | a0002c0002t0002g0196 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.348-984G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49479967 | |||||||
| chr6:49480385 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.348-566C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49480385 | |||||||
| chr6:49480541 | G | T | 2 | a0003c0003t0002g0226 a0003c0003t0002g0228 |
2 | HG01361.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.348-410G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 5/8 | chr6 | 49480541 | |||||||
| chr6:49481098 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.477+18G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481098 | |||||||
| chr6:49481213 | T | C | 1 | a0001c0001t0004g0120 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.477+133T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481213 | |||||||
| chr6:49481248 | G | C | 2 | a0002c0002t0002g0220 a0002c0002t0002g0221 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.477+168G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481248 | |||||||
| chr6:49481311 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.477+231C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481311 | |||||||
| chr6:49481343 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.477+263C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481343 | |||||||
| chr6:49481419 | G | A | 4 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0220 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+339G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481419 | |||||||
| chr6:49481465 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG00408.hp1 HG02155.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+385G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481465 | |||||||
| chr6:49481467 | G | A | 1 | a0003c0003t0003g0049 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.477+387G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481467 | |||||||
| chr6:49481532 | A | C | 1 | a0005c0005t0004g0158 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.477+452A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481532 | |||||||
| chr6:49481580 | G | C | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.477+500G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481580 | |||||||
| chr6:49481667 | G | C | 1 | a0001c0001t0001g0145 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.477+587G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481667 | |||||||
| chr6:49481680 | G | T | 1 | a0003c0003t0003g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.477+600G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481680 | |||||||
| chr6:49481832 | TCAGC | T | 54 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0041 others(51): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.477+754_477+757del others(4): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49481832 | ||||||
| chr6:49481838 | C | G | 54 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0041 others(51): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.477+758C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481838 | |||||||
| chr6:49481839 | T | A | 54 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0041 others(51): Show |
89 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.477+759T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481839 | |||||||
| chr6:49481918 | G | C | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.477+838G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49481918 | |||||||
| chr6:49482004 | G | A | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.477+924G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482004 | |||||||
| chr6:49482007 | G | A | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.477+927G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482007 | |||||||
| chr6:49482056 | G | A | 1 | a0003c0003t0003g0062 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.477+976G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482056 | |||||||
| chr6:49482137 | A | G | 1 | a0003c0003t0006g0171 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.477+1057A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482137 | |||||||
| chr6:49482177 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.477+1097C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482177 | |||||||
| chr6:49482223 | G | C | 1 | a0001c0001t0004g0101 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.477+1143G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482223 | |||||||
| chr6:49482286 | C | G | 1 | a0002c0002t0002g0033 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.477+1206C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482286 | |||||||
| chr6:49482335 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02080.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.477+1255C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482335 | |||||||
| chr6:49482540 | C | T | 1 | a0004c0004t0004g0038 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.477+1460C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482540 | |||||||
| chr6:49482628 | A | G | 231 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(228): Show |
353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.477+1548A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482628 | |||||||
| chr6:49482655 | CTCGGCGA | C | 108 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(105): Show |
145 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.477+1577_477+1583d others(9): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49482655 | ||||||
| chr6:49482657 | C | T | 58 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0041 others(55): Show |
93 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.477+1577C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482657 | |||||||
| chr6:49482679 | C | T | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.477+1599C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482679 | |||||||
| chr6:49482686 | C | T | 1 | a0003c0003t0003g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.477+1606C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482686 | |||||||
| chr6:49482698 | C | T | 1 | a0002c0002t0002g0217 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.477+1618C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482698 | |||||||
| chr6:49482829 | G | A | 1 | a0003c0003t0003g0049 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.477+1749G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482829 | |||||||
| chr6:49482868 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.477+1788G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49482868 | |||||||
| chr6:49483141 | A | G | 1 | a0001c0001t0004g0090 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.477+2061A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483141 | |||||||
| chr6:49483164 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.477+2084G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483164 | |||||||
| chr6:49483198 | A | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(163): Show |
238 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.477+2118A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483198 | |||||||
| chr6:49483289 | T | G | 2 | a0002c0002t0002g0179 a0002c0002t0002g0181 |
2 | HG02809.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.477+2209T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483289 | |||||||
| chr6:49483416 | G | A | 21 | a0003c0003t0002g0052 a0003c0003t0003g0007 a0003c0003t0003g0008 others(18): Show |
34 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.477+2336G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483416 | |||||||
| chr6:49483465 | G | C | 1 | a0003c0003t0003g0063 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.477+2385G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483465 | |||||||
| chr6:49483474 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(100): Show |
140 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.477+2394G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483474 | |||||||
| chr6:49483517 | G | C | 2 | a0002c0002t0002g0197 a0003c0003t0009g0232 |
2 | HG01099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.477+2437G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483517 | |||||||
| chr6:49483527 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(101): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.477+2447C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483527 | |||||||
| chr6:49483537 | G | A | 1 | a0003c0003t0006g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.477+2457G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483537 | |||||||
| chr6:49483649 | G | A | 1 | a0003c0003t0003g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.477+2569G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483649 | |||||||
| chr6:49483679 | C | T | 1 | a0001c0001t0001g0137 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.477+2599C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483679 | |||||||
| chr6:49483680 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.477+2600A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483680 | |||||||
| chr6:49483728 | C | G | 1 | a0002c0002t0002g0191 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.477+2648C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483728 | |||||||
| chr6:49483785 | G | A | 161 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(158): Show |
232 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.477+2705G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483785 | |||||||
| chr6:49483901 | G | T | 1 | a0002c0002t0002g0205 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.477+2821G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483901 | |||||||
| chr6:49483967 | A | G | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.477+2887A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49483967 | |||||||
| chr6:49484026 | T | C | 1 | a0002c0002t0002g0198 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.477+2946T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484026 | |||||||
| chr6:49484100 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.477+3020C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484100 | |||||||
| chr6:49484453 | T | A | 231 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(228): Show |
353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.477+3373T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484453 | |||||||
| chr6:49484522 | C | CA | 4 | a0003c0003t0003g0081 a0003c0003t0003g0082 a0003c0003t0003g0083 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.477+3443dupA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49484522 | ||||||
| chr6:49484673 | A | C | 1 | a0001c0001t0001g0110 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.477+3593A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484673 | |||||||
| chr6:49484720 | C | T | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-3632C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484720 | |||||||
| chr6:49484729 | C | T | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-3623C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484729 | |||||||
| chr6:49484733 | A | G | 4 | a0003c0003t0003g0081 a0003c0003t0003g0082 a0003c0003t0003g0083 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-3619A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484733 | |||||||
| chr6:49484815 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG02004.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.478-3537T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484815 | |||||||
| chr6:49484893 | G | A | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-3459G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484893 | |||||||
| chr6:49484932 | C | T | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-3420C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49484932 | |||||||
| chr6:49485131 | T | C | 2 | a0003c0003t0003g0064 a0003c0003t0003g0065 |
2 | HG02080.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.478-3221T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485131 | |||||||
| chr6:49485286 | A | G | 1 | a0003c0003t0003g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.478-3066A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485286 | |||||||
| chr6:49485313 | G | A | 4 | a0003c0003t0003g0081 a0003c0003t0003g0082 a0003c0003t0003g0083 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-3039G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485313 | |||||||
| chr6:49485369 | C | A | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.478-2983C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485369 | |||||||
| chr6:49485395 | C | A | 1 | a0002c0002t0002g0191 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.478-2957C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485395 | |||||||
| chr6:49485557 | A | T | 8 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 others(5): Show |
12 | HG01361.hp1 HG01884.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.478-2795A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485557 | |||||||
| chr6:49485680 | G | T | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-2672G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485680 | |||||||
| chr6:49485882 | A | G | 1 | a0002c0002t0002g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.478-2470A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485882 | |||||||
| chr6:49485923 | T | A | 158 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(155): Show |
229 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.478-2429T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485923 | |||||||
| chr6:49485938 | G | A | 51 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(48): Show |
97 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.478-2414G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485938 | |||||||
| chr6:49485959 | A | T | 101 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(98): Show |
136 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.478-2393A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485959 | |||||||
| chr6:49485984 | C | A | 1 | a0002c0002t0002g0037 | 2 | HG01346.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.478-2368C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485984 | |||||||
| chr6:49485991 | A | G | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-2361A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49485991 | |||||||
| chr6:49486017 | G | A | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-2335G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486017 | |||||||
| chr6:49486033 | C | T | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-2319C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486033 | |||||||
| chr6:49486052 | A | G | 4 | a0003c0003t0003g0081 a0003c0003t0003g0082 a0003c0003t0003g0083 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-2300A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486052 | |||||||
| chr6:49486119 | T | G | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-2233T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486119 | |||||||
| chr6:49486154 | G | A | 1 | a0003c0003t0003g0066 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.478-2198G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486154 | |||||||
| chr6:49486155 | G | A | 3 | a0002c0002t0002g0187 a0002c0002t0002g0200 a0002c0002t0008g0199 |
3 | HG01891.hp2 HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.478-2197G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486155 | |||||||
| chr6:49486174 | A | G | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-2178A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486174 | |||||||
| chr6:49486267 | C | G | 1 | a0003c0003t0003g0077 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.478-2085C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486267 | |||||||
| chr6:49486410 | T | A | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-1942T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486410 | |||||||
| chr6:49486568 | C | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(158): Show |
232 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.478-1784C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486568 | |||||||
| chr6:49486690 | T | G | 4 | a0002c0002t0002g0033 a0002c0002t0002g0176 a0002c0002t0007g0178 others(1): Show |
5 | HG00741.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1662T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486690 | |||||||
| chr6:49486723 | T | C | 5 | a0003c0003t0003g0007 a0003c0003t0003g0050 a0003c0003t0003g0055 others(2): Show |
10 | HG00323.hp2 HG00642.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.478-1629T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486723 | |||||||
| chr6:49486736 | T | G | 1 | a0004c0004t0004g0206 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.478-1616T>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486736 | |||||||
| chr6:49486881 | T | A | 1 | a0003c0003t0003g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.478-1471T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486881 | |||||||
| chr6:49486954 | C | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(88): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.478-1398C>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49486954 | |||||||
| chr6:49487121 | C | G | 4 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0002c0002t0002g0220 others(1): Show |
4 | HG02486.hp1 HG02647.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1231C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487121 | |||||||
| chr6:49487125 | C | G | 51 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(48): Show |
97 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.478-1227C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487125 | |||||||
| chr6:49487168 | A | AAAAGATG others(87): Show |
2 | a0001c0001t0001g0114 a0001c0001t0004g0028 |
3 | HG01106.hp2 NA18988.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.478-1183_478-1182i others(96): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487168 | ||||||
| chr6:49487168 | A | AAGATGGT others(85): Show |
4 | a0002c0002t0002g0033 a0002c0002t0002g0176 a0002c0002t0007g0178 others(1): Show |
5 | HG00741.hp1 HG02717.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1183_478-1182i others(94): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487168 | ||||||
| chr6:49487170 | T | A | 228 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(225): Show |
352 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(349): Show |
intron_variant | MODIFIER | c.478-1182T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487170 | |||||||
| chr6:49487172 | A | AAAAAAAA others(131): Show |
1 | a0001c0001t0001g0124 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.478-1174_478-1173i others(140): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(126): Show |
1 | a0001c0001t0001g0138 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.478-1174_478-1173i others(135): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(124): Show |
1 | a0001c0001t0001g0139 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.478-1174_478-1173i others(133): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(123): Show |
1 | a0001c0001t0001g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.478-1174_478-1173i others(132): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(121): Show |
1 | a0001c0001t0001g0151 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.478-1174_478-1173i others(130): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(120): Show |
6 | a0001c0001t0001g0030 a0001c0001t0001g0112 a0001c0001t0001g0115 others(3): Show |
7 | HG00423.hp2 HG01167.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(129): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(119): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0004g0087 |
6 | HG00140.hp2 HG01081.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(128): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(118): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0091 a0001c0001t0001g0096 others(4): Show |
8 | HG01255.hp2 HG01496.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(127): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(117): Show |
5 | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG00639.hp2 HG01192.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(126): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(116): Show |
6 | a0001c0001t0001g0092 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
7 | HG01069.hp1 HG01243.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(125): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(115): Show |
12 | a0001c0001t0001g0011 a0001c0001t0001g0027 a0001c0001t0001g0043 others(9): Show |
16 | HG00544.hp1 HG01099.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(124): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(114): Show |
20 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0095 others(17): Show |
32 | HG00438.hp1 HG00609.hp2 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(123): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(113): Show |
14 | a0001c0001t0001g0006 a0001c0001t0001g0025 a0001c0001t0001g0105 others(11): Show |
22 | HG00408.hp1 HG00639.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(122): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(112): Show |
10 | a0001c0001t0001g0100 a0001c0001t0001g0135 a0001c0001t0001g0144 others(7): Show |
11 | HG00323.hp1 HG00642.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(121): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(111): Show |
3 | a0001c0001t0004g0148 a0005c0005t0004g0157 a0005c0005t0004g0158 |
3 | HG02280.hp1 HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.478-1174_478-1173i others(120): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(110): Show |
3 | a0001c0001t0004g0013 a0002c0002t0002g0175 a0002c0002t0002g0221 |
5 | HG02615.hp2 HG02809.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(119): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(109): Show |
2 | a0001c0001t0004g0084 a0003c0003t0003g0085 |
2 | HG01891.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.478-1174_478-1173i others(118): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(106): Show |
1 | a0001c0001t0004g0029 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.478-1174_478-1173i others(115): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(105): Show |
1 | a0001c0001t0011g0111 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.478-1174_478-1173i others(114): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(103): Show |
1 | a0001c0001t0001g0106 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.478-1174_478-1173i others(112): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(102): Show |
1 | a0001c0001t0001g0137 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.478-1174_478-1173i others(111): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(101): Show |
3 | a0001c0001t0004g0101 a0003c0003t0003g0082 a0003c0003t0003g0173 |
3 | HG01243.hp1 HG01884.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.478-1174_478-1173i others(110): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(100): Show |
3 | a0001c0001t0001g0026 a0001c0001t0001g0107 a0001c0001t0004g0136 |
4 | HG02056.hp2 HG03486.hp2 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(109): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(99): Show |
6 | a0002c0002t0002g0190 a0002c0002t0002g0201 a0002c0002t0002g0214 others(3): Show |
6 | HG01934.hp2 HG01952.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(108): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(98): Show |
1 | a0002c0002t0002g0202 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.478-1174_478-1173i others(107): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(98): Show |
23 | a0002c0002t0002g0004 a0002c0002t0002g0015 a0002c0002t0002g0035 others(20): Show |
45 | HG00438.hp2 HG00544.hp2 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(107): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(97): Show |
2 | a0003c0003t0003g0064 a0003c0003t0003g0067 |
2 | HG02080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.478-1174_478-1173i others(106): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(97): Show |
28 | a0001c0001t0001g0230 a0002c0002t0002g0002 a0002c0002t0002g0016 others(25): Show |
53 | HG00140.hp1 HG00558.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(106): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(96): Show |
24 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0003g0001 others(21): Show |
45 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(105): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAA others(96): Show |
20 | a0001c0001t0001g0108 a0003c0003t0002g0226 a0003c0003t0002g0227 others(17): Show |
32 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(105): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAG others(95): Show |
1 | a0003c0003t0003g0072 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.478-1174_478-1173i others(104): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAAG others(95): Show |
6 | a0002c0002t0002g0179 a0002c0002t0002g0180 a0002c0002t0002g0181 others(3): Show |
7 | HG02145.hp2 HG02809.hp2 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-1174_478-1173i others(104): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAAGA others(94): Show |
4 | a0001c0001t0001g0109 a0002c0002t0002g0012 a0003c0003t0003g0078 others(1): Show |
7 | HG02109.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-1175_478-1174i others(103): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AAAAAGAT others(93): Show |
4 | a0001c0001t0004g0017 a0001c0001t0004g0042 a0002c0002t0002g0225 others(1): Show |
5 | HG01257.hp1 HG02451.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.478-1176_478-1175i others(102): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487172 | ||||||
| chr6:49487172 | A | AT | 6 | a0001c0001t0001g0114 a0001c0001t0004g0028 a0002c0002t0002g0033 others(3): Show |
8 | HG00741.hp1 HG01106.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1180_478-1179i others(3): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487172 | |||||||
| chr6:49487174 | A | T | 1 | a0002c0002t0005g0183 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.478-1178A>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487174 | |||||||
| chr6:49487224 | A | C | 1 | a0002c0002t0007g0178 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.478-1128A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487224 | |||||||
| chr6:49487285 | G | A | 58 | a0001c0001t0001g0069 a0003c0003t0002g0001 a0003c0003t0002g0041 others(55): Show |
93 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.478-1067G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487285 | |||||||
| chr6:49487454 | T | TAAAAAAA others(5): Show |
1 | a0003c0003t0003g0051 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.478-895_478-884dup others(12): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487454 | ||||||
| chr6:49487454 | T | TAAAAAAA others(6): Show |
5 | a0003c0003t0002g0052 a0003c0003t0003g0019 a0003c0003t0003g0020 others(2): Show |
7 | HG02451.hp2 NA18948.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-896_478-884dup others(13): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487454 | ||||||
| chr6:49487454 | T | TAAAAAAA others(7): Show |
24 | a0003c0003t0002g0041 a0003c0003t0002g0223 a0003c0003t0002g0226 others(21): Show |
37 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.478-897_478-884dup others(14): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487454 | ||||||
| chr6:49487454 | T | TAAAAAAA others(8): Show |
34 | a0001c0001t0001g0069 a0001c0001t0001g0114 a0001c0001t0001g0116 others(31): Show |
54 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.478-884_478-883ins others(15): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487454 | ||||||
| chr6:49487454 | T | TAAAAAAA others(9): Show |
86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(83): Show |
123 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.478-884_478-883ins others(16): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487454 | ||||||
| chr6:49487454 | T | TAAAAAAA others(10): Show |
13 | a0001c0001t0001g0103 a0001c0001t0001g0107 a0001c0001t0001g0115 others(10): Show |
13 | HG00423.hp2 HG01123.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-884_478-883ins others(17): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr6 | 49487454 | ||||||
| chr6:49487748 | T | C | 1 | a0003c0003t0003g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.478-604T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487748 | |||||||
| chr6:49487837 | G | A | 1 | a0002c0002t0002g0212 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.478-515G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487837 | |||||||
| chr6:49487885 | G | C | 2 | a0002c0002t0002g0033 a0002c0002t0002g0176 |
3 | HG00741.hp1 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.478-467G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49487885 | |||||||
| chr6:49488295 | G | A | 1 | a0003c0003t0003g0085 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.478-57G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 6/8 | chr6 | 49488295 | |||||||
| chr6:49488810 | G | A | 1 | a0001c0001t0004g0042 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.675+126G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49488810 | |||||||
| chr6:49488832 | G | A | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(114): Show |
163 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.675+148G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49488832 | |||||||
| chr6:49488840 | GTAGTC | G | 4 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0088 others(1): Show |
4 | HG02486.hp2 HG02970.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.675+161_675+165del others(5): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 49488840 | ||||||
| chr6:49488871 | CT | C | 11 | a0001c0001t0004g0084 a0001c0001t0004g0148 a0002c0002t0002g0192 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.675+201delT | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 49488871 | ||||||
| chr6:49489110 | G | A | 3 | a0003c0003t0002g0226 a0003c0003t0002g0227 a0003c0003t0002g0228 |
3 | HG01361.hp1 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.675+426G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489110 | |||||||
| chr6:49489284 | G | A | 1 | a0003c0003t0003g0050 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.675+600G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489284 | |||||||
| chr6:49489289 | G | C | 1 | a0002c0002t0002g0203 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.675+605G>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489289 | |||||||
| chr6:49489351 | A | G | 2 | a0001c0001t0004g0029 a0001c0001t0011g0111 |
3 | HG02257.hp2 HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.675+667A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489351 | |||||||
| chr6:49489487 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.675+803A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489487 | |||||||
| chr6:49489581 | T | A | 3 | a0002c0002t0002g0197 a0002c0002t0002g0204 a0002c0002t0002g0229 |
3 | HG01099.hp2 HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.675+897T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489581 | |||||||
| chr6:49489645 | GGCA | G | 3 | a0003c0003t0002g0226 a0003c0003t0002g0227 a0003c0003t0002g0228 |
3 | HG01361.hp1 HG01884.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.675+964_675+966del others(3): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 49489645 | ||||||
| chr6:49489893 | C | T | 1 | a0002c0002t0002g0200 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.675+1209C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489893 | |||||||
| chr6:49489952 | A | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(170): Show |
253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.675+1268A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489952 | |||||||
| chr6:49489964 | G | T | 26 | a0003c0003t0002g0001 a0003c0003t0003g0001 a0003c0003t0003g0022 others(23): Show |
47 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.675+1280G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49489964 | |||||||
| chr6:49490099 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.675+1415T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490099 | |||||||
| chr6:49490122 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(114): Show |
163 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.675+1438A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490122 | |||||||
| chr6:49490150 | A | G | 2 | a0002c0002t0002g0220 a0002c0002t0002g0221 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.675+1466A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490150 | |||||||
| chr6:49490205 | C | G | 39 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(36): Show |
76 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.675+1521C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490205 | |||||||
| chr6:49490217 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.675+1533G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490217 | |||||||
| chr6:49490384 | A | G | 39 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0015 others(36): Show |
76 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.675+1700A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490384 | |||||||
| chr6:49490385 | T | C | 1 | a0002c0002t0005g0182 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.675+1701T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490385 | |||||||
| chr6:49490544 | T | C | 2 | a0003c0003t0006g0171 a0003c0003t0006g0172 |
2 | HG02451.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.676-1600T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490544 | |||||||
| chr6:49490720 | A | C | 1 | a0001c0001t0001g0128 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.676-1424A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490720 | |||||||
| chr6:49490750 | A | G | 1 | a0003c0003t0003g0081 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.676-1394A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490750 | |||||||
| chr6:49490829 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.676-1315G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490829 | |||||||
| chr6:49490850 | C | CA | 3 | a0002c0002t0002g0012 a0002c0002t0002g0224 a0002c0002t0002g0225 |
6 | HG02109.hp2 HG02145.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-1292dupA | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 49490850 | ||||||
| chr6:49490945 | G | A | 1 | a0003c0003t0009g0232 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.676-1199G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49490945 | |||||||
| chr6:49491137 | A | G | 1 | a0003c0003t0003g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.676-1007A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491137 | |||||||
| chr6:49491214 | CTGTT | C | 3 | a0002c0002t0002g0174 a0002c0002t0002g0175 a0003c0003t0002g0228 |
3 | HG02486.hp1 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.676-927_676-924del others(4): Show |
CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr6 | 49491214 | ||||||
| chr6:49491269 | C | G | 3 | a0001c0001t0001g0127 a0001c0001t0001g0145 a0001c0001t0001g0153 |
3 | HG00639.hp2 HG01496.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.676-875C>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491269 | |||||||
| chr6:49491315 | T | C | 231 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(228): Show |
353 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(350): Show |
intron_variant | MODIFIER | c.676-829T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491315 | |||||||
| chr6:49491368 | T | A | 1 | a0003c0003t0003g0231 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.676-776T>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491368 | |||||||
| chr6:49491436 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.676-708A>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491436 | |||||||
| chr6:49491466 | G | T | 3 | a0002c0002t0002g0197 a0002c0002t0002g0204 a0002c0002t0002g0229 |
3 | HG01099.hp2 HG01192.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.676-678G>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491466 | |||||||
| chr6:49491537 | T | C | 2 | a0002c0002t0002g0016 a0002c0002t0002g0213 |
4 | NA18992.hp2 NA19058.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-607T>C | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491537 | |||||||
| chr6:49491569 | A | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0010 others(170): Show |
253 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.676-575A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491569 | |||||||
| chr6:49491631 | A | G | 1 | a0001c0001t0004g0080 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.676-513A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491631 | |||||||
| chr6:49491690 | C | T | 3 | a0003c0003t0003g0018 a0003c0003t0003g0044 a0003c0003t0003g0045 |
4 | HG02559.hp2 HG03139.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-454C>T | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49491690 | |||||||
| chr6:49492020 | G | A | 1 | a0002c0002t0002g0222 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.676-124G>A | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49492020 | |||||||
| chr6:49492078 | A | G | 27 | a0003c0003t0002g0001 a0003c0003t0003g0001 a0003c0003t0003g0022 others(24): Show |
48 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.676-66A>G | CENPQ | ENSG00000031691.7 | transcript | ENST00000335783.4 | protein_coding | 8/8 | chr6 | 49492078 |